Professor Nick Martin
Honorary Professor
School of Psychology
Book Chapters
Odintsova, Veronika, Willemsen, Gonneke, Dolan, Conor V., Hottenga, Jouke-Jan, Martin, Nicholas G., Slagboom, P. Eline, Ordoñana, Juan R. and Boomsma, Dorret I. (2022). Establishing a resource for genetic, epidemiological, and biomarker studies: the important role of twin registers. Twin research for everyone: from biology to health, epigenetics, and psychology. (pp. 163-188) edited by Adam D. Tarnoki, David L. Tarnoki, Jennifer R. Harris and Nancy L. Segal. Amsterdam, Netherlands: Elsevier. doi: 10.1016/B978-0-12-821514-2.00011-8
Shen, Kaikai, Dore, Vincent, Fripp, Jurgen, Rose, Stephen, McMahon, Katie L., de Zubicaray, Greig I., Martin, Nicholas G., Thompson, Paul M., Wright, Margaret J. and Salvado, Olivier (2018). Genetic correlation between cortical gray matter thickness and white matter connections. Imaging genetics. (pp. 85-100) edited by Adrian Dalca, Kayhan Batmanghelich, Mert Sabuncu and Li Shen. London, United Kingdom: Academic Press. doi: 10.1016/B978-0-12-813968-4.00005-5
Gillespie, Nathan A. and Martin, Nicholas G. (2014). Direction of causation models. Wiley StatsRef: Statistics Reference Online. (pp. *-*) Chichester, United Kingdom: John Wiley & Sons. doi: 10.1002/9781118445112.stat06685
Gillespie, Nathan A. and Martin, Nicholas G. (2014). Multivariate genetic analysis. Wiley StatsRef: statistics reference online. Chichester, United Kingdom: John Wiley & Sons. doi: 10.1002/9781118445112.stat06468
Zhan, L., Nie, Z., Ye, J., Wang, Y., Jin, Y., Jahanshad, N., Prasad, G., de Zubicaray, G. I., McMahan, K. L., Martin, N. G., Wright, M. J. and Thompson, P. M. (2014). Multiple stages classification of Alzheimer’s disease based on structural brain networks using generalized low rank approximations (GLRAM). Computational diffusion MRI: MICCAI Workshop, Boston, MA, USA, September 2014. (pp. 35-44) edited by Lauren O'Donnell, Gemma Nedjati-Gilani, Yogesh Rathi, Marco Reisert and Torben Schneider. Cham, Switzerland: Springer International Publishing. doi: 10.1007/978-3-319-11182-7_4
Eaves, Lindon J., Hatemi, Peter K., Heath, Andrew C. and Martin, Nicholas G. (2011). Modeling the cultural and biological inheritance of social and political behavior in twins and nuclear families. Man is by nature a political animal: evolution, biology, and politics. (pp. 101-184) edited by Peter K. Hatemi and Rose McDermott. Chicago, IL, United States: University of Chicago Press. doi: 10.7208/chicago/9780226319117.003.0005
Khytam Dawood, J. Michael Bailey and Nicholas G. Martin (2009). Genetic and Environmental Influences on Sexual Orientation. Handbook of Behavior Genetics. (pp. 269-279) edited by Kim, Yong-Kyu. United Sates: Springer New York. doi: 10.1007/978-0-387-76727-7_19
Journal Articles
Walker, Alicia, Karlsson, Robert, Szatkiewicz, Jin P., Thornton, Laura M., Yilmaz, Zeynep, Leppä, Virpi M., Savva, Androula, Lin, Tian, Sidorenko, Julia, McRae, Allan, Kirov, George, Davies, Helena L., Fundín, Bengt T., Chawner, Samuel J. R. A., Song, Jie, Borg, Stina, Wen, Jia, Watson, Hunna J., Munn-Chernoff, Melissa A., Baker, Jessica H., Gordon, Scott, Berrettini, Wade H., Brandt, Harry, Crawford, Steven, Halmi, Katherine A., Kaplan, Allan S., Kaye, Walter H., Mitchell, James, Strober, Michael ... Wray, Naomi R. (2024). Genome-wide copy number variation association study in anorexia nervosa. Molecular Psychiatry, 1-8. doi: 10.1038/s41380-024-02811-2
Curtis, Madeleine, Colodro-Conde, Lucia, Medland, Sarah E., Gordon, Scott, Martin, Nicholas G., Wade, Tracey D. and Cohen-Woods, Sarah (2024). Anorexia nervosa polygenic risk, beyond diagnoses: relationship with adolescent disordered eating and behaviors in an Australian female twin population. Psychological Medicine, 54 (13), 1-9. doi: 10.1017/s0033291724001727
García-Marín, Luis M., Campos, Adrian I., Diaz-Torres, Santiago, Rabinowitz, Jill A., Ceja, Zuriel, Mitchell, Brittany L., Grasby, Katrina L., Thorp, Jackson G., Agartz, Ingrid, Alhusaini, Saud, Ames, David, Amouyel, Philippe, Andreassen, Ole A., Arfanakis, Konstantinos, Arias-Vasquez, Alejandro, Armstrong, Nicola J., Athanasiu, Lavinia, Bastin, Mark E., Beiser, Alexa S., Bennett, David A., Bis, Joshua C., Boks, Marco P. M., Boomsma, Dorret I., Brodaty, Henry, Brouwer, Rachel M., Buitelaar, Jan K., Burkhardt, Ralph, Cahn, Wiepke, Calhoun, Vince D. ... Rentería, Miguel E. (2024). Genomic analysis of intracranial and subcortical brain volumes yields polygenic scores accounting for variation across ancestries. Nature Genetics, 56 (11), 1-12. doi: 10.1038/s41588-024-01951-z
Sidorenko, Julia, Couvy-Duchesne, Baptiste, Kemper, Kathryn E., Moen, Gunn-Helen, Bhatta, Laxmi, Åsvold, Bjørn Olav, Mägi, Reedik, Estonian Biobank Research Team, Ani, Alireza, Wang, Rujia, Nolte, Ilja M., Lifelines Cohort Study, Nolte, Ilja M., Gordon, Scott, Hayward, Caroline, Campbell, Archie, Benjamin, Daniel J., Cesarini, David, Evans, David M., Goddard, Michael E., Haley, Chris S., Porteous, David, Medland, Sarah E., Martin, Nicholas G., Snieder, Harold, Metspalu, Andres, Hveem, Kristian, Brumpton, Ben, Visscher, Peter M. and Yengo, Loic (2024). Genetic architecture reconciles linkage and association studies of complex traits. Nature Genetics, 56 (11), 2352-2360. doi: 10.1038/s41588-024-01940-2
Adams, Mark J., Thorp, Jackson G., Jermy, Bradley S., Kwong, Alex S. F., Kõiv, Kadri, Grotzinger, Andrew D., Nivard, Michel G., Marshall, Sally, Milaneschi, Yuri, Baune, Bernhard T., Müller-Myhsok, Bertram, Penninx, Brenda W. J. H., Boomsma, Dorret I., Levinson, Douglas F., Breen, Gerome, Pistis, Giorgio, Grabe, Hans J., Tiemeier, Henning, Berger, Klaus, Rietschel, Marcella, Magnusson, Patrik K., Uher, Rudolf, Hamilton, Steven P., Lucae, Susanne, Lehto, Kelli, Li, Qingqin S., Byrne, Enda M., Hickie, Ian B., Martin, Nicholas G. ... Derks, Eske M. (2024). Genome-wide meta-analysis of ascertainment and symptom structures of major depression in case-enriched and community cohorts. Psychological Medicine, 54 (12), 1-10. doi: 10.1017/s0033291724001880
Mosley, Philip E., van der Meer, Johan N., Hamilton, Lachlan H. W., Fripp, Jurgen, Parker, Stephen, Jeganathan, Jayson, Breakspear, Michael, Parker, Richard, Holland, Rebecca, Mitchell, Brittany L., Byrne, Enda, Hickie, Ian B., Medland, Sarah E., Martin, Nicholas G. and Cocchi, Luca (2024). Markers of positive affect and brain state synchrony discriminate melancholic from non-melancholic depression using naturalistic stimuli. Molecular Psychiatry. doi: 10.1038/s41380-024-02699-y
Ingold, Nathan, Seviiri, Mathias, Ong, Jue Sheng, Neale, Rachel E., Pandeya, Nirmala, Whiteman, David C., Olsen, Catherine M., Martin, Nicholas G., Duffy, David L., Khosrotehrani, Kiarash, Hayward, Nicholas, Montgomery, Grant W., MacGregor, Stuart and Law, Matthew H. (2024). Exploring the germline genetics of in situ and invasive cutaneous melanoma: a genome-wide association study meta-analysis. JAMA Dermatology, 160 (9), 964-971. doi: 10.1001/jamadermatol.2024.2601
Ciulkinyte, Austeja, Mountford, Hayley S., Fontanillas, Pierre, Aslibekyan, Stella, Auton, Adam, Babalola, Elizabeth, Bell, Robert K., Bielenberg, Jessica, Bowes, Jonathan, Bryc, Katarzyna, Chaudhary, Ninad S., Coker, Daniella, Das, Sayantan, DelloRusso, Emily, Elson, Sarah L., Eriksson, Nicholas, Filshtein, Teresa, Freyman, Will, Fuller, Zach, German, Chris, Granka, Julie M., Heilbron, Karl, Hernandez, Alejandro, Hicks, Barry, Hinds, David A., Jewett, Ethan M., Jiang, Yunxuan, Kukar, Katelyn, Kwong, Alan ... 23andMe Research Team (2024). Genetic neurodevelopmental clustering and dyslexia. Molecular Psychiatry. doi: 10.1038/s41380-024-02649-8
Kentistou, Katherine A., Kaisinger, Lena R., Stankovic, Stasa, Vaudel, Marc, Mendes de Oliveira, Edson, Messina, Andrea, Walters, Robin G., Liu, Xiaoxi, Busch, Alexander S., Helgason, Hannes, Thompson, Deborah J., Santoni, Federico, Petricek, Konstantin M., Zouaghi, Yassine, Huang-Doran, Isabel, Gudbjartsson, Daniel F., Bratland, Eirik, Lin, Kuang, Gardner, Eugene J., Zhao, Yajie, Jia, Raina Y., Terao, Chikashi, Riggan, Marjorie J., Bolla, Manjeet K., Yazdanpanah, Mojgan, Yazdanpanah, Nahid, Bradfield, Jonathan P., Broer, Linda, Campbell, Archie ... The China Kadoorie Biobank Collaborative Group (2024). Publisher Correction: Understanding the genetic complexity of puberty timing across the allele frequency spectrum. Nature Genetics, 56 (8), 1-2. doi: 10.1038/s41588-024-01857-w
Kentistou, Katherine A., Kaisinger, Lena R., Stankovic, Stasa, Vaudel, Marc, Mendes de Oliveira, Edson, Messina, Andrea, Walters, Robin G., Liu, Xiaoxi, Busch, Alexander S., Helgason, Hannes, Thompson, Deborah J., Santoni, Federico, Petricek, Konstantin M., Zouaghi, Yassine, Huang-Doran, Isabel, Gudbjartsson, Daniel F., Bratland, Eirik, Lin, Kuang, Gardner, Eugene J., Zhao, Yajie, Jia, Raina Y., Terao, Chikashi, Riggan, Marjorie J., Bolla, Manjeet K., Yazdanpanah, Mojgan, Yazdanpanah, Nahid, Bradfield, Jonathan P., Broer, Linda, Campbell, Archie ... The China Kadoorie Biobank Collaborative Group (2024). Understanding the genetic complexity of puberty timing across the allele frequency spectrum. Nature Genetics, 56 (7), 1-15. doi: 10.1038/s41588-024-01798-4
Dash, Genevieve F., Gizer, Ian R., Martin, Nicholas G. and Slutske, Wendy S. (2024). Differential etiologic associations of heroin use and prescription opioid misuse with psychopathology. Journal of Psychopathology and Clinical Science, 133 (5), 378-391. doi: 10.1037/abn0000921
Nievergelt, Caroline M., Maihofer, Adam X., Atkinson, Elizabeth G., Chen, Chia-Yen, Choi, Karmel W., Coleman, Jonathan R. I., Daskalakis, Nikolaos P., Duncan, Laramie E., Polimanti, Renato, Aaronson, Cindy, Amstadter, Ananda B., Andersen, Soren B., Andreassen, Ole A., Arbisi, Paul A., Ashley-Koch, Allison E., Austin, S. Bryn, Avdibegoviç, Esmina, Babić, Dragan, Bacanu, Silviu-Alin, Baker, Dewleen G., Batzler, Anthony, Beckham, Jean C., Belangero, Sintia, Benjet, Corina, Bergner, Carisa, Bierer, Linda M., Biernacka, Joanna M., Bierut, Laura J., Bisson, Jonathan I. ... HUNT All-In Psychiatry (2024). Genome-wide association analyses identify 95 risk loci and provide insights into the neurobiology of post-traumatic stress disorder. Nature Genetics, 56 (5), 792-808. doi: 10.1038/s41588-024-01707-9
Crouse, Jacob J., Park, Shin Ho, Byrne, Enda M., Mitchell, Brittany L., Scott, Jan, Medland, Sarah E., Lin, Tian, Wray, Naomi R., Martin, Nicholas G. and Hickie, Ian B. (2024). Patterns of stressful life events and polygenic scores for five mental disorders and neuroticism among adults with depression. Molecular Psychiatry, 29 (9), 1-9. doi: 10.1038/s41380-024-02492-x
Hatton, Alesha A., Cheng, Fei-Fei, Lin, Tian, Shen, Ren-Juan, Chen, Jie, Zheng, Zhili, Qu, Jia, Lyu, Fan, Harris, Sarah E., Cox, Simon R., Jin, Zi-Bing, Martin, Nicholas G., Fan, Dongsheng, Montgomery, Grant W., Yang, Jian, Wray, Naomi R., Marioni, Riccardo E., Visscher, Peter M. and McRae, Allan F. (2024). Genetic control of DNA methylation is largely shared across European and East Asian populations. Nature Communications, 15 (1) 2713, 1-12. doi: 10.1038/s41467-024-47005-0
Kiewa, Jacqueline, Meltzer-Brody, Samantha, Milgrom, Jeannette, Guintivano, Jerry, Hickie, Ian B, Whiteman, David C, Olsen, Catherine M, Medland, Sarah E, Martin, Nicholas G, Wray, Naomi R and Byrne, Enda M (2024). Comprehensive sex-stratified genetic analysis of 28 blood biomarkers and depression reveals a significant association between depression and low levels of total protein in females. Complex Psychiatry, 10 (1-4), 19-34. doi: 10.1159/000538058
Hur, Yoon-Mi, Martin, Nick, Oginni, Olakunle, Boomsma, Dorret, Hubers, Nikki and Mbarek, Hamdi (2024). Family History of Twinning and Fertility Traits in Nigerian Mothers of Dizygotic Twins. Twin Research and Human Genetics, 27 (1), 1-6. doi: 10.1017/thg.2024.2
Sterenborg, Rosalie B. T. M., Steinbrenner, Inga, Li, Yong, Bujnis, Melissa N., Naito, Tatsuhiko, Marouli, Eirini, Galesloot, Tessel E., Babajide, Oladapo, Andreasen, Laura, Astrup, Arne, Åsvold, Bjørn Olav, Bandinelli, Stefania, Beekman, Marian, Beilby, John P., Bork-Jensen, Jette, Boutin, Thibaud, Brody, Jennifer A., Brown, Suzanne J., Brumpton, Ben, Campbell, Purdey J., Cappola, Anne R., Ceresini, Graziano, Chaker, Layal, Chasman, Daniel I., Concas, Maria Pina, Coutinho de Almeida, Rodrigo, Cross, Simone M., Cucca, Francesco, Deary, Ian J. ... Regeneron Genetics Center (2024). Multi-trait analysis characterizes the genetics of thyroid function and identifies causal associations with clinical implications. Nature Communications, 15 (1) 888, 1-18. doi: 10.1038/s41467-024-44701-9
Scholz, Markus, Horn, Katrin, Pott, Janne, Wuttke, Matthias, Kühnapfel, Andreas, Nasr, M. Kamal, Kirsten, Holger, Li, Yong, Hoppmann, Anselm, Gorski, Mathias, Ghasemi, Sahar, Li, Man, Tin, Adrienne, Chai, Jin-Fang, Cocca, Massimiliano, Wang, Judy, Nutile, Teresa, Akiyama, Masato, Åsvold, Bjørn Olav, Bansal, Nisha, Biggs, Mary L., Boutin, Thibaud, Brenner, Hermann, Brumpton, Ben, Burkhardt, Ralph, Cai, Jianwen, Campbell, Archie, Campbell, Harry, Chalmers, John ... Pattaro, Cristian (2024). X-chromosome and kidney function: evidence from a multi-trait genetic analysis of 908,697 individuals reveals sex-specific and sex-differential findings in genes regulated by androgen response elements. Nature Communications, 15 (1) 586, 1-17. doi: 10.1038/s41467-024-44709-1
Meng, Xiangrui, Navoly, Georgina, Giannakopoulou, Olga, Levey, Daniel F., Koller, Dora, Pathak, Gita A., Koen, Nastassja, Lin, Kuang, Adams, Mark J., Rentería, Miguel E., Feng, Yanzhe, Gaziano, J. Michael, Stein, Dan J., Zar, Heather J., Campbell, Megan L., van Heel, David A., Trivedi, Bhavi, Finer, Sarah, McQuillin, Andrew, Bass, Nick, Chundru, V. Kartik, Martin, Hilary C., Huang, Qin Qin, Valkovskaya, Maria, Chu, Chia-Yi, Kanjira, Susan, Kuo, Po-Hsiu, Chen, Hsi-Chung, Tsai, Shih-Jen ... BioBank Japan Project (2024). Multi-ancestry genome-wide association study of major depression aids locus discovery, fine mapping, gene prioritization and causal inference. Nature Genetics, 56 (2), 222-233. doi: 10.1038/s41588-023-01596-4
Crouse, Jacob J., Park, Shin Ho, Byrne, Enda M., Mitchell, Brittany L., Chan, Karina, Scott, Jan, Medland, Sarah E., Martin, Nicholas G., Wray, Naomi R. and Hickie, Ian B. (2024). Evening chronotypes with depression report poorer outcomes of SSRIs: A survey-based study of self-ratings. Biological Psychiatry, 96 (1), 4-14. doi: 10.1016/j.biopsych.2023.12.023
Davis, Christal N., Gizer, Ian R., Agrawal, Arpana, Statham, Dixie J., Heath, Andrew C., Martin, Nicholas G. and Slutske, Wendy S. (2024). Genetic and shared environmental factors explain the association between adolescent polysubstance use and high school noncompletion. Psychology of Addictive Behaviors, 38 (1), 114-123. doi: 10.1037/adb0000915
Mbarek, Hamdi, Gordon, Scott D., Duffy, David L., Hubers, Nikki, Mortlock, Sally, Beck, Jeffrey J., Hottenga, Jouke-Jan, Pool, René, Dolan, Conor V., Actkins, Ky’Era V., Gerring, Zachary F., Van Dongen, Jenny, Ehli, Erik A., Iacono, William G., Mcgue, Matt, Chasman, Daniel I., Gallagher, C. Scott, Schilit, Samantha L. P., Morton, Cynthia C., Paré, Guillaume, Willemsen, Gonneke, Whiteman, David C., Olsen, Catherine M., Derom, Catherine, Vlietinck, Robert, Gudbjartsson, Daniel, Cannon-Albright, Lisa, Krapohl, Eva, Plomin, Robert ... Martin, Nicholas G. (2024). Genome-wide association study meta-analysis of dizygotic twinning illuminates genetic regulation of female fecundity. Human Reproduction, 39 (1), 240-257. doi: 10.1093/humrep/dead247
Perugini, Ambra, Fontanillas, Pierre, Gordon, Scott D., Fisher, Simon E., Martin, Nicholas G., Bates, Timothy C and Luciano, Michelle (2024). Dyslexia polygenic scores show heightened prediction of verbal working memory and arithmetic. Scientific Studies of Reading, 28 (5), 1-15. doi: 10.1080/10888438.2024.2365697
García-Marín, Luis M., Ogonowski, Natalia S., Han, Laura K.M., Maya-Martínez, Mateo, Mitchell, Brittany L., Schmaal, Lianne, Martin, Nicholas G. and Rentería, Miguel E. (2024). Investigating the genetic relationship of intracranial and subcortical brain volumes with depression and other psychiatric disorders. Imaging Neuroscience, 2, 1-16. doi: 10.1162/imag_a_00291
Zhou, Hang, Kember, Rachel L., Deak, Joseph D., Xu, Heng, Toikumo, Sylvanus, Yuan, Kai, Lind, Penelope A., Farajzadeh, Leila, Wang, Lu, Hatoum, Alexander S., Johnson, Jessica, Lee, Hyunjoon, Mallard, Travis T., Xu, Jiayi, Johnston, Keira J. A., Johnson, Emma C., Nielsen, Trine Tollerup, Galimberti, Marco, Dao, Cecilia, Levey, Daniel F., Overstreet, Cassie, Byrne, Enda M., Gillespie, Nathan A., Gordon, Scott, Hickie, Ian B., Whitfield, John B., Xu, Ke, Zhao, Hongyu, Huckins, Laura M. ... Million Veteran Program (2023). Multi-ancestry study of the genetics of problematic alcohol use in over 1 million individuals. Nature Medicine, 29 (12), 3184-3192. doi: 10.1038/s41591-023-02653-5
Guintivano, Jerry, Byrne, Enda M., Kiewa, Jacqueline, Yao, Shuyang, Bauer, Anna E., Aberg, Karolina A., Adams, Mark J., Campbell, Archie, Campbell, Megan L., Choi, Karmel W., Corfield, Elizabeth C., Havdahl, Alexandra, Hucks, Donald, Koen, Nastassja, Lu, Yi, Maegbaek, Merete L., Mullaer, Jimmy, Peterson, Roseann E., Raffield, Laura M., Sallis, Hannah M., Sealock, Julia M., Walker, Alicia, Watson, Hunna J., Xiong, Ying, Yang, Jessica M. K., Anney, Richard J. L., Gordon-Smith, Katherine, Hubbard, Leon, Jones, Lisa A. ... Sullivan, Patrick (2023). Meta-analyses of genome-wide association studies for postpartum depression. American Journal of Psychiatry, 180 (12), 884-895. doi: 10.1176/appi.ajp.20230053
Gordon, Scott D., Duffy, David L., Whiteman, David C., Olsen, Catherine M., McAloney, Kerrie, Adsett, Jessica M., Garden, Natalie A., Cross, Simone M., List-Armitage, Susan E., Brown, Joy, Beck, Jeffrey J., Mbarek, Hamdi, Medland, Sarah E., Montgomery, Grant W. and Martin, Nicholas G. (2023). GWAS of dizygotic twinning in an enlarged Australian sample of mothers of DZ twins. Twin Research and Human Genetics, 26 (6), 327-338. doi: 10.1017/thg.2023.45
Garcia-Marin, Luis M., Mulcahy, Aoibhe, Byrne, Enda M., Medland, Sarah E., Wray, Naomi R., Chafota, Freddy, Lind, Penelope A., Martin, Nicholas G., Hickie, Ian B., Rentería, Miguel E. and Campos, Adrian I. (2023). Discontinuation of antidepressant treatment: a retrospective cohort study on more than 20,000 participants. Annals of General Psychiatry, 22 (1) 49, 1-8. doi: 10.1186/s12991-023-00480-z
Ingold, N., Zhu, G., Duffy, D. L., Mothershaw, A., Martin, N. G., MacGregor, S. and Law, M. H. (2023). Counting nevi on the outer arm provides an accurate and feasible alternative to total body nevus count. Journal of the European Academy of Dermatology and Venereology, 37 (11), e1302-e1304. doi: 10.1111/jdv.19279
Lind, Penelope A., Siskind, Dan J., Hickie, Ian B, Colodro-Conde, Lucía, Cross, Simone, Parker, Richard, Martin, Nicholas G. and Medland, Sarah E. (2023). Preliminary results from the Australian Genetics of Bipolar Disorder Study: A nation-wide cohort. Australian and New Zealand Journal of Psychiatry, 57 (11), 1428-1442. doi: 10.1177/00048674231195571
Ong, Jue-Sheng, Seviiri, Mathias, Dusingize, Jean Claude, Wu, Yeda, Han, Xikun, Shi, Jianxin, Olsen, Catherine M., Neale, Rachel E., Thompson, John F., Saw, Robyn P. M., Shannon, Kerwin F., Mann, Graham J., Martin, Nicholas G., Medland, Sarah E., Gordon, Scott D., Scolyer, Richard A., Long, Georgina V., Iles, Mark M., Landi, Maria Teresa, Whiteman, David C., MacGregor, Stuart and Law, Matthew H. (2023). Uncovering the complex relationship between balding, testosterone and skin cancers in men. Nature Communications, 14 (1) 5962, 1-12. doi: 10.1038/s41467-023-41231-8
Mulder, Tessa A, Campbell, Purdey J, Taylor, Peter N, Peeters, Robin P, Wilson, Scott G, Medici, Marco, Dayan, Colin, Jaddoe, Vincent V W, Walsh, John P, Martin, Nicholas G, Tiemeier, Henning and Korevaar, Tim I M (2023). Genetic determinants of thyroid function in children. European Journal of Endocrinology, 189 (2), 164-174. doi: 10.1093/ejendo/lvad086
Gomez, Lina M., Mitchell, Brittany L., McAloney, Kerrie, Adsett, Jessica, Garden, Natalie, Wood, Madeline, Diaz-Torres, Santiago, Garcia-Marin, Luis M., Breakspear, Michael, Martin, Nicholas G. and Lupton, Michelle K. (2023). The effect of genetic predisposition to Alzheimer’s disease and related traits on recruitment bias in a study of cognitive aging. Twin Research and Human Genetics, 26 (3) PII S1832427423000269, 1-6. doi: 10.1017/thg.2023.26
Peng, Fuduan, Xiong, Ziyi, Zhu, Gu, Hysi, Pirro G., Eller, Ryan J., Wu, Sijie, Adhikari, Kaustubh, Chen, Yan, Li, Yi, Gonzalez-José, Rolando, Schüler-Faccini, Lavinia, Bortolini, Maria-Cátira, Acuña-Alonzo, Victor, Canizales-Quinteros, Samuel, Gallo, Carla, Poletti, Giovanni, Bedoya, Gabriel, Rothhammer, Francisco, Uitterlinden, André G., Ikram, M. Arfan, Nijsten, Tamar, Ruiz-Linares, Andrés, Wang, Sijia, Walsh, Susan, Spector, Timothy D., Martin, Nicholas G., Kayser, Manfred and Liu, Fan (2023). GWAs identify DNA variants influencing eyebrow thickness variation in Europeans and across continental populations. Journal of Investigative Dermatology, 143 (7), 1317-1322. doi: 10.1016/j.jid.2022.11.026
Chundru, V. Kartik, Marioni, Riccardo E., Pendergast, James G. D., Lin, Tian, Beveridge, Allan J., Martin, Nicholas G, Montgomery, Grant W., Hume, David A., Deary, Ian J., Visscher, Peter M., Wray, Naomi R. and McRae, Allan F. (2023). Rare genetic variants underlie outlying levels of DNA methylation and gene-expression. Human Molecular Genetics, 32 (11), 1912-1921. doi: 10.1093/hmg/ddad028
Graham, Sarah E., Clarke, Shoa L., Wu, Kuan-Han H., Kanoni, Stavroula, Zajac, Greg J. M., Ramdas, Shweta, Surakka, Ida, Ntalla, Ioanna, Vedantam, Sailaja, Winkler, Thomas W., Locke, Adam E., Marouli, Eirini, Hwang, Mi Yeong, Han, Sohee, Narita, Akira, Choudhury, Ananyo, Bentley, Amy R., Ekoru, Kenneth, Verma, Anurag, Trivedi, Bhavi, Martin, Hilary C., Hunt, Karen A., Hui, Qin, Klarin, Derek, Zhu, Xiang, Thorleifsson, Gudmar, Helgadottir, Anna, Gudbjartsson, Daniel F., Holm, Hilma ... Global Lipids Genetics Consortium (2023). Author Correction: The power of genetic diversity in genome-wide association studies of lipids. Nature, 618 (7965), E19-E20. doi: 10.1038/s41586-023-06194-2
García-Marín, Luis M., Reyes-Pérez, Paula, Diaz-Torres, Santiago, Medina-Rivera, Alejandra, Martin, Nicholas G., Mitchell, Brittany L. and Rentería, Miguel E. (2023). Shared molecular genetic factors influence subcortical brain morphometry and Parkinson’s disease risk. npj Parkinson's Disease, 9 (1) 73, 73. doi: 10.1038/s41531-023-00515-y
Johnson, Emma C., Colbert, Sarah M.C., Jeffries, Paul W., Tillman, Rebecca, Bigdeli, Tim B., Karcher, Nicole R., Chan, Grace, Kuperman, Samuel, Meyers, Jacquelyn L., Nurnberger, John I., Plawecki, Martin H., Degenhardt, Louisa, Martin, Nicholas G., Kamarajan, Chella, Schuckit, Marc A., Murray, Robin M., Dick, Danielle M., Edenberg, Howard J., D’Souza, Deepak Cyril, Di Forti, Marta, Porjesz, Bernice, Nelson, Elliot C. and Agrawal, Arpana (2023). Associations between cannabis use, polygenic liability for schizophrenia, and cannabis-related experiences in a sample of cannabis users. Schizophrenia Bulletin, 49 (3), 778-787. doi: 10.1093/schbul/sbac196
Dash, Genevieve F., Gizer, Ian R., Martin, Nicholas G. and Slutske, Wendy S. (2023). Specificity in genetic and environmental risk for prescription opioid misuse and heroin use. Psychological Medicine, 107 (2), 6828-6837. doi: 10.1017/s003329172300034x
Rahmioglu, Nilufer, Mortlock, Sally, Ghiasi, Marzieh, Møller, Peter L., Stefansdottir, Lilja, Galarneau, Geneviève, Turman, Constance, Danning, Rebecca, Law, Matthew H., Sapkota, Yadav, Christofidou, Paraskevi, Skarp, Sini, Giri, Ayush, Banasik, Karina, Krassowski, Michal, Lepamets, Maarja, Marciniak, Błażej, Nõukas, Margit, Perro, Danielle, Sliz, Eeva, Sobalska-Kwapis, Marta, Thorleifsson, Gudmar, Topbas-Selcuki, Nura F., Vitonis, Allison, Westergaard, David, Arnadottir, Ragnheidur, Burgdorf, Kristoffer S., Campbell, Archie, Cheuk, Cecilia S. K. ... The 23andMe Research Team (2023). The genetic basis of endometriosis and comorbidity with other pain and inflammatory conditions. Nature Genetics, 55 (3), 423-436. doi: 10.1038/s41588-023-01323-z
Campos, Adrian I., Ingold, Nathan, Huang, Yunru, Mitchell, Brittany L., Kho, Pik-Fang, Han, Xikun, García-Marín, Luis M., Ong, Jue-Sheng, 23andMe Research Team, Law, Matthew H., Yokoyama, Jennifer S., Martin, Nicholas G., Dong, Xianjun, Cuellar-Partida, Gabriel, MacGregor, Stuart, Aslibekyan, Stella and Rentería, Miguel E. (2023). Discovery of genomic loci associated with sleep apnoea risk through multi-trait GWAS analysis with snoring. Sleep, 46 (3) zsac308, 1-14. doi: 10.1093/sleep/zsac308
Bakker, Mark K., Kanning, Jos P., Abraham, Gad, Martinsen, Amy E., Winsvold, Bendik S., Zwart, John-Anker, Bourcier, Romain, Sawada, Tomonobu, Koido, Masaru, Kamatani, Yoichiro, Morel, Sandrine, Amouyel, Philippe, Debette, Stéphanie, Bijlenga, Philippe, Berrandou, Takiy, Ganesh, Santhi K., Bouatia-Naji, Nabila, Jones, Gregory, Bown, Matthew, Rinkel, Gabriel J.E., Veldink, Jan H., Ruigrok, Ynte M., Hege Aamodt, Anne, Heidi Skogholt, Anne, Brumpton, Ben M., Willer, Cristen J., Sandset, Else C., Kristoffersen, Espen S., Ellekjær, Hanne ... International Stroke Genetics Consortium (ISGC) Intracranial Aneurysm Working Group (2023). Genetic risk score for intracranial aneurysms: prediction of subarachnoid hemorrhage and role in clinical heterogeneity. Stroke, 54 (3), 810-818. doi: 10.1161/STROKEAHA.122.040715
Doust, Catherine, Fontanillas, Pierre, Eising, Else, Gordon, Scott D., Wang, Zhengjun, Alagöz, Gökberk, Molz, Barbara, Aslibekyan, Stella, Auton, Adam, Babalola, Elizabeth, Bell, Robert K., Bielenberg, Jessica, Bryc, Katarzyna, Bullis, Emily, Coker, Daniella, Partida, Gabriel Cuellar, Dhamija, Devika, Das, Sayantan, Elson, Sarah L., Filshtein, Teresa, Fletez-Brant, Kipper, Freyman, Will, Gandhi, Pooja M., Heilbron, Karl, Hicks, Barry, Hinds, David A., Jewett, Ethan M., Jiang, Yunxuan, Kukar, Katelyn ... Quantitative Trait Working Group of the GenLang Consortium (2023). Author Correction: Discovery of 42 genome-wide significant loci associated with dyslexia. Nature Genetics, 55 (3), 520-520. doi: 10.1038/s41588-023-01336-8
Weihs, Antoine, Chaker, Layal, Martin, Tiphaine Christiane, Braun, Kim V.E., Campbell, Purdey J, Cox, Simon R, Fornage, Myriam, Gieger, Christian, Grabe, Hans J, Grallert, Harald, Harris, Sarah E, Kühnel, Brigitte, Marioni, Riccardo E, Martin, Nicholas G, McCartney, Daniel L, McRae, Allan F, Meisinger, Christa, Meurs, Joyce van, Nano, Jana, Nauck, Matthias, Peters, Annette, Prokisch, Holger, Roden, Michael, Selvin, Elizabeth, Beekman, Marian, van Heemst, Diana, Slagboom, Eline P, Swenson, Brenton R, Tin, Adrienne ... Teumer, Alexander (2023). Epigenome-wide association study reveals CpG sites associated with thyroid function and regulatory effects on KLF9. Thyroid (ja), 301-311. doi: 10.1089/thy.2022.0373
Mathieson, Iain, Day, Felix R., Barban, Nicola, Tropf, Felix C., Brazel, David M., van Heemst, Diana, Vaez, Ahmad, van Zuydam, Natalie, Bitarello, Bárbara D., Gardner, Eugene J., Akimova, Evelina T., Azad, Ajuna, Bergmann, Sven, Bielak, Lawrence F., Boomsma, Dorret I., Bosak, Kristina, Brumat, Marco, Buring, Julie E., Cesarini, David, Chasman, Daniel I., Chavarro, Jorge E., Cocca, Massimiliano, Concas, Maria Pina, Davey Smith, George, Davies, Gail, Deary, Ian J., Esko, Tõnu, Faul, Jessica D., Franco, Oscar ... Perry, John R. B. (2023). Genome-wide analysis identifies genetic effects on reproductive success and ongoing natural selection at the FADS locus. Nature Human Behaviour, 7 (5), 790-801. doi: 10.1038/s41562-023-01528-6
Davis, Christal N., Gizer, Ian R., Lynskey, Michael T., Statham, Dixie J., Heath, Andrew C., Martin, Nicholas G. and Slutske, Wendy S. (2023). Adolescent substance use and high school noncompletion: exploring the nature of the relationship using a discordant twin design. Addiction, 118 (1), 167-176. doi: 10.1111/add.15996
Kanoni, Stavroula, Graham, Sarah E., Wang, Yuxuan, Surakka, Ida, Ramdas, Shweta, Zhu, Xiang, Clarke, Shoa L., Bhatti, Konain Fatima, Vedantam, Sailaja, Winkler, Thomas W., Locke, Adam E., Marouli, Eirini, Zajac, Greg J. M., Wu, Kuan-Han H., Ntalla, Ioanna, Hui, Qin, Klarin, Derek, Hilliard, Austin T., Wang, Zeyuan, Xue, Chao, Thorleifsson, Gudmar, Helgadottir, Anna, Gudbjartsson, Daniel F., Holm, Hilma, Olafsson, Isleifur, Hwang, Mi Yeong, Han, Sohee, Akiyama, Masato, Sakaue, Saori ... Peloso, Gina M. (2022). Implicating genes, pleiotropy, and sexual dimorphism at blood lipid loci through multi-ancestry meta-analysis. Genome Biology, 23 (1) 268, 1-42. doi: 10.1186/s13059-022-02837-1
Silventoinen, Karri, Piirtola, Maarit, Jelenkovic, Aline, Sund, Reijo, Tarnoki, Adam D., Tarnoki, David L., Medda, Emanuela, Nisticò, Lorenza, Toccaceli, Virgilia, Honda, Chika, Inui, Fujio, Tomizawa, Rie, Watanabe, Mikio, Sakai, Norio, Gatz, Margaret, Butler, David A., Lee, Jooyeon, Lee, Soo Ji, Sung, Joohon, Franz, Carol E., Kremen, William S., Lyons, Michael J., Derom, Catherine A., Vlietinck, Robert F., Loos, Ruth J. F., Tynelius, Per, Rasmussen, Finn, Martin, Nicholas G., Medland, Sarah E. ... Kaprio, Jaakko (2022). Smoking remains associated with education after controlling for social background and genetic factors in a study of 18 twin cohorts. Scientific Reports, 12 (1) 13148, 1-9. doi: 10.1038/s41598-022-17536-x
Gomez, Lina, Díaz-Torres, Santiago, Colodro-Conde, Lucía, Garcia-Marin, Luis M., Yap, Chloe X., Byrne, Enda M., Yengo, Loic, Lind, Penelope A., Wray, Naomi R., Medland, Sarah E., Hickie, Ian B., Lupton, Michelle K., Rentería, Miguel E., Martin, Nicholas G. and Campos, Adrian I. (2022). Phenotypic and genetic factors associated with donation of DNA and consent to record linkage for prescription history in the Australian Genetics of Depression Study. European Archives of Psychiatry and Clinical Neuroscience, 273 (6), 1359-1368. doi: 10.1007/s00406-022-01527-0
Doust, Catherine, Fontanillas, Pierre, Eising, Else, Gordon, Scott D., Wang, Zhengjun, Alagöz, Gökberk, Molz, Barbara, Aslibekyan, Stella, Auton, Adam, Babalola, Elizabeth, Bell, Robert K., Bielenberg, Jessica, Bryc, Katarzyna, Bullis, Emily, Coker, Daniella, Partida, Gabriel Cuellar, Dhamija, Devika, Das, Sayantan, Elson, Sarah L., Filshtein, Teresa, Fletez-Brant, Kipper, Freyman, Will, Gandhi, Pooja M., Heilbron, Karl, Hicks, Barry, Hinds, David A., Jewett, Ethan M., Jiang, Yunxuan, Kukar, Katelyn ... Quantitative Trait Working Group of the GenLang Consortium (2022). Discovery of 42 genome-wide significant loci associated with dyslexia. Nature Genetics, 54 (11), 1621-1629. doi: 10.1038/s41588-022-01192-y
Tielbeek, Jorim J., Uffelmann, Emil, Williams, Benjamin S., Colodro-Conde, Lucía, Gagnon, Éloi, Mallard, Travis T., Levitt, Brandt E., Jansen, Philip R., Johansson, Ada, Sallis, Hannah M., Pistis, Giorgio, Saunders, Gretchen R. B., Allegrini, Andrea G., Rimfeld, Kaili, Konte, Bettina, Klein, Marieke, Hartmann, Annette M., Salvatore, Jessica E., Nolte, Ilja M., Demontis, Ditte, Malmberg, Anni L. K., Burt, S. Alexandra, Savage, Jeanne E., Sugden, Karen, Poulton, Richie, Harris, Kathleen Mullan, Vrieze, Scott, McGue, Matt, Iacono, William G. ... Spit for Science Working Group (2022). Uncovering the genetic architecture of broad antisocial behavior through a genome-wide association study meta-analysis. Molecular Psychiatry, 27 (11), 4453-4463. doi: 10.1038/s41380-022-01793-3
Davis, Christal N., Gizer, Ian R., Colodro-Conde, Lucía, Statham, Dixie J., Martin, Nicholas G. and Slutske, Wendy S. (2022). Educational attainment polygenic scores: examining evidence for gene–environment interplay with adolescent alcohol, tobacco and cannabis use. Twin Research and Human Genetics, 25 (4-5) PII S1832427422000330, 187-195. doi: 10.1017/thg.2022.33
Boyce, Jessica O., Jackson, Victoria E., van Reyk, Olivia, Parker, Richard, Vogel, Adam P., Eising, Else, Horton, Sarah E., Gillespie, Nathan A., Scheffer, Ingrid E., Amor, David J., Hildebrand, Michael S., Fisher, Simon E., Martin, Nicholas G., Reilly, Sheena, Bahlo, Melanie and Morgan, Angela T. (2022). Self-reported impact of developmental stuttering across the lifespan. Developmental Medicine and Child Neurology, 64 (10), 1297-1306. doi: 10.1111/dmcn.15211
Watson, Hunna J., Thornton, Laura M., Yilmaz, Zeynep, Baker, Jessica H., Coleman, Jonathan R.I., Adan, Roger A.H., Alfredsson, Lars, Andreassen, Ole A., Ask, Helga, Berrettini, Wade H., Boehnke, Michael, Boehm, Ilka, Boni, Claudette, Buehren, Katharina, Bulant, Josef, Burghardt, Roland, Chang, Xiao, Cichon, Sven, Cone, Roger D., Courtet, Philippe, Crow, Scott, Crowley, James J., Danner, Unna N., de Zwaan, Martina, Dedoussis, George, DeSocio, Janiece E., Dick, Danielle M., Dikeos, Dimitris, Dina, Christian ... Bulik, Cynthia M. (2022). Common genetic variation and age of onset of anorexia nervosa. Biological Psychiatry Global Open Science, 2 (4), 368-378. doi: 10.1016/j.bpsgos.2021.09.001
Gallagher, C. S., Mäkinen, N., Harris, H. R., Rahmioglu, N., Uimari, O., Cook, J. P., Shigesi, N., Ferreira, T., Velez-Edwards, D. R., Edwards, T. L., Mortlock, S., Ruhioglu, Z., Day, F., Becker, C. M., Karhunen, V., Martikainen, H., Järvelin, M.-R., Cantor, R. M., Ridker, P. M., Terry, K. L., Buring, J. E., Gordon, S. D., Medland, S. E., Montgomery, G. W., Nyholt, D. R., Hinds, D. A., Tung, J. Y., Agee, Michelle, Alipanahi, Babak ... the 23andMe Research Team (2022). Author correction: Genome-wide association and epidemiological analyses reveal common genetic origins between uterine leiomyomata and endometriosis. Nature Communications, 13 (1) 5543, 5543. doi: 10.1038/s41467-022-33222-y
Wang, Zhe, Emmerich, Andrew, Pillon, Nicolas J., Moore, Tim, Hemerich, Daiane, Cornelis, Marilyn C., Mazzaferro, Eugenia, Broos, Siacia, Ahluwalia, Tarunveer S., Bartz, Traci M., Bentley, Amy R., Bielak, Lawrence F., Chong, Mike, Chu, Audrey Y., Berry, Diane, Dorajoo, Rajkumar, Dueker, Nicole D., Kasbohm, Elisa, Feenstra, Bjarke, Feitosa, Mary F., Gieger, Christian, Graff, Mariaelisa, Hall, Leanne M., Haller, Toomas, Hartwig, Fernando P., Hillis, David A., Huikari, Ville, Heard-Costa, Nancy, Holzapfel, Christina ... Lifelines Cohort Study (2022). Genome-wide association analyses of physical activity and sedentary behavior provide insights into underlying mechanisms and roles in disease prevention. Nature Genetics, 54 (9), 1332-1344. doi: 10.1038/s41588-022-01165-1
Aman, Asma M., García-Marín, Luis M., Thorp, Jackson G., Campos, Adrian I., Cuellar-Partida, Gabriel, Martin, Nicholas G.. and Rentería, Miguel E. (2022). Phenome-wide screening of the putative causal determinants of depression using genetic data. Human Molecular Genetics, 31 (17), 2887-2898. doi: 10.1093/hmg/ddac081
Mitchell, Brittany L., Hansell, Narelle K., McAloney, Kerrie, Martin, Nicholas G., Wright, Margaret J., Renteria, Miguel E. and Grasby, Katrina L. (2022). Polygenic influences associated with adolescent cognitive skills. Intelligence, 94 101680, 1-9. doi: 10.1016/j.intell.2022.101680
Eising, Else, Mirza-Schreiber, Nazanin, de Zeeuw, Eveline L., Wang, Carol A., Truong, Dongnhu T., Allegrini, Andrea G., Shapland, Chin Yang, Zhu, Gu, Wigg, Karen G., Gerritse, Margot L., Molz, Barbara, Alagöz, Gökberk, Gialluisi, Alessandro, Abbondanza, Filippo, Rimfeld, Kaili, van Donkelaar, Marjolein, Liao, Zhijie, Jansen, Philip R., Andlauer, Till F M, Bates, Timothy C., Bernard, Manon, Blokland, Kirsten, Bonte, Milene, Børglum, Anders D., Bourgeron, Thomas, Brandeis, Daniel, Ceroni, Fabiola, Csépe, Valéria, Dale, Philip S. ... Fisher, Simon E. (2022). Genome-wide analyses of individual differences in quantitatively assessed reading- and language-related skills in up to 34,000 people. Proceedings of the National Academy of Sciences of the United States of America, 119 (35) e2202764119, 1-12. doi: 10.1073/pnas.2202764119
Silventoinen, Karri, Li, Weilong, Jelenkovic, Aline, Sund, Reijo, Yokoyama, Yoshie, Aaltonen, Sari, Piirtola, Maarit, Sugawara, Masumi, Tanaka, Mami, Matsumoto, Satoko, Baker, Laura A., Tuvblad, Catherine, Tynelius, Per, Rasmussen, Finn, Craig, Jeffrey M., Saffery, Richard, Willemsen, Gonneke, Bartels, Meike, van Beijsterveldt, Catharina E. M., Martin, Nicholas G., Medland, Sarah E., Montgomery, Grant W., Lichtenstein, Paul, Krueger, Robert F., McGue, Matt, Pahlen, Shandell, Christensen, Kaare, Skytthe, Axel, Kyvik, Kirsten O. ... Kaprio, Jaakko (2022). Changing genetic architecture of body mass index from infancy to early adulthood: an individual based pooled analysis of 25 twin cohorts. International Journal of Obesity, 46 (10), 1901-1909. doi: 10.1038/s41366-022-01202-3
Xu, Jiayi, Johnson, Jessica S., Signer, Rebecca, Eating Disorders Working Group of the Psychiatric Genomics Consortium, Birgegård, Andreas, Jordan, Jennifer, Kennedy, Martin A., Landén, Mikael, Maguire, Sarah L., Martin, Nicholas G., Mortensen, Preben Bo, Petersen, Liselotte V., Thornton, Laura M., Bulik, Cynthia M. and Huckins, Laura M. (2022). Exploring the clinical and genetic associations of adult weight trajectories using electronic health records in a racially diverse biobank: a phenome-wide and polygenic risk study. The Lancet Digital Health, 4 (8), e604-e614. doi: 10.1016/S2589-7500(22)00099-1
Campos, Adrian I., Byrne, Enda M., Iorfino, Frank, Fabbri, Chiara, Hickie, Ian B., Lewis, Cathryn M., Wray, Naomi R., Medland, Sarah E., Rentería, Miguel E. and Martin, Nicholas G. (2022). Clinical, demographic, and genetic risk factors of treatment‐attributed suicidality in >10,000 Australian adults taking antidepressants. American Journal of Medical Genetics Part B: Neuropsychiatric Genetics, 189 (6), 196-206. doi: 10.1002/ajmg.b.32913
Whitfield, John B., Colodro-Conde, Lucía, Zhu, Gu, Timmers, Paul R. H. J., Joshi, Peter K., Montgomery, Grant W. and Martin, Nicholas G (2022). Co-inheritance of variation in all-cause mortality and biochemical risk factors. Twin Research and Human Genetics, 25 (3), 1-8. doi: 10.1017/thg.2022.25
Hansell, Narelle K., Strike, Lachlan T., van Eijk, Liza, O'Callaghan, Victoria, Martin, Nicholas G., de Zubicaray, Greig I., Thompson, Paul M., McMahon, Katie L. and Wright, Margaret J. (2022). Genetic specificity of hippocampal subfield volumes, relative to hippocampal formation, identified in 2148 young adult twins and siblings. Twin Research and Human Genetics, 25 (3) PII S1832427422000202, 129-139. doi: 10.1017/thg.2022.20
Kiewa, Jacqueline, Meltzer-Brody, Samantha, Milgrom, Jeannette, Bennett, Elizabeth, Mackle, Tracey, Guintivano, Jerry, Hickie, Ian B, Colodro-Conde, Lucia, Medland, Sarah E, Martin, Nick, Wray, Naomi and Byrne, Enda (2022). Lifetime prevalence and correlates of perinatal depression in a case-cohort study of depression. BMJ Open, 12 (8) e059300, 1-7. doi: 10.1136/bmjopen-2021-059300
Winkler, Thomas W., Rasheed, Humaira, Teumer, Alexander, Gorski, Mathias, Rowan, Bryce X., Stanzick, Kira J., Thomas, Laurent F., Tin, Adrienne, Hoppmann, Anselm, Chu, Audrey Y., Tayo, Bamidele, Thio, Chris H. L., Cusi, Daniele, Chai, Jin-Fang, Sieber, Karsten B., Horn, Katrin, Li, Man, Scholz, Markus, Cocca, Massimiliano, Wuttke, Matthias, van der Most, Peter J., Yang, Qiong, Ghasemi, Sahar, Nutile, Teresa, Li, Yong, Pontali, Giulia, Günther, Felix, Dehghan, Abbas, Correa, Adolfo ... VA Million Veteran Program (2022). Differential and shared genetic effects on kidney function between diabetic and non-diabetic individuals. Communications Biology, 5 (1) 580, 1-20. doi: 10.1038/s42003-022-03448-z
Crouse, Jacob J., Ho, Nicholas, Scott, Jan, Parker, Richard, Park, Shin Ho, Couvy-Duchesne, Baptiste, Mitchell, Brittany, Byrne, Enda M., Hermens, Daniel F., Medland, Sarah E., Martin, Nicholas G., Gillespie, Nathan A. and Hickie, Ian B. (2022). Dynamic networks of psychological symptoms, impairment, substance use, and social support: the evolution of psychopathology among emerging adults. European Psychiatry, 65 (1) e32, 1-24. doi: 10.1192/j.eurpsy.2022.23
Duffy, David L. and Martin, Nicholas G. (2022). The heritability of twinning in seven large historic pedigrees. Twin Research and Human Genetics, 25 (2), 1-4. doi: 10.1017/thg.2022.14
Martin, Nick (2022). Lindon Eaves: a personal memoir. Twin Research and Human Genetics, 25 (2), 97-100. doi: 10.1017/thg.2022.13
Johnson, Jessica S., Cote, Alanna C., Dobbyn, Amanda, Sloofman, Laura G., Xu, Jiayi, Cotter, Liam, Charney, Alexander W., Birgegård, Andreas, Jordan, Jennifer, Kennedy, Martin, Landén, Mikaél, Maguire, Sarah L., Martin, Nicholas G., Mortensen, Preben Bo, Thornton, Laura M., Bulik, Cynthia M., Huckins, Laura M. and Eating Disorders Working Group of the Psychiatric Genomics Consortium (2022). Mapping anorexia nervosa genes to clinical phenotypes. Psychological Medicine, 53 (6), 1-15. doi: 10.1017/s0033291721004554
Maihofer, Adam X., Choi, Karmel W., Coleman, Jonathan R. I., Daskalakis, Nikolaos P., Denckla, Christy A., Ketema, Elizabeth, Morey, Rajendra A., Polimanti, Renato, Ratanatharathorn, Andrew, Torres, Katy, Wingo, Aliza P., Zai, Clement C., Aiello, Allison E., Almli, Lynn M., Amstadter, Ananda B., Andersen, Soren B., Andreassen, Ole A., Arbisi, Paul A., Ashley-Koch, Allison E., Austin, S. Bryn, Avdibegovic, Esmina, Borglum, Anders D., Babic, Dragan, Bμkvad-Hansen, Marie, Baker, Dewleen G., Beckham, Jean C., Bierut, Laura J., Bisson, Jonathan I., Boks, Marco P. ... Nievergelt, Caroline M. (2022). Enhancing discovery of genetic variants for PTSD through integration of quantitative phenotypes and trauma exposure information. Biological Psychiatry, 91 (7), 626-636. doi: 10.1016/j.biopsych.2021.09.020
Dash, Genevieve F., Martin, Nicholas G. and Slutske, Wendy S. (2022). Childhood maltreatment and disordered gambling in adulthood: Disentangling causal and familial influences. Psychological Medicine, 52 (5), 1-10. doi: 10.1017/S0033291720002743
Kiewa, Jacqueline, Meltzer‐Brody, Samantha, Milgrom, Jeanette, Guintivano, Jerry, Hickie, Ian B., Whiteman, David C., Olsen, Catherine M., Colodro‐Conde, Lucía, Medland, Sarah E., Martin, Nicholas G., Wray, Naomi R. and Byrne, Enda M. (2022). Perinatal depression is associated with a higher polygenic risk for major depressive disorder than non-perinatal depression. Depression and Anxiety, 39 (3), 182-191. doi: 10.1002/da.23232
Rabinowitz, Jill A., Campos, Adrian I., Ong, Jue-Sheng, García-Marín, Luis M., Alcauter, Sarael, Mitchell, Brittany L, Grasby, Katrina L, Cuéllar-Partida, Gabriel, Gillespie, Nathan A, Huhn, Andrew S, Martin, Nicholas G, Thompson, Paul M, Medland, Sarah E, Maher, Brion S and Rentería, Miguel E (2022). Shared genetic etiology between cortical brain morphology and tobacco, alcohol, and cannabis use. Cerebral Cortex, 32 (4), 796-807. doi: 10.1093/cercor/bhab243
Finkel, Deborah, Zavala, Catalina, Franz, Carol E., Pahlen, Shandell, Gatz, Margaret, Pedersen, Nancy L., Finch, Brian K., Dahl Aslan, Anna, Catts, Vibeke S., Ericsson, Malin, Krueger, Robert F., Martin, Nicholas G., Mohan, Adith, Mosing, Miriam A., Prescott, Carol A. and Whitfield, Keith E. (2022). Financial strain moderates genetic influences on self-rated health: support for diathesis–stress model of gene–environment interplay. Biodemography and Social Biology, 67 (1), 1-13. doi: 10.1080/19485565.2022.2037069
Mitchell, Brittany L., Saklatvala, Jake R., Dand, Nick, Hagenbeek, Fiona A., Li, Xin, Min, Josine L., Thomas, Laurent, Bartels, Meike, Jan Hottenga, Jouke, Lupton, Michelle K., Boomsma, Dorret I., Dong, Xianjun, Hveem, Kristian, Løset, Mari, Martin, Nicholas G., Barker, Jonathan N., Han, Jiali, Smith, Catherine H., Rentería, Miguel E. and Simpson, Michael A. (2022). Genome-wide association meta-analysis identifies 29 new acne susceptibility loci. Nature Communications, 13 (1) 702, 702. doi: 10.1038/s41467-022-28252-5
Bivol, Svetlana, Mellick, George D., Gratten, Jacob, Parker, Richard, Mulcahy, Aoibhe, Mosley, Philip E., Poortvliet, Peter C., Campos, Adrian I., Mitchell, Brittany L., Garcia-Marin, Luis M., Cross, Simone, Ferguson, Mary, Lind, Penelope A., Loesch, Danuta Z., Visscher, Peter M., Medland, Sarah E., Scherzer, Clemens R., Martin, Nicholas G. and Rentería, Miguel E. (2022). Australian Parkinson’s Genetics Study (APGS): pilot (n=1532). BMJ Open, 12 (2) e052032, e052032. doi: 10.1136/bmjopen-2021-052032
Fazlollahi, Amir, Xia, Ying, Lupton, Michelle K., Raniga, Parnesh, Bourgeat, Pierrick, Martin, Nick, Dore, Vincent, Rose, Stephen, Salvado, Olivier, Breakspear, Michael and Fripp, Jurgen (2022). Early effects of amyloid-β on structural and vascular brain changes in mid-life cognitively unimpaired individuals. Alzheimer's and dementia : the journal of the Alzheimer's Association, 17, 1-3. doi: 10.1002/alz.052681
Campos, Adrian I., Byrne, Enda M., Mitchell, Brittany L., Wray, Naomi R., Lind, Penelope A., Licinio, Julio, Medland, Sarah E., Martin, Nicholas G., Hickie, Ian B. and Rentería, Miguel E. (2022). Impact of CYP2C19 metaboliser status on SSRI response: a retrospective study of 9500 participants of the Australian Genetics of Depression Study. The Pharmacogenomics Journal, 22 (2), 130-135. doi: 10.1038/s41397-022-00267-7
Li, Jinxi, Glover, James D., Zhang, Haiguo, Peng, Meifang, Tan, Jingze, Mallick, Chandana Basu, Hou, Dan, Yang, Yajun, Wu, Sijie, Liu, Yu, Peng, Qianqian, Zheng, Shijie C., Crosse, Edie I., Medvinsky, Alexander, Anderson, Richard A., Brown, Helen, Yuan, Ziyu, Zhou, Shen, Xu, Yanqing, Kemp, John P., Ho, Yvonne Y.W., Loesch, Danuta Z., Wang, Lizhong, Li, Yingxiang, Tang, Senwei, Wu, Xiaoli, Walters, Robin G., Lin, Kuang, Meng, Ruogu ... Wang, Sijia (2022). Limb development genes underlie variation in human fingerprint patterns. Cell, 185 (1), 95-112.e18. doi: 10.1016/j.cell.2021.12.008
Slutske, Wendy S., Davis, Christal N., Lynskey, Michael T., Heath, Andrew C. and Martin, Nicholas G. (2022). An Epidemiologic, Longitudinal, and Discordant-Twin Study of the Association Between Gambling Disorder and Suicidal Behaviors. Clinical Psychological Science, 10 (5), 901-919. doi: 10.1177/21677026211062599
Graham, Sarah E., Clarke, Shoa L., Wu, Kuan-Han H., Kanoni, Stavroula, Zajac, Greg J. M., Ramdas, Shweta, Surakka, Ida, Ntalla, Ioanna, Vedantam, Sailaja, Winkler, Thomas W., Locke, Adam E., Marouli, Eirini, Hwang, Mi Yeong, Han, Sohee, Narita, Akira, Choudhury, Ananyo, Bentley, Amy R., Ekoru, Kenneth, Verma, Anurag, Trivedi, Bhavi, Martin, Hilary C., Hunt, Karen A., Hui, Qin, Klarin, Derek, Zhu, Xiang, Thorleifsson, Gudmar, Helgadottir, Anna, Gudbjartsson, Daniel F., Holm, Hilma ... Global Lipids Genetics Consortium* (2021). The power of genetic diversity in genome-wide association studies of lipids. Nature, 600 (7890), 675-679. doi: 10.1038/s41586-021-04064-3
Melhuish Beaupre, Lindsay M., Tiwari, Arun K., Gonçalves, Vanessa F., Zai, Clement C., Marshe, Victoria S., Lewis, Cathryn M., Martin, Nicholas G., McIntosh, Andrew M., Adams, Mark J., Baune, Bernhard T., Levinson, Doug F., Boomsma, Dorret I., Penninx, Brenda W. J. H., Breen, Gerome, Hamilton, Steve, Awasthi, Swapnil, Ripke, Stephan, Jones, Lisa, Jones, Ian, Byrne, Enda M., Hickie, Ian B., Potash, James P., Shi, Jianxin, Weissman, Myrna M., Milaneschi, Yuri, Shyn, Stanley I., Geus, Eco J. C. de, Willemsen, Gonneke, Brown, Gregory M. and Kennedy, James L. (2021). Potential genetic overlap between insomnia and sleep symptoms in major depressive disorder: a polygenic risk score analysis. Frontiers in Psychiatry, 12 734077, 734077. doi: 10.3389/fpsyt.2021.734077
García-Marín, Luis M., Campos, Adrián I., Martin, Nicholas G., Cuéllar-Partida, Gabriel and Rentería, Miguel E. (2021). Phenome-wide analysis highlights putative causal relationships between self-reported migraine and other complex traits. Journal of Headache and Pain, 22 (1) 66, 66. doi: 10.1186/s10194-021-01284-w
Demontis, Ditte, Walters, Raymond K., Rajagopal, Veera M., Waldman, Irwin D., Grove, Jakob, Als, Thomas D., Dalsgaard, Søren, Ribasas, Marta, Bybjerg-Grauholm, Jonas, Bækvad-Hansen, Maria, Werge, Thomas, Nordentoft, Merete, Mors, Ole, Mortensen, Preben Bo, Andreassen, Ole A., Arranz, Maria Jesús, Banaschewski, Tobias, Bau, Claiton, Bellgrove, Mark, Biederman, Joseph, Brikell, Isabell, Buitelaar, Jan K., Burton, Christie L., Casas, Miguel, Crosbie, Jennifer, Doyle, Alysa E., Ebstein, Richard P., Elia, Josephine, Elizabeth, Corfield C. ... ADHD Working Group of the Psychiatric Genomics Consortium (PGC) (2021). Risk variants and polygenic architecture of disruptive behavior disorders in the context of attention-deficit/hyperactivity disorder. Nature Communications, 12 (1) 576. doi: 10.1038/s41467-020-20443-2
Bulik, Cynthia M., Thornton, Laura M., Parker, Richard, Kennedy, Hannah, Baker, Jessica H., MacDermod, Casey, Guintivano, Jerry, Cleland, Lana, Miller, Allison L., Harper, Lauren, Larsen, Janne T., Yilmaz, Zeynep, Grove, Jakob, Sullivan, Patrick F., Petersen, Liselotte V., Jordan, Jennifer, Kennedy, Martin A. and Martin, Nicholas G. (2021). The Eating Disorders Genetics Initiative (EDGI): study protocol. BMC Psychiatry, 21 (1) 234. doi: 10.1186/s12888-021-03212-3
Demontis, Ditte, Walters, Raymond K., Rajagopal, Veera M., Waldman, Irwin D., Grove, Jakob, Als, Thomas D., Dalsgaard, Søren, Ribasés, Marta, Bybjerg-Grauholm, Jonas, Bækvad-Hansen, Maria, Werge, Thomas, Nordentoft, Merete, Mors, Ole, Mortensen, Preben Bo, Andreassen, Ole A., Arranz, Maria Jesús, Banaschewski, Tobias, Bau, Claiton, Bellgrove, Mark, Biederman, Joseph, Brikell, Isabell, Buitelaar, Jan K., Burton, Christie L., Casas, Miguel, Crosbie, Jennifer, Doyle, Alysa E., Ebstein, Richard P., Elia, Josephine, Elizabeth, Corfield C. ... Børglum, Anders D. (2021). Author Correction: Risk variants and polygenic architecture of disruptive behavior disorders in the context of attention-deficit/hyperactivity disorder (Nature Communications, (2021), 12, 1, (576), 10.1038/s41467-020-20443-2). Nature Communications, 12 (1) 1166. doi: 10.1038/s41467-021-21566-w
Dash, Genevieve F., Martin, Nicholas G. and Slutske, Wendy S. (2021). Big Five personality traits and illicit drug use: Specificity in trait–drug associations. Psychology of Addictive Behaviors, 37 (2), 318-330. doi: 10.1037/adb0000793
Campos, Adrian I., Mulcahy, Aoibhe, Thorp, Jackson G., Wray, Naomi R., Byrne, Enda M., Lind, Penelope A., Medland, Sarah E., Martin, Nicholas G., Hickie, Ian B. and Rentería, Miguel E. (2021). Understanding genetic risk factors for common side effects of antidepressant medications. Communications Medicine, 1 (1) 45, 1-10. doi: 10.1038/s43856-021-00046-8
Arends, Rachel M., Pasman, Joëlle A., Verweij, Karin J.H., Derks, Eske M., Gordon, Scott D., Hickie, Ian, Thomas, Nathaniel S., Aliev, Fazil, Zietsch, Brendan P., van der Zee, Matthijs D., Mitchell, Brittany L., Martin, Nicholas G., Dick, Danielle M., Gillespie, Nathan A., de Geus, Eco J.C., Boomsma, Dorret I., Schellekens, Arnt F.A. and Vink, Jacqueline M. (2021). Associations between the CADM2 gene, substance use, risky sexual behavior, and self-control: A phenome-wide association study. Addiction Biology, 26 (6) e13015, e13015. doi: 10.1111/adb.13015
Nolan, James, Campbell, Purdey J, Brown, Suzanne J, Zhu, Gu, Gordon, Scott, Lim, Ee Mun, Joseph, John, Cross, Simone M, Panicker, Vijay, Medland, Sarah E, Melton, Phillip E, Beilin, Lawrence J, Mori, Trevor A, Mullin, Benjamin H, Pennell, Craig E, Wang, Carol A, Dudbridge, Frank, Walsh, John P, Martin, Nicholas G and Wilson, Scott G (2021). Genome-wide analysis of thyroid function in Australian adolescents highlights SERPINA7 and NCOA3. European Journal of Endocrinology, 185 (5), 743-753. doi: 10.1530/EJE-21-0614
Mitchell, Brittany L., Campos, Adrian I., Whiteman, David C., Olsen, Catherine M., Gordon, Scott D., Walker, Adam J., Dean, Olivia M., Berk, Michael, Hickie, Ian B., Medland, Sarah E., Wray, Naomi R., Martin, Nicholas G. and Byrne, Enda M. (2021). The Australian Genetics of Depression Study: new risk loci and dissecting heterogeneity between subtypes. Biological Psychiatry, 92 (3), 227-235. doi: 10.1016/j.biopsych.2021.10.021
O'Callaghan, Victoria S., Hansell, Narelle K., Guo, Wei, Carpenter, Joanne S., Shou, Haochang, Strike, Lachlan T., Crouse, Jacob J., McAloney, Kerrie, McMahon, Katie L., Byrne, Enda M., Burns, Jane M., Martin, Nicholas G., Hickie, Ian B., Merikangas, Kathleen R. and Wright, Margaret J. (2021). Genetic and environmental influences on sleep-wake behaviours in adolescence. Sleep Advances, 2 (1) zpab018, zpab018. doi: 10.1093/sleepadvances/zpab018
Coventry, William L., Gillespie, Nathan A., Heath, Andrew C. and Martin, Nicholas G. (2021). Genetic and environmental influences on perceived social support: differences by sex and relationship. Twin Research and Human Genetics, 24 (5) PII S1832427421000438, 251-263. doi: 10.1017/thg.2021.43
Beck, Jeffrey J., Pool, René, Van De Weijer, Margot, Chen, Xu, Krapohl, Eva, Gordon, Scott D., Nygaard, Marianne, Debrabant, Birgit, Palviainen, Teemu, Van Der Zee, Matthijs D., Baselmans, Bart, Finnicum, Casey T., Yi, Lu, Lundström, Sebastian, Van Beijsterveldt, Toos, Christiansen, Lene, Heikkilä, Kauko, Kittelsrud, Julie, Loukola, Anu, Ollikainen, Miina, Christensen, Kaare, Martin, Nicholas G., Plomin, Robert, Nivard, Michel, Bartels, Meike, Dolan, Conor, Willemsen, Gonneke, De Geus, Eco, Almqvist, Catarina ... Hottenga, Jouke-Jan (2021). Genetic meta-analysis of twin birth weight shows high genetic correlation with singleton birth weight. Human Molecular Genetics, 30 (19), 1894-1905. doi: 10.1093/hmg/ddab121
Tanha, Hamzeh M., Medland, Sarah, Martin, Nicholas G. and Nyholt, Dale R. (2021). Genetic correlation analysis does not associate male pattern baldness with COVID-19. Journal of the American Academy of Dermatology, 85 (4), 971-973. doi: 10.1016/j.jaad.2021.05.009
Tanha, Hamzeh M, Martin, Nicholas G, Whitfield, John B, Nyholt, Dale R, Gormley, Padhraig, Anttila, Verneri, Winsvold, Bendik S, Palta, Priit, Esko, Tonu, Pers, Tune H, Farh, Kai-How, Cuenca-Leon, Ester, Muona, Mikko, Furlotte, Nicholas A, Kurth, Tobias, Ingason, Andres, McMahon, George, Ligthart, Lannie, Terwindt, Gisela M, Kallela, Mikko, Freilinger, Tobias M, Ran, Caroline, Gordon, Scott G, Stam, Anine H, Steinberg, Stacy, Borck, Guntram, Koiranen, Markku, Quaye, Lydia, Adams, Hieab H H ... Palotie, Aarno (2021). Association and genetic overlap between clinical chemistry tests and migraine. Cephalalgia, 41 (11-12), 1208-1221. doi: 10.1177/03331024211018131
van Dongen, Jenny, Gordon, Scott D., McRae, Allan F., Odintsova, Veronika V., Mbarek, Hamdi, Breeze, Charles E., Sugden, Karen, Lundgren, Sara, Castillo-Fernandez, Juan E., Hannon, Eilis, Moffitt, Terrie E., Hagenbeek, Fiona A., van Beijsterveldt, Catharina E. M., Jan Hottenga, Jouke, Tsai, Pei-Chien, van Dongen, Jenny, Hottenga, Jouke-Jan, McRae, Allan F., Sugden, Karen, Castillo-Fernandez, Juan E., Hannon, Eilis, Moffitt, Terrie E., Hottenga, Jouke-Jan, de Geus, Eco J. C., Spector, Timothy D., Min, Josine L., Hemani, Gibran, Ehli, Erik A., Paul, Franziska ... Genetics of DNA Methylation Consortium (2021). Identical twins carry a persistent epigenetic signature of early genome programming. Nature Communications, 12 (1) 5618, 5618. doi: 10.1038/s41467-021-25583-7
Martin, Joanna, Asjadi, Kimiya, Hubbard, Leon, Kendall, Kimberley, Pardiñas, Antonio F., Jermy, Bradley, Lewis, Cathryn M., Baune, Bernhard T., Boomsma, Dorret I., Hamilton, Steven P., Lucae, Susanne, Magnusson, Patrik K., Martin, Nicholas G., McIntosh, Andrew M., Mehta, Divya, Mors, Ole, Mullins, Niamh, Penninx, Brenda W. J. H., Preisig, Martin, Rietschel, Marcella, Jones, Ian, Walters, James T. R., Rice, Frances, Thapar, Anita, O’Donovan, Michael and Major Depressive Disorder Working Group of the Psychiatric Genomics Consortium (2021). Examining sex differences in neurodevelopmental and psychiatric genetic risk in anxiety and depression. PLoS One, 16 (9) e0248254, e0248254. doi: 10.1371/journal.pone.0248254
Min, Josine L., Hemani, Gibran, Hannon, Eilis, Dekkers, Koen F., Castillo-Fernandez, Juan, Luijk, René, Carnero-Montoro, Elena, Lawson, Daniel J., Burrows, Kimberley, Suderman, Matthew, Bretherick, Andrew D., Richardson, Tom G., Klughammer, Johanna, Iotchkova, Valentina, Sharp, Gemma, Al Khleifat, Ahmad, Shatunov, Aleksey, Iacoangeli, Alfredo, McArdle, Wendy L., Ho, Karen M., Kumar, Ashish, Söderhäll, Cilla, Soriano-Tárraga, Carolina, Giralt-Steinhauer, Eva, Kazmi, Nabila, Mason, Dan, McRae, Allan F., Corcoran, David L., Sugden, Karen ... BIOS Consortium (2021). Genomic and phenotypic insights from an atlas of genetic effects on DNA methylation. Nature Genetics, 53 (9), 1311-1321. doi: 10.1038/s41588-021-00923-x
Tapmeier, Thomas T., Rahmioglu, Nilufer, Lin, Jianghai, De Leo, Bianca, Obendorf, Maik, Raveendran, Muthuswamy, Fischer, Oliver M., Bafligil, Cemsel, Guo, Manman, Harris, Ronald Alan, Hess-Stumpp, Holger, Laux-Biehlmann, Alexis, Lowy, Ernesto, Lunter, Gerton, Malzahn, Jessica, Martin, Nicholas G., Martinez, Fernando O., Manek, Sanjiv, Mesch, Stefanie, Montgomery, Grant W., Morris, Andrew P., Nagel, Jens, Simmons, Heather A., Brocklebank, Denise, Shang, Catherine, Treloar, Susan, Wells, Graham, Becker, Christian M., Oppermann, Udo ... Zondervan, Krina T. (2021). Neuropeptide S receptor 1 is a nonhormonal treatment target in endometriosis. Science Translational Medicine, 13 (608) eabd6469, 1-12. doi: 10.1126/scitranslmed.abd6469
Mitchell, Brittany L., Thorp, Jackson G., Wu, Yeda, Campos, Adrian I., Nyholt, Dale R., Gordon, Scott D., Whiteman, David C., Olsen, Catherine M., Hickie, Ian B., Martin, Nicholas G., Medland, Sarah E., Wray, Naomi R. and Byrne, Enda M. (2021). Polygenic risk scores derived from varying definitions of depression and risk of depression. JAMA Psychiatry, 78 (10), 1152-1160. doi: 10.1001/jamapsychiatry.2021.1988
Hemani, Gibran, Powell, Joseph E., Wang, Huanwei, Shakhbazov, Konstantin, Westra, Harm-Jan, Esko, Tonu, Henders, Anjali K., McRae, Allan F., Martin, Nicholas G., Metspalu, Andres, Franke, Lude, Montgomery, Grant W., Goddard, Michael E., Gibson, Greg, Yang, Jian and Visscher, Peter M. (2021). Phantom epistasis between unlinked loci. Nature, 596 (7871), E1-E3. doi: 10.1038/s41586-021-03765-z
Ruth, Katherine S., Day, Felix R., Hussain, Jazib, Martínez-Marchal, Ana, Aiken, Catherine E., Azad, Ajuna, Thompson, Deborah J., Knoblochova, Lucie, Abe, Hironori, Tarry-Adkins, Jane L., Gonzalez, Javier Martin, Fontanillas, Pierre, Claringbould, Annique, Bakker, Olivier B., Sulem, Patrick, Walters, Robin G., Terao, Chikashi, Turon, Sandra, Horikoshi, Momoko, Lin, Kuang, Onland-Moret, N. Charlotte, Sankar, Aditya, Hertz, Emil Peter Thrane, Timshel, Pascal N., Shukla, Vallari, Borup, Rehannah, Olsen, Kristina W., Aguilera, Paula, Ferrer-Roda, Mònica ... Perry, John R. B. (2021). Genetic insights into biological mechanisms governing human ovarian ageing. Nature, 596 (7872), 393-397. doi: 10.1038/s41586-021-03779-7
Campos, Adrian I., Kho, Pik, Vazquez-Prada, Karla X., García-Marín, Luis M., Martin, Nicholas G., Cuéllar-Partida, Gabriel and Rentería, Miguel E. (2021). Genetic susceptibility to pneumonia: a GWAS meta-analysis between the UK Biobank and FinnGen. Twin Research and Human Genetics, 24 (3) PII S183242742100027X, 145-154. doi: 10.1017/thg.2021.27
Ip, Hill F., van der Laan, Camiel M., Krapohl, Eva M. L., Brikell, Isabell, Sánchez-Mora, Cristina, Nolte, Ilja M., St Pourcain, Beate, Bolhuis, Koen, Palviainen, Teemu, Zafarmand, Hadi, Colodro-Conde, Lucía, Gordon, Scott, Zayats, Tetyana, Aliev, Fazil, Jiang, Chang, Wang, Carol A., Saunders, Gretchen, Karhunen, Ville, Hammerschlag, Anke R., Adkins, Daniel E., Border, Richard, Peterson, Roseann E., Prinz, Joseph A., Thiering, Elisabeth, Seppälä, Ilkka, Vilor-Tejedor, Natàlia, Ahluwalia, Tarunveer S., Day, Felix R., Hottenga, Jouke-Jan ... Boomsma, Dorret I. (2021). Genetic association study of childhood aggression across raters, instruments, and age. Translational Psychiatry, 11 (1) 413, 413. doi: 10.1038/s41398-021-01480-x
Campos, Adrián I., Ngo, Trung Thanh, Medland, Sarah E., Wray, Naomi R., Hickie, Ian B., Byrne, Enda M., Martin, Nicholas G. and Rentería, Miguel E. (2021). Genetic risk for chronic pain is associated with lower antidepressant effectiveness: converging evidence for a depression subtype. Australian and New Zealand Journal of Psychiatry, 56 (9) ARTN 00048674211031491, 1-10. doi: 10.1177/00048674211031491
Fieder, Martin, Mitchell, Brittany L., Gordon, Scott, Huber, Susanne and Martin, Nicholas G. (2021). Ethnic Identity and Genome Wide Runs of Homozygosity. Behavior Genetics, 51 (4), 405-413. doi: 10.1007/s10519-021-10053-z
Bainomugisa, Charlotte K., Sutherland, Heidi G., Parker, Richard, Mcrae, Allan F., Haupt, Larisa M., Griffiths, Lyn R., Heath, Andrew, Nelson, Elliot C., Wright, Margaret J., Hickie, Ian B., Martin, Nicholas G., Nyholt, Dale R. and Mehta, Divya (2021). Using monozygotic twins to dissect common genes in posttraumatic stress disorder and migraine. Frontiers in Neuroscience, 15 678350, 678350. doi: 10.3389/fnins.2021.678350
Mullins, Niamh, Forstner, Andreas J., O'Connell, Kevin S., Coombes, Brandon, Coleman, Jonathan R I, Qiao, Zhen, Als, Thomas D., Bigdeli, Tim B., Børte, Sigrid, Bryois, Julien, Charney, Alexander W., Drange, Ole Kristian, Gandal, Michael J., Hagenaars, Saskia P., Ikeda, Masashi, Kamitaki, Nolan, Kim, Minsoo, Krebs, Kristi, Panagiotaropoulou, Georgia, Schilder, Brian M., Sloofman, Laura G., Steinberg, Stacy, Trubetskoy, Vassily, Winsvold, Bendik S., Won, Hong-Hee, Abramova, Liliya, Adorjan, Kristina, Agerbo, Esben, Al Eissa, Mariam ... Andreassen, Ole A. (2021). Genome-wide association study of more than 40,000 bipolar disorder cases provides new insights into the underlying biology. Nature genetics, 53 (6), 817-829. doi: 10.1038/s41588-021-00857-4
Scott, Jan, Crouse, Jacob J., Ho, Nicholas, Iorfino, Frank, Martin, Nicholas, Parker, Richard, McGrath, John, Gillespie, Nathan A., Medland, Sarah and Hickie, Ian B. (2021). Early expressions of psychopathology and risk associated with trans-diagnostic transition to mood and psychotic disorders in adolescents and young adults. PLoS ONE, 16 (6 June) e0252550, 1-17. doi: 10.1371/journal.pone.0252550
García-Marín, Luis M., Campos, Adrián I., Kho, Pik-Fang, Martin, Nicholas G., Cuéllar-Partida, Gabriel and Rentería, Miguel E. (2021). Phenome-wide screening of GWAS data reveals the complex causal architecture of obesity. Human Genetics, 140 (8), 1253-1265. doi: 10.1007/s00439-021-02298-9
Hwang, Liang-Dar, Mitchell, Brittany L., Medland, Sarah E., Martin, Nicholas G., Neale, Michael C. and Evans, David M. (2021). Correction to: The augmented Classical Twin Design: incorporating genome‐wide identity by descent sharing into twin studies in order to model violations of the equal environments assumption. Behavior Genetics, 51 (4), 441-442. doi: 10.1007/s10519-021-10065-9
Crouse, Jacob J., Ho, Nicholas, Scott, Jan, Martin, Nicholas G., Couvy-Duchesne, Baptiste, Hermens, Daniel F., Parker, Richard, Gillespie, Nathan A., Medland, Sarah E. and Hickie, Ian B. (2021). Days out of role and somatic, anxious-depressive, hypo-manic, and psychotic-like symptom dimensions in a community sample of young adults. Translational Psychiatry, 11 (1) 285, 285. doi: 10.1038/s41398-021-01390-y
Garvert, Linda, Baune, Bernhard T, Berger, Klaus, Boomsma, Dorret I, Breen, Gerome, Greinacher, Andreas, Hamilton, Steven P, Levinson, Douglas F, Lewis, Cathryn M, Lucae, Susanne, Magnusson, Patrik K E, Martin, Nicholas G, McIntosh, Andrew M, Mors, Ole, Müller-Myhsok, Bertram, Penninx, Brenda W J H, Perlis, Roy H, Pistis, Giorgio, Potash, James B, Preisig, Martin, Rietschel, Marcella, Shi, Jianxin, Smoller, Jordan W, Tiemeier, Henning, Uher, Rudolf, Völker, Uwe, Völzke, Henry, Weissman, Myrna M, Grabe, Hans J and Van der Auwera, Sandra (2021). The association between genetically determined ABO blood types and major depressive disorder. Psychiatry Research, 299 113837, 113837. doi: 10.1016/j.psychres.2021.113837
Dash, Genevieve F., Martin, Nicholas G., Agrawal, Arpana, Lynskey, Michael T. and Slutske, Wendy S. (2021). Typologies of illicit drug use in mid-adulthood: a quasi-longitudinal latent class analysis in a community-based sample of twins. Addiction, 116 (5), 1101-1112. doi: 10.1111/add.15225
Lafontaine, Nicole, Campbell, Purdey J., Castillo-Fernandez, Juan E., Mullin, Shelby, Lim, Ee Mun, Kendrew, Phillip, Lewer, Michelle, Brown, Suzanne J., Huang, Rae-Chi, Melton, Phillip E., Mori, Trevor A., Beilin, Lawrence J., Dudbridge, Frank, Spector, Tim D., Wright, Margaret J., Martin, Nicholas G., McRae, Allan F., Panicker, Vijay, Zhu, Gu, Walsh, John P., Bell, Jordana T. and Wilson, Scott G. (2021). Epigenome-wide association study of thyroid function traits identifies novel associations of fT3 with KLF9 and DOT1L. The Journal of Clinical Endocrinology and Metabolism, 106 (5), e2191-e2202. doi: 10.1210/clinem/dgaa975
Thorp, Jackson G., Campos, Adrian I., Grotzinger, Andrew D., Gerring, Zachary F., An, Jiyuan, Ong, Jue-Sheng, Wang, Wei, Shringarpure, Suyash, Byrne, Enda M., MacGregor, Stuart, Martin, Nicholas G., Medland, Sarah E., Middeldorp, Christel M. and Derks, Eske M. (2021). Symptom-level modelling unravels the shared genetic architecture of anxiety and depression. Nature Human Behaviour, 5 (10), 1432-1442. doi: 10.1038/s41562-021-01094-9
Roughan, William H., Campos, Adrián I., García-Marín, Luis M., Cuéllar-Partida, Gabriel, Lupton, Michelle K., Hickie, Ian B., Medland, Sarah E., Wray, Naomi R., Byrne, Enda M., Ngo, Trung Thanh, Martin, Nicholas G. and Rentería, Miguel E. (2021). Comorbid chronic pain and depression: shared risk factors and differential antidepressant effectiveness. Frontiers in Psychiatry, 12 643609, 1-13. doi: 10.3389/fpsyt.2021.643609
Loesch, Danuta Z., Duffy, David L., Martin, Nicholas G., Tassone, Flora, Atkinson, Anna and Storey, Elsdon (2021). 'Essential Tremor' Phenotype in FMR1 Premutation/Gray Zone Sibling Series: Exploring Possible Genetic Modifiers. Twin Research and Human Genetics, 24 (2), 95-102. doi: 10.1017/thg.2021.10
Simcoe, Mark, Valdes, Ana, Liu, Fan, Furlotte, Nicholas A., Evans, David M., Hemani, Gibran, Ring, Susan M., Smith, George Davey, Duffy, David L., Zhu, Gu, Gordon, Scott D., Medland, Sarah E., Vuckovic, Dragana, Girotto, Giorgia, Sala, Cinzia, Catamo, Eulalia, Concas, Maria Pina, Brumat, Marco, Gasparini, Paolo, Toniolo, Daniela, Cocca, Massimiliano, Robino, Antonietta, Yazar, Seyhan, Hewitt, Alex, Wu, Wenting, Kraft, Peter, Hammond, Christopher J., Shi, Yuan, Chen, Yan ... the International Visible Trait Genetics Consortium (2021). Genome-wide association study in almost 195,000 individuals identifies 50 previously unidentified genetic loci for eye color. Science Advances, 7 (11) abd1239, eabd1239. doi: 10.1126/sciadv.abd1239
Campos, Adrian I., Thompson, Paul M., Veltman, Dick J., Pozzi, Elena, van Veltzen, Laura S., Jahanshad, Neda, Adams, Mark J., Baune, Bernhard T., Berger, Klaus, Brosch, Katharina, Bülow, Robin, Connolly, Colm G., Dannlowski, Udo, Davey, Christopher G., de Zubicaray, Greig I., Dima, Danai, Erwin-Grabner, Tracy, Evans, Jennifer W., Fu, Cynthia H.Y., Gotlib, Ian H., Goya-Maldonado, Roberto, Grabe, Hans J., Grotegerd, Dominik, Harris, Matthew A., Harrison, Ben J., Hatton, Sean N., Hermesdorf, Marco, Hickie, Ian B., Ho, Tiffany C. ... Rentería, Miguel E. (2021). Brain correlates of suicide attempt in 18,925 participants across 18 international cohorts. Biological Psychiatry, 90 (4), 243-252. doi: 10.1016/j.biopsych.2021.03.015
Sherva, Richard, Zhu, Congcong, Wetherill, Leah, Edenberg, Howard J., Johnson, Emma, Degenhardt, Louisa, Agrawal, Arpana, Martin, Nicholas G., Nelson, Elliot, Kranzler, Henry R., Gelernter, Joel and Farrer, Lindsay A. (2021). Genome-wide association study of phenotypes measuring progression from first cocaine or opioid use to dependence reveals novel risk genes. Exploration of Medicine, 2 (1), 60-73. doi: 10.37349/emed.2021.00032
Scott, Jan, Crouse, Jacob J., Ho, Nicholas, Carpenter, Joanne, Martin, Nicholas, Medland, Sarah, Parker, Richard, Byrne, Enda, Couvy-Duchesne, Baptiste, Mitchell, Brittany, Merikangas, Kathleen, Gillespie, Nathan A. and Hickie, Ian (2021). Can network analysis of self-reported psychopathology shed light on the core phenomenology of bipolar disorders in adolescents and young adults?. Bipolar Disorders, 23 (6), 584-594. doi: 10.1111/bdi.13067
Gharahkhani, Puya, NEIGHBORHOOD consortium, Jorgenson, Eric, Hysi, Pirro, Khawaja, Anthony P., Pendergrass, Sarah, Han, Xikun, Ong, Jue Sheng, Hewitt, Alex W., Segrè, Ayellet V., Rouhana, John M., Hamel, Andrew R., Igo, Robert P., Choquet, Helene, Qassim, Ayub, Josyula, Navya S., Cooke Bailey, Jessica N., Bonnemaijer, Pieter W. M., Iglesias, Adriana, Siggs, Owen M., Young, Terri L., Vitart, Veronique, Thiadens, Alberta A. H. J., Karjalainen, Juha, Uebe, Steffen, Melles, Ronald B., Nair, K. Saidas, Luben, Robert, Simcoe, Mark ... 23 and Me Research Team (2021). Genome-wide meta-analysis identifies 127 open-angle glaucoma loci with consistent effect across ancestries. Nature Communications, 12 (1) 1258, 1-16. doi: 10.1038/s41467-020-20851-4
Frangou, Sophia, Modabbernia, Amirhossein, Williams, Steven C. R., Papachristou, Efstathios, Doucet, Gaelle E., Agartz, Ingrid, Aghajani, Moji, Akudjedu, Theophilus N., Albajes-Eizagirre, Anton, Alnaes, Dag, Alpert, Kathryn I, Andersson, Micael, Andreasen, Nancy C, Andreassen, Ole A, Asherson, Philip, Banaschewski, Tobias, Bargallo, Nuria, Baumeister, Sarah, Baur-Streubel, Ramona, Bertolino, Alessandro, Bonvino, Aurora, Boomsma, Dorret I, Borgwardt, Stefan, Bourque, Josiane, Brandeis, Daniel, Breier, Alan, Brodaty, Henry, Brouwer, Rachel M, Buitelaar, Jan K ... Dima, Danai (2021). Cortical thickness across the lifespan: Data from 17,075 healthy individuals aged 3-90 years. Human Brain Mapping, 43 (1) hbm.25364, 431-451. doi: 10.1002/hbm.25364
Hwang, Liang-Dar, Mitchell, Brittany L., Medland, Sarah E., Martin, Nicholas G., Neale, Michael C. and Evans, David M. (2021). The augmented Classical Twin Design: incorporating genome‐wide identity by descent sharing into twin studies in order to model violations of the equal environments assumption. Behavior Genetics, 51 (3), 223-236. doi: 10.1007/s10519-021-10044-0
Dima, Danai, Modabbernia, Amirhossein, Papachristou, Efstathios, Doucet, Gaelle E., Agartz, Ingrid, Aghajani, Moji, Akudjedu, Theophilus N., Albajes-Eizagirre, Anton, Alnaes, Dag, Alpert, Kathryn I., Andersson, Micael, Andreasen, Nancy C., Andreassen, Ole A., Asherson, Philip, Banaschewski, Tobias, Bargallo, Nuria, Baumeister, Sarah, Baur-Streubel, Ramona, Bertolino, Alessandro, Bonvino, Aurora, Boomsma, Dorret I., Borgwardt, Stefan, Bourque, Josiane, Brandeis, Daniel, Breier, Alan, Brodaty, Henry, Brouwer, Rachel M., Buitelaar, Jan K., Busatto, Geraldo F. ... Karolinska Schizophrenia Project (KaSP) (2021). Subcortical volumes across the lifespan: Data from 18,605 healthy individuals aged 3-90 years. Human Brain Mapping, 43 (1) hbm.25320, 452-469. doi: 10.1002/hbm.25320
Mitchell, Brittany L., Kirk, Katherine M., McAloney, Kerrie, Wright, Margaret J., Davenport, Tracey A., Hermens, Daniel F., Scott, James G., McGrath, John J., Gillespie, Nathan A., Carpenter, Joanne S., O’Callaghan, Victoria S., Medland, Sarah, Christensen, Helen, Martin, Nicholas G., Burns, Jane M. and Hickie, Ian B. (2021). 16Up: Outline of a study investigating wellbeing and information and communication technology use in adolescent twins. Twin Research and Human Genetics, 23 (6) PII S1832427420000833, 1-13. doi: 10.1017/thg.2020.83
Whitfield, John B., Colodro-Conde, Lucía, Timmers, Paul R. H. J., Joshi, Peter K., Montgomery, Grant W. and Martin, Nicholas G. (2021). Comparison of Familial, Polygenic and Biochemical Predictors of Mortality. Twin Research and Human Genetics, 23 (6), 307-315. doi: 10.1017/thg.2020.89
Dash, Genevieve F., Martin, Nicholas G., Agrawal, Arpana, Lynskey, Michael T. and Slutske, Wendy S. (2021). Are prescription misuse and illicit drug use etiologically distinct? A genetically-informed analysis of opioids and stimulants. Psychological Medicine, 52 (14), 3176-3183. doi: 10.1017/S0033291720005267
García-Marín, Luis M., Campos, Adrián I., Martin, Nicholas G., Cuéllar-Partida, Gabriel and Rentería, Miguel E. (2021). Inference of causal relationships between sleep-related traits and 1,527 phenotypes using genetic data. Sleep, 44 (1) zsaa154. doi: 10.1093/sleep/zsaa154
Li, Zhixiu, Wu, Xin, Leo, Paul J., De Guzman, Erika, Akkoc, Nurullah, Breban, Maxime, MacFarlane, Gary J., Mahmoudi, Mahdi, Marzo-Ortega, Helena, Anderson, Lisa K., Wheeler, Lawrie, Chou, Chung-Tei, Harrison, Andrew A., Stebbings, Simon, Jones, Gareth T., Bang, So-Young, Wang, Geng, Jamshidi, Ahmadreza, Farhadi, Elham, Song, Jing, Lin, Li, Li, Mengmeng, Wei, James Cheng-Chung, Martin, Nicholas G., Wright, Margaret J., Lee, MinJae, Wang, Yuqin, Zhan, Jian, Zhang, Jin-San ... Brown, Matthew A (2021). Polygenic Risk Scores have high diagnostic capacity in ankylosing spondylitis. Annals of the Rheumatic Diseases, 80 (9) annrheumdis-2020- 219446, annrheumdis-2020. doi: 10.1136/annrheumdis-2020-219446
Van Dongen, Jenny, Gordon, Scott D., Odintsova, Veronika V., McRae, Allan F., Robinson, Wendy P., Hall, Judith G., Boomsma, Dorret I. and Martin, Nicholas G. (2021). Examining the Vanishing Twin Hypothesis of Neural Tube Defects: Application of an Epigenetic Predictor for Monozygotic Twinning. Twin Research and Human Genetics, 24 (3) PII S1832427421000256, 155-159. doi: 10.1017/thg.2021.25
Medland, Sarah E., Grasby, Katrina L., Jahanshad, Neda, Painter, Jodie N., Colodro-Conde, Lucía, Bralten, Janita, Hibar, Derrek P., Lind, Penelope A., Pizzagalli, Fabrizio, Thomopoulos, Sophia I., Stein, Jason L., Franke, Barbara, Martin, Nicholas G. and Thompson, Paul M. (2020). Ten years of enhancing neuro-imaging genetics through meta-analysis: an overview from the ENIGMA Genetics Working Group. Human Brain Mapping, 43 (1), 292-299. doi: 10.1002/hbm.25311
Silventoinen, Karri, Jelenkovic, Aline, Sund, Reijo, Latvala, Antti, Honda, Chika, Inui, Fujio, Tomizawa, Rie, Watanabe, Mikio, Sakai, Norio, Rebato, Esther, Busjahn, Andreas, Tyler, Jessica, Hopper, John L., Ordoñana, Juan R., Sánchez-Romera, Juan F., Colodro-Conde, Lucia, Calais-Ferreira, Lucas, Oliveira, Vinicius C., Ferreira, Paulo H., Medda, Emanuela, Nisticò, Lorenza, Toccaceli, Virgilia, Derom, Catherine A., Vlietinck, Robert F., Loos, Ruth J. F., Siribaddana, Sisira H., Hotopf, Matthew, Sumathipala, Athula, Rijsdijk, Fruhling ... Kaprio, Jaakko (2020). Genetic and environmental variation in educational attainment: an individual-based analysis of 28 twin cohorts. Scientific Reports, 10 (1) 12681, 12681. doi: 10.1038/s41598-020-69526-6
Laisk, Triin, Soares, Ana Luiza G., Ferreira, Teresa, Painter, Jodie N., Censin, Jenny C., Laber, Samantha, Bacelis, Jonas, Chen, Chia-Yen, Lepamets, Maarja, Lin, Kuang, Liu, Siyang, Millwood, Iona Y., Ramu, Avinash, Southcombe, Jennifer, Andersen, Marianne S., Yang, Ling, Becker, Christian M., Børglum, Anders D., Gordon, Scott D., Bybjerg-Grauholm, Jonas, Helgeland, Øyvind, Hougaard, David M., Jin, Xin, Johansson, Stefan, Juodakis, Julius, Kartsonaki, Christiana, Kukushkina, Viktorija, Lind, Penelope A., Metspalu, Andres ... Lindgren, Cecilia M. (2020). The genetic architecture of sporadic and multiple consecutive miscarriage. Nature Communications, 11 (1) 5980, 1-12. doi: 10.1038/s41467-020-19742-5
Guo, Yanjun, Rist, Pamela M., Daghlas, Iyas, Giulianini, Franco, Gormley, Padhraig, Anttila, Verneri, Winsvold, Bendik S., Palta, Priit, Esko, Tonu, Pers, Tune H., Farh, Kai-How, Cuenca-Leon, Ester, Muona, Mikko, Furlotte, Nicholas A., Kurth, Tobias, Ingason, Andres, McMahon, George, Ligthart, Lannie, Terwindt, Gisela M., Kallela, Mikko, Freilinger, Tobias M., Ran, Caroline, Gordon, Scott G., Stam, Anine H., Steinberg, Stacy, Borck, Guntram, Koiranen, Markku, Quaye, Lydia, Adams, Hieab H. H. ... Chasman, Daniel I. (2020). A genome-wide cross-phenotype meta-analysis of the association of blood pressure with migraine. Nature Communications, 11 (1) 3368. doi: 10.1038/s41467-020-17002-0
Lupton, Michelle K., Robinson, Gail A., Adam, Robert J, Rose, Stephen, Byrne, Gerard J., Salvado, Olivier, Pachana, Nancy A., Almeida, Osvaldo P., McAloney, Kerrie, Gordon, Scott D., Raniga, Parnesh, Fazlollahi, Amir, Xia, Ying, Ceslis, Amelia, Sonkusare, Saurabh, Zhang, Qing, Kholghi, Mahnoosh, Karunanithi, Mohan, Mosley, Philip E., Lv, Jinglei, Borne, Léonie, Adsett, Jessica, Garden, Natalie, Fripp, Jurgen, Martin, Nicholas G., Guo, Christine C. and Breakspear, Michael (2020). A prospective cohort study of prodromal Alzheimer’s disease: Prospective Imaging Study of Ageing: genes, brain and behaviour (PISA). NeuroImage: Clinical, 29 102527, 102527. doi: 10.1016/j.nicl.2020.102527
Whitfield, John B., Zhu, Gu, Landers, J. George and Martin, Nicholas G. (2020). Pessimism is associated with greater all-cause and cardiovascular mortality, but optimism is not protective. Scientific Reports, 10 (1) 12609, 1-7. doi: 10.1038/s41598-020-69388-y
Trevisan, Rodrigo, Pérez, Osvaldo, Schmitz, Nathan, Diers, Brian and Martin, Nicolas (2020). High-throughput phenotyping of soybean maturity using time series UAV imagery and convolutional neural networks. Remote Sensing, 12 (21) 3617, 1-19. doi: 10.3390/rs12213617
Xue, Sen, Kidd, Michael P., Le, Anh.T., Kirk, Kathy and Martin, Nicholas G. (2020). The role of locus of control in adulthood outcomes: Evidence from Australian twins. Journal of Economic Behavior and Organization, 179, 566-588. doi: 10.1016/j.jebo.2020.09.018
Ho, Yvonne Y. W., Mina-Vargas, Angela, Zhu, Gu, Brims, Mark, Mcnevin, Dennis, Montgomery, Grant W., Martin, Nicholas G., Medland, Sarah E. and Painter, Jodie N. (2020). Comparison of genome-wide association scans for quantitative and observational measures of human hair curvature. Twin Research and Human Genetics, 23 (5) PII S183242742000078X, 271-277. doi: 10.1017/thg.2020.78
Dash, Genevieve F., Martin, Nicholas G., Lynskey, Michael T. and Slutske, Wendy S. (2020). Sex differences in the relative influence of marital status and parenthood on alcohol use disorder symptoms: a multilevel discordant twin design. Journal of Abnormal Psychology, 129 (7), 737-747. doi: 10.1037/abn0000611
Erzurumluoglu, A. Mesut, Liu, Mengzhen, Jackson, Victoria E., Barnes, Daniel R., Datta, Gargi, Melbourne, Carl A., Young, Robin, Batini, Chiara, Surendran, Praveen, Jiang, Tao, Adnan, Sheikh Daud, Afaq, Saima, Agrawal, Arpana, Altmaier, Elisabeth, Antoniou, Antonis C., Asselbergs, Folkert W., Baumbach, Clemens, Bierut, Laura, Bertelsen, Sarah, Boehnke, Michael, Bots, Michiel L., Brazel, David M, Chambers, John C., Chang-Claude, Jenny, Chen, Chu, Corley, Janie, Chou, Yi-Ling, David, Sean P., de Boer, Rudolf A. ... CHD Exome+ consortium (2020). Meta-analysis of up to 622,409 individuals identifies 40 novel smoking behaviour associated genetic loci. Molecular Psychiatry, 25 (10), 2392-2409. doi: 10.1038/s41380-018-0313-0
Cuellar-Partida, Gabriel, Tung, Joyce Y., Eriksson, Nicholas, Albrecht, Eva, Aliev, Fazil, Andreassen, Ole A., Barroso, Inês, Beckmann, Jacques S., Boks, Marco P., Boomsma, Dorret I., Boyd, Heather A., Breteler, Monique M. B., Campbell, Harry, Chasman, Daniel I., Cherkas, Lynn F., Davies, Gail, de Geus, Eco J. C., Deary, Ian J., Deloukas, Panos, Dick, Danielle M., Duffy, David L., Eriksson, Johan G., Esko, Tõnu, Feenstra, Bjarke, Geller, Frank, Gieger, Christian, Giegling, Ina, Gordon, Scott D., Han, Jiali ... Medland, Sarah E. (2020). Genome-wide association study identifies 48 common genetic variants associated with handedness. Nature Human Behaviour, 5 (1), 59-70. doi: 10.1038/s41562-020-00956-y
Pizzagalli, Fabrizio, Auzias, Guillaume, Yang, Qifan, Mathias, Samuel R., Faskowitz, Joshua, Boyd, Joshua D., Amini, Armand, Rivière, Denis, McMahon, Katie L., de Zubicaray, Greig I., Martin, Nicholas G., Mangin, Jean-François, Glahn, David C., Blangero, John, Wright, Margaret J., Thompson, Paul M., Kochunov, Peter and Jahanshad, Neda (2020). The reliability and heritability of cortical folds and their genetic correlations across hemispheres. Communications Biology, 3 (1) 510, 510. doi: 10.1038/s42003-020-01163-1
Schermer, Julie Aitken, Colodro-Conde, Lucía, Grasby, Katrina L., Hickie, Ian B., Burns, Jane, Ligthart, Lannie, Willemsen, Gonneke, Trull, Timothy J., Martin, Nicholas G. and Boomsma, Dorret I. (2020). Genetic and environmental causes of individual differences in borderline personality disorder features and loneliness are partially shared. Twin Research and Human Genetics, 23 (4) PII S1832427420000626, 214-220. doi: 10.1017/thg.2020.62
D'Urso, Shannon, Rajbhandari, Dorrilyn, Peach, Elizabeth, De Guzman, Erika, Li, Qiang, Medland, Sarah E., Gordon, Scott D., Martin, Nicholas G., Ligthart, Symen, Brown, Matthew A., Powell, Joseph, McArthur, Colin, Rhodes, Andrew, Meyer, Jason, Finfer, Simon, Myburgh, John, Blumenthal, Antje, Cohen, Jeremy, Venkatesh, Balasubramanian, Cuellar-Partida, Gabriel and Evans, David M. (2020). Septic shock: a genomewide association study and polygenic risk score analysis. Twin Research and Human Genetics, 23 (4) PII S1832427420000602, 204-213. doi: 10.1017/thg.2020.60
Hagenaars, Saskia P., Coleman, Jonathan R. I., Choi, Shing Wan, Gaspar, Héléna, Adams, Mark J., Howard, David M., Hodgson, Karen, Traylor, Matthew, Air, Tracy M., Andlauer, Till F. M., Arolt, Volker, Baune, Bernhard T., Binder, Elisabeth B., Blackwood, Douglas H. R., Boomsma, Dorret I., Campbell, Archie, Cearns, Micah, Czamara, Darina, Dannlowski, Udo, Domschke, Katharina, de Geus, Eco J. C., Hamilton, Steven P., Hayward, Caroline, Hickie, Ian B., Hottenga, Jouke Jan, Ising, Marcus, Jones, Ian, Jones, Lisa, Kutalik, Zoltan ... Lewis, Cathryn M. (2020). Genetic comorbidity between major depression and cardio‐metabolic traits, stratified by age at onset of major depression. American Journal of Medical Genetics Part B: Neuropsychiatric Genetics, 183 (6) ajmg.b.32807, 309-330. doi: 10.1002/ajmg.b.32807
Campos, Adrian I., Verweij, Karin J. H., Statham, Dixie J., Madden, Pamela A. F., Maciejewski, Dominique F., Davis, Katrina A. S., John, Ann, Hotopf, Matthew, Heath, Andrew C., Martin, Nicholas G. and Rentería, Miguel E. (2020). Genetic aetiology of self-harm ideation and behaviour. Scientific Reports, 10 (1) 9713, 9713. doi: 10.1038/s41598-020-66737-9
Karagiannis, Tanya T., Cleary, John P., Gok, Busra, Henderson, Andrew J., Martin, Nicholas G., Yajima, Masanao, Nelson, Elliot C. and Cheng, Christine S. (2020). Single cell transcriptomics reveals opioid usage evokes widespread suppression of antiviral gene program. Nature Communications, 11 (1) 2611, 2611. doi: 10.1038/s41467-020-16159-y
Byrne, Enda M., Kirk, Katherine M., Medland, Sarah E., McGrath, John J., Colodro-Conde, Lucia, Parker, Richard, Cross, Simone, Sullivan, Lenore, Statham, Dixie J., Levinson, Douglas F., Licinio, Julio, Wray, Naomi R, Hickie, Ian B. and Martin, Nicholas G. (2020). Cohort profile: the Australian genetics of depression study. BMJ Open, 10 (5) e032580, e032580. doi: 10.1136/bmjopen-2019-032580
Mitchell, Brittany L., Cuéllar-Partida, Gabriel, Grasby, Katrina L., Campos, Adrian I., Strike, Lachlan T., Hwang, Liang-Dar, Okbay, Aysu, Thompson, Paul M., Medland, Sarah E., Martin, Nicholas G., Wright, Margaret J. and Rentería, Miguel E. (2020). Educational attainment polygenic scores are associated with cortical total surface area and regions important for language and memory. NeuroImage, 212 116691, 116691. doi: 10.1016/j.neuroimage.2020.116691
Chang, Lun-Hsien, Ong, Jue-Sheng, An, Jiyuan, Verweij, Karin J.H., Vink, Jacqueline M., Pasman, Joëlle, Liu, Mengzhen, MacGregor, Stuart, Cornelis, Marilyn C., Martin, Nicholas G. and Derks, Eske M. (2020). Investigating the genetic and causal relationship between initiation or use of alcohol, caffeine, cannabis and nicotine. Drug and Alcohol Dependence, 210 107966, 107966. doi: 10.1016/j.drugalcdep.2020.107966
Landi, Maria Teresa, GenoMEL Consortium, Bishop, D. Timothy, MacGregor, Stuart, Machiela, Mitchell J., Stratigos, Alexander J., Ghiorzo, Paola, Brossard, Myriam, Calista, Donato, Choi, Jiyeon, Fargnoli, Maria Concetta, Zhang, Tongwu, Rodolfo, Monica, Trower, Adam J., Menin, Chiara, Martinez, Jacobo, Hadjisavvas, Andreas, Song, Lei, Stefanaki, Irene, Scolyer, Richard, Yang, Rose, Goldstein, Alisa M., Potrony, Miriam, Kypreou, Katerina P., Pastorino, Lorenza, Queirolo, Paola, Pellegrini, Cristina, Cattaneo, Laura, Zawistowski, Matthew ... MelaNostrum Consortium (2020). Genome-wide association meta-analyses combining multiple risk phenotypes provide insights into the genetic architecture of cutaneous melanoma susceptibility. Nature Genetics, 52 (5), 494-504. doi: 10.1038/s41588-020-0611-8
Revez, Joana A., Lin, Tian, Qiao, Zhen, Xue, Angli, Holtz, Yan, Zhu, Zhihong, Zeng, Jian, Wang, Huanwei, Sidorenko, Julia, Kemper, Kathryn E., Vinkhuyzen, Anna A. E., Frater, Julanne, Eyles, Darryl, Burne, Thomas H. J., Mitchell, Brittany, Martin, Nicholas G., Zhu, Gu, Visscher, Peter M., Yang, Jian, Wray, Naomi R. and McGrath, John J. (2020). Genome-wide association study identifies 143 loci associated with 25 hydroxyvitamin D concentration. Nature Communications, 11 (1) 1647, 1-12. doi: 10.1038/s41467-020-15421-7
Campbell, Purdey J., Brown, Suzanne J., Kendrew, Phillip, Lewer, Michelle, Lim, Ee Mun, Joseph, John, Cross, Simone M., Wright, Margaret J., Martin, Nicholas G., Wilson, Scott G. and Walsh, John P. (2020). Changes in thyroid function across adolescence: a longitudinal study. The Journal of Clinical Endocrinology and Metabolism, 105 (4) ARTN dgz331, e1162-e1170. doi: 10.1210/clinem/dgz331
Cai, Na, Revez, Joana A., Adams, Mark J., Andlauer, Till F. M., Breen, Gerome, Byrne, Enda M., Clarke, Toni-Kim, Forstner, Andreas J., Grabe, Hans J., Hamilton, Steven P., Levinson, Douglas F., Lewis, Cathryn M., Lewis, Glyn, Martin, Nicholas G., Milaneschi, Yuri, Mors, Ole, Müller-Myhsok, Bertram, Penninx, Brenda W. J. H., Perlis, Roy H., Pistis, Giorgio, Potash, James B., Preisig, Martin, Shi, Jianxin, Smoller, Jordan W., Streit, Fabien, Tiemeier, Henning, Uher, Rudolf, Van der Auwera, Sandra, Viktorin, Alexander ... Flint, Jonathan (2020). Minimal phenotyping yields genome-wide association signals of low specificity for major depression. Nature Genetics, 52 (4), 437-447. doi: 10.1038/s41588-020-0594-5
Grasby, Katrina L., Jahanshad, Neda, Painter, Jodie N., Colodro-Conde, Lucía, Bralten, Janita, Hibar, Derrek P., Lind, Penelope A., Pizzagalli, Fabrizio, Ching, Christopher R. K., McMahon, Mary Agnes B., Shatokhina, Natalia, Zsembik, Leo C. P., Thomopoulos, Sophia I., Zhu, Alyssa H., Strike, Lachlan T., Agartz, Ingrid, Alhusaini, Saud, Almeida, Marcio A. A., Alnæs, Dag, Amlien, Inge K., Andersson, Micael, Ard, Tyler, Armstrong, Nicola J., Ashley-Koch, Allison, Atkins, Joshua R., Bernard, Manon, Brouwer, Rachel M., Buimer, Elizabeth E. L., Bülow, Robin ... Medland, Sarah E. (2020). The genetic architecture of the human cerebral cortex. Science, 367 (6484) aay6690, 1-17. doi: 10.1126/science.aay6690
Fan, Qiao, Pozarickij, Alfred, Tan, Nicholas Y. Q., Guo, Xiaobo, Verhoeven, Virginie J. M., Vitart, Veronique, Guggenheim, Jeremy A., Miyake, Masahiro, Tideman, J. Willem L., Khawaja, Anthony P., Zhang, Liang, MacGregor, Stuart, Höhn, René, Chen, Peng, Biino, Ginevra, Wedenoja, Juho, Saffari, Seyed Ehsan, Tedja, Milly S., Xie, Jing, Lanca, Carla, Wang, Ya Xing, Sahebjada, Srujana, Mazur, Johanna, Mirshahi, Alireza, Martin, Nicholas G., Yazar, Seyhan, Pennell, Craig E., Yap, Maurice, Haarman, Annechien E. G. ... Evans, David M. (2020). Genome-wide association meta-analysis of corneal curvature identifies novel loci and shared genetic influences across axial length and refractive error. Communications Biology, 3 (1) 133, 133. doi: 10.1038/s42003-020-0802-y
Ong, Jue-Sheng, Hwang, Liang-Dar, Zhong, Victor W., An, Jiyuan, Gharahkhani, Puya, Breslin, Paul A. S., Wright, Margaret J., Lawlor, Deborah A., Whitfield, John, MacGregor, Stuart, Martin, Nicholas G. and Corneli, Marilyn C. (2020). Author Correction: Understanding the role of bitter taste perception in coffee, tea and alcohol consumption through Mendelian randomization. Scientific Reports, 10 (1) 4778, 4778. doi: 10.1038/s41598-020-60488-3
Buchwald, Jadwiga, Chenoweth, Meghan J., Palviainen, Teemu, Zhu, Gu, Benner, Christian, Gordon, Scott, Korhonen, Tellervo, Ripatti, Samuli, Madden, Pamela A. F., Lehtimäki, Terho, Raitakari, Olli T., Salomaa, Veikko, Rose, Richard J., George, Tony P., Lerman, Caryn, Pirinen, Matti, Martin, Nicholas G., Kaprio, Jaakko, Loukola, Anu and Tyndale, Rachel F. (2020). Genome-wide association meta-analysis of nicotine metabolism and cigarette consumption measures in smokers of European descent. Molecular Psychiatry, 26 (6), 2212-2223. doi: 10.1038/s41380-020-0702-z
Li, Chen, Stoma, Svetlana, Lotta, Luca A., Warner, Sophie, Albrecht, Eva, Allione, Alessandra, Arp, Pascal P., Broer, Linda, Buxton, Jessica L., Da Silva Couto Alves, Alexessander, Deelen, Joris, Fedko, Iryna O., Gordon, Scott D., Jiang, Tao, Karlsson, Robert, Kerrison, Nicola, Loe, Taylor K., Mangino, Massimo, Milaneschi, Yuri, Miraglio, Benjamin, Pervjakova, Natalia, Russo, Alessia, Surakka, Ida, van der Spek, Ashley, Verhoeven, Josine E., Amin, Najaf, Beekman, Marian, Blakemore, Alexandra I., Canzian, Federico ... Codd, Veryan (2020). Genome-wide association analysis in humans links nucleotide metabolism to Leukocyte Telomere Length. American Journal of Human Genetics, 106 (3), 389-404. doi: 10.1016/j.ajhg.2020.02.006
Taylor, Andrew, Catchpole, Anthony, Day, Martin P., Hill, Sarah, Martin, Nicholas and Patriarca, Marina (2020). Atomic spectrometry update: Review of advances in the analysis of clinical and biological materials, foods and beverages. Journal of Analytical Atomic Spectrometry, 35 (3), 426-454. doi: 10.1039/d0ja90005b
Polimanti, Renato, Walters, Raymond K., Johnson, Emma C., McClintick, Jeanette N., Adkins, Amy E., Adkins, Daniel E., Bacanu, Silviu-Alin, Bierut, Laura J., Bigdeli, Tim B., Brown, Sandra, Bucholz, Kathleen K., Copeland, William E., Costello, E. Jane, Degenhardt, Louisa, Farrer, Lindsay A, Foroud, Tatiana M., Fox, Louis, Goate, Alison M., Grucza, Richard, Hack, Laura M., Hancock, Dana B., Hartz, Sarah M., Heath, Andrew C., Hewitt, John K., Hopfer, Christian J., Johnson, Eric O., Kendler, Kenneth S., Kranzler, Henry R., Krauter, Kenneth ... Gelernter, Joel (2020). Leveraging genome-wide data to investigate differences between opioid use vs. opioid dependence in 41,176 individuals from the Psychiatric Genomics Consortium. Molecular Psychiatry, 25 (8), 1673-1687. doi: 10.1038/s41380-020-0677-9
Campos, Adrián I., García-Marín, Luis M., Byrne, Enda M., Martin, Nicholas G., Cuéllar-Partida, Gabriel and Rentería, Miguel E. (2020). Insights into the aetiology of snoring from observational and genetic investigations in the UK Biobank. Nature Communications, 11 (1) 817, 817. doi: 10.1038/s41467-020-14625-1
Duffy, David L., Jagirdar, Kasturee, Lee, Katie J., McWhirter, Seamus R., McMeniman, Erin K., De’Ambrosis, Brian, Pflugfelder, Annette, Rayner, Jenna E., Whiteman, David C., Brown, Matthew A., Martin, N.G., Smithers, B.M., Schaider, Helmut, Soyer, H. Peter and Sturm, Richard A. (2020). Genes determining nevus count and dermoscopic appearance in Australian melanoma cases and controls. Journal of Investigative Dermatology, 140 (2), 498-501.e17. doi: 10.1016/j.jid.2019.05.032
Dash, Genevieve F., Davis, Christal N., Martin, Nicholas G., Statham, Dixie J., Lynskey, Michael T. and Slutske, Wendy S. (2020). High-intensity drinking in adult Australian twins. Alcoholism: Clinical and Experimental Research, 44 (2), 522-531. doi: 10.1111/acer.14262
Doust, Catherine, Gordon, Scott D., Garden, Natalie, Fisher, Simon E., Martin, Nicholas G., Bates, Timothy C. and Luciano, Michelle (2020). The Association of Dyslexia and Developmental Speech and Language Disorder Candidate Genes with Reading and Language Abilities in Adults. Twin Research and Human Genetics, 23 (1), 23-32. doi: 10.1017/thg.2020.7
Craig, Jamie E., Han, Xikun, Qassim, Ayub, Hassall, Mark, Cooke Bailey, Jessica N., Kinzy, Tyler G., Khawaja, Anthony P., An, Jiyuan, Marshall, Henry, Gharahkhani, Puya, Igo, Robert P., Graham, Stuart L., Healey, Paul R., Ong, Jue-Sheng, Zhou, Tiger, Siggs, Owen, Law, Matthew H., Souzeau, Emmanuelle, Ridge, Bronwyn, Hysi, Pirro G., Burdon, Kathryn P., Mills, Richard A., Landers, John, Ruddle, Jonathan B., Agar, Ashish, Galanopoulos, Anna, White, Andrew J. R., Willoughby, Colin E., Andrew, Nicholas H. ... MacGregor, Stuart (2020). Multitrait analysis of glaucoma identifies new risk loci and enables polygenic prediction of disease susceptibility and progression. Nature Genetics, 52 (2), 160-166. doi: 10.1038/s41588-019-0556-y
Cox, Jiayi W., Sherva, Richard M., Lunetta, Kathryn L., Johnson, Emma C., Martin, Nicholas G., Degenhardt, Louisa, Agrawal, Arpana, Nelson, Elliot C., Kranzler, Henry R., Gelernter, Joel and Farrer, Lindsay A. (2020). Genome-wide association study of opioid cessation. Journal of Clinical Medicine, 9 (1) 180, 180. doi: 10.3390/jcm9010180
Munn-Chernoff, Melissa A., Johnson, Emma C., Chou, Yi-Ling, Coleman, Jonathan R.I., Thornton, Laura M., Walters, Raymond K., Yilmaz, Zeynep, Baker, Jessica H., Hübel, Christopher, Gordon, Scott, Medland, Sarah E., Watson, Hunna J., Gaspar, Héléna A., Bryois, Julien, Hinney, Anke, Leppä, Virpi M., Mattheisen, Manuel, Ripke, Stephan, Yao, Shuyang, Giusti-Rodríguez, Paola, Hanscombe, Ken B., Adan, Roger A.H., Alfredsson, Lars, Ando, Tetsuya, Andreassen, Ole A., Berrettini, Wade H., Boehm, Ilka, Boni, Claudette, Boraska Perica, Vesna ... Agrawal, Arpana (2020). Shared genetic risk between eating disorder- and substance-use-related phenotypes: evidence from genome-wide association studies. Addiction Biology, 26 (1) e12880, e12880. doi: 10.1111/adb.12880
Scott, Jan, Martin, Nicholas G., Parker, Richard, Couvy-Duchesne, Baptiste, Medland, Sarah E. and Hickie, Ian (2020). Prevalence of self-reported subthreshold phenotypes of major mental disorders and their association with functional impairment, treatment and full-threshold syndromes in a community-residing cohort of young adults. Early Intervention in Psychiatry, 15 (2) eip.12942, 306-313. doi: 10.1111/eip.12942
Mitchell, Brittany L., Thorp, Jackson G., Evans, David M., Nyholt, Dale R., Martin, Nicholas G. and Lupton, Michelle K. (2020). Exploring the genetic relationship between hearing impairment and Alzheimer's disease. Alzheimer's and Dementia: Diagnosis, Assessment and Disease Monitoring, 12 (1) e12108, 1-10. doi: 10.1002/dad2.12108
Swiatkowska, Ilona, Martin, Nicholas G., Henckel, Johann, Apthorp, Hugh, Hamshere, Jane and Hart, Alister J. (2020). Blood and plasma titanium levels associated with well-functioning hip implants. Journal of Trace Elements in Medicine and Biology, 57, 9-17. doi: 10.1016/j.jtemb.2019.09.005
Lee, Phil H., Anttila, Verneri, Won, Hyejung, Feng, Yen-Chen A., Rosenthal, Jacob, Zhu, Zhaozhong, Tucker-Drob, Elliot M., Nivard, Michel G., Grotzinger, Andrew D., Posthuma, Danielle, Wang, Meg M.-J., Yu, Dongmei, Stahl, Eli A., Walters, Raymond K., Anney, Richard J.L., Duncan, Laramie E., Ge, Tian, Adolfsson, Rolf, Banaschewski, Tobias, Belangero, Sintia, Cook, Edwin H., Coppola, Giovanni, Derks, Eske M., Hoekstra, Pieter J., Kaprio, Jaakko, Keski-Rahkonen, Anna, Kirov, George, Kranzler, Henry R., Luykx, Jurjen J. ... Smoller, Jordan W. (2019). Genomic relationships, novel loci, and pleiotropic mechanisms across eight psychiatric disorders. Cell, 179 (7), 1469-1482.e11. doi: 10.1016/j.cell.2019.11.020
Jia, Tianye, Chu, Congying, Liu, Yun, van Dongen, Jenny, Papastergios, Evangelos, Armstrong, Nicola J., Bastin, Mark E., Carrillo-Roa, Tania, den Braber, Anouk, Harris, Mathew, Jansen, Rick, Liu, Jingyu, Luciano, Michelle, Ori, Anil P. S., Roiz Santiañez, Roberto, Ruggeri, Barbara, Sarkisyan, Daniil, Shin, Jean, Sungeun, Kim, Tordesillas Gutiérrez, Diana, van’t Ent, Dennis, Ames, David, Artiges, Eric, Bakalkin, Georgy, Banaschewski, Tobias, Bokde, Arun L. W., Brodaty, Henry, Bromberg, Uli, Brouwer, Rachel ... Desrivières, Sylvane (2019). Epigenome-wide meta-analysis of blood DNA methylation and its association with subcortical volumes: findings from the ENIGMA Epigenetics Working Group. Molecular Psychiatry, 26 (8), 1-12. doi: 10.1038/s41380-019-0605-z
Chang, Lun-Hsien, Whitfield, John B., Liu, Mengzhen, Medland, Sarah E., Hickie, Ian B., Martin, Nicholas G., Verhulst, Brad, Heath, Andrew C., Madden, Pamela A., Statham, Dixie J., Gillespie, Nathan A. and GSCAN Consortium (2019). Associations between polygenic risk for tobacco and alcohol use and liability to tobacco and alcohol use, and psychiatric disorders in an independent sample of 13,999 Australian adults. Drug and Alcohol Dependence, 205 107704, 107704. doi: 10.1016/j.drugalcdep.2019.107704
Kendler, Kenneth S., Gardner, Charles O., Neale, Michael C., Aggen, Steve, Heath, Andrew, Colodro-Conde, Lucía, Couvyduchesne, Baptiste, Byrne, Enda M., Martin, Nicholas G. and Gillespie, Nathan A. (2019). Shared and specific genetic risk factors for lifetime major depression, depressive symptoms and neuroticism in three population-based twin samples. Psychological Medicine, 49 (16), 2745-2753. doi: 10.1017/S003329171800377X
Silventoinen, K., Jelenkovic, A., Yokoyama, Y., Sund, R., Sugawara, M., Tanaka, M., Matsumoto, S., Bogl, L. H., Freitas, D. L., Maia, J. A., Hjelmborg, J. V.B., Aaltonen, S., Piirtola, M., Latvala, A., Calais-Ferreira, L., Oliveira, V. C., Ferreira, P. H., Ji, F., Ning, F., Pang, Z., Ordoñana, J. R., Sánchez-Romera, J. F., Colodro-Conde, L., Burt, S. A., Klump, K. L., Martin, N. G., Medland, S. E., Montgomery, G. W., Kandler, C. ... Kaprio, J. (2019). The CODATwins Project: the current status and recent findings of COllaborative Project of Development of Anthropometrical Measures in Twins. Twin Research and Human Genetics, 22 (6) PII S1832427419000355, 1-9. doi: 10.1017/thg.2019.35
Davis, Christal N., Slutske, Wendy S., Martin, Nicholas G., Agrawal, Arpana and Lynskey, Michael T. (2019). Identifying subtypes of cannabis users based on simultaneous polysubstance use. Drug and Alcohol Dependence, 205 107696, 1-7. doi: 10.1016/j.drugalcdep.2019.107696
Hur, Yoon-Mi, Jeong, Hoe-Uk, Kang, Man Chull, Ajose, Frances, Kim, Jong Woo, Beck, Jeffrey J., Hottenga, Jouke-Jan, Mbarek, Hamdi, Finnicum, Casey T., Ehli, Erik A., Martin, Nicholas G., De Geus, Eco J., Boomsma, Dorret I., Davies, Gareth E. and Bates, Timothy (2019). The Nigerian Twin and Sibling Registry: An Update. Twin Research and Human Genetics, 22 (6), 637-640. doi: 10.1017/thg.2019.110
Xiong, Ziyi, Dankova, Gabriela, Howe, Laurence J., Lee, Myoung Keun, Hysi, Pirro G., de Jong, Markus A., Zhu, Gu, Adhikari, Kaustubh, Li, Dan, Li, Yi, Pan, Bo, Feingold, Eleanor, Marazita, Mary L., Shaffer, John R., McAloney, Kerrie, Xu, Shu-Hua, Jin, Li, Wang, Sijia, de Vrij, Femke Ms, Lendemeijer, Bas, Richmond, Stephen, Zhurov, Alexei, Lewis, Sarah, Sharp, Gemma C., Paternoster, Lavinia, Thompson, Holly, Gonzalez-Jose, Rolando, Bortolini, Maria Catira, Canizales-Quinteros, Samuel ... Kayser, Manfred (2019). Novel genetic loci affecting facial shape variation in humans. eLife, 8 e49898. doi: 10.7554/eLife.49898
Ye, Lin, Zhu, Gu, Martin, Nick and Liu, Yangyang (2019). The Relationship Between Adolescents’ Personality and Neurasthenia: A Comparison of Australian and Chinese. Journal of Early Adolescence, 39 (9), 1337-1342. doi: 10.1177/0272431618824710
Clark, David W., Okada, Yukinori, Moore, Kristjan H. S., Mason, Dan, Pirastu, Nicola, Gandin, Ilaria, Mattsson, Hannele, Barnes, Catriona L. K., Lin, Kuang, Zhao, Jing Hua, Deelen, Patrick, Rohde, Rebecca, Schurmann, Claudia, Guo, Xiuqing, Giulianini, Franco, Zhang, Weihua, Medina-Gomez, Carolina, Karlsson, Robert, Bao, Yanchun, Bartz, Traci M., Baumbach, Clemens, Biino, Ginevra, Bixley, Matthew J., Brumat, Marco, Chai, Jin-Fang, Corre, Tanguy, Cousminer, Diana L., Dekker, Annelot M., Eccles, David A. ... Wilson, James F. (2019). Associations of autozygosity with a broad range of human phenotypes. Nature Communications, 10 (1) 4957, 4957. doi: 10.1038/s41467-019-12283-6
Van Der Meer, Dennis, Sønderby, Ida E., Kaufmann, Tobias, Walters, G. Bragi, Abdellaoui, Abdel, Ames, David, Amunts, Katrin, Andersson, Micael, Armstrong, Nicola J., Bernard, Manon, Blackburn, Nicholas B., Blangero, John, Boomsma, Dorret I., Brodaty, Henry, Brouwer, Rachel M., Bülow, Robin, Cahn, Wiepke, Calhoun, Vince D., Caspers, Svenja, Cavalleri, Gianpiero L., Ching, Christopher R. K., Cichon, Sven, Ciufolini, Simone, Corvin, Aiden, Crespo-Facorro, Benedicto, Curran, Joanne E., Dalvie, Shareefa, Dazzan, Paola, De Geus, Eco J. C. ... Andreassen, Ole A. (2019). Association of copy number variation of the 15q11.2 BP1-BP2 region with cortical and subcortical morphology and cognition. JAMA Psychiatry, 77 (4), 1-11. doi: 10.1001/jamapsychiatry.2019.3779
Gallagher, C. S., Mäkinen, N., Harris, H. R., Rahmioglu, N., Uimari, O., Cook, J. P., Shigesi, N., Ferreira, T., Velez-Edwards, D. R., Edwards, T. L., Mortlock, S., Ruhioglu, Z., Day, F., Becker, C. M., Karhunen, V., Martikainen, H., Järvelin, M.-R., Cantor, R. M., Ridker, P. M., Terry, K. L., Buring, J. E., Gordon, S. D., Medland, S. E., Montgomery, G. W., Nyholt, D. R., Hinds, D. A., Tung, J. Y., Perry, J. R. B., Lind, P. A. ... Morton, C. C. (2019). Genome-wide association and epidemiological analyses reveal common genetic origins between uterine leiomyomata and endometriosis. Nature Communications, 10 (1) 4857, 4857. doi: 10.1038/s41467-019-12536-4
Satizabal, Claudia L., Adams, Hieab H. H., Hibar, Derrek P., White, Charles C., Knol, Maria J., Stein, Jason L., Scholz, Markus, Sargurupremraj, Muralidharan, Jahanshad, Neda, Roshchupkin, Gennady V., Smith, Albert V., Bis, Joshua C., Jian, Xueqiu, Luciano, Michelle, Hofer, Edith, Teumer, Alexander, van der Lee, Sven J., Yang, Jingyun, Yanek, Lisa R., Lee, Tom V., Li, Shuo, Hu, Yanhui, Koh, Jia Yu, Eicher, John D., Desrivières, Sylvane, Arias-Vasquez, Alejandro, Chauhan, Ganesh, Athanasiu, Lavinia, Rentería, Miguel E. ... Ikram, M. Arfan (2019). Genetic architecture of subcortical brain structures in 38,851 individuals. Nature Genetics, 51 (11), 1624-1636. doi: 10.1038/s41588-019-0511-y
Nievergelt, Caroline M., Maihofer, Adam X., Klengel, Torsten, Atkinson, Elizabeth G., Chen, Chia-Yen, Choi, Karmel W., Coleman, Jonathan R. I., Dalvie, Shareefa, Duncan, Laramie E., Gelernter, Joel, Levey, Daniel F., Logue, Mark W., Polimanti, Renato, Provost, Allison C., Ratanatharathorn, Andrew, Stein, Murray B., Torres, Katy, Aiello, Allison E., Almli, Lynn M., Amstadter, Ananda B., Andersen, Søren B., Andreassen, Ole A., Arbisi, Paul A., Ashley-Koch, Allison E., Austin, S. Bryn, Avdibegovic, Esmina, Babić, Dragan, Bækvad-Hansen, Marie, Baker, Dewleen G. ... Koenen, Karestan C. (2019). International meta-analysis of PTSD genome-wide association studies identifies sex- and ancestry-specific genetic risk loci. Nature Communications, 10 (1) 4558, 4558. doi: 10.1038/s41467-019-12576-w
Tin, Adrienne, Marten, Jonathan, Halperin Kuhns, Victoria L., Li, Yong, Wuttke, Matthias, Kirsten, Holger, Sieber, Karsten B., Qiu, Chengxiang, Gorski, Mathias, Yu, Zhi, Giri, Ayush, Sveinbjornsson, Gardar, Li, Man, Chu, Audrey Y., Hoppmann, Anselm, O’Connor, Luke J., Prins, Bram, Nutile, Teresa, Noce, Damia, Akiyama, Masato, Cocca, Massimiliano, Ghasemi, Sahar, van der Most, Peter J., Horn, Katrin, Xu, Yizhe, Fuchsberger, Christian, Sedaghat, Sanaz, Afaq, Saima, Amin, Najaf ... Köttgen, Anna (2019). Target genes, variants, tissues and transcriptional pathways influencing human serum urate levels. Nature Genetics, 51 (10), 1459-1474. doi: 10.1038/s41588-019-0504-x
van Velzen, Laura S., Kelly, Sinead, Isaev, Dmitry, Aleman, Andre, Aftanas, Lyubomir I., Bauer, Jochen, Baune, Bernhard T., Brak, Ivan V., Carballedo, Angela, Connolly, Colm G., Couvy-Duchesne, Baptiste, Cullen, Kathryn R., Danilenko, Konstantin V., Dannlowski, Udo, Enneking, Verena, Filimonova, Elena, Förster, Katharina, Frodl, Thomas, Gotlib, Ian H., Groenewold, Nynke A., Grotegerd, Dominik, Harris, Mathew A., Hatton, Sean N., Hawkins, Emma L., Hickie, Ian B., Ho, Tiffany C., Jansen, Andreas, Kircher, Tilo, Klimes-Dougan, Bonnie ... Schmaal, Lianne (2019). White matter disturbances in major depressive disorder: a coordinated analysis across 20 international cohorts in the ENIGMA MDD working group. Molecular Psychiatry, 25 (7), 1511-1525. doi: 10.1038/s41380-019-0477-2
Van der Spek, Ashley, Broer, Linda, Draisma, Harmen H. M., Pool, René, Albrecht, Eva, Beekman, Marian, Mangino, Massimo, Raag, Mait, Nyholt, Dale R., Dharuri, Harish K., Codd, Veryan, Amin, Najaf, de Geus, Eco J. C., Deelen, Joris, Demirkan, Ayse, Yet, Idil, Fischer, Krista, Haller, Toomas, Henders, Anjali K., Isaacs, Aaron, Medland, Sarah E., Montgomery, Grant W., Mooijaart, Simon P., Strauch, Konstantin, Suchiman, H. Eka D., Vaarhorst, Anika A. M., van Heemst, Diana, Wang-Sattler, Rui, Whitfield, John B. ... Gieger, Christian (2019). Metabolomics reveals a link between homocysteine and lipid metabolism and leukocyte telomere length: the ENGAGE consortium. Scientific Reports, 9 (1) 11623, 11623. doi: 10.1038/s41598-019-47282-6
Glanville, Kylie P., Coleman, Jonathan R. I., Hanscombe, Ken B., Euesden, Jack, Choi, Shing Wan, Purves, Kirstin L., Breen, Gerome, Air, Tracy M., Andlauer, Till F. M., Baune, Bernhard T., Binder, Elisabeth B., Blackwood, Douglas H. R., Boomsma, Dorret I., Buttenschøn, Henriette N., Colodro-Conde, Lucía, Dannlowski, Udo, Direk, Nese, Dunn, Erin C., Forstner, Andreas J., de Geus, Eco J. C., Grabe, Hans J., Hamilton, Steven P., Jones, Ian, Jones, Lisa A., Knowles, James A., Kutalik, Zoltán, Levinson, Douglas F., Lewis, Glyn, Lind, Penelope A. ... Børglum, Anders D. (2019). Classical human leukocyte antigen alleles and C4 haplotypes are not significantly associated With depression. Biological Psychiatry, 87 (5), 419-430. doi: 10.1016/j.biopsych.2019.06.031
Beck, Jeffrey J., Hottenga, Jouke-Jan, Mbarek, Hamdi, Finnicum, Casey T., Ehli, Erik A., Hur, Yoon-Mi, Martin, Nicholas G., De Geus, Eco J.C., Boomsma, Dorret I. and Davies, Gareth E. (2019). Genetic Similarity Assessment of Twin-Family Populations by Custom-Designed Genotyping Array. Twin Research and Human Genetics, 22 (4), 210-219. doi: 10.1017/thg.2019.41
Kfrerer, Marisa L., Martin, Nicholas G. and Schermer, Julie Aitken (2019). A behavior genetic analysis of the relationship between humor styles and depression. Humor, 32 (3), 417-431. doi: 10.1515/humor-2017-0098
Evangelou, Evangelos, Gao, He, Chu, Congying, Ntritsos, Georgios, Blakeley, Paul, Butts, Andrew R., Pazoki, Raha, Suzuki, Hideaki, Koskeridis, Fotios, Yiorkas, Andrianos M., Karaman, Ibrahim, Elliott, Joshua, Luo, Qiang, Aeschbacher, Stefanie, Bartz, Traci M., Baumeister, Sebastian E., Braund, Peter S., Brown, Michael R., Brody, Jennifer A., Clarke, Toni-Kim, Dimou, Niki, Faul, Jessica D., Homuth, Georg, Jackson, Anne U., Kentistou, Katherine A., Joshi, Peter K., Lemaitre, Rozenn N., Lind, Penelope A., Lyytikäinen, Leo-Pekka ... Elliott, Paul (2019). New alcohol-related genes suggest shared genetic mechanisms with neuropsychiatric disorders. Nature Human Behaviour, 3 (9), 950-961. doi: 10.1038/s41562-019-0653-z
Gillespie, Nathan A., Bates, Timothy C., Hickie, Ian B., Medland, Sarah E., Verhulst, Brad, Kirkpatrick, Robert M., Kendler, Kenneth S., Martin, Nicholas G. and Benotsch, Eric G. (2019). Genetic and environmental risk factors in the non-medical use of over-the-counter or prescribed analgesics, and their relationship to major classes of licit and illicit substance use and misuse in a population-based sample of young adult twins. Addiction, 114 (12) add.14750, 2229-2240. doi: 10.1111/add.14750
Watson, Hunna J., Yilmaz, Zeynep, Thornton, Laura M., Hübel, Christopher, Coleman, Jonathan R. I., Gaspar, Héléna A., Bryois, Julien, Hinney, Anke, Leppä, Virpi M., Mattheisen, Manuel, Medland, Sarah E., Ripke, Stephan, Yao, Shuyang, Giusti-Rodríguez, Paola, Hanscombe, Ken B., Purves, Kirstin L., Adan, Roger A. H., Alfredsson, Lars, Ando, Tetsuya, Andreassen, Ole A., Baker, Jessica H., Berrettini, Wade H., Boehm, Ilka, Boni, Claudette, Perica, Vesna Boraska, Buehren, Katharina, Burghardt, Roland, Cassina, Matteo, Cichon, Sven ... Bulik, Cynthia M. (2019). Genome-wide association study identifies eight risk loci and implicates metabo-psychiatric origins for anorexia nervosa. Nature Genetics, 51 (8), 1207-1214. doi: 10.1038/s41588-019-0439-2
Peng, Fuduan, Zhu, Gu, Hysi, Pirro G., Eller, Ryan J., Chen, Yan, Li, Yi, Hamer, Merel A., Zeng, Changqing, Hopkins, Racquel L., Jacobus, Case L., Wallace, Paige L., Uitterlinden, André G., Ikram, M. Arfan, Nijsten, Tamar, Duffy, David L., Medland, Sarah E., Spector, Timothy D., Walsh, Susan, Martin, Nicholas G., Liu, Fan and Kayser, Manfred (2019). Genome-Wide Association Studies Identify Multiple Genetic Loci Influencing Eyebrow Color Variation in Europeans. Journal of Investigative Dermatology, 139 (7), 1601-1605. doi: 10.1016/j.jid.2018.12.029
Pardiñas, Antonio F., Holmans, Peter, Pocklington, Andrew J., Escott-Price, Valentina, Ripke, Stephan, Carrera, Noa, Legge, Sophie E., Bishop, Sophie, Cameron, Darren, Hamshere, Marian L., Han, Jun, Hubbard, Leon, Lynham, Amy, Mantripragada, Kiran, Rees, Elliott, MacCabe, James H., McCarroll, Steven A., Baune, Bernhard T., Breen, Gerome, Byrne, Enda M., Dannlowski, Udo, Eley, Thalia C., Hayward, Caroline, Martin, Nicholas G., McIntosh, Andrew M., Plomin, Robert, Porteous, David J., Wray, Naomi R., Caballero, Armando ... Walters, James T. R. (2019). Publisher Correction: Common schizophrenia alleles are enriched in mutation-intolerant genes and in regions under strong background selection. Nature Genetics, 51 (7), 1193-1193. doi: 10.1038/s41588-019-0450-7
Davis, Christal N., Slutske, Wendy S., Martin, Nicholas G., Agrawal, Arpana and Lynskey, Michael T. (2019). Genetic and environmental influences on gambling disorder liability: A replication and combined analysis of two twin studies. Psychological Medicine, 49 (10), 1705-1712. doi: 10.1017/S0033291718002325
Pasman, Joëlle A., Verweij, Karin J. H., Gerring, Zachary, Stringer, Sven, Sanchez-Roige, Sandra, Treur, Jorien L., Abdellaoui, Abdel, Nivard, Michel G., Baselmans, Bart M. L., Ong, Jue-Sheng, Ip, Hill F., van der Zee, Matthijs D., Bartels, Meike, Day, Felix R., Fontanillas, Pierre, Elson, Sarah L., de Wit, Harriet, Davis, Lea K., MacKillop, James, Derringer, Jaime L., Branje, Susan J. T., Hartman, Catharina A., Heath, Andrew C., van Lier, Pol A. C., Madden, Pamela A. F., Mägi, Reedik, Meeus, Wim, Montgomery, Grant W., Oldehinkel, A. J. ... Vink, Jacqueline M. (2019). Author Correction: GWAS of lifetime cannabis use reveals new risk loci, genetic overlap with psychiatric traits, and a causal effect of schizophrenia liability. Nature Neuroscience, 22 (7), 1196-1196. doi: 10.1038/s41593-019-0402-7
Hwang, Liang-Dar, Lin, Cailu, Gharahkhani, Puya, Cuellar-Partida, Gabriel, Ong, Jue-Sheng, An, Jiyuan, Gordon, Scott D., Zhu, Gu, MacGregor, Stuart, Lawlor, Deborah A., Breslin, Paul A. S., Wright, Margaret J., Martin, Nicholas G. and Reed, Danielle R. (2019). New insight into human sweet taste: a genome-wide association study of the perception and intake of sweet substances. The American Journal of Clinical Nutrition, 109 (6), 1724-1737. doi: 10.1093/ajcn/nqz043
Davis, Christal N., Slutske, Wendy S., Martin, Nicholas G., Agrawal, Arpana and Lynskey, Michael T. (2019). Genetic Epidemiology of Liability for Alcohol-Induced Blacking and Passing Out. Alcoholism: Clinical and Experimental Research, 43 (6) acer.14045, 1103-1112. doi: 10.1111/acer.14045
Brazel, David M., Jiang, Yu, Hughey, Jordan M., Turcot, Valérie, Zhan, Xiaowei, Gong, Jian, Batini, Chiara, Weissenkampen, J. Dylan, Liu, MengZhen, Surendran, Praveen, Young, Robin, Barnes, Daniel R., Nielsen, Sune Fallgaard, Rasheed, Asif, Samuel, Maria, Zhao, Wei, Kontto, Jukka, Perola, Markus, Caslake, Muriel, de Craen, Anton J.M., Trompet, Stella, Uria-Nickelsen, Maria, Malarstig, Anders, Reily, Dermot F., Hoek, Maarten, Vogt, Thomas, Jukema, J. Wouter, Sattar, Naveed, Ford, Ian ... Vrieze, Scott (2019). Exome Chip Meta-analysis Fine Maps Causal Variants and Elucidates the Genetic Architecture of Rare Coding Variants in Smoking and Alcohol Use. Biological Psychiatry, 85 (11), 946-955. doi: 10.1016/j.biopsych.2018.11.024
Wuttke, Matthias, Li, Yong, Li, Man, Sieber, Karsten B., Feitosa, Mary F., Gorski, Mathias, Tin, Adrienne, Wang, Lihua, Chu, Audrey Y., Hoppmann, Anselm, Kirsten, Holger, Giri, Ayush, Chai, Jin-Fang, Sveinbjornsson, Gardar, Tayo, Bamidele O., Nutile, Teresa, Fuchsberger, Christian, Marten, Jonathan, Cocca, Massimiliano, Ghasemi, Sahar, Xu, Yizhe, Horn, Katrin, Noce, Damia, van der Most, Peter J., Sedaghat, Sanaz, Yu, Zhi, Akiyama, Masato, Afaq, Saima, Ahluwalia, Tarunveer S. ... Pattaro, Cristian (2019). A catalog of genetic loci associated with kidney function from analyses of a million individuals. Nature Genetics, 51 (6), 957-972. doi: 10.1038/s41588-019-0407-x
Jahanshad, Neda, Faskowitz, Joshua I., Roshchupkin, Gennady, Hibar, Derrek, Gutman, Boris A, Tustison, Nicholas J., Adams, Hieab H. H., Niessen, Wiro, Vernooij, Meike W, Ikram, M Arfan, Zwiers, Marcel P., Vasquez, Alejandro Arias, Franke, Barbara, Kroll, Jennifer L., Mwangi, Benson, Soares, Jair C, Ing, Alex, Desrivieres, Sylvane, Schumann, Gunter, Hansell, Narelle K, de Zubicaray, Greig I., McMahon, Katie L., Martin, Nicholas G., Wright, Margaret J. and Thompson, Paul M. (2019). Multi-site meta-analysis of morphometry. IEEE/ACM Transactions on Computational Biology and Bioinformatics, 16 (5) 3370702, 1-1. doi: 10.1109/TCBB.2019.2914905
Davies, Gail, Lam, Max, Harris, Sarah E., Trampush, Joey W., Luciano, Michelle, Hill, W. David, Hagenaars, Saskia P., Ritchie, Stuart J., Marioni, Riccardo E., Fawns-Ritchie, Chloe, Liewald, David C. M., Okely, Judith A., Ahola-Olli, Ari V., Barnes, Catriona L. K., Bertram, Lars, Bis, Joshua C., Burdick, Katherine E., Christoforou, Andrea, DeRosse, Pamela, Djurovic, Srdjan, Espeseth, Thomas, Giakoumaki, Stella, Giddaluru, Sudheer, Gustavson, Daniel E., Hayward, Caroline, Hofer, Edith, Ikram, M. Arfan, Karlsson, Robert, Knowles, Emma ... Deary, Ian J. (2019). Author correction: Study of 300,486 individuals identifies 148 independent genetic loci influencing general cognitive function. Nature Communications, 10 (1) 2068, 2068. doi: 10.1038/s41467-019-10160-w
Stahl, Eli A., Breen, Gerome, Forstner, Andreas J., McQuillin, Andrew, Ripke, Stephan, Trubetskoy, Vassily, Mattheisen, Manuel, Wang, Yunpeng, Coleman, Jonathan R. I., Gaspar, Héléna A., de Leeuw, Christiaan A., Steinberg, Stacy, Pavlides, Jennifer M. Whitehead, Trzaskowski, Maciej, Byrne, Enda M., Pers, Tune H., Holmans, Peter A., Richards, Alexander L., Abbott, Liam, Agerbo, Esben, Akil, Huda, Albani, Diego, Alliey-Rodriguez, Ney, Als, Thomas D., Anjorin, Adebayo, Antilla, Verneri, Awasthi, Swapnil, Badner, Judith A., Bækvad-Hansen, Marie ... Sklar, Pamela (2019). Genome-wide association study identifies 30 loci associated with bipolar disorder. Nature Genetics, 51 (5), 793-803. doi: 10.1038/s41588-019-0397-8
Polimanti, Renato, Peterson, Roseann E., Ong, Jue-Sheng, MacGregor, Stuart, Edwards, Alexis C., Clarke, Toni-Kim, Frank, Josef, Gerring, Zachary, Gillespie, Nathan A., Lind, Penelope A., Maes, Hermine H., Martin, Nicholas G., Mbarek, Hamdi, Medland, Sarah E., Streit, Fabian, Agrawal, Arpana, Edenberg, Howard J., Kendler, Kenneth S., Lewis, Cathryn M., Sullivan, Patrick F., Wray, Naomi R., Gelernter, Joel and Derks, Eske M. (2019). Evidence of causal effect of major depression on alcohol dependence: Findings from the psychiatric genomics consortium. Psychological Medicine, 49 (07), 1-9. doi: 10.1017/S0033291719000667
Hwang, Liang-Dar, Strike, Lachlan T, Couvy-Duchesne, Baptiste, de Zubicaray, Greig I, McMahon, Katie, Breslin, Paul A. S., Reed, Danielle R., Martin, Nicholas G. and Wright, Margaret J. (2019). Associations between brain structure and perceived intensity of sweet and bitter tastes. Behavioural Brain Research, 363, 103-108. doi: 10.1016/j.bbr.2019.01.046
Swiatkowska, Ilona, Martin, Nicholas and Hart, Alister J. (2019). Blood titanium level as a biomarker of orthopaedic implant wear. Journal of Trace Elements in Medicine and Biology, 53, 120-128. doi: 10.1016/j.jtemb.2019.02.013
Lazaroo, Nikita K., Bates, Timothy C., Hansell, Narelle K., Wright, Margaret J., Martin, Nicholas G. and Luciano, Michelle (2019). Genetic structure of IQ, phonemic decoding skill, and academic achievement. Frontiers in Genetics, 10 (MAR) 195, 195. doi: 10.3389/fgene.2019.00195
Kochunov, Peter, Patel, Binish, Ganjgahi, Habib, Donohue, Brian, Ryan, Meghann, Hong, Elliot L., Chen, Xu, Adhikari, Bhim, Jahanshad, Neda, Thompson, Paul M., Van't Ent, Dennis, den Braber, Anouk, de Geus, Eco J. C., Brouwer, Rachel M., Boomsma, Dorret, Pol, Hilleke E. Hulshoff, de Zubicaray, Greig, McMahon, Katie L., Martin, Nicholas G., Wright, Margaret J. and Nichols, Thomas E. (2019). Homogenizing estimates of heritability among SOLAR-Eclipse, OpenMx, APACE, and FPHI software packages in neuroimaging data. Frontiers in Neuroinformatics, 13 16, 16. doi: 10.3389/fninf.2019.00016
Dudding, Tom, Haworth, Simon, Lind, Penelope A., Sathirapongsasuti, J. Fah, Tung, Joyce Y., Mitchell, Ruth, Colodro-Conde, Lucía, Medland, Sarah E., Gordon, Scott, Elsworth, Benjamin, Paternoster, Lavinia, Franks, Paul W., Thomas, Steven J., Martin, Nicholas G. and Timpson, Nicholas J. (2019). Genome wide analysis for mouth ulcers identifies associations at immune regulatory loci. Nature Communications, 10 (1) 1052, 1052. doi: 10.1038/s41467-019-08923-6
Whitfield, John B., Zhu, Gu, Madden, Pamela A. F., Montgomery, Grant W., Heath, Andrew C. and Martin, Nicholas G. (2019). Biomarker and genomic risk factors for liver function test abnormality in hazardous drinkers. Alcoholism: Clinical and Experimental Research, 43 (3), 473-482. doi: 10.1111/acer.13949
Taylor, Andrew, Barlow, Nicola, Day, Martin P., Hill, Sarah, Martin, Nicholas and Patriarca, Marina (2019). Atomic Spectrometry Update: Review of adVances in the analysis of clinical and biological materials, foods and beverages. Journal of Analytical Atomic Spectrometry, 34 (3), 426-459. doi: 10.1039/c9ja90004g
Liu, Mengzhen, Jiang, Yu, Wedow, Robbee, Li, Yue, Brazel, David M., Chen, Fang, Datta, Gargi, Davila-Velderrain, Jose, McGuire, Daniel, Tian, Chao, Zhan, Xiaowei, Choquet, Hélène, Docherty, Anna R., Faul, Jessica D., Foerster, Johanna R., Fritsche, Lars G., Gabrielsen, Maiken Elvestad, Gordon, Scott D., Haessler, Jeffrey, Hottenga, Jouke-Jan, Huang, Hongyan, Jang, Seon-Kyeong, Jansen, Philip R., Ling, Yueh, Mägi, Reedik, Matoba, Nana, McMahon, George, Mulas, Antonella, Orrù, Valeria ... Vrieze, Scott (2019). Association studies of up to 1.2 million individuals yield new insights into the genetic etiology of tobacco and alcohol use. Nature Genetics, 51 (2), 237-244. doi: 10.1038/s41588-018-0307-5
Chang, Lun-Hsien, Couvy-Duchesne, Baptiste, Liu, Mengzhen, Medland, Sarah E., Verhulst, Brad, Benotsch, Eric G., Hickie, Ian B., Martin, Nicholas G., Gillespie, Nathan A. and GSCAN Consortium (2019). Association between polygenic risk for tobacco or alcohol consumption and liability to licit and illicit substance use in young Australian adults. Drug and Alcohol Dependence, 197, 271-279. doi: 10.1016/j.drugalcdep.2019.01.015
Trzaskowski, Maciej, Mehta, Divya, Peyrot, Wouter J., Hawkes, David, Davies, Daniel, Howard, David M., Kemper, Kathryn E., Sidorenko, Julia, Maier, Robert, Ripke, Stephan, Mattheisen, Manuel, Baune, Bernhard T., Grabe, Hans J., Heath, Andrew C., Jones, Lisa, Jones, Ian, Madden, Pamela A.F., McIntosh, Andrew M., Breen, Gerome, Lewis, Cathryn M., Børglum, Anders D., Sullivan, Patrick F., Martin, Nicholas G., Kendler, Kenneth S., Levinson, Douglas F. and Wray, Naomi R. (2019). Quantifying between-cohort and between-sex genetic heterogeneity in major depressive disorder. American Journal of Medical Genetics Part B: Neuropsychiatric Genetics, 180 (6), 439-447. doi: 10.1002/ajmg.b.32713
Richmond-Rakerd, Leah S., Trull, Timothy J., Gizer, Ian R., McLaughlin, Kristin, Scheiderer, Emily M., Nelson, Elliot C., Agrawal, Arpana, Lynskey, Michael T., Madden, Pamela A.F., Heath, Andrew C., Statham, Dixie J. and Martin, Nicholas G. (2019). Common genetic contributions to high-risk trauma exposure and self-injurious thoughts and behaviors. Psychological Medicine, 49 (3), 421-430. doi: 10.1017/S0033291718001034
Schermer, Julie Aitken and Martin, Nicholas G. (2019). A behavior genetic analysis of personality and loneliness. Journal of Research in Personality, 78, 133-137. doi: 10.1016/j.jrp.2018.11.011
Bates, Timothy C., Maher, Brion S., Colodro-Conde, Lucía, Medland, Sarah E., McAloney, Kerrie, Wright, Margaret J., Hansell, Narelle K., Okbay, Aysu, Kendler, Kenneth S., Martin, Nicholas G. and Gillespie, Nathan A. (2019). Social competence in parents increases children's educational attainment: Replicable genetically-mediated effects of parenting revealed by non-transmitted DNA. Twin Research and Human Genetics, 22 (01), 1-3. doi: 10.1017/thg.2018.75
Duffy, David L., Zhu, Gu, Li, Xin, Sanna, Marianna, Iles, Mark M., Jacobs, Leonie C., Evans, David M., Yazar, Seyhan, Beesley, Jonathan, Law, Matthew H., Kraft, Peter, Visconti, Alessia, Taylor, John C., Liu, Fan, Wright, Margaret J., Henders, Anjali K., Bowdler, Lisa, Glass, Dan, Ikram, M. Arfan, Uitterlinden, André G., Madden, Pamela A., Heath, Andrew C., Nelson, Elliot C., Green, Adele C., Chanock, Stephen, Barrett, Jennifer H., Brown, Matthew A., Hayward, Nicholas K., MacGregor, Stuart ... Martin, Nicholas G. (2019). Publisher correction: Novel pleiotropic risk loci for melanoma and nevus density implicate multiple biological pathways. Nature Communications, 10 (1) 299, 299. doi: 10.1038/s41467-018-08078-w
Iglesias, Adriana I., Mishra, Aniket, Vitart, Veronique, Bykhovskaya, Yelena, Höhn, René, Springelkamp, Henriët, Cuellar-Partida, Gabriel, Gharahkhani, Puya, Bailey, Jessica N. Cooke, Willoughby, Colin E., Li, Xiaohui, Yazar, Seyhan, Nag, Abhishek, Khawaja, Anthony P., Polašek, Ozren, Siscovick, David, Mitchell, Paul, Tham, Yih Chung, Haines, Jonathan L., Kearns, Lisa S., Hayward, Caroline, Shi, Yuan, van Leeuwen, Elisabeth M., Taylor, Kent D., Bonnemaijer, Pieter, Rotter, Jerome I., Martin, Nicholas G., Zeller, Tanja, Mills, Richard A. ... MacGregor, Stuart (2019). Author correction: Cross-ancestry genome-wide association analysis of corneal thickness strengthens link between complex and Mendelian eye diseases. Nature Communications, 10 (1) 155, 155. doi: 10.1038/s41467-018-07819-1
Morris, Andrew P., Le, Thu H., Wu, Haojia, Akbarov, Artur, van der Most, Peter J., Hemani, Gibran, Smith, George Davey, Mahajan, Anubha, Gaulton, Kyle J., Nadkarni, Girish N., Valladares-Salgado, Adan, Wacher-Rodarte, Niels, Mychaleckyj, Josyf C., Dueker, Nicole D., Guo, Xiuqing, Hai, Yang, Haessler, Jeffrey, Kamatani, Yoichiro, Stilp, Adrienne M., Zhu, Gu, Cook, James P., Ärnlöv, Johan, Blanton, Susan H., de Borst, Martin H., Bottinger, Erwin P., Buchanan, Thomas A., Cechova, Sylvia, Charchar, Fadi J., Chu, Pei-Lun ... Franceschini, Nora (2019). Trans-ethnic kidney function association study reveals putative causal genes and effects on kidney-specific disease aetiologies. Nature Communications, 10 (1) 29, 29. doi: 10.1038/s41467-018-07867-7
Demontis, Ditte, Walters, Raymond K., Martin, Joanna, Mattheisen, Manuel, Als, Thomas D., Agerbo, Esben, Baldursson, Gísli, Belliveau, Rich, Bybjerg-Grauholm, Jonas, Bækvad-Hansen, Marie, Cerrato, Felecia, Chambert, Kimberly, Churchhouse, Claire, Dumont, Ashley, Eriksson, Nicholas, Gandal, Michael, Goldstein, Jacqueline I., Grasby, Katrina L., Grove, Jakob, Gudmundsson, Olafur O., Hansen, Christine S., Hauberg, Mads Engel, Hollegaard, Mads V., Howrigan, Daniel P., Huang, Hailiang, Maller, Julian B., Martin, Alicia R., Martin, Nicholas G., Moran, Jennifer ... Kemp, John P. (2019). Discovery of the first genome-wide significant risk loci for attention deficit/hyperactivity disorder. Nature Genetics, 51 (1), 63-75. doi: 10.1038/s41588-018-0269-7
Mitchell, Brittany L., Zhu, Gu, Medland, Sarah E., Renteria, Miguel. E., Eyles, Darryl W., Grasby, Katrina L., McGrath, John J. and Martin, Nicholas G. (2019). Half the genetic variance in vitamin D concentration is shared with skin colour and sun exposure genes. Behavior Genetics, 49 (4), 386-398. doi: 10.1007/s10519-019-09954-x
Mitchell, Brittany L., Campos, Adrian I., Rentería, Miguel E., Parker, Richard, Sullivan, Lenore, McAloney, Kerrie, Couvy-Duchesne, Baptiste, Medland, Sarah E., Gillespie, Nathan A., Scott, Jan, Zietsch, Brendan P., Lind, Penelope A., Martin, Nicholas G. and Hickie, Ian B. (2019). Twenty-Five and Up (25Up) Study: A New Wave of the Brisbane Longitudinal Twin Study. Twin Research and Human Genetics, 22 (03) PII S1832427419000276, 154-163. doi: 10.1017/thg.2019.27
Dash, Genevieve F., Slutske, Wendy S., Martin, Nicholas G., Statham, Dixie J., Agrawal, Arpana and Lynskey, Michael T. (2019). Big Five Personality Traits and Alcohol, Nicotine, Cannabis, and Gambling Disorder Comorbidity. Psychology of Addictive Behaviors, 33 (4), 420-429. doi: 10.1037/adb0000468
Davis, Christal N., Slutske, Wendy S., Piasecki, Thomas M., Martin, Nicholas G. and Lynskey, Michael T. (2019). Comparing the Potential Causal Influence of Two Indicators of Early Alcohol Use on Later Alcohol Use Disorder Symptoms. Journal of Abnormal Psychology, 129 (3), 256-265. doi: 10.1037/abn0000474
Björnmalm, Mattias, Wong, Lok Man, Wojciechowski, Jonathan P., Penders, Jelle, Horgan, Conor C., Booth, Marsilea A., Martin, Nicholas G., Sattler, Susanne and Stevens, Molly M. (2019). In vivo biocompatibility and immunogenicity of metal-phenolic gelation. Chemical Science, 10 (43), 10179-10194. doi: 10.1039/c9sc03325d
Hayward, Tanisha A., Zhu, Gu, Warrington, Nicole M., Wong, Yide, Ryan, Rachael Y.M., Murray, Abella M., Haigh, Oscar, Martin, Nicholas G., Miles, John J. and Evans, David M. (2018). Antibody response to common human viruses is shaped by genetic factors. Journal of Allergy and Clinical Immunology, 143 (4), 1640-1643. doi: 10.1016/j.jaci.2018.11.039
McRae, Allan F., Marioni, Riccardo E., Shah, Sonia, Yang, Jian, Powell, Joseph E., Harris, Sarah E., Gibson, Jude, Henders, Anjali K., Bowdler, Lisa, Painter, Jodie N., Murphy, Lee, Martin, Nicholas G., Starr, John M., Wray, Naomi R., Deary, Ian J., Visscher, Peter M. and Montgomery, Grant W. (2018). Identification of 55,000 replicated DNA methylation QTL. Scientific Reports, 8 (1) 17605, 17605. doi: 10.1038/s41598-018-35871-w
Martin, Nicholas (2018). Getting to the genetic and environmental roots of educational inequality. npj Science of Learning, 3 (1) 4. doi: 10.1038/s41539-018-0021-1
Guintivano, Jerry, Krohn, Holly, Lewis, Carol, Byrne, Enda M., Henders, Anjali K., Ploner, Alexander, Kirk, Katherine, Martin, Nicholas G., Milgrom, Jeannette, Wray, Naomi R., Sullivan, Patrick F. and Meltzer-Brody, Samantha (2018). PPD ACT: an app-based genetic study of postpartum depression. Translational Psychiatry, 8 (1) 260, 260. doi: 10.1038/s41398-018-0305-5
Walters, Raymond K., Polimanti, Renato, Johnson, Emma C., McClintick, Jeanette N., Adams, Mark J., Adkins, Amy E., Aliev, Fazil, Bacanu, Silviu-Alin, Batzler, Anthony, Bertelsen, Sarah, Biernacka, Joanna M., Bigdeli, Tim B., Chen, Li-Shiun, Clarke, Toni-Kim, Chou, Yi-Ling, Degenhardt, Franziska, Docherty, Anna R., Edwards, Alexis C., Fontanillas, Pierre, Foo, Jerome C., Fox, Louis, Frank, Josef, Giegling, Ina, Gordon, Scott, Hack, Laura M., Hartmann, Annette M., Hartz, Sarah M., Heilmann-Heimbach, Stefanie, Herms, Stefan ... Agrawal, Arpana (2018). Transancestral GWAS of alcohol dependence reveals common genetic underpinnings with psychiatric disorders. Nature Neuroscience, 21 (12), 1656-1669. doi: 10.1038/s41593-018-0275-1
Ong, Jue-Sheng, Hwang, Liang-Dar, Zhong, Victor W., An, Jiyuan, Gharahkhani, Puya, Breslin, Paul A. S., Wright, Margaret J., Lawlor, Deborah A., Whitfield, John, MacGregor, Stuart, Martin, Nicholas G. and Cornelis, Marilyn C. (2018). Understanding the role of bitter taste perception in coffee, tea and alcohol consumption through Mendelian randomization. Scientific Reports, 8 (1) 16414, 16414. doi: 10.1038/s41598-018-34713-z
Couvy-Duchesne, Baptiste, Strike, Lachlan T., McMahon, Katie L., de Zubicaray, Greig I., Thompson, Paul M., Martin, Nicholas G., Medland, Sarah E. and Wright, Margaret J. (2018). A fast method for estimating statistical power of multivariate GWAS in real case scenarios: examples from the field of imaging genetics. Behavior Genetics, 49 (1), 112-121. doi: 10.1007/s10519-018-9936-9
Duffy, David L., Zhu, Gu, Li, Xin, Sanna, Marianna, Iles, Mark M., Jacobs, Leonie C., Evans, David M., Yazar, Seyhan, Beesley, Jonathan, Law, Matthew H., Kraft, Peter, Visconti, Alessia, Taylor, John C., Lui, Fan, Wright, Margaret J., Henders, Anjali K., Bowdler, Lisa, Glass, Dan, Ikram, Arfan M., Uitterlinden, André G., Madden, Pamela A., Heath, Andrew C., Nelson, Elliot C., Green, Adele C., Chanock, Stephen, Barrett, Jennifer H., Brown, Matthew A., Hayward, Nicholas K., MacGregor, Stuart ... Martin, Nicholas G. (2018). Novel pleiotropic risk loci for melanoma and nevus density implicate multiple biological pathways. Nature Communications, 9 (1) 4774, 4774. doi: 10.1038/s41467-018-06649-5
Minică, Camelia C., Verweij, Karin J. H., van der Most, Peter J., Mbarek, Hamdi, Bernard, Manon, van Eijk, Kristel R., Lind, Penelope A., Liu, Meng Zhen, Maciejewski, Dominique F., Palviainen, Teemu, Sánchez-Mora, Cristina, Sherva, Richard, Taylor, Michelle, Walters, Raymond K., Abdellaoui, Abdel, Bigdeli, Timothy B., Branje, Susan J. T., Brown, Sandra A., Casas, Miguel, Corley, Robin P., Smith, George Davey, Davies, Gareth E., Ehli, Erik A., Farrer, Lindsay, Fedko, Iryna O., Garcia-Martínez, Iris, Gordon, Scott D., Hartman, Catharina A., Heath, Andrew C. ... Derks, Eske M. (2018). Genome-wide association meta-analysis of age at first cannabis use. Addiction, 113 (11), 2073-2086. doi: 10.1111/add.14368
Pośpiech, Ewelina, Chen, Yan, Kukla-Bartoszek, Magdalena, Breslin, Krystal, Aliferi, Anastasia, Andersen, Jeppe D., Ballard, David, Chaitanya, Lakshmi, Freire-Aradas, Ana, van der Gaag, Kristiaan J., Girón-Santamaría, Lorena, Gross, Theresa E., Gysi, Mario, Huber, Gabriela, Mosquera-Miguel, Ana, Muralidharan, Charanya, Skowron, Małgorzata, Carracedo, Ángel, Haas, Cordula, Morling, Niels, Parson, Walther, Phillips, Christopher, Schneider, Peter M., Sijen, Titia, Syndercombe-Court, Denise, Vennemann, Marielle, Wu, Sijie, Xu, Shuhua, Jin, Li ... EUROFORGEN NoE Consortium (2018). Towards broadening Forensic DNA Phenotyping beyond pigmentation: Improving the prediction of head hair shape from DNA. Forensic Science International: Genetics, 37, 241-251. doi: 10.1016/j.fsigen.2018.08.017
Ligthart, Symen, Vaez, Ahmad, Võsa, Urmo, Stathopoulou, Maria G., de Vries, Paul S., Prins, Bram P., Van der Most, Peter J., Tanaka, Toshiko, Naderi, Elnaz, Rose, Lynda M., Wu, Ying, Karlsson, Robert, Barbalic, Maja, Lin, Honghuang, Pool, René, Zhu, Gu, Macé, Aurélien, Sidore, Carlo, Trompet, Stella, Mangino, Massimo, Sabater-Lleal, Maria, Kemp, John P., Abbasi, Ali, Kacprowski, Tim, Verweij, Niek, Smith, Albert V., Huang, Tao, Marzi, Carola, Feitosa, Mary F. ... Alizadeh, Behrooz Z. (2018). Genome analyses of >200,000 individuals identify 58 loci for chronic inflammation and highlight pathways that link inflammation and complex disorders. American Journal of Human Genetics, 103 (5), 691-706. doi: 10.1016/j.ajhg.2018.09.009
Thornton, Laura M., Munn-Chernoff, Melissa A., Baker, Jessica H., Juréus, Anders, Parker, Richard, Henders, Anjali K., Larsen, Janne T., Petersen, Liselotte, Watson, Hunna J., Yilmaz, Zeynep, Kirk, Katherine M., Gordon, Scott, Leppä, Virpi M., Martin, Felicity C., Whiteman, David C., Olsen, Catherine M., Werge, Thomas M., Pedersen, Nancy L., Kaye, Walter, Bergen, Andrew W., Halmi, Katherine A., Strober, Michael, Kaplan, Allan S., Woodside, D. Blake, Mitchell, James, Johnson, Craig L., Brandt, Harry, Crawford, Steven, Horwood, L. John ... Bulik, Cynthia M. (2018). The Anorexia Nervosa Genetics Initiative (ANGI): overview and methods. Contemporary Clinical Trials, 74, 61-69. doi: 10.1016/j.cct.2018.09.015
Niemi, Mari E. K., Martin, Hilary C., Rice, Daniel L., Gallone, Giuseppe, Gordon, Scott, Kelemen, Martin, McAloney, Kerrie, McRae, Jeremy, Radford, Elizabeth J., Yu, Sui, Gecz, Jozef, Martin, Nicholas G., Wright, Caroline F., Fitzpatrick, David R., Firth, Helen V., Hurles, Matthew E. and Barrett, Jeffrey C. (2018). Common genetic variants contribute to risk of rare severe neurodevelopmental disorders. Nature, 562 (7726), 268-271. doi: 10.1038/s41586-018-0566-4
de Jong, Simone, Abdalla Diniz, Mateus Jose, Saloma, Andiara, Gadelha, Ary, Santoro, Marcos L., Ota, Vanessa K., Noto, Cristiano, Curtis, Charlesg, Newhouse, Stephen J., Patel, Hamel, Hall, Lynsey S., O'Reilly, Paul F., Belangero, Sintia, Bressan, Rodrigo A., Breen, Gerome, Wray, Naomi R., Ripke, Stephan, Mattheisen, Manuel, Trzaskowski, Maciej, Byrne, Enda M., Abdellaoui, Abdel, Adams, Mark J., Agerbo, Esben, Air, Tracy M., Andlauer, Till F. M., Bacanu, Silviu-Alin, Baekvad-Hansen, Marie, Beekman, Aartjan T. F., Bigdeli, Tim B. ... Major Depressive Disorder and Bipolar Disorder Working Groups of the Psychiatric Genomics Consortium (2018). Applying polygenic risk scoring for psychiatric disorders to a large family with bipolar disorder and major depressive disorder. Communications Biology, 1 (163) 163. doi: 10.1038/s42003-018-0155-y
Hwang, Liang-Dar, Gharahkhani, Puya, Breslin, Paul A. S., Gordon, Scott D., Zhu, Gu, Martin, Nicholas G., Reed, Danielle R. and Wright, Margaret J. (2018). Bivariate genome-wide association analysis strengthens the role of bitter receptor clusters on chromosomes 7 and 12 in human bitter taste. BMC Genomics, 19 (678) 678, 678. doi: 10.1186/s12864-018-5058-2
Loehlin, John C., Wright, Margaret J., Hansell, Narelle K. and Martin, Nicholas G. (2018). Are there distinct cognitive types?. Intelligence, 70, 7-11. doi: 10.1016/j.intell.2018.07.002
MacGregor, Stuart, Ong, Jue-Sheng, An, Jiyuan, Han, Xikun, Zhou, Tiger, Siggs, Owen M., Law, Matthew H., Souzeau, Emmanuelle, Sharma, Shiwani, Lynn, David J., Beesley, Jonathan, Sheldrick, Bronwyn, Mills, Richard A., Landers, John, Ruddle, Jonathan B., Graham, Stuart L., Healey, Paul R., White, Andrew J. R., Casson, Robert J., Best, Stephen, Grigg, John R., Goldberg, Ivan, Powell, Joseph E., Whiteman, David C., Radford-Smith, Graham L., Martin, Nicholas G., Montgomery, Grant W., Burdon, Kathryn P., Mackey, David A. ... Hewitt, Alex W. (2018). Genome-wide association study of intraocular pressure uncovers new pathways to glaucoma. Nature Genetics, 50 (8), 1067-1071. doi: 10.1038/s41588-018-0176-y
Chang, Lun-Hsien, Couvy-Duchesne, Baptiste, Medland, Sarah E., Gillespie, Nathan A., Hickie, Ian B., Parker, Richard and Martin, Nicholas G. (2018). The genetic relationship between psychological distress, somatic distress, affective disorders, and substance use in young Australian adults: a multivariate twin study. Twin Research and Human Genetics, 21 (5), 347-360. doi: 10.1017/thg.2018.33
Piirtola, Maarit, Jelenkovic, Aline, Latvala, Antti, Sund, Reijo, Honda, Chika, Inui, Fujio, Watanabe, Mikio, Tomizawa, Rie, Iwatani, Yoshinori, Ordoñana, Juan R., Sánchez-Romera, Juan F., Colodro-Conde, Lucia, Tarnoki, Adam D., Tarnoki, David L., Martin, Nicholas G., Montgomery, Grant W., Medland, Sarah E., Rasmussen, Finn, Tynelius, Per, Tan, Qihua, Zhang, Dongfeng, Pang, Zengchang, Rebato, Esther, Stazi, Maria A., Fagnani, Corrado, Brescianini, Sonia, Busjahn, Andreas, Harris, Jennifer R., Brandt, Ingunn ... Silventoinen, Karri (2018). Association of current and former smoking with body mass index: a study of smoking discordant twin pairs from 21 twin cohorts. PLoS One, 13 (7) e0200140, e0200140. doi: 10.1371/journal.pone.0200140
Liu, Yangyang, Gillespie, Nathan A., Ye, Lin, Zhu, Gu, Duffy, David L. and Martin, Nicholas G. (2018). The relationship between personality and somatic and psychological distress: a comparison of Chinese and Australian adolescents. Behavior Genetics, 48 (4), 315-322. doi: 10.1007/s10519-018-9905-3
Ellingson, Jarrod M., Slutske, Wendy S., Vergés, Alvaro, Littlefield, Andrew K., Statham, Dixie J. and Martin, Nicholas G. (2018). A multivariate behavior genetic investigation of dual-systems models of alcohol involvement. Journal of Studies on Alcohol and Drugs, 79 (4), 617-626. doi: 10.15288/JSAD.2018.79.617
Smit, Dirk J. A., Wright, Margaret J., Meyers, Jacquelyn L., Martin, Nicholas G., Ho, Yvonne Y. W., Malone, Stephen M., Zhang, Jian, Burwell, Scott J., Chorlian, David B., de Geus, Eco J. C., Denys, Damiaan, Hansell, Narelle K., Hottenga, Jouke-Jan, McGue, Matt, van Beijsterveldt, Catharina E. M., Jahanshad, Neda, Thompson, Paul M., Whelan, Christopher D., Medland, Sarah E., Porjesz, Bernice, Lacono, William G. and Boomsma, Dorret I. (2018). Genome-wide association analysis links multiple psychiatric liability genes to oscillatory brain activity. Human Brain Mapping, 39 (11), 4183-4195. doi: 10.1002/hbm.24238
Savage, Jeanne E., Jansen, Philip R., Stringer, Sven, Watanabe, Kyoko, Bryois, Julien, de Leeuw, Christiaan A., Nagel, Mats, Awasthi, Swapnil, Barr, Peter B., Coleman, Jonathan R. I., Grasby, Katrina L., Hammerschlag, Anke R., Kaminski, Jakob A., Karlsson, Robert, Krapohl, Eva, Lam, Max, Nygaard, Marianne, Reynolds, Chandra A., Trampush, Joey W., Young, Hannah, Zabaneh, Delilah, Hägg, Sara, Hansell, Narelle K., Karlsson, Ida K., Linnarsson, Sten, Montgomery, Grant W., Muñoz-Manchado, Ana B., Quinlan, Erin B., Schumann, Gunter ... Posthuma, Danielle (2018). Genome-wide association meta-analysis in 269,867 individuals identifies new genetic and functional links to intelligence. Nature Genetics, 50 (7), 912-919. doi: 10.1038/s41588-018-0152-6
Verhulst, Brad, Neale, Michael C., Eaves, Lindon J., Medland, Sarah E., Heath, Andrew C., Martin, Nicholas G. and Maes, Hermine H. (2018). Extended twin study of alcohol use in Virginia and Australia. Twin Research and Human Genetics, 21 (3), 163-178. doi: 10.1017/thg.2018.21
Odintsova, Veronika V., Willemsen, Gonneke, Dolan, Conor V., Hottenga, Jouke-Jan, Martin, Nicholas G., Slagboom, P. Eline, Ordoñana, Juan R. and Boomsma, Dorret I. (2018). Establishing a twin register: an invaluable resource for (behavior) genetic, epidemiological, biomarker, and ‘omics’ studies. Twin Research and Human Genetics, 21 (3), 239-252. doi: 10.1017/thg.2018.23
Maes, Hermine H., Morley, Kate, Neale, Michael C., Kendler, Kenneth S., Heath, Andrew C., Eaves, Lindon J. and Martin, Nicholas G. (2018). Cross-cultural comparison of genetic and cultural transmission of smoking initiation using an extended twin kinship model. Twin Research and Human Genetics, 21 (3), 179-190. doi: 10.1017/thg.2018.22
Cuellar Partida, Gabriel, Laurin, Charles, Ring, Susan M., Gaunt, Tom R., McRae, Allan, Visscher, Peter M., Montgomery, Grant W., Martin, Nicholas G., Hemani, Gibran, Suderman, Matthew, Relton, Caroline L., Davey Smith, George and Evans, David M. (2018). Genome-wide survey of parent-of-origin effects on DNA methylation identifies candidate imprinted loci in humans. Human Molecular Genetics, 27 (16), 2927-2939. doi: 10.1093/hmg/ddy206
Bartels, Meike, Hendriks, Anne, Mauri, Matteo, Krapohl, Eva, Whipp, Alyce, Bolhuis, Koen, Conde, Lucia Colodro, Luningham, Justin, Fung Ip, Hill, Hagenbeek, Fiona, Roetman, Peter, Gatej, Raluca, Lamers, Audri, Nivard, Michel, van Dongen, Jenny, Lu, Yi, Middeldorp, Christel, van Beijsterveldt, Toos, Vermeiren, Robert, Hankemeijer, Thomas, Kluft, Cees, Medland, Sarah, Lundström, Sebastian, Rose, Richard, Pulkkinen, Lea, Vuoksimaa, Eero, Korhonen, Tellervo, Martin, Nicholas G., Lubke, Gitta ... Boomsma, Dorret I. (2018). Childhood aggression and the co-occurrence of behavioural and emotional problems: results across ages 3-16 years from multiple raters in six cohorts in the EU-ACTION project. European Child & Adolescent Psychiatry, 27 (9), 1-17. doi: 10.1007/s00787-018-1169-1
Visconti, Alessia, Duffy, David L., Liu, Fan, Zhu, Gu, Wu, Wenting, Chen, Yan, Hysi, Pirro G., Zeng, Changqing, Sanna, Marianna, Iles, Mark M., Kanetsky, Peter A., Demenais, Florence, Hamer, Merel A., Uitterlinden, Andre G., Ikram, M. Arfan, Nijsten, Tamar, Martin, Nicholas G., Kayser, Manfred, Spector, Tim D., Han, Jiali, Bataille, Veronique and Falchi, Mario (2018). Genome-wide association study in 176,678 Europeans reveals genetic loci for tanning response to sun exposure. Nature Communications, 9 (1) 1684. doi: 10.1038/s41467-018-04086-y
Wray, Naomi R., Ripke, Stephan, Mattheisen, Manuel, Trzaskowski, Maciej, Byrne, Enda M., Abdellaoui, Abdel, Adams, Mark J., Agerbo, Esben, Air, Tracy M., Andlauer, Till M. F., Bacanu, Silviu-Alin, Baekvad-Hansen, Marie, Beekman, Aartjan F. T., Bigdeli, Tim B., Binder, Elisabeth B., Blackwood, Douglas R. H., Bryois, Julien, Buttenschon, Henriette N., Bybjerg-Grauholm, Jonas, Cai, Na, Castelao, Enrique, Christensen, Jane Hvarregaard, Clarke, Toni-Kim, Coleman, Jonathan I. R., Colodro-Conde, Lucia, Couvy-Duchesne, Baptiste, Craddock, Nick, Crawford, Gregory E., Crowley, Cheynna A. ... Sullivan, Patrick F. (2018). Genome-wide association analyses identify 44 risk variants and refine the genetic architecture of major depression. Nature Genetics, 50 (5), 668-+. doi: 10.1038/s41588-018-0090-3
Gillespie, Nathan A., Neale, Michael C., Bates, Timothy C., Eyler, Lisa T., Fennema-Notestine, Christine, Vassileva, Jasmin, Lyons, Michael J., Prom-Wormley, Elizabeth C., McMahon, Katie L., Thompson, Paul M., de Zubicaray, Greig., Hickie, Ian B., McGrath, John J., Strike, Lachlan T., Rentería, Miguel E., Panizzon, Matthew S., Martin, Nicholas G., Franz, Carol E., Kremen, William S. and Wright, Margaret J. (2018). Testing associations between cannabis use and subcortical volumes in two large population-based samples. Addiction, 113 (9), 1661-1672. doi: 10.1111/add.14252
Hysi, Pirro G., Valdes, Ana M., Liu, Fan, Furlotte, Nicholas A., Evans, David M., Bataille, Veronique, Visconti, Alessia, Hemani, Gibran, McMahon, George, Ring, Susan M., Smith, George Davey, Duffy, David L., Zhu, Gu, Gordon, Scott D., Medland, Sarah E., Lin, Bochao D., Willemsen, Gonneke, Jan Hottenga, Jouke, Vuckovic, Dragana, Girotto, Giorgia, Gandin, Ilaria, Sala, Cinzia, Concas, Maria Pina, Brumat, Marco, Gasparini, Paolo, Toniolo, Daniela, Cocca, Massimiliano, Robino, Antonietta, Yazar, Seyhan ... Spector, Timothy D. (2018). Genome-wide association meta-analysis of individuals of European ancestry identifies new loci explaining a substantial fraction of hair color variation and heritability. Nature Genetics, 50 (5), 652-656. doi: 10.1038/s41588-018-0100-5
Warrington, Nicole M., Shevroja, Enisa, Hemani, Gibran, Hysi, Pirro G., Jiang, Yunxuan, Auton, Adam, Boer, Cindy G., Mangino, Massimo, Wang, Carol A., Kemp, John P., McMahon, George, Medina-Gomez, Carolina, Hickey, Martha, Trajanoska, Katerina, Wolke, Dieter, Ikram, Arfan M., 23 and Me Research Team, Montgomery, Grant W., Felix, Janine F., Wright, Margaret J., Mackey, David A., Jaddoe, Vincent W., Martin, Nicholas G., Tung, Joyce Y., Davey Smith, George, Pennell, Craig E., Spector, Tim D., van Meurs, Joyce, Rivadeneira, Fernando ... Evans, David M. (2018). Genome-wide association study identifies nine novel loci for 2D:4D finger ratio, a putative retrospective biomarker of testosterone exposure in utero. Human Molecular Genetics, 27 (11), 2025-2038. doi: 10.1093/hmg/ddy121
Painter, Jodie N., O'Mara, Tracy A., Morris, Andrew P., Cheng, Timothy H. T., Gorman, Maggie, Martin, Lynn, Hodson, Shirley, Jones, Angela, Martin, Nicholas G., Gordon, Scott, Henders, Anjali K, Attia, John, McEvoy, Mark, Holliday, Elizabeth G., Scott, Rodney J, Webb, Penelope M., Fasching, Peter A.., Beckmann, Matthias W, Ekici, Arif B, Hein, Alexander, Rübner, Matthias, Hall, Per, Czene, Kamila, Dörk, Thilo, Dürst, Matthias, Hillemanns, Peter, Runnebaum, Ingo, Lambrechts, Diether, Amant, Frederic ... Spurdle, Amanda B (2018). Genetic overlap between endometriosis and endometrial cancer: evidence from cross-disease genetic correlation and GWAS meta-analyses. Cancer Medicine, 7 (5), 1978-1987. doi: 10.1002/cam4.1445
Couvy-Duchesne, Baptiste, O'Callaghan, Victoria, Parker, Richard, Mills, Natalie, Kirk, Katherine M., Scott, Jan, Vinkhuyzen, Anna., Hermens, Daniel F., Lind, Penelope A., Davenport, Tracey A., Burns, Jane M., Connell, Melissa, Zietsch, Brendan P., Scott, James, Wright, Margaret J., Medland, Sarah E., McGrath, John, Martin, Nicholas G., Hickie, Ian B. and Gillespie, Nathan A. (2018). Nineteen and Up study (19Up): Understanding pathways to mental health disorders in young Australian twins. BMJ Open, 8 (3) e018959, 1-13. doi: 10.1136/bmjopen-2017-018959
Bates, Timothy C., Maher, Brion S., Medland, Sarah E., McAloney, Kerrie, Wright, Margaret J., Hansell, Narelle K., Kendler, Kenneth S., Martin, Nicholas G. and Gillespie, Nathan A. (2018). The Nature of Nurture: Using a Virtual-Parent Design to Test Parenting Effects on Children's Educational Attainment in Genotyped Families. Twin Research and Human Genetics, 21 (2), 73-83. doi: 10.1017/thg.2018.11
Wu, Yang, Zeng, Jian, Zhang, Futao, Zhu, Zhihong, Qi, Ting, Zheng, Zhili, Lloyd-Jones, Luke R., Marioni, Riccardo E., Martin, Nicholas G., Montgomery, Grant W., Deary, Ian J., Wray, Naomi R., Visscher, Peter M., McRae, Allan F. and Yang, Jian (2018). Integrative analysis of omics summary data reveals putative mechanisms underlying complex traits. Nature Communications, 9 (918) 918, 918. doi: 10.1038/s41467-018-03371-0
Mühleisen, Thomas W., Reinbold, Céline S., Forstner, Andreas J., Abramova, Lilia I., Alda, Martin, Babadjanova, Gulja, Bauer, Michael, Brennan, Paul, Chuchalin, Alexander, Cruceanu, Cristiana, Czerski, Piotr M., Degenhardt, Franziska, Fischer, Sascha B., Fullerton, Janice M., Gordon, Scott D., Grigoroiu-Serbanescu, Maria, Grof, Paul, Hauser, Joanna, Hautzinger, Martin, Herms, Stefan, Hoffmann, Per, Kammerer-Ciernioch, Jutta, Khusnutdinova, Elza, Kogevinas, Manolis, Krasnov, Valery, Lacour, André, Laprise, Catherine, Leber, Markus, Lissowska, Jolanta ... Cichon, Sven (2018). Gene set enrichment analysis and expression pattern exploration implicate an involvement of neurodevelopmental processes in bipolar disorder. Journal of Affective Disorders, 228, 20-25. doi: 10.1016/j.jad.2017.11.068
Taylor, Andrew, Barlow, Nicola, Day, Martin P., Hill, Sarah, Martin, Nicholas and Patriarca, Marina (2018). Atomic spectrometry update: review of advances in the analysis of clinical and biological materials, foods and beverages. Journal of Analytical Atomic Spectrometry, 33 (3), 338-382. doi: 10.1039/c8ja90005a
Binz, T. M., Rietschel, L., Streit, F., Hofmann, M., Gehrke, J., Herdener, M., Quednow, B. B., Martin, N. G., Rietschel, M., Kraemer, T. and Baumgartner, M. R. (2018). Endogenous cortisol in keratinized matrices: systematic determination of baseline cortisol levels in hair and the influence of sex, age and hair color. Forensic Science International, 284, 33-38. doi: 10.1016/j.forsciint.2017.12.032
Pardiñas, Antonio F, Holmans, Peter, Pocklington, Andrew J, Escott-Price, Valentina, Ripke, Stephan, Carrera, Noa, Legge, Sophie E, Bishop, Sophie, Cameron, Darren, Hamshere, Marian L, Han, Jun, Hubbard, Leon, Lynham, Amy, Mantripragada, Kiran, Rees, Elliott, MacCabe, James H, McCarroll, Steven A, Baune, Bernhard T, Breen, Gerome, Byrne, Enda M., Dannlowski, Udo, Eley, Thalia C, Hayward, Caroline, Martin, Nicholas G., McIntosh, Andrew M, Plomin, Robert, Porteous, David J, Wray, Naomi R, Caballero, Armando ... CRESTAR Consortium (2018). Common schizophrenia alleles are enriched in mutation-intolerant genes and in regions under strong background selection. Nature Genetics, 50 (3), 381-389. doi: 10.1038/s41588-018-0059-2
Gharahkhani, Puya, Burdon, Kathryn P., Cooke Bailey, Jessica N, Hewitt, Alex W., Law, Matthew H., Pasquale, Louis R., Kang, Jae H., Haines, Jonathan L., Souzeau, Emmanuelle, Zhou, Tiger, Siggs, Owen M., Landers, John, Awadalla, Mona, Sharma, Shiwani, Mills, Richard A., Ridge, Bronwyn, Lynn, David, Casson, Robert, Graham, Stuart L., Goldberg, Ivan, White, Andrew, Healey, Paul R., Grigg, John, Lawlor, Mitchell, Mitchell, Paul, Ruddle, Jonathan, Coote, Michael, Walland, Mark, Best, Stephen ... NEIGHBORHOOD consortium (2018). Analysis combining correlated glaucoma traits identifies five new risk loci for open-angle glaucoma. Scientific reports, 8 (1) 3124, 3124. doi: 10.1038/s41598-018-20435-9
Liu, Fan, Chen, Yan, Zhu, Gu, Hysi, Pirro G., Wu, Sijie, Adhikari, Kaustubh, Breslin, Krystal, Pośpiech, Ewelina, Hamer, Merel A., Peng, Fuduan, Muralidharan, Charanya, Acuna-Alonzo, Victor, Canizales-Quinteros, Samuel, Bedoya, Gabriel, Gallo, Carla, Poletti, Giovanni, Rothhammer, Francisco, Bortolini, Maria Catira, Gonzalez-Jose, Rolando, Zeng, Changqing, Xu, Shuhua, Jin, Li, Uitterlinden, André G., Arfan Ikram, M., van Duijn, Cornelia M., Nijsten, Tamar, Walsh, Susan, Branicki, Wojciech, Wang, Sijia ... Kayser, Manfred (2018). Meta-analysis of genome-wide association studies identifies 8 novel loci involved in shape variation of human head hair. Human Molecular Genetics, 27 (3), 559-575. doi: 10.1093/hmg/ddx416
Loehlin, John C. and Martin, Nicholas G. (2018). Personality types: a twin study. Personality and Individual Differences, 122, 99-103. doi: 10.1016/j.paid.2017.10.012
Chang, H., Hoshina, N., Zhang, C., Ma, Y., Cao, H., Wang, Y., Wu, D. D., Bergen, S. E., Landén, M., Hultman, C. M., Preisig, M., Kutalik, Z., Castelao, E., Grigoroiu-Serbanescu, M., Forstner, A. J., Strohmaier, J., Hecker, J., Schulze, T. G., Müller-Myhsok, B., Reif, A., Mitchell, P. B., Martin, N. G., Schofield, P. R., Cichon, S., Nöthen, M. M., Walter, H., Erk, S., Heinz, A., Amin, N. ... MooDS Bipolar Consortium (2018). The protocadherin 17 gene affects cognition, personality, amygdala structure and function, synapse development and risk of major mood disorders. Molecular Psychiatry, 23 (2), 400-412. doi: 10.1038/mp.2016.231
Crist, R. C., Doyle, G. A., Nelson, E. C., Degenhardt, L., Martin, N. G., Montgomery, G. W., Saxon, A. J., Ling, W. and Berrettini, W. H. (2018). A polymorphism in the OPRM1 3'-untranslated region is associated with methadone efficacy in treating opioid dependence. The Pharmacogenomics Journal, 18 (1), 173-179. doi: 10.1038/tpj.2016.89
Couvy-Duchesne, Baptiste, Strike, Lachlan T., de Zubicaray, Greig I., McMahon, Katie L., Thompson, Paul M., Hickie, Ian B., Martin, Nicholas G. and Wright, Margaret J. (2018). Lingual Gyrus Surface Area Is Associated with Anxiety-Depression Severity in Young Adults: A Genetic Clustering Approach. eNeuro, 5 (1) e0153-17.2017, 1-14. doi: 10.1523/ENEURO.0153-17.2017
Lupton, Michelle K., Medland, Sarah E., Gordon, Scott D., Goncalves, Tabatha, MacGregor, Stuart, Mackey, David A., Young, Terri L., Duffy, David L., Visscher, Peter M., Wray, Naomi R., Nyholt, Dale R., Bain, Lisa, Ferreira, Manuel A., Henders, Anjali K., Wallace, Leanne, Montgomery, Grant W., Wright, Margaret J. and Martin, Nicholas G. (2018). Accuracy of inferred APOE genotypes for a range of genotyping arrays and imputation reference panels. Journal of Alzheimer's Disease, 64 (1), 49-54. doi: 10.3233/JAD-171104
Whitfield, John B., Heath, Andrew C., Madden, Pamela A. F., Landers, J. George and Martin, Nicholas G. (2018). Effects of high alcohol intake, alcohol-related symptoms and smoking on mortality. Addiction, 113 (1), 158-166. doi: 10.1111/add.14008
Scott, Jan, Davenport, Tracey A., Parker, Richard, Hermens, Daniel F., Lind, Penelope A., Medland, Sarah E., Wright, Margaret J., Martin, Nicholas G., Gillespie, Nathan A. and Hickie, Ian B. (2017). Pathways to depression by age 16 years: Examining trajectories for self-reported psychological and somatic phenotypes across adolescence. Journal of Affective Disorders, 230, 1-6. doi: 10.1016/j.jad.2017.12.007
Joshi, Peter K., Pirastu, Nicola, Kentistou, Katherine A., Fischer, Krista, Hofer, Edith, Schraut, Katharina E., Clark, David W., Nutile, Teresa, Barnes, Catriona L. K., Timmers, Paul R. H. J., Shen, Xia, Gandin, Ilaria, McDaid, Aaron F., Hansen, Thomas Folkmann, Gordon, Scott D., Giulianini, Franco, Boutin, Thibaud S., Abdellaoui, Abdel, Zhao, Wei, Medina-Gomez, Carolina, Bartz, Traci M., Trompet, Stella, Lange, Leslie A., Raffield, Laura, Van Der Spek, Ashley, Galesloot, Tessel E., Proitsi, Petroula, Yanek, Lisa R., Bielak, Lawrence F. ... Wilson, James F. (2017). Genome-wide meta-analysis associates HLA-DQA1/DRB1 and LPA and lifestyle factors with human longevity. Nature Communications, 8 (1) 910, 910. doi: 10.1038/s41467-017-00934-5
Tielbeek, Jorim J., Johansson, Ada, Polderman, Tinca J.C., Rautiainen, Marja-Riitta, Jansen, Philip, Taylor, Michelle, Tong, Xiaoran, Lu, Qing, Burt, Alexandra S., Tiemeier, Henning, Viding, Essi, Plomin, Robert, Martin, Nicholas G., Heath, Andrew C., Madden, Pamela A.F., Montgomery, Grant, Beaver, Kevin M., Waldman, Irwin, Gelernter, Joel, Kranzler, Henry R., Farrer, Lindsay A., Perry, John R.B., Munafò, Marcus, LoParo, Devon, Paunio, Tiina, Tiihonen, Jari, Mous, Sabine E., Pappa, Irene, De Leeuw, Christiaan ... Broad Antisocial Behavior Consortium (2017). Genome-wide association studies of a broad spectrum of antisocial behavior. JAMA Psychiatry, 74 (12), 1242-1250. doi: 10.1001/jamapsychiatry.2017.3069
Xiao, Xiao, Wang, Lu, Wang, Chuang, Yuan, Ti-Fei, Zhou, Dongsheng, Zheng, Fanfan, Li, Lingyi, Grigoroiu-Serbanescu, Maria, Ikeda, Masashi, Iwata, Nakao, Takahashi, Atsushi, Kamatani, Yoichiro, Kubo, Michiaki, Preisig, Martin, Kutalik, Zoltán, Castelao, Enrique, Pistis, Giorgio, Amin, Najaf, Van Duijn, Cornelia M., Forstner, Andreas J., Strohmaier, Jana, Hecker, Julian, Schulze, Thomas G., Müller-Myhsok, Bertram, Reif, Andreas, Mitchell, Philip B., Martin, Nicholas G., Schofield, Peter R., Cichon, Sven ... MooDS Bipolar Consortium (2017). Common variants at 2q11.2, 8q21.3, and 11q13.2 are associated with major mood disorders. Translational Psychiatry, 7 (12) 1273. doi: 10.1038/s41398-017-0019-0
Mina-Vargas, Angela, Colodro-Conde, Lucía, Grasby, Katrina, Zhu, Gu, Gordon, Scott, Medland, Sarah E. and Martin, Nicholas G. (2017). Heritability and GWAS analyses of acne in australian adolescent twins. Twin Research and Human Genetics, 20 (6), 541-549. doi: 10.1017/thg.2017.58
Ong, Jue-Sheng, Hwang, Liang-Dar, Cuellar-Partida, Gabriel, Martin, Nicholas G., Chenevix-Trench, Georgia, Quinn, Michael C. J., Cornelis, Marilyn C., Gharahkhani, Puya, Webb, Penelope M., MacGregor, Stuart and Ovarian Cancer Association Consortium (2017). Assessment of moderate coffee consumption and risk of epithelial ovarian cancer: a Mendelian randomization study. International Journal of Epidemiology, 47 (2), 450-459. doi: 10.1093/ije/dyx236
Agrawal, A., Chou, Y.- L., Carey, C. E., Baranger, D. A. A., Zhang, B., Sherva, R., Wetherill, L., Kapoor, M., Wang, J.-.C., Bertelsen, S., Anokhin, A. P., Hesselbrock, V., Kramer, J., Lynskey, M. T., Meyers, J. L., Nurnberger, J. I., Rice, J. P., Tischfield, J., Bierut, L. J., Degenhardt, L., Farrer, L. A., Gelernter, J., Hariri, A. R., Heath, A. C., Kranzler, H. R., Madden, P. A. F., Martin, N. G., Montgomery, G. W., Porjesz, B. ... Nelson, E. C. (2017). Genome-wide association study identifies a novel locus for cannabis dependence. Molecular Psychiatry, 23 (5), 1293-1302. doi: 10.1038/mp.2017.200
Mills, Natalie T., Maier, Robert, Whitfield, John B., Wright, Margaret J., Colodro-Conde, Lucia, Byrne, Enda M., Scott, James G., Byrne, Gerard J., Hansell, Narelle K., Vinkhuyzen, Anna A. E., CouvyDuchesne, Baptiste, Montgomery, Grant W., Henders, Anjali K., Martin, Nicholas G., Wray, Naomi R. and Benyamin, Beben (2017). Investigating the relationship between iron and depression. Journal of Psychiatric Research, 94, 148-155. doi: 10.1016/j.jpsychires.2017.07.006
Zhong, Kaiyin, Zhu, Gu, Jing, Xiaoxi, Hendriks, A. Emile J., Drop, Sten L. S., Ikram, M. Arfan, Gordon, Scott, Zeng, Changqing, Uitterlinden, Andre G., Martin, Nicholas G., Liu, Fan and Kayser, Manfred (2017). Genome-wide compound heterozygote analysis highlights alleles associated with adult height in Europeans. Human Genetics, 136 (11-12), 1407-1417. doi: 10.1007/s00439-017-1842-3
Schermer, Julie Aitken, Martin, Rod A., Vernon, Philip A., Martin, Nicholas G., Conde, Lucia Colodro, Statham, Dixie and Lynskey, Michael T. (2017). Lonely people tend to make fun of themselves: A behavior genetic analysis of humor styles and loneliness. Personality and Individual Differences, 117, 71-73. doi: 10.1016/j.paid.2017.05.042
Silventoinen, Karri, Jelenkovic, Aline, Latvala, Antti, Sund, Reijo, Yokoyama, Yoshie, Ullemar, Vilhelmina, Almqvist, Catarina, Derom, Catherine A., Vlietinck, Robert F., Loos, Ruth J. F., Kandler, Christian, Honda, Chika, Inui, Fujio, Iwatani, Yoshinori, Watanabe, Mikio, Rebato, Esther, Stazi, Maria A., Fagnani, Corrado, Brescianini, Sonia, Hur, Yoon-Mi, Jeong, Hoe-Uk, Cutler, Tessa L., Hopper, John L., Busjahn, Andreas, Saudino, Kimberly J., Ji, Fuling, Ning, Feng, Pang, Zengchang, Rose, Richard J. ... Kaprio, Jaakko (2017). Education in twins and their parents across birth cohorts over 100 years: an individual-level pooled analysis of 42-twin cohorts. Twin Research and Human Genetics, 20 (5), 395-405. doi: 10.1017/thg.2017.49
Guadalupe, Tulio, Mathias, Samuel R., vanErp, Theo G. M., Whelan, Christopher D., Zwiers, Marcel P., Abe, Yoshinari, Abramovic, Lucija, Agartz, Ingrid, Andreassen, Ole A., Arias-Vásquez, Alejandro, Aribisala, Benjamin S., Armstrong, Nicola J., Arolt, Volker, Artiges, Eric, Ayesa-Arriola, Rosa, Baboyan, Vatche G., Banaschewski, Tobias, Barker, Gareth, Bastin, Mark E., Baune, Bernhard T., Blangero, John, Bokde, Arun L.W., Boedhoe, Premika S.W., Bose, Anushree, Brem, Silvia, Brodaty, Henry, Bromberg, Uli, Brooks, Samantha, Büchel, Christian ... Francks, Clyde (2017). Human subcortical brain asymmetries in 15,847 people worldwide reveal effects of age and sex. Brain Imaging and Behavior, 11 (5), 1497-1514. doi: 10.1007/s11682-016-9629-z
Macé, Aurélien, Tuke, Marcus A., Deelen, Patrick, Kristiansson, Kati, Mattsson, Hannele, Nõukas, Margit, Sapkota, Yadav, Schick, Ursula, Porcu, Eleonora, Rüeger, Sina, McDaid, Aaron F., Porteous, David, Winkler, Thomas W., Salvi, Erika, Shrine, Nick, Liu, Xueping, Ang, Wei Q., Zhang, Weihua, Feitosa, Mary F., Venturini, Cristina, Van Der Most, Peter J., Rosengren, Anders, Wood, Andrew R., Beaumont, Robin N., Jones, Samuel E., Ruth, Katherine S., Yaghootkar, Hanieh, Tyrrell, Jessica, Havulinna, Aki S. ... Kutalik, Zoltán (2017). CNV-association meta-analysis in 191,161 European adults reveals new loci associated with anthropometric traits. Nature Communications, 8 (1) 744, 744. doi: 10.1038/s41467-017-00556-x
Tropf, Felix C., Lee, S Hong, Verweij, Renske M., Stulp, Gert, van der Most, Peter J., de Vlaming, Ronald, Bakshi, Andrew, Briley, Daniel A., Rahal, Charles, Hellpap, Robert, Nyman, Anastasia, Esko, Tõnu, Metspalu, Andres, Medland, Sarah E., Martin, Nicholas G., Barban, Nicola, Snieder, Harold, Robinson, Matthew R. and Mills, Melinda C. (2017). Hidden heritability due to heterogeneity across seven populations. Nature Human Behaviour, 1 (10), 757-765. doi: 10.1038/s41562-017-0195-1
Lee, Anthony J., Hibbs, Courtney, Wright, Margaret J., Martin, Nicholas G., Keller, Matthew C. and Zietsch, Brendan P. (2017). Assessing the accuracy of perceptions of intelligence based on heritable facial features. Intelligence, 64, 1-8. doi: 10.1016/j.intell.2017.06.002
Law, Matthew H., Medland, Sarah E., Zhu, Gu, Yazar, Seyhan, Vinuela, Ana, Wallace, Leanne, Shekar, Sri Niranjan, Duffy, David L., Bataille, Veronique, Glass, Dan, Spector, Tim D., Wood, Diane, MuTHER Consortium, Gordon, Scott D., Barbour, Julie M., Henders, Anjali K., Hewitt, Alex W., Montgomery, Grant W., Sturm, Richard A., Mackey, David A., Green, Adele C., Martin, Nicholas G. and MacGregor, Stuart (2017). Genome-Wide Association shows that pigmentation genes play a role in skin aging. Journal of Investigative Dermatology, 137 (9), 1887-1894. doi: 10.1016/j.jid.2017.04.026
Chang, Hong, Li, Lingyi, Peng, Tao, Grigoroiu-Serbanescu, Maria, Bergen, Sarah E., Landén, Mikael, Hultman, Christina M., Forstner, Andreas J., Strohmaier, Jana, Hecker, Julian, Schulze, Thomas G., Müller-Myhsok, Bertram, Reif, Andreas, Mitchell, Philip B., Martin, Nicholas G., Cichon, Sven, Nöthen, Markus M., Jamain, Stéphane, Leboyer, Marion, Bellivier, Frank, Etain, Bruno, Kahn, Jean-Pierre, Henry, Chantal, Rietschel, Marcella, Backlund, Lena, Frisén, Louise, Lavebratt, Catharina, Schalling, Martin, Ösby, Urban ... MooDS Consortium (2017). Identification of a bipolar disorder vulnerable gene CHDH at 3p21.1. Molecular Neurobiology, 54 (7), 5166-5176. doi: 10.1007/s12035-016-0041-x
Agrawal, Arpana, Nelson, Elliot C., Bucholz, Kathleen K., Tillman, Rebecca, Grucza, Richard A., Statham, Dixie J., Madden, Pamela A. F., Martin, Nicholas G., Heath, Andrew C. and Lynskey, Michael T. (2017). Major depressive disorder, suicidal thoughts and behaviours, and cannabis involvement in discordant twins: a retrospective cohort study. The Lancet Psychiatry, 4 (9), 706-714. doi: 10.1016/S2215-0366(17)30280-8
Silventoinen, Karri, Jelenkovic, Aline, Sund, Reijo, Yokoyama, Yoshie, Hur, Yoon-Mi, Cozen, Wendy, Hwang, Amie E., Mack, Thomas M., Honda, Chika, Inui, Fujio, Iwatani, Yoshinori, Watanabe, Mikio, Tomizawa, Rie, Pietilainen, Kirsi H., Rissanen, Aila, Siribaddana, Sisira H., Hotopf, Matthew, Sumathipala, Athula, Rijsdijk, Fruhling, Tan, Qihua, Zhang, Dongfeng, Pang, Zengchang, Piirtola, Maarit, Aaltonen, Sari, Oncel, Sevgi Y., Aliev, Fazil, Rebato, Esther, Hjelmborg, Jacob B., Christensen, Kaare ... Kaprio, Jaakko (2017). Differences in genetic and environmental variation in adult BMI by sex, age, time period, and region: an individual-based pooled analysis of 40 twin cohorts. American Journal of Clinical Nutrition, 106 (2), 457-466. doi: 10.3945/ajcn.117.153643
Couvy-Duchesne, Baptiste, Davenport, Tracey A., Martin, Nicholas G., Wright, Margaret J. and Hickie, Ian B. (2017). Validation and psychometric properties of the Somatic and Psychological HEalth REport (SPHERE) in a young Australian-based population sample using non-parametric item response theory. BMC Psychiatry, 17 (1) 279, 279. doi: 10.1186/s12888-017-1420-1
Park, Shin-Ho, Guastella, Adam J., Lynskey, Michael, Agrawal, Arpana, Constantino, John N., Medland, Sarah E., Song, Yun Ju C., Martin, Nicholas G. and Colodro-Conde, Lucía (2017). Neuroticism and the Overlap between Autistic and ADHD Traits: Findings from a Population Sample of Young Adult Australian Twins. Twin Research and Human Genetics, 20 (4), 319-329. doi: 10.1017/thg.2017.38
Deutsch, Arielle R., Slutske, Wendy S., Lynskey, Michael T., Bucholz, Kathleen K., Madden, Pamela A. F., Heath, Andrew C. and Martin, Nicholas G. (2017). From alcohol initiation to tolerance to problems: Discordant twin modeling of a developmental process. Development and Psychopathology, 29 (3), 845-861. doi: 10.1017/S0954579416000523
Lee, Anthony J., Wright, Margaret J., Martin, Nicholas G., Keller, Matthew C. and Zietsch, Brendan P. (2017). Facial trustworthiness is associated with heritable aspects of face shape. Adaptive Human Behavior and Physiology, 3 (4), 351-364. doi: 10.1007/s40750-017-0073-0
Rivera, Natalia V., Hagemann-Jensen, Michael, Ferreira, Manuel A. R., Kullberg, Susanna, Eklund, Anders, Martin, Nicholas G., Padyukov, Leonid and Grunewald, Johan (2017). Common variants of T-cells contribute differently to phenotypic variation in sarcoidosis. Scientific Reports, 7 (1) 5623. doi: 10.1038/s41598-017-05754-7
Colodro-Conde, L., Couvy-Duchesne, B., Zhu, G., Coventry, W. L., Byrne, E. M., Gordon, S., Wright, M. J., Montgomery, G. W., Madden, P. A. F., Ripke, S., Eaves, L. J., Heath, A. C., Wray, N. R., Medland, S. E. and Martin, N. G. (2017). A direct test of the diathesis–stress model for depression. Molecular Psychiatry, 23 (7), 1590-1596. doi: 10.1038/mp.2017.130
Lupton, Michelle K., Benyamin, Beben, Proitsi, Petroula, Nyholt, Dale R., Ferreira, Manuel A., Montgomery, Grant W., Heath, Andrew C., Madden, Pamela A., Medland, Sarah E., Gordon, Scott D., Lovestone, Simon, Tsolaki, Magda, Kloszewska, Iwona, Soininen, Hilkka, Mecocci, Patrizia, Vellas, Bruno, Powell, John F., Bush, Ashley I., Wright, Margaret J., Martin, Nicholas G. and Whitfield, John B. (2017). No genetic overlap between circulating iron levels and Alzheimer's disease. Journal of Alzheimers Disease, 59 (1), 85-99. doi: 10.3233/JAD-170027
Luciano, Michelle, Hagenaars, Saskia P. , Cox, Simon R. , Hill, William David , Davies, Gail , Harris, Sarah E. , Deary, Ian J. , Evans, David M. , Martin, Nicholas G. , Wright, Margaret J. and Bates, Timothy C. (2017). Single Nucleotide Polymorphisms Associated with Reading Ability Show Connection to Socio-Economic Outcomes. Behavior Genetics, 47 (5), 469-479. doi: 10.1007/s10519-017-9859-x
Smolkina, M., Morley, K. I., Rijsdijk, F., Agrawal, A., Bergin, J. E., Nelson, E. C., Statham, D., Martin, N. G. and Lynskey, M. T. (2017). Cannabis and Depression: A Twin Model Approach to Co-morbidity. Behavior Genetics, 47 (4), 394-404. doi: 10.1007/s10519-017-9848-0
Witt, S. H., Streit, F., Jungkunz, M., Frank, J., Awasthi, S., Reinbold, C. S., Treutlein, J., Degenhardt, F., Forstner, A. J., Heilmann-Heimbach, S., Dietl, L., Schwarze, C. E., Schendel, D., Strohmaier, J., Abdellaoui, A., Adolfsson, R., Air, T. M., Akil, H., Alda, M., Alliey-Rodriguez, N., Andreassen, O. A., Babadjanova, G., Bass, N. J., Bauer, M., Baune, B. T., Bellivier, F., Bergen, S., Bethell, A., Biernacka, J. M. ... Rietschel, M. (2017). Genome-wide association study of borderline personality disorder reveals genetic overlap with bipolar disorder, major depression and schizophrenia.. Translational psychiatry, 7 (6), e1155-e1155. doi: 10.1038/tp.2017.115
Brouwer, Rachel M., Panizzon, Matthew S., Glahn, David C., Hibar, David P., Hua, Xue, Jahanshad, Neda, Abramovic, Lucija, de Zubicaray, Greig I., Franz, Carol E., Hansell, Narelle K., Hickie, Ian B., Koenis, Marinka M. G., Martin, Nicholas G., Mather, Karen A., McMahon, Katie L., Schnack, Hugo G., Strike, Lachlan T., Swagerman, Suzanne C., Thalamuthu, Anbupalam, Wen, Wei, Gilmore, John H., Gogtay, Nitin, Kahn, Rene S., Sachdev, Perminder S., Wright, Margaret J., Boomsma, Dorret I., Kremen, William S., Thompson, Paul M. and Hulshoff Pol, Hilleke E. (2017). Genetic influences on individual differences in longitudinal changes in global and subcortical brain volumes: results of the ENIGMA plasticity working group. Human Brain Mapping, 8 (9), 4444-4458. doi: 10.1002/hbm.23672
Kirk, Katherine M., Martin, Felicity C., Mao, Amy, Parker, Richard, Maguire, Sarah, Thornton, Laura M., Zhu, Gu, McAloney, Kerrie, Freeman, Jeremy L., Hay, Phillipa, Madden, Sloane, Morgan, Christine, Russell, Janice, Sawyer, Susan M., Hughes, Elizabeth K., Fairweather-Schmidt, A. Kate, Fursland, Anthea, McCormack, Julie, Wagg, Fiona, Jordan, Jennifer, Kennedy, Martin A., Ward, Warren, Wade, Tracey D., Bulik, Cynthia M. and Martin, Nicholas G. (2017). The Anorexia Nervosa Genetics Initiative: study description and sample characteristics of the Australian and New Zealand arm. Australian and New Zealand Journal of Psychiatry, 51 (6), 583-594. doi: 10.1177/0004867417700731
Corfield, Elizabeth C., Martin, Nicholas G. and Nyholt, Dale R. (2017). Familiality and heritability of fatigue in an Australian twin sample. Twin Research and Human Genetics, 20 (3), 208-215. doi: 10.1017/thg.2017.22
Sapkota, Yadav, Steinthorsdottir, Valgerdur, Morris, Andrew P., Fassbender, Amelie, Rahmioglu, Nilufer, De Vivo, Immaculata, Buring, Julie E., Zhang, Futao, Edwards, Todd L., Jones, Sarah, Dorien, O., Peterse, Danielle, Rexrode, Kathryn M., Ridker, Paul M., Schork, Andrew J., MacGregor, Stuart, Martin, Nicholas G., Becker, Christian M., Adachi, Sosuke, Yoshihara, Kosuke, Enomoto, Takayuki, Takahashi, Atsushi, Kamatani, Yoichiro, Matsuda, Koichi, Kubo, Michiaki, Thorleifsson, Gudmar, Geirsson, Reynir T., Thorsteinsdottir, Unnur, Wallace, Leanne M. ... Nyholt, Dale R. (2017). Meta-analysis identifies five novel loci associated with endometriosis highlighting key genes involved in hormone metabolism. Nature Communications, 8 (1) 15539, 15539. doi: 10.1038/ncomms15539
Corfield, E. C., Yang, Y., Martin, N. G. and Nyholt, D. R. (2017). A continuum of genetic liability for minor and major depression. Translational Psychiatry, 7 (5) e1131, e1131-e1131. doi: 10.1038/tp.2017.99
Duncan, Laramie, Yilmaz, Zeynep, Gaspar, Helena, Walters, Raymond, Goldstein, Jackie, Anttila, Verneri, Bulik-Sullivan, Brendan, Ripke, Stephan, Thornton, Laura, Hinney, Anke, Daly, Mark, Sullivan, Patrick F., Zeggini, Eleftheria, Breen, Gerome, Bulik, Cynthia M., Duncan, Laramie, Yilmaz, Zeynep, Gaspar, Héléna, Walters, Raymond, Goldstein, Jackie, Anttila, Verneri, Bulik-Sullivan, Brendan, Ripke, Stephan, Adan, Roger, Alfredsson, Lars, Ando, Tetsuya, Andreassen, Ole, Aschauer, Harald, Baker, Jessica ... Eating Disorders Working Group of the Psychiatric Genomics Consortium (2017). Significant locus and metabolic genetic correlations revealed in genome-wide association study of anorexia nervosa. American Journal of Psychiatry, 174 (9), 850-858. doi: 10.1176/appi.ajp.2017.16121402
Renteria, M. E., Schmaal, L., Hibar, D. P., Couvy-Duchesne, B., Strike, L. T., Mills, N. T., de Zubicaray, G. I., McMahon, K. L., Medland, S. E., Gillespie, N. A., Hatton, S. N., Lagopoulos, J., Veltman, D. J., van der Wee, N., van Erp, T. G. M., Wittfeld, K., Grabe, H. J., Block, A., Hegenscheid, K., Voelzke, H., Veer, I. M., Walter, H., Schnell, K., Schramm, E., Normann, C., Schoepf, D., Konrad, C., Zurowski, B., Godlewska, B. R. ... Hickie, I. B. (2017). Subcortical brain structure and suicidal behaviour in major depressive disorder: a meta-analysis from the ENIGMA-MDD working group. Translational Psychiatry, 7 (5) e1116, e1116-e1116. doi: 10.1038/tp.2017.84
Haycock, Philip C., Burgess, Stephen, Nounu, Aayah, Zheng, Jie, Okoli, George N., Bowden, Jack, Wade, Kaitlin Hazel, Timpson, Nicholas J., Evans, David M., Willeit, Peter, Aviv, Abraham, Gaunt, Tomr., Hemani, Gibran, Mangino, Massimo, Ellis, Hayley Patricia, Kurian, Kathreena M., Pooley, Karen A., Eeles, Rosalind A., Lee, Jeffrey E., Fang, Shenying, Chen, Wei V., Law, Matthew H., Bowdler, Lisa M., Iles, Mark M., Yang, Qiong, Worrall, Bradford B., Markus, Hugh Stephen, Hung, Rayjean J., Amos, Chris I. ... Smith, George Davey (2017). Association between telomere length and risk of cancer and non-neoplastic diseases a Mendelian randomization study. JAMA Oncology, 3 (5), 636-651. doi: 10.1001/jamaoncol.2016.5945
Bogl, Leonie H., Jelenkovic, Aline, Vuoksimaa, Eero, Ahrenfeldt, Linda, Pietiläinen, Kirsi H., Stazi, Maria A., Fagnani, Corrado, D’Ippolito, Cristina, Hur, Yoon-Mi, Jeong, Hoe-Uk, Silberg, Judy L., Eaves, Lindon J., Maes, Hermine H., Bayasgalan, Gombojav, Narandalai, Danshiitsoodol, Cutler, Tessa L., Kandler, Christian, Jang, Kerry L., Christensen, Kaare, Skytthe, Axel, Kyvik, Kirsten O., Cozen, Wendy, Hwang, Amie E., Mack, Thomas M., Derom, Catherine A., Vlietinck, Robert F., Nelson, Tracy L., Whitfield, Keith E., Corley, Robin P. ... Kaprio, Jaakko (2017). Does the sex of one’s co-twin affect height and BMI in adulthood? A study of dizygotic adult twins from 31 cohorts. Biology of Sex Differences, 8 (1) 14. doi: 10.1186/s13293-017-0134-x
Graff, Mariaelisa, Scott, Robert A., Justice, Anne E., Young, Kristin L., Feitosa, Mary F., Barata, Llilda, Winkler, Thomas W., Chu, Audrey Y., Mahajan, Anubha, Hadley, David, Xue, Luting, Workalemahu, Tsegaselassie, Heard-Costa, Nancy L., den Hoed, Marcel, Ahluwalia, Tarunveer S., Qi, Qibin, Ngwa, Julius S., Renström, Frida, Quaye, Lydia, Eicher, John D., Hayes, James E., Cornelis, Marilyn, Kutalik, Zoltan, Lim, Elise, Luan, Jian’an, Huffman, Jennifer E., Zhang, Weihua, Zhao, Wei, Griffin, Paula J. ... Kilpeläinen, Tuomas O. (2017). Genome-wide physical activity interactions in adiposity ― a meta-analysis of 200,452 adults. PLoS Genetics, 13 (4) e1006528, e1006528. doi: 10.1371/journal.pgen.1006528
Justice, Anne E., Winkler, Thomas W., Feitosa, Mary F., Graff, Misa, Fisher, Virginia A., Young, Kristin, Barata, Llilda, Deng, Xuan, Czajkowski, Jacek, Hadley, David, Ngwa, Julius S., Ahluwalia, Tarunveer S., Chu, Audrey Y., Heard-Costa, Nancy L., Lim, Elise, Perez, Jeremiah, Eicher, John D., Kutalik, Zolta'n, Xue, Luting, Mahajan, Anubha, Renström, Frida, Wu, Joseph, Qi, Qibin, Ahmad, Shafqat, Alfred, Tamuno, Amin, Najaf, Bielak, Lawrence F., Bonnefond, Amelie, Bragg, Jennifer ... Cupples, L. Adrienne (2017). Genome-wide meta-analysis of 241,258 adults accounting for smoking behaviour identifies novel loci for obesity traits. Nature Communications, 8 (1) 14977, 14977. doi: 10.1038/ncomms14977
Hagg, S., Zhan, Y., Karlsson, R., Gerritsen, L., Ploner, A., van der Lee, S. J., Broer, L., Deelen, J., Marioni, R. E., Wong, A., Lundquist, A., Zhu, G., Hansell, N. K., Sillanpaa, E., Fedko, I. O., Amin, N. A., Beekman, M., de Craen, A. J. M., Degerman, S., Harris, S. E., Kan, K-J, Martin-Ruiz, C. M., Montgomery, G. W., Adolfsson, A. N., Reynolds, C. A., Samani, N. J., Suchiman, H. E. D., Viljanen, A., von Zglinicki, T. ... Pedersen, N. L. (2017). Short telomere length is associated with impaired cognitive performance in European ancestry cohorts. Translational Psychiatry, 7 (4) e1100, 983-992. doi: 10.1038/tp.2017.73
Culverhouse, R. C., Saccone, N. L., Horton, A. C., Ma, Y., Anstey, K. J., Banaschewski, T., Burmeister, M., Cohen-Woods, S., Etain, B., Fisher, H. L., Goldman, N., Guillaume, S., Horwood, J., Juhasz, G., Lester, K. J., Mandelli, L., Middeldorp, C. M., Olie, E., Villafuerte, S., Air, T. M., Araya, R., Bowes, L., Burns, R., Byrne, E. M., Coffey, C., Coventry, W. L., Gawronski, K. A. B., Glei, D., Hatzimanolis, A. ... Bierut, L. J. (2017). Collaborative meta-analysis finds no evidence of a strong interaction between stress and 5-HTTLPR genotype contributing to the development of depression. Molecular Psychiatry, 23 (1), 133-142. doi: 10.1038/mp.2017.44
Day, Felix R., Thompson, Deborah J., Helgason, Hannes, Chasman, Daniel I., Finucane, Hilary, Sulem, Patrick, Ruth, Katherine S., Whalen, Sean, Sarkar, Abhishek K., Albrecht, Eva, Altmaier, Elisabeth, Amini, Marzyeh, Barbieri, Caterina M., Boutin, Thibaud, Campbell, Archie, Demerath, Ellen, Giri, Ayush, He, Chunyan, Hottenga, Jouke J., Karlsson, Robert, Kolcic, Ivana, Loh, Po-Ru, Lunetta, Kathryn L., Mangino, Massimo, Marco, Brumat, McMahon, George, Medland, Sarah E., Nolte, Ilja M., Noordam, Raymond ... Perry, John R. B. (2017). Genomic analyses identify hundreds of variants associated with age at menarche and support a role for puberty timing in cancer risk. Nature Genetics, 49 (6), 834-841. doi: 10.1038/ng.3841
Ferreira, Manuel A. R., Jansen, Rick, Willemsen, Gonneke, Penninx, Brenda, Bain, Lisa M., Vicente, Cristina T., Revez, Joana A., Matheson, Melanie C., Hui, Jennie, Tung, Joyce Y., Baltic, Svetlana, Le Souef, Peter, Montgomery, Grant W., Martin, Nicholas G., Robertson, Colin F., James, Alan, Thompson, Philip J., Boomsma, Dorret I., Hopper, John L., Hinds, David A., Werder, Rhiannon B., Phipps, Simon and and the Australian Asthma Genetics Consortium Collaborators (2017). Gene-based analysis of regulatory variants identifies 4 putative novel asthma risk genes related to nucleotide synthesis and signaling. Journal of Allergy and Clinical Immunology, 139 (4), 1148-1157. doi: 10.1016/j.jaci.2016.07.017
Smith, Kevin B., Alford, John R., Hibbing, John R., Martin, Nicholas G. and Hatemi, Peter K. (2017). Intuitive ethics and political orientations: testing moral foundations as a theory of political ideology. American Journal of Political Science, 61 (2), 424-437. doi: 10.1111/ajps.12255
Bigdeli, T. B., Ripke, S., Peterson, R. E., Trzaskowski, M., Bacanu, S-A, Abdellaoui, A., Andlauer, T. F. M., Beekman, A. T. F., Berger, K., Blackwood, D. H. R., Boomsma, D. I., Breen, G., Buttenschon, H. N., Byrne, E. M., Cichon, S., Clarke, T-K, Couvy-Duchesne, B., Craddock, N., de Geus, E. J. C., Degenhardt, F., Dunn, E. C., Edwards, A. C., Fanous, A. H., Forstner, A. J., Frank, J., Gill, M., Gordon, S. D., Grabe, H. J., Hamilton, S. P. ... Kendler, K. S. (2017). Genetic effects influencing risk for major depressive disorder in China and Europe. Translational Psychiatry, 7 (3) e1074, e1074-e1074. doi: 10.1038/tp.2016.292
Heilmann-Heimbach, Stefanie, Herold, Christine, Hochfeld, Lara M., Hillmer, Axel M., Nyholt, Dale R., Hecker, Julian, Javed, Asif, Chew, Elaine G. Y., Pechlivanis, Sonali, Drichel, Dmitriy, Heng, Xiu Ting, Del Rosario, Ricardo C.-H., Fier, Heide L., Paus, Ralf, Rueedi, Rico, Galesloot, Tessel E., Moebus, Susanne, Anhalt, Thomas, Prabhakar, Shyam, Li, Rui, Kanoni, Stavroula, Papanikolaou, George, Kutalik, Zoltán, Deloukas, Panos, Philpott, Michael P., Waeber, Gérard, Spector, Tim D., Vollenweider, Peter, Kiemeney, Lambertus A. L. M. ... Nöthen, Markus M. (2017). Meta-analysis identifies novel risk loci and yields systematic insights into the biology of male-pattern baldness. Nature Communications, 8 (1) 14694, 14694. doi: 10.1038/ncomms14694
Daley, G. M., Duffy, D. L., Pflugfelder, A., Jagirdar, K., Lee, K. J., Yong, X. L., Eigentler, T. K., Weide, B., Smithers, B. M., Martin, N. G., Garbe, C., Soyer, H. P. and Sturm, R. A. (2017). GSTP1 does not modify MC1R effects on melanoma risk. Experimental Dermatology, 26 (8), 730-733. doi: 10.1111/exd.13114
Forstner, Andreas J., Hecker, Julian, Hofmann, Andrea, Maaser, Anna, Reinbold, Céline S., Mühleisen, Thomas W., Leber, Markus, Strohmaier, Jana, Degenhardt, Franziska, Treutlein, Jens, Mattheisen, Manuel, Schumacher, Johannes, Streit, Fabian, Meier, Sandra, Herms, Stefan, Hoffmann, Per, Lacour, André, Witt, Stephanie H., Reif, Andreas, Müller-Myhsok, Bertram, Lucae, Susanne, Maier, Wolfgang, Schwarz, Markus, Vedder, Helmut, Kammerer-Ciernioch, Jutta, Pfennig, Andrea, Bauer, Michael, Hautzinger, Martin, Moebus, Susanne ... Nöthen, Markus M. (2017). Identification of shared risk loci and pathways for bipolar disorder and schizophrenia. PLoS ONE, 12 (2) e0171595, e0171595. doi: 10.1371/journal.pone.0171595
Hibar, Derrek P., Adams, Hieab H. H., Jahanshad, Neda, Chauhan, Ganesh, Stein, Jason L., Hofer, Edith, Renteria, Miguel E., Bis, Joshua C., Arias-Vasquez, Alejandro, Ikram, M. Kamran, Desrivieres, Sylvane, Vernooij, Meike W., Abramovic, Lucija, Alhusaini, Saud, Amin, Najaf, Andersson, Micael, Arfanakis, Konstantinos, Aribisala, Benjamin S., Armstrong, Nicola J., Athanasiu, Lavinia, Axelsson, Tomas, Beecham, Ashley H., Beiser, Alexa, Bernard, Manon, Blanton, Susan H., Bohlken, Marc M., Boks, Marco P., Bralten, Janita, Brickman, Adam M. ... Ikram, M. Arfan (2017). Novel genetic loci associated with hippocampal volume. Nature Communications, 8 (1) 13624, 13624. doi: 10.1038/ncomms13624
Mann, Frank D., Engelhardt, Laura, Briley, Daniel A., Grotzinger, Andrew D., Patterson, Megan W., Tackett, Jennifer L., Strathan, Dixie B., Heath, Andrew, Lynskey, Michael, Slutske, Wendy, Martin, Nicholas G., Tucker-Drob, Elliot M. and Harden, K. Paige (2017). Sensation seeking and impulsive traits as personality endophenotypes for antisocial behavior: evidence from two independent samples. Personality and Individual Differences, 105, 30-39. doi: 10.1016/j.paid.2016.09.018
Fejzo, Marlena Schoenberg, Myhre, Ronny, Colodro-Conde, Lucía, MacGibbon, Kimber W, Sinsheimer, Janet S., Reddy, M. V. Prasad Linga, Pajukanta, Paivi, Nyholt, Dale R., Wright, Margaret J., Martin, Nicholas G., Engel, Stephanie M., Medland, Sarah E., Magnus, Per and Mullin, Patrick M. (2017). Genetic analysis of hyperemesis gravidarum reveals association with intracellular calcium release channel (RYR2). Molecular and Cellular Endocrinology, 439 (C), 308-316. doi: 10.1016/j.mce.2016.09.017
Benyamin, Beben, Maihofer, Adam X., Schork, Andrew J., Hamilton, Bruce A., Rao, Fangwen, Schmid-Schonbein, Geert W., Zhang, Kuixing, Mahata, Manjula, Stridsberg, Mats, Schork, Nicholas J., Biswas, Nilima, Hook, Vivian Y., Wei, Zhiyun, Montgomery, Grant W., Martin, Nicholas G., Nievergelt, Caroline M., Whitfield, John B. and O'Connor, Daniel T. (2017). Identification of novel loci affecting circulating chromogranins and related peptides. Human Molecular Genetics, 26 (1), 233-242. doi: 10.1093/hmg/ddw380
Zeng, Yanni, Navarro, Pau, Shirali, Masoud, Howard, David M., Adams, Mark J., Hall, Lynsey S., Clarke, Toni-Kim, Thomson, Pippa A., Smith, Blair H., Murray, Alison, Padmanabhan, Sandosh, Hayward, Caroline, Boutin, Thibaud, MacIntyre, Donald J., Lewis, Cathryn M., Wray, Naomi R., Mehta, Divya, Penninx, Brenda W. J. H., Milaneschi, Yuri, Baune, Bernhard T., Air, Tracy, Hottenga, Jouke-Jan, Mbarek, Hamdi, Castelao, Enrique, Pistis, Giorgio, Schulze, Thomas G., Streit, Fabian, Forstner, Andreas J., Byrne, Enda M. ... McIntosh, Andrew M. (2016). Genome-wide regional heritability mapping identifies a locus within the TOX2 gene associated with major depressive disorder. Biological Psychiatry, 82 (5), 312-321. doi: 10.1016/j.biopsych.2016.12.012
Roshchupkin, Gennady V., Gutman, Boris A., Vernooij, Meike W., Jahanshad, Neda, Martin, Nicholas G., Hofman, Albert, McMahon, Katie L., van der Lee, Sven J., Van Duijn, Cornelia M., de Zubicaray, Greig I., Uitterlinden, Andre´ G., Wright, Margaret J., Niessen, Wiro J., Thompson, Paul M., Ikram, M. Arfan and Adams, Hieab H.H. (2016). Heritability of the shape of subcortical brain structures in the general population. Nature Communications, 7 (1) 13738, 1-8. doi: 10.1038/ncomms13738
Corfield, Elizabeth C., Martin, Nicholas G. and Nyholt, Dale R. (2016). Shared genetic factors in the co-occurrence of depression and fatigue. Twin Research and Human Genetics, 19 (6), 610-618. doi: 10.1017/thg.2016.79
Li, Ming, Huang, Liang, Grigoroiu-Serbanescu, Maria, Bergen, Sarah E., Landén, Mikael, Hultman, Christina M., Forstner, Andreas J., Strohmaier, Jana, Hecker, Julian, Schulze, Thomas G., Müller-Myhsok, Bertram, Reif, Andreas, Mitchell, Philip B., Martin, Nicholas G., Cichon, Sven, Nöthen, Markus M., Alkelai, Anna, Lerer, Bernard, Jamain, Stéphane, Leboyer, Marion, Bellivier, Frank, Etain, Bruno, Kahn, Jean-Pierre, Henry, Chantal, Rietschel, Marcella, MooDS Consortium, and The Swedish Bipolar Study Group, (2016). Convergent lines of evidence support LRP8 as a susceptibility gene for psychosis. Molecular Neurobiology, 53 (10), 6608-6619. doi: 10.1007/s12035-015-9559-6
Lee, P. H., Baker, J. T., Holmes, A. J., Jahanshad, N., Ge, T., Jung, J. -Y., Cruz, Y., Manoach, D. S., Hibar, D. P., Faskowitz, J., McMahon, K. L., De Zubicaray, G. I., Martin, N. H., Wright, M. J., Ongur, D., Buckner, R., Roffman, J., Thompson, P. M. and Smoller, J. W. (2016). Partitioning heritability analysis reveals a shared genetic basis of brain anatomy and schizophrenia. Molecular Psychiatry, 21 (12), 1680-1689. doi: 10.1038/mp.2016.164
Boyle, Gregory J., Stankov, Lazar, Martin, Nicholas G., Petrides, K. V., Eysenck, Michael W. and Ortet, Generos (2016). Hans J. Eysenck and Raymond B. Cattell on intelligence and personality. Personality and Individual Differences, 103, 40-47. doi: 10.1016/j.paid.2016.04.029
Loehlin, John C., Hansell, Narelle K., Wright, Margaret J. and Martin, Nicholas G. (2016). Genetic and environmental contributions to cognitive structure in Australian twins: a reappraisal. Intelligence, 59, 24-31. doi: 10.1016/j.intell.2016.05.007
Hwang, Liang-Dar, Breslin, Paul A. S., Reed, Danielle R., Zhu, Gu, Martin, Nicholas G. and Wright, Margaret J. (2016). Is the association between sweet and bitter perception due to genetic variation?. Chemical Senses, 41 (9), 737-744. doi: 10.1093/chemse/bjw083
Zhou, Yuan, Zhu, Gu, Charlesworth, Jac C., Simpson, Steve, Rubicz, Rohina, Göring, Harald H.H., Patsopoulos, Nikolaos A., Laverty, Caroline, Wu, Feitong, Henders, Anjali, Ellis, Jonathan J., Van Der Mei, Ingrid, Montgomery, Grant W., Blangero, John, Curran, Joanne E., Johnson, Matthew P., Martin, Nicholas G., Nyholt, Dale R. and Taylor, Bruce V. (2016). Genetic loci for Epstein-Barr virus nuclear antigen-1 are associated with risk of multiple sclerosis. Multiple Sclerosis, 22 (13), 1655-1664. doi: 10.1177/1352458515626598
Ebejer, Jane L., Medland, Sarah E., van der Werf, Julius, Lynskey, Michael, Martin, Nicholas G. and Duffy, David L. (2016). Variation in latent classes of adult attention–deficit hyperactivity disorder by sex and environmental adversity. Journal of Attention Disorders, 20 (11), 934-945. doi: 10.1177/1087054713506261
Corfield, Elizabeth C., Martin, Nicholas G. and Nyholt, Dale R. (2016). Co-occurrence and symptomatology of fatigue and depression. Comprehensive Psychiatry, 71, 1-10. doi: 10.1016/j.comppsych.2016.08.004
Few, Lauren R., Grant, Julia D., Nelson, Elliot C., Trull, Timothy J., Grucza, Richard A., Bucholz, Kathleen K., Verweij, Karin J. H., Martin, Nicholas G., Statham, Dixie J., Madden, Pamela A. F., Heath, Andrew C., Lynskey, Michael T. and Agrawal, Arpana (2016). Cannabis involvement and nonsuicidal self-injury: A discordant twin approach. Journal of Studies on Alcohol and Drugs, 77 (6), 873-880. doi: 10.15288/jsad.2016.77.873
Kassam, Irfahan, Qi, Tuan, Lloyd-Jones, Luke, Holloway, Alexander, Bonder, Marc Jan, Henders, Anjali K., Martin, Nicholas G., Powell, Joseph E., Franke, Lude, Montgomery, Grant W., Visscher, Peter M. and McRae, Allan F. (2016). Evidence for mitochondrial genetic control of autosomal gene expression. Human Molecular Genetics, 25 (24), 5332-5338. doi: 10.1093/hmg/ddw347
Adams, Hieab H. H., Hibar, Derrek P., Chouraki, Vincent, Stein, Jason L., Nyquist, Paul A., Renteria, Miguel E., Trompet, Stella, Arias-Vasquez, Alejandro, Seshadri, Sudha, Desrivieres, Sylvane, Beecham, Ashley H., Jahanshad, Neda, Wittfeld, Katharina, Van der Lee, Sven J., Abramovic, Lucija, Alhusaini, Saud, Amin, Najaf, Andersson, Micael, Arfanakis, Konstantinos, Aribisala, Benjamin S., Armstrong, Nicola J., Athanasiu, Lavinia, Axelsson, Tomas, Beiser, Alexa, Bernard, Manon, Bis, Joshua C., Blanken, Laura M. E., Blanton, SusanH., Bohlken, Marc M. ... Thompson, Paul M. (2016). Novel genetic loci underlying human intracranial volume identified through genome-wide association. Nature Neuroscience, 19 (12), 1569-1582. doi: 10.1038/nn.4398
Rietschel, Liz, Streit, Fabian, Zhu, Gu, McAloney, Kerrie, Kirschbaum, Clemens, Frank, Josef, Hansell, Narelle K., Wright, Margaret J., McGrath, John J., Witt, Stephanie H., Rietschel, Marcella and Martin, Nicholas G. (2016). Hair cortisol and its association with psychological risk factors for psychiatric disorders: a pilot study in adolescent twins. Twin Research and Human Genetics, 19 (5), 438-446. doi: 10.1017/thg.2016.50
Amin, Najaf, Allebrandt, Karla V., van der Spek, Ashley, Müller-Myhsok, Bertram, Hek, Karin, Teder-Laving, Maris, Hayward, Caroline, Esko, Tõnu, van Mill, Josine G., Mbarek, Hamdi, Watson, Nathaniel F., Melville, Scott A., Del Greco, Fabiola M., Byrne, Enda M., Oole, Edwin, Kolcic, Ivana, Chen, Ting-hsu, Evans, Daniel S., Coresh, Josef, Vogelzangs, Nicole, Karjalainen, Juha, Willemsen, Gonneke, Gharib, Sina A., Zgaga, Lina, Mihailov, Evelin, Stone, Katie L., Campbell, Harry, Brouwer, Rutger W. W., Demirkan, Ayse ... van Duijn, Cornelia M. (2016). Genetic variants in RBFOX3 are associated with sleep latency. European Journal of Human Genetics, 24 (10), 1488-1495. doi: 10.1038/ejhg.2016.31
Middeldorp, Christel M., Hammerschlag, Anke R., Ouwens, Klaasjan G., Groen-Blokhuis, Maria M., St Pourcain, Beate, Greven, Corina U., Pappa, Irene, Tiesler, Carla M. T., Ang, Wei, Nolte, Ilja M., Vilor-Tejedor, Natalia, Bacelis, Jonas, Ebejer, Jane L., Zhao, Huiying, Davies, Gareth E., Ehli, Erik A., Evans, David M., Fedko, Iryna O., Guxens, Monica, Hottenga, Jouke-Jan, Hudziak, James J., Jugessur, Astanand, Kemp, John P., Krapohl, Eva, Martin, Nicholas G., Murcia, Mario, Myhre, Ronny, Ormel, Johan, Ring, Susan M. ... Boomsma, Dorret I. (2016). A genome-wide association meta-analysis of attention-deficit/hyperactivity disorder symptoms in population-based pediatric cohorts. Journal of the American Academy of Child and Adolescent Psychiatry, 55 (10), 896-905.e6. doi: 10.1016/j.jaac.2016.05.025
Hwang, Liang-Dar, Cuellar-Partida, Gabriel, Ong, Jue-Sheng, Breslin, Paul A. S., Reed, Danielle R., Macgregor, Stuart, Gharahkhani, Puya, Martin, Nicholas G. and Renteria, Miguel E. (2016). Sweet taste perception is associated with body mass index at the phenotypic and genotypic level. Twin Research and Human Genetics, 19 (5), 465-471. doi: 10.1017/thg.2016.60
Richmond-Rakerd, Leah S., Slutske, Wendy S., Lynskey, Michael T., Agrawal, Arpana, Madden, Pamela A. F., Bucholz, Kathleen K., Heath, Andrew C., Statham, Dixie J. and Martin, Nicholas G. (2016). Age at first use and later substance use disorder: shared genetic and environmental pathways for nicotine, alcohol, and cannabis. Journal of Abnormal Psychology, 125 (7), 946-959. doi: 10.1037/abn0000191
Otowa, T., Hek, K., Lee, M., Byrne, E. M., Mirza, S. S., Nivard, M. G., Bigdeli, T., Aggen, S. H., Adkins, D., Wolen, A., Fanous, A., Keller, M. C., Castelao, E., Kutalik, Z., Der Auwera, S. V., Homuth, G., Nauck, M., Teumer, A., Milaneschi, Y., Hottenga, J. -J., Direk, N., Hofman, A., Uitterlinden, A., Mulder, C. L., Henders, A. K., Medland, S. E., Gordon, S., Heath, A. C., Madden, P. A. F. ... Hettema, J. M. (2016). Meta-analysis of genome-wide association studies of anxiety disorders. Molecular Psychiatry, 21 (10), 1391-1399. doi: 10.1038/mp.2015.197
Ellingson, J. M., Richmond-Rakerd, L. S., Statham, D. J., Martin, N. G. and Slutske, W. S. (2016). Most of the genetic covariation between major depressive and alcohol use disorders is explained by trait measures of negative emotionality and behavioral control. Psychological Medicine, 46 (14), 2919-2930. doi: 10.1017/S0033291716001525
Blokland, Gabriella A. M., Wallace, Angus K., Hansell, Narelle K., Thompson, Paul M., Hickie, Ian B., Montgomery, Grant W., Martin, Nicholas G., McMahon, Katie L., de Zubicaray, Greig I. and Wright, Margaret J. (2016). Genome-wide association study of working memory brain activation. International Journal of Psychophysiology, 115, 98-111. doi: 10.1016/j.ijpsycho.2016.09.010
Sherlock, James M., Verweij, Karin J. H., Murphy, Sean C., Heath, Andrew C., Martin, Nicholas G. and Zietsch, Brendan P. (2016). The role of genes and environment in degree of partner self-similarity. Behavior Genetics, 47 (1), 1-11. doi: 10.1007/s10519-016-9808-0
Maciejewski, Dominique F., Renteria, Miguel E., Abdellaoui, Abdel, Medland, Sarah E., Few, Lauren R., Gordon, Scott D., Madden, Pamela A. F., Montgomery, Grant, Trull, Timothy J., Heath, Andrew C., Statham, Dixie J., Martin, Nicholas G., Zietsch, Brendan P. and Verweij, Karin J. H. (2016). The association of genetic predisposition to depressive symptoms with non-suicidal and suicidal self-injuries. Behavior Genetics, 47 (1), 1-8. doi: 10.1007/s10519-016-9809-z
Mahajan, Anubha, Rodan, Aylin R., Le, Thu H., Gaulton, Kyle J., Haessler, Jeffrey, Stilp, Adrienne M., Kamatani, Yoichiro, Zhu, Gu, Sofer, Tamar, Puri, Sanjana, Schellinger, Jeffrey N., Chu, Pei-Lun, Cechova, Sylvia, van Zuydam, Natalie, Arnlov, Johan, Flessner, Michael F., Giedraitis, Vilmantas, Heath, Andrew C., Kubo, Michiaki, Larsson, Anders, Lindgren, Cecilia M., Madden, Pamela A.F., Montgomery, Grant W., Papanicolaou, George J., Reiner, Alex P., Sundström, Johan, Thornton, Timothy A., Lind, Lars, Ingelsson, Erik ... Franceschini, Nora (2016). Trans-ethnic fine mapping highlights kidney-function genes linked to salt sensitivity. American Journal of Human Genetics, 99 (3), 636-646. doi: 10.1016/j.ajhg.2016.07.012
Ho, Yvonne Y. W., Brims, Mark, McNevin, Dennis, Spector, Timothy D., Martin, Nicholas G. and Medland, Sarah E. (2016). Variation and heritability in hair diameter and curvature in an Australian twin sample. Twin Research and Human Genetics, 19 (4), 351-358. doi: 10.1017/thg.2016.45
Lang, M., Leménager, T., Streit, F., Fauth-Bühler, M., Frank, J., Juraeva, D., Witt, S. H., Degenhardt, F., Hofmann, A., Heilmann-Heimbach, S., Kiefer, F., Brors, B., Grabe, H. J., John, U., Bischof, A., Bischof, G., Völker, U., Homuth, G., Beutel, M., Lind, P. A., Medland, S. E., Slutske, W. S., Martin, N. G., Völzke, H., Nöthen, M. M., Meyer, C., Rumpf, H. J., Wurst, F. M., Rietschel, M. and Mann, K. F. (2016). Genome-wide association study of pathological gambling. European Psychiatry, 36, 38-46. doi: 10.1016/j.eurpsy.2016.04.001
Yang, Yuanhao, Zhao, Huiying, Heath, Andrew C., Madden, Pamela A. F., Martin, Nicholas G. and Nyholt, Dale R. (2016). Shared genetic factors underlie migraine and depression. Twin Research and Human Genetics, 19 (4), 341-350. doi: 10.1017/thg.2016.46
Yang, Yuanhao, Zhao, Huiying, Heath, Andrew C., Madden, Pamela A. F., Martin, Nicholas G. and Nyholt, Dale R. (2016). Familial aggregation of migraine and depression: insights from a large Australian twin sample. Twin Research and Human Genetics, 19 (4), 312-321. doi: 10.1017/thg.2016.43
Gormley, Padhraig, Anttila, Verneri, Winsvold, Bendik S., Palta, Priit, Esko, Tonu, Pers, Tune H., Farh, Kai-How, Cuenca-Leon, Ester, Muona, Mikko, Furlotte, Nicholas A., Kurth, Tobias, Ingason, Andres, McMahon, George, Ligthart, Lannie, Terwindt, Gisela M., Kallela, Mikko, Freilinger, Tobias M., Ran, Caroline, Gordon, Scott G., Stam, Anine H., Steinberg, Stacy, Borck, Guntram, Koiranen, Markku, Quaye, Lydia, Adams, Hieab H. H., Lehtimäki, Terho, Sarin, Antti-Pekka, Wedenoja, Juho, Hinds, David A. ... Palotie, Aarno (2016). Meta-analysis of 375,000 individuals identifies 38 susceptibility loci for migraine. Nature Genetics, 48 (8), 856-866. doi: 10.1038/ng.3598
Direk, Nese, Williams, Stephanie, Smith, Jennifer A., Ripke, Stephan, Air, Tracy, Amare, Azmeraw T., Amin, Najaf, Baune, Bernhard T., Bennett, David A., Blackwood, Douglas H. R., Boomsma, Dorret, Breen, Gerome, Buttenschon, Henriette N., Byrne, Enda M., Borglum, Anders D., Castelao, Enrique, Cichon, Sven, Clarke, Toni-Kim, Cornelis, Marilyn C., Dannlowski, Udo, De Jager, Philip L., Demirkan, Ayse, Domenici, Enrico, van Duijn, Cornelia M., Dunn, Erin C., Eriksson, Johan G., Esko, Tonu, Faul, Jessica D., Ferrucci, Luigi ... Sullivan, Patrick F. (2016). An analysis of two genome-wide association meta-analyses identifies a new locus for broad depression phenotype. Biological Psychiatry, 82 (5), 322-329. doi: 10.1016/j.biopsych.2016.11.013
Silventoinen, Karri, Jelenkovic, Aline, Sund, Reijo, Hur, Yoon-Mi, Yokoyama, Yoshie, Honda, Chika, Hjelmborg, Jacob B., Moller, Soren, Ooki, Syuichi, Aaltonen, Sari, Ji, Fuling, Ning, Feng, Pang, Zengchang, Rebato, Esther, Busjahn, Andreas, Kandler, Christian, Saudino, Kimberly J., Jang, Kerry L., Cozen, Wendy, Hwang, Amie E., MacK, Thomas M., Gao, Wenjing, Yu, Canqing, Li, Liming, Corley, Robin P., Huibregtse, Brooke M., Christensen, Kaare, Skytthe, Axel, Kyvik, Kirsten O. ... Kaprio, Jaakko (2016). Genetic and environmental effects on body mass index from infancy to the onset of adulthood: an individual-based pooled analysis of 45 twin cohorts participating in the COllaborative project of Development of Anthropometrical measures in Twins (CODATwins) study. American Journal of Clinical Nutrition, 104 (2), 371-379. doi: 10.3945/ajcn.116.130252
Revez, J. A., Matheson, M. C., Hui, J., Baltic, S., James, A., Upham, J. W., Dharmage, S., Thompson, P. J., Martin, N. G., Hopper, J. L. and Ferreira, M. A. R. (2016). Identification of STOML2 as a putative novel asthma risk gene associated with IL6R. Allergy, 71 (7), 1020-1030. doi: 10.1111/all.12869
Jelenkovic, Aline, Sund, Reijo, Hur, Yoon-Mi, Yokoyama, Yoshie, Hjelmborg, Jacob V. B., Miller, Soren, Honda, Chika, Magnusson, Patrik K. E., Pedersen, Nancy L., Ooki, Syuichi, Aaltonen, Sari, Stazi, Maria A., Fagnani, Corrado, D'Ippolito, Cristina, Freitas, Duarte L., Maia, Jose Antonio, Ji, Fuling, Ning, Feng, Pang, Zengchang, Rebato, Esther, Busjahn, Andreas, Kandler, Christian, Saudino, Kimberly J., Jang, Kerry L., Cozen, Wendy, Hwang, Amie E., Mack, Thomas M., Gao, Wenjing, Yu, Canqing ... Silventoinen, Karri (2016). Genetic and environmental influences on height from infancy to early adulthood: An individual-based pooled analysis of 45 twin cohorts. Scientific Reports, 6 (1) 28496. doi: 10.1038/srep28496
Shen, Kai-Kai, Dore, Vincent, Rose, Stephen, Fripp, Jurgen, McMahon, Katie L., de Zubicaray, Greig I., Martin, Nicholas G., Thompson, Paul M., Wright, Margaret J. and Salvado, Olivier (2016). Heritability and genetic correlation between the cerebral cortex and associated white matter connections. Human Brain Mapping, 37 (6), 2331-2347. doi: 10.1002/hbm.23177
Cheng, Timothy H. T., Thompson, Deborah J., O'Mara, Tracy A., Painter, Jodie N., Glubb, Dylan M., Flach, Susanne, Lewis, Annabelle, French, Juliet D., Freeman-Mills, Luke, Church, David, Gorman, Maggie, Martin, Lynn, Hodgson, Shirley, Webb, Penelope M., Attia, John, Holliday, Elizabeth G., McEvoy, Mark, Scott, Rodney J., Henders, Anjali K., Martin, Nicholas G., Montgomery, Grant W., Nyholt, Dale R., Ahmed, Shahana, Healey, Catherine S., Shah, Mitul, Dennis, Joe, Fasching, Peter A., Beckmann, Matthias W., Hein, Alexander ... Spurdle, Amanda B. (2016). Five endometrial cancer risk loci identified through genome-wide association analysis. Nature Genetics, 48 (6), 667-674. doi: 10.1038/ng.3562
Parmar, Priyakumari Ganesh, Taal, H. Rob, Timpson, Nicholas J., Thiering, Elisabeth, Lehtimaki, Terho, Marinelli, Marcella, Lind, Penelope A., Howe, Laura D., Verwoert, Germaine, Aalto, Ville, Uitterlinden, Andre G., Briollais, Laurent, Evans, Dave M., Wright, Margie J., Newnham, John P., Whitfield, John B., Lyytikainen, Leo-Pekka, Rivadeneira, Fernando, Boomsma, Dorrett I., Viikari, Jorma, Gillman, Matthew W., St Pourcain, Beate, Hottenga, Jouke-Jan, Montgomery, Grant W., Hofman, Albert, Kahonen, Mika, Martin, Nicholas G., Tobin, Martin D., Raitakari, Ollie ... Palmer, Lyle J. (2016). International genome-wide association study consortium identifies novel loci associated with blood pressure in children and adolescents. Circulation: Cardiovascular Genetics, 9 (3), 266-278. doi: 10.1161/CIRCGENETICS.115.001190
Zhao, Huiying, Eising, Else, De Vries, Boukje, Vijfhuizen, Lisanne S., Anttila, Verneri, Winsvold, Bendik S., Kurth, Tobias, Stefansson, Hreinn, Kallela, Mikko, Malik, Rainer, Stam, Anine H., Arfan Ikram, M., Ligthart, Lannie, Freilinger, Tobias, Alexander, Michael, Müller-Myhsok, Bertram, Schreiber, Stefan, Meitinger, Thomas, Aromas, Arpo, Eriksson, Johan G., Boomsma, Dorret I., Van Duijn, Cornelia M., Zwart, John-Anker, Quaye, Lydia, Kubisch, Christian, Dichgans, Martin, Wessman, Maija, Stefansson, Kari, Chasman, Daniel I. ... Nyholt, Dale R. (2016). Gene-based pleiotropy across migraine with aura and migraine without aura patient groups. Cephalalgia, 36 (7), 648-657. doi: 10.1177/0333102415591497
Smith, D. J., Escott-Price, V., Davies, G., Bailey, M. E. S., Colodro-Conde, L., Ward, J., Vedernikov, A., Marioni, R., Cullen, B., Lyall, D., Hagenaars, S. P., Liewald, D. C. M., Luciano, M., Gale, C. R., Ritchie, S. J., Hayward, C., Nicholl, B., Bulik-Sullivan, B., Adams, M., Couvy-Duchesne, B., Graham, N., Mackay, D., Evans, J., Smith, B. H., Porteous, D. J., Medland, S. E., Martin, N. G., Holmans, P., McIntosh, A. M. ... O'Donovan, M. C. (2016). Genome-wide analysis of over 106000 individuals identifies 9 neuroticism-associated loci. Molecular Psychiatry, 21 (6), 749-757. doi: 10.1038/mp.2016.49
Mbarek, Hamdi, Steinberg, Stacy, Nyholt, Dale R., Gordon, Scott D., Miller, Michael B., McRae, Allan F, Hottenga, Jouke Jan, Day, Felix R., Willemsen, Gonneke, de Geus, Eco J., Davies, Gareth E, Martin, Hilary C, Penninx, Brenda W, Jansen, Rick, McAloney, Kerrie, Vink, Jacqueline M., Kaprio, Jaakko, Plomin, Robert, Spector, Tim D., Magnusson, Patrik K., Reversade, Bruno, Harris, R. Alan, Aagaard, Kjersti, Kristjansson, Ragnar P., Olafsson, Isleifur, Eyjolfsson, Gudmundur Ingi, Sigurdardottir, Olof, Iacono, William G., Lambalk, Cornelis B ... Boomsman, Dorret I. (2016). Identification of common genetic variants influencing spontaneous dizygotic twinning and female fertility. American Journal of Human Genetics, 98 (5), 898-908. doi: 10.1016/j.ajhg.2016.03.008
van Beijsterveldt, C. E.M., Overbeek, L. I.H., Rozendaal, L., McMaster, M. T.B., Glasner, T. J., Bartels, M., Vink, J. M., Martin, N. G., Dolan, C. V. and Boomsma, D. I. (2016). Chorionicity and heritability estimates from twin studies: the prenatal environment of twins and their resemblance across a large number of traits. Behavior Genetics, 46 (3), 304-314. doi: 10.1007/s10519-015-9745-3
Read, Jazlyn, Symmons, Judith, Palmer, Jane M., Montgomery, Grant W., Martin, Nicholas G. and Hayward, Nicholas K. (2016). Increased incidence of bladder cancer, lymphoid leukaemia, and myeloma in a cohort of Queensland melanoma families. Familial Cancer, 15 (4), 651-663. doi: 10.1007/s10689-016-9907-3
Shakhbazov, Konstantin, Powell, Joseph E., Hemani, Gibran, Henders, Anjali K., Martin, Nicholas G., Visscher, Peter M., Montgomery, Grant W. and McRae, Allan F. (2016). Shared genetic control of expression and methylation in peripheral blood. BMC Genomics, 17 (1) 278, 278. doi: 10.1186/s12864-016-2498-4
Ho, Yvonne Y. W., Evans, David M., Montgomery, Grant W., Henders, Anjali K., Kemp, John P., Timpson, Nicholas J., Pourcain, Beate St., Heath, Andrew C., Madden, Pamela A. F., Loesch, Danuta Z., McNevin, Dennis, Daniel, Runa, Davey-Smith, George, Martin, Nicholas G. and Medland, Sarah E. (2016). Common genetic variants influence whorls in fingerprint patterns. Journal of Investigative Dermatology, 136 (4), 859-862. doi: 10.1016/j.jid.2015.10.062
Lupton, Michelle K., Strike, Lachlan, Hansell, Narelle K., Wen, Wei, Mather, Karen A., Armstrong, Nicola J., Thalamuthu, Anbupalam, McMahon, Katie L., de Zubicaray, Greig I., Assareh, Amelia A., Simmons, Andrew, Proitsi, Petroula, Powell, John F., Montgomery, Grant W., Hibar, Derrek P., Westman, Eric, Tsolaki, Magda, Kloszewska, Iwona, Soininen, Hilkka, Mecocci, Patrizia, Velas, Bruno, Lovestone, Simon, Brodaty, Henry, Ames, David, Trollor, Julian N., Martin, Nicholas G., Thompson, Paul M., Sachdev, Perminder S. and Wright, Margaret J. (2016). The effect of increased genetic risk for Alzheimer's disease on hippocampal and amygdala volume. Neurobiology of Aging, 40, 68-77. doi: 10.1016/j.neurobiolaging.2015.12.023
Yokoyama, Yoshie, Jelenkovic, Aline, Sund, Reijo, Sung, Joohon, Hopper, John L., Ooki, Syuichi, Heikkila, Kauko, Aaltonen, Sari, Tarnoki, Adam D., Tarnoki, David L., Willemsen, Gonneke, Bartels, Meike, van Beijsterveldt, Toos C. E. M., Saudino, Kimberly J., Cutler, Tessa L., Nelson, Tracy L., Whitfield, Keith E., Wardle, Jane, Llewellyn, Clare H., Fisher, Abigail, He, Mingguang, Ding, Xiaohu, Bjerregaard-Andersen, Morten, Beck-Nielsen, Henning, Sodemann, Morten, Song, Yun-Mi, Yang, Sarah, Lee, Kayoung, Jeong, Hoe-Uk ... Silventoinen, Karri (2016). Twin's Birth-Order Differences in Height and Body Mass Index From Birth to Old Age: A Pooled Study of 26 Twin Cohorts Participating in the CODATwins Project. Twin Research and Human Genetics, 19 (2), 112-124. doi: 10.1017/thg.2016.11
Kapoor, M., Chou, Y-L, Edenberg, H. J., Foroud, T., Martin, N. G., Madden, P A F, Wang, J. C., Bertelsen, S., Wetherill, L., Brooks, A., Chan, G., Hesselbrock, V., Kuperman, S., Medland, S. E., Montgomery, G., Tischfield, J., Whitfield, J. B., Bierut, L. J., Heath, A. C., Bucholz, K. K., Goate, A. M. and Agrawal, A. (2016). Genome-wide polygenic scores for age at onset of alcohol dependence and association with alcohol-related measures. Translational Psychiatry, 6 (3) e761, e761-e761. doi: 10.1038/tp.2016.27
Schmaal, L., Hibar, D. P., Samann, P. G., Hall, G. B., Baune, B. T., Jahanshad, N., Cheung, J. W., van Erp, T. G. M., Bos, D., Ikram, M. A., Vernooij, M. W., Niessen, W. J., Tiemeier, H., Hofman, A., Wittfeld, K., Grabe, H. J., Janowitz, D., Bulow, R., Selonke, M., Volzke, H., Grotegerd, D., Dannlowski, U., Arolt, V., Opel, N., Heindel, W., Kugel, H., Hoehn, D., Czisch, M., Couvy-Duchesne, B. ... Veltman, D. J. (2016). Cortical abnormalities in adults and adolescents with major depression based on brain scans from 20 cohorts worldwide in the ENIGMA Major Depressive Disorder Working Group. Molecular Psychiatry, 22 (6), 900-909. doi: 10.1038/mp.2016.60
Stringer, S., Minică, C. C., Verweij, K. J. H., Mbarek, H., Bernard, M., Derringer, J., van Eijk, K. R., Isen, J. D., Loukola, A., Maciejewsk, D. F., Mihailov, E., van der Most, P. J., Sánchez-Mora, C., Roos, L., Sherva, R., Walters, R., Ware, J. J., Abdellaoui, A., Bigdeli, T. B., Branje, S. J. T., Brown, S. A., Bruinenberg, M., Casas, M., Esko, T., Garcia-Martinez, I., Gordon, S. D., Harris, J. M., Hartman, C. A., Henders, A. K. ... Vink, J. M. (2016). Genome-wide association study of lifetime cannabis use based on a large meta-analytic sample of 32 330 subjects from the International Cannabis Consortium. Translational Psychiatry, 6 (3) e769, e769-e769. doi: 10.1038/tp.2016.36
Schwantes-An, Tae-Hwi, Zhang, Juan, Chen, Li-Shiun, Hartz, Sarah M., Culverhouse, Robert C., Chen, Xiangning, Coon, Hilary, Frank, Josef, Kamens, Helen M., Konte, Bettina, Kovanen, Leena, Latvala, Antti, Legrand, Lisa N., Maher, Brion S., Melroy, Whitney E., Nelson, Elliot C., Reid, Mark W., Robinson, Jason D., Shen, Pei-Hong, Yang, Bao-Zhu, Andrews, Judy A., Aveyard, Paul, Beltcheva, Olga, Brown, Sandra A., Cannon, Dale S., Cichon, Sven, Corley, Robin P., Dahmen, Norbert, Degenhardt, Louisa ... Saccone, Nancy L. (2016). Association of the OPRM1 Variant rs1799971 (A118G) with Non-Specific Liability to Substance Dependence in a Collaborative de novo Meta-Analysis of European-Ancestry Cohorts. Behavior Genetics, 46 (2), 151-169. doi: 10.1007/s10519-015-9737-3
Clarke, T-K, Lupton, M. K., Fernandez-Pujals, A. M., Starr, J., Davies, G., Cox, S., Pattie, A., Liewald, D. C., Hall, L. S., MacIntyre, D. J., Smith, B. H., Hocking, L. J., Padmanabhan, S., Thomson, P. A., Hayward, C., Hansell, N. K., Montgomery, G. W., Medland, S. E., Martin, N. G., Wright, M. J., Porteous, D. J., Deary, I. J. and McIntosh, A. M. (2016). Common polygenic risk for autism spectrum disorder (ASD) is associated with cognitive ability in the general population. Molecular Psychiatry, 21 (3), 419-425. doi: 10.1038/mp.2015.12
Hines, Lindsey A., Morley, Katherine I., Strang, John, Agrawal, Arpana, Nelson, Elliot C., Statham, Dixie, Martin, Nicholas G. and Lynskey, Michael T. (2016). Onset of opportunity to use cannabis and progression from opportunity to dependence: are influences consistent across transitions?. Drug and Alcohol Dependence, 160, 57-64. doi: 10.1016/j.drugalcdep.2015.12.032
Kristjansson, Sean, Mccutcheon, Vivia V., Agrawal, Arpana, Lynskey, Michael T., Conroy, Elizabeth, Statham, Dixie J., Madden, Pamela A. F., Henders, Anjali K., Todorov, Alexandre A., Bucholz, Kathleen K., Degenhardt, Louisa, Martin, Nicholas G., Heath, Andrew C. and Nelson, Elliot C. (2016). The variance shared across forms of childhood trauma is strongly associated with liability for psychiatric and substance use disorders. Brain and Behavior, 6 (2) ARTN e00432, 1-11. doi: 10.1002/brb3.432
Werner, K. B., McCutcheon, V. V., Challa, M., Agrawal, A., Lynskey, M. T., Conroy, E., Statham, D. J., Madden, P. A.F., Henders, A. K., Todorov, A. A., Heath, A. C., Degenhardt, L., Martin, N. G., Bucholz, K. K. and Nelson, E. C. (2016). The association between childhood maltreatment, psychopathology, and adult sexual victimization in men and women: results from three independent samples. Psychological Medicine, 46 (3), 563-573. doi: 10.1017/S0033291715002056
Li, Ming, Luo, Xiong-Jian, Landén, Mikael, Bergen, Sarah E., Hultman, Christina M., Li, Xiao, Zhang, Wen, Yao, Yong-Gang, Zhang, Chen, Liu, Jiewei, Mattheisen, Manuel, Cichon, Sven, Mühleisen, Thomas W., Degenhardt, Franziska A., Nöthen, Markus M., Schulze, Thomas G., Grigoroiu-Serbanescu, Maria, Li, Hao, Fuller, Chris K., Chen, Chunhui, Dong, Qi, Chen, Chuansheng, Jamain, Stéphane, Leboyer, Marion, Bellivier, Frank, Etain, Bruno, Kahn, Jean-Pierre, Henry, Chantal, Preisig, Martin ... The Swedish Bipolar Study Group (2016). Impact of a cis-associated gene expression SNP on chromosome 20q11.22 on bipolar disorder susceptibility, hippocampal structure and cognitive performance. British Journal of Psychiatry, 208 (2), 128-137. doi: 10.1192/bjp.bp.114.156976
Thompson, Deborah J., O'Mara, Tracy A., Glubb, Dylan M., Painter, Jodie N., Cheng, Timothy, Folkerd, Elizabeth, Doody, Deborah, Dennis, Joe, Webb, Penelope M., Gorman, Maggie, Martin, Lynn, Hodgson, Shirley, Michailidou, Kyriaki, Tyrer, Jonathan P., Maranian, Mel J., Hall, Per, Czene, Kamila, Darabi, Hatef, Li, Jingmei, Fasching, Peter A., Hein, Alexander, Beckmann, Matthias W., Ekici, Arif B., Doerk, Thilo, Hillemanns, Peter, Duerst, Matthias, Runnebaum, Ingo, Zhao, Hui, Depreeuw, Jeroen ... Spurdle, Amanda B. (2016). CYP19A1 fine-mapping and Mendelian randomization: estradiol is causal for endometrial cancer. Endocrine-Related Cancer, 23 (2), 77-91. doi: 10.1530/ERC-15-0386
Lee, S., Duffy, D.L., Mcclenahan, P., Lee, K. J., McEniery, E., Burke, B., Jagirdar, K., Martin, N.G., Sturm, R.A., Soyer, H.P. and Schaider, H. (2016). Heritability of naevus patterns in an adult twin cohort from the Brisbane Twin Registry: A cross-sectional study. British Journal of Dermatology, 174 (2), 356-363. doi: 10.1111/bjd.14291
Long, Elizabeth C., Verhulst, Brad, Neale, Michael C., Lind, Penelope A., Hickie, Ian B., Martin, Nicholas G. and Gillespie, Nathan A. (2016). The Genetic and Environmental Contributions to Internet Use and Associations with Psychopathology: A Twin Study. Twin Research and Human Genetics, 19 (1), 1-9. doi: 10.1017/thg.2015.91
Nambron, Rajasree, Silajdžić, Edina, Kalliolia, Eirini, Ottolenghi, Chris, Hindmarsh, Peter, Hill, Nathan R., Costelloe, Seán J., Martin, Nicholas G., Positano, Vincenzo, Watt, Hilary C., Frost, Chris, Björkqvist, Maria and Warner, Thomas T. (2016). A metabolic study of Huntington's disease. PLoS ONE, 11 (1) e0146480, e0146480. doi: 10.1371/journal.pone.0146480
Couvy-Duchesne, Baptiste, Ebejer, Jane L., Gillespie, Nathan A., Duffy, David L., Hickie, Ian B., Thompson, Paul M., Martin, Nicholas G., de Zubicaray, Greig I., McMahon, Katie L., Medland, Sarah E. and Wright, Margaret J. (2016). Head motion and inattention/hyperactivity share common genetic influences: Implications for fMRI studies of ADHD. PLoS One, 11 (1) e0146271, 1-19. doi: 10.1371/journal.pone.0146271
Shan, Zuyao Y., Vinkhuyzen, Anna A. E., Thompson, Paul M., McMahon, Katie L., Blokland, Gabriella A.M., de Zubicaray, Greig I., Calhoun, Vince, Martin, Nicholas G., Visscher, Peter M., Wright, Margaret J. and Reutens, David C. (2016). Genes influence the amplitude and timing of brain hemodynamic responses. NeuroImage, 124 (Part A), 663-671. doi: 10.1016/j.neuroimage.2015.09.016
Lee, Anthony J., Mitchem, Dorian G., Wright, Margaret J., Martin, Nicholas G., Keller, Matthew C. and Zietsch, Brendan P. (2016). Facial averageness and genetic quality: Testing heritability, genetic correlation with attractiveness, and the paternal age effect. Evolution and Human Behavior, 37 (1), 61-66. doi: 10.1016/j.evolhumbehav.2015.08.003
Hill, W. D., Davies, G., Liewald, D. C., Payton, A., McNeil, C. J., Whalley, L. J., Horan, M., Ollier, W., Starr, J. M., Pendleton, N., Hansel, N. K., Montgomery, G. W., Medland, S. E., Martin, N. G., Wright, M. J., Bates, T. C. and Deary, I. J. (2016). Examining non-syndromic autosomal recessive intellectual disability (NS-ARID) genes for an enriched association with intelligence differences. Intelligence, 54, 80-89. doi: 10.1016/j.intell.2015.11.005
Few, Lauren R., Miller, Joshua D., Grant, Julia D., Maples, Jessica, Trull, Timothy J., Nelson, Elliot C., Oltmanns, Thomas F., Martin, Nicholas G., Lynskey, Michael T. and Agrawal, Arpana (2016). Trait-based assessment of borderline personality disorder using the NEO five-factor inventory: phenotypic and genetic support. Psychological Assessment, 28 (1), 39-50. doi: 10.1037/pas0000142
Schmaal, L., Veltman, D. J., van Erp, T. G. M., Sämann, P. G., Frodl, T., Jahanshad, N., Loehrer, E., Tiemeier, H., Hofman, A., Niessen, W. J., Vernooij, M. W., Ikram, M. A., Wittfeld, K., Grabe, H. J., Block, A., Hegenscheid, K., Völzke, H., Hoehn, D., Czisch, M., Lagopoulos, J., Hatton, S. N., Hickie, I. B., Goya-Maldonado, R., Krämer, B., Gruber, O., Couvy-Duchesne, B., Rentería, M. E., Strike, L. T., Mills, N. T. ... Hibar, D. P. (2016). Subcortical brain alterations in major depressive disorder: findings from the ENIGMA Major Depressive Disorder working group. Molecular Psychiatry, 21 (6), 806-812. doi: 10.1038/mp.2015.69
Bui, Masato, Benyamin, Beben, Shah, Sonia, Henders, Anjali K., Martin, Nicholas G., Montgomery, Grant W. and McRae, Allan F. (2015). Sharing a placenta is associated with a greater similarity in DNA methylation in monochorionic versus dichorionic twin pars in blood at age 14. Twin Research and Human Genetics, 18 (6), 680-685. doi: 10.1017/thg.2015.87
Grant, J. D., Lynskey, M. T., Madden, P. A.F., Nelson, E. C., Few, L. R., Bucholz, K. K., Statham, D. J., Martin, N. G., Heath, A. C. and Agrawal, A. (2015). The role of conduct disorder in the relationship between alcohol, nicotine and cannabis use disorders. Psychological Medicine, 45 (16), 3505-3515. doi: 10.1017/S0033291715001518
Marenholz, Ingo, Esparza-Gordillo, Jorge, Ruschendorf, Franz, Bauerfeind, Anja, Strachan, David P., Spycher, Ben D., Baurecht, Hansjorg, Margaritte-Jeannin, Patricia, Saaf, Annika, Kerkhof, Marjan, Ege, Markus, Baltic, Svetlana, Matheson, Melanie C., Li, Jin, Michel, Sven, Ang, Wei Q., McArdle, Wendy, Arnold, Andreas, Homuth, Georg, Demenais, Florence, Bouzigon, Emmanuelle, Soderhall, Cilla, Pershagen, Goran, De Jongste, Johan C., Postma, Dirkje S., Braun-Fahrlander, Charlotte, Horak, Elisabeth, Ogorodova, Ludmila M., Puzyrev, Valery P. ... Lee, Young Ae (2015). Meta-analysis identifies seven susceptibility loci involved in the atopic March. Nature Communications, 6 (1) 8804, 8804.1-8804.8. doi: 10.1038/ncomms9804
Sinclair, Benjamin, Hansell, Narelle K., Blokland, Gabriella A. M., Martin, Nicholas G., Thompson, Paul M., Breakspear, Michael, de Zubicaray, Greig I., Wright, Margret J. and McMahon, Katie L. (2015). Heritability of the network architecture of intrinsic brain functional connectivity. NeuroImage, 121, 243-252. doi: 10.1016/j.neuroimage.2015.07.048
Carey, Caitlin E., Agrawal, Arpana, Zhang, Bo, Conley, Emily D., Degenhardt, Louisa, Heath, Andrew C., Li, Daofeng, Lynskey, Michael T., Martin, Nicholas G., Montgomery, Grant W., Wang, Ting, Bierut, Laura J., Hariri, Ahmad R., Nelson, Elliot C. and Bogdan, Ryan (2015). Monoacylglycerol lipase (MGLL) polymorphism rs604300 interacts with childhood adversity to predict cannabis dependence symptoms and amygdala habituation: Evidence from an endocannabinoid system-level analysis. Journal of Abnormal Psychology, 124 (4), 860-877. doi: 10.1037/abn0000079
Franic, Sanja, Groen-Blokhuis, Maria M., Dolan, Conor V., Kattenberg, Mathijs V., Pool, Rene, Xiao, Xiangjun, Scheet, Paul A., Ehli, Erik A., Davies, Gareth E., van der Sluis, Sophie, Abdellaoui, Abdel, Hansell, Narelle K., Martin, Nicholas G., Hudziak, James J., van Beijsterveldt, Catherina E. M., Swagerman, Suzanne C., Pol, Hilleke E. Hulshoff, de Geus, Eco J. C., Bartels, Meike, Ropers, H. Hilger, Hottenga, Jouke-Jan and Boomsma, Dorret I. (2015). Intelligence: Shared genetic basis between Mendelian disorders and a polygenic trait. European Journal of Human Genetics, 23 (10), 1378-1383. doi: 10.1038/ejhg.2015.3
Kalliolia, Eirini, Silajdžic, Edina, Nambron, Rajasree, Costelloe, Seán J., Martin, Nicholas G., Hill, Nathan R., Frost, Chris, Watt, Hilary C., Hindmarsh, Peter, Björkqvist, Maria and Warner, Thomas T. (2015). A 24-hour study of the Hypothalamo-pituitary axes in Huntington's disease. PLoS ONE, 10 (10) e0138848, e0138848. doi: 10.1371/journal.pone.0138848
Hancock, Dana B., Levy, Joshua L., Gaddis, Nathan C., Glasheen, Cristie, Saccone, Nancy L., Page, Grier P., Hulse, Gary K., Wildenauer, Dieter, Kelty, Erin A., Schwab, Sibylle G., Degenhardt, Louisa, Martin, Nicholas G., Montgomery, Grant W., Attia, John, Holliday, Elizabeth G., McEvoy, Mark, Scott, Rodney J., Bierut, Laura J., Nelson, Elliot C., Kral, Alex H. and Johnson, Eric O. (2015). Cis-expression quantitative trait loci mapping reveals replicable associations with heroin addiction in OPRM1. Biological Psychiatry, 78 (7), 474-484. doi: 10.1016/j.biopsych.2015.01.003
Jelenkovic, Aline, Yokoyama, Yoshie, Sund, Reijo, Honda, Chika, Bogl, Leonie H., Aaltonen, Sari, Ji, Fuling, Ning, Feng, Pang, Zengchang, Ordonana, Juan R., Sanchez-Romera, Juan F., Colodro-Conde, Lucia, Burt, S. Alexandra, Klump, Kelly L., Medland, Sarah E., Montgomery, Grant W., Kandler, Christian, McAdams, Tom A., Eley, Thalia C., Gregory, Alice M., Saudino, Kimberly J., Dubois, Lise, Boivin, Michel, Tarnoki, Adam D., Tarnoki, David L., Haworth, Claire M. A., Plomin, Robert, Oncel, Sevgi Y., Aliev, Fazil ... Silventoinen, Karri (2015). Zygosity differences in height and body mass index of twins from infancy to old age: a study of the CODATwins project. Twin Research and Human Genetics, 18 (5), 557-570. doi: 10.1017/thg.2015.57
Winkler, Thomas W., Justice, Anne E., Graff, Mariaelisa, Barata, Llilda, Feitosa, Mary F., Chu, Su, Czajkowski, Jacek, Esko, Tonu, Fall, Tove, Kilpelainen, Tuomas O., Lu, Yingchang, Magi, Reedik, Mihailov, Evelin, Pers, Tune H., Rueeger, Sina, Teumer, Alexander, Ehret, Georg B., Ferreira, Teresa, Heard-Costa, Nancy L., Karjalainen, Juha, Lagou, Vasiliki, Mahajan, Anubha, Neinast, Michael D., Prokopenko, Inga, Simino, Jeannette, Teslovich, Tanya M., Jansen, Rick, Westra, Harm-Jan, White, Charles C. ... Loos, Ruth J. F. (2015). The influence of age and sex on genetic associations with adult body size and shape: a large-scale genome-wide interaction study. PL o S Genetics, 11 (10) e1005378, 1-42. doi: 10.1371/journal.pgen.1005378
Howrigan, D.P., Simonson, M.A., Davies, G., Harris, S.E., Tenesa, A., Starr, J.M., Liewald, D.C., Deary, I.J., McRae, A., Wright, M.J., Montgomery, G.W., Hansell, N., Martin, N.G., Payton, A., Horan, M., Ollier, W.E., Abdellaoui, A., Boomsma, D.I., DeRosse, P., Knowles, E.E.M., Glahn, D.C., Djurovic, S., Melle, I., Andreassen, O.A., Christoforou, A., Steen, V.M., Hellard, S.L., Sundet, K., Reinvang, I. ... Keller, M.C. (2015). Genome-wide autozygosity is associated with lower general cognitive ability. Molecular Psychiatry, 21 (6), 837-843. doi: 10.1038/mp.2015.120
Robinson, Matthew R., Hemani, Gibran, Medina-Gomez, Carolina, Mezzavilla, Massimo, Esko, Tonu, Shakhbazov, Konstantin, Powell, Joseph E., Vinkhuyzen, Anna, Berndt, Sonja I., Gustafsson, Stefan, Justice, Anne E., Kahali, Bratati, Locke, Adam E., Pers, Tune H., Vedantam, Sailaja, Wood, Andrew R., van Rheenen, Wouter, Andreassen, Ole A., Gasparini, Paolo, Metspalu, Andres, van den Berg, Leonard H., Veldink, Jan H., Rivadeneira, Fernando, Werge, Thomas M., Abecasis, Goncalo R., Boomsma, Dorret I., Chasman, Daniel I., de Geus, Eco J. C., Frayling, Timothy M. ... Visscher, Peter M. (2015). Population genetic differentiation of height and body mass index across Europe. Nature Genetics, 47 (11), 1357-1361. doi: 10.1038/ng.3401
van Den Berg, Stephanie M., de Moor, Marleen H.M., Verweij, Karin J.H., Krueger, Robert F., Luciano, Michelle, Arias Vasquez, Alejandro, Matteson, Lindsay K., Derringer, Jaime, Esko, Tonu, Amin, Najaf, Gordon, Scott D., Hansell, Narelle K., Hart, Amy B., Seppala, Ilkka, Huffman, Jennifer, Konte, Bettina, Lahti, Jari, Lee, Minyoung, Miller, Mike, Nutile, Teresa, Tanaka, Toshiko, Teumer, Alexander, Viktorin, Alexander, Wedenoja, Juho, Abdellaoui, Abdel, Abecasis, Goncalo R., Adkins, Daniel E., Agrawal, Arpana, Allik, Juri ... Boomsma, Dorret I. (2015). Meta-analysis of Genome-Wide Association Studies for Extraversion: Findings from the Genetics of Personality Consortium. Behavior Genetics, 46 (2), 170-182. doi: 10.1007/s10519-015-9735-5
Law, Matthew H., Bishop, D. Timothy, Lee, Jeffrey E., Brossard, Myriam, Martin, Nicholas G., Moses, Eric K., Song, Fengju, Barrett, Jennifer H., Kumar, Rajiv, Easton, Douglas F., Pharoah, Paul D. P., Swerdlow, Anthony J., Kypreou, Katerina P., Taylor, John C., Harland, Mark, Randerson-Moor, Juliette, Akslen, Lars A., Andresen, Per A., Avril, Marie-Franoise, Azizi, Esther, Scarra, Giovanna Bianchi, Brown, Kevin M., Debniak, Tadeusz, Duffy, David L., Elder, David E., Fang, Shenying, Friedman, Eitan, Galan, Pilar, Ghiorzo, Paola ... Iles, Mark M. (2015). Genome-wide meta-analysis identifies five new susceptibility loci for cutaneous malignant melanoma. Nature Genetics, 47 (9), 987-995. doi: 10.1038/ng.3373
Haysom, Hannah J., Mitchem, Dorian G., Lee, Anthony J., Wright, Margaret J., Martin, Nicholas G., Keller, Matthew C. and Zietsch, Brendan P. (2015). A test of the facultative calibration/reactive heritability model of extraversion. Evolution and Human Behavior, 36 (5), 414-419. doi: 10.1016/j.evolhumbehav.2015.03.002
Wade, Tracey D., Fairweather-Schmidt, A. Kate, Zhu, Gu and Martin, Nicholas G. (2015). Does shared genetic risk contribute to the co-occurrence of eating disorders and suicidality?. International Journal of Eating Disorders, 48 (6), 684-691. doi: 10.1002/eat.22421
Aoude, Lauren G., Heitzer, Ellen, Johansson, Peter, Gartside, Michael, Wadt, Karin, Pritchard, Antonia L., Palmer, Jane M., Symmons, Judith, Gerdes, Anne-Marie, Montgomery, Grant W., Martin, Nicholas G., Tomlinson, Ian, Kearsey, Stephen and Hayward, Nicholas K. (2015). POLE mutations in families predisposed to cutaneous melanoma. Familial Cancer, 14 (4), 621-628. doi: 10.1007/s10689-015-9826-8
Silventoinen, Karri, Jelenkovic, Aline, Sund, Reijo, Honda, Chika, Aaltonen, Sari, Yokoyama, Yoshie, Tarnoki, Adam D., Tarnoki, David L., Ning, Feng, Ji, Fuling, Pang, Zengchang, Ordonana, Juan R., Sanchez-Romera, Juan F., Colodro-Conde, Lucia, Burt, S. Alexandra, Klump, Kelly L., Medland, Sarah E., Montgomery, Grant W., Kandler, Christian, McAdams, Tom A., Eley, Thalia C., Gregory, Alice M., Saudino, Kimberly J., Dubois, Lise, Boivin, Michel, Haworth, Claire M. A., Plomin, Robert, Oncel, Sevgi Y., Aliev, Fazil ... Kaprio, Jaakko (2015). The CODATwins project: the cohort description of collaborative project of development of anthropometrical measures in twins to study macro-environmental variation in genetic and environmental effects on anthropometric traits. Twin Research and Human Genetics, 18 (4), 348-360. doi: 10.1017/thg.2015.29
Nelson, E. C., Agrawal, A., Heath, A. C., Bogdan, R., Sherva, R., Zhang, B., Al-Hasani, R., Bruchas, M. R., Chou, Y.-L., Demers, C. H., Carey, C. E., Conley, E. D., Fakira, A. K., Farrer, L. A., Goate, A., Gordon, S., Henders, A. K., Hesselbrock, V., Kapoor, M., Lynskey, M. T., Madden, P. A. F., Moron, J. A., Rice, J. P., Saccone, N. L., Schwab, S. G., Shand, F. L., Todorov, A. A., Wallace, L., Wang, T. ... Montgomery, G. W. (2015). Evidence of CNIH3 involvement in opioid dependence. Molecular Psychiatry, 21 (5), 608-614. doi: 10.1038/mp.2015.102
Liu, Fan, Visser, Mijke, Duffy, David L., Hysi, Pirro G., Jacobs, Leonie C., Lao, Oscar, Zhong, Kaiyin, Walsh, Susan, Chaitanya, Lakshmi, Wollstein, Andreas, Zhu, Gu, Montgomery, Grant W., Henders, Anjali K., Mangino, Massimo, Glass, Daniel, Bataille, Veronique, Sturm, Richard A., Rivadeneira, Fernando, Hofman, Albert, van IJcken, Wilfred F. J., Uitterlinden, André G., Palstra, Robert-Jan T. S., Spector, Timothy D., Martin, Nicholas G., Nijsten, Tamar E. C. and Kayser, Manfred (2015). Genetics of skin color variation in Europeans: genome-wide association studies with functional follow-up. Human Genetics, 134 (8), 823-835. doi: 10.1007/s00439-015-1559-0
Hwang, Liang-Dar, Zhu, Gu, Breslin, Paul A. S., Reed, Danielle R., Martin, Nicholas G. and Wright, Margaret J. (2015). A common genetic influence on human intensity ratings of sugars and high-potency sweeteners. Twin Research and Human Genetics, 18 (4), 361-367. doi: 10.1017/thg.2015.42
Sapkota, Yadav, Attia, John, Gordon, Scott D., Henders, Anjali K., Holliday, Elizabeth G., Rahmioglu, Nilufer, MacGregor, Stuart, Martin, Nicholas G., McEvoy, Mark, Morris, Andrew P., Scott, Rodney J., Zondervan, Krina T., Montgomery, Grant W. and Nyholt, Dale R. (2015). Genetic burden associated with varying degrees of disease severity in endometriosis. Molecular Human Reproduction, 21 (7), 594-602. doi: 10.1093/molehr/gav021
De Moor, Marleen H.M, Van Den Berg, Stephanie M, Verweij, Karin J.H, Krueger, Robert F, Luciano, Michelle, Arias Vasquez, Alejandro, Matteson, Lindsay K, Derringer, Jaime, Esko, Tonu, Amin, Najaf, Gordon, Scott D, Hansell, Narelle K, Hart, Amy B, Seppala, Ilkka, Huffman, Jennifer E, Konte, Bettina, Lahti, Jari, Lee, Minyoung, Miller, Mike, Nutile, Teresa, Tanaka, Toshiko, Teumer, Alexander, Viktorin, Alexander, Wedenoja, Juho, Abecasis, Goncalo R, Adkins, Daniel E, Agrawal, Arpana, Allik, Juri, Appel, Katja ... Boomsma, Dorret I (2015). Meta-analysis of genome-wide association studies for neuroticism, and the polygenic association with major depressive disorder. JAMA Psychiatry, 72 (7), 642-650. doi: 10.1001/jamapsychiatry.2015.0554
Cuellar-Partida, Gabriel, Springelkamp, Henriet, Lucas, Sionne E. M., Yazar, Seyhan, Hewitt, Alex W., Iglesias, Adriana I., Montgomery, Grant W., Martin, Nicholas G., Pennell, Craig E., van Leeuwen, Elisabeth M., Verhoeven, Virginie J. M., Hofman, Albert, Uitterlinden, Andre G., Ramdas, Wishal D., Wolfs, Roger. C. W., Vingerling, Johannes R., Brown, Matthew A., Mills, Richard A., Craig, Jamie E., Klaver, Caroline C. W., van Duijn, Cornelia M., Burdon, Kathryn P., MacGregor, Stuart and Mackey, David A. (2015). WNT10A exonic variant increases the risk of keratoconus by decreasing corneal thickness. Human Molecular Genetics, 24 (17), 5060-5068. doi: 10.1093/hmg/ddv211
Koning, Pierre, Webbink, Dinand and Martin, Nicholas G. (2015). The effect of education on smoking behavior: new evidence from smoking durations of a sample of twins. Empirical Economics, 48 (4), 1479-1497. doi: 10.1007/s00181-014-0842-6
Hatemi, Peter K., Smith, Kevin, Alford, John R., Martin, Nicholas G. and Hibbing, John R. (2015). The genetic and environmental foundations of political, psychological, social, and economic behaviors: a panel study of twins and families. Twin Research and Human Genetics, 18 (3), 243-255. doi: 10.1017/thg.2015.13
Loehlin, John C., Bartels, Meike, Boomsma, Dorret I., Bratko, Denis, Martin, Nicholas G., Nichols, Robert C. and Wright, Margaret J. (2015). Is there a genetic correlation between general factors of intelligence and personality?. Twin Research and Human Genetics, 18 (3), 234-242. doi: 10.1017/thg.2015.28
Rossi, Roberta Elisa, Garcia-Hernandez, Jorge, Meyer, Tim, Thirlwell, Christina, Watkins, Jennifer, Martin, Nicholas Guy, Caplin, Martyn Evan and Toumpanakis, Christos (2015). Chromogranin A as a predictor of radiological disease progression in neuroendocrine tumours. Annals of Translational Medicine, 3 (9) ARTN 118. doi: 10.3978/j.issn.2305-5839.2015.04.23
Mitchem, Dorian G., Zietsch, Brendan P., Wright, Margaret J., Martin, Nicholas G., Hewitt, John K. and Keller, Matthew C. (2015). No relationship between intelligence and facial attractiveness in a large, genetically informative sample. Evolution and Human Behavior, 36 (3), 240-247. doi: 10.1016/j.evolhumbehav.2014.11.009
Fall, Tove, Hagg, Sara, Ploner, Alexander, Maegi, Reedik, Fischer, Krista, Draisma, Harmen H. M., Sarin, Antti-Pekka, Benyamin, Beben, Ladenvall, Claes, Akerlund, Mikael, Kals, Mart, Esko, Tonu, Nelson, Christopher P., Kaakinen, Marika, Huikari, Ville, Mangino, Massimo, Meirhaeghe, Aline, Kristiansson, Kati, Nuotio, Marja-Liisa, Kobl, Michael, Grallert, Harald, Dehghan, Abbas, Kuningas, Maris, de Vries, Paul S., de Bruijn, Renee F. A. G., Willems, Sara M., Heikkila, Kauko, Silventoinen, Karri, Pietilainen, Kirsi H. ... Ingelsson, Erik (2015). Age- and sex-specific causal effects of adiposity on cardiovascular risk factors. Diabetes, 64 (5), 1841-1852. doi: 10.2337/db14-0988
Meier, Madeline H., Gillespie, Nathan A., Hansell, Narelle K., Hewitt, Alex W., Hickie, Ian B., Lu, Yi, McGrath, John, MacGregor, Stuart, Medland, Sarah E., Sun, Cong, Wong, Tien Y., Wright, Margaret J., Zhu, Gu, Martin, Nicholas G. and Mackey, David A. (2015). Retinal microvessels reflect familial vulnerability to psychotic symptoms: A comparison of twins discordant for psychotic symptoms and controls. Schizophrenia Research, 164 (1-3), 47-52. doi: 10.1016/j.schres.2015.01.045
Kochunov, Peter, Jahanshad, Neda, Marcus, Daniel, Winkler, Anderson, Sprooten, Emma, Nichols, Thomas E, Wright, Susan N, Hong, L. Elliot, Patel, Binish, Behrens, Timothy, Jbabdi, Saad, Andersson, Jesper, Lenglet, Christophe, Yacoub, Essa, Moeller, Steen, Auerbach, Eddie, Ugurbil, Kamil, Sotiropoulos, Stamatios N, Brouwer, Rachel M, Landman, Bennett, Lemaitre, Herve, den Braber, Anouk, Zwiers, Marcel P, Ritchie, Stuart, van Hulzen, Kimm, Almasy, Laura, Curran, Joanne, deZubicaray, Greig I, Duggirala, Ravi ... Van Essen, David C (2015). Heritability of fractional anisotropy in human white matter: A comparison of Human Connectome Project and ENIGMA-DTI data. NeuroImage, 111, 300-311. doi: 10.1016/j.neuroimage.2015.02.050
Wilmut, Ian, Leslie, Stephen, Martin, Nicholas G., Peschanski, Marc, Rao, Mahendra, Trounson, Alan, Turner, David, Turner, Marc L., Yamanaka, Shinya and Taylor, Craig J. (2015). Development of a global network of induced pluripotent stem cell haplobanks. Regenerative Medicine, 10 (3), 235-238. doi: 10.2217/RME.15.1
Delforterie, M. J., Lynskey, M. T., Huizink, A. C., Creemers, H. E., Grant, J. D., Few, L. R., Glowinski, A. L., Statham, D. J., Trull, T. J., Bucholz, K. K., Madden, P. A. F., Martin, N. G., Heath, A. C. and Agrawal, A. (2015). The relationship between cannabis involvement and suicidal thoughts and behaviors. Drug and Alcohol Dependence, 150, 98-104. doi: 10.1016/j.drugalcdep.2015.02.019
Springelkamp, Henriet, Iglesias, Adriana I., Cuellar-Partida, Gabriel, Amin, Najaf, Burdon, Kathryn P., van Leeuwen, Elisabeth M., Gharahkhani, Puya, Mishra, Aniket, van der Lee, Sven J., Hewitt, Alex W., Rivadeneira, Fernando, Viswanathan, Ananth C., Wolfs, Roger C. W., Martin, Nicholas G., Ramdas, Wishal D., van Koolwijk, Leonieke M., Pennell, Craig E., Vingerling, Johannes R., Mountain, Jenny E., Uitterlinden, Andre G., Hofman, Albert, Mitchell, Paul, Lemij, Hans G., Wang, Jie Jin, Klaver, Caroline C. W., Mackey, David A., Craig, Jamie E., van Duijn, Cornelia M. and MacGregor, Stuart (2015). ARHGEF12 influences the risk of glaucoma by increasing intraocular pressure. Human Molecular Genetics, 24 (9), 2689-2699. doi: 10.1093/hmg/ddv027
Santulli, Gaetano, Pagano, Gennaro, Sardu, Celestino, Xie, Wenjun, Reiken, Steven, D'Ascia, Salvatore Luca, Cannone, Michele, Marziliano, Nicola, Trimarco, Bruno, Guise, Theresa A., Lacampagne, Alain and Marks, Andrew R. (2015). Calcium release channel RyR2 regulates insulin release and glucose homeostasis. Journal of Clinical Investigation, 125 (5), 1968-1978. doi: 10.1172/JCI79273
Hibar, Derrek P, Stein, Jason L, Renteria, Miguel E, Arias-Vasquez, Alejandro, Desrivieres, Sylvane, Jahanshad, Neda, Toro, Roberto, Wittfeld, Katharina, Abramovic, Lucija, Andersson, Micael, Aribisala, Benjamin S, Armstrong, Nicola J, Bernard, Manon, Bohlken, Marc M, Boks, Marco P, Bralten, Janita, Brown, Andrew A, Mallar Chakravarty M., Chen, Qiang, Ching, Christopher R.K., Cuellar-Partida, Gabriel, Den Braber, Anouk, Giddaluru, Sudheer, Goldman, Aaron L, Grimm, Oliver, Guadalupe, Tulio, Hass, Johanna, Woldehawariat, Girma, Holmes, Avram J ... Medland, Sarah E (2015). Common genetic variants influence human subcortical brain structures. Nature, 520 (7546), 224-229. doi: 10.1038/nature14101
Strohmaier, Jana, van Dongen, Jenny, Willemsen, Gonneke, Nyholt, Dale R., Zhu, Gu, Codd, Veryan, Novakovic, Boris, Hansell, Narelle, Wright, Margaret J., Rietschel, Liz, Streit, Fabian, Henders, Anjali K., Montgomery, Grant W., Samani, Nilesh J., Gillespie, Nathan A., Hickie, Ian B., Craig, Jeffrey M., Saffery, Richard, Boomsma, Dorret I., Rietschel, Marcella and Martin, Nicholas G. (2015). Low birth weight in MZ twins discordant for birth weight is associated with shorter telomere length and lower IQ, but not anxiety/depression in later life. Twin Research and Human Genetics, 18 (2), 198-209. doi: 10.1017/thg.2015.3
Hansell, Narelle K., Halford, Graeme S., Andrews, Glenda, Shum, David H. K., Harris, Sarah E., Davies, Gail, Franic, Sanja, Christoforou, Andrea, Zietsch, Brendan, Painter, Jodie, Medland, Sarah E., Ehli, Erik A., Davies, Gareth E., Steen, Vidar M., Lundervold, Astri J., Reinvang, Ivar, Montgomery, Grant W., Espeseth, Thomas, Pol, Hilleke E. Hulshoff, Starr, John M., Martin, Nicholas G., Le Hellard, Stephanie, Boomsma, Dorret I., Deary, Ian J. and Wright, Margaret J. (2015). Genetic basis of a cognitive complexity metric. PLoS One, 10 (4) e0123886, 1-19. doi: 10.1371/journal.pone.0123886
Aoude, Lauren G., Gartside, Michael, Johansson, Peter, Palmer, Jane M., Symmons, Judith, Martin, Nicholas G., Montgomery, Grant W. and Hayward, Nicholas K. (2015). Prevalence of germline BAP1, CDKN2A, and CDK4 mutations in an australian population-based sample of cutaneous melanoma cases. Twin Research and Human Genetics, 18 (2), 126-133. doi: 10.1017/thg.2015.12
Zimmermann, E., Angquist, L. H., Mirza, S. S., Zhao, J. H., Chasman, D. I., Fischer, K., Qi, Q., Smith, A. V., Thinggaard, M., Jarczok, M. N., Nalls, M. A., Trompet, S., Timpson, N. J., Schmidt, B., Jackson, A. U., Lyytikainen, L. P., Verweij, N., Mueller-Nurasyid, M., Vikstrom, M., Marques-Vidal, P., Wong, A., Meidtner, K., Middelberg, R. P., Strawbridge, R. J., Christiansen, L., Kyvik, K. O., Hamsten, A., Jaaskelainen, T., Tjonneland, A. ... Montgomery, G. W. (2015). Is the adiposity-associated FTO gene variant related to all-cause mortality independent of adiposity? Meta-analysis of data from 169,551 Caucasian adults. Obesity Reviews, 16 (4), 327-340. doi: 10.1111/obr.12263
Benyamin, Beben, Esko, Tonu, Ried, Janina S., Radhakrishnan, Aparna, Vermeulen, Sita H., Traglia, Michela, Goegele, Martin, Anderson, Denise, Broer, Linda, Podmore, Clara, Luan, Jianan, Kutalik, Zoltan, Sanna, Serena, van der Meer, Peter, Tanaka, Toshiko, Wang, Fudi, Westra, Harm-Jan, Franke, Lude, Mihailov, Evelin, Milani, Lili, Haelldin, Jonas, Winkelmann, Juliane, Meitinger, Thomas, Thiery, Joachim, Peters, Annette, Waldenberger, Melanie, Rendon, Augusto, Jolley, Jennifer, Sambrook, Jennifer ... Whitfield, John B. (2015). Novel loci affecting iron homeostasis and their effects in individuals at risk for hemochromatosis (vol 5, 4926, 2014). Nature Communications, 6 (1) 6542, 1-1. doi: 10.1038/ncomms7542
Warrington, Nicole M., Zhu, Gu, Dy, Veronica, Heath, Andrew C., Madden, Pamela A. F., Hemani, Gibran, Kemp, John P., Mcmahon, George, St Pourcain, Beate, Timpson, Nicholas J., Taylor, Caroline M., Golding, Jean, Lawlor, Debbie A., Steer, Colin, Montgomery, Grant W., Martin, Nicholas G., Smith, George Davey, Evans, David M. and Whitfield, John B. (2015). Genome-wide association study of blood lead shows multiple associations near ALAD. Human Molecular Genetics, 24 (13) ddv112, 3871-3879. doi: 10.1093/hmg/ddv112
Painter J.N., O'Mara T.A., Batra J., Cheng T., Lose F.A., Dennis J., Michailidou K., Tyrer J.P., Ahmed S., Ferguson K., Healey C.S., Kaufmann S., Hillman K.M., Walpole C., Moya L., Pollock P., Jones A., Howarth K., Martin L., Gorman M., Hodgson S., De Polanco M.M.E., Sans M., Carracedo A., Castellvi-Bel S., Rojas-Martinez A., Santos E., Teixeira M.R., Carvajal-Carmona L. ... Spurdle A.B. (2015). Fine-mapping of the HNF1B multicancer locus identifies candidate variants that mediate endometrial cancer risk. Human Molecular Genetics, 24 (5), 1478-1492. doi: 10.1093/hmg/ddu552
Mangino, Massimo, Christiansen, Lene, Stone, Rivka, Hunt, Steven C., Horvath, Kent, Eisenberg, Dan T. A., Kimura, Masayuki, Petersen, Inge, Kark, Jeremy D., Herbig, Utz, Reiner, Alex P., Benetos, Athanase, Codd, Veryan, Nyholt, Dale R., Sinnreich, Ronit, Christensen, Kaare, Nassar, Hisham, Hwang, Shih-Jen, Levy, Daniel, Bataille, Veronique, Fitzpatrick, Annette L., Chen, Wei, Berenson, Gerald S., Samani, Nilesh J., Martin, Nicholas G., Tishkoff, Sarah, Schork, Nicholas J., Kyvik, Kirsten Ohm, Dalgard, Christine ... Aviv, Abraham (2015). DCAF4, a novel gene associated with leucocyte telomere length. Journal of Medical Genetics, 52 (3), 157-162. doi: 10.1136/jmedgenet-2014-102681
Sanfilippo, Paul G., Wilkinson, Colleen H., Ruddle, Jonathan B., Zhu, Gu, Martin, Nicholas G., Hewitt, Alex W. and Mackey, David A. (2015). Don't it make your brown eyes blue? A comparison of iris colour across latitude in Australian twins. Clinical and Experimental Optometry, 98 (2), 172-176. doi: 10.1111/cxo.12209
Costelloe, Seán J., Theocharidou, Eleni, Tsochatzis, Emmanuel, Thalassinos, Evangelos, Martin, Nicholas, Fede, Guiseppe, Thomas, Michael and Burroughs, Anthony K. (2015). Hepascore and hyaluronic acid as markers of fibrosis in liver disease of mixed aetiology. European Journal of Gastroenterology and Hepatology, 27 (3), 313-320. doi: 10.1097/MEG.0000000000000267
Glaz, Barry, Wiersma, Jochum, Hernandez, Jose A., Martin, Nicolas F. and Yeater, Kathleen M. (2015). Introduction to the statistical concepts symposium section: Selected review topics to improve our understanding and use of statistics. Agronomy Journal, 107 (2), 691-691. doi: 10.2134/agronj14.0888
Colodro-Conde, Lucia, Zhu, Gu, Power, Robert A., Henders, Anjali, Heath, Andrew C., Madden, Pamela A. F., Montgomery, Grant W., Medland, Sarah, Ordonana, Juan R. and Martin, Nicholas G. (2015). A twin study of breastfeeding with a preliminary genome-wide association scan. Twin Research and Human Genetics, 18 (1), 61-72. doi: 10.1017/thg.2014.74
Mills, Natalie T., Wright, Margaret J., Henders, Anjali K., Eyles, Darryl W., Baune, Bernhard T., McGrath, John J., Byrne, Edna M., Hansell, Narelle K., Birosova, Eva, Scott, James G., Martin, Nicholas G., Montgomery, Grant W., Wray, Naomi R. and Vinkhuyzen, Anna A. E. (2015). Heritability of Transforming Growth Factor-β1 and Tumor Necrosis Factor-Receptor Type 1 Expression and Vitamin D Levels in Healthy Adolescent Twins. Twin Research and Human Genetics, 18 (1), 28-35. doi: 10.1017/thg.2014.70
Mcrae, Allan F., Visscher, Peter M., Montgomery, Grant W. and Martin, Nicholas G. (2015). Large autosomal copy-number differences within unselected monozygotic twin pairs are rare. Twin Research and Human Genetics, 18 (1), 13-18. doi: 10.1017/thg.2014.85
Aoude, Lauren G., Pritchard, Antonia L., Robles-Espinoza, Carla Daniela, Wadt, Karin, Harland, Mark, Choi, Jiyeon, Gartside, Michael, Quesada, Victor, Johansson, Peter, Palmer, Jane M., Ramsay, Andrew J., Zhang, Xijun, Jones, Kristine, Symmons, Judith, Holland, Elizabeth A., Schmid, Helen, Bonazzi, Vanessa, Woods, Susan, Dutton-Regester, Ken, Stark, Mitchell S., Snowden, Helen, van Doom, Remco, Montgomery, Grant W., Martin, Nicholas G., Keane, Thomas M., Lopez-Otin, Carlos, Gerdes, Anne-Marie, Olsson, Hakan, Ingvar, Christian ... Hayward, Nicholas K. (2015). Nonsense mutations in the shelterin complex genes ACD and TERF2IP in familial melanoma. Journal of the National Cancer Institute, 107 (2) dju408, 1-7. doi: 10.1093/jnci/dju408
Marioni, Riccardo E., Shah, Sonia, McRae, Allan F., Chen, Brian H., Colicino, Elena, Harris, Sarah E., Gibson, Jude, Henders, Anjali K., Redmond, Paul, Cox, Simon R., Pattie, Alison, Corley, Janie, Murphy, Lee, Martin, Nicholas G., Montgomery, Grant W., Feinberg, Andrew P., Fallin, M. Daniele, Multhaup, Michael L., Jaffe, Andrew E., Joehanes, Roby, Schwartz, Joel, Just, Allan C., Lunetta, Kathryn L., Murabito, Joanne M., Starr, John M., Horvath, Steve, Baccarelli, Andrea A., Levy, Daniel, Visscher, Peter M. ... Deary, Ian J. (2015). DNA methylation age of blood predicts all-cause mortality in later life. Genome Biology, 16 (1) 25, 25.1-25.12. doi: 10.1186/s13059-015-0584-6
O'Dushlaine, Colm, Rossin, Lizzy, Lee, Phil H., Duncan, Laramie, Parikshak, Neelroop N., Newhouse, Stephen, Ripke, Stephan, Neale, Benjamin M., Purcell, Shaun M., Posthuma, Danielle, Nurnberger, John I., Lee, S. Hong, Faraone, Stephen V., Perlis, Roy H., Mowry, Bryan J, Thapar, Anita, Goddard, Michael E., Witte, John S., Absher, Devin, Agartz, Ingrid, Akil, Huda, Amin, Farooq, Andreassen, Ole A., Anjorin, Adebayo, Anney, Richard, Anttila, Verneri, Arking, Dan E., Asherson, Philip, Azevedo, Maria H. ... Breen, Gerome (2015). Psychiatric genome-wide association study analyses implicate neuronal, immune and histone pathways. Nature Neuroscience, 18 (2), 199-209. doi: 10.1038/nn.3922
Sapkota, Yadav, Low, Siew-Kee, Attia, John, Gordon, Scott D., Henders, Anjali K., Holliday, Elizabeth G., MacGregor, Stuart, Martin, Nicholas G., McEvoy, Mark, Morris, Andrew P., Takahashi, Atsushi, Scott, Rodney J., Kubo, Michiaki, Zondervan, Krina T., Montgomery, Grant W. and Nyholt, Dale R. (2015). Association between endometriosis and the interleukin 1A (IL1A) locus. Human Reproduction, 30 (1), 239-248. doi: 10.1093/humrep/deu267
Ebejer, J. L., Medland, S. E., van der Werf, J., Wright, M. J., Henders, A. K., Gillespie, N. A., Hickie, I. B., Martin, N. G. and Duffy, D. L. (2015). Contrast Effects and Sex Influence Maternal and Self-Report Dimensional Measures of Attention-Deficit Hyperactivity Disorder. Behavior Genetics, 45 (1), 35-50. doi: 10.1007/s10519-014-9670-x
Slutske, Wendy S., Piasecki, Thomas M., Deutsch, Arielle R., Statham, Dixie J. and Martin, Nicholas G. (2015). Telescoping and gender differences in the time course of disordered gambling: evidence from a general population sample. Addiction, 110 (1), 144-151. doi: 10.1111/add.12717
Hines, Lindsey A., Morley, Katherine I., Strang, John, Agrawal, Arpana, Nelson, Elliot C., Statham, Dixie, Martin, Nicholas G. and Lynskey, Michael T. (2015). The association between speed of transition from initiation to subsequent use of cannabis and later problematic cannabis use, abuse and dependence. Addiction, 110 (8), 1311-1320. doi: 10.1111/add.12963
Gottlieb, D. J., Hek, K., Chen, T. H., Watson, N. F., Eiriksdottir, G., Byrne, E. M., Cornelis, M., Warby, S. C., Bandinelli, S., Cherkas, L., Evans, D. S., Grabe, H. J., Lahti, J., Li, M., Lehtimaki, T., Lumley, T., Marciante, K. D., Perusse, L., Psaty, B. M., Robbins, J., Tranah, G. J., Vink, J. M., Wilk, J. B., Stafford, J. M., Bellis, C., Biffar, R., Bouchard, C., Cade, B., Curhan, G. C. ... Tiemeier, H. (2014). Novel loci associated with usual sleep duration: the CHARGE Consortium Genome-Wide Association Study. Molecular Psychiatry, 20 (10), 1232-1239. doi: 10.1038/mp.2014.133
Savage, Jeanne E., Slutske, Wendy S. and Martin, Nicholas G. (2014). Personality and gambling involvement: a person-centered approach. Psychology of Addictive Behaviors, 28 (4), 1198-1211. doi: 10.1037/a0037413
Slutske, Wendy S., Deutsch, Arielle R., Richmond-Rakerd, Leah S., Chernyavskiy, Pavel, Statham, Dixie J. and Martin, Nicholas G. (2014). Test of a potential causal influence of earlier age of gambling initiation on gambling involvement and disorder: a multilevel discordant twin design. Psychology of Addictive Behaviors, 28 (4), 1177-1189. doi: 10.1037/a0035356
Loehlin, John C. and Martin, Nicholas G. (2014). The genetic correlation between procrastination and impulsivity. Twin Research and Human Genetics, 17 (6), 512-515. doi: 10.1017/thg.2014.60
Martin, Nicholas J. and Cooper, Helen J. (2014). Challenges and opportunities in mass spectrometric analysis of proteins from dried blood spots. Expert Review of Proteomics, 11 (6), 685-695. doi: 10.1586/14789450.2014.965158
Few, Lauren R., Grant, Julia D., Trull, Timothy J., Statham, Dixie J., Martin, Nicholas G., Lynskey, Michael T. and Agrawal, Arpana (2014). Genetic variation in personality traits explains genetic overlap between borderline personality features and substance use disorders. Addiction, 109 (12), 2118-2127. doi: 10.1111/add.12690
Slutske, Wendy S., Piasecki, Thomas M., Nathanson, Lisa, Statham, Dixie J. and Martin, Nicholas G. (2014). Genetic influences on alcohol-related hangover. Addiction, 109 (12), 2027-2034. doi: 10.1111/add.12699
Evangelou, Evangelos, Kerkhos, Hanneke J., Styrkarsdottir, Unnur, Ntzani, Evangelia E., Bos, Steffan D., Esko, Tonu, Evans, Daniel S., Metrustry, Sarah, Panoutsopoulou, Kalliope, Ramos, Yolande F. M., Thorleifsson, Gudmar, Tsilides, Konstantinos K., arcOGEN Consortium, Arden, Nigel, Aslam, Nadim, Bellamy, Nicholas, Birrell, Fraser, Blanco, Francisco J., Carr, Andrew, Chapman, Kay, Day-Williams, Aaron G., Deloukas, Panos, Doherty, Michael, Engstrom, Gunnar, Helgadottir, Hafdis T., Hoffman, Albert, Ingvarsson, Thorvaldur, Jonsson, Helgi, Keis, Aime ... Valdes, Anna M. (2014). A meta-analysis of genome-wide association studies identifies novel variants associated with osteoarthritis of the hip. Annals of the Rheumatic Diseases, 73 (12), 2130-2136. doi: 10.1136/annrheumdis-2012-203114
Dennis, Emily L., Jahanshad, Neda, Braskie, Meredith N., Warstadt, Nicholus M., Hibar, Derrek P., Kohannim, Omid, Nir, Talia M., McMahon, Katie L., de Zubicaray, Greig I., Montgomery, Grant W., Martin, Nicholas G., Toga, Arthur W., Wright, Margaret J. and Thompson, Paul M. (2014). Obesity gene NEGR1 associated with white matter integrity in healthy young adults. Neuroimage, 102 (Part 2), 548-557. doi: 10.1016/j.neuroimage.2014.07.041
Wood, Andrew R., Esko, Tonu, Yang, Jian, Vedantam, Sailaja, Pers, Tune H., Gustafsson, Stefan, Chu, Audrey Y., Estrada, Karol, Luan, Jian'an, Kutalik, Zoltan, Amin, Najaf, Buchkovich, Martin L., Croteau-Chonka, Damien C., Day, Felix R., Duan, Yanan, Fall, Tove, Fehrmann, Rudolf, Ferreira, Teresa, Jackson, Anne U., Karjalainen, Juha, Lo, Ken Sin, Locke, Adam E., Magi, Reedik, Mihailov, Evelin, Porcu, Evelin, Randall, Joshua C., Scherag, Andre, Vinkhuyzen, Anne A. E., Westra, Harm-Jan ... Frayling, Timothy M. (2014). Defining the role of common variation in the genomic and biological architecture of adult human height. Nature Genetics, 46 (11), 1173-1186. doi: 10.1038/ng.3097
Li, Qing, Wojciechowski, Robert, Simpson, Claire L., Hysi, Pirro G., Verhoeven, Virginie J. M., Ikram, Mohammad Kamran, Hohn, Rene, Vitart, Veronique, Hewitt, Alex W., Oexle, Konrad, Makela, Kari-Matti, MacGregor, Stuart, Pirastu, Mario, Fan, Qiao, Cheng, Ching-Yu, St Pourcain, Beate, McMahon, George, Kemp, John P., Northstone, Kate, Rahi, Jugnoo S., Cumberland, Phillippa M., Martin, Nicholas G., Sanfilippo, Paul G., Lu, Yi, Wang, Ya Xing, Hayward, Caroline, Polasek, Ozren, Campbell, Harry, Bencic, Goran ... Guggenheim, Jeremy A. (2014). Genome-wide association study for refractive astigmatism reveals genetic co-determination with spherical equivalent refractive error: the CREAM consortium. Human Genetics, 134 (2), 131-146. doi: 10.1007/s00439-014-1500-y
Meier, Madeline H., Gillespie, Nathan A., Hansell, Narelle K., Hewitt, Alex W., Hickie, Ian B., Lu, Yi, MacGregor, Stuart, Medland, Sarah E., Sun, Cong, Wong, Tien Y., Wright, Margaret J., Zhu, Gu, Martin, Nicholas G. and Mackey, David A. (2014). Associations between depression and anxiety symptoms and retinal vessel caliber in adolescents and young adults. Psychosomatic Medicine, 76 (9), 732-738. doi: 10.1097/PSY.0000000000000117
Warstadt, Nicholus M., Dennis, Emily L., Jahanshad, Neda, Kohannim, Omid, Nir, Talia M., McMahon, Katie L., de Zubicaray, Greig I., Montgomery, Grant W., Henders, Anjali K., Martin, Nicholas G., Whitfield, John B., Jack, Clifford R. Jr., Bernstein, Matt A., Weiner, Michael W., Toga, Arthur W., Wright, Margaret J., Thompson, Paul M. and for the Alzheimer’s Disease Neuroimaging Initiative (ADNI) (2014). Serum cholesterol and variant in cholesterol-related gene CETP predict white matter microstructure. Neurobiology of Aging, 35 (11), 2504-2513. doi: 10.1016/j.neurobiolaging.2014.05.024
Shah, Sonia, McRae, Allan F., Marioni, Riccardo E., Harris, Sarah E., Gibson, Jude, Henders, Anjali K., Redmond, Paul, Cox, Simon R., Pattie, Alison, Corley, Janie, Murphy, Lee, Martin, Nicholas G., Montgomery, Grant W., Starr, John M., Wray, Naomi R., Deary, Ian J. and Visscher, Peter M. (2014). Genetic and environmental exposures constrain epigenetic drift over the human life course. Genome Research, 24 (11), 1725-1733. doi: 10.1101/gr.176933.114
Rietschel, Liz, Zhu, Gu, Kirschbaum, Clemens, Strohmaier, Jana, Wuest, Stefan, Rietschel, Marcella and Martin, Nicholas G. (2014). Perceived stress has genetic influences distinct from neuroticism and depression. Behavior Genetics, 44 (6), 639-645. doi: 10.1007/s10519-013-9636-4
Rentería, M. E., Hansell, N. K., Strike, L. T., McMahon, K. L., de Zubicaray, G. I., Hickie, Ian B., Thompson, Paul M., Martin, N. G., Medland, S. E. and Wright, M. J. (2014). Genetic architecture of subcortical brain regions: common and region-specific genetic contributions. Genes, Brain and Behavior, 13 (8), 821-830. doi: 10.1111/gbb.12177
Benyamin, Beben, Esko, Tonu, Ried, Janina S., Radhakrishnan, Aparna, Vermeulen, Sita H., Traglia, Michela, Goegele, Martin, Anderson, Denise, Broer, Linda, Podmore, Clara, Luan, Jian'an, Kutalik, Zoltan, Sanna, Serena, van der Meer, Peter, Tanaka, Toshiko, Wang, Fudi, Westra, Harm-Jan, Franke, Lude, Mihailov, Evelin, Milani, Lili, Haeldin, Jonas, Winkelmann, Juliane, Meitinger, Thomas, Thiery, Joachim, Peters, Annette, Waldenberger, Melanie, Rendon, Augusto, Jolley, Jennifer, Sambrook, Jennifer ... Whitfield, John B. (2014). Novel loci affecting iron homeostasis and their effects in individuals at risk for hemochromatosis. Nature Communications, 5 (1) 5926, 4926.1-4926.10. doi: 10.1038/ncomms5926
Shen, Kai-Kai, Rose, Stephen, Fripp, Jurgen, McMahon, Katie L., de Zubicaray, Greig I., Martin, Nicholas G., Thompson, Paul M., Wright, Margaret J. and Salvado, Olivier (2014). Investigating brain connectivity heritability in a twin study using diffusion imaging data. Neuroimage, 100, 628-641. doi: 10.1016/j.neuroimage.2014.06.041
Hemani, Gibran, Shakhbazov, Konstantin, Westra, Harm-Jan, Esko, Tonu, Henders, Anjali K., McRae, Allan F., Yang, Jian, Gibson, Greg, Martin, Nicholas G., Metspalu, Andres, Franke, Lude, Montgomery, Grant W., Visscher, Peter M. and Powell, Joseph E. (2014). Another explanation for apparent epistasis: reply. Nature, 514 (7520), E5-E6. doi: 10.1038/nature13692
Le, Anh T., Miller, Paul W., Slutske, Wendy S. and Martin, Nicholas G. (2014). Attitudes toward economic risk and occupational choice. Industrial Relations, 53 (4), 568-592. doi: 10.1111/irel.12054
Hysi, Pirro G., Cheng, Ching-Yu, Springelkamp, Henriet, Macgregor, Stuart, Bailey, Jessica N. Cooke, Wojciechowski, Robert, Vitart, Veronique, Nag, Abhishek, Hewitt, Alex W., Hohn, Rene, Venturini, Cristina, Mirshahi, Alireza, Ramdas, Wishal D., Thorleifsson, Gudmar, Vithana, Eranga, Khor, Chiea-Chuen, Stefansson, Arni B., Liao, Jiemin, Haines, Jonathan L., Amin, Najaf, Wang, Ya Xing, Wild, Philipp S., Ozel, Ayse B., Li, Jun Z., Fleck, Brian W., Zeller, Tanja, Staffieri, Sandra E., Teo, Yik-Ying, Cuellar-Partida, Gabriel ... Aung, Tin (2014). Genome-wide analysis of multi-ancestry cohorts identifies new loci influencing intraocular pressure and susceptibility to glaucoma. Nature Genetics, 46 (10), 1126-1130. doi: 10.1038/ng.3087
Rietveld, Cornelius A., Esko, Tonu, Davies, Gail, Pers, Tune H., Turley, Patrick, Benyamin, Beben, Chabris, Christopher F., Emilsson, Valur, Johnson, Andrew D., Lee, James J., De Leeuw, Christiaan, Marioni, Riccardo E., Medland, Sarah E., Miller, Michael B., Rostapshova, Olga, Van Der Lee, Sven J., Vinkhuyzen, Anna A. E., Amin, Najaf, Conley, Dalton, Derringer, Jaime, Van Duijn, Cornelia M., Fehrmann, Rudolf, Franke, Lude, Glaeser, Edward L., Hansell, Narelle K., Hayward, Caroline, Iacono, William G., Ibrahim-Verbaas, Carla, Jaddoe, Vincent ... Koellinger, Philipp D. (2014). Common genetic variants associated with cognitive performance identified using the proxy-phenotype method. Proceedings of the National Academy of Sciences of the United States of America, 111 (38), 13790-13794. doi: 10.1073/pnas.1404623111
Rietveld, Cornelius A., Esko, Tonu, Davies, Gail, Pers, Tune H., Turley, Patrick, Benyamin, Beben, Chabris, Christopher F., Emilsson, Valur, Johnson, Andrew D., Lee, James J., de Leeuw, Christiaan, Marioni, Riccardo E., Medland, Sarah E., Miller, Michael B., Rostapshova, Olga, van der Lee, Sven J., Vinkhuyzen, Anna A. E., Amin, Najaf, Conley, Dalton, Derringer, Jaime, van Duijn, Cornelia M., Fehrmann, Rudolf, Franke, Lude, Glaeser, Edward L., Hansell, Narelle K., Hayward, Caroline, Iacono, William G., Ibrahim-Verbaas, Carla, Jaddoe, Vincent ... Koellinger, Philipp D. (2014). Common genetic variants associated with cognitive performance identified using the proxy-phenotype method (vol 111, pg 13790, 2014). Proceedings of the National Academy of Sciences of the United States of America, 112 (4), E380-E380. doi: 10.1073/pnas.1424631112
Song, Fengju, Amos, Christopher I., Lee, Jeffrey E., Lian, Christine G., Fang, Shenying, Liu, Hongliang, MacGregor, Stuart, Iles, Mark M., Law, Matthew H., Lindeman, Neal I., Montgomery, Grant W., Duffy, David L., Cust, Anne E., Jenkins, Mark A., Whiteman, David C., Kefford, Richard F., Giles, Graham G., Armstrong, Bruce K., Aitken, Joanne F., Hopper, John L., Brown, Kevin M., Martin, Nicholas G., Mann, Graham J., Bishop, D. Timothy, Bishop, Julia A. Newton, Kraft, Peter, Qureshi, Abrar A., Kanetsky, Peter A., Hayward, Nicholas K. ... Han, Jiali (2014). Identification of a melanoma susceptibility locus and somatic mutation in TET2. Carcinogenesis, 35 (9) bgu140, 2097-2101. doi: 10.1093/carcin/bgu140
Heath, Andrew C., Waldron, Mary C., Martin, Nicholas G., Nelson, Elliot C., Bucholz, Kathleen K. and Madden, Pamela A. F. (2014). Human mate selection and addiction: A conceptual critique. Behavior Genetics, 44 (5), 419-426. doi: 10.1007/s10519-014-9669-3
Hibar, Derrek P., Stein, Jason L., Jahanshad, Neda, Kohannim, Omid, Hua, Xue, Toga, Arthur W., McMahon, Katie L., de Zubicaray, Greig I., Martin, Nicholas G., Wright, Margaret J., Alzheimer’s Disease Neuroimaging Initiative, Weiner, Michael W. and Thompson, Paul M. (2014). Genome-wide interaction analysis reveals replicated epistatic effects on brain structure. Neurobiology of Aging, 36 (S1), S151-S158. doi: 10.1016/j.neurobiolaging.2014.02.033
Metrustry, Sarah J., Edwards, Mark H., Medland, Sarah E., Holloway, John W., Montgomery, Grant W., Martin, Nicholas G., Spector, Tim D., Cooper, Cyrus and Valdes, Ana M. (2014). Variants close to NTRK2 gene are associated with birth weight in female twins. Twin Research and Human Genetics, 17 (4), 254-261. doi: 10.1017/thg.2014.34
Byrne, Edna M., Carrillo-Roa, Tania, Penninx, Brenda W. J. H., Sallis, Hannah M., Viktorin, Alexander, Chapman, Brett, Henders, Anjali K., Pergadia, Michele L., Heath, Andrew C., Madden, Pamela A. F., Sullivan, Patrick F., Boschloo, Lynn, van Grootheest, Gerard, McMahon, George, Lawlor, Debbie A., Landen, Mikael, Lichtenstein, Paul, Magnusson, Patrik K. E., Evans, David M., Montgomery, Grant W., Boomsma, Dorret I., Martin, Nicholas G., Meltzer-Brody, Samantha and Wray, Naomi R. (2014). Applying polygenic risk scores to postpartum depression. Archives of Women's Mental Health, 17 (6), 519-528. doi: 10.1007/s00737-014-0428-5
Kochunov, Peter, Jahanshad, Neda, Sprooten, Emma, Nichols, Thomas E., Mandl, René C., Almasy, Laura, Booth, Tom, Brouwer, Rachel M., Curran, Joanne E., de Zubicaray, Greig I., Dimitrova, Rali, Duggirala, Ravi, Fox, Peter T., Hong, L. Elliot, Landman, Bennett A., Lemaitre, Hervé, Lopez, Lorna M., Martin, Nicholas G., McMahon, Katie L., Mitchell, Braxton D., Olvera, Rene L., Peterson, Charles P., Starr, John M., Sussmann, Jessika E., Toga, Arthur W., Wardlaw, Joanna M., Wright, Margaret J., Wright, Susan N., Bastin, Mark E. ... Glahn, David C. (2014). Multi-site study of additive genetic effects on fractional anisotropy of cerebral white matter: comparing meta and megaanalytical approaches for data pooling. Neuroimage, 95, 136-150. doi: 10.1016/j.neuroimage.2014.03.033
Nelson, Elliot C., Heath, Andrew C., Lynskey, Michael T., Agrawal, Arpana, Henders, Anjali K., Bowdler, Lisa M., Todorov, Alexandre A., Madden, Pamela A. F., Moore, Elizabeth, Degenhardt, Louisa, Martin, Nicholas G. and Montgomery, Grant W. (2014). PTSD risk associated with a functional DRD2 polymorphism in heroin-dependent cases and controls is limited to amphetamine-dependent individuals. Addiction Biology, 19 (4), 700-707. doi: 10.1111/adb.12062
van den Berg, Stephanie M., de Moor, Marleen H. M., McGue, Matt, Pettersson, Erik, Terracciano, Antonio, Verweij, Karin J. H., Amin, Najaf, Derringer, Jaime, Esko, Tonu, van Grootheest, Gerard, Hansell, Narelle K., Huffman, Jennifer, Konte, Bettina, Lahti, Jari, Luciano, Michelle, Matteson, Lindsay K., Viktorin, Alexander, Wouda, Jasper, Agrawal, Arpana, Allik, Jueri, Bierut, Laura, Broms, Ulla, Campbell, Harry, Smith, George Davey, Eriksson, Johan G., Ferrucci, Luigi, Franke, Barbera, Fox, Jean-Paul, de Geus, Eco J. C. ... Boomsma, Dorret I. (2014). Harmonization of neuroticism and extraversion phenotypes across inventories and cohorts in the Genetics of Personality Consortium: an application of item response theory. Behavior Genetics, 44 (4), 295-313. doi: 10.1007/s10519-014-9654-x
Aoude, Lauren G., Xu, Mai, Zhao, Zhen Zhen, Kovacs, Michael, Palmer, Jane M., Johansson, Peter, Symmons, Judith, Trent, Jeffrey M., Martin, Nicholas G., Montgomery, Grant W., Brown, Kevin M. and Hayward, Nicholas K. (2014). Assessment of PALB2 as a candidate melanoma susceptibility gene. PLoS One, 9 (6) e100683, e100683.1-e100683.7. doi: 10.1371/journal.pone.0100683
Jagirdar, Kasturee, Smit, Darren J., Ainger, Stephen A., Lee, Katie J., Brown, Darren L., Chapman, Brett, Zhao, Zhen Zhen, Montgomery, Grant W., Martin, Nicholas G., Stow, Jennifer L., Duffy, David L. and Sturm, Richard A. (2014). Molecular analysis of common polymorphisms within the human Tyrosinase locus and genetic association with pigmentation traits. Pigment Cell and Melanoma Research, 27 (4), 552-564. doi: 10.1111/pcmr.12253
Maciejewski, Dominique F., Creemers, Hanneke E., Lynskey, Michael T., Madden, Pamela A. F., Heath, Andrew C., Statham, Dixie J., Martin, Nicholas G. and Verweij, Karin J. H. (2014). Overlapping genetic and environmental influences on nonsuicidal self-injury and suicidal ideation different outcomes, same etiology?. Jama Psychiatry, 71 (6), 699-705. doi: 10.1001/jamapsychiatry.2014.89
Thompson, Paul M., Stein, Jason L., Medland, Sarah E., Hibar, Derrek P., Arias Vasquez, Alejandro, Renteria, Miguel E., Toro, Roberto, Jahanshad, Neda, Schumann, Gunter, Franke, Barbara, Wright, Margaret J., Martin, Nicholas G., Agartz, Ingrid, Alda, Martin, Alhusaini, Saud, Almasy, Laura, Almeida, Jorge, Alpert, Kathryn, Andreasen, Nancy C., Andreassen, Ole A., Apostolova, Liana G., Appel, Katja, Armstrong, Nicola J., Aribisala, Benjamin, Bastin, Mark E., Bauer, Michael, Bearden, Carrie E., Bergmann, Ørjan, Binder, Elisabeth B. ... Saguenay Youth Study (SYS) Group (2014). The ENIGMA Consortium: large-scale collaborative analyses of neuroimaging and genetic data. Brain Imaging and Behavior, 8 (2), 153-182. doi: 10.1007/s11682-013-9269-5
McRae, Allan F., Powell, Joseph E., Henders, Anjali K., Bowdler, Lisa, Hemani, Gibran, Shah, Sonia, Painter, Jodie N., Martin, Nicholas G., Visscher, Peter M. and Montgomery, Grant W. (2014). Contribution of genetic variation to transgenerational inheritance of DNA methylation. Genome Biology, 15 (5) ARTN R73, 1-10. doi: 10.1186/gb-2014-15-5-r73
Purrington, Kristen S., Slager, Susan, Eccles, Diana, Yannoukakos, Drakoulis, Fasching, Peter A., Miron, Penelope, Carpenter, Jane, Chang-Claude, Jenny, Martin, Nicholas G., Montgomery, Grant W., Kristensen, Vessela, Anton-Culver, Hoda, Goodfellow, Paul, Tapper, William J., Rafiq, Sajjad, Gerty, Susan M., Durcan, Lorraine, Konstantopoulou, Irene, Fostira, Florentia, Vratimos, Athanassios, Apostolou, Paraskevi, Konstanta, Irene, Kotoula, Vassiliki, Lakis, Sotiris, Dimopoulos, Meletios A., Skarlos, Dimosthenis, Pectasides, Dimitrios, Fountzilas, George, Beckmann, Matthias W. ... Couch, Fergus J. (2014). Genome-wide association study identifies 25 known breast cancer susceptibility loci as risk factors for triple-negative breast cancer. Carcinogenesis, 35 (5), 1012-1019. doi: 10.1093/carcin/bgt404
Hatemi, Peter K., Medland, Sarah E., Klemmensen, Robert, Oskarsson, Sven, Littvay, Levente, Dawes, Christopher T., Verhulst, Brad, McDermott, Rose, Norgaard, Asbjorn Sonne, Klofstad, Casey A., Christensen, Kaare, Johannesson, Magnus, Magnusson, Patrik K. E., Eaves, Lindon J. and Martin, Nicholas G. (2014). Genetic influences on political ideologies: Twin analyses of 19 measures of political ideologies from five democracies and genome-wide findings from three populations. Behavior Genetics, 44 (3), 282-294. doi: 10.1007/s10519-014-9648-8
Martin, Nick (2014). Lindon eaves: The astonishing decade. Behavior Genetics, 44 (3), 193-197. doi: 10.1007/s10519-013-9613-y
Davies, Matthew N., Krause, Lutz, Bell, Jordana T., Gao, Fei, Ward, Kirsten J., Wu, Honglong, Lu, Hanlin, Liu, Yuan, Tsai, Pei-Chein, Collier, David A., Murphy, Therese, Dempster, Emma, Mill, Jonathan, UK Brain Expression Consortium, Battle, Alexis, Mostafavi, Sara, Zhu, Xiaowei, Henders, Anjali, Byrne, Enda, Wray, Naomi R., Martin, Nicholas G., Spector, Tim D. and Wang, Jun (2014). Hypermethylation in the ZBTB20 gene is associated with major depressive disorder. Genome Biology, 15 (4) R56, R56.1-R56.12. doi: 10.1186/gb-2014-15-4-r56
Dennis, Emily L., Jahanshad, Neda, McMahon, Katie L., de Zubicaray, Greig I., Martin, Nicholas G., Hickie, Ian B., Toga, Arthur W., Wright, Margaret J. and Thompson, Paul M. (2014). Development of insula connectivity between ages 12 and 30 revealed by high angular resolution diffusion imaging. Human Brain Mapping, 35 (4), 1790-1800. doi: 10.1002/hbm.22292
Roussotte, Florence F., Jahanshad, Neda, Hibar, Derrek P., Sowell, Elizabeth R., Kohannim, Omid, Barysheva, Marina, Hansell, Narelle K., McMahon, Katie L., de Zubicaray, Greig I., Montgomery, Grant W., Martin, Nicholas G., Wright, Margaret J., Toga, Arthur W., Jack Jr, Clifford R., Weiner, Michael W., Thompson, Paul M. and ADNI (2014). A commonly carried genetic variant in the delta opioid receptor gene, OPRD1, is associated with smaller regional brain volumes: replication in elderly and young populations. Human Brain Mapping, 35 (4), 1226-1236. doi: 10.1002/hbm.22247
Karcher, Nicole R., Slutske, Wendy S., Kerns, John G., Piasecki, Thomas M. and Martin, Nicholas G. (2014). Sex differences in magical ideation: A community-based twin study. Personality Disorders-Theory Research and Treatment, 5 (2), 212-219. doi: 10.1037/per0000040
Kubarych, Thomas S., Kendler, Kenneth S., Aggen, Steven H., Estabrook, Ryne, Edwards, Alexis C., Clark, Shaunna L., Martin, Nicholas G., Hickie, Ian B., Neale, Michael C. and Gillespie, Nathan A. (2014). Comparing factor, class, and mixture models of cannabis initiation and DSM cannabis use disorder criteria, including craving, in the Brisbane longitudinal twin study. Twin Research and Human Genetics, 17 (2), 89-98. doi: 10.1017/thg.2014.9
Shand, Fiona L., Day, Carolyn, Rawlinson, William, Degenhardt, Louisa, Martin, Nicholas G. and Nelson, Elliot C. (2014). Hepatitis C testing and status among opioid substitution treatment clients in New South Wales. Australian and New Zealand Journal of Public Health, 38 (2), 160-164. doi: 10.1111/1753-6405.12173
Lafortune, Marjolaine, Gagnon, Jean-Francois, Martin, Nicolas, Latreille, Veronique, Dube, Jonathan, Bouchard, Maude, Bastien, Celyne and Carrier, Julie (2014). Sleep spindles and rapid eye movement sleep as predictors of next morning cognitive performance in healthy middle-aged and older participants. Journal of Sleep Research, 23 (2), 159-167. doi: 10.1111/jsr.12108
Albrecht, Eva, Sillanpaa, Elina, Karrasch, Stefan, Alves, Alexessander Couto, Codd, Veryan, Hovatta, Iiris, Buxton, Jessica L., Nelson, Christopher P., Broer, Linda, Hagg, Sara, Mangino, Massimo, Willemsen, Gonneke, Surakka, Ida, Ferreira, Manuel A. R., Amin, Najaf, Oostra, Ben A., Backmand, Hell M., Peltonen, Markku, Sarna, Seppo, Rantanen, Taina, Sipila, Sarianna, Korhonen, Tellervo, Madden, Pamela A. F., Gieger, Christian, Jorres, Rudolf A., Heinrich, Joachim, Behr, Juergen, Huber, Rudolf M., Peters, Annette ... Schulz, Holger (2014). Telomere length in circulating leukocytes is associated with lung function and disease. European Respiratory Journal, 43 (4), 983-992. doi: 10.1183/09031936.00046213
Muehleisen, Thomas W., Leber, Markus, Schulze, Thomas G., Strohmaier, Jana, Degenhardt, Franziska, Treutlein, Jens, Mattheisen, Manuel, Forstner, Andreas J., Schumacher, Johannes, Breuer, Rene, Meier, Sandra, Herms, Stefan, Hoffmann, Per, Lacour, Andre, Witt, Stephanie H., Reif, Andreas, Mueller-Myhsok, Bertram, Lucae, Susanne, Maier, Wolfgang, Schwarz, Markus, Vedder, Helmut, Kammerer-Ciernioch, Jutta, Pfennig, Andrea, Bauer, Michael, Hautzinger, Martin, Moebus, Susanne, Priebe, Lutz, Czerski, Piotr M., Hauser, Joanna ... Cichon, Sven (2014). Genome-wide association study reveals two new risk loci for bipolar disorder. Nature Communications, 5 (3339) 3339, 1-8. doi: 10.1038/ncomms4339
De Alwis, Duneesha, Agrawal, Arpana, Reiersen, Angela M., Constantino, John N., Henders, Anjali, Martin, Nicholas G. and Lynskey, Michael T. (2014). ADHD symptoms, autistic traits, and substance use and misuse in adult Australian twins. Journal of Studies On Alcohol and Drugs, 75 (2), 211-221. doi: 10.15288/jsad.2014.75.211
Fede, Giuseppe, Spadaro, Luisa, Tomaselli, Tania, Privitera, Graziella, Scicali, Roberto, Vasianopoulou, Panayota, Thalassinos, Evangelos, Martin, Nicholas, Thomas, Michael, Purrello, Francesco and Burroughs, Andrew Kenneth (2014). Comparison of total cortisol, free cortisol, and surrogate markers of free cortisol in diagnosis of adrenal insufficiency in patients with stable cirrhosis. Clinical Gastroenterology and Hepatology, 12 (3), 504-512. doi: 10.1016/j.cgh.2013.08.028
Shan, Zuyao Y., Wright, Margaret J., Thompson, Paul M., McMahon, Katie L., Blokland, Gabriella G. A. M., de Zubicaray, Greig I., Martin, Nicholas G., Vinkhuyzen, Anna A. E. and Reutens, David C. (2014). Modeling of the hemodynamic responses in block design fMRI studies. Journal of Cerebral Blood Flow and Metabolism, 34 (2), 316-324. doi: 10.1038/jcbfm.2013.200
Blokland, Gabriëlla A. M., McMahon, Katie L., Thompson, Paul M., Hickie, Ian B., Martin, Nicholas G., de Zubicaray, Greig I. and Wright, Margaret J. (2014). Genetic effects on the cerebellar role in working memory: same brain, different genes?. NeuroImage, 86, 392-403. doi: 10.1016/j.neuroimage.2013.10.006
Ligthart, Lannie, Hottenga, Jouke-Jan, Lewis, Cathryn M., Farmer, Anne E., Craig, Ian W., Breen, Gerome, Willemsen, Gonneke, Vink, Jacqueline M., Middeldorp, Christel M., Byrne, Enda M., Heath, Andrew C., Madden, Pamela A. F., Pergadia, Michele L., Montgomery, Grant W., Martin, Nicholas G., Penninx, Brenda W. J. H., McGuffin, Peter, Boomsma, Dorret I. and Nyholt, Dale R. (2014). Genetic risk score analysis indicates migraine with and without comorbid depression are genetically different disorders. Human Genetics, 133 (2), 173-186. doi: 10.1007/s00439-013-1370-8
Richmond-Rakerd, Leah S., Slutske, Wendy S., Heath, Andrew C. and Martin, Nicholas G. (2014). Genetic and environmental influences on the ages of drinking and gambling initiation: evidence for distinct aetiologies and sex differences. Addiction, 109 (2), 323-331. doi: 10.1111/add.12310
Jahanshad, Neda, Kochunov, Peter V., Sprooten, Emma, Mandl, Rene C., Nichols, Thomas E., Almasy, Laura, Blangero, John, Brouwer, Rachel M., Curran, Joanne E., de Zubicaray, Greig I., Duggirala, Ravi, Fox, Peter T., Hong, L. Elliot, Landman, Bennett A., Martin, Nicholas G., McMahon, Katie L., Medland, Sarah E., Mitchell, Braxton D., Olvera, Rene L., Peterson, Charles P., Starr, John M., Sussmann, Jessika E., Toga, Arthur W., Wardlaw, Joanna M., Wright, Margaret J., Pol, Hilleke E. Hulshoff, Bastin, Mark E., McIntosh, Andrew M., Deary, Ian J. ... Glahn, David C. (2014). Multi-site genetic analysis of diffusion images and voxelwise heritability analysis: A pilot project of the ENIGMA-DTI working group (vol 81, pg 455, 2013). Neuroimage, 90, 470-471. doi: 10.1016/j.neuroimage.2013.12.053
Hill, W. D., Davies, G., Van De Lagemaat, L. N., Christoforou, A., Marioni, R. E., Fernandes, C. P. D., Liewald, D. C., Croning, M. D. R., Payton, A., Craig, L. C. A., Whalley, L. J., Horan, M., Ollier, W., Hansell, N. K., Wright, M. J., Martin, N. G., Montgomery, G. W., Steen, V. M., Le Hellard, S., Espeseth, T., Lundervold, A. J., Reinvang, I., Starr, J. M., Pendleton, N., Grant, S. G. N., Bates, T. C. and Deary, I. J. (2014). Human cognitive ability is influenced by genetic variation in components of postsynaptic signalling complexes assembled by NMDA receptors and MAGUK proteins. Translational Psychiatry, 4 (1) e341, 1-8. doi: 10.1038/tp.2013.114
Oh, Gabriel, Wang, Sun-Chong, Pal, Mrinal, Chen, Zheng Fei, Khare, Tarang, Tochigi, Mamoru, Ng, Catherine, Yang, Yeqing A., Kwan, Andrew, Kaminsky, Zachary A., Mill, Jonathan, Gunasinghe, Cerisse, Tackett, Jennifer L., Gottesman, Irving I., Willemsen, Gonneke, de Geus, Eco J. C., Vink, Jacqueline M., Slagboom, P. Eline, Wray, Naomi R., Heath, Andrew C., Montgomery, Grant W., Turecki, Gustavo, Martin, Nicholas G., Boomsma, Dorret I., McGuffin, Peter, Kustra, Rafal and Petronis, Art (2014). DNA modification study of major depressive disorder: beyond locus-by-locus comparisons. Biological Psychiatry, 77 (3), 246-255. doi: 10.1016/j.biopsych.2014.06.016
Painter, Jodie N., Nyholt, Dale R, Krause, Lutz, Zhao, Zhen Z., Chapman, Brett, Zhang, Christine, Medland, Sarah, Martin, Nicholas G., Kennedy, Stephen, Treloar, Susan, Zondervan, Krina and Montgomery, Grant W. (2014). Common variants in the CYP2C19 gene are associated with susceptibility to endometriosis. Fertility and Sterility, 102 (2), 496-502.e5. doi: 10.1016/j.fertnstert.2014.04.015
Power, R. A., Verweij, K. J. H., Zuhair, M., Montgomery, G. W., Henders, A. K., Heath, A. C., Madden, P. A. F., Medland, S. E., Wray, N. R. and Martin, N. G. (2014). Genetic predisposition to schizophrenia associated with increased use of cannabis. Molecular Psychiatry, 19 (11), 1201-1204. doi: 10.1038/mp.2014.51
Nelson, Elliot C., Lynskey, Michael T., Heath, Andrew C., Wray, Naomi, Agrawal, Arpana, Shand, Fiona L., Henders, Anjali K., Wallace, Leanne, Todorov, Alexandre A., Schrage, Andrew J., Madden, Pamela A. F., Degenhardt, Louisa, Martin, Nicholas G. and Montgomery, Grant W. (2014). Association of OPRD1 polymorphisms with heroin dependence in a large case-control series. Addiction Biology, 19 (1), 111-121. doi: 10.1111/j.1369-1600.2012.00445.x
Byrne, Enda M., Heath, Andrew C., Madden, Pamela A. F., Pergadia, Michele L., Hickie, Ian B., Montgomery, Grant W., Martin, Nicholas G. and Wray, Naomi R. (2014). Testing the role of circadian genes in conferring risk for psychiatric disorders. American Journal of Medical Genetics, Part B: Neuropsychiatric Genetics, 165 (3), 254-260. doi: 10.1002/ajmg.b.32230
Li, M., Luo, X-j, Rietschel, M., Lewis, C. M., Mattheisen, M., Mueller-Myhsok, B., Jamain, S., Leboyer, M., Landen, M., Thompson, P. M., Cichon, S., Noethen, M. M., Schulze, T. G., Sullivan, P. F., Bergen, S. E., Donohoe, G., Morris, D. W., Hargreaves, A., Gill, M., Corvin, A., Hultman, C., Toga, A. W., Shi, L., Lin, Q., Shi, H., Gan, L., Meyer-Lindenberg, A., Czamara, D., Henry, C. ... Su, B. (2014). Allelic differences between Europeans and Chinese for CREB1 SNPs and their implications in gene expression regulation, hippocampal structure and function, and bipolar disorder susceptibility. Molecular Psychiatry, 19 (4), 452-461. doi: 10.1038/mp.2013.37
Lee, Anthony J., Mitchem, Dorian G., Wright, Margaret J., Martin, Nicholas G., Keller, Matthew C. and Zietsch, Brendan P. (2014). Genetic factors that increase male facial masculinity decrease facial attractiveness of female relatives. Psychological Science, 25 (2), 476-484. doi: 10.1177/0956797613510724
Couvy-Duchesne, Baptiste, Blokland, Gabriëlla A.M., Hickie, Ian B., Thompson, Paul M., Martin, Nicholas G., de Zubicaray, Greig I., McMahon, Katie L. and Wright, Margaret J. (2014). Heritability of head motion during resting state functional MRI in 462 healthy twins. Neuroimage, 102 (2), 424-434. doi: 10.1016/j.neuroimage.2014.08.010
Plug, Erik, Webbink, Dinand and Martin, Nick (2014). Sexual orientation, prejudice, and segregation. Journal of Labor Economics, 32 (1), 123-159. doi: 10.1086/673315
Prasad, Gautam, Joshi, Shantanu H., Jahanshad, Neda, Villalon-Reina, Julio, Aganj, Iman, Lenglet, Christophe, Guillermo Sapiro, McMahon, Katie L., de Zubicaray, Greig I., Martin, Nicholas G., Wright, Margaret J., Toga, Arthur W. and Thompson, Paul M. (2014). Automatic clustering and population analysis of white matter tracts using maximum density paths. NeuroImage, 97, 284-295. doi: 10.1016/j.neuroimage.2014.04.033
Loukola, A., Wedenoja, J., Keskitalo-Vuokko, K., Broms, U., Korhonen, T., Ripatti, S., Sarin, A-P, Pitkaniemi, J., He, L., Happola, A., Heikkila, K., Chou, Y-L, Pergadia, M. L., Heath, A. C., Montgomery, G. W., Martin, N. G., Madden, P. A. F. and Kaprio, J. (2014). Genome-wide association study on detailed profiles of smoking behavior and nicotine dependence in a twin sample. Molecular Psychiatry, 19 (5), 615-624. doi: 10.1038/mp.2013.72
Steinberg, S., de Jong, S., Mattheisen, M., Costas, J., Demontis, D., Jamain, S., Pietilainen, O. P. H., Lin, K., Papiol, S., Huttenlocher, J., Sigurdsson, E., Vassos, E., Giegling, I., Breuer, R., Fraser, G., Walker, N., Melle, I., Djurovic, S., Agartz, I., Tuulio-Henriksson, A., Suvisaari, J., Lonnqvist, J., Paunio, T., Olsen, L., Hansen, T., Ingason, A., Pirinen, M., Strengman, E., Hougaard, D. M. ... Stefansson, K. (2014). Common variant at 16p11.2 conferring risk of psychosis. Molecular Psychiatry, 19 (1), 108-114. doi: 10.1038/mp.2012.157
Hoggart, C. J., Venturini, G., Mangino, M., Gomez, F., Ascari, G., Zhao, J.H., Teumer, A., Winkler, T. W., Tsernikova, N., Luan, J., Mihailov, E., Ehret, G. B., Zhang, W., Lamparter, D., Esko, T., Mace, A., Rueger, S., Bochud, P.-Y., Barcella, M., Dauvilliers, Y., Benyamin, B., Evans, D. M., Hayward, C., Lopez, M. F., Franke, L., Russo, A., Heid, I. M., Salvi, E., Vendantam, S. ... Kutalik Z. (2014). Novel Approach Identifies SNPs in SLC2A10 and KCNK9 with Evidence for Parent-of-Origin Effect on Body Mass Index. PLoS Genetics, 10 (7) e1004508, 1-12. doi: 10.1371/journal.pgen.1004508
Robles-Espinoza, Carla Daniela, Harland, Mark, Ramsay, Andrew J, Aoude, Lauren G, Quesada, Víctor, Ding, Zhihao, Pooley, Karen A, Pritchard, Antonia L, Tiffen, Jessamy C, Petljak, Mia, Palmer, Jane M, Symmons, Judith, Johansson, Peter, Stark, Mitchell S., Gartside, Michael G, Snowden, Helen, Montgomery, Grant W, Martin, Nicholas G, Liu, Jimmy Z, Choi, Jiyeon, Makowski, Matthew, Brown, Kevin M, Dunning, Alison M, Keane, Thomas M, Lopez-Otin, Carlos, Gruis, Nelleke A, Hayward, Nicholas K, Bishop, D Timothy, Newton-Bishop, Julia A and Adams, David J (2014). POT1 loss-of-function variants predispose to familial melanoma. Nature Genetics, 46 (5), 478-481. doi: 10.1038/ng.2947
Waldron, Mary, Grant, Julia D., Bucholz, Kathleen K., Lynskey, Michael T., Slutske, Wendy S., Glowinski, Anne L., Henders, Anjali, Statham, Dixie J., Martin, Nicholas G. and Heath, Andrew C. (2014). Parental separation and early substance involvement: results from children of alcoholic and cannabis dependent twins. Drug and Alcohol Dependence, 134 (1), 78-84. doi: 10.1016/j.drugalcdep.2013.09.010
Deutsch, Arielle R., Slutske, Wendy S., Heath, Andrew C., Madden, Pamela A. F. and Martin, Nicholas G. (2014). Substance use and sexual intercourse onsets in adolescence: A genetically informative discordant twin design. Journal of Adolescent Health, 54 (1), 114-116. doi: 10.1016/j.jadohealth.2013.07.013
Ferreira, Manuel A. R., Matheson, Melanie C., Tang, Clara S., Granell, Raquel, Ang, Wei., Hui, Jennie, Kiefer, Amy K., Duffy, David L., Baltic, Svetlana, Danoy, Patrick, Bui, Minh, Price, Loren, Sly, Peter D., Eriksson, Nicholas, Madden, Pamela A., Abraham, Michael J. A., Holt, Patrick G., Heath, p Andrew C., Hunter, Michael, Musk, Bill, Robertson, Colin F., Le Souef, Peter, Montgomery, Grant W., Henderson, A. John, Tung, Joyce Y., Dharmage, Shyamali C., Brown, Matthew A., James, Alan, Thompson, Philip J. ... Australian Asthma Genetics Consortium Collaborators (2013). Genome-wide association analysis identifies 11 risk variants associated with the asthma with hay fever phenotype. Journal of Allergy And Clinical Immunology, 133 (6), 1564-1571. doi: 10.1016/j.jaci.2013.10.030
Wang, Jiping, Carvajal-Carmona, Luis G., Chu, Jen-Hwa, Zauber, Ann G., Kubo, Michikai, Matsuda, Koichi, Dunlop, Malcolm, Houlston, Richard S., Sieber, Oliver, Lipton, Lara, Gibbs, Peter, Martin, Nicholas G., Montgomery, Grant W., Young, Joanne, Baird, Paul N., Ratain, Mark J., Nakamura, Yusuke, Weiss, Scott T., Tomlinson, Ian and Bertagnolli, Monica M. (2013). Germline variants and advanced colorectal adenomas: adenoma prevention with celecoxib trial genome-wide association study. Clinical Cancer Research, 19 (23), 6430-6437. doi: 10.1158/1078-0432.CCR-13-0550
Stephens, Sarah H., Hartz, Sarah M., Hoft, Nicole R., Saccone, Nancy L., Corley, Robin C., Hewitt, John K., Hopfer, Christian J., Breslau, Naomi, Coon, Hilary, Chen, Xiangning, Ducci, Francesca, Dueker, Nicole, Franceschini, Nora, Frank, Josef, Han, Younghun, Hansel, Nadia N., Jiang, Chenhui, Korhonen, Tellervo, Lind, Penelope A., Liu, Jason, Lyytikaeinen, Leo-Pekka, Michel, Martha, Shaffer, John R., Short, Susan E., Sun, Juzhong, Teumer, Alexander, Thompson, John R., Vogelzangs, Nicole, Vink, Jacqueline M. ... Ehringer, Marissa A. (2013). Distinct loci in the CHRNA5/CHRNA3/CHRNB4 gene cluster are associated with onset of regular smoking. Genetic Epidemiology, 37 (8), 846-859. doi: 10.1002/gepi.21760
Verweij, Karin J. H., Huizink, Anja C., Agrawal, Arpana, Martin, Nicholas G. and Lynskey, Michael T. (2013). Is the relationship between early-onset cannabis use and educational attainment causal or due to common liability?. Drug and Alcohol Dependence, 133 (2), 580-586. doi: 10.1016/j.drugalcdep.2013.07.034
Braskie, Meredith N., Kohannim, Omid, Jahanshad, Neda, Chiang, Ming-Chang, Barysheva, Marina, Toga, Arthur W., Ringman, John M., Montgomery, Grant W., McMahon, Katie L., de Zubicaray, Greig I., Martin, Nicholas G., Wright, Margaret J. and Thompson, Paul M. (2013). Relation between variants in the neurotrophin receptor gene, NTRK3, and white matter integrity in healthy young adults. Neuroimage, 82, 146-153. doi: 10.1016/j.neuroimage.2013.05.095
Mitchem, Dorian G., Purkey, Alicia M., Grebe, Nicholas M., Carey, Gregory, Garver-Apgar, Christine E., Bates, Timothy C., Arden, Rosalind, Hewitt, John K., Medland, Sarah E., Martin, Nicholas G., Zietsch, Brendan P. and Keller, Matthew C. (2013). Estimating the sex-specific effects of genes on facial attractiveness and sexual dimorphism. Behavior Genetics, 44 (3), 270-281. doi: 10.1007/s10519-013-9627-5
Sletten, Tracey L., Rajaratnam, Shantha M. W., Wright, Margaret J., Zhu, Gu, Naismith, Sharon, Martin, Nicholas G. and Hickie, Ian (2013). Genetic and environmental contributions to sleep-wake behavior in 12-year-old twins. Sleep, 36 (11), 1715-1722. doi: 10.5665/sleep.3136
Hemani, Gibran, Yang, Jian, Vinkhuyzen, Anna, Powell, Joseph E., Willemsen, Gonneke, Hottenga, Jouke-Jan, Abdellaoui, Abdel, Mangino, Massimo, Valdes, Ana M., Medland, Sarah E., Madden, Pamela A., Heath, Andrew C., Henders, Anjali K., Nyholt, Dale R., de Geus, Eco J. C., Magnusson, Patrik K. E., Ingelsson, Erik, Montgomery, Grant W., Spector, Timothy D., Boomsma, Dorret I., Pedersen, Nancy L., Martin, Nicholas G. and Visscher, Peter M. (2013). Inference of the Genetic Architecture Underlying BMI and Height with the Use of 20,240 Sibling Pairs. American Journal of Human Genetics, 93 (5), 865-875. doi: 10.1016/j.ajhg.2013.10.005
Willer C.J., Schmidt E.M., Sengupta S., Peloso G.M., Gustafsson S., Kanoni S., Ganna A., Chen J., Buchkovich M.L., Mora S., Beckmann J.S., Bragg-Gresham J.L., Chang H.-Y., Demirkan A., Den Hertog H.M., Do R., Donnelly L.A., Ehret G.B., Esko T., Feitosa M.F., Ferreira T., Fischer K., Fontanillas P., Fraser R.M., Freitag D.F., Gurdasani D., Heikkila K., Hypponen E., Isaacs A. ... Abecasis G.R. (2013). Discovery and refinement of loci associated with lipid levels. Nature Genetics, 45 (11), 1274-1285. doi: 10.1038/ng.2797
Ellingson, Jarrod M., Verges, Alvaro, Littlefield, Andrew K., Martin, Nicholas G. and Slutske, Wendy S. (2013). Are bottom-up and top-down traits in dual-systems models of risky behavior genetically distinct?. Behavior Genetics, 43 (6), 480-490. doi: 10.1007/s10519-013-9615-9
Perkins, Adam M., Cserjesi, Renata, Ettinger, Ulrich, Kumari, Veena, Martin, Nicholas G. and Arden, Rosalind (2013). Personality and occupational markers of 'solid citizenship' are associated with having fewer children. Personality and Individual Differences, 55 (8), 871-876. doi: 10.1016/j.paid.2013.07.011
Wang, J-C, Foroud, T., Hinrichs, A. L., Le, N. X. H., Bertelsen, S., Budde, J. P., Harari, O., Koller, D. L., Wetherill, L., Agrawal, A., Almasy, L., Brooks, A. I., Bucholz, K., Dick, D., Hesselbrock, V., Johnson, E. O., Kang, S., Kapoor, M., Kramer, J., Kuperman, S., Madden, P. A. F., Manz, N., Martin, N. G., McClintick, J. N., Montgomery, G. W., Nurnberger, J. I., Rangaswamy, M., Rice, J., Schuckit, M. ... Goate, A. M. (2013). A genome-wide association study of alcohol-dependence symptom counts in extended pedigrees identifies C15orf53. Molecular Psychiatry, 18 (11), 1218-1224. doi: 10.1038/mp.2012.143
Do, Ron, Willer, Cristen J., Schmidt, Ellen M., Sengupta, Sebanti, Gao, Chi, Peloso, Gina M., Gustafsson, Stefan, Kanoni, Stavroula, Ganna, Andrea, Chen, Jin, Buchkovich, Martin L., Mora, Samia, Beckmann, Jacques S., Bragg-Gresham, Jennifer L., Chang, Hsing-Yi, Demirkan, Ayse, Den Hertog, Heleen M., Donnelly, Louise A., Ehret, Georg B., Esko, Tonu, Feitosa, Mary F., Ferreira, Teresa, Fischer, Krista, Fontanillas, Pierre, Fraser, Ross M., Freitag, Daniel F., Gurdasani, Deepti, Heikkila, Kauko, Hyppoenen, Elina ... Kathiresan, Sekar (2013). Common variants associated with plasma triglycerides and risk for coronary artery disease. Nature Genetics, 45 (11), 1345-1352. doi: 10.1038/ng.2795
Turner, Marc, Leslie, Stephen, Martin, Nicholas G., Peschanski, Marc, Rao, Mahendra, Taylor, Craig J., Trounson, Alan, Turner, David, Yamanaka, Shinya and Wilmut, Ian (2013). Toward the development of a global induced pluripotent stem cell library. Cell Stem Cell, 13 (4), 382-384. doi: 10.1016/j.stem.2013.08.003
Revez, J. A., Bain, L., Chapman, B., Powell, J. E., Jansen, R., Duffy, D. L., Tung, J. Y., AAGC Collaborators, Penninx, B. W., Visscher, P. M., De Geus, E. J. C., Boomsma, D. I., Hinds, D. A., Martin, N. G., Montgomery, G. W., Ferreira, M. A. R., Danoy, Patrick and Brown, Matthew A. (2013). A new regulatory variant in the interleukin-6 receptor gene associates with asthma risk. Genes and Immunity, 14 (7), 441-446. doi: 10.1038/gene.2013.38
Wade, Tracey D., Gordon, Scott, Medland, Sarah, Bulik, Cynthia M., Heath, Andrew C., Montgomery, Grant W. and Martin, Nicholas G. (2013). Genetic variants associated with disordered eating. International Journal of Eating Disorders, 46 (6), 594-608. doi: 10.1002/eat.22133
Lee, S. Hong, Ripke, Stephan, Neale, Benjamin M., Faraone, Stephen V., Purcell, Shaun M., Perlis, Roy H., Mowry, Bryan J., Thapar, Anita, Goddard, Michael E., Witte, John S., Absher, Devin, Agartz, Ingrid, Akil, Huda, Amin, Farooq, Andreassen, Ole A., Anjorin, Adebayo, Anney, Richard, Anttila, Verneri, Arking, Dan E., Asherson, Philip, Azevedo, Maria H., Backlund, Lena, Badner, Judith A., Bailey, Anthony J., Banaschewski, Tobias, Barchas, Jack D., Barnes, Michael R., Barrett, Thomas B., Bass, Nicholas ... Wray, Naomi R. (2013). Genetic relationship between five psychiatric disorders estimated from genome-wide SNPs. Nature Genetics, 45 (9), 984-995. doi: 10.1038/ng.2711
Deutsch, Arielle R., Slutske, Wendy S., Richmond-Rakerd, Leah S., Chernyavskiy, Pavel, Heath, Andrew C. and Martin, Nicholas G. (2013). Causal influence of age at first drink on alcohol involvement in adulthood and its moderation by familial context. Journal of Studies On Alcohol and Drugs, 74 (5), 703-713. doi: 10.15288/jsad.2013.74.703
Munn-Chernoff, Melissa A., Duncan, Alexis E., Grant, Julia D., Wade, Tracey D., Agrawal, Arpana, Bucholz, Kathleen K., Madden, Pamela A. F., Martin, Nicholas G. and Heath, Andrew C. (2013). A twin study of alcohol dependence, binge eating, and compensatory behaviors. Journal of Studies On Alcohol and Drugs, 74 (5), 664-673. doi: 10.15288/jsad.2013.74.664
Fernández-Rhodes, Lindsay, Demerath, Ellen W., Cousminer, Diana L., Tao, Ran, Dreyfus, Jill G., Esko, Tõnu, Smith, Albert V., Gudnason, Vilmundur, Harris, Tamara B., Launer, Lenore, McArdle, Patrick F., Yerges-Armstrong, Laura M., Elks, Cathy E., Strachan, David P., Kutalik, Zoltán, Vollenweider, Peter, Feenstra, Bjarke, Boyd, Heather A., Metspalu, Andres, Mihailov, Evelin, Broer, Linda, Zillikens, M. Carola, Oostra, Ben, van Duijn, Cornelia M., Lunetta, Kathryn L., Perry, John R. B., Murray, Anna, Koller, Daniel L., Lai, Dongbing ... Franceschini, Nora (2013). Association of adiposity genetic variants with menarche timing in 92,105 women of European descent. American Journal of Epidemiology, 178 (3), 451-460. doi: 10.1093/aje/kws473
Rentería, Miguel E., Coolen, Marcel W., Statham, Aaron L., Choi, R. Seong Min, Qu, Wenjia, Campbell, Megan J., Smith, Sara, Henders, Anjali K., Montgomery, Grant W., Clark, Susan J., Martin, Nicholas G. and Medland, Sarah E. (2013). GWAS of DNA methylation variation within imprinting control regions suggests parent-of-origin association. Twin Research and Human Genetics, 16 (4), 767-781. doi: 10.1017/thg.2013.30
Bønnelykke, Klaus, Matheson, Melanie C., Pers, Tune H., Granell, Raquel, Strachan, David P., Alves, Alexessander Couto, Linneberg, Allan, Curtin, John A., Warrington, Nicole M., Standl, Marie, Kerkhof, Marjan, Jonsdottir, Ingileif, Bukvic, Blazenka K., Kaakinen, Marika, Sleimann, Patrick, Thorleifsson, Gudmar, Thorsteinsdottir, Unnur, Schramm, Katharina, Baltic, Svetlana, Kreiner-Møller, Eskil, Simpson, Angela, St Pourcain, Beate, Coin, Lachlan, Hui, Jennie, Walters, Eugene H., Tiesler, Carla M. T., Duffy, David L., Jones, Graham, Ring, Susan M. ... Brown, Matthew A. (2013). Meta-analysis of genome-wide association studies identifies ten loci influencing allergic sensitization. Nature Genetics, 45 (8), 902-906. doi: 10.1038/ng.2694
Verweij, K. J. H., Agrawal, A., Nat, N. O., Creemers, H. E., Huizink, A. C., Martin, N. G. and Lynskey, M. T. (2013). A genetic perspective on the proposed inclusion of cannabis withdrawal in DSM-5. Psychological Medicine, 43 (8), 1713-1722. doi: 10.1017/S0033291712002735
Brant, Angela M., Munakata, Yuko, Boomsma, Dorret I., DeFries, John C., Haworth, Claire M. A., Keller, Matthew C., Martin, Nicholas G., McGue, Matthew, Petrill, Stephen A., Plomin, Robert, Wadsworth, Sally J., Wright, Margaret J. and Hewitt, John K. (2013). The nature and nurture of high IQ: an extended sensitive period for intellectual development. Psychological Science, 24 (8), 1487-1495. doi: 10.1177/0956797612473119
Heilmann, S., Nyholt, D. R., Brockschmidt, F. F., Hillmer, A. M., Herold, C., Becker, T., Martin, N. G. and Noethen, M. M. (2013). No genetic support for a contribution of prostaglandins to the aetiology of androgenetic alopecia. British Journal of Dermatology, 169 (1), 222-224. doi: 10.1111/bjd.12292
Fall, Tove, Hägg, Sara, Maegi, Reedik, Ploner, Alexander, Fischer, Krista, Horikoshi, Momoko, Sarin, Antti-Pekka, Thorleifsson, Gudmar, Ladenvall, Claes, Kals, Mart, Kuningas, Maris, Draisma, Harmen H. M., Ried, Janina S., van Zuydam, Natalie R., Huikari, Ville, Mangino, Massimo, Sonestedt, Emily, Benyamin, Beben, Nelson, Christopher P., Rivera, Natalia V., Kristiansson, Kati, Shen, Huei-yi, Havulinna, Aki S., Dehghan, Abbas, Donnelly, Louise A., Kaakinen, Marika, Nuotio, Marja-Liisa, Robertson, Neil, de Bruijn, Renee F. A. G. ... Prokopenko, Inga (2013). The role of adiposity in cardiometabolic traits: a Mendelian randomization analysis. PLoS Medicine, 10 (6) e1001474, e1001474.1-e1001474.15. doi: 10.1371/journal.pmed.1001474
Haefors, Jenni, Loukola, Anu, Pitkaeemi, Janne, Broms, Ulla, Maennistoe, Satu, Salomaa, Veikko, Helioevaara, Markku, Lehtimaeki, Terho, Raitakari, Olli, Madden, Pamela A. F., Heath, Andrew C., Montgomery, Grant W., Martin, Nicholas G., Korhonen, Tellervo and Kaprio, Jaakko (2013). Scrutiny of the CHRNA5-CHRNA3-CHRNB4 smoking behavior locus reveals a novel association with alcohol use in a Finnish population based study. International Journal of Molecular Epidemiology and Genetics, 4 (2), 109-119.
Sim X., Jensen R.A., Ikram M.K., Cotch M.F., Li X., MacGregor S., Xie J., Smith A.V., Boerwinkle E., Mitchell P., Klein R., Klein B.E.K., Glazer N.L., Lumley T., McKnight B., Psaty B.M., de Jong P.T.V.M., Hofman A., Rivadeneira F., Uitterlinden A.G., van Duijn C.M., Aspelund T., Eiriksdottir G., Harris T.B., Jonasson F., Launer L.J., Attia J., Baird P.N., Harrap S. ... Wong T.Y. (2013). Genetic Loci for Retinal Arteriolar Microcirculation. PLoS ONE, 8 (6) e65804, e65804.1-e65804.12. doi: 10.1371/journal.pone.0065804
Rietveld, Cornelius A., Medland, Sarah E., Derringer, Jaime, Yang, Jian, Esko, Tonu, Martin, Nicolas W., Westra, Harm-Jan, Shakhbazov, Konstantin, Abdellaoui, Abdel, Agrawal, Arpana, Albrecht, Eva, Alizadeh, Behrooz Z., Amin, Najaf, Bamard, John, Baumeister, Sebastian E., Benke, Kelly S., Bielak, Lawrence F., Boatman, Jeffrey A., Boyle, Patricia A., Davies, Gail, De Leeuw, Christiaan, Eklund, Niina, Evans, Daniel S., Ferhmann, Rudolf, Fischer, Krista, Gieger, Christian, Gjessing, Hakon K., Haegg, Sara, Harris, Jennifer R. ... Koellinger, Philipp D. (2013). GWAS of 126,559 individuals identifies genetic variants associated with educational attainment. Science, 340 (6139), 1467-1471. doi: 10.1126/science.1235488
Byrne, E. M., Carrillo-Roa, T., Henders, A. K., Bowdler, L., McRae, A. F., Heath, A. C., Martin, N. G., Montgomery, G. W., Krause, L. and Wray, N. R. (2013). Monozygotic twins affected with major depressive disorder have greater variance in methylation than their unaffected co-twin. Translational Psychiatry, 3 (6) e269, e269.1-e269.6. doi: 10.1038/tp.2013.45
Randall, Joshua C., Winkler, Thomas W., Kutalik, Zoltan, Berndt, Sonja I., Jackson, Anne U., Monda, Keri L., Kilpelaeinen, Tuomas O., Esko, Tonu, Maegi, Reedik, Li, Shengxu, Workalemahu, Tsegaselassie, Feitosa, Mary F., Croteau-Chonka, Damien C., Day, Felix R., Fall, Tove, Ferreira, Teresa, Gustafsson, Stefan, Locke, Adam E., Mathieson, Iain, Scherag, Andre, Vedantam, Sailaja, Wood, Andrew R., Liang, Liming, Steinthorsdottir, Valgerdur, Thorleifsson, Gudmar, Dermitzakis, Emmanouil T., Dimas, Antigone S., Karpe, Fredrik, Min, Josine L. ... MAGIC Investigators (2013). Sex-stratified Genome-wide Association Studies Including 270,000 Individuals Show Sexual Dimorphism in Genetic Loci for Anthropometric Traits. Plos Genetics, 9 (6) e1003500, e1003500.1-e1003500.19. doi: 10.1371/journal.pgen.1003500
den Hoed, Marcel, Eijgelsheim, Mark, Esko, Tonu, Brundel, Bianca J. J. M., Peal, David S., Evans, David M., Nolte, Ilja M., Segre, Ayellet V., Holm, Hilma, Handsaker, Robert E., Westra, Harm-Jan, Johnson, Toby, Isaacs, Aaron, Yang, Jian, Lundby, Alicia, Zhao, Jing Hua, Kim, Young Jin, Go, Min Jin, Almgren, Peter, Bochud, Murielle, Boucher, Gabrielle, Cornelis, Marilyn C., Gudbjartsson, Daniel, Hadley, David, van der Harst, Pim, Hayward, Caroline, den Heijer, Martin, Igl, Wilmar, Jackson, Anne U. ... Loos, Ruth J. F. (2013). Identification of heart rate-associated loci and their effects on cardiac conduction and rhythm disorders. Nature Genetics, 45 (6), 621-634. doi: 10.1038/ng.2610
Richmond-Rakerd, Leah S., Slutske, Wendy S., Heath, Andrew C. and Martin, Nicholas G. (2013). Effects of sibship size and composition on younger brothers' and sisters' alcohol use initiation: findings from an Australian twin sample. Alcoholism-Clinical and Experimental Research, 37 (6), 1016-1024. doi: 10.1111/acer.12052
Schermer, Julie Aitken, Martin, Rod A., Martin, Nicholas G., Lynskey, Michael and Vernon, Philip A. (2013). The general factor of personality and humor styles. Personality and Individual Differences, 54 (8), 890-893. doi: 10.1016/j.paid.2012.12.026
Heilmann, Stefanie, Kiefer, Amy K., Fricker, Nadine, Drichel, Dmitriy, Hillmer, Axel M., Herold, Christine, Tung, Joyce Y., Eriksson, Nicholas, Redler, Silke, Betz, Regina C., Li, Rui, Karason, Ari, Nyholt, Dale R., Song, Kijoung, Vermeulen, Sita H., Kanoni, Stavroula, Dedoussis, George, Martin, Nicholas G., Kiemeney, Lambertus A., Mooser, Vincent, Stefansson, Kari, Richards, J. Brent, Becker, Tim, Brockschmidt, Felix F., Hinds, David A. and Noethen, Markus M. (2013). Androgenetic alopecia: identification of four genetic risk loci and evidence for the contribution of WNT signaling to its etiology. Journal of Investigative Dermatology, 133 (6), 1489-1496. doi: 10.1038/jid.2013.43
Byrne, Enda M., Gehrman, Philip R., Medland, Sarah E., Nyholt, Dale R., Heath, Andrew C., Madden, Pamela A. F., Hickie, Ian B., Van Duijn, Cornelia M., Henders, Anjali K., Montgomery, Grant W., Martin, Nicholas G., Wray, Naomi R. and The Chronogen Consortium (2013). A genome-wide association study of sleep habits and insomnia. American Journal of Medical Genetics Part B: Neuropsychiatric Genetics, 162 (5), 439-451. doi: 10.1002/ajmg.b.32168
Evans, David M., Zhu, Gu, Dy, Veronica, Heath, Andrew C., Madden, Pamela A. F., Kemp, John P., McMahon, George, St Pourcain, Beate, Timpson, Nicholas J., Golding, Jean, Lawlor, Debbie A., Steer, Colin, Montgomery, Grant W., Martin, Nicholas G, Smith, George Davey and Whitfield, John B. (2013). Genome-wide association study identifies loci affecting blood copper, selenium and zinc.. Human Molecular Genetics, 22 (19), 3998-4006. doi: 10.1093/hmg/ddt239
Molenaar, Dylan, van der Sluis, Sophie, Boomsma, Dorret I., Haworth, Claire M. A., Hewitt, John K., Martin, Nicholas G., Plomin, Robert, Wright, Margaret J. and Dolan, Conor V. (2013). Genotype by environment interactions in cognitive ability: a survey of 14 studies from four countries covering four age groups. Behavior Genetics, 43 (3), 208-219. doi: 10.1007/s10519-012-9581-7
Powell, Joseph E., Henders, Anjali K., McRae, Allan F., Kim, Jinhee, Hemani, Gibran, Martin, Nicholas G., Dermitzakis, Emmanouil T., Gibson, Greg, Montgomery, Grant W. and Visscher, Peter M. (2013). Congruence of additive and non-additive effects on gene expression estimated from pedigree and SNP data. PLoS Genetics, 9 (5) e1003502, e1003502.1-e1003502.10. doi: 10.1371/journal.pgen.1003502
Lind, Penelope A., Zhu, Gu, Montgomery, Grant W., Madden, Pamela A. F., Heath, Andrew C., Martin, Nicholas G. and Slutske, Wendy S. (2013). Genome-wide association study of a quantitative disordered gambling trait. Addiction Biology, 18 (3), 511-522. doi: 10.1111/j.1369-1600.2012.00463.x
McRae, Allan F., Wright, Margaret J., Hansell, Narelle K., Montgomery, Grant W. and Martin, Nicholas G. (2013). No association between general cognitive ability and rare copy number variation. Behavior Genetics, 43 (3), 202-207. doi: 10.1007/s10519-013-9587-9
Berndt, Sonja I., Gustafsson, Stefan, Maegi, Reedik, Ganna, Andrea, Wheeler, Eleanor, Feitosa, Mary F., Justice, Anne E., Monda, Keri L., Croteau-Chonka, Damien C., Day, Felix R., Esko, Tonu, Fall, Tove, Ferreira, Teresa, Gentilini, Davide, Jackson, Anne U., Luan, Jian'an, Randall, Joshua C., Vedantam, Sailaja, Willer, Cristen J., Winkler, Thomas W., Wood, Andrew R., Workalemahu, Tsegaselassie, Hu, Yi-Juan, Lee, Sang Hong, Liang, Liming, Lin, Dan-Yu, Min, Josine L., Neale, Benjamin M., Thorleifsson, Gudmar ... Ingelsson, Erik (2013). Genome-wide meta-analysis identifies 11 new loci for anthropometric traits and provides insights into genetic architecture. Nature Genetics, 45 (5), 501-U69. doi: 10.1038/ng.2606
Ellingson, Jarrod M., Slutske, Wendy S., Richmond-Rakerd, Leah S. and Martin, Nicholas G. (2013). Investigating the influence of prenatal androgen exposure and sibling effects on alcohol use and alcohol use disorder in females from opposite-sex twin pairs. Alcoholism-Clinical and Experimental Research, 37 (5), 868-876. doi: 10.1111/acer.12035
Keating, Brendan, Bansal, Aruna T., Walsh, Susan, Millman, Jonathan, Newman, Jonathan, Kidd, Kenneth, Budowle, Bruce, Eisenberg, Arthur, Donfack, Joseph, Gasparini, Paolo, Budimlija, Zoran, Henders, Anjali K., Chandrupatla, Hareesh, Duffy, David L., Gordon, Scott D., Hysi, Pirro, Liu, Fan, Medland, Sarah E., Rubin, Laurence, Martin, Nicholas G., Spector, Timothy D. and Kayser, Manfred (2013). First all-in-one diagnostic tool for DNA intelligence: genome-wide inference of biogeographic ancestry, appearance, relatedness, and sex with the Identitas v1 Forensic Chip. International Journal of Legal Medicine, 127 (3), 559-572. doi: 10.1007/s00414-012-0788-1
Verweij, K. J. H., Yang, J., Lahti, J., Veijola, J., Hintsanen, M., Pulkki-Raback, L., Heinonen, K., Pouta, A., Pesonen, A. -K., Widen, E., Taanila, A., Isohanni, M., Miettunen, J., Palotie, A., Penke, L., Service, S. K., Heath, A. C., Montgomery, G. W., Raitakari, O., Kaehoenen, M., Viikari, J., Raeikkoenen, K., Eriksson, J. G., Keltikangas-Jaervinen, L., Lehtimaeki, T., Martin, N. G., Jaervelin, M. -R., Visscher, P. M., Keller, M. C. and Zietsch, B. P. (2013). Correction: Maintenance of variation in human personality: testing evolutionary models by estimating heritability due to common causal variants and investigating the effect of distant inbreeding (vol 66, pg 3238, 2012). Evolution, 67 (5), 1537-1537. doi: 10.1111/evo.12095
Keller, Matthew C., Garver-Apgar, Christine E., Wright, Margaret J., Martin, Nicholas G., Corley, Robin P., Stallings, Michael C., Hewitt, John K. and Zietsch, Brendan P. (2013). The genetic correlation between height and IQ: shared genes or assortative mating?. PLoS Genetics, 9 (4) e1003451, e1003451.1-e1003451.10. doi: 10.1371/journal.pgen.1003451
Whitfield, John B., Heath, Andrew C., Madden, Pamela A. F., Pergadia, Michele L., Montgomery, Grant W. and Martin, Nicholas G. (2013). Metabolic and biochemical effects of low-to-moderate alcohol consumption. Alcoholism: Clinical and Experimental Research, 37 (4), 575-586. doi: 10.1111/acer.12015
Major Depressive Disorder Working Group of the Psychiatric GWAS Consortium, Wray, Naomi, Byrne, Enda M., Martin, Nicholas G., Gordon, Scott D., Henders, Anjali K., Montgomery, Grant M., Nyholt, Dale R. and Middeldorp, Christel M. (2013). A mega-analysis of genome-wide association studies for major depressive disorder. Molecular Psychiatry, 18 (4), 497-511. doi: 10.1038/mp.2012.21
Loehlin, John C. and Martin, Nicholas G. (2013). General and supplementary factors of personality in genetic and environmental correlation matrices. Personality and Individual Differences, 54 (6), 761-766. doi: 10.1016/j.paid.2012.12.014
Zubanov, N., Webbink, H. D. and Martin, N. G. (2013). The effect of schooling on problem drinking: evidence from Australian twins. Applied Economics, 45 (12), 1583-1599. doi: 10.1080/00036846.2011.631897
Slutske, Wendy S., Ellingson, Jarrod M., Richmond-Rakerd, Leah S., Zhu, Gu and Martin, Nicholas G. (2013). Shared genetic vulnerability for disordered gambling and alcohol use disorder in men and women: evidence from a national community-based Australian twin study. Twin Research and Human Genetics, 16 (2), 525-534. doi: 10.1017/thg.2013.11
Jahanshad, Neda, Rajagopalan, Priya, Hua, Xue, Hibar, Derrek P., Nir, Talia M., Toga, Arthur W., Jack, Jr, Clifford R., Saykin, Andrew J., Green, Robert C., Weiner, Michael W., Medland, Sarah E., Montgomery, Grant W., Hansell, Narelle K., McMahon, Katie L., de Zubicaray, Greig I., Martin, Nicholas G., Wright, Margaret J., Thompson, Paul M. and The Alzheimer’s Disease Neuroimaging Initiative (2013). Genome-wide scan of healthy human connectome discovers SPON1 gene variant influencing dementia severity. Proceedings of the National Academy of Sciences of the United States of America, 110 (12), 4768-4773. doi: 10.1073/pnas.1216206110
Ramasamy, Adaikalavan, Kuokkanen, Mikko, Vedantam, Sailaja, Gajdos, Zofia K., Alves, Alexessander Couto, Lyon, Helen N., Ferreira, Manuel A. R., Strachan, David P., Zhao, Jing Hua, Abramson, Michael J., Brown, Matthew A., Coin, Lachlan, Dharmage, Shyamali C., Duffy, David L., Haahtela, Tari, Heath, Andrew C., Janson, Christer, Kähönen, Mika, Khaw, Kay-Tee, Laitinen, Jaana, Souef, Peter Le, Lehtimäki, Terho, Madden, Pamela A. F., Marks, Guy B., Martin, Nicholas G., Matheson, Melanie C., Palmer, Cameron D., Palotie, Aarno, Pouta, Anneli ... Hirschhorn, Joel N. (2013). Correction: Genome-wide association studies of asthma in population-based cohorts confirm known and suggested loci and identify an additional association near HLA (PLoS ONE). PLoS ONE, 8 (3), 1-1. doi: 10.1371/annotation/9630862b-4676-4b82-9869-8d8fbb2a2e65
Nelson, Elliot C., Lynskey, Michael T., Heath, Andrew C., Wray, Naomi, Agrawal, Arpana, Shand, Fiona L., Henders, Anjali K., Wallace, Leanne, Todorov, Alexandre A., Schrage, Andrew J., Saccone, Nancy L., Madden, Pamela A. F., Degenhardt, Louisa, Martin, Nicholas G. and Montgomery, Grant W. (2013). ANKK1, TTC12, and NCAM1 polymorphisms and heroin dependence: importance of considering drug exposure. JAMA Psychiatry, 70 (3), 325-333. doi: 10.1001/jamapsychiatry.2013.282
Panagopoulos, Vassilis N., Trull, Timothy J., Glowinski, Anne L., Lynskey, Michael T., Heath, Andrew C., Agrawal, Arpana, Henders, Anjali K., Wallace, Leanne, Todorov, Alexandre A., Madden, Pamela A. F., Moore, Elizabeth, Degenhardt, Louisa, Martin, Nicholas G., Montgomery, Grant W. and Nelson, Elliot C. (2013). Examining the association of NRXN3 SNPs with borderline personality disorder phenotypes in heroin dependent cases and socio-economically disadvantaged controls. Drug and Alcohol Dependence, 128 (3), 187-193. doi: 10.1016/j.drugalcdep.2012.11.011
Agrawal, Arpana, Madden, Pamela A. F., Martin, Nicholas G. and Lynskey, Michael T. (2013). Do early experiences with cannabis vary in cigarette smokers?. Drug and Alcohol Dependence, 128 (3), 255-259. doi: 10.1016/j.drugalcdep.2012.09.002
Lu, Yi, Vitart, Veronique, Burdon, Kathryn P., Khor, Chiea Chuen, Bykhovskaya, Yelena, Mirshahi, Alireza, Hewitt, Alex W., Koehn, Demelza, Hysi, Pirro G., Ramdas, Wishal D., Zeller, Tanja, Vithana, Eranga N., Cornes, Belinda K., Tay, Wan-Ting, Tai, E. Shyong, Cheng, Ching-Yu, Liu, Jianjun, Foo, Jia-Nee, Saw, Seang Mei, Thorleifsson, Gudmar, Stefansson, Kari, Dimasi, David P., Mills, Richard A., Mountain, Jenny, Ang, Wei, Hoehn, Rene, Verhoeven, Virginie J. M., Grus, Franz, Wolfs, Roger ... Wong, Tien Y. (2013). Genome-wide association analyses identify multiple loci associated with central corneal thickness and keratoconus. Nature Genetics, 45 (2), 155-163. doi: 10.1038/ng.2506
Wade, Tracey D., Hansell, Narelle K., Crosby, Ross D., Bryant-Waugh, Rachel, Treasure, Janet, Nixon, Reginald, Byrne, Susan and Martin, Nicholas G. (2013). A study of changes in genetic and environmental influences on weight and shape concern across adolescence. Journal of Abnormal Psychology, 122 (1), 119-130. doi: 10.1037/a0030290
Koettgen, Anna, Albrecht, Eva, Teumer, Alexander, Vitart, Veronique, Krumsiek, Jan, Hundertmark, Claudia, Pistis, Giorgio, Ruggiero, Daniela, O'Seaghdha, Conall M., Haller, Toomas, Yang, Qiong, Tanaka, Toshiko, Johnson, Andrew D., Kutalik, Zoltan, Smith, Albert V., Shi, Julia, Struchalin, Maksim, Middelberg, Rita P. S., Brown, Morris J., Gaffo, Angelo L., Pirastu, Nicola, Li, Guo, Hayward, Caroline, Zemunik, Tatijana, Huffman, Jennifer, Yengo, Loic, Zhao, Jing Hua, Demirkan, Ayse, Feitosa, Mary F. ... Gieger, Christian (2013). Genome-wide association analyses identify 18 new loci associated with serum urate concentrations. Nature Genetics, 45 (2), 145-154. doi: 10.1038/ng.2500
Webbink, Dinand, Koning, Pierre, Vujić, Sunčica and Martin, Nicholas G. (2013). Why are criminals less educated than non-criminals? Evidence from a cohort of young Australian twins. Journal of Law Economics & Organization, 29 (1), 115-144. doi: 10.1093/jleo/ews014
Slutske, Wendy S., Cho, Seung Bin, Piasecki, Thomas M. and Martin, Nicholas G. (2013). Genetic overlap between personality and risk for disordered gambling: evidence from a national community-based Australian twin study. Journal of Abnormal Psychology, 122 (1), 250-255. doi: 10.1037/a0029999
Martin, Nicolas, Lafortune, Marjolaine, Godbout, Jonathan, Barakat, Marc, Robillard, Rebecca, Poirier, Gaetan, Bastien, Celyne and Carrier, Julie (2013). Topography of age-related changes in sleep spindles. Neurobiology of Aging, 34 (2), 468-476. doi: 10.1016/j.neurobiolaging.2012.05.020
Codd, Veryan, Nelson, Christopher P., Albrecht, Eva, Mangino, Massimo, Deelen, Joris, Buxton, Jessica L., Hottenga, Jouke Jan, Fischer, Krista, Esko, Tonu, Surakka, Ida, Broer, Linda, Nyholt, Dale R., Leach, Irene Mateo, Salo, Perttu, Hagg, Sara, Matthews, Mary K., Palmen, Jutta, Norata, Giuseppe D., O'Reilly, Paul F., Saleheen, Danish, Amin, Najaf, Balmforth, Anthony J., Beekman, Marian, de Boer, Rudolf A., Bohringer, Stefan, Braund, Peter S., Burton, Paul R., de Craen, Anton J. M., Denniff, Matthew ... Samani, Nilesh J. (2013). Identification of seven loci affecting mean telomere length and their association with disease. Nature Genetics, 45 (4), 422-427. doi: 10.1038/ng.2528
Anttila, Verneri, Winsvold, Bendik S., Gormley, Padhraig, Kurth, tobias, Bettella, Francesco, McMahon, george, Kallela, mikko, Malik, Rainer, De Vries, Boukje, Terwindt, Gisela, Medland, Sarah E., Todt, Unda, McArdle, Wendy L., Quaye, Lydia, Koiranen, Markku, Ikram, M. Arfan, Lehtimaki, Terho, Stam, Anine H., Ligthart, Lannie, Wedenoja, Juho, Dunham, Ian, Neale, Benjamin M., Palta, Priit, Hamalainen, Eija, Schurks, Markus, Rose, Lynda M., Buring, Julie E., Ridker, Paul M., Steinberg, Stacy ... Palotie, Aarno (2013). Genome-wide meta-analysis identifies new susceptibility loci for migraine. Nature Genetics, 45 (8), 912-917. doi: 10.1038/ng.2676
Broer, Linda, Codd, Veryan, Nyholt, Dale R., Deelen, Joris, Mangino, Massimo, Willemsen, Gonneke, Albrecht, Eva, Amin, Najaf, Beekman, Marian, de Geus, Eco J. C., Henders, Anjali, Nelson, Christopher P., Steves, Claire J., Wright, Margie J., de Craen, Anton J. M., Isaacs, Aaron, Matthews, Mary, Moayyeri, Alireza, Montgomery, Grant W., Oostra, Ben A., Vink, Jacqueline M., Spector, Tim D., Slagboom, P. Eline, Martin, Nicholas G., Samani, Nilesh J., van Duijn, Cornelia M. and Boomsma, Dorret I. (2013). Meta-analysis of telomere length in 19 713 subjects reveals high heritability, stronger maternal inheritance and a paternal age effect. European Journal of Human Genetics, 21 (10), 1163-1168. doi: 10.1038/ejhg.2012.303
Gillespie, Nathan A., Henders, Anjali K., Davenport, Tracy A., Hermens, Daniel F., Wright, Margie J., Martin, Nicholas G. and Hickie, Ian B. (2013). The Brisbane Longitudinal Twin Study: pathways to cannabis use, abuse, and dependence project - current status, preliminary results, and future directions. Twin Research and Human Genetics, 16 (1), 21-33. doi: 10.1017/thg.2012.111
Evans, David M., Brion, Marie Jo A., Paternoster, Lavinia, Kemp, John P., McMahon, George, Munafo, Marcus, Whitfield, John B., Medland, Sarah E., Montgomery, Grant W., The GIANT consortium, The CRP consortium, The TAG Consortium, Timpson, Nicholas J., St. Pourcain, Beate, Lawlor, Debbie A., Martin, Nicholas G., Dehghan, Abbas, Hirschhorn, Joel and Davey Smith, George (2013). Mining the Human Phenome Using Allelic Scores That Index Biological Intermediates. PLoS Genetics, 9 (10) e1003919, e1003919.1-e1003919.15. doi: 10.1371/journal.pgen.1003919
Goldinger, Anita, Henders, Anjali K., McRae, Allan F., Martin, Nicholas G., Gibson, Greg, Montgomery, Grant W., Visscher, Peter M. and Powell, Joseph E. (2013). Genetic and nongenetic variation revealed for the principal components of human gene expression. Genetics, 195 (3), 1117-1128. doi: 10.1534/genetics.113.153221
Garcia-Closas M., Couch F.J., Lindstrom S., Michailidou K., Schmidt M.K., Brook M.N., Orr N., Rhie S.K., Riboli E., Feigelson H.S., Le Marchand L., Buring J.E., Eccles D., Miron P., Fasching P.A., Brauch H., Chang-Claude J., Carpenter J., Godwin A.K., Nevanlinna H., Giles G.G., Cox A., Hopper J.L., Bolla M.K., Wang Q., Dennis J., Dicks E., Howat W.J., Schoof N. ... Kraft P. (2013). Genome-wide association studies identify four ER negative-specific breast cancer risk loci. Nature Genetics, 45 (4), 392-398. doi: 10.1038/ng.2561
Iles M.M., Law M.H., Stacey S.N., Han J., Fang S., Pfeiffer R., Harland M., MacGregor S., Taylor J.C., Aben K.K., Akslen L.A., Avril M.-F., Azizi E., Bakker B., Benediktsdottir K.R., Bergman W., Scarra G.B., Brown K.M., Calista D., Chaudru V., Fargnoli M.C., Cust A.E., Demenais F., De Waal A.C., Debniak T., Elder D.E., Friedman E., Galan P., Ghiorzo P. ... Barrett J.H. (2013). A variant in FTO shows association with melanoma risk not due to BMI. Nature Genetics, 45 (4), 428-432. doi: 10.1038/ng.2571
Amin, Najaf, Hottenga, Jouke-Jan, Hansell, Narelle K., Janssens, A. Cecile J. W., de Moor, Marleen H. M., Madden, Pamela A. F., Zorkoltseva, Irina V., Penninx, Brenda W., Terracciano, Antonio, Uda, Manuela, Tanaka, Toshiko, Esko, Tonu, Realo, Anu, Ferrucci, Luigi, Luciano, Michelle, Davies, Gail, Metspalu, Andres, Abecasis, Goncalo R., Deary, Ian J., Raikkonen, Katri, Bierut, Laura J., Costa, Paul T., Saviouk, Viatcheslav, Zhu, Gu, Kirichenko, Anatoly V., Isaacs, Aaron, Aulchenko, Yurii S., Willemsen, Gonneke, Heath, Andrew C. ... van Duijn, Cornelia M. (2013). Refining genome-wide linkage intervals using a meta-analysis of genome-wide association studies identifies loci influencing personality dimensions. European Journal of Human Genetics, 21 (8), 876-882. doi: 10.1038/ejhg.2012.263
Luciano, M., Evans, D. M., Hansell, N. K., Medland, S. E., Montgomery, G. W., Martin, N. G., Wright, M. J. and Bates, T. C. (2013). A genome-wide association study for reading and language abilities in two population cohorts. Genes, Brain and Behavior, 12 (6), 645-652. doi: 10.1111/gbb.12053
Ebejer, Jane L., Duffy, David L., van der Werf, Julius, Wright, Margaret J., Montgomery, Grant, Gillespie, Nathan A., Hickie, Ian B., Martin, Nicholas G. and Medland, Sarah E. (2013). Genome-wide association study of inattention and hyperactivity-impulsivity measured as quantitative traits. Twin Research and Human Genetics, 16 (2), 560-574. doi: 10.1017/thg.2013.12
Hibar, Derrek P., Stein, Jason L., Ryles, April B., Kohannim, Omid, Jahanshad, Neda, Medland, Sarah E., Hansell, Narelle K., McMahon, Katie L., de Zubicaray, Greig I., Montgomery, Grant W., Martin, Nicholas G., Wright, Margaret J., Saykin, Andrew J., Jack, lifford R., Weiner, Michael W., Toga, Arthur W. and Thompson, Paul M. (2013). Genome-wide association identifies genetic variants associated with lentiform nucleus volume in N = 1345 young and elderly subjects. Brain Imaging and Behavior, 7 (2), 102-115. doi: 10.1007/s11682-012-9199-7
Jahanshad, Neda, Kochunov, Peter V., Sprooten, Emma, Mandl, René C., Nichols, Thomas E., Almassy, Laura, Blangero, John, Brouwer, Rachel M., Curran, Joanne E., de Zubicaray, Greig I., Duggirala, Ravi, Fox, Peter T., Hong, L. Elliot, Landman, Bennett A., Martin, Nicholas G., McMahon, Katie L., Medland, Sarah E., Mitchell, Braxton D., Olvera, Rene L., Peterson, Charles P., Starr, John M., Sussmann, Jessika E., Toga, Arthur W., Wardlaw, Joanna M., Wright, Margaret J., Hulshoff Pol, Hilleke E., Bastind, Mark E., McIntosh, Andrew M., Deary, Ian J. ... Glahn, David C. (2013). Multi-site genetic analysis of diffusion images and voxelwise heritability analysis: a pilot project of the ENIGMA–DTI working group. NeuroImage, 81, 455-469. doi: 10.1016/j.neuroimage.2013.04.061
Porter, J. B., Elalfy, M. S., Taher, A. T., Aydinok, Y., Chan, L. L., Lee, S. H., Sutcharitchan, P., Habr, D., Martin, N. and El-Beshlawy, A. (2013). Efficacy and safety of deferasirox at low and high iron burdens: results from the EPIC magnetic resonance imaging substudy. Annals of Hematology, 92 (2), 211-219. doi: 10.1007/s00277-012-1588-x
Siddiq, Afshan, Couch, Fergus J., Chen, Gary K., Lindstrom, Sara, Eccles, Diana, Millikan, Robert C., Michailidou, Kyriaki, Stram, Daniel O., Beckmann, Lars, Rhie, Suhn Kyong, Ambrosone, Christine B., Aittomaki, Kristiina, Amiano, Pilar, Apicella, Carmel, Baglietto, Laura, Bandera, Elisa V., Beckmann, Matthias W., Berg, Christine D., Bernstein, Leslie, Blomqvist, Carl, Brauch, Hiltrud, Brinton, Louise, Bui, Quang M., Buring, Julie E., Buys, Saundra S., Campa, Daniele, Carpenter, Jane E., Chasman, Daniel I., Chang-Claude, Jenny ... Vachon, Celine M. (2012). A meta-analysis of genome-wide association studies of breast cancer identifies two novel susceptibility loci at 6q14 and 20q11. Human Molecular Genetics, 21 (24), 5373-5384. doi: 10.1093/hmg/dds381
Harari, Oscar, Wang, Jen-Chyong, Bucholz, Kathleen, Edenberg, Howard J., Heath, Andrew, Martin, Nicholas G., Pergadia, Michele L., Montgomery, Grant, Schrage, Andrew, Bierut, Laura J., Madden, Pamela F. and Goate, Alison M. (2012). Pathway analysis of smoking quantity in multiple GWAS identifies cholinergic and sensory pathways. Plos One, 7 (12) e50913, e50913. doi: 10.1371/journal.pone.0050913
van der Harst, Pim, Zhang, Weihua, Leach, Irene Mateo, Rendon, Augusto, Verweij, Niek, Sehmi, Joban, Paul, Dirk S., Elling, Ulrich, Allayee, Hooman, Li, Xinzhong, Radhakrishnan, Aparna, Tan, Sian-Tsung, Voss, Katrin, Weichenberger, Christian X., Albers, Cornelis A., Al-Hussani, Abtehale, Asselbergs, Folkert W., Ciullo, Marina, Danjou, Fabrice, Dina, Christian, Esko, Tonu, Evans, David M., Franke, Lude, Goegele, Martin, Hartiala, Jaana, Hersch, Micha, Holm, Hilma, Hottenga, Jouke-Jan, Kanoni, Stavroula ... Chambers, John C. (2012). Seventy-five genetic loci influencing the human red blood cell. Nature, 492 (7429), 369-375. doi: 10.1038/nature11677
Gillespie, Nathan A., Gehrman, Philip, Byrne, Enda M., Kendler, Kenneth S., Heath, Andrew C. and Martin, Nicholas G. (2012). Modeling the direction of causation between cross-sectional measures of disrupted sleep, anxiety and depression in a sample of male and female Australian twins. Journal of Sleep Research, 21 (6), 675-683. doi: 10.1111/j.1365-2869.2012.01026.x
Lind, Penelope A., Macgregor, Stuart, Heath, Andrew C., Madden, Pamela A. F., Montgomery, Grant W., Martin, Nicholas G. and Whitfield, John B. (2012). Association between in vivo alcohol metabolism and genetic variation in pathways that metabolize the carbon skeleton of ethanol and NADH reoxidation in the Alcohol Challenge Twin Study. Alcoholism: Clinical and Experimental Research, 36 (12), 2074-2085. doi: 10.1111/j.1530-0277.2012.01829.x
Schermerhorn, Alice C., D'Onofrio, Brian M., Slutske, Wendy S., Emery, Robert E., Turkheimer, Eric, Harden, K. Paige, Heath, Andrew C. and Martin, Nicholas G. (2012). Offspring ADHD as a risk factor for parental marital problems: controls for genetic and environmental confounds. Twin Research and Human Genetics, 15 (6), 700-713. doi: 10.1017/thg.2012.55
Li, Ming, Wang, Yi, Zheng, Xue-bin, Ikeda, Masashi, Iwata, Nakao, Luo, Xiong-jian, Chong, Siow-Ann, Lee, Jimmy, Rietschel, Marcella, Zhang, Fengyu, Mueller-Myhsok, Bertram, Cichon, Sven, Weinberger, Daniel R., Mattheisen, Manuel, Schulze, Thomas G., Martin, Nicholas G., Mitchell, Philip B., Schofield, Peter R., Liu, Jian-jun and Su, Bing (2012). Meta-analysis and brain imaging data support the involvement of VRK2 (rs2312147) in schizophrenia susceptibility. Schizophrenia Research, 142 (1-3), 200-205. doi: 10.1016/j.schres.2012.10.008
Martin, Nick (2012). Liberal neutrality and charitable purposes. Political Studies, 60 (4), 936-952. doi: 10.1111/j.1467-9248.2011.00942.x
Nyholt, Dale R., Low, Siew-Kee, Anderson, Carl A., Painter, Jodie N., Uno, Satoko, Morris, Andrew P., MacGregor, Stuart, Gordon, Scott D., Henders, Anjali K., Martin, Nicholas G., Attia, John, Holliday, Elizabeth G., McEvoy, Mark, Scott, Rodney J., Kennedy, Stephen H., Treloar, Susan A., Missmer, Stacey A., Adachi, Sosuke, Tanaka, Kenichi, Nakamura, Yusuke, Zondervan, Krina T., Zembutsu, Hitoshi and Montgomery, Grant W. (2012). Genome-wide association meta-analysis identifies new endometriosis risk loci. Nature Genetics, 44 (12), 1355-1359. doi: 10.1038/ng.2445
Zhang, K., Rao, F., Miramontes-Gonzalez, J. P., Hightower, C. M., Vaught, B., Chen, Y., Greenwood, T. A., Schork, A. J., Wang, L., Mahata, M., Stridsberg, M., Khandrika, S., Biswas, N., Fung, M. M., Waalen, J., Middelberg, R. P., Heath, A. C., Montgomery, G. W., Martin, N. G., Whitfield, J. B., Baker, D. G., Schork, N. J., Nievergelt, C. M. and O'Connor, D. T. (2012). Neuropeptide Y (NPY): Genetic Variation in the Human Promoter Alters Glucocorticoid Signaling, Yielding Increased NPY Secretion and Stress Responses (vol 60, pg 1678, 2012). Journal of the American College of Cardiology, 60 (21), 2261-2261. doi: 10.1016/j.jacc.2012.10.002
Asselbergs, Folkert W., Guo, Yiran, van Iperen, Erik P. A., Sivapalaratnam, Suthesh, Tragante, Vinicius, Lanktree, Matthew B., Lange, Leslie A., Almoguera, Berta, Appelman, Yolande E., Barnard, John, Baumert, Jens, Beitelshees, Amber L., Bhangale, Tushar R., Chen, Yii-Der Ida, Gaunt, Tom R., Gong, Yan, Hopewell, Jemma C., Johnson, Toby, Kleber, Marcus E., Langaee, Taimour Y., Li, Mingyao, Li, Yun R., Liu, Kiang, McDonough, Caitrin W., Meijs, Matthijs El., Middelberg, Rita P. S., Musunuru, Kiran, Nelson, Christopher P., O'Connell, Jeffery R. ... Drenos, Fotios (2012). Large-scale gene-centric meta-analysis across 32 studies identifies multiple lipid loci. American Journal of Human Genetics, 91 (5), 823-838. doi: 10.1016/j.ajhg.2012.08.032
Boraska, Vesna, Jeroncic, Ana, Colonna, Vincenza, Southam, Lorraine, Nyholt, Dale R., Rayner, Nigel William, Perry, John R. B., Toniolo, Daniela, Albrecht, Eva, Ang, Wei, Bandinelli, Stefania, Barbalic, Maja, Barroso, Ines, Beckmann, Jacques S., Biffar, Reiner, Boomsma, Dorret, Campbell, Harry, Corre, Tanguy, Erdmann, Jeanette, Esko, Tonu, Fischer, Krista, Franceschini, Nora, Frayling, Timothy M., Girotto, Giorgia, Gonzalez, Juan R., Harris, Tamara B., Heath, Andrew C., Heid, Iris M., Hoffmann, Wolfgang ... Zeggini, Eleftheria (2012). Genome-wide meta-analysis of common variant differences between men and women. Human Molecular Genetics, 21 (21) dds304, 4805-4815. doi: 10.1093/hmg/dds304
Agrawal, A., Verweij, K. J. H., Gillespie, N. A., Heath, A. C., Lessov-Schlaggar, C. N., Martin, N. G., Nelson, E. C., Slutske, W. S., Whitfield, J. B. and Lynskey, M. T. (2012). The genetics of addiction - a translational perspective. Translational Psychiatry, 2 e140. doi: 10.1038/tp.2012.54
Lee, P. H., Perlis, R. H., Jung, J-Y, Byrne, E. M., Rueckert, E., Siburian, R., Haddad, S., Mayerfeld, C. E., Heath, A. C., Pergadia, M. L., Madden, P. A. F., Boomsma, D. I., Penninx, B. W., Sklar, P., Martin, N. G., Wray, N. R., Purcell, S. M. and Smoller, J. W. (2012). Multi-locus genome-wide association analysis supports the role of glutamatergic synaptic transmission in the etiology of major depressive disorder. Translational Psychiatry, 2 (11) e184, e184.1-e184.9. doi: 10.1038/tp.2012.95
Bergin, Jocilyn E., Neale, Michael C., Eaves, Lindon J., Martin, Nicholas G., Heath, Andrew C. and Maes, Hermine H. (2012). Genetic and environmental transmission of body mass index fluctuation. Behavior Genetics, 42 (6), 867-874. doi: 10.1007/s10519-012-9567-5
McCutcheon, V. V., Grant, J. D., Heath, A. C., Bucholz, K. K., Sartor, C. E., Nelson, E. C., Madden, P. A. F. and Martin, N. G. (2012). Environmental influences predominate in remission from alcohol use disorder in young adult twins. Psychological Medicine, 42 (11), 2421-2431. doi: 10.1017/S003329171200044X
Agrawal, A., Verweij, K. J. H., Gillespie, N. A., Heath, A. C., Lessov-Schlaggar, C. N., Martin, N. G., Nelson, E. C., Slutske, W. S., Whitfield, J. B. and Lynskey, M. T. (2012). Erratum: The genetics of addiction - a translational perspective (Translational Psychiatry (2012) 2 (e140) DOI: 10.1038/tp.2012.54). Translational Psychiatry, 2 (11) e193, e193-e193. doi: 10.1038/tp.2012.129
Zhang, Kuixing, Rao, Fangwen, Miramontes-Gonzalez, Jose Pablo, Hightower, C. Makena, Vaught, Brian, Chen, Yuhong, Greenwood, Tiffany A., Schork, Andrew J., Wang, Lei, Mahata, Manjula, Stridsberg, Mats, Khandrika, Srikrishna, Biswas, Nilima, Fung, Maple M., Waalen, Jill, Middelberg, Rita P., Heath, Andrew C., Montgomery, Grant W., Martin, Nicholas G., Whitfield, John B., Baker, Dewleen G., Schork, Nicholas J., Nievergelt, Caroline M. and O'Connor, Daniel T. (2012). Neuropeptide Y (NPY): genetic variation in the human promoter alters glucocorticoid signaling, yielding increased NPY secretion and stress responses. Journal of the American College of Cardiology, 60 (17), 1678-1689. doi: 10.1016/j.jacc.2012.06.042
Ebejer, Jane L., Medland, Sarah E., van der Werf, Julius, Gondro, Cedric, Henders, Anjali K., Lynskey, Michael, Martin, Nicholas G. and Duffy, David L. (2012). Attention deficit hyperactivity disorder in Australian adults: prevalence, persistence, conduct problems and disadvantage. Plos One, 7 (10) e47404, e47404. doi: 10.1371/journal.pone.0047404
Eggert, Stacey L., Huyck, Karen L., Somasundaram, Priya, Kavalla, Raghava, Stewart, Elizabeth A., Lu, Ake T., Painter, Jodie N., Montgomery, Grant W., Medland, Sarah E., Nyholt, Dale R., Treloar, Susan A., Zondervan, Krina T., Heath, Andrew C., Madden, Pamela A. F., Rose, Lynda, Buring, Julie E., Ridker, Paul M., Chasman, Daniel I., Martin, Nicholas G., Cantor, Rita M. and Morton, Cynthia C. (2012). Genome-wide linkage and association analyses implicate FASN in predisposition to uterine leiomyomata. American Journal of Human Genetics, 91 (4), 621-628. doi: 10.1016/j.ajhg.2012.08.009
Tielbeek, Jorim J., Medland, Sarah E., Benyamin, Beben, Byrne, Enda M., Heath, Andrew C., Madden, Pamela A. F., Martin, Nicholas G., Wray, Naomi R. and Verweij, Karin J. H. (2012). Unraveling the genetic etiology of adult antisocial behavior: a genome-wide association study. PLoS One, 7 (10) e45086, e1005378-e1005378. doi: 10.1371/journal.pone.0045086
Verweij, Karin J. H., Yang, Jian, Lahti, Jari, Veijola, Juha, Hintsanen, Mirka, Pulkki-Raback, Laura, Heinonen, Kati, Pouta, Anneli, Pesonen, Anu-Katriina, Widen, Elisabeth, Taanila, Anja, Isohanni, Matti, Miettunen, Jouko, Palotie, Aarno, Penke, Lars, Service, Susan K., Heath, Andrew C., Montgomery, Grant W., Raitakari, Olli, Kahonen, Mika, Viikari, Jorma, Raikkonen, Katri, Eriksson, Johan G., Keltikangas-Jarvinen, Liisa, Lehtimaki, Terho, Martin, Nicholas G., Jarvelin, Marjo-Riitta, Visscher, Peter M., Keller, Matthew C. and Zietsch, Brendan P. (2012). Maintenance of genetic variation in human personality: testing evolutionary models by estimating heritability due to common causal variants and investigating the effect of distant inbreeding. Evolution, 66 (10), 3238-3251. doi: 10.1111/j.1558-5646.2012.01679.x
Surakka, Ida, Whitfield, John B., Perola, Markus, Visscher, Peter M., Montgomery, Grant W., Falchi, Mario, Willemsen, Gonneke, de Geus, Eco J. C., Magnusson, Patrik K. E., Christensen, Kaare, Sorensen, Thorild I. A., Pietilainen, Kirsi H., Rantanen, Taina, Silander, Kaisa, Widen, Elisabeth, Muilu, Juhu, Rahman, Iffat, Liljedahl, Ulrika, Syvanen, Ann-Christine, Palotie, Aarno, Kaprio, Jaakko, Kyvik, Kirsten O., Pedersen, Nancy L., Boomsma, Dorret I., Spector, Tim, Martin, Nicolas G., Ripatti, Samuli and Peltonen, Leena (2012). A genome-wide association study of monozygotic twin-pairs suggests a locus related to variability of serum high-density lipoprotein cholesterol. Twin Research and Human Genetics, 15 (6), 691-699. doi: 10.1017/thg.2012.63
Mishra, Aniket, Yazar, Seyhan, Hewitt, Alex W., Mountain, Jenny A., Ang, Wei, Pennell, Craig E., Martin, Nicholas G., Montgomery, Grant W., Hammond, Christopher J., Young, Terri L., Macgregor, Stuart and Mackey, David A. (2012). Genetic variants near PDGFRA are associated with corneal curvature in Australians. Investigative Ophthalmology and Visual Science, 53 (11), 7131-7136. doi: 10.1167/iovs.12-10489
Baughman, H. M., Giammarco, E. A., Veselka, Livia, Schermer, Julie A., Martin, Nicholas G., Lynskey, Michael and Vernon, Phillip A. (2012). A behavioral genetic study of humor styles in an Australian sample. win Research and Human Genetics, 15 (5), 663-667. doi: 10.1017/thg.2012.23
Sanfilippo, Paul G., Hammond, Christopher J., Staffieri, Sandra E., Kearns, Lisa S., Liew, S. H. Melissa, Barbour, Julie M., Hewitt, Alex W., Ge, Dongliang, Snieder, Harold, MacKinnon, Jane R., Brown, Shayne A., Lorenz, Birgit, Spector, Tim D., Martin, Nicholas G., Wilmer, Jeremy B. and Mackeymo, David A. (2012). Heritability of strabismus: genetic influence is specific to eso-deviation and independent of refractive error. Twin Research and Human Genetics, 15 (5), 624-630. doi: 10.1017/thg.2012.22
Lynskey, Michael T., Agrawal, Arpana, Henders, Anjali, Nelson, Elliot C., Madden, Pamela A. F. and Martin, Nicholas G. (2012). An Australian twin study of cannabis and other illicit drug use and misuse, and other psychopathology. Twin Research and Human Genetics, 15 (5), 631-641. doi: 10.1017/thg.2012.41
Yang, Jian, Loos, Ruth J., Powell, Joseph E., Medland, Sarah E, Speliotes, Elizabeth K., Chasman, Daniel I., Rose, Lynda M., Thorleifsson, Gudmar, Steinthorsdottir, Valgerdur, Magi, Reedik, Waite, Lindsay, Vernon Smith, Albert, Yerges-Armstrong, Laura M., Monda, Keri L., Hadley, David, Mahajan, Anubha, Li, Guo, Kapur, Karen, Vitart, Veronique, Huffman, Jennifer E., Wang, Sophie R., Palmer, Cameron, Esko, To˜nu, Fischer, Krista, Hua Zhao, Jing, Demirkan, Ayse, Isaacs, Aaron, Feitosa, Mary F., Luan, Jian’an ... Visscher, Peter (2012). FTO genotype is associated with phenotypic variability of body mass index. Nature, 490 (7419), 267-272. doi: 10.1038/nature11401
Liu, Fan, van der Lijn, Fedde, Schurmann, Claudia, Zhu, Gu, Chakravarty, M. Mallar, Hysi, Pirro G., Wollstein, Andreas, Lao, Oscar, de Bruijne, Marleen, Ikram, M. Arfan, van der Lugt, Aad, Rivadeneira, Fernando, Uitterlinden, Andre G., Hofman, Albert, Niessen, Wiro J., Homuth, Georg, de Zubicaray, Greig, McMahon, Katie L., Thompson, Paul M., Daboul, Amro, Puls, Ralf, Hegenscheid, Katrin, Bevan, Liisa, Pausova, Zdenka, Medland, Sarah E., Montgomery, Grant W., Wright, Margaret J., Wicking, Carol A., Boehringer, Stefan ... Kayser, Manfred for the International Visible Trait Genetics (VisiGen) Consortium (2012). A Genome-Wide Association Study Identifies Five Loci Influencing Facial Morphology in Europeans. PLoS Genetics, 8 (9) e1002932, e1002932.1-e1002932.13. doi: 10.1371/journal.pgen.1002932
Ramasamy, Adaikalavan, Kuokkanen, Mikko, Vedantam, Sailaja, Gajdos, Zofia K., Alves, Alexessander Couto, Lyon, Helen N., Ferreira, Manuel A. R., Strachan, David P., Zhao, Jing Hua, Abramson, Michael J., Brown, Matthew A., Coin, Lachlan, Dharmage, Shyamali C., Duffy, David L., Haahtela, Tari, Heath, Andrew C., Janson, Christer, Kahonen, Mika, Khaw, Kay-Tee, Laitinen, Jaana, Le Souef, Peter, Lehtimaki, Terho, Madden, Pamela A. F., Marks, Guy B., Martin, Nicholas G., Matheson, Melanie C., Palmer, Cameron D., Palotie, Aarno, Pouta, Anneli ... Hirschhorn, Joel N. (2012). Genome-Wide Association Studies of Asthma in Population-Based Cohorts Confirm Known and Suggested Loci and Identify an Additional Association near HLA. PLoS One, 7 (9 Article No. e44008) e44008, e44008-1-e44008-10. doi: 10.1371/journal.pone.0044008
Braskie, Meredith N., Jahanshad, Neda, Toga, Arthur W., McMahon, Katie L, de Zubicaray, Greig I., Martin, Nicholas G., Wright, Margaret J. and Thompson, Paul M. (2012). How a common variant in the growth factor receptor gene, NTRK1, affects white matter. BioArchitecture, 2 (5), 1-4. doi: 10.4161/bioa.22190
Mosing, Miriam A., Mellanby, Jane, Martin, Nicholas G. and Wright, Margaret J. (2012). Genetic and environmental influences on analogical and categorical verbal and spatial reasoning in 12-year old twins. Behavior Genetics, 42 (5), 722-731. doi: 10.1007/s10519-012-9540-3
Luciano, Michelle, Huffman, Jennifer E., Arias-Vasquez, Alejandro, Vinkhuyzen, Anna A. E., Middeldorp, Christel M., Giegling, Ina, Payton, Antony, Davies, Gail, Zgaga, Lina, Janzing, Joost, Ke, Xiayi, Galesloot, Tessel, Hartmann, Annette M., Ollier, William, Tenesa, Albert, Hayward, Caroline, Verhagen, Maaike, Montgomery, Grant W., Hottenga, Jouke-Jan, Konte, Bettina, Starr, John M., Vitart, Veronique, Vos, Pieter E., Madden, Pamela A. F., Willemsen, Gonneke, Konnerth, Heike, Horan, Michael A., Porteous, David J., Campbell, Harry ... Deary, Ian J. (2012). Genome-wide association uncovers shared genetic effects among personality traits and mood states. American Journal of Medical Genetics Part B: Neuropsychiatric Genetics, 159B (6), 684-695. doi: 10.1002/ajmg.b.32072
Macare, Christine, Bates, Timothy C., Heath, Andrew C., Martin, Nicholas G. and Ettinger, Ulrich (2012). Substantial genetic overlap between schizotypy and neuroticism: a twin study. Behavior Genetics, 42 (5), 732-742. doi: 10.1007/s10519-012-9558-6
van Dongen, Jenny, Slagboom, P. Eline, Draisma, Harmen H. M., Martin, Nicholas G. and Boomsma, Dorret I. (2012). The continuing value of twin studies in the omics era. Nature Reviews Genetics, 13 (9), 640-653. doi: 10.1038/nrg3243
Martin, Nicholas G. (2012). Commentary: discussion of 'The history of twins, as a criterion of the relative powers of nature And nurture' by Francis Galton (1875). International Journal of Epidemiology, 41 (4) dys110, 917-919. doi: 10.1093/ije/dys110
Lafortune, Marjolaine, Gagnon, Jean-Francois, Latreille, Veronique, Vandewalle, Gilles, Martin, Nicolas, Filipini, Daniel, Doyon, Julien and Carrier, Julie (2012). Reduced slow-wave rebound during daytime recovery sleep in middle-aged subjects. Plos One, 7 (8) e43224, e43224. doi: 10.1371/journal.pone.0043224
Hartz, Sarah M., Short, Susan E., Saccone, Nancy L., Culverhouse, Robert, Chen, LiShiun, Schwantes-An, Tae-Hwi, Coon, Hilary, Han, Younghun, Stephens, Sarah H., Sun, Juzhong, Chen, Xiangning, Ducci, Francesca, Dueker, Nicole, Franceschini, Nora, Frank, Josef, Geller, Frank, Guobjartsson, Daniel, Hansel, Nadia N., Jiang, Chenhui, Keskitalo-Vuokko, Kaisu, Liu, Zhen, Lyytikainen, Leo-Pekka, Michel, Martha, Rawal, Rajesh, Hum, Sc, Rosenberger, Albert, Scheet, Paul, Shaffer, John R., Teumer, Alexander ... Bierut, Laura J. (2012). Increased genetic vulnerability to smoking at CHRNA5 in early-onset smokers. Archives of General Psychiatry, 69 (8), 854-861. doi: 10.1001/archgenpsychiatry.2012.124
Kohannim, Omid, Hibar, Derrek P., Stein, Jason L., Jahanshad, Neda, Hua, Xue, Rajagopalan, Priya, Toga, Arthur W., Jack Jr., Clifford R., Weiner, Michael W., de Zubicaray, Greig I., McMahon, Katie L., Hansell, Narelle K., Martin, Nicholas G., Margaret J. Wright, Thompson, Paul M. and The Alzheimer’s Disease Neuroimaging Initiative (2012). Discovery and replication of gene influences on brain structure using LASSO regression. Frontiers in Neuroscience, 6 (AUG) Article 115, 115.1-115.13. doi: 10.3389/fnins.2012.00115
Webbink, Dinand, Vujić, Sunčica, Koning, Pierre and Martin, Nicholas G. (2012). The effect of childhood conduct disorder on human capital. Health Economics, 21 (8), 928-945. doi: 10.1002/hec.1767
Verweij, Karin J. H., Vinkhuyzen, Anna A. E., Benyamin, Beben, Lynskey, Michael T., Quaye, Lydia, Agrawal, Arpana, Gordon, Scott D., Montgomery, Grant W., Madden, Pamela A. F., Heath, Andrew C., Spector, Andrew C., Martin, Nicholas G. and Medland, Sarah E. (2012). The genetic aetiology of cannabis use initiation: a meta-analysis of genome-wide association studies and a SNP-based heritability estimation. Addiction Biology, 18 (5), 846-850. doi: 10.1111/j.1369-1600.2012.00478.x
Agrawal, Arpana, Nelson, Elliot C., Littlefield, Andrew K., Bucholz, Kathleen K., Degenhardt, Louisa, Henders, Anjali K., Madden, Pamela A. F., Martin, Nicholas G., Montgomery, Grant W., Pergadia, Michele L., Sher, Kenneth J., Heath, Andrew C. and Lynskey, Michael T. (2012). Cannabinoid receptor genotype moderation of the effects of childhood physical abuse on anhedonia and depression. Archives of General Psychiatry, 69 (7), 732-740. doi: 10.1001/archgenpsychiatry.2011.2273
McQuillan, Ruth, Eklund, Niina, Pirastu, Nicola, Kuningas, Maris, McEvoy, Brian P., Esko, Tonu, Corre, Tanguy, Davies, Gail, Kaakinen, Marika, Lyytikainen, Leo-Pekka, Kristiansson, Kati, Havulinna, Aki S., Gogele, Martin, Vitart, Veronique, Tenesa, Albert, Aulchenko, Yurii, Hayward, Caroline, Johansson, Asa, Boban, Mladen, Ulivi, Sheila, Robino, Antonietta, Boraska, Vesna, Igl, Wilmar, Wild, Sarah H., Zgaga, Lina, Amin, Najaf, Theodoratou, Evropi, Polasek, Ozren, Girotto, Giorgia ... Wilson, James F. (2012). Evidence of inbreeding depression on human height. Plos Genetics, 8 (7) e1002655, e1002655. doi: 10.1371/journal.pgen.1002655
Byrne, Enda M., Johnson, Julie, McRae, Allan F., Nyholt, Dale R., Medland, Sarah E., Gehrman, Philip R., Heath, Andrew C., Madden, Pamela A. F., Montgomery, Grant W., Chenevix-Trench, Georgia and Martin, Nicholas G. (2012). A genome-wide association study of caffeine-related sleep disturbance: confirmation of a role for a common variant in the adenosine receptor. Sleep, 35 (7), 967-975. doi: 10.5665/sleep.1962
Lee, Teresa, Mosing, Miriam A., Henry, Julie D., Trollor, Julian N., Ames, David, Martin, Nicholas G., Wright, Margaret J., Sachdev, Perminder S. and OATS Research Team (2012). Genetic influences on four measures of executive functions and their covariation with general cognitive ability: The Older Australian Twins Study. Behavior Genetics, 42 (4), 528-538. doi: 10.1007/s10519-012-9526-1
Bloom, A. Joseph, Harari, Oscar, Martinez, Maribel, Madden, Pamela A. F., Martin, Nicholas G., Montgomery, Grant W., Rice, John P., Murphy, Sharon E., Bierut, Laura J. and Goate, Alison (2012). Use of a predictive model derived from in vivo endophenotype measurements to demonstrate associations with a complex locus, CYP2A6. Human Molecular Genetics, 21 (13) dds114, 3050-3062. doi: 10.1093/hmg/dds114
Chiang, Ming-Chang, Barysheva, Marina, McMahon, Katie L., de Zubicaray, Greig I., Johnson, Kori, Montgomery, Grant W., Martin, Nicholas G., Toga, Arthur W., Wright, Margaret J., Shapshak, Paul and Thompson, Paul M. (2012). Gene network effects on brain microstructure and intellectual performance identified in 472 twins. Journal of Neuroscience, 32 (25), 8732-8745. doi: 10.1523/JNEUROSCI.5993-11.2012
Hibar, Derrek P., Jahanshad, Neda, Stein, Jason L., Kohannim, Omid, Toga, Arthur W., Medland, Sarah E., Hansell, Narelle K., McMahon, Katie L., de Zubicaray, Greig I., Montgomery, Grant W., Martin, Nicholas G., Wright, Margaret J. and Thompson, Paul M. (2012). Alzheimer's disease risk gene, GAB2, is associated with regional brain volume differences in 755 young healthy twins. Twin Research and Human Genetics, 15 (3), 286-295. doi: 10.1017/thg.2012.15
Li, Rui, Brockschmidt, Felix F., Kiefer, Amy K., Stefansson, Hreinn, Nyholt, Dale R., Song, Kijoung, Vermeulen, Sita H., Kanoni, Stavroula, Glass, Daniel, Medland, Sarah E., Dimitriou, Maria, Waterworth, Dawn, Tung, Joyce Y., Geller, Frank, Heilmann, Stefanie, Hillmer, Axel M., Bataille, Veronique, Eigelshoven, Sibylle, Hanneken, Sandra, Moebus, Susanne, Herold, Christine, den Heijer, Martin, Montgomery, Grant W., Deloukas, Panos, Eriksson, Nicholas, Heath, Andrew C., Becker, Tim, Sulem, Patrick, Mangino, Massimo ... Richards, J. Brent (2012). Six novel susceptibility loci for early-onset androgenetic alopecia and their unexpected association with common diseases. PLoS Genetics, 8 (5) e1002746, 222-224. doi: 10.1371/journal.pgen.1002746
Vinkhuyzen, A. A. E., Pedersen, N. L., Yang, J., Lee, S. H., Magnusson, P. K. E., Iacono, W. G., McGue, M., Madden, P. A. F., Heath, A. C., Luciano, M., Payton, A., Horan, M., Ollier, W., Pendleton, N., Deary, I. J., Montgomery, G. W., Martin, N. G., Visscher, P. M. and Wray, N. R. (2012). Common SNPs explain some of the variation in the personality dimensions of neuroticism and extraversion (vol 2, e125, 2012). Translational Psychiatry, 2 (5) e125, e125-e125. doi: 10.1038/tp.2012.49
Service, S. K., Verweij, K. J. H., Lahti, J., Congdon, E., Ekelund, J., Hintsanen, M., Raikkonen, K., Lehtimaki, T., Kahonen, M., Widen, E., Taanila, A., Veijola, J., Heath, A. C., Madden, P. A. F., Montgomery, G. W., Sabatti, C., Jarvelin, M-R, Palotie, A., Raitakari, O., Viikari, J., Martin, N. G., Eriksson, J. G., Keltikangas-Jarvinen, L., Wray, N. R. and Freimer, N. B. (2012). A genome-wide meta-analysis of association studies of Cloninger's Temperament Scales. Translational Psychiatry, 2 (5) e116, e116-e116. doi: 10.1038/tp.2012.37
Verweij, Karin J. H., Zietsch, Brendan P., Liu, Jimmy Z., Medland, Sarah E., Lynskey, Michael T., Madden, Pamela A. F., Agrawal, Arpana, Montgomery, Grant W., Heath, Andrew C. and Martin, Nicholas G. (2012). No association of candidate genes with cannabis use in a large sample of Australian twin families. Addiction Biology, 17 (3), 687-690. doi: 10.1111/j.1369-1600.2011.00320.x
Bis, Joshua C., DeCarli, Charles, Smith, Albert Vernon, van der Lijn, Fedde, Crivello, Fabrice, Fornage, Myriam, Debette, Stephanie, Shulman, Joshua M., Schmidt, Helena, Srikanth, Velandai, Schuur, Maaike, Yu, Lei, Choi, Seung-Hoan, Sigurdsson, Sigurdur, Verhaaren, Benjamin F. J., DeStefano, Anita L., Lambert, Jean-Charles, Jack, Clifford R., Struchalin, Maksim, Stankovich, Jim, Ibrahim-Verbaas, Carla A., Fleischman, Debta, Zijdenbos, Alex, den Heijer, Tom, Mazoyer, Bernard, Coker, Laura H., Enzinger, Christian, Danoy, Patrick, Amin, Najaf ... Cohorts Heart Aging Res Genomic Ep (2012). Common variants at 12q14 and 12q24 are associated with hippocampal volume. Nature Genetics, 44 (5), 545-551. doi: 10.1038/ng.2237
Braskie, Meredith N., Jahanshad, Neda, Stein, Jason L., Barysheva, Marina, Johnson, Kori, McMahon, Katie L., de Zubicaray, Greig I., Martin, Nicholas G., Wright, Margaret J., Ringman, John M., Toga, Arthur W. and Thompson, Paul M. (2012). Relationship of a variant in the NTRK1 gene to white matter microstructure in young adults. The Journal of Neuroscience, 32 (17), 5964-5972. doi: 10.1523/JNEUROSCI.5561-11.2012
Middelberg, Rita P. S., Heath, Andrew C., Madden, Pamela A. F., Montgomery, Grant W., Martin, Nicholas G. and Whitfield, John B. (2012). Evidence of differential allelic effects between adolescents and adults for plasma high-density lipoprotein. PLoS ONE, 7 (4) e35605, e35605. doi: 10.1371/journal.pone.0035605
Webb, Bradley T., Guo, An-Yuan, Maher, Brion S., Zhao, Zhongming, van den Oord, Edwin J., Kendler, Kenneth S., Riley, Brien P., Gillespie, Nathan A., Prescott, Carol A., Middeldorp, Christel M., Willemsen, Gonneke, de Geus, Eco J. C., Hottenga, Jouke-Jan, Boomsma, Dorret I., Slagboom, Eline P., Wray, Naomi R., Montgomery, Grant W., Martin, Nicholas G., Wright, Margie J., Heath, Andrew C., Madden, Pamela A., Gelernter, Joel, Knowles, James A., Hamilton, Steven P., Weissman, Myrna M., Fyer, Abby J., Huezo-Diaz, Patricia, McGuffin, Peter, Farmer, Anne ... Hettema, John M. (2012). Meta-analyses of genome-wide linkage scans of anxiety-related phenotypes. European Journal of Human Genetics, 20 (10), 1078-1084. doi: 10.1038/ejhg.2012.47
Jahanshad, Neda, Kohannim, Omid, Hibar, Derrek P., Stein, Jason L., McMahon, Katie L., de Zubicaray, Greig I., Medland, Sarah E., Montgomery, Grant W., Whitfield, John B., Martin, Nicholas G., Wright, Margaret J., Toga, Arthur W. and Thompson, Paul M. (2012). Brain structure in healthy adults is related to serum transferrin and the H63D polymorphism in the HFE gene. Proceedings of the National Academy of Sciences of USA, 109 (14), E851-E859. doi: 10.1073/pnas.1105543109
Powell, Joseph E., Henders, Anjali K., McRae, Allan F., Caracella, Anthony, Smith, Sara, Wright, Margaret J., Whitfield, John B., Dermitzakis, Emmanouil T., Martin, Nicholas G., Visscher, Peter M. and Montgomery, Grant W. (2012). The Brisbane systems genetics study: genetical genomics meets complex trait genetics. PLoS One, 7 (4) e35430, e35430.1-e35430.9. doi: 10.1371/journal.pone.0035430
Vinkhuyzen, A. A. E., Pedersen, N. L., Yang, J., Lee, S. H., Magnusson, P. K. E., Iacono, W. G., McGue, M., Madden, P. A. F., Heath, A. C., Luciano, M., Payton, A., Horan, M., Ollier, W., Pendleton, N., Deary, I. J., Montgomery, G. W., Martin, N. G., Visscher, P. M. and Wray, N. R. (2012). Common SNPs explain some of the variation in the personality dimensions of neuroticism and extraversion. Translational Psychiatry, 2 (e102) 201227, e102-e102. doi: 10.1038/tp.2012.27
Dennis, Emily L., Jahanshad, Neda, Rudie, Jeffrey D., Brown, Jesse A., Johnson, Kori, McMahon, Katie L., de Zubicaray, Greig I., Montgomery, Grant, Martin, Nicholas G., Wright, Margaret J., Bookheimer, Susan Y., Dapretto, Mirella, Toga, Arthur W. and Thompson, Paul M. (2012). Altered structural brain connectivity in healthy carriers of the autism risk gene, CNTNAP2. Brain Connectivity, 1 (6), 447-460. doi: 10.1089/brain.2011.0064
Yang, Jian, Ferreira, Teresa, Morris, Andrew P., Medland, Sarah E., Madden, Pamela A. F., Heath, Andrew C., Martin, Nicholas G., Montgomery, Grant W., Weedon, Michael N., Loos, Ruth J., Frayling, Timothy M., McCarthy, Mark I., Hirschhorn, Joel N., Goddard, Michael E., Visscher, Peter M., Genetic Invest ANthropometric Trai and DIAbet Genetics Replication Meta-A (2012). Conditional and joint multiple-SNP analysis of GWAS summary statistics identifies additional variants influencing complex traits. Nature Genetics, 44 (4), 369-375. doi: 10.1038/ng.2213
Lee, Teresa, Mosing, Miriam A., Henry, Julie D., Trollor, Julian N., Ames, David, Martin, Nicholas G., Wright, Margaret J. and Sachdev, Perminder S. (2012). Genetic Influences on Four Measures of Executive Functions and Their Covariation with General Cognitive Ability: The Older Australian Twins Study (vol 42, pg 528, 2012). Behavior Genetics, 42 (4), 539-540. doi: 10.1007/s10519-012-9536-z
Powell, Joseph E., Henders, Anjali K., McRae, Allan F., Wright, Margaret J., Martin, Nicholas G., Dermitzakis, Emmanouil T., Montgomery, Grant W. and Visscher, Peter M. (2012). Genetic control of gene expression in whole blood and lymphoblastoid cell lines is largely independent. Genome Research, 22 (3), 456-466. doi: 10.1101/gr.126540.111
Zietsch, B. P., Verweij, K. J. H., Heath, A. C., Madden, P. A. F., Martin, N. G., Nelson, E. C. and Lynskey, M. T. (2012). Do shared etiological factors contribute to the relationship between sexual orientation and depression?. Psychological Medicine, 42 (3), 521-532. doi: 10.1017/S0033291711001577
Luciano, Michelle, Lopez, Lorna M., de Moor, Marleen H. M., Harris, Sarah E., Davies, Gail, Nutile, Teresa, Krueger, Robert F., Esko, Tonu, Schlessinger, David, Toshiko, Tanaka, Derringer, Jaime L., Realo, Anu, Hansell, Narelle K., Pergadia, Michele L., Pesonen, Anu-Katriina, Sanna, Serena, Terracciano, Antonio, Madden, Pamela A. F., Penninx, Brenda, Spinhoven, Philip, Hartman, Catherina A., Oostra, Ben A., Janssens, A. Cecile J. W., Eriksson, Johan G., Starr, John M., Cannas, Alessandra, Ferrucci, Luigi, Metspalu, Andres, Wright, Margeret J. ... Deary, Ian J. (2012). Longevity candidate genes and their association with personality traits in the elderly. American Journal of Medical Genetics Part B: Neuropsychiatric Genetics, 159 B (2), 192-200. doi: 10.1002/ajmg.b.32013
Hatemi, Peter K., McDermott, Rose, Bailey, J. Michael and Martin, Nicholas G. (2012). The different effects of gender and sex on vote choice. Political Research Quarterly, 65 (1), 76-92. doi: 10.1177/1065912910391475
Sartor, Carolyn E., Grant, Julia D., Lynskey, Michael T., McCutcheon, Vivia V., Waldron, Mary, Statham, Dixie J., Bucholz, Kathleen K., Madden, Pamela A. F., Heath, Andrew C., Martin, Nicholas G. and Nelson, Elliot C. (2012). Common heritable contributions to low-risk trauma, high-risk trauma, posttraumatic stress disorder, and major depression. Archives of General Psychiatry, 69 (3), 293-299. doi: 10.1001/archgenpsychiatry.2011.1385
Duarte-Carvajalino, Julio M., Jahanshad, Neda, Lenglet, Christophe, McMahon, Katie L., de Zubicaray, Greig I., Martin, Nicholas G., Wright, Margaret J., Thompson, Paul M. and Sapiro, Guillermo (2012). Hierarchical topological network analysis of anatomical human brain connectivity and differences related to sex and kinship. NeuroImage, 59 (4), 3784-3804. doi: 10.1016/j.neuroimage.2011.10.096
Spain, Sarah L., Carvajal-Carmona, Luis G., Howarth, Kimberley M., Jones, Angela M., Su, Zhan, Cazier, Jean-Baptiste, Williams, Jennet, Aaltonen, Lauri A., Pharoah, Paul, Kerr, David J., Cheadle, Jeremy, Li, Li, Casey, Graham, Vodicka, Pavel, Sieber, Oliver, Lipton, Lara, Gibbs, Peter, Martin, Nicholas G., Montgomery, Grant W., Young, Joanne, Baird, Paul N., Morreau, Hans, van Wezel, Tom, Ruiz-Ponte, Clara, Fernandez-Rozadilla, Ceres, Carracedo, Angel, Castells, Antoni, Castellvi-Bel, Sergi, Dunlop, Malcolm ... Tomlinson, Ian P. M. (2012). Refinement of the associations between risk of colorectal cancer and polymorphisms on chromosomes 1q41 and 12q13.13. Human Molecular Genetics, 21 (4) ddr523, 934-946. doi: 10.1093/hmg/ddr523
Dubois, Lise, Kyvik, Kirsten Ohm, Girard, Manon, Tatone-Tokuda, Fabiola, Perusse, Daniel, Hjelmborg, Jacob, Skytthe, Axel, Rasmussen, Finn, Wright, Margaret J., Lichtenstein, Paul and Martin, Nicholas G. (2012). Genetic and environmental contributions to weight, height, and BMI from birth to 19 years of age: An international study of over 12,000 twin pairs. PLoS ONE, 7 (2) e30153, e30153. doi: 10.1371/journal.pone.0030153
Law, Matthew H., Montgomery, Grant W., Brown, Kevin M., Martin, Nicholas G., Mann, Graham J., Hayward, Nicholas K., MacGregor, Stuart and Q-MEGA and AMFS Investigators (2012). Meta-analysis combining new and existing data sets confirms that the TERT-CLPTM1L locus influences melanoma risk. Journal of Investigative Dermatology, 132 (2), 485-487. doi: 10.1038/jid.2011.322
Martin, Nicholas G., Li, Ka Wah, Murray, Heather, Putt, Wendy, Packard, Chris J. and Humphries, Steve E. (2012). The effects of a single nucleotide polymorphism in SLCO1B1 on the pharmacodynamics of pravastatin. British Journal of Clinical Pharmacology, 73 (2), 303-306. doi: 10.1111/j.1365-2125.2011.04090.x
Knaapila, Antti, Zhu, Gu, Medland, Sarah E., Wysocki, Charles J., Montgomery, Grant W., Martin, Nicholas G., Wright, Margaret J. and Reed, Danielle R. (2012). A genome-wide study on the perception of the odorants androstenone and galaxolide. Chemical Senses, 37 (6), 541-552. doi: 10.1093/chemse/bjs008
Middelberg, Rita P., Benyamin, Beben, de Moor, Marleen H. M., Warrington, Nicole M., Gordon, Scott, Henders, Anjali K., Medland, Sarah E., Nyholt, Dale R., de Geus, Eco J. C., Hottenga, Jouke J., Willemsen, Gonneke, Beilin, Lawrence J., Mori, Trevor A., Wright, Margaret J., Heath, Andrew C., Madden, Pamela A. F., Boomsma, Dorret I., Pennell, Craig E., Montgomery, Grant W., Martin, Nicholas G. and Whitfield, John B. (2012). Loci affecting gamma-glutamyl transferase in adults and adolescents show age x SNP interaction and cardiometabolic disease associations. Human Molecular Genetics, 21 (2) ddr478, 446-455. doi: 10.1093/hmg/ddr478
Mosing, Miriam A., Medland, Sarah E., McRae, Allan, Landers, Joseph George, Wright, Margaret J. and Martin, Nicholas G. (2012). Genetic influences on life span and its relationship to personality: A 16-year follow-up study of a sample of aging twins. Psychosomatic Medicine, 74 (1), 16-22. doi: 10.1097/PSY.0b013e3182385784
Dennis, Emily L., Jahanshad, Neda, McMahon, Katie L., de Zubicaray, Greig I., Martin, Nicholas G., Hickie, Ian B., Toga, Arthur W., Wright, Margaret J. and Thompson, Paul M. (2012). Development of brain structural connectivity between ages 12 and 30: a 4-tesla diffusion imaging study in 439 adolescents and adults. NeuroImage, 64 (1), 671-684. doi: 10.1016/j.neuroimage.2012.09.004
Rao, Fangwen, Chiron, Stephane, Wei, Zhiyun, Fung, Maple M., Chen, Yuqing, Wen, Gen, Khandrika, Srikrishna, Ziegler, Michael G., Benyamin, Beben, Montgomery, Grant, Whitfield, John B., Martin, Nicholas G., Waalen, Jill, Hamiltoni, Bruce A., Mahata, Sushil K. and O'Connor, Daniel T. (2012). Genetic variation within a metabolic motif in the chromogranin A promoter: Pleiotropic influence on cardiometabolic risk traits in twins. American Journal of Hypertension, 25 (1), 29-40. doi: 10.1038/ajh.2011.163
Lee, Teresa, Mosing, Miriam A., Henry, Julie D., Trollor, Julian N., Lammel, Andrea, Ames, David, Martin, Nicholas G., Wright, Margaret J. and Sachdev, Perminder S. (2012). Genetic influences on five measures of processing speed and their covariation with general cognitive ability in the elderly: The older Australian twins study. Behavior Genetics, 42 (1), 96-106. doi: 10.1007/s10519-011-9474-1
Miller, Geoffrey, Zhu, Gu, Wright, Margaret J., Hansell, Narelle K. and Martin, Nicholas G. (2012). The heritability and genetic correlates of mobile phone use: a twin study of consumer behavior. Twin Research and Human Genetics, 15 (1), 97-106. doi: 10.1375/twin.15.1.97
de Moor, M. H. M., Costa, P. T., Terracciano, A., Krueger, R. F., de Geus, E. J. C., Toshiko, T., Penninx, B. W. J. H., Esko, T., Madden, P. A. F., Derringer, J., Amin, N., Willemsen, G., Hottenga, J.-J., Distel, M. A., Uda, M., Sanna, S., Spinhoven, P., Hartman, C. A., Sullivan, P., Realo, A., Allik, J., Heath, A. C., Pergadia, M. L., Agrawal, A., Lin, P., Grucza, R., Nutile, T., Ciullo, M., Rujescu, D. ... Boomsma, D. I. (2012). Meta-analysis of genome-wide association studies for personality. Molecular Psychiatry, 17 (3), 337-349. doi: 10.1038/mp.2010.128
Hansell, N. K., Wright, M. J., Medland, S. E., Davenprot, T. A., Wray, N. R., Martin, N. G. and Hickie, I. B. (2012). Genetic co-morbidity between neuroticism, anxiety/depression and somatic distress in a population sample of adolescent and young adult twins. Psychological Medicine, 42 (6), 1249-1260. doi: 10.1017/S0033291711002431
Wray, N. R., Pergadia, M. L., Blackwood, D. H. R., Penninx, B. W. J. H., Gordon, S. D., Nyholt, D. R., Ripke, S., MacIntyre, D. J., McGhee, K. A., MacLean, A. W., Smit, J. H., Hottenga, J. J., Willemsen, G., Middeldorp, C. M., De Geus, E. J. C., Lewis, C. M., McGuffin, P., Hickie, I. B., Van Den Oord, E. J. C. G., Liu, J. Z., MacGregor, S., McEvoy, B. P., Byrne, E. M., Medland, S. E., Statham, D. J., Henders, A. K., Heath, A. C., Montgomery, G. W., Martin, N. G. ... Sullivan, P. F. (2012). Genome-wide association study of major depressive disorder: New results, meta-analysis, and lessons learned. Molecular Psychiatry, 17 (1), 36-48. doi: 10.1038/mp.2010.109
Kohannim, Omid, Jahanshad, Neda, Braskie, Meredith N., Stein, Jason L., Chiang, Ming-Chang, Reese. April H., Hibar, Derrek P., Toga, Arthur W., McMahon, Katie L., de Zubicaray, Greig I., Medland, Sarah E., Montgomery, Grant W., Martin, Nicholas G., Wright. Margaret J. and Thompson, Paul M. (2012). Predicting white matter integrity from multiple common genetic variants. Neuropsychopharmacology, 37 (9), 2012-2019. doi: 10.1038/npp.2012.49
Porter, John, Bowden, Donald K., Economou, Marina, Troncy, Jacques, Ganser, Arnold, Habr, Dany, Martin, Nicolas, Gater, Adam, Rofail, Diana, Abetz-Webb, Linda, Lau, Helen and Cappellini, Maria Domenica (2012). Health-related quality of life, treatment satisfaction, adherence and persistence in beta-thalassemia and myelodysplastic syndrome patients with iron overload receiving deferasirox: Results from the EPIC clinical trial. Anemia, 2012 297641, 1-10. doi: 10.1155/2012/297641
Loehlin, John C., Medland, Sarah E. and Martin, Nicholas G. (2012). Is CAG sequence length in the androgen receptor gene correlated with finger-length ratio?. Personality and Individual Differences, 52 (2), 224-227. doi: 10.1016/j.paid.2011.09.009
Stolk L., Perry J.R.B., Chasman D.I., He C., Mangino M., Sulem P., Barbalic M., Broer L., Byrne E.M., Ernst F., Esko T., Franceschini N., Gudbjartsson D.F., Hottenga J.-J., Kraft P., McArdle P.F., Porcu E., Shin S.-Y., Smith A.V., Van Wingerden S., Zhai G., Zhuang W.V., Albrecht E., Alizadeh B.Z., Aspelund T., Bandinelli S., Lauc L.B., Beckmann J.S., Boban M. ... Lunetta K.L. (2012). Meta-analyses identify 13 loci associated with age at menopause and highlight DNA repair and immune pathways. Nature Genetics, 44 (3), 260-268. doi: 10.1038/ng.1051
Amos, Christopher I., Wang, Li-E, Lee, Jeffrey E., Gershenwald, Jeffrey E., Chen, Wei V., Fang, Shenying, Kosoy, Roman, Zhang, Mingfeng, Qureshi, Abrar A., Vattathil, Selina, Schacherer, Christopher W., Gardner, Julie M., Wang, Yuling, Bishop, D. Tim, Barrett, Jennifer H., MacGregor, Stuart, Hayward, Nicholas K., Martin, Nicholas G., Duffy, David L., Mann, Graham J., Cust, Anne, Hopper, John, Brown, Kevin M., Grimm, Elizabeth A., Xu, Yaji, Han, Younghun, Jing, Kaiyan, McHugh, Caitlin, Laurie, Cathy C. ... Wei, Qingyi (2011). Genome-wide association study identifies novel loci predisposing to cutaneous melanoma. Human Molecular Genetics, 20 (24) ddr415, 5012-5023. doi: 10.1093/hmg/ddr415
Gieger, Christian, Radhakrishnan, Aparna, Cvejic, Ana, Tang, Weihong, Porcu, Eleonora, Pistis, Giorgio, Serbanovic-Canic, Jovana, Elling, Ulrich, Goodall, Alison H., Labrune, Yann, Lopez, Lorna M., Magi, Reedik, Meacham, Stuart, Okada, Yukinori, Pirastu, Nicola, Sorice, Rossella, Teumer, Alexander, Voss, Katrin, Zhang, Weihua, Ramirez-Solis, Ramiro, Bis, Joshua C., Ellinghaus, David, Gogele, Martin, Hottenga, Jouke-Jan, Langenberg, Claudia, Kovacs, Peter, O'Reilly, Paul F., Shin, So-Youn, Esko, Tonu ... Soranzo, Nicole (2011). New gene functions in megakaryopoiesis and platelet formation. Nature, 480 (7376), 201-208. doi: 10.1038/nature10659
Segal, Nancy L., Turkheimer, Eric, Gottesman, Irving I., Gatz, Margaret and Martin, Nicholas G. (2011). The value of twin studies: a response to Slate magazine. Twin Research and Human Genetics, 14 (6), 593-597. doi: 10.1375/twin.14.6.593
Yokoyama, Satoru, Woods, Susan L., Boyle, Glen M., Aoude, Lauren G., MacGregor, Stuart, Zismann, Victoria, Gartside, Michael, Cust, Anne E., Haq, Rizwan, Harland, Mark, Taylor, John C., Duffy, David L., Holohan, Kelly, Dutton-Regester, Ken, Palmer, Jane M., Bonazzi, Vanessa, Stark, Mitchell S., Symmons, Judith, Law, Matthew H., Schmidt, Christopher, Lanagan, Cathy, O'Connor, Linda, Holland, Elizabeth A., Schmid, Helen, Maskiell, Judith A., Jetann, Jodie, Ferguson, Megan, Jenkins, Mark A., Kefford, Richard F. ... Brown, Kevin M. (2011). A novel recurrent mutation in MITF predisposes to familial and sporadic melanoma. Nature, 480 (7375), 99-103. doi: 10.1038/nature10630
Benyamin, Beben, Middelberg, Rita P., Lind, Penelope A., Valle, Anne M., Gordon, Scott, Nyholt, Dale R., Medland, Sarah E., Henders, Anjali K., Heath, Andrew C., Madden, Pamela A. F., Visscher, Peter M., O'Connor, Daniel T., Montgomery, Grant W., Martin, Nicholas G. and Whitfield, John B. (2011). GWAS of butyrylcholinesterase activity identifies four novel loci, independent effects within BCHE and secondary associations with metabolic risk factors. Human Molecular Genetics, 20 (22) ddr375, 4504-4514. doi: 10.1093/hmg/ddr375
Loehlin, John C. and Martin, Nicholas G. (2011). What does a general factor of personality look like in unshared environmental variance?. Personality and Individual Differences, 51 (7), 862-865. doi: 10.1016/j.paid.2011.07.021
MacGregor, Stuart, Montgomery, Grant W., Liu, Jimmy Z., Zhao, Zhen Zhen, Henders, Anjali K., Stark, Mitchell, Schmid, Helen, Holland, Elizabeth A., Duffy, David L., Zhang, Mingfeng, Painter, Jodie N., Nyholt, Dale R., Maskiell, Judith A., Jetann, Jodie, Ferguson, Megan, Cust, Anne E., Jenkins, Mark A., Whiteman, David C., Olsson, Hakan, Puig, Susana, Bianchi-Scarra, Giovanna, Hansson, Johan, Demenais, Florence, Landi, Maria Teresa, Debniak, Tadeusz, Mackie, Rona, Azizi, Esther, Bressac-de Paillerets, Brigitte, Goldstein, Alisa M. ... Hayward, Nicholas K. (2011). Genome-wide association study identifies a new melanoma susceptibility locus at 1q21.3. Nature Genetics, 43 (11), 1114-1118. doi: 10.1038/ng.958
Terracciano, A., Esko, T., Sutin, A. R., de Moor, M. H. M., Meirelles, O., Zhu, G., Tanaka, T., Giegling, I., Nutile, T., Realo, A., Allik, J., Hansell, N. K., Wright, M. J., Montgomery, G. W., Willemsen, G., Hottenga, J-J, Friedl, M., Ruggiero, D., Sorice, R., Sanna, S., Cannas, A., Raikkonen, K., Widen, E., Palotie, A., Eriksson, J. G., Cucca, F., Krueger, R. F., Lahti, J., Luciano, M. ... Uda, M. (2011). Meta-analysis of genome-wide association studies identifies common variants in CTNNA2 associated with excitement-seeking. Translational Psychiatry, 1 (10) e49, e49-e49. doi: 10.1038/tp.2011.42
Coolen, Marcel W., Statham, Aaron L., Qu, Wenjia, Campbell, Megan J., Henders, Anjali K., Montgomery, Grant W., Martin, Nick G. and Clark, Susan J. (2011). Impact of the genome on the epigenome is manifested in DNA methylation patterns of imprinted regions in monozygotic and dizygotic twins. PLoS ONE, 6 (10) e25590, 1-12. doi: 10.1371/journal.pone.0025590
Kvaskoff, Marina, Whiteman, David C., Zhao, Zhen Z., Montgomery, Grant W., Martin, Nicholas G., Hayward, Nicholas K. and Duffy, David L. (2011). Polymorphisms in nevus-associated genes MTAP, PLA2G6, and IRF4 and the risk of invasive cutaneous melanoma. Twin Research and Human Genetics, 14 (5), 422-432. doi: 10.1375/twin.14.5.422
Sachdev, Perminder S., Lee, Teresa, Lammel, Andrea, Crawford, John, Trollor, Julian N., Wright, Margaret J., Brodaty, Henry, Ames, David, Martin, Nicholas G. and OATS Research Team (2011). Cognitive functioning in older twins: The older Australian twins study. Australasian Journal on Ageing, 30 (Supp. 2), 17-23. doi: 10.1111/j.1741-6612.2011.00534.x
Stevens, Kristen N., Vachon, Celine M., Lee, Adam M., Slager, Susan, Lesnick, Timothy, Olswold, Curtis, Fasching, Peter A., Miron, Penelope, Eccles, Diana, Carpenter, Jane E., Godwin, Andrew K., Ambrosone, Christine, Winqvist, Robert, Brauch, Hiltrud, Schmidt, Marjanka K., Cox, Angela, Cross, Simon S., Sawyer, Elinor, Hartmann, Arndt, Beckmann, Matthias W., Schulz-Wendtland, Ruediger, Ekici, Arif B., Tapper, William J., Gerty, Susan M., Durcan, Lorraine, Graham, Nikki, Hein, Rebecca, Nickels, Stephan, Flesch-Janys, Dieter ... Couch, Fergus J. (2011). Common breast cancer susceptibility loci are associated with triple-negative breast cancer. Cancer Research, 71 (19), 6240-6249. doi: 10.1158/0008-5472.CAN-11-1266
Surakka, Ida, Isaacs, Aaron, Karssen, Lennart C., Laurila, Pirkka-Pekka P., Middelberg, Rita P. S., Tikkanen, Emmi, Ried, Janina S., Lamina, Claudia, Mangino, Massimo, Igl, Wilmar, Hottenga, Jouke-Jan, Lagou, Vasiliki, van der Harst, Pim, Leach, Irene Mateo, Esko, Tonu, Kutalik, Zoltan, Wainwright, Nicholas W., Struchalin, Maksim V., Sarin, Antti-Pekka, Kangas, Antti J., Viikari, Jorma S., Perola, Markus, Rantanen, Taina, Petersen, Ann-Kristin, Soininen, Pasi, Johansson, Asa, Soranzo, Nicole, Heath, Andrew C., Papamarkou, Theodore ... Ripatti, Samuli (2011). A genome-wide screen for interactions reveals a new locus on 4p15 modifying the effect of waist-to-hip ratio on total cholesterol. PLoS Genetics, 7 (10) e1002333, e1002333. doi: 10.1371/journal.pgen.1002333
Luong, Hein T. T., Chaplin, Justin, McRae, Allan F., Medland, Sarah E., Willemsen, Gonneke, Nyholt, Dale R., Henders, Anjali K., Hoekstra, Chantal, Duffy, David L., Martin, Nicholas G., Boomsma, Dorret I., Montgomery, Grant W. and Painter, Jodie N. (2011). Variation in BMPR1B, TGFRB1 and BMPR2 and control of dizygotic twinning. Twin Research and Human Genetics, 14 (5), 408-416. doi: 10.1375/twin.14.5.408
Middelberg, Rita P. S., Ferreira, Manuel A. R., Henders, Anjali K., Heath, Andrew C., Madden, Pamela A. F., Montgomery, Grant W., Martin, Nicholas G. and Whitfield, John B. (2011). Genetic variants in LPL, OASL and TOMM40/APOE-C1-C2-C4 genes are associated with multiple cardiovascular-related traits. BMC Medical Genetics, 12 (123) 123, 1-9. doi: 10.1186/1471-2350-12-123
Heath, Andrew C., Whitfield, John B., Martin, Nicholas G., Pergadia, Michele L., Goate, Alison M., Lind, Penelope A., McEvoy, Brian P., Schrage, Andrew J., Grant, Julia D., Chou, Yi-Ling, Zhu, Rachel, Henders, Anjali K., Medland, Sarah E., Gordon, Scott D., Nelson, Elliot C., Agrawal, Arpana, Nyholt, Dale R., Bucholz, Kathleen K., Madden, Pamela A. F. and Montgomery, Grant W. (2011). A quantitative-trait genome-wide association study of alcoholism risk in the community: findings and implications. Biological Psychiatry, 70 (6), 513-518. doi: 10.1016/j.biopsych.2011.02.028
Kutalik, Zoltan, Benyamin, Beben, Bergmann, Sven, Mooser, Vincent, Waeber, Gerard, Montgomery, Grant W., Martin, Nicholas G., Madden, Pamela A. F., Heath, Andrew C., Beckmann, Jacques S., Vollenweider, Peter, Marques-Vidal, Pedro and Whitfield, John B. (2011). Genome-wide association study identifies two loci strongly affecting transferrin glycosylation. Human Molecular Genetics, 20 (18) ddr272, 3710-3717. doi: 10.1093/hmg/ddr272
Stein, J. L., Hibar, D. P., Madsen, S. K., Khamis, M, McMahon, K. L., de Zubicaray, G. I., Hansell, N. K., Montgomery, G. W., Martin, N. G., Wright, M. J., Saykin, A. J., Jack Jr, C. R., Weiner. M. W., Toga. A. W., Thompson, P. M. and The Alzheimer’s Disease Neuroimaging Initiative (2011). Discovery and replication of dopamine-related gene effects on caudate volume in young and elderly populations (N=1198) using genome-wide search. Molecular Psychiatry, 16 (9), 927-937. doi: 10.1038/mp.2011.32
Ferreira, Manuel A. R., Matheson, Melanie C., Duffy, David L., Marks, Guy B., Hui, Jennie, Le Souef, Peter, Danoy, Patrick, Baltic, Svetlana, Nyholt, Dale R., Jenkins, Mark, Hayden, Catherine, Willemsen, Gonneke, Ang, Wei, Kuokkanen, Mikko, Beilby, John, Cheah, Faang, de Geus, Eco J.C., Ramasamy, Adaikalavan, Vedantam, Sailaka, Salomaa, Veikko, Madden, Pamela A., Heath, Andrew C., Hopper, John L., Visscher, Peter M., Musk, Bill, Leeder, Stephen R., Jarvelin, Marjo-Riitta, Pennell, Craig, Boomsma, Dorret I. ... Wright, Margaret J. (2011). Identification of IL6R and chromosome 11q13.5 as risk loci for asthma. Lancet, 378 (9795), 1006-1014. doi: 10.1016/S0140-6736(11)60874-X
Stein, J. L., Hibar, D. P., Madsen, S. K., Khamis, M., McMahon, K. L., De Zubicaray, G. I., Hansell, N. K., Montgomery, G. W., Martin, N. G., Wright, M. J., Saykin, A. J., Jack, C. R., Weiner, M. W., Toga, A. W. and Thompson, P. M. (2011). Genome-wide association reveals dopamine-related genetic effects on caudate volume. Molecular Psychiatry, 16 (9), 881-881. doi: 10.1038/mp.2011.98
Amin, N., Byrne, E., Johnson, J., Chenevix-Trench, G., Walter, S., Nolte, I. M., kConFab Investigators, Vink, J.M., Rawal, R., Mangino, M., Teumer, A., Keers, J. C., Verwoert, G., Baumeister, S., Biffar, R., Petersmann, A., Dahmen, N., Doering, A., Isaacs, A., Broer, L., Wray, N. R., Montgomery, G. W., Levy, D., Psaty, B. M., Gudnason, V., Chakravarti, A., Sulem, P., Gudbjartsson, D. F., Kiemeney, L. A. ... van Duijn, C. M. (2011). Genome-wide association analysis of coffee drinking suggests association with CYP1A1/CYP1A2 and NRCAM. Molecular Psychiatry, 17 (11), 1116-1129. doi: 10.1038/mp.2011.101
Larsson, Mats, Duffy, David L., Zhu, Gu, Liu, Jimmy Z., Macgregor, Stuart, McRae, Allan F., Wright, Margaret J., Sturm, Richard A., Mackey, David A., Montgomery, Grant W., Martin, Nicholas G. and Medland, Sarah E. (2011). GWAS findings for human iris patterns: Associations with variants in genes that influence normal neuronal pattern development. American Journal of Human Genetics, 89 (2), 334-343. doi: 10.1016/j.ajhg.2011.07.011
Maugeri, Narelle, Powell, Joseph E., 't Hoen, Peter A. C., de Geus, Eco J. C., Willemsen, Gonneke, Kattenberg, Mathijs, Henders, Anjali K., Wallace, Leanne, Penninx, Brenda, Hottenga, Jouke-Jan, Medland, Sarah E., Saviouk, Viatcheslav, Martin, Nicholas G., Visscher, Peter M., van Ommen, Gert-Jan B., Frazer, Ian H., Boomsma, Dorret I., Montgomery, Grant W. and Ferreira, Manuel A. R (2011). LPAR1 and ITGA4 Regulate Peripheral Blood Monocyte Counts. Human Mutation, 32 (8), 873-876. doi: 10.1002/humu.21536
Zietsch, Brendan P., Miller, Geoffrey F., Bailey, J. Michael and Martin, Nicholas G. (2011). Female orgasm rates are largely independent of other traits: Implications for "female orgasmic disorder" and evolutionary theories of orgasm. Journal of Sexual Medicine, 8 (8), 2305-2316. doi: 10.1111/j.1743-6109.2011.02300.x
Le, Anh T., Miller, Paul W., Slutske, Wendy S. and Martin, Nicholas G. (2011). Attitudes towards economic risk and the gender pay gap. Labour Economics, 18 (4), 555-561. doi: 10.1016/j.labeco.2010.12.007
Bedi, Saaniya, Nelson, Elliot C., Lynskey, Michael T., McCutcheon, Vivia V., Heath, Andrew C., Madden, Pamela A. F. and Martin, Nicholas G. (2011). Risk for suicidal thoughts and behavior after childhood sexual abuse in women and men. Suicide and Life-Threatening Behavior, 41 (4), 406-415. doi: 10.1111/j.1943-278X.2011.00040.x
Slutske, Wendy S., Zhu, Gu, Meier, Madeline H. and Martin, Nicholas G. (2011). Disordered gambling as defined by the diagnostic and statistical manual of mental disorders and the South Oaks Gambling Screen: evidence for a common etiologic structure. Journal of Abnormal Psychology, 120 (3), 743-751. doi: 10.1037/a0022879
Blokland, Gabriella A. M., McMahon, Katie L., Thompson, Paul M., Martin, Nicholas G., de Zubicaray, Greig I. and Wright, Margaret J. (2011). Heritability of working memory brain activation. Journal of Neuroscience, 31 (30), 10882-10890. doi: 10.1523/JNEUROSCI.5334-10.2011
Yang, Jian, Weedon, Michael N., Purcell, Shaun, Lettre, Guillaume, Estrada, Karol, Willer, Cristen J., Smith, Albert V., Ingelsson, Erik, O'Connell, Jeffrey R., Mangino, Massimo, Maegi, Reedik, Madden, Pamela A., Heath, Andrew C., Nyholt, Dale R., Martin, Nicholas G., Montgomery, Grant W., Frayling, Timothy M., Hirschhorn, Joel N., McCarthy, Mark I., Goddard, Michael E. and Visscher, Peter M. (2011). Genomic inflation factors under polygenic inheritance. European Journal of Human Genetics, 19 (7), 807-812. doi: 10.1038/ejhg.2011.39
Demirkan, Ayse, Amin, Najaf, Isaacs, Aaron, Jarvelin, Marjo-Riitta, Whitfield, John B., Wichmann, Heinz-Erich, Kyvik, Kirsten Ohm, Rudan, Igor, Gieger, Christian, Hicks, Andrew A., Johansson, Asa, Hottenga, Jouke-Jan, Smith, Johannes J., Wild, Sarah H., Pedersen, Nancy L., Willemsen, Gonneke, Mangino, Massimo, Hayward, Caroline, Uitterlinden, Andre G., Hofman, Albert, Witteman, Jacqueline, Montgomery, Grant W., Pietilainen, Kirsi H., Rantanen, Taina, Kaprio, Jaakko, Doering, Angela, Pramstaller, Peter P., Gyllensten, Ulf, de Geus, Eco J. C. ... van Duijn, Cornelia M. (2011). Genetic architecture of circulating lipid levels. European Journal of Human Genetics, 19 (7), 813-819. doi: 10.1038/ejhg.2011.21
Theodoraki, A., Jones, G., Parker, J., Woolman, E., Martin, N., Perera, S., Thomas, M., Bunn, C., Khoo, B., Bouloux, P. M. and Vanderpump, M. P. J. (2011). Performance of a third-generation TSH-receptor antibody in a UK clinic. Clinical Endocrinology, 75 (1), 127-133. doi: 10.1111/j.1365-2265.2011.04022.x
Slutske, Wendy S., Bascom, Elise N., Meier, Madeline H., Medland, Sarah E. and Martin, Nicholas G. (2011). Sensation seeking in females from opposite-versus same-sex twin pairs: hormone transfer or sibling imitation?. Behavior Genetics, 41 (4), 533-542. doi: 10.1007/s10519-010-9416-3
Singh, A. L., D'Onofrio, B. M., Slutske, W. S., Turkheimer, E., Emery, R. E., Harden, K. P., Heath, A. C., Madden, P. A. F., Statham, D. J. and Martin, N. G. (2011). Parental depression and offspring psychopathology: a Children of Twins study. Psychological Medicine, 41 (7), 1385-1395. doi: 10.1017/S0033291710002059
Sanfilippo, Paul G., Medland, Sarah E., Hewitt, Alex W., Kearns, Lisa S., Ruddle, Jonathan B., Sun, Cong, Hammond, Christopher J., Young, Terri L., Martin, Nicholas G. and Mackey, David A. (2011). Ophthalmic phenotypes and the representativeness of twin data for the general population. Investigative Ophthalmology & Visual Science, 52 (8), 5565-5572. doi: 10.1167/iovs.11-7258
Luciano, Michelle, Montgomery, Grant W., Martin, Nicholas G., Wright, Margaret J. and Bates, Timothy C. (2011). SNP sets and reading ability: testing confirmation of a 10-SNP set in a population sample. Twin Research and Human Genetics, 14 (3), 228-232. doi: 10.1375/twin.14.3.228
Martin, Nicolas W., Medland, Sarah E., Verweij, Karin J. H., Lee, S. Hong, Nyholt, Dale R., Madden, Pamela A., Heath, Andrew C., Montgomery, Grant W., Wright, Margaret J. and Martin, Nicholas G. (2011). Educational Attainment: A Genome Wide Association Study in 9538 Australians. PLoS One, 6 (6) e20128, e20128.1-e20128.8. doi: 10.1371/journal.pone.0020128
Painter, Jodie N., Nyholt, Dale R., Morris, Andrew, Zhao, Zhen Z., Henders, Anjali K., Lambert, Ann, Wallace, Leanne, Martin, Nicholas G., Kennedy, Stephen H., Treloar, Susan A., Zondervan, Krina T. and Montgomery, Grant W. (2011). High-density fine-mapping of a chromosome 10q26 linkage peak suggests association between endometriosis and variants close to CYP2C19. Fertility and Sterility, 95 (7), 2236-2240. doi: 10.1016/j.fertnstert.2011.03.062
Burdon, Kathryn P., Macgregor, Stuart, Hewitt, Alex W., Sharma, Shiwani, Chidlow, Glyn, Mills, Richard A., Danoy, Patrick, Casson, Robert, Viswanathan, Ananth C., Liu, Jimmy Z., Landers, John, Henders, Anjali K., Wood, John, Souzeau, Emmanuelle, Crawford, April, Leo, Paul, Wang, Jie Jin, Rochtchina, Elena, Nyholt, Dale R., Martin, Nicholas G., Montgomery, Grant W., Mitchell, Paul, Brown, Matthew A., Mackey, David A. and Craig, Jamie E. (2011). Genome-wide association study identifies susceptibility loci for open angle glaucoma at TMCO1 and CDKN2B-AS1. Nature Genetics, 43 (6), 574-578. doi: 10.1038/ng.824
Benyamin, Beben, Montgomery, Grant W., Martin, Nicholas G. and Whitfield, John B. (2011). Transferrin saturation and mortality. Clinical Chemistry, 57 (6), 921-923. doi: 10.1373/clinchem.2011.162784
Beam, Christopher R., Horn, Erin E., Hunt, Stacy Karagis, Emery, Robert E., Turkheimer, Eric and Martin, Nick (2011). Revisiting the effect of marital support on depressive symptoms in mothers and fathers: a genetically informed study. Journal of Family Psychology, 25 (3), 336-344. doi: 10.1037/a0023758
Gehrman, Philip R., Byrne, Enda, Gillespie, Nathan and Martin, Nicholas G. (2011). Genetics of insomnia. Sleep Medicine Clinics, 6 (2), 191-202. doi: 10.1016/j.jsmc.2011.03.003
Schumann, Gunter, Coin, Lachlan J., Lourdusamy, Anbarasu, Charoen, Pimphen, Berger, Karen H., Stacey, David, Desrivieres, Sylvane, Aliev, Fazil A., Khan, Anokhi A., Amin, Najaf, Aulchenko, Yurii S., Bakalkin, Georgy, Bakker, Stephan J., Balkau, Beverley, Beulens, Joline W., Bilbao, Ainhoa, de Boer, Rudolf A., Beury, Delphine, Bots, Michiel L., Breetvelt, Elemi J., Cauchi, Stephane, Cavalcanti-Proenca, Christine, Chambers, John C., Clarke, Toni-Kim, Dahmen, Norbert, de Geus, Eco J., Dick, Danielle, Ducci, Francesca, Easton, Alanna ... Elliott, Paul (2011). Genome-wide association and genetic functional studies identify autism susceptibility candidate 2 gene (AUTS2) in the regulation of alcohol consumption (vol 108, pg 7119, 2011). Proceedings of the National Academy of Sciences of the United States of America, 108 (22), 9316-9316. doi: 10.1073/pnas.1106917108
Braskie, Meredith N., Jahanshad, Neda, Stein, Jason L., Barysheva, Marina, McMahon, Katie L., de Zubicaray, Greig I., Martin, Nicholas G., Wright, Margaret J., Ringman, John M., Toga, Arthur W. and Thompson, Paul M. (2011). Common Alzheimer's disease risk variant within the CLU gene affects white matter microstructure in young adults. The Journal of Neuroscience, 31 (18), 6764-6770. doi: 10.1523/JNEUROSCI.5794-10.2011
Zietsch, Brendan P., Verweij, Karin J. H., Heath, Andrew C. and Martin, Nicholas G. (2011). Variation in human mate choice: Simultaneously investigating heritability, parental influence, sexual imprinting, and assortative mating. The American Naturalist, 177 (5), 605-616. doi: 10.1086/659629
Meier, Madeline H., Slutske, Wendy S., Heath, Andrew C. and Martin, Nicholas G. (2011). Sex differences in the genetic and environmental influences on childhood conduct disorder and adult antisocial behavior. Journal of Abnormal Psychology, 120 (2), 377-388. doi: 10.1037/a0022303
Schumann, Gunter, Coin, Lachlan J., Lourdusamy, Anbarasu, Charoen, Pimphen, Berger, Karen H., Stacey, David, Desrivieres, Sylvane, Aliev, Fazil A., Khan, Anokhi A., Amin, Najaf, Aulchenko, Yurii S., Bakalkin, Georgy, Bakker, Stephan J., Balkau, Beverley, Beulens, Joline W., Bilbao, Ainhoa, de Boer, Rudolf A., Beury, Delphine, Bots, Michiel L., Breetvelt, Elemi J., Cauchi, Stéphane, Cavalcanti-Proenca, Christine, Chambers, John C., Clarke, Toni-Kim, Dahmen, Norbert, de Geus, Eco J., Dick, Danielle, Ducci, Francesca, Easton, Alanna ... Elliott, Paul (2011). Genome-wide association and genetic functional studies identify autism susceptibility candidate 2 gene (AUTS2) in the regulation of alcohol consumption. Proceedings of the National Academy of Sciences of the United States of America, 108 (17), 7119-7124. doi: 10.1073/pnas.1017288108
Webbink, Dinand, Martin, Nicholas G. and Visscher, Peter M. (2011). Does teenage childbearing reduce investment in human capital?. Journal of Population Economics, 24 (2), 701-730. doi: 10.1007/s00148-009-0270-7
Painter, Jodie N., Anderson, Carl A., Nyholt, Dale R., Macgregor, Stuart, Lin, Jianghai, Lee, Sang Hong, Lambert, Ann, Zhao, Zhen Z., Roseman, Fenella, Guo, Qun, Gordon, Scott D., Wallace, Leanne, Henders, Anjali K., Visscher, Peter M., Kraft, Peter, Martin, Nicholas G., Morris, Andrew P., Treloar, Susan A., Kennedy, Stephen H., Missmer, Stacey A., Montgomery, Grant W. and Zondervan, Krina T. (2011). Genome-wide association study identifies a locus at 7p15.2 associated with endometriosis. Obstetrical and Gynecological Survey, 66 (4), 214-216. doi: 10.1097/OGX.0b013e318210cea1
Alford, John R., Hatemi, Peter K., Hibbing, John R., Martin, Nicholas G. and Eaves, Lindon J. (2011). The politics of mate choice. The Journal of Politics, 73 (2), 362-379. doi: 10.1017/S0022381611000016
Loehlin, John C. and Martin, Nicholas G. (2011). Corrigendum to: "The general factor of personality: questions and elaborations" [J. Res. Pers. 45 (2011) 44-49]. Journal of Research in Personality, 45 (2), 258-258. doi: 10.1016/j.jrp.2011.02.010
Waldron, Mary, Heath, Andrew C., Lynskey, Michael T., Bucholz, Kathleen K., Madden, Pamela A. F. and Martin, Nicholas G. (2011). Alcoholic marriage: later start, sooner end. Alcoholism: Clinical and Experimental Research, 35 (4), 632-642. doi: 10.1111/j.1530-0277.2010.01381.x
Ferreira, Manuel A. R., McRae, Allan F., Medland, Sarah E., Nyholt, Dale R., Gordon, Scott D., Wright, Margaret J., Henders, Anjali K., Madden, Pamela A., Visscher, Peter M., Wray, Naomi R., Heath, Andrew C., Montgomery, Grant W., Duffy, David L. and Martin, Nicholas G. (2011). Association between ORMDL3, IL1RL1 and a deletion on chromosome 17q21 with asthma risk in Australia. European Journal of Human Genetics, 19 (4), 458-464. doi: 10.1038/ejhg.2010.191
Cichon, Sven, Muehleisen, Thomas W., Degenhardt, Franziska A., Mattheisen, Manuel, Miro, Xavier, Strohmaier, Jana, Steffens, Michael, Meesters, Christian, Herms, Stefan, Weingarten, Moritz, Priebe, Lutz, Haenisch, Britta, Aexander, Michael, Vollmer, Jennifer, Breuer, Rene, Schmael, Christine, Tessmann, Peter, Moebus, Susanne, Wichmann, H. -Erich, Schreiber, Stefan, Mueller-Myhsok, Bertram, Lucae, Susanne, Jamain, Stephane, Leboyer, Marion, Bellivier, Frank, Etain, Bruno, Henry, Chantal, Kahn, Jean-Pierre, Heath, Simon ... Noethen, Markus M. (2011). Genome-wide association study identifies genetic variation in neurocan as a susceptibility factor for bipolar disorder. American Journal of Human Genetics, 88 (3), 372-381. doi: 10.1016/j.ajhg.2011.01.017
Speliotes, Elizabeth K., Yerges-Armstrong, Laura M., Wu, Jun, Hernaez, Ruben, Kim, Lauren J., Palmer, Cameron D., Gudnason, Vilmundur, Eiriksdottir, Gudny, Garcia, Melissa E., Launer, Lenore J., Nalls, Michael A., Clark, Jeanne M., Mitchell, Braxton D., Shuldiner, Alan R., Butler, Johannah L., Tomas, Marta, Hoffmann, Udo, Hwang, Shih-Jen, Massaro, Joseph M., O'Donnell, Christopher J., Sahani, Dushyant V., Salomaa, Veikko, Schadt, Eric E., Schwartz, Stephen M., Siscovick, David S., NASH CRN, GIANT Consortium, MAGIC Investigators, Voight, Benjamin F. ... Coin, Lachlan (2011). Genome-wide association analysis identifies variants associated with nonalcoholic fatty liver disease that have distinct effects on metabolic traits. PLoS Genetics, 7 (3) e1001324, e1001324.1-e1001324.14. doi: 10.1371/journal.pgen.1001324
Luciano, Michelle, Hansell, Narelle K., Lahti, Jari, Davies, Gail, Medland, Sarah E., Raikkonen, Katri, Tenesa, Albert, Widen, Elisabeth, McGhee, Kevin A., Palotie, Aarno, Liewald, David, Porteous, David J., Starr, John M., Montgomery, Grant W., Martin, Nicholas G., Eriksson, Johan G., Wright, Margaret J. and Deary, Ian J. (2011). Whole genome association scan for genetic polymorphisms influencing information processing speed. Biological Psychology, 86 (3), 193-202. doi: 10.1016/j.biopsycho.2010.11.008
Chiang, M. C., Barysheva, M., Toga, A. W., Medland, S. E., Hansel, N. K., James, M. R., McMahon, K. L., de Zubicaray, G. I., Martin, N. G., Wright, M. J. and Thompson, P. M. (2011). BDNF gene effects on brain circuitry replicated in 455 twins. NeuroImage, 55 (2), 448-454. doi: 10.1016/j.neuroimage.2010.12.053
Cichon, Sven, Muehleisen, Thomas W., Degenhardt, Franziska A., Mattheisen, Manuel, Miro, Xavier, Strohmaier, Jana, Steffens, Michael, Meesters, Christian, Herms, Stefan, Weingarten, Moritz, Priebe, Lutz, Haenisch, Britta, Alexander, Michael, Vollmer, Jennifer, Breuer, Rene, Schmael, Christine, Tessmann, Peter, Moebus, Susanne, Wichmann, H. -Erich, Schreiber, Stefan, Mueller-Myhsok, Bertram, Lucae, Susanne, Jamain, Stephane, Leboyer, Marion, Bellivier, Frank, Etain, Bruno, Henry, Chantal, Kahn, Jean-Pierre, Heath, Simon ... Noethen, Markus M. (2011). Genome-wide Association Study Identifies Genetic Variation in Neurocan as a Susceptibility Factor for Bipolar Disorder (vol 88, pg 372, 2011). American Journal of Human Genetics, 88 (3), 396-396. doi: 10.1016/j.ajhg.2011.03.001
Joshi, A.A., Lepore, N., Joshi, S.H., Lee, A.D., Barysheva, M., Stein, J.L., McMahon, K.L., Johnson, K., de Zubicaray, G.I., Martin, N.G., Wright, M.J., Toga, A.W. and Thompson, P.M. (2011). The contribution of genes to cortical thickness and volume. NeuroReport, 22 (3), 101-105. doi: 10.1097/WNR.0b013e3283424c84
Barakat, M., Doyon, J., Debas, K., Vandewalle, G., Morin, A., Poirier, G., Martin, N., Lafortune, M., Karni, A., Ungerleider, L. G., Benali, H. and Carrier, J. (2011). Fast and slow spindle involvement in the consolidation of a new motor sequence. Behavioural Brain Research, 217 (1), 117-121. doi: 10.1016/j.bbr.2010.10.019
Chiang, MC, McMahon, KL, de Zubicaray, GI, Martin, NG, Hickie, I, Toga, AW, Wright, MJ and Thompson, PM (2011). Genetics of white matter development: A DTI study of 705 twins and their siblings aged 12 to 29. NeuroImage, 54 (3), 2308-2317. doi: 10.1016/j.neuroimage.2010.10.015
Zietsch, Brendan P., Verweij, Karin J. H., Bailey, J. Michael, Wright, Margaret J. and Martin, Nicholas G. (2011). Sexual orientation and psychiatric vulnerability: A twin study of neuroticism and psychoticism. Archives of Sexual Behavior, 40 (1), 133-142. doi: 10.1007/s10508-009-9508-4
Ngo, Trung T., Mitchell, Philip B., Martin, Nicholas G. and Miller, Steven M. (2011). Psychiatric and genetic studies of binocular rivalry: an endophenotype for bipolar disorder?. Acta Neuropsychiatrica, 23 (1), 37-42. doi: 10.1111/j.1601-5215.2010.00510.x
Carrier, Julie, Viens, Isabelle, Poirier, Gaétan , Robillard, Rébecca , Lafortune, Marjolaine, Vandewalle, Gilles, Martin, Nicolas, Barakat, Marc, Paquet, Jean and Filipini, Daniel (2011). Sleep slow wave changes during the middle years of life. European Journal of Neuroscience, 33 (4), 758-766. doi: 10.1111/j.1460-9568.2010.07543.x
Fahy, Samantha J., Sun, Cong, Zhu, Gu, Healey, Paul R., Spector, Tim D., Martin, Nicolas G., Mitchell, Paul, Wong, Tien Y., Mackey, David A., Hammond, Christopher J. and Andrew, Toby (2011). The relationship between retinal arteriolar and venular calibers is genetically mediated, and each is associated with risk of cardiovascular disease. Investigative Ophthalmology & Visual Science, 52 (2), 975-981. doi: 10.1167/iovs.10-5927
Loehlin, John C. and Martin, Nicholas G. (2011). The general factor of personality: questions and elaborations. Journal of Research in Personality, 45 (1), 44-49. doi: 10.1016/j.jrp.2010.11.008
Vink, Jacqueline M., Boomsma, Dorret I., Medland, Sarah E., de Moor, Marleen H. M., Stubbe, Janine H., Cornes, Belinda K., Martin, Nicholas G., Skytthea, Axel, Kyvik, Kirsten O., Rose, Richard J., Kujala, Urho M., Kaprio, Jaakko, Harris, Jennifer R., Pedersen, Nancy L., Cherkas, Lynn, Spector, Tim D. and de Geus, Eco J. C. (2011). Variance components models for physical activity with age as modifier: a comparative twin study in seven countries. Twin Research and Human Genetics, 14 (1), 25-34. doi: 10.1375/twin.14.1.25
Siskind, Victor, Hughes, Maria Celia B., Palmer, Jane M., Symmons, Judith M., Aitken, Joanne F., Martin, Nicholas G., Hayward, Nicholas K. and Whiteman, David C. (2011). Nevi, family history, and fair skin increase the risk of second primary melanoma. The Journal of Investigative Dermatology, 131 (2), 461-467. doi: 10.1038/jid.2010.298
Hatemi, Peter K., Gillespie, Nathan A., Eaves, Lindon J., Maher, Brion S., Webb, Bradley T., Heath, Andrew C., Medland, Sarah E., Smyth, David C., Beeby, Harry N., Gordon, Scott D., Montgomery, Grant W., Zhu, Ghu, Byrne, Enda M. and Martin, Nicholas G. (2011). A genome-wide analysis of liberal and conservative political attitudes. Journal of Politics, 73 (1), 271-285. doi: 10.1017/S0022381610001015
Barrett, Jennifer H., Iles, Mark M., Harland, Mark, Taylor, John C., Aitken, Joanne F., Andresen, Per Arne, Akslen, Lars A., Armstrong, Bruce K., Avril, Marie-Francoise, Azizi, Esther, Bakker, Bert, Bergman, Wilma, Bianchi-Scarrà, Giovanna, Bressac-de Paillerets, Brigitte, Calista, Donato, Cannon-Albright, Lisa A., Corda, Eve, Cust, Anne E., Dębniak, Tadeusz, Duffy, David, Dunning, Alison M., Easton, Douglas F., Friedman, Eitan, Galan, Pilar, Ghiorzo, Paola, Giles, Graham G., Hansson, Johan, Hocevar, Marko, Höiom, Veronica ... Bishop, D. Timothy (2011). Genome-wide association study identifies three new melanoma susceptibility loci. Nature Genetics, 43 (11), 1108-1113. doi: 10.1038/ng.959
Martin, Nicolas W., Benyamin, Beben, Hansell, Narelle K., Montgomery, Grant W., Martin, Nicholas G., Wright, Margaret J. and Bates, Timothy C. (2011). Cognitive function in adolescence: Testing for interactions between breast-feeding and FADS2 polymorphisms. Journal of the American Academy of Child and Adolescent Psychiatry, 50 (1), 55-62.e4. doi: 10.1016/j.jaac.2010.10.010
Painter, JN, Anderson, CA, Nyholt, DR, Macgregor, S, Lin, JH, Lee, SH, Lambert, A, Zhao, ZZ, Roseman, F, Guo, Q, Gordon, SD, Wallace, L, Henders, AK, Visscher, PM, Kraft, P, Martin, NG, Morris, AP, Treloar, SA, Kennedy, SH, Missmer, SA, Montgomery, GW and Zondervan, KT (2011). Genome-wide association study identifies a locus at 7p15.2 associated with endometriosis. Nature Genetics, 43 (1), 51-54. doi: 10.1038/ng.731
Wade, T. D., Zhu, G. and Martin, N. G. (2011). Undue influence of weight and shape: Is it distinct from body dissatisfaction and concern about weight and shape?. Psychological Medicine, 41 (4), 819-828. doi: 10.1017/S0033291710001066
Vinkhuyzen, A. A. E., Dumenil, T., Ryan, L., Gordon, S. D., Henders, A. K., Madden, P. A. F., Heath, A. C., Montgomery, G. W., Martin, N. G. and Wray, N. R. (2011). Identification of tag haplotypes for 5HTTLPR for different genome-wide SNP platforms. Molecular Psychiatry, 16 (11), 1073-1075. doi: 10.1038/mp.2011.68
Pergadia, Michele L., Glowinski, Anne L., Wray, Naomi, Agrawal, Arpana, Saccone, Scott F., Loukola, Anu, Broms, Ulla, Koronen, Tellervo, Penninx, Brenda W. J. H., Grant, Julia D., Nelson, Elliot C., Henders, Anjali K., Schrage, Andrew J., Chou, Yi-Ling, Keskitalo-Vuokko, Kaisu, Zhu, Qin, Gordon, Scott D., Vink, Jacqueline M., de Geus, Eco J. C., MacGregor, Stuart, Liu, Jimmy Z., Willemsen, Gonneke, Medland, Sarah E., Boomsma, Dorret I., Montgomery, Grant W., Rice, John P., Goate, Alison M., Heath, Andrew, C, Martin, Nicholas G. and Madden, Pamela A. F. (2011). A 3p26-3p25 genetic linkage finding for DSM-IV major depression in heavy smoking families. American Journal Psychiatry, 168 (8), 848-852. doi: 10.1176/appi.ajp.2011.10091319
Rizzi, Thais S., Arias-Vasquez, Alejandro, Rommelse, Nanda, Kuntsi, Jonna, Anney, Richard, Asherson, Philip, Buitelaar, Jan, Banaschewski, Tobias, Ebstein, Richard, Ruano, Dina, van der Sluis, Sophie, Markunas, Christina A., Garrett, Melanie E., Ashley-Koch, Allison E., Kollins, Scott H., Anastopoulos, Arthur D., Hansell, Narelle K., Wright, Margaret J., Montgomery, Grant W., Martin, Nicholas G., Harris, Sarah E., Davies, Gail, Tenesa, Albert, Porteous, David J., Starr, John M., Deary, Ian J., St. Pourcain, Beate, Smith, George Davey, Timpson, Nicholas J. ... Posthuma, Danielle (2011). The ATXN1 and TRIM31 genes are related to intelligence in an ADHD background: evidence from a large collaborative study totaling 4,963 subjects. American Journal of Medical Genetics, Part B: Neuropsychiatric Genetics, 156 (2), 145-157. doi: 10.1002/ajmg.b.31149
Bates, Timothy C., Luciano, Michelle, Medland, Sarah E., Montgomery, Grant W., Wright, Margaret J. and Martin, Nicholas G. (2011). Genetic variance in a component of the language acquisition device: ROBO1 polymorphisms associated with phonological buffer deficits. Behavior Genetics, 41 (1), 50-57. doi: 10.1007/s10519-010-9402-9
Middeldorp, C. M., de Moor, M. H. M., McGrath, L. M., Gordon, S. D., Blackwood, D. H., Costa, P. T., Terracciano, A., Krueger, R. F., de Geus, E. J. C., Nyholt, D. R., Tanaka, T., Esko, T., Madden, P. A. F., Derringer, J., Amin, N., Willemsen, G., Hottenga, J-J., Distel, M. A., Uda, M., Sanna, S., Spinhoven, P., Hartman, C. A, Ripke, S., Sullivan, P. F., Realo, A., Allik, J., Heath, A. C., Pergadia, M. L., Agrawal, A. ... Boomsma, D. I. (2011). The genetic association between personality and major depression or bipolar disorder. A polygenic score analysis using genome-wide association data. Translational Psychiatry, 1 (10) e50, e50.1-e50.8. doi: 10.1038/tp.2011.45
Elks, C. E., Perry, J. R. B., Sulem, P., Chasman, D. I., Franceschini, N., He, C. Y., Lunetta, K. L., Visser, J. A., Byrne, E. M., Cousminer, D. L., Gudbjartsson, D. F., Esko, T., Feenstra, B., Hottenga, J. J., Koller, D. L., Kutalik, Z., Lin, P., Mangino, M., Marongiu, M., McArdle, P. F., Smith, A. V., Stolk, L., Van Wingerden, S. H., Zhao, J. H., Albrecht, E., Corre, T., Ingelsson, E., Hayward, C., Magnusson, P. K. E. ... GIANT Consortium (2010). Thirty new loci for age at menarche identified by a meta-analysis of genome-wide association studies. Nature Genetics, 42 (12), 1077-1085. doi: 10.1038/ng.714
Sprangers, Mirjam A. G., Bartels, Meike, Veenhoven, Ruut, Baas, Frank, Martin, Nicholas G., Mosing, Miriam, Movsas, Benjamin, Ropka, Mary E., Shinozaki, Gen, Swaab, Dick and The GENEQOL Consortium (2010). Which patient will feel down, which will be happy? The need to study the genetic disposition of emotional states. Quality of Life Research, 19 (10), 1429-1437. doi: 10.1007/s11136-010-9652-2
Sun, Cong, Ponsonby, Anne-Louise, Brown, Shayne A., Kearns, Lisa S., Mackinnon, Jane R., Barbour, Julie M., Ruddle, Jonathan B., Wright, Margaret J., Martin, Nicholas G., Dwyer, Terence and Mackey, David A. (2010). Associations of birth weight with ocular biometry, refraction, and glaucomatous endophenotypes: The Australian twins eye study. American Journal of Ophthalmology, 150 (6), 909-916. doi: 10.1016/j.ajo.2010.06.028
Slutske, Wendy S., Piasecki, Thomas M., Blaszczynski, Alex and Martin, Nicholas G. (2010). Pathological gambling recovery in the absence of abstinence. Addiction, 105 (12), 2169-2175. doi: 10.1111/j.1360-0443.2010.03080.x
Bates, T. C., Lind, P. A., Luciano, M., Montgomery, G. W., Martin, N. G. and Wright, M. J. (2010). Dyslexia and DYX1C1: Deficits in reading and spelling associated with a missense mutation. Molecular Psychiatry, 15 (12), 1190-1196. doi: 10.1038/mp.2009.120
Reed, Danielle R., Zhu, Gu, Breslin, Paul A. S., Duke, Fujiko F., Henders, Anjali K., Campbell, Megan J., Montgomery, Grant W., Medland, Sarah E., Martin, Nicholas G. and Wright, Margaret J. (2010). The perception of quinine taste intensity is associated with common genetic variants in a bitter receptor cluster on chromosome 12. Human Molecular Genetics, 19 (21) ddq324, 4278-4285. doi: 10.1093/hmg/ddq324
Haworth, Cma, Wright, MJ, Luciano, M, Martin, NG, de Geus, EJC, van Beijsterveldt, CEM, Bartels, M, Posthuma, D, Boomsma, DI, Davis, OSP, Kovas, Y, Corley, RP, DeFries, JC, Hewitt, JK, Olson, RK, Rhea, SA, Wadsworth, SJ, Iacono, WG, McGue, M, Thompson, LA, Hart, SA, Petrill, SA, Lubinski, D and Plomin, R (2010). The heritability of general cognitive ability increases linearly from childhood to young adulthood. Molecular Psychiatry, 15 (11), 1112-1120. doi: 10.1038/mp.2009.55
Elizabeth K Speliotes, Cristen J Willer, Sonja I Berndt, Keri L Monda, Gudmar Thorleifsson, Anne U Jackson, Hana Lango Allen, Cecilia M Lindgren, Jian'an Luan, Reedik Magi, Joshua C Randall, Sailaja Vedantam, Thomas W Winkler, Lu Qi, Tsegaselassie Workalemahu, Iris M Heid, Valgerdur Steinthorsdottir, Heather M Stringham, Michael N Weedon, Eleanor Wheeler, Andrew R Wood, Teresa Ferreira, Robert J Weyant, Ayellet V Segre, Karol Estrada, Liming Liang, James Nemesh, Ju-Hyun Park, Stefan Gustafsson ... Ruth J F Loos (2010). Association analyses of 249,796 individuals reveal 18 new loci associated with body mass index. Nature Genetics, 42 (11), 937-948. doi: 10.1038/ng.686
Allen, Hana Lango, Estrada, Karol, Lettre, Guillaume, Berndt, Sonja I., Weedon, Michael N., Rivadeneira, Fernando, Willer, Cristen J., Jackson, Anne U., Vedantam, Sailaja, Raychaudhuri, Soumya, Nyholt, Dale, Martin, Nicholas G., Montgomery, Grant W. and Visscher, Peter M. (2010). Hundreds of variants clustered in genomic loci and biological pathways affect human height. Nature, 467 (7317), 832-838. doi: 10.1038/nature09410
Ikram, M. Kamran, Sim, Xueling, Jensen, Richard A., Cotch, Mary Frances, Hewitt, Alex W., Ikram, M. Arfan, Wang, Jie Jin, Klein, Ronald, Klein, Barbara E. K., Breteler, Monique M. B., Cheung, Ning, Liew, Gerald, Mitchell, Paul, Uitterlinden, Andrew G., Rivadeneira, Fernando, Hofman, Albert, de Jong, Paulus T. V. M., van Kuijn, Cornelia M., Kao, Linda, Cheng, Ching-Yu, Smith, Albert Vernon, Glazer, Nicole L., Lumley, Thomas, McKnight, Barbara, Psaty, Bruce M., Jonasson, Fridbert, Eiriksdottir, Gudny, Aspelund, Thor, Global BPgen Consortium ... Wong, Tien Y. (2010). Four novel Loci (19q13, 6q24, 12q24, and 5q14) influence the microcirculation in vivo. PLoS Genetics, 6 (10) e1001184, 1-12. doi: 10.1371/journal.pgen.1001184
Antoniou, Antonis C., Wang, Xianshu, Fredericksen, Zachary S., McGuffog, Lesley, Tarrell, Robert, Sinilnikova, Olga M., Healey, Sue, Morrison, Jonathan, Kartsonaki,Christiana, Lesnick, Timothy, Ghoussaini, Maya, Barrowdale, Daniel, Peock, Susan, Cook, Margaret, Oliver, Clare, Frost, Debra, Eccles, Diana, Evans, D. Gareth, Eeles, Ros, Izatt, Louise, Chu, Carol, Douglas, Fiona, Paterson, Joan, Stoppa-Lyonnet, Dominique, Houdayer, Claude, Mazoyer, Sylvie, Giraud, Sophie, Lasset, Christine, Remenieras, Audrey ... Lakhani, Sunil (2010). A locus on 19p13 modifies risk of breast cancer in BRCA1 mutation carriers and is associated with hormone receptor–negative breast cancer in the general population. Nature Genetics, 42 (10), 885-892. doi: 10.1038/ng.669
Aung, Hnin T., Harrison, Dion K., Findlay, Ian, Mattick, John S., Martin, Nicholas G. and Carroll, Bernard J. (2010). Stringent programming of DNA methylation in humans. Twin Research and Human Genetics, 13 (5), 405-411. doi: 10.1375/twin.13.5.405
Wade, Tracey D., Zhu, Gu and Martin, Nicholas G. (2010). Body mass index and breast size in women: Same or different genes?. Twin Research and Human Genetics, 13 (5), 450-454. doi: 10.1375/twin.13.5.450
Verweij, Kjh, Zietsch, BP, Medland, SE, Gordon, SD, Benyamin, B, Nyholt, DR, McEvoy, BP, Sullivan, PF, Heath, AC, Madden, PAF, Henders, AK, Montgomery, GW, Martin, NG and Wray, NR (2010). A genome-wide association study of Cloninger’s temperament scales: Implications for the evolutionary genetics of personality. Biological Psychology, 85 (2), 306-317. doi: 10.1016/j.biopsycho.2010.07.018
Hysi, Pirro G., Young, Terri L., Mackey, David A., Andrew, Toby, Fernandez-Medarde, Alberto, Solouki, Abbas M., Hewitt, Alex W., Macgregor, Stuart, Vingerling, Johannes R., Li, Yi-Ju, Ikram, M. Kamran, Fai, Lee Yiu, Sham, Pak C., Manyes, Lara, Porteros, Angel, Lopes, Margarida C., Carbonaro, Francis, Fahy, Samantha J., Martin, Nicholas G., van Diujn, Cornelia M., Spector, Timothy D., Rahi, Jugnoo S., Santos, Eugenio, Klaver, Caroline C. W. and Hammond, Christopher J. (2010). A genome-wide association study for myopia and refractive error identifies a susceptibility locus at 15q25. Nature Genetics, 42 (10), 902-905. doi: 10.1038/ng.664
Thorleifsson, Gudmar, Walters, G. Bragi, Hewitt, Alex W., Masson, Gisli, Helgason, Agnar, DeWan, Andrew, Sigurdsson, Asgeir, Jonasdottir, Adalbjorg, Gudjonsson, Sigurjon A., Magnusson, Kristinn P., Stefansson, Hreinn, Lam, Dennis S. C., Tam, Pancy O. S., Gudmundsdottir, Gudrun J., Southgate, Laura, Burdon, Kathryn P., Gottfredsdottir, Maria Soffia, Aldred, Micheala A., Mitchell, Paul, St Clair, David, Collier, David A., Tang, Nelson, Sveinsson, Orn, Macgregor, Stuart, Martin, Nicholas G., Cree, Angela J., Gibson, Jane, MacLeod, Alex, Jacob, Aby ... Stefansson, Kari (2010). Common variants near CAV1 and CAV2 are associated with primary open-angle glaucoma. Nature Genetics, 42 (10), 906-910. doi: 10.1038/ng.661
Verhulst, Brad, Hatemi, Peter K. and Martin, Nicholas G. (2010). The nature of the relationship between personality traits and political attitudes. Personality and Individual Differences, 49 (4), 306-316. doi: 10.1016/j.paid.2009.11.013
Teslovich, Tanya M., Musunuru, Kiran, Smith, Albert V., Edmondson, Andrew C., Stylianou, Ioannis M., Koseki, Masahiro, Pirruccello, James P., Ripatti, Samuli, Chasman, Daniel I., Willer, Cristen J., Johansen, Christopher T., Fouchier, Sigrid W., Isaacs, Aaron, Peloso, Gina M., Barbalic, Maja, Ricketts, Sally L., Bis, Joshua C., Aulchenko, Yurii S., Thorleifsson, Gudmar, Feitosa, Mary F., Chambers, John, Orho-Melander, Marju, Melander, Olle, Johnson, Toby, Li, Xiaohui, Guo, Xiuqing, Li, Mingyao, Cho, Yoon Shin, Go, Min Jin ... Kathiresan, Sekar (2010). Biological, clinical and population relevance of 95 loci for blood lipids. Nature, 466 (7307), 707-713. doi: 10.1038/nature09270
Saccone, Nancy L., Culverhouse, Robert C., Schwantes-An, Tae-Hwi, Cannon, Dale S., Chen, Xiangning, Cichon, Sven, Giegling, Ina, Han, Shizhong, Han, Younghun, Keskitalo-Vuokko, Kaisu, Kong, Xiangyang, Landi, Maria Teresa, Ma, Jennie Z., Short, Susan E., Stephens, Sarah H., Stevens, Victoria L., Sun, Lingwei, Wang, Yufei, Wenzlaff, Angela S., Aggen, Steven H., Breslau, Naomi, Broderick, Peter, Chatterjee, Nilanjan, Chen, Jingchun, Heath, Andrew C., Heliovaara, Markku, Hoft, Nicole R., Hunter, David J., Jensen, Majken K. ... Bierut, Laura J. (2010). Multiple independent loci at chromosome 15q25.1 affect smoking quantity: A meta-analysis and comparison with lung cancer and COPD. PLoS Genetics, 6 (8) ARTN e1001053, 1-16. doi: 10.1371/journal.pgen.1001053
Thompson, Paul M., Martin, Nicholas G. and Wright, Margaret J. (2010). Imaging genomics. Current Opinion in Neurology, 23 (4), 368-373. doi: 10.1097/WCO.0b013e32833b764c
Distel, Marijn A., Willemsen, Gonneke, Ligthart, Lannie, Derom, Catherine A., Martin, Nicholas G., Neale, Michael C., Trull, Timothy J. and Boomsma, Dorret I. (2010). Genetic covariance structure of the four main features of borderline personality disorder. Journal of Personality Disorders, 24 (4), 427-444. doi: 10.1521/pedi.2010.24.4.427
Pergadia, Michele L., Agrawal, Arpana, Heath, Andrew C., Martin, Nicholas G., Bucholz, Kathleen K. and Madden, Pamela A. F. (2010). Nicotine withdrawal symptoms in adolescent and adult twins. Twin Research And Human Genetics, 13 (4), 359-369. doi: 10.1375/twin.13.4.359
Slutske, Wendy S., Piasecki, Thomas M., Ellingson, Jarrod M. and Martin, Nicholas G. (2010). The family history method in disordered gambling research: A comparison of reports obtained from discordant twin pairs. Twin Research and Human Genetics, 13 (4), 340-346. doi: 10.1375/twin.13.4.340
Le, Anh T., Miller, Paul W., Slutske, Wendy S. and Martin, Nicholas G. (2010). Are attitudes towards economic risk heritable? Analyses using the Australian twin study of gambling. Twin Research And Human Genetics, 13 (4), 330-339. doi: 10.1375/twin.13.4.330
Mosing, Miriam A., Pedersen, Nancy L., Martin, Nicholas G. and Wright, Margaret J. (2010). Sex differences in the genetic architecture of optimism and health and their interrelation: A study of Australian and Swedish twins. Twin Research And Human Genetics, 13 (4), 322-329. doi: 10.1375/twin.13.4.322
Mosing, Miriam A., Verweij, Karin J. H., Medland, Sarah E., Painter, Jodie, Gordon, Scott D., Heath, Andrew C., Madden, Pamela A., Montgomery, Grant W. and Martin, Nicholas G. (2010). A genome-wide association study of self-rated health. Twin Research and Human Genetics, 13 (4), 398-403. doi: 10.1375/twin.13.4.398
Jahanshad, Neda, Lee, Agatha D., Barysheva, Marina, McMahon, Katie L., de Zubicaray, Greig I., Martin, Nicholas G., Wright, Margaret J., Toga, Arthur W. and Thompson, Paul M. (2010). Genetic influences on brain asymmetry: A DTI study of 374 twins and siblings. NeuroImage, 52 (2), 455-469. doi: 10.1016/j.neuroimage.2010.04.236
Smit, Dirk J. A., Luciano, Michelle, Bartels, Meike, van Beijsterveldt, Catharine E. M., Wright, Margaret J., Hansell, Narelle K., Brunner, Han G., Estourgie-van Burk, G. Frederiek, de Geus, Eco J. C., Martin, Nicholas G. and Boomsma, Dorret I. (2010). Heritability of head size in Dutch and Australian twin families at ages 0-50 years. Twin Research And Human Genetics, 13 (4), 370-380. doi: 10.1375/twin.13.4.370
Foley, Debra L., Morley, Katherine I., Madden, Pamela A. F., Heath, Andrew C., Whitfield, John B. and Martin, Nicholas G. (2010). Major depression and the metabolic syndrome. Twin Research and Human Genetics, 13 (4), 347-358. doi: 10.1375/twin.13.4.347
Liu, Jimmy Z., McRae, Allan F., Nyholt, Dale R., Medland, Sarah E., Wray, Naomi R., Brown, Kevin M., AMFS Investigators, Hayward, Nicholas K., Montgomery, Grant W., Visscher, Peter M., Martin, Nicholas G. and Macgregor, Stuart (2010). A versatile gene-based test for genome-wide association studies. American Journal of Human Genetics, 87 (1), 139-145. doi: 10.1016/j.ajhg.2010.06.009
Hatemi, Peter K., Hibbing, John R., Medland, Sarah E., Keller, Matthew C., Alford, John R., Smith, Kevin B., Martin, Nicholas G. and Eaves, Lindon J. (2010). Not by twins alone: Using the extended family design to investigate genetic influence on political beliefs. American Journal of Political Science, 54 (3), 798-814. doi: 10.1111/j.1540-5907.2010.00461.x
Macgregor, Stuart, Hewitt, Alex W., Hysi, Pirro G., Ruddle, Jonathan B., Medland, Sarah E., Henders, Anjali K., Gordon, Scott D., Andrew, Toby, McEvoy, Brian, Sanfilippo, Paul G., Carbonaro, Francis, Tah, Vikas, Li, Yi Ju, Bennett, Sonya L., Craig, Jamie E., Montgomery, Grant W., Tran-Viet, Khanh-Nhat, Brown, Nadean L., Spector, Timothy D., Martin, Nicholas G., Young, Terri L., Hammond, Christopher J. and Mackey, David A. (2010). Genome-wide association identifies ATOH7 as a major gene determining human optic disc size. Human Molecular Genetics, 19 (13) ddq144, 2716-2724. doi: 10.1093/hmg/ddq144
Duffy, David L., Iles, Mark M., Glass, Dan, Zhu, Gu, Barrett, Jennifer H., Hoiom, Veronica, Zhao, Zhen Z., Sturm, Richard A., Soranzo, Nicole, Hammond, Chris, Kvaskoff, Marina, Whiteman, David C., Mangino, Massimo, Hansson, Johan, Newton-Bishop, Julia A., Bataille, Veronique, Hayward, Nicholas K., Martin, Nicholas G., Bishop, D. Timothy, Spector, Timothy D. and Montgomery, Grant W. (2010). IRF4 variants have age-specific effects on nevus count and predispose to melanoma. American Journal of Human Genetics, 87 (1), 6-16. doi: 10.1016/j.ajhg.2010.05.017
Yang, Jian, Benyamin, Beben, McEvoy, Brian P., Gordon, Scott, Henders, Anjali K., Nyholt, Dale R., Madden, Pamela A., Heath, Andrew C., Martin, Nicholas G., Montgomery, Grant W., Goddard, Michael E. and Visscher, Peter M. (2010). Common SNPs explain a large proportion of the heritability for human height. Nature Genetics, 42 (7), 565-569. doi: 10.1038/ng.608
Slutske, Wendy S., Zhu, Gu, Meier, Madeline H. and Martin, Nicholas G. (2010). Genetic and environmental influences on disordered gambling in men and women. Archives of General Psychiatry, 67 (6), 624-630. doi: 10.1001/archgenpsychiatry.2010.51
Whitfield, John B., Dy, Veronica, McQuilty, Robert, Zhu, Gu, Heath, Andrew C., Montgomery, Grant W. and Martin, Nicholas G. (2010). Genetic effects on toxic and essential elements in humans: Arsenic, cadmium, copper, lead, mercury, selenium, and zinc in erythrocytes. Environmental Health Perspectives, 118 (6), 776-782. doi: 10.1289/ehp.0901541
Sturgis, Patrick, Read, Sanna, Hatemi, Peter K., Zhu, Gu, Trull, Tim, Wright, Margaret J. and Martin, Nicholas G. (2010). A genetic basis for social trust?. Political Behavior, 32 (2), 205-230. doi: 10.1007/s11109-009-9101-5
Ellingson, Jarrod M., Slutske, Wendy S. and Martin, Nicholas G. (2010). The reliability and validity of the family history method for assessing pathological gambling and gambling involvement. Psychology of Addictive Behaviors, 24 (2), 292-299. doi: 10.1037/a0018126
Painter, Jodie N., Willemsen, Gonneke, Nyholt, Dale, Hoekstra, Chantal, Duffy, David L., Henders, Anjali K., Wallace, Leanne, Healey, Sue, Cannon-Albright, Lisa A., Skolnick, Mark, Martin, Nicholas G., Boomsma, Dorret I. and Montgomery, Grant W. (2010). A genome wide linkage scan for dizygotic twinning in 525 families of mothers of dizygotic twins. Human Reproduction, 25 (6), 1569-1580. doi: 10.1093/humrep/deq084
Lind, Penelope A., Luciano, Michelle, Wright, Margaret J., Montgomery, Grant W., Martin, Nicholas G. and Bates, Timothy C. (2010). Dyslexia and DCDC2: Normal variation in reading and spelling is associated with DCDC2 polymorphisms in an Australian population sample. European Journal of Human Genetics, 18 (6), 668-673. doi: 10.1038/ejhg.2009.237
Lu, Yi, Dimasi, David P., Hysi, Pirro G., Hewitt, Alex W., Burdon, Kathryn P., Toh, Tze'Yo, Ruddle, Jonathan B., Li, Yi Ju, Mitchell, Paul, Healey, Paul R., Montgomery, Grant W., Hansell, Narelle, Spector, Timothy D., Martin, Nicholas G., Young, Terri L., Hammond. Christopher J., Macgregor, Stuart, Craig, Jamie E. and Mackey, David A. (2010). Common genetic variants near the brittle cornea syndrome locus ZNF469 influence the blinding disease risk factor central corneal thickness. PLoS Genetics, 6 (5) ARTN e1000947, e1000947.1-e1000947.10. doi: 10.1371/journal.pgen.1000947
Liu, Fan, Wollstein, Andreas, Hysi, Pirro G., Ankra-Badu, Georgina A., Spector, Timothy D., Park, Daniel, Zhu, Gu, Larsson, Mats, Duffy, David L., Montgomery, Grant W., Mackey, David A., Walsh, Susan, Lao, Oscar, Hofman, Albert, Rivadeneira, Fernando, Vingerling, Johannes R., Uitterlinden, Andrew G., Martin, Nicholas G., Hammond, Christopher J. and Kayser, Manfred (2010). Digital quantification of human eye color highlights genetic association of three new loci. PLoS Genetics, 6 (5) ARTN e1000934, e1000934-1-e1000934-15. doi: 10.1371/journal.pgen.1000934
Thorgeirsson, Thorgeir E., Gudbjartsson, Daniel F., Surakka, Ida, Vink, Jacqueline M., Amin, Najaf, Geller, Frank, Sulem, Patrick, Rafnar, Thorunn, Esko, Tōnu, Walter, Stefan, Gieger, Christian, Rawal, Rajesh, Mangino, Massimo, Prokopenko, Inga, Mägi, Reedik, Keskitalo, Kaisu, Gudjonsdottir, Iris H., Gretarsdottir, Solveig, Stefansson, Hreinn, Thompson, John R., Aulchenko, Yurii S., Nelis, Mari, Aben, Katja K., den Heijer, Martin, Dirksen, Asger, Ashraf, Haseem, Soranzo, Nicole, Valdes, Ana M., Steves, Claire ... Stefansson, Kari (2010). Sequence variants at CHRNB3-CHRNA6 and CYP2A6 affect smoking behavior. Nature Genetics, 42 (5), 448-454. doi: 10.1038/ng.573
Medland, Sarah E., Zayats,Tetyana, Glaser, Beate, Nyholt, Dale R., Gordon,Scott D., Wright, Margaret J., Montgomery, Grant W., Campbell, Megan J., Henders, Anjali K., Timpson, Nicholas J., Peltonen, Leena, Wolke, Dieter, Ring, Susan M., Deloukas, Panos, Martin, Nicholas G., Smith, George Davey and Evans, David M. (2010). A variant in LIN28B is Associated with 2D:4D finger-length ratio, a putative retrospective biomarker of prenatal testosterone exposure. American Journal of Human Genetics, 86 (4), 519-525. doi: 10.1016/j.ajhg.2010.02.017
Liu, Jimmy Z., Medland, Sarah E., Wright, Margaret J., Henders, Anjali K., Heath, Andrew C., Madden, Pamela A. F., Duncan, Alexis, Montgomery, Grant W., Martin, Nicholas G. and McRae, Allan F. (2010). Genome-wide association study of height and body mass index in Australian twin families. Twin Research And Human Genetics, 13 (2), 179-193. doi: 10.1375/twin.13.2.179
Nelson, Elliot C., Lynskey, Michael T., Heath, Andrew C., Madden, Pamela A. F. and Martin, Nicholas G. (2010). A Family Study of Adult Twins with and without a History of Childhood Abuse: Stability of Retrospective Reports of Maltreatment and Associated Family Measures. Twin Research and Human Genetics, 13 (2), 121-130. doi: 10.1375/twin.13.2.121
Sartor, Carolyn E., Grant, Julia D., Bucholz, Kathleen K., Madden, Pamela A. F., Heath, Andrew C., Agrawal, Arpana, Whitfield, John B., Statham, Dixie J., Martin, Nicholas G. and Lynkey, Michael T. (2010). Common genetic contributions to alcohol and cannabis use and dependence symptomatology. Alcoholism: Clinical and Experimental Research, 34 (3), 545-554. doi: 10.1111/j.1530-0277.2009.01120.x
Verweij, Karin J. H., Zietsch, Brendan P., Lynskey, Michael T., Medland, Sarah E., Neale, Michael C., Martin, Nicholas G., Boomsma, Dorret I. and Vink, Jacqueline M. (2010). Genetic and environmental influences on cannabis use initiation and problematic use: A meta-analysis of twin studies. Addiction, 105 (3), 417-430. doi: 10.1111/j.1360-0443.2009.02831.x
M. A. R. Ferreira, N. A. Oates, J. van Vliet, Z. Z. Zhao, M. Ehrich, N. G. Martin, G. W. Montgomery, E. Whitelaw and D. L. Duffy (2010). Characterization of the methylation patterns of MS4A2 in atopic cases and controls. ALLERGY, 65 (3), 333-337. doi: 10.1111/j.1398-9995.2009.02135.x
Miller, Steven M., Hansell, Narelle K., Ngo, Trung T., Liu, Guang B., Pettigrew, John D., Martin, Nicholas G. and Wright, Margaret J. (2010). Genetic contribution to individual variation in binocular rivalry rate. Proceedings of the National Academy of Sciences of the United States of America, 107 (6), 2664-2668. doi: 10.1073/pnas.0912149107
McCutcheon, Vivia V., Heath, Andrew C., Nelson, Elliot C., Bucholz, Kathleen K., Madden, Pamela A. F. and Martin, Nicholas G. (2010). Clustering of trauma and associations with single and co-occurring depression and panic attack over twenty years. Twin Research And Human Genetics, 13 (1), 57-65. doi: 10.1375/twin.13.1.57
Duffy, David L., Zhao, Zhen Z., Sturm, Richard A., Hayward, Nicholas K., Martin, Nicholas G. and Montgomery, Grant W. (2010). Multiple pigmentation gene polymorphisms account for a substantial proportion of risk of cutaneous malignant melanoma. Journal of Investigative Dermatology, 130 (2), 520-528. doi: 10.1038/jid.2009.258
Lind, Penelope A., Macgregor, Stuart, Vink, Jacqueline M., Pergadia, Michele L., Hansell, Narelle K., de Moor, Marleen H. M., Smit, August B., Hottenga, Jouke-Jan, Richter, Melinda M., Heath, Andrew C., Martin, Nicholas G., Willemsen, Gonneke, de Geus, Eco J. C., Vogelzangs,Nicole, Penninx, Brenda W., Whitfield, John B., Montgomery, Grant W., Boomsma, Dorret I. and Madden, Pamela A. F. (2010). A genomewide association study of nicotine and alcohol dependence in Australian and Dutch populations. Twin Research And Human Genetics, 13 (1), 10-29. doi: 10.1375/twin.13.1.10
Ferreira, Mar, Mangino, M, Brumme, CJ, Zhao, ZZ, Medland, SE, Wright, MJ, Nyholt, DR, Gordon, S, Campbell, M, McEvoy, BP, Henders, A, Evans, DM, Lanchbury, JS, Pereyra, F, Walker, BD, Haas, DW, Soranzo, N, Spector, TD, de Bakker, PIW, Frazer, IH, Montgomery, GW, Martin, NG and Int HIV Controllers Study (2010). Quantitative trait loci for CD4:CD8 lymphocyte ratio are associated with risk of type 1 diabetes and HIV-1 immune control. American Journal of Human Genetics, 86 (1), 88-92. doi: 10.1016/j.ajhg.2009.12.008
Webbink, Dinand, Martin, Nicholas G. and Visscher, Peter M. (2010). Does education reduce the probability of being overweight?. Journal of Health Economics, 29 (1), 29-38. doi: 10.1016/j.jhealeco.2009.11.013
Nelson, Elliot C., Agrawal, Arpana, Pergadia, Michele L., Wang, Jen C., Whitfield, John B., Saccone, F. Scott, Kern, Jason, Grant, Julia D., Schrage, Andrew J., Rice, John P., Montgomery, Grant W., Heath, Andrew C, Goate, Alison M., Martin, Nicholas G. and Madden, Pamela A. F. (2010). H2 haplotype at chromosome 17q21.31 protects against childhood sexual abuse-associated risk for alcohol consumption and dependence. Addiction Biology, 15 (1), 1-11. doi: 10.1111/j.1369-1600.2009.00181.x
Bouzigon, Emmanuelle, Forabosco, Paola, Koppelman, Gerard H., Cookson, William O. C. M., Dizier, Marie-Helene, Duffy, David L., Evans, David M., Ferreira, Manuel A. R., Kere, Juha, Laitinen, Tarja, Malerba, Giovanni, Meyers, Deborah A., Moffatt, Miriam, Martin, Nicholas G, Ng, Mandy Y., Pignatti, Pier Franco, Wjst, Mathias, Kauffmann, Francine, Demenais, Florence and Lewis, Cathryn M. (2010). Meta-analysis of 20 genome-wide linkage studies evidenced new regions linked to asthma and atopy. European Journal of Human Genetics, 18 (6), 700-706. doi: 10.1038/ejhg.2009.224
Zietsch, B. P., Verweij, K. J. H., Bailey, J. M., Wright, M. J. and Martin, N. G. (2010). Genetic and environmental influences on risky sexual behaviour and its relationship with personality. Behavior Genetics, 40 (1), 12-21. doi: 10.1007/s10519-009-9300-1
Hansell, Narelle K., Agrawal, Arpana, Whitfield, John B., Morley, Katherine I., Gordon, Scott D., Lind, Penelope A., Pergadia, Michele L., Montgomery, Grant W., Madden, Pamela A. F., Todd, Richard D., Heath, Andrew C. and Martin, Nicholas G. (2010). Linkage analysis of alcohol dependence symptoms in the community. Alcoholism: Clinical and Experimental Research, 34 (1), 158-163. doi: 10.1111/j.1530-0277.2009.01077.x
Dawood, Khytam, Bailey, J. Michael and Martin, Nicholas G. (2010). Genetic and Environmental Influences on Sexual Orientation. Handbook of Behavior Genetics, 269-279. doi: 10.1007/978-0-387-76727-7_19
Marijn A. Distel, Timothy J. Trull, Gonneke Willemsen, Jacqueline M. Vink, Catherine A. Derom, Michael Lynskey, Nicholas G. Martin and Dorret I. Boomsm (2009). The Five-Factor Model of Personality and Borderline Personality Disorder: A Genetic Analysis of Comorbidity. BIOLOGICAL PSYCHIATRY, 66 (12), 1131-1138. doi: 10.1016/j.biopsych.2009.07.017
Sachdev, Perminder S., Lammel, Andrea, Trollor, Julian N., Lee, Teresa, Wright, Margaret J., Ames, David, Wen, Wei, Martin, Nicholas G., Brodaty, Henry, Schofield, Peter R. and OATS Research Team (2009). A comprehensive neuropsychiatric study of elderly twins: The Older Australian Twins Study. Twin Research and Human Genetics, 12 (6), 573-582. doi: 10.1375/twin.12.6.573
Medland, S, Nyholt, D, Painter, JN, McEnvoy, BP, Allan McRae, Zhu, G, Gordon, SD, Ferreira, MAR, Wright, MJ, Henders, AK, Campbell MJ, Duffy, D, Hansell, N K, Macgregor, S, Slutske, WS, Heath, AC, Montgomery, GW and Martin, NG (2009). Common Variants in the Trichohyalin Gene Are Associated with Straight Hair in Europeans. American Journal of Human Genetics, 85 (5), 750-755. doi: 10.1016/j.ajhg.2009.10.009
William L. Coventry, Michael R. James, Lindon J. Eaves, Scott D. Gordon, Nathan A. Gillespie, Leanne Ryan, Andrew C. Heath, Grant W. Montgomery, Nicholas G. Martin and Naomi R. Wray (2009). Do 5HTTLPR and stress interact in risk for depression and suicidality? Item response analyses of a large sample. American Journal of Medical Genetics. Part B: Neuropsychiatric Genetics, 153b (3), 757-765. doi: 10.1002/ajmg.b.31044
Ferreira, MAR, Hottenga, JJ, Warrington, NM, Medland, SE, Willemsen, G, Lawrence, RW, Gordon, S, de Geus, EJC, Henders, AK, Smit, JH, Campbell, MJ, Wallace, L, Evans, DM, Wright, MJ, Nyholt, DR, James, AL, Beilby, JP, Penninx, BW, Palmer, LJ, Frazer, IH, Montgomery, GW, Martin, NG and Boomsma, DI (2009). Sequence Variants in Three Loci Influence Monocyte Counts and Erythrocyte Volume. AMERICAN JOURNAL OF HUMAN GENETICS, 85 (5), 745-749. doi: 10.1016/j.ajhg.2009.10.005
Benyamin, B, Ferreira, MAR, Willemsen, G, Gordon, S, Middelberg, RPS, McEvoy, BP, Hottenga, JJ, Henders, AK, Campbell, MJ, Wallace, L, Frazer, IH, Heath, AC, de Geus, EJC, Nyholt, DR, Visscher, PM, Penninx, BW, Boomsma, DI, Martin, NG, Montgomery, GW and Whitfield, JB (2009). Common variants in TMPRSS6 are associated with iron status and erythrocyte volume. Nature Genetics, 41 (11), 1173-1175. doi: 10.1038/ng.456
Mosing, Miriam A., Zietsch, Brendan P., Shekar, Sri N., Wright, Margaret J. and Martin, Nicholas G. (2009). Genetic and environmental influences on optimism and its relationship to mental and self-rated health: A study of aging twins. Behavior Genetics, 39 (6), 597-604. doi: 10.1007/s10519-009-9287-7
Julia D. Grant, Arpana Agrawal, Kathleen K. Bucholz, Pamela A.F. Madden, Michele L. Pergadia, Elliot C. Nelson, Michael T. Lynskey, Richard D. Todd, Alexandre A. Todorov, Narelle K. Hansell, John B. Whitfield, Nicholas G. Martin and Andrew C. Heath (2009). Alcohol consumption indices of genetic risk for alcohol dependence. Biological Psychiatry, 66 (8), 795-800. doi: 10.1016/j.biopsych.2009.05.018
Ferreira, M. A. R., Zhao, Z. Z., Thomsen, S. F., James, M., Evans, D. M., Postmus, P. E., Kyvik, K. O., Backer, V., Boomsma, D. I., Martin, N. G., Montgomery, G. W. and Duffy, D. L. (2009). Association and interaction analyses of eight genes under asthma linkage peaks. Allergy, 64 (11), 1623-1628. doi: 10.1111/j.1398-9995.2009.02091.x
Sarah E. Medland, Gu Zhu and Nicholas G. Martin (2009). Estimating the Heritability of Hair Curliness in Twins of European Ancestry. Twin Research and Human Genetics, 12 (5), 514-518. doi: 10.1375/twin.12.5.514
David A. Mackey, Jane R. MacKinnon, Shayne A. Brown, Lisa S. Kearns, Jonathan B. Ruddle, Paul G. Sanfilippo, Cong Sun, Christopher J. Hammond, Terri L. Young, Nicholas G. Martin and Alex W. Hewitt (2009). Twins Eye Study in Tasmania (TEST): Rationale and Methodology to Recruit and Examine Twins. Twin Research and Human Genetics, 12 (5), 441-454. doi: 10.1375/twin.12.5.441
Mary Waldron, Nicholas G. Martin and Andrew C. Heath (2009). Parental Alcoholism and Offspring Behavior Problems: Findings in Australian Children of Twins. Twin Research and Human Genetics, 12 (5), 433-440. doi: 10.1375/twin.12.5.433
Wendy S. Slutske, Alex Blaszczynski and Nicholas G. Martin (2009). Sex Differences in the Rates of Recovery, Treatment-Seeking, and Natural Recovery in Pathological Gambling: Results From an Australian Community-Based Twin Survey. Twin Research and Human Genetics, 12 (5), 425-432. doi: 10.1375/twin.12.5.425
Sun, Cong, Zhu, Gu, Wong, Tien Y, Hewitt, Alex W, Ruddle, Jonathan B, Hodgson, Lauren, Montgomery, Grant W, Young, Terri L, Hammond, Christopher J, Craig, Jamie E, Martin, Nicholas G, He, Mingguang and Mackey, David A. (2009). Quantitative Genetic Analysis of the Retinal Vascular Caliber: The Australian Twins Eye Study. Hypertension, 54 (4), 788-795. doi: 10.1161/HYPERTENSIONAHA.109.132902
E. M. Byrne, A. F. McRae, D. L. Duffy, Z. Z. Zhao, N. G. Martin, J. B. Whitfield, P. M. Visscher and G. W. Montgomery (2009). Family-based mitochondrial association study of traits related to type 2 diabetes and the metabolic syndrome in adolescents. Diabetologia, 52 (11), 2359-2368. doi: 10.1007/s00125-009-1510-9
Arpana Agrawal, Carolyn E. Sartor, Michael T. Lynskey, Julia D. Grant, Michele L. Pergadia, Richard Grucza, Kathleen K. Bucholz, Elliot C. Nelson, Pamela A. F. Madden, Nicholas G. Martin and Andrew C. Heath (2009). Evidence for an Interaction Between Age at First Drink and Genetic Influences on DSM-IV Alcohol Dependence Symptoms. Alcoholism: Clinical and Experimental Research, 33 (12), 2047-2056. doi: 10.1111/j.1530-0277.2009.01044.x
Byrne, EM, McRae, AF, Duffy, DL, Zhao, ZZ, Martin, NG, Wright, MJ, Montgomery, GW and Visscher, PM (2009). Association Study of Common Mitochondrial Variants and Cognitive Ability. BEHAVIOR GENETICS, 39 (5), 504-512. doi: 10.1007/s10519-009-9276-x
Shekar, SN, Duffy, DL, Youl, P, Baxter, AJ, Kvaskoff, M, Whiteman, DC, Green, AC, Hughes, MC, Hayward, NK, Coates, M and Martin, NG (2009). A Population-Based Study of Australian Twins with Melanoma Suggests a Strong Genetic Contribution to Liability. Journal of Investigative Dermatology, 129 (9), 2211-2219. doi: 10.1038/jid.2009.48
Mary Waldron, , , ,, ,, Andrew C. Heath, Michael T. Lynskey, Elliot C. Nelson, Kathleen K. Bucholz, Pamela A.F. Madden and Nicholas G. Martin (2009). Smoking and Illicit Drug Use Associations With Early Versus Delayed Reproduction: Findings in a Young Adult Cohort of Australian Twins. Journal of Studies on Alcohol and Drugs, 70 (5), 786-796. doi: 10.15288/jsad.2009.70.786
J Kettunen, M Perola, N G Martin, B K Cornes, S G Wilson, G W Montgomery, B Benyamin, J R Harris, D Boomsma, G Willemsen, J-J Hottenga, P E Slagboom, K Christensen, K O Kyvik, T I A Sørensen, N L Pedersen, P K E Magnusson, T Andrew, T D Spector, E Widen, K Silventoinen, J Kaprio, A Palotie and L Peltonen (2009). Multicenter dizygotic twin cohort study confirms two linkage susceptibility loci for body mass index at 3q29 and 7q36 and identifies three further potential novel loci. International Journal of Obesity, 33 (11), 1235-1242. doi: 10.1038/ijo.2009.168
Naomi R. Wray, Michael R. James, Scott D. Gordon, Troy Dumenil, Leanne Ryan, William L. Coventry, Dixie J. Statham, Michele L. Pergadia, Pamela A.F. Madden, Andrew C. Heath, Grant W. Montgomery and Nicholas G. Martin (2009). Accurate, Large-Scale Genotyping of 5HTTLPR and Flanking Single Nucleotide Polymorphisms in an Association Study of Depression, Anxiety, and Personality Measures. Biological Psychiatry, 66 (5), 468-476. doi: 10.1016/j.biopsych.2009.04.030
Hatemi, Peter K., Alford, John R., Hibbing, John R., Martin, Nicholas G. and Eaves, Lindon J. (2009). Is There a "Party" in Your Genes?. Political Research Quarterly, 62 (3), 584-600. doi: 10.1177/1065912908327606
Carolyn E. Sartor, Michael T. Lynskey, Kathleen K. Bucholz, Pamela A. F. Madden, Nicholas G. Martin and Andrew C. Heath (2009). Timing of first alcohol use and alcohol dependence: evidence of common genetic influences. Addiction, 104 (9), 1512-1518. doi: 10.1111/j.1360-0443.2009.02648.x
Matthew C. Keller, Allan F. McRae, Julie M. McGaughran, Peter M. Visscher, Nicholas G. Martin and Grant W. Montgomery (2009). Non-pathological paternal isodisomy of chromosome 2 detected from a genome-wide SNP scan.. American Journal of Medical Genetics. Part A, 149A (8), 1823-1826. doi: 10.1002/ajmg.a.32973
Falchi, M, Bataille, V, Hayward, NK, Duffy, DL, Bishop, JAN, Pastinen, T, Cervino, A, Zhao, ZZ, Deloukas, P, Soranzo, N, Elder, DE, Barrett, JH, Martin, NG, Bishop, DT, Montgomery, GW and Spector, TD (2009). Genome-wide association study identifies variants at 9p21 and 22q13 associated with development of cutaneous nevi. Nature Genetics, 41 (8), 915-919. doi: 10.1038/ng.410
Bishop, DT, Demenais, F, Iles, MM, Harland, M, Taylor, JC, Corda, E, Randerson-Moor, J, Aitken, JF, Avril, MF, Azizi, E, Bakker, B, Bianchi-Scarra, G, Bressac-de Paillerets, B, Calista, D, Cannon-Albright, LA, Chin-A-Woeng, T, Debniak, T, Galore-Haskel, G, Ghiorzo, P, Gut, I, Hansson, J, Hocevar, M, Hoiom, V, Hopper, JL, Ingvar, C, Kanetsky, PA, Kefford, RF, Landi, MT, Lang, J ... Bishop, JAN (2009). Genome-wide association study identifies three loci associated with melanoma risk. Nature Genetics, 41 (8), 920-925. doi: 10.1038/ng.411
Claire M. A. Haworth, Margaret J. Wright, Nicolas W. Martin, Nicholas G. Martin, Dorret I. Boomsma, Meike Bartels, Danielle Posthuma, Oliver S. P. Davis, Angela M. Brant, Robin P. Corley, John K. Hewitt, William G. Iacono, Matthew McGue, Lee A. Thompson, Sara A. Hart, Stephen A. Petrill, David Lubinski and Robert Plomin (2009). A Twin Study of the Genetics of High Cognitive Ability Selected from 11,000 Twin Pairs in Six Studies from Four Countries. Behavior Genetics, 39 (4), 359-370. doi: 10.1007/s10519-009-9262-3
Martin, Nicolas W., Hansell, Narelle K., Wainwright, Mark A., Shekar, Sri N., Medland, Sarah E., Bates, Timothy C., Burt, Jennifer S., Martin, Nicholas G. and Wright, Margaret J. (2009). Genetic covariation between the author recognition test and reading and verbal abilities: What can we learn from the analysis of high performance?. Behavior Genetics, 39 (4), 417-426. doi: 10.1007/s10519-009-9275-y
Hatemi, Peter K., Funk, Carolyn L., Medland, Sarah E., Maes, Hermine M., Silberg, Judy L., Martin, Nicholas G. and Eaves, Lindon J. (2009). Genetic and Environmental Transmission of Political Attitudes Over a Life Time. Journal of Politics, 71 (3), 1141-1156. doi: 10.1017/S0022381609090938
Sprangers, Mirjam A. G., Sloan, Jeff A., Veenhoven, Ruut, Cleeland, Charles S., Halyard, Michele Y., Abertnethy, Amy R., Baas, Frank, Barsevick, Andrea M., Bartels, Meike, Boomsma, Dorret I., Chauhan, Cynthia, Dueck, Amylou C., Frost, Marlene H., Hall, Per, Klepstad, Pal, Martin, Nicholas G., Miaskowski, Christine, Mosing, Miriam, Movsas, Benjamin, Van Noorden, Cornelis J. F., Patrick, Donald L., Pedersen, Nancy L., Ropka, Mary E., Shi, Quiling, Shinozaki, Gen, Singh, Jasvinder A., Yang, Ping and Zwinderman, Ailko H. (2009). The Establishment of the GENEQOL Consortium to Investigate the Genetic Disposition of Patient-Reported Quality-of-Life Outcomes. Twin Research and Human Genetics, 12 (3), 301-311. doi: 10.1375/twin.12.3.301
Cornes, Belinda K., Medland, Sarah E., Lind, Penelope A., Nyholt, Dale R., Montgomery, Grant W. and Martin, Nicholas G. (2009). Genetic variation in female BMI increases with number of children born but failure to replicate association between GN beta 3 variants and increased BMI in parous females. Twin Research and Human Genetics, 12 (3), 276-285. doi: 10.1375/twin.12.3.276
Penelope A. Lind, Michelle Luciano, Michael A. Horan, Riccardo E. Marioni, Margaret J. Wright, Timothy C. Bates, Patrick Rabbitt, Sarah E. Harris, Yvonne Davidson, Ian J. Deary, Linda Gibbons, Andrew Pickles, William Ollier, Neil Pendleton, Jackie F. Price, Antony Payton and Nicholas G. Martin (2009). No Association Between Cholinergic Muscarinic Receptor 2 (CHRM2) Genetic Variation and Cognitive Abilities in Three Independent Samples. Behavior Genetics, 39 (5), 513-523. doi: 10.1007/s10519-009-9274-z
Brian P. McEvoy, Grant W. Montgomery, Allan F. McRae, Samuli Ripatti, Markus Perola, Tim D. Spector, Lynn Cherkas, Kourosh R. Ahmadi, Dorret Boomsma, Gonneke Willemsen, Jouke J. Hottenga, Nancy L. Pedersen, Patrik K.E. Magnusson, Kirsten Ohm Kyvik, Kaare Christensen, Jaakko Kaprio, Kauko Heikkilä, Aarno Palotie, Elisabeth Widen, Juha Muilu, Ann-Christine Syvänen, Ulrika Liljedahl, Orla Hardiman, Simon Cronin, Leena Peltonen, Nicholas G. Martin and Peter M. Visscher (2009). Geographical structure and differential natural selection among North European populations. Genome Research, 19 (5), 804-814. doi: 10.1101/gr.083394.108
Marijn A. Distel, Irene Rebollo-Mesa, Gonneke Willemsen, Catherine A. Derom, Timothy J. Trull, Nicholas G. Martin and Dorret I. Boomsma (2009). Familial Resemblance of Borderline Personality Disorder Features: Genetic or Cultural Transmission?. PLoS One, 4 (4) e5334, e5334. doi: 10.1371/journal.pone.0005334
Carla Chia Ming Chen, Jonathan M. Keith, Dale R. Nyholt, Nicholas G. Martin and Kerrie L. Mengersen (2009). Bayesian latent trait modeling of migraine symptom data. Human Genetics, 126 (2), 277-288. doi: 10.1007/s00439-009-0671-4
Christopher Oldmeadow, Kerrie Mengersen, Nicholas Martin and David L. Duffy (2009). Heritability and Linkage Analysis of Appendicitis Utilizing Age at Onset. Twin Research and Human Genetics, 12 (2), 150-157. doi: 10.1375/twin.12.2.150
Zhao, ZZ, Duffy, DL, Thomas, SA, Martin, NG, Hayward, NK and Montgomery, GW (2009). Polymorphisms in the syntaxin 17 gene are not associated with human cutaneous malignant melanoma. Melanoma Research, 19 (2), 80-85. doi: 10.1097/CMR.0b013e328322fc45
Loehlin, JC, Medland, SE and Martin, NG (2009). Relative Finger Lengths, Sex Differences, and Psychological Traits. Archives of Sexual Behavior, 38 (2), 298-305. doi: 10.1007/s10508-007-9303-z
Chen, Carla C. M., Mengersen, Kerrie L., Keith, Jonathan M., Martin, Nicholas G. and Nyholt, Dale R. (2009). Linkage and heritability analysis of migraine symptom groupings: A comparison of three different clustering methods on twin data. Human Genetics, 125 (5-6), 591-604. doi: 10.1007/s00439-009-0652-7
Jacqueline M. Vink1, August B. Smit, Eco J.C. de Geus, Patrick Sullivan, Gonneke Willemsen, Jouke-Jan Hottenga, Johannes H. Smit, Witte J. Hoogendijk, Frans G. Zitman, Leena Peltonen, Jaakko Kaprio, Nancy L. Pedersen, Patrik K. Magnusson, Tim D. Spector, Kirsten Ohm Kyvik, Katherine I. Morley, Andrew C. Heath, Nicholas G. Martin, Rudi G.J. Westendorp, P. Eline Slagboom, Henning Tiemeier, Albert Hofman, Andre G. Uitterlinden, Yurii S. Aulchenko, Najaf Amin, Cornelia van Duijn, Brenda W. Penninx and Dorret I. Boomsma (2009). Genome-wide Association Study of Smoking Initiation and Current Smoking. American Journal of Human Genetics, 84 (3), 367-379. doi: 10.1016/j.ajhg.2009.02.001
Madeline H. Meier, Wendy S. Slutske, Andrew C. Heath and Nicholas G. Martin (2009). The Role of Harsh Discipline in Explaining Sex Differences in Conduct Disorder: a Study of Opposite-Sex Twin Pairs. Journal of Abnormal Child Psychology, 37 (5), 653-664. doi: 10.1007/s10802-009-9309-1
Agrawal, Arpana, Pergadia, Michele L., Balasubramanian, Sumitra, Saccone, Scott F., Hinrichs, Anthony L., Saccone, Nancy L., Breslau, Naomi, Johnson, Eric O., Hatsukami, Dorothy, Martin, Nicholas G., Montgomery, Grant W., Goate, Alison M., Rice, John P., Bierut, Laura J. and Madden, Pamela A.F. (2009). Further evidence for an association between the gamma-aminobutyric acid receptor A, subunit 4 genes on chromosome 4 and Fagerstrom test for nicotine dependence. Addiction, 104 (3), 471-477. doi: 10.1111/j.1360-0443.2008.02445.x
Nelson, E. C., Agrawal, A., Pergadia, M. L., Lynskey, M. T., Todorov, A. A., Wang, J. C., Todd, R. D., Martin, N. G., Heath, A. C., Goate, A. M., Montgomery, G. W. and Madden, P. A. F. (2009). Association of childhood trauma exposure and GABRA2 polymorphisms with risk of posttraumatic stress disorder in adults. Molecular Psychiatry, 14 (3), 234-235. doi: 10.1038/mp.2008.81
M. Luciano, F. Miyajima, P. A. Lind, T. C. Bates, M. Horan, S. E. Harris, M. J. Wright, W. E. Ollier, C. Hayward, N. Pendleton, A. J. Gow, P. M. Visscher, J. M. Starr, I. J. Deary, N. G. Martin and A. Payton (2009). Variation in the dysbindin gene and normal cognitive function in three independent population samples. Genes, Brain and Behavior, 8 (2), 218-227. doi: 10.1111/j.1601-183X.2008.00462.x
Tracey D. Wade, Susan A. Treloar, Andrew C. Heath and Nicholas G. Martin (2009). An examination of the overlap between genetic and environmental risk factors for intentional weight loss and overeating. International Journal of Eating Disorders, 42 (6), 492-497. doi: 10.1002/eat.20668
Andrew J. Birley, Michael R. James, Peter A. Dickson, Grant W. Montgomery, Andrew C. Heath, Nicholas G. Martin and John B. Whitfield (2009). ADH single nucleotide polymorphism associations with alcohol metabolism in vivo. Human Molecular Genetics, 18 (8), 1533-1542. doi: 10.1093/hmg/ddp060
Nyholt, Dale R., Gillespie, Nathan G., Merikangas, Kathleen R., Treloar, Susan A., Martin, Nicholas G. and Montgomery, Grant W. (2009). Common genetic influences underlie comorbidity of migraine and endometriosis. Genetic Epidemiology, 33 (2), 105-113. doi: 10.1002/gepi.20361
Wendy S. Slutske, Madeline H. Meier, Gu Zhu, Dixie J. Statham, Alex Blaszczynski and Nicholas G. Martin (2009). The Australian twin study of gambling (OZ-GAM): Rationale, sample description, predictors of participation, and a first look at sources of individual differences in gambling involvement. Twin Research and Human Genetics, 12 (1), 63-78. doi: 10.1375/twin.12.1.63
Hermine H. Maes, Michael C. Neale, Sarah E. Medland, Matthew C. Keller, Nicholas G. Martin, Andrew C. Heath and Lindon J. Eaves (2009). Flexible Mx Specification of Various Extended Twin Kinship Designs. Twin Research and Human Genetics, 12 (1), 26-34. doi: 10.1375/twin.12.1.26
Stuart Macgregor, Penelope A. Lind, Kathleen K. Bucholz, Narelle K. Hansell, Pamela A.F. Madden, Melinda M. Richter, Grant W. Montgomery, Nicholas G. Martin, Andrew C. Heath and John B. Whitfield (2009). Associations of ADH and ALDH2 gene variation with self report alcohol reactions, consumption and dependence: an integrated analysis. Human Molecular Genetics, 18 (3), 580-593. doi: 10.1093/hmg/ddn372
Verweij, K. J. H., Zietsch, B. P., Bailey, J. M. and Martin, N. G. (2009). Shared aetiology of risky sexual behaviour and adolescent misconduct : Genetic and environmental influences. Genes, Brain And Behavior, 8 (1), 107-113. doi: 10.1111/j.1601-183X.2008.00456.x
Michele L. Pergadia, Arpana Agrawal, Anu Loukola, Grant W. Montgomery, Ulla Broms, Scott F. Saccone, Jen C. Wang, Alexandre A. Todorov, Kauko Heikkilä, Dixie J. Statham, Anjali K. Henders, Megan J. Campbell, John P. Rice, Richard D. Todd, Andrew C. Heath, Alison M. Goate, Leena Peltonen, Jaakko Kaprio, Nicholas G. Martin and Pamela A.F. Madden (2009). Genetic linkage findings for DSM-IV nicotine withdrawal in two populations. American Journal of Medical Genetics. Part B: Neuropsychiatric Genetics, 150b (7), 950-959. doi: 10.1002/ajmg.b.30924
Narelle K. Hansell, Arpana Agrawal, John B. Whitfield, Katherine I. Morley, Scott D. Gordon, Penelope A. Lind, Michele L. Pergadia, Grant W. Montgomery, Pamela A. F. Madden, Richard D. Todd, Andrew C. Heath and Nicholas G. Martin (2009). Can We Identify Genes For Alcohol Consumption In Samples Ascertained For Heterogeneous Purposes?. Alcoholism: Clinical and Experimental Research, 33 (4), 729-739. doi: 10.1111/j.1530-0277.2008.00890.x
Zachary A Kaminsky, Thomas Tang, Sun-Chong Wang, Carolyn Ptak, Gabriel H T Oh, Albert H C Wong, Laura A Feldcamp, Carl Virtanen, Jonas Halfvarson, Curt Tysk, Allan F McRae, Peter M Visscher, Grant W Montgomery, Irving I Gottesman, Nicholas G Martin and Art Petronis (2009). DNA methylation profiles in monozygotic and dizygotic twins. Nature Genetics, 41 (2), 240-245. doi: 10.1038/ng.286
Beben Benyamin, Allan F. McRae, Gu Zhu, Scott Gordon, Anjali K. Henders, Aarno Palotie, Leena Peltonen, Nicholas G. Martin, Grant W. Montgomery, John B. Whitfield and Peter M. Visscher (2009). Variants in TF and HFE Explain 40% of Genetic Variation in Serum-Transferrin Levels. American Journal of Human Genetics, 84 (1), 60-65. doi: 10.1016/j.ajhg.2008.11.011
Medland, Sarah E., Duffy, David L., Wright, Margaret J., Geffen, Gina M., Hay, David A., Levy, Florence, Van-Beijsterveldt, Catherina E.M., Willemsen, Gonneke, Townsend, Grant C., White, Vicki, Hewitt, Alex W., Mackey, David A., Bailey, J. Michael, Slutske, Wendy S., Nyholt, Dale R., Treloar, Susan A., Martin, Nicholas G. and Boomsma, Dorret I. (2009). Genetic influences on handedness: Data from 25,732 Australian and Dutch twin families. Neuropsychologia, 47 (2), 330-337. doi: 10.1016/j.neuropsychologia.2008.09.005
Psychiatric GWAS Consortium Coordinating Committee, Martin, N., Wray, N., Mowry, B. and Holliday, E. (2009). Genomewide Association Studies: History, Rationale, and Prospects for Psychiatric Disorders. American Journal of Psychiatry, 166 (5), 540-556. doi: 10.1176/appi.ajp.2008.08091354
Yurii S Aulchenko, Samuli Ripatti, Ida Lindqvist, Dorret Boomsma, Iris M Heid, Peter P Pramstaller, Brenda W J H Penninx, A Cecile J W Janssens, James F Wilson, Tim Spector, Nicholas G Martin, Nancy L Pedersen, Kirsten Ohm Kyvik, Jaakko Kaprio, Albert Hofman, Nelson B Freimer, Marjo-Riitta Jarvelin, Ulf Gyllensten, Harry Campbell, Igor Rudan, Åsa Johansson, Fabio Marroni, Caroline Hayward, Veronique Vitart, Inger Jonasson, Cristian Pattaro, Alan Wright, Nick Hastie, Irene Pichler ... Jouke-Jan Hottenga (2009). Loci influencing lipid levels and coronary heart disease risk in 16 European population cohorts. Nature Genetics, 41 (1), 47-55. doi: 10.1038/ng.269
V. V. McCutcheon, A. C. Heath, E. C. Nelson, K. K. Bucholz, P. A. F. Madden and N. G. Martin (2009). Accumulation of trauma over time and risk for depression in a twin sample. Psychological Medicine, 39 (3), 431-441. doi: 10.1017/S0033291708003759
Cornes, B., Lind, P. A., Medland, S. E., Montgomery, G. W ., Nyholt, D. R. and Martin, N. G . (2009). Replication of the association of common rs9939609 variant of FTO with increased BMI in an Australian adult twin population but no evidence for gene by environment (G × E) interaction. International Journal of Obesity, 33 (1), 75-79. doi: 10.1038/ijo.2008.223
Sullivan, P. F., de Geus, E. J. C., Willemsen, G., James, M. R., Smit, J. H., Zandbelt, T., Martin, N. G., Wray, N. R., Boomsma, D. I. and Penninx, B. W. J. H. (2009). Genome-wide association for major depressive disorder: a possible role for the presynaptic protein piccolo. Molecular Psychiatry, 14 (4), 359-375. doi: 10.1038/mp.2008.125
De Zubicaray, Greig I., Chiang, Ming-Chang, McMahon, Katie L., Shattuck, David W., Toga, Arthur W., Martin, Nicholas G., Wright, Margaret J. and Thompson, Paul M. (2008). Meeting the challenges of neuroimaging genetics. Brian Imaging and Behavior, 2 (4), 258-263. doi: 10.1007/s11682-008-9029-0
Reiersen, Angela M., Constantino, John N., Grimmer, Marisa, Martin, Nicholas G. and Todd, Richard D. (2008). Evidence for shared genetic influences on self-reported ADHD and autistic symptoms in young adult Australian twins. Twin Research and Human Genetics, 11 (6), 579-585. doi: 10.1375/twin.11.6.579
Middelberg, Rita P., Gordon, Scott D., Zhu, Gu, McRae, Allan, Montgomery, Grant W., Martin, Nicholas G. and Whitfield, John B. (2008). Linkage and Association Analyses of Longitudinally Measured Lipid Phenotypes in Adolescence. Twin Research and Human Genetics, 11 (6), 603-620. doi: 10.1375/twin.11.6.603
Agrawal, Arpana, Morley, Katherine I., Hansell, Narelle K., Pergadia, Michele L., Montgomery, Grant W., Statham, Dixie J., Todd, Richard D., Madden, Pamela A. F., Heath, Andrew C., Whitfield, John, Martin, Nicholas G. and Lynskey, Michael T. (2008). Autosomal linkage analysis for cannabis use behaviors in Australian adults. Drug and Alcohol Dependence, 98 (3), 185-190. doi: 10.1016/j.drugalcdep.2008.05.009
Hillmer, Axel M., Brockschmidt, Felix F., Hanneken, Sandra, Eigelshoven, Sibylle, Steffens, Michael, Flaquer, Antonia, Herms, Stefan, Becker, Tim, Kortuem, Anne-Katrin, Nyholt, Dale R., Zhao, Zhen Zhen, Montgomery, Grant W., Martin, Nicholas G., Muehleisen, Thomas W., Alblas, Margrieta A., Moebus, Susanne, Joeckel, Karl-Heinz, Broecker-Preuss, Martina, Erbel, Raimund, Reinartz, Roman, Betz, Regina C., Cichon, Sven, Propping, Peter, Baur, Max P., Wienker, Thomas F., Kruse, Roland and Noethen, Markus M. (2008). Susceptibility variants for male-pattern baldness on chromosome 20p11. Nature Genetics, 40 (11), 1279-1281. doi: 10.1038/ng.228
Nyholt, Dale R., LaForge, K. Steven, Kallela, Mikko, Alakurtti, Kirsi, Anttila, Verneri, Farkkila, Markus, Hamalainen, Eija, Kaprio, Jaakko, Kaunisto, Mari A., Heath, Andrew C., Montgomery, Grant W., Goebel, Hartmut, Todt, Unda, Ferrari, Michel D., Launer, Lenore J., Frants, Rune R., Terwindt, Gisela M., de Vries, Boukje, Verschuren, W. M. Monique, Brand, Jan, Freilinger, Tobias, Pfaffenrath, Volker, Straube, Andreas, Ballinger, Dennis G., Zhan, Yiping, Daly, Mark J., Cox, David R., Dichgans, Martin, van den Maagdenberg, Arn M. J. M. ... Palotie, Aarno (2008). A high-density association screen of 155 ion transport genes for involvement with common migraine. Human Molecular Genetics, 17 (21), 3318-3331. doi: 10.1093/hmg/ddn227
Bates, Timothy C., Luciano, Michelle, Lind, Penelope A., Wright, Margaret J., Montgomery, Grant W. and Martin, Nicholas G. (2008). Recently-derived variants of brain-size genes ASPM, MCPH1, CDK5RAP and BRCA1 not associated with general cognition, reading or language. Intelligence, 36 (6), 689-693. doi: 10.1016/j.intell.2008.04.001
Zietsch, Brendan P., Morley, Katherine I., Shekar, Sri N., Verweij, Karin J. H., Keller, Matthew C., Macgregor, Stuart, Wright, Margaret J., Bailey, J. Michael and Martin, Nicholas G. (2008). Genetic factors predisposing to homosexuality may increase mating success in heterosexuals. Evolution and Human Behavior, 29 (6), 424-433. doi: 10.1016/j.evolhumbehav.2009.07.002
Byrne, Enda M., Mcrae, Allan F., Zhao, Zhen-Zhen, Martin, Nicholas G., Montgomery, Grant W. and Visscher, Peter M. (2008). The use of common mitochondrial variants to detect and characterise population structure in the Australian population: Implications for genome-wide association studies. European Journal of Human Genetics, 16 (11), 1396-1403. doi: 10.1038/ejhg.2008.117
Agrawal, Arpana, Lynskey, Michael T., Pergadia, Michele L., Bucholz, Kathleen K., Heath, Andrew C., Martin, Nicholas G. and Madden, Pamela A. F. (2008). Early cannabis use and DSM-IV nicotine dependence: A twin study. Addiction, 103 (11), 1896-1904. doi: 10.1111/j.1360-0443.2008.02354.x
Waldron, Mary, Heath, Andrew C., Bucholz, Kathleen K., Madden, Pamela A. F. and Martin, Nicholas G. (2008). Alcohol Dependence and Reproductive Onset: Findings in Two Australian Twin Cohorts. Alcoholism-Clinical and Experimental Research, 32 (11), 1865-1874. doi: 10.1111/j.1530-0277.2008.00771.x
Anderson, Carl A., Zhu, Gu, Falchi, Mario, van den Berg, Stéphanie M., Treloar, Susan A., Spector, Timothy D., Martin, Nicholas G., Boomsma, Dorret I., Visscher, Peter M. and Montgomery, Grant W. (2008). A genome-wide linkage scan for age at menarche in three populations of European descent. Journal of Clinical Endocrinology and Metabolism., 93 (10), 3965-3970. doi: 10.1210/jc.2007-2568
Lind, Penelope A., Macgregor, Stuart, Agrawal, Arpana, Montgomery, Grant W., Heath, Andrew C., Martin, Nicholas G. and Whitfield, John B. (2008). The role of GABRA2 in alcohol dependence, smoking, and illicit drug use in an Australian population sample. Alcoholism: Clinical and Experimental Research, 32 (10), 1721-1731. doi: 10.1111/j.1530-0277.2008.00768.x
Wade, T. D., Treloar, S. and Martin, N. G. (2008). Shared and unique risk factors between lifetime purging and objective binge eating: A twin study. Psychological Medicine, 38 (10), 1455-1464. doi: 10.1017/S0033291708002791
Zhao, Zhen Zhen, Painter, Jodie N., Palmer, James S., Webb, Penelope M., Hayward, Nicholas K., Whiteman, David C., Boomsma, Dorret I., Martin, Nicholas G., Duffy, David L. and Montgomery, Grant W. (2008). Variation in bone morphogenetic protein 15 is not associated with spontaneous human dizygotic twinning. Human Reproduction, 23 (10), 2372-2379. doi: 10.1093/humrep/den268
Macgregor, Stuart, Hottenga, Jouke-Jan, Lind, Penelope A., Suchiman, H. Eka D., Willemsen, Gonneke, Slagboom, P. Eline, Montgomery, Grant W., Martin, Nicholas G., Visscher, Peter M. and Boomsma, Dorret I. (2008). Vitamin D receptor gene polymorphisms have negligible effect on human height. Twin Research and Human Genetics, 11 (5), 488-494. doi: 10.1375/twin.11.5.488
Hur, Y-M, Kaprio, J., Iacono, W. G., Boomsma, D. I., McGgue, M., Silventoinen, K., Martin, N. G., Luciano, M., Visscher, P. M., Rose, R. J., He, M., Ando, J., Ooki, S., Nonaka, K., Lin, C. C. H., Lajunen, H. R., Cornes, B. K., Bartels, M., van Beijsterveldt, C. E. M., Cherny, S. S. and Mitchell, K. (2008). Genetic influences on the difference in variability of height, weight and body mass index between Caucasian and East Asian adolescent twins. International Journal of Obesity, 32 (10), 1455-1467. doi: 10.1038/ijo.2008.144
Schermer, Julie Aitken, Feather, N. T., Zhu, Gu and Martin, Nicholas G. (2008). Phenotypic, Genetic, and Environmental Properties of the Portrait Values Questionnaire. Twin Research and Human Genetics, 11 (5), 531-537. doi: 10.1375/twin.11.5.531
Distel, M. A., Trull, T. J., Derom, C. A., Thiery, E. W., Grimmer, M. A., Martin, N. G., Willemsen, G. and Boomsma, D. I. (2008). Heritability of borderline personality disorder features is similar across three countries. Psychological Medicine, 38 (9), 1219-1229. doi: 10.1017/S0033291707002024
Lundmark, Per E., Liljedahl, Ulrika, Boomsma, Dorret I., Mannila, Heikki, Martin, Nicholas G., Palotie, Aarno, Peltonen, Leena, Perola, Markus, Spector, Tim D. and Syvanen, Ann-Christine (2008). Evaluation of HapMap data in six populations of European descent. European Journal of Human Genetics, 16 (9), 1142-1150. doi: 10.1038/ejhg.2008.77
Slutske, Wendy S., D'Onofrio, Brian M., Turkheimer, Eric, Emery, Robert E., Harden, K. Paige, Heath, Andrew C. and Martin, Nicholas G. (2008). Searching for an environmental effect of parental alcoholism on offspring alcohol use disorder: A genetically informed study of children of alcoholics. Journal of Abnormal Psychology, 117 (3), 534-551. doi: 10.1037/a0012907
Oldmeadow, Chris, Wood, Ian, Mengersen, Kerrie, Visscher, Peter M., Martin, Nicholas G. and Duffy, David L. (2008). Investigation of the relationship between smoking and appendicitis in Australian twins. Annals of Epidemiology, 18 (8), 631-636. doi: 10.1016/j.annepidem.2008.04.004
Wright, A. D., Martin, N. and Dodson, P. M. (2008). Homocysteine, folates, and the eye. Eye, 22 (8), 989-993. doi: 10.1038/sj.eye.6703061
Martin, Nick (2008). Welcome - Human genetics society of Australasia. Twin Research and Human Genetics, 11 (4), III-III. doi: 10.1375/twin.11.4.iii
O'Connor, Daniel T., Zhu, Gu, Rao, Fangwen, Taupenot, Laurent, Fung, Maple M., Das, Madhusudan, Mahata, Sushil K., Mahata, Manjula, Wang, Lei, Zhang, Kuixing, Greenwood, Tiffany A., Shih, Pei-an Betty, Cockburn, Myles G, Ziegler, Michael G., Stridsberg, Mats, Martin, Nicholas G. and Whitfield, John B. (2008). Heritability and genome-wide linkage in US and Australian twins identify novel genomic regions controlling chromogranin A. Circulation, 118 (3), 247-257. doi: 10.1161/CIRCULATIONAHA.107.709105
Middeldorp, CM, Sullivan, PF, Wray, NR, Hottenga, JJ, de Geus, EJC, van den Berg, M, Montgomery, GW, Coventry, WL, Statham, DJ, Andrews, G, Slagboom, PE, Boomsma, DI and Martin, NG (2008). Suggestive linkage on chromosome 2, 8, and 17 for lifetime major depression. American Journal of Medical Genetics Part B: Neuropsychiatric Genetics, 150B (3), 352-358. doi: 10.1002/ajmg.b.30817
Whitfield, John B., Day, Veronica, Madden, Pamela A. F., Heath, Andrew C., Martin, Nicholas G. and Montgomery, Grant W. (2008). Measuring carbohydrate-deficient transferrin by direct immunoassay: factors affecting diagnostic sensitivity for excessive alcohol intake. Clinical Chemistry, 54 (7), 1158-1165. doi: 10.1373/clinchem.2007.101733
Webbink, Dinand, Martin, Nicholas G. and Visscher, Peter M. (2008). Does teenage childbearing increase smoking, drinking and body size?. Journal of Health Economics, 27 (4), 888-903. doi: 10.1016/j.jhealeco.2008.02.005
Brown, K. M., MacGregor, S., Montgomery, G. W., Craig, D. W., Zhao, Z. Z., Iyadurai, K., Henders, A. K., Homer, N., Campbell, M. J., Stark, M., Thomas, S., Schmid, H., Maskiell, J. A., Jetann, J., Ferguson, M., Stephan, D. A., Cust, A. E., Whiteman, D. C., Green, A., Olsson, H., Puig, S., Ghiorzo, P., Hansson, J., Demenais, F., Goldstein, A. M., Gruis, N. A., Elder, D. E., Newton Bishop, J., Kefford, R. F. ... Hayward, N. (2008). Common sequence variants on 20q11.22 confer melanoma susceptibility. Nature Genetics, 40 (7), 838-840. doi: 10.1038/ng.163
Agrawal, Arpana, Pergadia, Michele. L., Saccone, Scott F., Lynskey, Michael T., Wang, Jen C., Martin, Nicholas G., Statham, Dixie, Henders, Anjali, Campbell, Megan, Garcia, Robertino, Broms, Ulla, Todd, Richard D., Goate, Alison M., Rice, John, Kaprio, Jaakko, Heath, Andrew C., Montgomery, Grant W. and Madden, Pamela A. F. (2008). An autosomal linkage scan for cannabis use disorders in the nicotine addiction genetics project. Archives of General Psychiatry, 65 (6), 713-722. doi: 10.1001/archpsyc.65.6.713
Agrawal, Arpana, Pergadia, Michele L., Saccone, Scott F., Hinrichs, Anthony L., Lessov-Schlaggar, Christina N., Saccone, Nancy L., Neuman, Rosalind J., Breslau, Naomi, Johnson, Eric, Hatsukami, Dorothy, Montgomery, Grant W., Heath, Andrew C., Martin, Nicholas G., Goate, Alison M., Rice, John P., Bierut, Laura J. and Madden, Pamela A. F. (2008). Gamma-aminobutyric acid receptor genes and nicotine dependence: Evidence for association from a case-control study. Addiction, 103 (6), 1027-1038. doi: 10.1111/j.1360-0443.2008.02236.x
Wainwright, Mark A., Wright, Margaret J., Luciano, Michelle, Geffen, Gina M. and Martin, Nicholas G. (2008). Genetic covariation among facets of openness to experience and general cognitive ability. Twin Research and Human Genetics, 11 (3), 275-286. doi: 10.1375/twin.11.3.275
Zhu, Gu, Hewitt, Alex W., Ruddle, Jonathan B., Kearns, Lisa S., Brown, Shayne A., Mackinnon, Jane R., Chen, Christine Y., Hammond, Christopher J., Craig, Jamie E., Montgomery, Grant W., Martin, Nicholas G. and Mackey, David A. (2008). Genetic Dissection of Myopia Evidence for Linkage of Ocular Axial Length to Chromosome 5q. Ophthalmology, 115 (6), 1053-1057. doi: 10.1016/j.ophtha.2007.08.013
Conference Papers
Ceja, Zuriel, Edwards, Alexis, Martin, Nick, Hickie, Ian, Medland, Sarah E. and Rentería, Miguel E. (2024). Genetic And Psychological Predictors Of Suicidal Behavior: Insights From Polygenic Risk Scores And Mental Health Diagnoses. World Congress of Psychiatric Genetics WCPG 2024, Singapore, 15-19 October 2024. Amsterdam, Netherlands: Elsevier. doi: 10.1016/j.euroneuro.2024.08.324
Werwath, Kathryn, Lawn, Rebecca, Salem, Madeleine, Li, Tayden, Gordon, Scott, Shen, Hanyang, Mitchell, Brittany, Kung, Benson, Stafford, Ciera, Vemuri, Mytilee, Ratanatharathorn, Andrew, Meijsen, Joeri, Medland, Sarah E., Martin, Nicholas G. and Duncan, Laramie (2024). Trans-ancestry GWAS Of Hot Flushes Reveals Potent Treatment Target, Overlap With Psychiatric Disorders, And Cell Types Matching Known Hot Flash Neurons. World Congress of Psychiatric Genetics WCPG 2024, Singapore, 15-19 October 2024. Amsterdam, Netherlands: Elsevier. doi: 10.1016/j.euroneuro.2024.08.207
Lind, Penelope A., Martin, Nicholas G. and Medland, Sarah E. (2024). A Genome-wide Association Meta-analysis Of Lithium Response Including The Recently Recruited Australian Genetics Of Bipolar Disorder Study. World Congress of Psychiatric Genetics WCPG 2024, Singapore, 15-19 October 2024. Amsterdam, Netherlands: Elsevier. doi: 10.1016/j.euroneuro.2024.08.458
Mitchell, Brittany, Martin, Nick and Medland, Sarah E. (2024). Genetic And Environmental Predictors Of Treatment Resistant Depression. World Congress of Psychiatric Genetics WCPG 2024, Singapore, 15-19 October 2024. Amsterdam, Netherlands: Elsevier. doi: 10.1016/j.euroneuro.2024.08.067
Lupton, Michelle K., Gomez, Lina, Mitchell, Brittany L., Adsett, Jessica, García‐Marín, Luis M., Renteria, Miguel E., McAloney, Kerrie, Ceslis, Amelia, Thienel, Renate, Robinson, Gail, Breakspear, Michael and Martin, Nicholas G (2023). Poorer online cognitive performance is associated with genetic risk for Alzheimer’s disease and brain phenotypes in healthy mid‐life and older adults. AAIC 2023 Abstracts, Amsterdam, Netherlands, 16-20 July 2023. Hoboken, NJ USA: Wiley. doi: 10.1002/alz.078078
Thienel, Renate, Borne, Léonie, Faucher, Caroline, Robinson, Gail, Fripp, Jurgen, Giorgio, Joseph, Martin, Nicholas G., Breakspear, Michael and Lupton, Michelle K. (2023). Can an online battery match in‐person cognitive testing in predicting age‐related cortical changes. Alzheimer’s Association International Conference AAIC 2023, Amsterdam, Netherlands, 16-20 July 2023. Hoboken, NJ United States: John Wiley & Sons. doi: 10.1002/alz.074476
Mitchell, Brittany, Morosoli, José, Martin, Nicholas G., Lind, Penelope A., Hickie, Ian B., Medland, Sarah E. and Wray, Naomi (2023). Characterising antidepressant usage based on electronic prescription records in the Australian Genetics of Depression Study. World Congress of Psychiatric Genetics (WCPG), Montreal, Canada, 10-14 October 2023. Amsterdam, Netherlands: Elsevier. doi: 10.1016/j.euroneuro.2023.08.422
Ma, X., Shah, A., Fairlie, T., Martin, N., Jones, M., Koloski, N., Morrison, M. and Holtmann, G. (2023). Small intestinal bacterial overgrowth in patients with intestinal failure: A systematic review and meta-analysis. Gastroenterological Society of Australia (GESA) Australian Gastroenterology Week (AGW) 2023, Brisbane, QLD Australia, 2-5 September 2023. Richmond, VIC Australia: John Wiley & Sons.
Kholghi, Mahnoosh, Fazlollahi, Amir, Lupton, Michelle K., Bourgeat, Pierrick, Zhang, Qing, Martin, Nicholas G., Breakspear, Michael, Fripp, Jurgen and PISA (Prospective Imaging Study of Aging: Genes, Brain and Behaviour) (2023). The association between sleep restlessness and neuroimaging biomarkers of Alzheimer’s Disease in mid‐life to older adults and patients. Alzheimer's Association International Conference (AAIC) 2022, San Diego, CA United States, 31 July - 4 August 2022. Hoboken, NJ United States: John Wiley & Sons. doi: 10.1002/alz.062017
Mitchell, B., Saklatvala, J., Martin, N.G., Smith, C., Barker, J., Renteria, M. and Simpson, M. (2022). Exploring the relationship between acne and mental health. 51st Annual ESDR Meeting, Amsterdam, Netherlands, 28 September-1 October 2022. Oxford, United Kingdom: Elsevier. doi: 10.1016/j.jid.2022.09.318
Hopkins, Kristen L., Lind, Penelope A., Mitchell, Brittany L., Whiteman, David C., Olsen, Catherine M., Siskind, Dan J., Hickie, Ian B., Martin, Nicholas G. and Medland, Sarah E. (2022). Can polygenic Risk Scores Predict Who Will Receive or Respond Better to Electroconvulsive Therapy for Treatment of Major Depressive Disorder?. 51st Annual Meeting of the Behavior-Genetics-Association (BGA), Los Angeles Ca, Jun 22-25, 2022. NEW YORK: SPRINGER.
Medland, Sarah E., Mitchell, Brittany, Campos, Adrian, Whiteman, David C., Olsen, Catherine M., Siskind, Dan J., Hickie, Ian, Lind, Penelope A. and Martin, Nicholas G. (2022). Challenges to Incorporating Polygenic Risk Scores in Clinical Mental Health Practice. 51st Annual Meeting of the Behavior-Genetics-Association (BGA), Los Angeles Ca, Jun 22-25, 2022. NEW YORK: SPRINGER.
Campos, Adrian I., Garcia-Marin, Luis M., Christensen, Helen, Batterham, Philip J., van Velzen, Laura S., Schmaal, Lianne, Rabinowitz, Jill A., Jahanshad, Neda, Martin, Nicholas G., Cuellar-Partida, Gabriel, Ruderfer, Douglas M., Mullins, Niamh and Renteria, Miguel E. (2022). Genomics Driven Screening for Causal Determinants of Suicide Attempt. SOBP 77th Annual Scientific Meeting, New Orleans, LA United States, 28-30 April 2022. Philadelphia, PA United States: Elsevier.
Lupton, Michelle K., McAloney, Kerrie, Ceslis, Amelia, Robinson, Gail, Thienel, Renate, Breakspear, Michael and Martin, Nicholas G. (2021). The use of online testing to assess cognitive differences in healthy individuals at high genetic risk of Alzheimer's disease. 2021 Alzheimer's Association International Conference, Denver, CO United States, 26 - 30 July 2021. Hoboken, NJ United States: John Wiley & Sons. doi: 10.1002/alz.055369
Thorp, Jackson G., Campos, Adrian I., Grotzinger, Andrew D., Gerring, Zachary, An, Jiyuan, Ong, Jue-Sheng, Wang, Wei, Shringarpure, Suyash, Byrne, Enda M., MacGregor, Stuart, Martin, Nicholas G., Medland, Sarah E., Middeldorp, Christel M. and Derks, Eske M. (2020). Symptom-level genetic modelling identifies novel risk loci and unravels the shared genetic architecture of anxiety and depression. 50th Annual Meeting of the Behavior-Genetics-Association (BGA), Electr Network, Jun 26, 2020. NEW YORK: SPRINGER.
Campos, Adrián I., Roughan, William H., García-Marin, Luis M., Cuéllar-Partida, Gabriel, Lupton, Michelle K., Hickie, Ian B., Medland, Sarah E., Wray, Naomi R., Byrne, Enda M., Ngo, Trung T., Martin, Nicholas G. and Rentería, Miguel E. (2020). The relationship between comorbid chronic pain and poorer self-reported antidepressant efficacy is partly mediated by genetics. Virtual 2020 World Congress of Psychiatric Genetics (WCPG), Online, 16–22 October 2020.
Hubel, C., Watson, H. J., Yilmaz, Z., Landen, M., Martin, N. G., Mortensen, P., Sullivan, P. F., Breen, G. and Bulik, C. M. (2019). Anorexia nervosa genome-wide association study identifies eight loci and implicates psychiatric and metabolic origins. 52nd Conference of the European-Society-of-Human-Genetics (ESHG), Gothenburg Sweden, Jun 15-18, 2019. LONDON: NATURE PUBLISHING GROUP.
Hwang, Liang-Dar, Gharahkhani, Puya, Zhu, Gu, Gordon, Scott D., Breslin, Paul A. S., Martin, Nicholas G., Reed, Danielle R. and Wright, Margaret J. (2018). Replication and discovery of genetic variants influencing human bitter taste perception. 39th Annual Meeting of the Association for Chemoreception Sciences, Bonita Springs, FL, United States, 26 - 29 April 2017. Oxford, United Kingdom: Oxford University Press. doi: 10.1093/chemse/bjy003
Cuéllar-Partida, Gabriel, Ngo, Trung T., Couvy-Duchesne, Baptiste, Rentería, Miguel E., Colodro Conde, Lucia, Gordon, Scott D., Hansell, Narelle K., Medland, Sarah E., Wright, Margaret J. and Martin, Nicholas G. (2017). A perceptual endophenotype for mental illness: Characterising normal genetic variation in the trait. BLiSS 2017 — Brisbane Life Science ECR Symposium, Translational Research Institute, Brisbane, 24 November 2017.
Ngo, Trung T., Cuéllar-Partida, Gabriel, Couvy-Duchesne, Baptiste, Rentería, Miguel E., Colodro Conde, Lucia, Gordon, Scott D., Hansell, Narelle K., Medland, Sarah E., Wright, Margaret J. and Martin, Nicholas G. (2017). GWAS of complementary perceptual endophenotype measures: How do they rate?. Australasian Society for Bipolar & Depressive Disorders (ASBDD) 2017 Conference, Deakin Edge, Melbourne, 15–17 September 2017.
Dennis, Emily L., Rashid, Faisal, Faskowitz, Josh, Jin, Yan, McMahon, Katie L., de Zubicaray, Greig I., Martin, Nicholas G., Hickie, Ian B., Wright, Margaret J., Jahanshad, Neda and Thompson, Paul M. (2017). Mapping age effects along fiber tracts in young adults. 2017 IEEE 14th International Symposium on Biomedical Imaging (ISBI 2017),, Melbourne, VIC, Australia, 18-21 April 2017. NEW YORK: IEEE. doi: 10.1109/ISBI.2017.7950478
Pizzagalli, Fabrizio, Auzias, Guillaume, Kochunov, Peter, Faskowitz, Joshua I., McMahon, Katie L., De Zubicaray, Greig I., Martin, Nicholas G., Wright, Margaret J., Jahanshad, Neda and Thompson, Paul M. (2016). Genetic analysis of cortical sulci in 1,009 adults. 2016 IEEE 13th International Symposium on Biomedical Imaging: From Nano to Macro, ISBI 2016, Prague, Czech Republic, 13-16 April 2016. Piscataway, NJ, United States: Institute of Electrical and Electronics Engineers. doi: 10.1109/ISBI.2016.7493395
Shen, Kaikai, Dore, Vincent, Rose, Stephen, Fripp, Jurgen, McMahon, Katie L., de Zubicaray, Greig I., Martin, Nicholas G., Thompson, Paul M., Wright, Margaret J. and Salvado, Olivier (2015). Heritability analysis of surface-based cortical thickness estimation on a large twin cohort. Medical Imaging 2015: Image Processing, Orlando, Florida, United States, Feb 24-26, 2015. Bellingham, WA United States: SPIE. doi: 10.1117/12.2081677
Zhan, L., Jahanshad, N., Faskowitz, J., Zhu, D., Prasad, G., Martin, N. G., de Zubicaray, G. I., McMahon, K. L., Wright, M. J. and Thompson, P. M. (2015). Heritability of brain network topology in 853 twins and siblings. IEEE 12th International Symposium on Biomedical Imaging, New York, United States, Apr 16-19, 2015. Piscataway, NJ, United States: IEEE. doi: 10.1109/ISBI.2015.7163908
Zhu, Dajiang, Zhan, Liang, Faskowitz, Joshua, Daianu, Madelaine, Jahanshad, Neda, De Zubicaray, Greig I., McMahon, Katie L., Martin, Nicholas G., Wright, Margaret J. and Thompson, Paul M. (2015). Genetic analysis of structural brain connectivity using DICCCOL models of diffusion MRI in 522 twins. IEEE 12th International Symposium on Biomedical Imaging, New York, United States, Apr 16-19, 2015. Piscataway, NJ, United States: IEEE. doi: 10.1109/ISBI.2015.7164080
Hwang, Liang-Dar, Zhu, Gu, Wright, Margaret J., Martin, Nicholas G., Reed, Danielle R. and Breslin, Paul A. S. (2015). Genetic Modeling of Human Intensity Ratings of Four Sweeteners. 15th Scientific Meeting of the Australasian Association for ChemoSensory Science (AACSS), Brisbane, QLD Australia, 03-05 December 2014. Oxford, United Kingdom: Oxford University Press. doi: 10.1093/chemse/bjv008
Warstadt, Nicholus M., Jahanshad, Neda, Dennis, Emily L., Kohannim, Omid, McMahon, Katie L., de Zubicaray, Greig I., Montgomery, Grant W., Henders, Anjali K., Martin, Nicholas G., Whitfield, John B., Wright, Margaret J. and Thompson, Paul M. (2014). Identifying candidate gene effects by restricting search space in a multivariate genetic analysis of white matter microstructure. Biomedical Imaging ISBI, Beijing, China, 29 April - 2 May, 2014. Piscataway, NJ, United States: IEEE. doi: 10.1109/ISBI.2014.6867881
Jahanshad, Neda, Kochunov, Peter, Nichols, Thomas E., Sprooten, Emma, Mandl, Rene C., Almasy, Laura, Brouwer, Rachel M., Curran, Joanne E., de Zubicaray, Greig I., Dimitrova, Rali, Fox, Peter T., Hong, L. Elliot, Landman, Bennett A., Lemaitre, Herve, Lopez, Lorna, Martin, Nicholas G., McMahon, Katie L., Mitchell, Braxton D., Olvera, Rene L., Peterson, Charles P., Sussmann, Jessika E., Toga, Arthur W., Wardlaw, Joanna M., Wright, Margaret J., Wright, Susan N., Bastin, Mark E., McIntosh, Andrew M., Boomsma, Dorret I., Kahn, Rene S. ... Thompson, Paul M. (2014). Combining meta- and mega- analytic approaches for multi-site diffusion imaging based genetic studies: From the ENIGMA-DTI working group. 11th IEEE International Symposium on Biomedical Imaging (ISBI), Beijing, Peoples Republic of China, 29 April-02 May 2014. Piscataway, NJ., United States: IEEE. doi: 10.1109/ISBI.2014.6868099
Mitchem, Dorian, Purkey, Alicia, Grebe, Nicholas, Carey, Greg, Garver-Apgar, Christine, Bates, Timothy, Arden, Rosalind, Hewitt, John, Medland, Sarah, Martin, Nick G., Zietsch, Brendan and Keller, Matthew (2013). Estimating the sex-specific effects of genes on facial attractiveness and sexual dimorphism. 43rd Annual Meeting of the Behavior-Genetics-Association, Marseille France, Jun 28-Jul 02, 2013. NEW YORK: SPRINGER.
Jin, Yan, Shi, Yonggang, Zhan, Liang, de Zubicaray, Greig I., McMahon, Katie L., Martin, Nicholas G., Wright, Margaret J. and Thompson, Paul M. (2013). Labeling white matter tracts in hardi by fusing multiple tract atlases with applications to genetics. 2013 IEEE 10th International Symposium on Biomedical Imaging: From Nano to Macro, ISBI 2013, San Francisco, CA, United States, 7-11 April 2013. Piscataway, NJ, United States: IEEE. doi: 10.1109/ISBI.2013.6556524
Zhan, Liang, Jahanshad, Neda, Jin, Yan, Toga, Arthur W., McMahon, Katie L., de Zubicaray, Greig I., Martin, Nicholas G., Wright, Margaret J. and Thompson, Paul M. (2013). Brain network efficiency and topology depend on the fiber tracking method: 11 tractography algorithms compared in 536 subjects. 2013 IEEE 10th International Symposium on Biomedical Imaging: From Nano to Macro, ISBI 2013, San Francisco, CA, United States, 7-11 April 2013. Piscataway, NJ, United States: IEEE. doi: 10.1109/ISBI.2013.6556679
Jahanshad, Neda, Bhatt, Priya, Hibar, Derrek P., Villalon, Julio E., Nir, Talia M., Toga, Arthur W., Jack Jr., Clifford R., Bernstein, Matt A. B, Weiner, Michael W., McMahon, Katie L., de Zubicaray, Greig I., Martin, Nicholas G., Wright, Margaret J. and Thompson, Paul M. (2013). Bivariate genome-wide association study of genetically correlated neuroimaging phenotypes from DTI and MRI through a seemingly unrelated regression model. 3rd International Workshop on Multimodal Brain Image Analysis, MBIA 2013, Held in Conjunction with the 16th International Conference on Medical Image Computing and Computer Assisted Intervention, MICCAI 2013, Nagoya, Japan, 22 September 2013. Heidelberg, Germany: Springer. doi: 10.1007/978-3-319-02126-3_19
Ebejer, Jane, Medland, Sarah, Martin, Nick G., Wright, Margaret, Montgomery, Grant, Powell, Joseph, Visscher, Peter and Duffy, David (2013). Clarification of varying genetic expression and structure within adolescent monozygotic and dizygotic twins discordant for high and low attention and activity. 43rd Annual Meeting of the Behavior-Genetics-Association, Marseille France, 28 June-02 July 2013. New York, NY United States: Springer New York LLC. doi: 10.1007/s10519-013-9623-9
Jahanshad, Neda, Kochunov, Peter, Glahn, David C., Blangero, John, Nichols, Thomas E., McMahon, Katie L., de Zubicaray, Greig I., Martin, Nicholas G., Wright, Margaret J., Jack, Jr., Clifford R., Bernstein, Matt A., Weiner, Michael W., Toga, Arthur W. and Thompson, Paul M. (2013). Power estimates for voxel-based genetic association studies using diffusion imaging. MMBC 2013: Mathematical Methods for Brain Connectivity. Held in conjunction with MICCAI 2013: The 16th International Conference on Medical Image Computing and Computer Assisted Intervention Workshops, Nagoya, Japan, 22 September, 2013. Cham, Switzerland: Springer International Publishing. doi: 10.1007/978-3-319-02475-2_21
Hibar, Derrek P., Medland, Sarah E., Stein, Jason L., Kim, Sungeun, Shen, Li, Saykin, Andrew J., de Zubicaray, Greig I., McMahon, Katie L, Montgomery, Grant W., Martin, Nicholas G., Wright, Margaret J., Djurovic, Srdjan, Agartz, Ingrid A., Andreassen, Ole A. and Thompson, Paul M. (2013). Genetic clustering on the hippocampal surface for genome-wide association studies. 16th International Conference on Medical Image Computing and Computer Assisted Intervention, MICCAI 2013, Nagoya, Japan, 22-26 September 2013. Berlin, Germany: Springer. doi: 10.1007/978-3-642-40763-5_85
Hibar, Derrek P., Stein, Jason L., Jahanshad, Neda, Kohannim, Omid, Toga, Arthur W., McMahon, Katie L., de Zubicaray, Greig I., Montgomery, Grant W., Martin, Nicholas G., Wright, Margaret J., Weiner, Michael W. and Thompson, Paul M. (2013). Exhaustive search of the SNP-SNP interactome identifies epistatic effects on brain volume in two cohorts. 16th International Conference on Medical Image Computing and Computer Assisted Intervention, MICCAI 2013, Nagoya, Japan, 22-26 September 2013. Berlin, Germany: Springer. doi: 10.1007/978-3-642-40760-4_75
Jahanshad, Neda, Kohannim, Omid, Toga, Arthur W., McMahon, Katie L., de Zubicaray, Greig I., Hansell, Narelle K., Montgomery, Grant W., Martin, Nicholas G., Wright, Margaret J. and Thompson, Paul M. (2012). Diffusion imaging protocol effects on genetic associations. International Symposium on Biomedical Imaging, Barcelona, Spain, 2-5 May 2012. NEW YORK: IEEE. doi: 10.1109/ISBI.2012.6235712
Daianu, Madelaine, Jahanshad, Neda, Dennis, Emily L., Toga, Arthur W., McMahon, Katie L., de Zubicaray, Greig I., Martin, Nicholas G., Wright, Margaret J., Hickie, Ian B. and Thompson, Paul M. (2012). Left versus right hemisphere differences in brain connectivity: 4-Tesla HARDI tractography in 569 twins. 9th IEEE International Symposium on Biomedical Imaging (ISBI) - From Nano to Macro, Barcelona Spain, 2 - 5 May 2012. Piscataway, NJ, United States: IEEE (Institute for Electrical and Electronic Engineers). doi: 10.1109/ISBI.2012.6235601
Jin, Yan, Shi, Yonggang, Zhan, Liang, Li, Junning, de Zubicaray, Greig I., McMahon, Katie L., Martin, Nicholas G., Wright, Margaret J. and Thompson, Paul M. (2012). Automatic population HARDI white matter tract clustering by label fusion of multiple tract atlases. Second International Multimodal Brain Image Analysis Workshop (MBIA 2012) in Conjunction with MICCAI 2012, Nice, France, 1 - 5 October 2012. Heidelberg, Germany: Springer. doi: 10.1007/978-3-642-33530-3_12
Joshi, S. H., Joshi, A. A., Gutman, B., Toga, A. W., McMahon, K., de Zubicaray, G., Martin, N., Wright, M. and Thompson, P. M. (2012). Genetic influences on sulcal patterns of the brain. 9th International Symposium on Biomedical Imaging, Barcelona, Spain, 2 - 5 May 2012. Piscataway, NJ, United States: IEEE (Institute for Electrical and Electronic Engineers). doi: 10.1109/ISBI.2012.6235572
Dennis, Emily L., Jahanshad, Neda, Toga, Arthur W., Johnson, Kori, McMahon, Katie L., de Zubicaray, Greig I., Montgomery, Grant W., Martin, Nicholas G., Wright, Margaret J. and Thompson, Paul M. (2012). Changes in Anatomical Brain Connectivity Between Ages 12 and 30: A HARDI Study of 484 Adolescents and Adults. 9th IEEE International Symposium on Biomedical Imaging, Barcelona, Spain, 2-5 May 2012. Piscataway NJ, United States: IEEE. doi: 10.1109/ISBI.2012.6235695
Wheland, D., Joshi, A., McMahon, K., Hansell, N., Martin, N., Wright, M., Thompson, P., Shattuck, D. and Leahy, R. (2012). Robust identification of partial-correlation based networks with applications to cortical thickness data. 9th IEEE International Symposium on Biomedical Imaging: From Nano to Macro, ISBI 2012, Barcelona, Spain, 2 - 5 May 2012. Piscataway, NJ United States: I E E E. doi: 10.1109/ISBI.2012.6235869
Jahanshad, Neda, Hibar, Derrek, Ryles, April, Toga, Arthur W., McMahon, Katie L., de Zubicaray, Greig I., Hansel, Narelle K., Montgomery, Grant W., Martin, Nicholas G., Wright, Margaret J. and Thompson, Paul M. (2012). Discovery of genes that affect human brain connectivity: a genome-wide analysis of the connectome. 9th International Symposium on Biomedical Imaging, Barcelona, Spain, 2-5 May 2012. Piscataway, NJ, United States: IEEE (Institute for Electrical and Electronic Engineers). doi: 10.1109/ISBI.2012.6235605
Miller, S. M., Hansell, N. K., Ngo, T. T., Liu, G. B., Pettigrew, J. D., Wright, M. J. and Martin, N. G. (2012). Genetic contribution to individual variation in binocular rivalry, an endophenotype for bipolar disorder. 5th Biennial Conference of the International-Society-for-Bipolar-Disorders, Istanbul, Turkey, 14-17 March 2012. Malden, MA, United States: Wiley-Blackwell. doi: 10.1111/j.1399-5618.2012.00981.x
Dennis, Emily L., Jahanshad, Neda, Toga, Arthur W., McMahon, Katie L., de Zubicaray, Greig I., Martin, Nicholas G., Wright, Margaret J. and Thompson, Paul M. (2012). Test-retest reliability of graph theory measures of structural brain connectivity. 15th International Conference on Medical Image Computing and Computer Assisted Intervention (MICCAI 2012), Nice, France, 1-5 October 2012. Springer: Heidelberg, Germany. doi: 10.1007/978-3-642-33454-2_38
Chiang, Ming-Chang, Barysheva, Marina, McMahon, Katie L., de Zubicaray, Greig I., Johnson, Kori, Martin, Nicholas G., Toga, Arthur W., Wright, Margaret J. and Thompson, Paul M. (2011). Hierarchical clustering of the genetic connectivity matrix reveals the network topology of gene action on brain microstructure: An N=531 twin study. 2011 IEEE 8th International Symposium on Biomedical Imaging (ISBI 2011), Chicago, United States, 30 March - 2 April 2011. Piscataway, NJ, United States: IEEE. doi: 10.1109/ISBI.2011.5872533
Jahanshad, Neda, Aganj, Iman, Lenglet, Christophe, Joshi, Anand, Jin, Yan, Barysheva, Marina, McMahon, Katie L., de Zubicaray, Greig I., Martin, Nicholas G., Wright Margaret J., Toga, Arthur W., Sapiro, Guillermo and Thompson, Paul M. (2011). Sex differences in the human connectome: 4-Tesla High Angular Resolution Diffusion Imaging (HARDI) tractography in 234 young adult twins. 2011 IEEE 8th International Symposium on Biomedical Imaging (ISBI 2011), Chicago, United States, 30 March - 2 April 2011. Piscataway, NJ, United States: IEEE. doi: 10.1109/ISBI.2011.5872558
Jin, Yan, Shi, Yonggang, Joshi, Shantanu, Jahanshad, Neda, Zhan, Lian, de Zubicaray, Greig I., McMahon, Katie L., Martin, Nicholas G., Wright, Margaret J., Toga, Arthur W. and Thompson, Paul M. (2011). Heritability of white matter fiber tract shapes: A HARDI study of 198 twins. Multimodal Brain Image Analysis: First International Workshop, MBIA 2011. Held in Conjunction with MICCAI 2011, Toronto, Canada, 18-22 September 2011. Heidelberg, Germany: Springer. doi: 10.1007/978-3-642-24446-9_5
Prasad, Gautam, Joshi, Shantanu H,, Jahanshad, Neda, Villalon, Julio, Aganj, Iman, Lenglet, Christophe, Sapiro, Guillermo, McMahon, Katie L., de Zubicaray, Greig I., Martin, Nicholas G., Wright, Margaret J., Toga, Arthur W and Thompson, Paul M. (2011). White matter tract analysis in 454 adults using maximum density paths. CDMRI'11 - Workshop on Computational Diffusion MRI, Toronto, Canada, 22 September 2011.
Prasad, Gautam, Joshi, Anand A., Feng, Albert, Barysheva, Marina, McMahon, Katie L., de Zubicaray, Greig I., Martin, Nicholas G., Wright, Margaret J., Toga, Arthur W., Terzopoulos, Demetri and Thompson, Paul M. (2011). Brain segmentation using deformable organisms and error learning. 3rd MICCAI Workshop on Mathematical Foundations of Computational Anatomy (MFCA 2011), Toronto, Canada, 22 September 2011. Toronto, Canada: MFCA.
Le, Anh T., Miller, Paul W., Slutske, Wendy S. and Martin, Nicholas G. (2011). Opportunity and Educational Outcomes in Australia. 39th Australian Conference of Economists, Sydney Australia, 27-29 September 2010. Richmond, VIC., Australia: Wiley-Blackwell Publishing. doi: 10.1111/j.1475-4932.2011.00749.x
Staffieri, S. E., Ruddle, J. B., Hewitt, A. W., Kearns, L. S., Sanfilippo, P. G., MacGregor, S., Martin, N. G., Young, T. L., Hammond, C. J. and Mackey, D. A. (2010). Genome Wide Analysis Identifies Putative Loci Associated With Interpupillary Distance. ROCKVILLE: ASSOC RESEARCH VISION OPHTHALMOLOGY INC.
Kearns, L. S., Hewitt, A. W., Ruddle, J. B., Bigault, O., Staffieri, S. E., Sanfillipo, P., Martin, N. G., Hammond, C. J., Young, T. L. and Mackey, D. A. (2010). Up to What Age is a Cyclopleged Refraction Required? Results From the Twins Eye Study Tasmania(TEST). ROCKVILLE: ASSOC RESEARCH VISION OPHTHALMOLOGY INC.
Aganj, Iman, Jahanshad, Neda, Lenglet, Christophe, Toga, Arthur W., McMahon, Katie L., de Zubicaray, Greig I., Wright, Margaret J., Martin, Nicholas G., Sapiro, Guillermo and Thompson, Paul M. (2010). Relating fiber crossing in HARDI to intellectual function. 16th annual meeting of the Organization for Human Brain Mapping, Barcelona, Spain, 6-10 June 2010.
Zietsch, B. P., Verweij, K. J. H., Bailey, J. M., Wright, M. J. and Martin, N. G. (2010). Psychiatric vulnerability in nonheterosexuals. The 40th Annual Behavior Genetics Association meeting, Seoul, Korea, 2-5 June 2010. New York, NY, U.S.A.: Springer New York. doi: 10.1007/s10519-010-9392-7
Hansell, Narelle K., Hickie, Ian B., Davenport, Tracey A., Hadzi-Pavlovic, Dusan, Wray, Naomi R., Martin, Nicholas G. and Wright, Margaret J. (2010). A study of genetic influence on SPHERE (somatic and psychological health report) measures collected in adolescents and young adults. 40th Annual Meeting of Behavior Genetics Association, Pennsylvania, PA, U.S.A., May 2009. New York, NY, U.S.A.: Springer New York LLC. doi: 10.1007/s10519-010-9392-7
Brant, Angela M., Boomsma, Dorret I., Corley, Robin P., DeFries, John C., Haworth, Clare M. A., Hewitt, John K., Martin, Nicholas G., McGue, Matthew, Petrill, Stephen A., Plomin, Robert, Wadsworth, Sally J. and Wright, Margaret J. (2010). Ability and heritability: Investigating the continuous effect of IQ score on IQ etiology in multiple samples. The 40th Annual Behavior Genetic Association Meeting, Seoul, Korea, 2- 5 June 2010. New York, NY, U.S.A.: Springer New York LLC. doi: 10.1007/s10519-010-9392-7
Bates, Timothy C., Luciano, Michelle, Montgomery, Grant W., Wright, Margaret J. and Martin, Nicholas G. (2010). Genes for a component of the language acquisition mechanism: ROBO1 polymorphisms associated with phonological buffer deficits. Behavior Genetics Association 40th Annual Meeting, Seoul, Korea, 2-5 June 2010. New York, U.S.A.: Springer New York LLC. doi: 10.1007/s10519-010-9392-7
Martin, N., Madden, P., Pergadia, M., Nelson, E., Bucholz, K., Whitfield, J.B., Montgomery, G. and Heath, G. (2010). Genomewide association study of quantitative alcohol phenotypes in community-ascertained families. 2010 World Congress on International Society for Biomedical Research on Alcoholism, Paris, France, 13-16 September 2010. Hoboken, NJ, U.S.A.: Wiley-Blackwell Publishing. doi: 10.1111/j.1530-0277.2010.01292_3.x
Medland, S. E., Nyholt, D. R., Painter, J. N., McEvoy, B. P., McRae, A. F., Montgomery, G. W. and Martin, N. G. (2010). Common variants in the Trichohyalin gene are associated with straight hair in Europeans genetics and genodermatoses. 6th World Congress for Hair Research, Cairns, QLD, Australia, 16-19 June 2010. Oxford, United Kingdom: Wiley-Blackwell. doi: 10.1111/j.1600-0625.2010.01097.x
Zhan, Liang, Leow, Alex D., Jahanshad, Neda, Lee, Agatha D., Barysheva, Marina, Toga, Arthur W., McMahon, Katie L., de Zubicaray, Greig I., Martin, Nicholas G., Wright, Margaret J. and Thompson, Paul M. (2010). Genetic analysis of high angular resolution diffusion images (HARDI). MICCAI 2010 Workshop on Computational Diffusion MRI, Beijiing, China, 20-24 September 2010. Berlin, Germany: Springer.
Lee, Agatha D., Leporé, Natasha, de Leeuw, Jan, Brun, Caroline C., Barysheva, Marina, McMahon, Katie L., de Zubicaray, Greig I., Martin, Nicholas G., Wright, Margaret J. and Thompson, Paul M. (2010). Multivariate variance-components analysis in DTI. 2010 7th IEEE International Symposium on Biomedical Imaging: From Nano to Macro, Rotterdam, Netherlands, 14-17 April 2010. Piscataway, NJ, U.S.A.: I E E E. doi: 10.1109/ISBI.2010.5490199
Patel, V, Chiang, MC, Thompson, PM, McMahon, KL, de Zubicaray, GI, Martin, NG, Wright, MJ and Toga, AW (2010). Scalar connectivity measures from fast-marching tractography reveal heritability of white matter architecture. ISBI 2010 7th IEEE International Symposium on Biomedical Imaging: From Nano to Macro, Rotterdam, Netherlands, 14-17 April 2010. Piscataway, NJ, U.S.A.: Institute of Electrical and Electronic Engineers (IEEE). doi: 10.1109/ISBI.2010.5490187
Lepore, Natasha, Brun, Caroline, Descoteaux, Maxime, Lee, Agatha D., Barysheva, Marina, Chou, Yi-Yu, de Zubicaray, Greig, McMahon, Katie, Wright, Margaret J., Martin, Nicholas G., Gee, James C. and Thompson, Paul M. (2010). Multivariate group-wise genetic analysis of white matter integrity using orientation distribution functions. MICCAI Workshop on Computational Diffusion MRI, Beijiing, China, 20-24 September 2010.
Verweij, Kjh, Zietsch, BP, Lynskey, MT, Heath, AC and Martin, NG (2010). Examining the relationship between sexual orientation and depression: overlapping genetic and early environmental influences. 40th Annual Meeting of Behavior-Genetics-Association, Pennsylvania PA, MAY, 2009.
Mosing, MA, Wright, MJ, Pedersen, Nancy L. and Martin, NG (2010). Genetic influences on optimism and its relationship to health. 40th Annual Meeting of Behavior-Genetics-Association, Pennsylvania PA, MAY, 2009.
Blokland, G, McMahon, K, Thompson, P, Martin, N, de Zubicaray, G and Wright, MJ (2010). Heritability of FMRI response in young adult twins. 40th Annual Meeting of Behavior-Genetics-Association, Pennsylvania PA, MAY, 2009. NEW YORK: SPRINGER.
Mosing, Miriam A., Gordon, Scott D., Medland, Sarah E., Statham, Dixie J., Nelson, Elliot C., Heath, Andrew C., Martin, Nicholas G. and Wray, Naomi R. (2009). Genetic and Environmental Influences on the Co-morbidity Between Depression, Panic Disorder, Agoraphobia, and Social Phobia: A Twin Study. United States: John Wiley & Sons, Inc.. doi: 10.1002/da.20611
Valle, A. M., Radic, Z., Rana, B. K., Whitfield, J. B., O'Connor, D. T., Martin, N. G. and Taylor, P. (2008). The cholinesterases: Analysis by pharmacogenomics in man. 9th International Meeting on Cholinesterases, Suzhou Peoples R China, May 06-10, 2007. CLARE: ELSEVIER IRELAND LTD. doi: 10.1016/j.cbi.2008.04.042
Data Collection
Wright, Margaret Jane, Martin, Nicholas and Hickie, Ian (2017). Data for the psychometric analysis reported in "Validation and psychometric properties of the Somatic and Psychological HEalth REport (SPHERE) in a young Australian-based population sample using non-parametric Item Response Theory". The University of Queensland. (Dataset) doi: 10.14264/uql.2017.647