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2022 Journal Article Lifetime prevalence and correlates of perinatal depression in a case-cohort study of depressionKiewa, 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 |
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2022 Conference Publication Differentiation of unipolar and bipolar depression based on clinical features: a systematic review and meta-analysis.Hopkins, Kristen, Siskind, Dan, McMahon, Laura, Philips, Elise, Lind, Penelope, Medland, Sarah and Warren, Nicola (2022). Differentiation of unipolar and bipolar depression based on clinical features: a systematic review and meta-analysis.. The 24th Annual Conference of the International Society for Bipolar Disorders, Online, 10–12 June 2022. Hoboken, NJ United States: Wiley-Blackwell. |
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2022 Journal Article Dynamic networks of psychological symptoms, impairment, substance use, and social support: the evolution of psychopathology among emerging adultsCrouse, 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 |
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2022 Journal Article Within-sibship genome-wide association analyses decrease bias in estimates of direct genetic effectsHowe, Laurence J., Nivard, Michel G., Morris, Tim T., Hansen, Ailin F., Rasheed, Humaira, Cho, Yoonsu, Chittoor, Geetha, Ahlskog, Rafael, Lind, Penelope A., Palviainen, Teemu, van der Zee, Matthijs D., Cheesman, Rosa, Mangino, Massimo, Wang, Yunzhang, Li, Shuai, Klaric, Lucija, Ratliff, Scott M., Bielak, Lawrence F., Nygaard, Marianne, Giannelis, Alexandros, Willoughby, Emily A., Reynolds, Chandra A., Balbona, Jared V., Andreassen, Ole A., Ask, Helga, Baras, Aris, Bauer, Christopher R., Boomsma, Dorret I., Campbell, Archie ... Within Family Consortium (2022). Within-sibship genome-wide association analyses decrease bias in estimates of direct genetic effects. Nature Genetics, 54 (5), 581-592. doi: 10.1038/s41588-022-01062-7 |
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2022 Journal Article Genetic variants associated with longitudinal changes in brain structure across the lifespanBrouwer, Rachel M., Klein, Marieke, Grasby, Katrina L., Schnack, Hugo G., Jahanshad, Neda, Teeuw, Jalmar, Thomopoulos, Sophia I., Sprooten, Emma, Franz, Carol E., Gogtay, Nitin, Kremen, William S., Panizzon, Matthew S., Olde Loohuis, Loes M., Whelan, Christopher D., Aghajani, Moji, Alloza, Clara, Alnæs, Dag, Artiges, Eric, Ayesa-Arriola, Rosa, Barker, Gareth J., Bastin, Mark E., Blok, Elisabet, Bøen, Erlend, Breukelaar, Isabella A., Bright, Joanna K., Buimer, Elizabeth E. L., Bülow, Robin, Cannon, Dara M., Ciufolini, Simone ... the IMAGEN Consortium (2022). Genetic variants associated with longitudinal changes in brain structure across the lifespan. Nature Neuroscience, 25 (4), 421-432. doi: 10.1038/s41593-022-01042-4 |
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2022 Journal Article DNA methylation in peripheral tissues and left-handednessOdintsova, Veronika V., Suderman, Matthew, Hagenbeek, Fiona A., Caramaschi, Doretta, Hottenga, Jouke-Jan, Pool, René, Dolan, Conor V., Ligthart, Lannie, van Beijsterveldt, Catharina E M, Willemsen, Gonneke, de Geus, Eco J C, Beck, Jeffrey J., Ehli, Erik A., Cuellar-Partida, Gabriel, Evans, David M., Medland, Sarah E., Relton, Caroline L., Boomsma, Dorret I. and van Dongen, Jenny (2022). DNA methylation in peripheral tissues and left-handedness. Scientific Reports, 12 (1) 5606, 5606. doi: 10.1038/s41598-022-08998-0 |
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2022 Journal Article Genetic and environmental influences on biological essentialism, heuristic thinking, need for closure, and conservative values: insights from a survey and twin studyMorosoli, J. J., Barlow, F. K., Colodro-Conde, L. and Medland, S. E. (2022). Genetic and environmental influences on biological essentialism, heuristic thinking, need for closure, and conservative values: insights from a survey and twin study. Behavior Genetics, 52 (3), 170-183. doi: 10.1007/s10519-022-10101-2 |
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2022 Journal Article censusADHD Study: an Australian-wide medication-based recruitment study for Attention-Deficit/Hyperactivity DisorderLind, Penelope A. and Medland, Sarah E. (2022). censusADHD Study: an Australian-wide medication-based recruitment study for Attention-Deficit/Hyperactivity Disorder. Australian & New Zealand Journal of Psychiatry, 57 (2) ARTN 00048674221089234, 1-12. doi: 10.1177/00048674221089234 |
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2022 Journal Article Perinatal depression is associated with a higher polygenic risk for major depressive disorder than non-perinatal depressionKiewa, 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 |
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2022 Journal Article Shared genetic etiology between cortical brain morphology and tobacco, alcohol, and cannabis useRabinowitz, 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 |
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2022 Journal Article Subtly altered topological asymmetry of brain structural covariance networks in autism spectrum disorder across 43 datasets from the ENIGMA consortiumSha, Zhiqiang, van Rooij, Daan, Anagnostou, Evdokia, Arango, Celso, Auzias, Guillaume, Behrmann, Marlene, Bernhardt, Boris, Bolte, Sven, Busatto, Geraldo F., Calderoni, Sara, Calvo, Rosa, Daly, Eileen, Deruelle, Christine, Duan, Meiyu, Duran, Fabio Luis Souza, Durston, Sarah, Ecker, Christine, Ehrlich, Stefan, Fair, Damien, Fedor, Jennifer, Fitzgerald, Jacqueline, Floris, Dorothea L., Franke, Barbara, Freitag, Christine M., Gallagher, Louise, Glahn, David C., Haar, Shlomi, Hoekstra, Liesbeth, Jahanshad, Neda ... Francks, Clyde (2022). Subtly altered topological asymmetry of brain structural covariance networks in autism spectrum disorder across 43 datasets from the ENIGMA consortium. Molecular Psychiatry, 27 (4), 2114-2125. doi: 10.1038/s41380-022-01452-7 |
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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 |
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2022 Journal Article Impact of CYP2C19 metaboliser status on SSRI response: a retrospective study of 9500 participants of the Australian Genetics of Depression StudyCampos, 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 |
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2022 Journal Article Limb development genes underlie variation in human fingerprint patternsLi, 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 |
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2022 Journal Article Bridging the gap: Short structural variants in the genetics of anorexia nervosaBerthold, Natasha, Pytte, Julia, Bulik, Cynthia M., Tschochner, Monika, Medland, Sarah E. and Akkari, Patrick Anthony (2022). Bridging the gap: Short structural variants in the genetics of anorexia nervosa. International Journal of Eating Disorders, 55 (6), 747-753. doi: 10.1002/eat.23716 |
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2022 Conference Publication Effects of ApoE4 and ApoE2 genotypes on subcortical magnetic susceptibility and microstructure in 27,535 participants from the UK BiobankNir, Talia M., Zhu, Alyssa H., Gari, Iyad Ba, Dixon, Daniel, Islam, Tasfiya, Villalon-Reina, Julio E., Medland, Sarah E., Thompson, Paul M. and Jahanshad, Neda (2022). Effects of ApoE4 and ApoE2 genotypes on subcortical magnetic susceptibility and microstructure in 27,535 participants from the UK Biobank. Pacific Symposium on Biocomputing 2022, Kohala Coast, HI United States, 3 – 7 January 2022. Singapore: World Scientific Publishing. doi: 10.1142/9789811250477_0012 |
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2021 Journal Article Comparing empirical kinship derived heritability for imaging genetics traits in the UK biobank and human connectome projectGao, Si, Donohue, Brian, Hatch, Kathryn S., Chen, Shuo, Ma, Tianzhou, Ma, Yizhou, Kvarta, Mark D., Bruce, Heather, Adhikari, Bhim M., Jahanshad, Neda, Thompson, Paul M., Blangero, John, Hong, L. Elliot, Medland, Sarah E., Ganjgahi, Habib, Nichols, Thomas E. and Kochunov, Peter (2021). Comparing empirical kinship derived heritability for imaging genetics traits in the UK biobank and human connectome project. NeuroImage, 245 118700, 1-11. doi: 10.1016/j.neuroimage.2021.118700 |
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2021 Journal Article Large-scale genetic investigation reveals genetic liability to multiple complex traits influencing a higher risk of ADHDGarcía-Marín, Luis M., Campos, Adrián I., Cuéllar-Partida, Gabriel, Medland, Sarah E., Kollins, Scott H. and Rentería, Miguel E. (2021). Large-scale genetic investigation reveals genetic liability to multiple complex traits influencing a higher risk of ADHD. Scientific Reports, 11 (1) 22628, 22628. doi: 10.1038/s41598-021-01517-7 |
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2021 Journal Article Trauma and posttraumatic stress disorder modulate polygenic predictors of hippocampal and amygdala volumeZheng, Yuanchao, Garrett, Melanie E., Sun, Delin, Clarke-Rubright, Emily K., Haswell, Courtney C., Maihofer, Adam X., Elman, Jeremy A., Franz, Carol E., Lyons, Michael J., Kremen, William S., Peverill, Matthew, Sambrook, Kelly, McLaughlin, Katie A., Davenport, Nicholas D., Disner, Seth, Sponheim, Scott R., Andrew, Elpiniki, Korgaonkar, Mayuresh, Bryant, Richard, Varkevisser, Tim, Geuze, Elbert, Coleman, Jonathan, Beckham, Jean C., Kimbrel, Nathan A., Sullivan, Danielle, Miller, Mark, Hayes, Jasmeet, Verfaellie, Mieke, Wolf, Erika ... Morey, Rajendra A. (2021). Trauma and posttraumatic stress disorder modulate polygenic predictors of hippocampal and amygdala volume. Translational Psychiatry, 11 (1) 637, 637. doi: 10.1038/s41398-021-01707-x |
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2021 Journal Article Understanding genetic risk factors for common side effects of antidepressant medicationsCampos, 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 |
