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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 Dissecting the shared genetic architecture of suicide attempt, psychiatric disorders, and known risk factorsMullins, Niamh, Kang, JooEun, Campos, Adrian I., Coleman, Jonathan R I, Edwards, Alexis C., Galfalvy, Hanga, Levey, Daniel F., Lori, Adriana, Shabalin, Andrey, Starnawska, Anna, Su, Mei-Hsin, Watson, Hunna J., Adams, Mark, Awasthi, Swapnil, Gandal, Michael, Hafferty, Jonathan D., Hishimoto, Akitoyo, Kim, Minsoo, Okazaki, Satoshi, Otsuka, Ikuo, Ripke, Stephan, Ware, Erin B., Bergen, Andrew W., Berrettini, Wade H., Bohus, Martin, Brandt, Harry, Chang, Xiao, Chen, Wei J., Chen, Hsi-Chung ... Ruderfer, Douglas M. (2022). Dissecting the shared genetic architecture of suicide attempt, psychiatric disorders, and known risk factors. Biological Psychiatry, 91 (3), 313-327. doi: 10.1016/j.biopsych.2021.05.029 |
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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 Deleterious Genetic Variation Across the NOD Signaling Pathway Is Associated With Reduced <i>NFKB Signaling</i> Transcription and Upregulation of Alternative Inflammatory Transcripts in Pediatric Inflammatory Bowel DiseaseAshton, James J., Boukas, Konstantinos, Stafford, Imogen S., Cheng, Guo, Haggarty, Rachel, Coelho, Tracy A. F., Batra, Akshay, Afzal, Nadeem A., Williams, Anthony P., Polak, Marta E., Beattie, R. Mark and Ennis, Sarah (2022). Deleterious Genetic Variation Across the NOD Signaling Pathway Is Associated With Reduced NFKB Signaling Transcription and Upregulation of Alternative Inflammatory Transcripts in Pediatric Inflammatory Bowel Disease. Inflammatory Bowel Diseases, 28 (6), 912-922. doi: 10.1093/ibd/izab318 |
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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 Exome sequencing identifies a disease variant of the mitochondrial ATP-Mg/Pi carrier SLC25A25 in two families with kidney stonesJabalameli, M. Reza, Fitzpatrick, Fiona M., Colombo, Roberto, Howles, Sarah A., Leggatt, Gary, Walker, Valerie, Wiberg, Akira, Kunji, Edmund R. S. and Ennis, Sarah (2021). Exome sequencing identifies a disease variant of the mitochondrial ATP-Mg/Pi carrier SLC25A25 in two families with kidney stones. Molecular Genetics and Genomic Medicine, 9 (12) e1749, 1-14. doi: 10.1002/mgg3.1749 |
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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 |
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2021 Journal Article Educational attainment of same-sex and opposite-sex dizygotic twins: an individual-level pooled study of 19 twin cohortsSilventoinen, Karri, Bogl, Leonie H., Jelenkovic, Aline, Vuoksimaa, Eero, Latvala, Antti, Li, Weilong, Tan, Qihua, Zhang, Dongfeng, Pang, Zengchang, Ordoñana, Juan R., Sánchez-Romera, Juan F., Colodro-Conde, Lucia, Willemsen, Gonneke, Bartels, Meike, van Beijsterveldt, Catharina E.M., Rebato, Esther, Corley, Robin P., Huibregtse, Brooke M., Hopper, John L., Tyler, Jessica, Duncan, Glen E., Buchwald, Dedra, Silberg, Judy L., Maes, Hermine H., Kandler, Christian, Cozen, Wendy, Hwang, Amie E., Mack, Thomas M., Nelson, Tracy L. ... Kaprio, Jaakko (2021). Educational attainment of same-sex and opposite-sex dizygotic twins: an individual-level pooled study of 19 twin cohorts. Hormones and Behavior, 136 105054, 1-6. doi: 10.1016/j.yhbeh.2021.105054 |
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2021 Journal Article Genome-wide analysis of thyroid function in Australian adolescents highlights SERPINA7 and NCOA3Nolan, James, Campbell, Purdey J, Brown, Suzanne J, Zhu, Gu, Gordon, Scott, Lim, Ee Mun, Joseph, John, Cross, Simone M, Panicker, Vijay, Medland, Sarah E, Melton, Phillip E, Beilin, Lawrence J, Mori, Trevor A, Mullin, Benjamin H, Pennell, Craig E, Wang, Carol A, Dudbridge, Frank, Walsh, John P, Martin, Nicholas G and Wilson, Scott G (2021). Genome-wide analysis of thyroid function in Australian adolescents highlights SERPINA7 and NCOA3. European Journal of Endocrinology, 185 (5), 743-753. doi: 10.1530/EJE-21-0614 |
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2021 Journal Article The Australian Genetics of Depression Study: new risk loci and dissecting heterogeneity between subtypesMitchell, 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 |
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2021 Journal Article Investigating perceived heritability of mental health disorders and attitudes toward genetic testing in the United States, United Kingdom, and AustraliaMorosoli, José Juan, Colodro‐Conde, Lucía, Barlow, Fiona Kate and Medland, Sarah E. (2021). Investigating perceived heritability of mental health disorders and attitudes toward genetic testing in the United States, United Kingdom, and Australia. American Journal of Medical Genetics Part B: Neuropsychiatric Genetics, 186 (6), 341-352. doi: 10.1002/ajmg.b.32875 |
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2021 Journal Article Total body water in full-term and preterm newborns: systematic review and meta-analysisYoung, Aneurin, Brown, Lisa K., Ennis, Sarah, Beattie, R. Mark and Johnson, Mark John (2021). Total body water in full-term and preterm newborns: systematic review and meta-analysis. Archives of Disease in Childhood-Fetal and Neonatal Edition, 106 (5), F542-F548. doi: 10.1136/archdischild-2020-321112 |
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2021 Journal Article Polygenic risk scores derived from varying definitions of depression and risk of depressionMitchell, Brittany L., Thorp, Jackson G., Wu, Yeda, Campos, Adrian I., Nyholt, Dale R., Gordon, Scott D., Whiteman, David C., Olsen, Catherine M., Hickie, Ian B., Martin, Nicholas G., Medland, Sarah E., Wray, Naomi R. and Byrne, Enda M. (2021). Polygenic risk scores derived from varying definitions of depression and risk of depression. JAMA Psychiatry, 78 (10), 1152-1160. doi: 10.1001/jamapsychiatry.2021.1988 |
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2021 Journal Article Genetic insights into biological mechanisms governing human ovarian ageingRuth, Katherine S., Day, Felix R., Hussain, Jazib, Martínez-Marchal, Ana, Aiken, Catherine E., Azad, Ajuna, Thompson, Deborah J., Knoblochova, Lucie, Abe, Hironori, Tarry-Adkins, Jane L., Gonzalez, Javier Martin, Fontanillas, Pierre, Claringbould, Annique, Bakker, Olivier B., Sulem, Patrick, Walters, Robin G., Terao, Chikashi, Turon, Sandra, Horikoshi, Momoko, Lin, Kuang, Onland-Moret, N. Charlotte, Sankar, Aditya, Hertz, Emil Peter Thrane, Timshel, Pascal N., Shukla, Vallari, Borup, Rehannah, Olsen, Kristina W., Aguilera, Paula, Ferrer-Roda, Mònica ... Perry, John R. B. (2021). Genetic insights into biological mechanisms governing human ovarian ageing. Nature, 596 (7872), 393-397. doi: 10.1038/s41586-021-03779-7 |
