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2022 Journal Article Smoking remains associated with education after controlling for social background and genetic factors in a study of 18 twin cohortsSilventoinen, 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 |
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2022 Journal Article Phenotypic and genetic factors associated with donation of DNA and consent to record linkage for prescription history in the Australian Genetics of Depression StudyGomez, 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 |
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2022 Conference Publication Can polygenic Risk Scores Predict Who Will Receive or Respond Better to Electroconvulsive Therapy for Treatment of Major Depressive Disorder?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. |
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2022 Conference Publication Challenges to Incorporating Polygenic Risk Scores in Clinical Mental Health PracticeMedland, 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. |
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2022 Journal Article Uncovering the genetic architecture of broad antisocial behavior through a genome-wide association study meta-analysisTielbeek, 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 |
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2022 Journal Article Genetic map of regional sulcal morphology in the human brain from UK biobank dataSun, Benjamin B., Loomis, Stephanie J., Pizzagalli, Fabrizio, Shatokhina, Natalia, Painter, Jodie N., Foley, Christopher N., Sun, Benjamin, Tsai, Ellen, Bronson, Paola, Sexton, David, John, Sally, Marshall, Eric, Patel, Mehool, Duraisamy, Saranya, Swan, Timothy, Baird, Dennis, Chen, Chia-Yen, Eaton, Susan, Gagnon, Jake, Gao, Feng, Gubbels, Cynthia, Huang, Yunfeng, Kupelian, Varant, Li, Kejie, Liu, Dawei, Loomis, Stephanie, McLaughlin, Helen, Mitchell, Adele, Jensen, Megan E. ... Biogen Biobank Team (2022). Genetic map of regional sulcal morphology in the human brain from UK biobank data. Nature Communications, 13 (1) 6071, 1-13. doi: 10.1038/s41467-022-33829-1 |
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2022 Conference Publication Exploring genetic heterogeneity of depression: scalar and non-scalar SNP effects in the genetics of mild versus severe depressionMartin, Nick, Mitchell, Brittany, Medland, Sarah, Byrne, Enda, Wray, Naomi, Whiteman, David, Olsen, Catherine and Hickie, Ian (2022). Exploring genetic heterogeneity of depression: scalar and non-scalar SNP effects in the genetics of mild versus severe depression. World Congress of Psychiatric Genetics (WCPG), Florence, Italy, 13-17 September 2022. Amsterdam, Netherlands: Elsevier. doi: 10.1016/j.euroneuro.2022.07.099 |
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2022 Conference Publication Exploring the genome-wide genetic overlap between anxiety and fear disorderster Kuile, Abigail, Mitchell, Brittany, Peel, Alicia, Mundy, Jessica, Hubel, Christopher, Zvrskovec, Johan, Palmos, Alish, Coleman, Jonathan, Davies, Molly, Martin, Nick, Byrne, Enda M., Medland, Sarah E., Wray, Naomi R., Adey, Brett N., Lee, Sang Hyuck, Furtjes, Anna E., Morneau-Vaillancourt, Genevieve, Purves, Kirstin, Skelton, Megan, Hotopf, Matthew, Smith, Daniel J., Veale, David, Armour, Cherie, McIntosh, Andrew, Walters, James T. R., Jones, Ian R., Hirsch, Colette R., Kalsi, Gursharan, Breen, Gerome and Eley, Thalia (2022). Exploring the genome-wide genetic overlap between anxiety and fear disorders. World Congress of Psychiatric Genetics (WCPG), Florence, Italy, 13-17 September 2022. Amsterdam, Netherlands: Elsevier. doi: 10.1016/j.euroneuro.2022.07.014 |
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2022 Journal Article Author correction: Genome-wide association and epidemiological analyses reveal common genetic origins between uterine leiomyomata and endometriosisGallagher, 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 |
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2022 Journal Article Genome-wide association analyses of physical activity and sedentary behavior provide insights into underlying mechanisms and roles in disease preventionWang, 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 |
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2022 Journal Article NOD2 in Crohn's disease-unfinished businessAshton, James J., Seaby, Eleanor G., Beattie, R. Mark and Ennis, Sarah (2022). NOD2 in Crohn's disease-unfinished business. Journal of Crohn's and Colitis, 17 (3), 450-458. doi: 10.1093/ecco-jcc/jjac124 |
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2022 Journal Article Genome-wide meta-analyses reveal novel loci for verbal short-term memory and learningLahti, Jari, Tuominen, Samuli, Yang, Qiong, Pergola, Giulio, Ahmad, Shahzad, Amin, Najaf, Armstrong, Nicola J., Beiser, Alexa, Bey, Katharina, Bis, Joshua C., Boerwinkle, Eric, Bressler, Jan, Campbell, Archie, Campbell, Harry, Chen, Qiang, Corley, Janie, Cox, Simon R., Davies, Gail, De Jager, Philip L., Derks, Eske M., Faul, Jessica D., Fitzpatrick, Annette L., Fohner, Alison E., Ford, Ian, Fornage, Myriam, Gerring, Zachary, Grabe, Hans J., Grodstein, Francine, Gudnason, Vilmundur ... Räikkönen, Katri (2022). Genome-wide meta-analyses reveal novel loci for verbal short-term memory and learning. Molecular Psychiatry, 27 (11), 4419-4431. doi: 10.1038/s41380-022-01710-8 |
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2022 Journal Article De novo putative loss-of-function variants in TAF4 are associated with a neuro-developmental disorderJanssen, Beau D. E., van den Boogaard, Marie-Jose H., Lichtenbelt, Klaske, Seaby, Eleanor G., Stals, Karen, Ellard, Sian, Newbury-Ecob, Ruth, Dixit, Abhijit, Roht, Laura, Pajusalu, Sander, Ounap, Katrin, Firth, Helen, Buckley, Michael, Wilson, Meredith, Roscioli, Tony, Tidwell, Timothy, Mao, Rong, Ennis, Sarah, Holwerda, Sjoerd J., van Gassen, Koen and van Jaarsveld, Richard H. (2022). De novo putative loss-of-function variants in TAF4 are associated with a neuro-developmental disorder. Human Mutation, 43 (12), 1844-1851. doi: 10.1002/humu.24444 |
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2022 Journal Article Changing genetic architecture of body mass index from infancy to early adulthood: an individual based pooled analysis of 25 twin cohortsSilventoinen, 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 |
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2022 Journal Article A gene-to-patient approach uplifts novel disease gene discovery and identifies 18 putative novel disease genesSeaby, Eleanor G., Smedley, Damian, Tavares, Ana Lisa Taylor, Brittain, Helen, van Jaarsveld, Richard H., Baralle, Diana, Rehm, Heidi L., O'Donnell-Luria, Anne and Ennis, Sarah (2022). A gene-to-patient approach uplifts novel disease gene discovery and identifies 18 putative novel disease genes. Genetics in Medicine, 24 (8), 1697-1707. doi: 10.1016/j.gim.2022.04.019 |
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2022 Journal Article Event-based modeling in temporal lobe epilepsy demonstrates progressive atrophy from cross-sectional dataLopez, Seymour M., Aksman, Leon M., Oxtoby, Neil P., Vos, Sjoerd B., Rao, Jun, Kaestner, Erik, Alhusaini, Saud, Alvim, Marina, Bender, Benjamin, Bernasconi, Andrea, Bernasconi, Neda, Bernhardt, Boris, Bonilha, Leonardo, Caciagli, Lorenzo, Caldairou, Benoit, Caligiuri, Maria Eugenia, Calvet, Angels, Cendes, Fernando, Concha, Luis, Conde-Blanco, Estefania, Davoodi-Bojd, Esmaeil, de Bézenac, Christophe, Delanty, Norman, Desmond, Patricia M., Devinsky, Orrin, Domin, Martin, Duncan, John S., Focke, Niels K., Foley, Sonya ... for the ENIGMA- Epilepsy Working Group (2022). Event-based modeling in temporal lobe epilepsy demonstrates progressive atrophy from cross-sectional data. Epilepsia, 63 (8), 2081-2095. doi: 10.1111/epi.17316 |
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2022 Journal Article Clinical, demographic, and genetic risk factors of treatment‐attributed suicidality in >10,000 Australian adults taking antidepressantsCampos, 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 |
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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 A Systematic Review of Artificial Intelligence and Machine Learning Applications to Inflammatory Bowel Disease, with Practical Guidelines for InterpretationStafford, Imogen S., Gosink, Mark M., Mossotto, Enrico, Ennis, Sarah and Hauben, Manfred (2022). A Systematic Review of Artificial Intelligence and Machine Learning Applications to Inflammatory Bowel Disease, with Practical Guidelines for Interpretation. Inflammatory Bowel Diseases, 28 (10), 1573-1583. doi: 10.1093/ibd/izac115 |
