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2022

Journal Article

Genome-wide analyses of individual differences in quantitatively assessed reading- and language-related skills in up to 34,000 people

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

Genome-wide analyses of individual differences in quantitatively assessed reading- and language-related skills in up to 34,000 people

2022

Journal Article

Changing genetic architecture of body mass index from infancy to early adulthood: an individual based pooled analysis of 25 twin cohorts

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

Changing genetic architecture of body mass index from infancy to early adulthood: an individual based pooled analysis of 25 twin cohorts

2022

Journal Article

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

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

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

2022

Journal Article

Clinical, demographic, and genetic risk factors of treatment‐attributed suicidality in >10,000 Australian adults taking antidepressants

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

Clinical, demographic, and genetic risk factors of treatment‐attributed suicidality in >10,000 Australian adults taking antidepressants

2022

Journal Article

Co-inheritance of variation in all-cause mortality and biochemical risk factors

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

Co-inheritance of variation in all-cause mortality and biochemical risk factors

2022

Journal Article

Genetic specificity of hippocampal subfield volumes, relative to hippocampal formation, identified in 2148 young adult twins and siblings

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

Genetic specificity of hippocampal subfield volumes, relative to hippocampal formation, identified in 2148 young adult twins and siblings

2022

Journal Article

Lifetime prevalence and correlates of perinatal depression in a case-cohort study of depression

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

Lifetime prevalence and correlates of perinatal depression in a case-cohort study of depression

2022

Journal Article

Differential and shared genetic effects on kidney function between diabetic and non-diabetic individuals

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

Differential and shared genetic effects on kidney function between diabetic and non-diabetic individuals

2022

Journal Article

Dynamic networks of psychological symptoms, impairment, substance use, and social support: the evolution of psychopathology among emerging adults

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

Dynamic networks of psychological symptoms, impairment, substance use, and social support: the evolution of psychopathology among emerging adults

2022

Journal Article

The heritability of twinning in seven large historic pedigrees

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

The heritability of twinning in seven large historic pedigrees

2022

Journal Article

Lindon Eaves: a personal memoir

Martin, Nick (2022). Lindon Eaves: a personal memoir. Twin Research and Human Genetics, 25 (2), 97-100. doi: 10.1017/thg.2022.13

Lindon Eaves: a personal memoir

2022

Journal Article

Mapping anorexia nervosa genes to clinical phenotypes

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) PII S0033291721004554, 1-15. doi: 10.1017/s0033291721004554

Mapping anorexia nervosa genes to clinical phenotypes

2022

Journal Article

Childhood maltreatment and disordered gambling in adulthood: Disentangling causal and familial influences

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

Childhood maltreatment and disordered gambling in adulthood: Disentangling causal and familial influences

2022

Journal Article

Enhancing discovery of genetic variants for PTSD through integration of quantitative phenotypes and trauma exposure information

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

Enhancing discovery of genetic variants for PTSD through integration of quantitative phenotypes and trauma exposure information

2022

Journal Article

Perinatal depression is associated with a higher polygenic risk for major depressive disorder than non-perinatal depression

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

Perinatal depression is associated with a higher polygenic risk for major depressive disorder than non-perinatal depression

2022

Journal Article

Shared genetic etiology between cortical brain morphology and tobacco, alcohol, and cannabis use

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

Shared genetic etiology between cortical brain morphology and tobacco, alcohol, and cannabis use

2022

Journal Article

Financial strain moderates genetic influences on self-rated health: support for diathesis–stress model of gene–environment interplay

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

Financial strain moderates genetic influences on self-rated health: support for diathesis–stress model of gene–environment interplay

2022

Journal Article

Genome-wide association meta-analysis identifies 29 new acne susceptibility loci

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

Genome-wide association meta-analysis identifies 29 new acne susceptibility loci

2022

Journal Article

Australian Parkinson’s Genetics Study (APGS): pilot (n=1532)

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

Australian Parkinson’s Genetics Study (APGS): pilot (n=1532)

2022

Journal Article

Impact of CYP2C19 metaboliser status on SSRI response: a retrospective study of 9500 participants of the Australian Genetics of Depression Study

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

Impact of CYP2C19 metaboliser status on SSRI response: a retrospective study of 9500 participants of the Australian Genetics of Depression Study