Book Chapters
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). Multivariate genetic analysis. Wiley StatsRef: statistics reference online. Chichester, United Kingdom: John Wiley & Sons. doi: 10.1002/9781118445112.stat06468
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
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. (2013). Modeling the cultural and biological inheritance of social and political behavior in twins and nuclear families. Man is by nature a political animal. (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
Gillespie, N. A. and Martin, N. G. (2006). Neuroticism as a genetic marker for mood and anxiety. Biology of Personality & Individual Differences. (pp. 225-250) edited by T. Canli. New York, U.S.A.: Guilford Press.
Journal Articles
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
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. doi: 10.1038/s41380-022-01793-3
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), 1-9. doi: 10.1038/s41588-022-01192-y
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), 1-9. doi: 10.1017/thg.2022.33
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
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, 101680. doi: 10.1016/j.intell.2022.101680
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
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
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
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
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, 580. doi: 10.1038/s42003-022-03448-z
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 : the official journal of the International Society for Twin Studies, 25 (3), 129-139. doi: 10.1017/thg.2022.20
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
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
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, 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
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
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
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
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
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, 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
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
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. 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
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). doi: 10.1093/sleepadvances/zpab018
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
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, 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
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