2024 Journal Article Genetic architecture of the structural connectomeWainberg, Michael, Forde, Natalie J., Mansour, Salim, Kerrebijn, Isabel, Medland, Sarah E., Hawco, Colin and Tripathy, Shreejoy J. (2024). Genetic architecture of the structural connectome. Nature Communications, 15 (1) 1962, 1-20. doi: 10.1038/s41467-024-46023-2 |
2024 Journal Article Comprehensive sex-stratified genetic analysis of 28 blood biomarkers and depression reveals a significant association between depression and low levels of total protein in femalesKiewa, 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 |
2024 Journal Article Scientific clickbait: Examining media coverage and readability in genome-wide association researchMorosoli, José J., Colodro-Conde, Lucía, Barlow, Fiona Kate and Medland, Sarah E. (2024). Scientific clickbait: Examining media coverage and readability in genome-wide association research. PLoS One, 19 (1) e0296323, 1-16. doi: 10.1371/journal.pone.0296323 |
2024 Journal Article Changes in sleep patterns in people with a history of depression during the COVID-19 pandemic: a natural experimentShin, Mirim, Crouse, Jacob J., Byrne, Enda M., Mitchell, Brittany L., Lind, Penelope, Parker, Richard, Tonini, Emiliana, Carpenter, Joanne S., Wray, Naomi R., Colodro-Conde, Lucia, Medland, Sarah E. and Hickie, Ian B. (2024). Changes in sleep patterns in people with a history of depression during the COVID-19 pandemic: a natural experiment. BMJ Mental Health, 27 (1) e301067, e301067. doi: 10.1136/bmjment-2024-301067 |
2024 Journal Article Evening chronotypes with depression report poorer outcomes of SSRIs: A survey-based study of self-ratingsCrouse, 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 |
2024 Journal Article Genome-wide association study meta-analysis of dizygotic twinning illuminates genetic regulation of female fecundityMbarek, 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 |
2023 Journal Article GWAS of dizygotic twinning in an enlarged Australian sample of mothers of DZ twinsGordon, 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 |
2023 Journal Article Discontinuation of antidepressant treatment: a retrospective cohort study on more than 20,000 participantsGarcia-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 |
2023 Journal Article Preliminary results from the Australian Genetics of Bipolar Disorder Study: A nation-wide cohortLind, 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 |
2023 Journal Article Uncovering the complex relationship between balding, testosterone and skin cancers in menOng, 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 |
2023 Conference Publication Genetics of EEG Oscillations Reveal Novel Biological Insights Into The Links Between Brain Structure, Brain Function, and BehaviorJawinski, Philippe, Meyers, Jacquelyn, Garcia, José Morosoli, Thompson, Paul, Medland, Sarah E. and Smit, Dirk J.A. (2023). Genetics of EEG Oscillations Reveal Novel Biological Insights Into The Links Between Brain Structure, Brain Function, and Behavior. World Congress of Psychiatric Genetics (WCPG), Montreal, QC Canada, 10-14 October 2023. Amsterdam, Netherlands: Elsevier. doi: 10.1016/j.euroneuro.2023.08.141 |
2023 Conference Publication Characterising antidepressant usage based on electronic prescription records in the Australian Genetics of Depression StudyMitchell, 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 |
2023 Journal Article Educational attainment, health outcomes and mortality: a within-sibship Mendelian randomization studyHowe, Laurence J., Rasheed, Humaira, Jones, Paul R., Boomsma, Dorret I., Evans, David M., Giannelis, Alexandros, Hayward, Caroline, Hopper, John L., Hughes, Amanda, Lahtinen, Hannu, Li, Shuai, Lind, Penelope A., Martin, Nicholas G., Martikainen, Pekka, Medland, Sarah E., Morris, Tim T., Nivard, Michel G., Pingault, Jean-Baptiste, Silventoinen, Karri, Smith, Jennifer A., Willoughby, Emily A., Wilson, James F., Ahlskog, Rafael, Andreassen, Ole A., Ask, Helga, Campbell, Archie, Cheesman, Rosa, Cho, Yoonsu, Christensen, Kaare ... Within Family Consortium (2023). Educational attainment, health outcomes and mortality: a within-sibship Mendelian randomization study. International Journal of Epidemiology, 52 (5), 1579-1591. doi: 10.1093/ije/dyad079 |
2023 Conference Publication Progress and promise of neurogenetics methods to study PTSDMorey, Rajendra, Logue, Mark, Maihofer, Adam X., Nievergelt, Caroline, Ashley-Koch, Allison, Garrett, Melanie, Haswell, Courtney, Mufford, Maryanne, Dalvie, Shareefa, Katrinli, Seyma, Medland, Sarah E. and Thompson, Paul (2023). Progress and promise of neurogenetics methods to study PTSD. World Congress of Psychiatric Genetics (WCPG), Montreal, Canada, 10-14 October 2023. Amsterdam, Netherlands: Elsevier. doi: 10.1016/j.euroneuro.2023.08.082 |
2023 Journal Article Beyond the Global Brain Differences: Intra-individual Variability Differences in 1q21.1 Distal and 15q11.2 BP1-BP2 Deletion CarriersBoen, Rune, Kaufmann, Tobias, van der Meer, Dennis, Frei, Oleksandr, Agartz, Ingrid, Ames, David, Andersson, Micael, Armstrong, Nicola J., Artiges, Eric, Atkins, Joshua R., Bauer, Jochen, Benedetti, Francesco, Boomsma, Dorret I., Brodaty, Henry, Brosch, Katharina, Buckner, Randy L., Cairns, Murray J., Calhoun, Vince, Caspers, Svenja, Cichon, Sven, Corvin, Aiden P., Facorro, Benedicto Crespo, Dannlowski, Udo, David, Friederike S., de Geus, Eco J.C., de Zubicaray, Greig I., Desrivières, Sylvane, Doherty, Joanne L., Donohoe, Gary ... Sonderby, Ida E. (2023). Beyond the Global Brain Differences: Intra-individual Variability Differences in 1q21.1 Distal and 15q11.2 BP1-BP2 Deletion Carriers. Biological Psychiatry, 95 (2), 147-160. doi: 10.1016/j.biopsych.2023.08.018 |
2023 Journal Article Effects of semaglutide on body weight in clozapine-treated people with schizophrenia and obesity: study protocol for a placebo-controlled, randomised multicentre trial (COaST)Siskind, Dan, Baker, Andrea, Russell, Anthony, Warren, Nicola, Robinson, Gail, Parker, Stephen, Medland, Sarah, Kisely, Steve, Hager, Tineka and Arnautovska, Urska (2023). Effects of semaglutide on body weight in clozapine-treated people with schizophrenia and obesity: study protocol for a placebo-controlled, randomised multicentre trial (COaST). BJPsych Open, 9 (4) e136, 1-6. doi: 10.1192/bjo.2023.532 |
2023 Journal Article A genotype-to-phenotype approach suggests under-reporting of single nucleotide variants in nephrocystin-1 (NPHP1) related disease (UK 100,000 Genomes Project)Leggatt, Gary, Cheng, Guo, Narain, Sumit, Briseno-Roa, Luis, Annereau, Jean-Philippe, Gast, Christine, Gilbert, Rodney D. and Ennis, Sarah (2023). A genotype-to-phenotype approach suggests under-reporting of single nucleotide variants in nephrocystin-1 (NPHP1) related disease (UK 100,000 Genomes Project). Scientific Reports, 13 (1) 9369, 1-12. doi: 10.1038/s41598-023-32169-4 |
2023 Journal Article “Echoes of a dark past” is a history of maternal childhood maltreatment a perinatal risk factor for pregnancy and postpartum trauma experiences? A longitudinal studyMackle, Tracey, Colodro-Conde, Lucía, de Dassel, Therese, Braun, Anastasia, Pope, Adele, Bennett, Elizabeth, Kothari, Alka, Bruxner, George, Medland, Sarah E. and Patterson, Sue (2023). “Echoes of a dark past” is a history of maternal childhood maltreatment a perinatal risk factor for pregnancy and postpartum trauma experiences? A longitudinal study. BMC Pregnancy and Childbirth, 23 (1) 397, 1-12. doi: 10.1186/s12884-023-05714-2 |
2023 Conference Publication Childhood Trauma Exposure and PTSD Diagnosis Interact With Polygenic Determinants of Hippocampal and Amygdala VolumeLogue, Mark, Zheng, Yuanchao, Garrett, Melanie, Maihofer, Adam, Clarke, Emily, Haswell, Courtney, Sun, Delin, Peverill, Matthew, McLaughlin, Katie, Sambrook, Kelly, Davenport, Nicholas, Disner, Seth, Korgaonkar, Mayuresh, Bryant, Richard, Varkevisser, Tim, Geuze, Elbert, Beckham, Jean, Kimbrel, Nathan, Coleman, Jonathan, Sullivan, Danielle, Wolf, Erika, Hayes, Jasmeet, Verfaellie, Mieke, Salat, David, Spielberg, Jeffrey M., McGlinchey, Regina, Milberg, William, Medland, Sarah E., Nievergelt, Caroline ... Morey, Rajendra (2023). Childhood Trauma Exposure and PTSD Diagnosis Interact With Polygenic Determinants of Hippocampal and Amygdala Volume. 78th Annual Meeting of the Society of Biological Psychiatry, San Diego, CA United States, 27-29 April 2023. Philadelphia, PA United States: Elsevier. doi: 10.1016/j.biopsych.2023.02.056 |
2023 Journal Article A palindrome-like structure on 16p13.3 is associated with the formation of complex structural variations and SRRM2 haploinsufficiencyPagnamenta, Alistair T. T., Yu, Jing, Willis, Tracey A. A., Hashim, Mona, Seaby, Eleanor G. G., Walker, Susan, Xian, Jiaqi, Cheng, Emily W. Y., Tavares, Ana Lisa Taylor, Forzano, Francesca, Cox, Helen, Dabir, Tabib, Brady, Angela F. F., Ghali, Neeti, Atanur, Santosh S. S., Ennis, Sarah, Baralle, Diana and Taylor, Jenny C. C. (2023). A palindrome-like structure on 16p13.3 is associated with the formation of complex structural variations and SRRM2 haploinsufficiency. Human Mutation, 2023 6633248, 1-9. doi: 10.1155/2023/6633248 |