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2023 Journal Article Counting nevi on the outer arm provides an accurate and feasible alternative to total body nevus countIngold, N., Zhu, G., Duffy, D. L., Mothershaw, A., Martin, N. G., MacGregor, S. and Law, M. H. (2023). Counting nevi on the outer arm provides an accurate and feasible alternative to total body nevus count. Journal of the European Academy of Dermatology and Venereology, 37 (11), e1302-e1304. doi: 10.1111/jdv.19279 |
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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 |
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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 |
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2023 Journal Article Genetic determinants of thyroid function in childrenMulder, Tessa A, Campbell, Purdey J, Taylor, Peter N, Peeters, Robin P, Wilson, Scott G, Medici, Marco, Dayan, Colin, Jaddoe, Vincent V W, Walsh, John P, Martin, Nicholas G, Tiemeier, Henning and Korevaar, Tim I M (2023). Genetic determinants of thyroid function in children. European Journal of Endocrinology, 189 (2), 164-174. doi: 10.1093/ejendo/lvad086 |
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2023 Journal Article The effect of genetic predisposition to Alzheimer’s disease and related traits on recruitment bias in a study of cognitive agingGomez, Lina M., Mitchell, Brittany L., McAloney, Kerrie, Adsett, Jessica, Garden, Natalie, Wood, Madeline, Diaz-Torres, Santiago, Garcia-Marin, Luis M., Breakspear, Michael, Martin, Nicholas G. and Lupton, Michelle K. (2023). The effect of genetic predisposition to Alzheimer’s disease and related traits on recruitment bias in a study of cognitive aging. Twin Research and Human Genetics, 26 (3) PII S1832427423000269, 1-6. doi: 10.1017/thg.2023.26 |
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2023 Journal Article GWAs identify DNA variants influencing eyebrow thickness variation in Europeans and across continental populationsPeng, Fuduan, Xiong, Ziyi, Zhu, Gu, Hysi, Pirro G., Eller, Ryan J., Wu, Sijie, Adhikari, Kaustubh, Chen, Yan, Li, Yi, Gonzalez-José, Rolando, Schüler-Faccini, Lavinia, Bortolini, Maria-Cátira, Acuña-Alonzo, Victor, Canizales-Quinteros, Samuel, Gallo, Carla, Poletti, Giovanni, Bedoya, Gabriel, Rothhammer, Francisco, Uitterlinden, André G., Ikram, M. Arfan, Nijsten, Tamar, Ruiz-Linares, Andrés, Wang, Sijia, Walsh, Susan, Spector, Timothy D., Martin, Nicholas G., Kayser, Manfred and Liu, Fan (2023). GWAs identify DNA variants influencing eyebrow thickness variation in Europeans and across continental populations. Journal of Investigative Dermatology, 143 (7), 1317-1322. doi: 10.1016/j.jid.2022.11.026 |
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2023 Journal Article Rare genetic variants underlie outlying levels of DNA methylation and gene-expressionChundru, V. Kartik, Marioni, Riccardo E., Pendergast, James G. D., Lin, Tian, Beveridge, Allan J., Martin, Nicholas G, Montgomery, Grant W., Hume, David A., Deary, Ian J., Visscher, Peter M., Wray, Naomi R. and McRae, Allan F. (2023). Rare genetic variants underlie outlying levels of DNA methylation and gene-expression. Human Molecular Genetics, 32 (11), 1912-1921. doi: 10.1093/hmg/ddad028 |
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2023 Journal Article Author Correction: The power of genetic diversity in genome-wide association studies of lipidsGraham, Sarah E., Clarke, Shoa L., Wu, Kuan-Han H., Kanoni, Stavroula, Zajac, Greg J. M., Ramdas, Shweta, Surakka, Ida, Ntalla, Ioanna, Vedantam, Sailaja, Winkler, Thomas W., Locke, Adam E., Marouli, Eirini, Hwang, Mi Yeong, Han, Sohee, Narita, Akira, Choudhury, Ananyo, Bentley, Amy R., Ekoru, Kenneth, Verma, Anurag, Trivedi, Bhavi, Martin, Hilary C., Hunt, Karen A., Hui, Qin, Klarin, Derek, Zhu, Xiang, Thorleifsson, Gudmar, Helgadottir, Anna, Gudbjartsson, Daniel F., Holm, Hilma ... Global Lipids Genetics Consortium (2023). Author Correction: The power of genetic diversity in genome-wide association studies of lipids. Nature, 618 (7965), E19-E20. doi: 10.1038/s41586-023-06194-2 |
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2023 Journal Article Shared molecular genetic factors influence subcortical brain morphometry and Parkinson’s disease riskGarcía-Marín, Luis M., Reyes-Pérez, Paula, Diaz-Torres, Santiago, Medina-Rivera, Alejandra, Martin, Nicholas G., Mitchell, Brittany L. and Rentería, Miguel E. (2023). Shared molecular genetic factors influence subcortical brain morphometry and Parkinson’s disease risk. npj Parkinson's Disease, 9 (1) 73, 73. doi: 10.1038/s41531-023-00515-y |
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2023 Journal Article Associations between cannabis use, polygenic liability for schizophrenia, and cannabis-related experiences in a sample of cannabis usersJohnson, Emma C., Colbert, Sarah M.C., Jeffries, Paul W., Tillman, Rebecca, Bigdeli, Tim B., Karcher, Nicole R., Chan, Grace, Kuperman, Samuel, Meyers, Jacquelyn L., Nurnberger, John I., Plawecki, Martin H., Degenhardt, Louisa, Martin, Nicholas G., Kamarajan, Chella, Schuckit, Marc A., Murray, Robin M., Dick, Danielle M., Edenberg, Howard J., D’Souza, Deepak Cyril, Di Forti, Marta, Porjesz, Bernice, Nelson, Elliot C. and Agrawal, Arpana (2023). Associations between cannabis use, polygenic liability for schizophrenia, and cannabis-related experiences in a sample of cannabis users. Schizophrenia Bulletin, 49 (3), 778-787. doi: 10.1093/schbul/sbac196 |
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2023 Journal Article Specificity in genetic and environmental risk for prescription opioid misuse and heroin useDash, Genevieve F., Gizer, Ian R., Martin, Nicholas G. and Slutske, Wendy S. (2023). Specificity in genetic and environmental risk for prescription opioid misuse and heroin use. Psychological Medicine, 107 (2), 6828-6837. doi: 10.1017/s003329172300034x |
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2023 Journal Article The genetic basis of endometriosis and comorbidity with other pain and inflammatory conditionsRahmioglu, Nilufer, Mortlock, Sally, Ghiasi, Marzieh, Møller, Peter L., Stefansdottir, Lilja, Galarneau, Geneviève, Turman, Constance, Danning, Rebecca, Law, Matthew H., Sapkota, Yadav, Christofidou, Paraskevi, Skarp, Sini, Giri, Ayush, Banasik, Karina, Krassowski, Michal, Lepamets, Maarja, Marciniak, Błażej, Nõukas, Margit, Perro, Danielle, Sliz, Eeva, Sobalska-Kwapis, Marta, Thorleifsson, Gudmar, Topbas-Selcuki, Nura F., Vitonis, Allison, Westergaard, David, Arnadottir, Ragnheidur, Burgdorf, Kristoffer S., Campbell, Archie, Cheuk, Cecilia S. K. ... The 23andMe Research Team (2023). The genetic basis of endometriosis and comorbidity with other pain and inflammatory conditions. Nature Genetics, 55 (3), 423-436. doi: 10.1038/s41588-023-01323-z |
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2023 Journal Article Genetic risk score for intracranial aneurysms: prediction of subarachnoid hemorrhage and role in clinical heterogeneityBakker, Mark K., Kanning, Jos P., Abraham, Gad, Martinsen, Amy E., Winsvold, Bendik S., Zwart, John-Anker, Bourcier, Romain, Sawada, Tomonobu, Koido, Masaru, Kamatani, Yoichiro, Morel, Sandrine, Amouyel, Philippe, Debette, Stéphanie, Bijlenga, Philippe, Berrandou, Takiy, Ganesh, Santhi K., Bouatia-Naji, Nabila, Jones, Gregory, Bown, Matthew, Rinkel, Gabriel J.E., Veldink, Jan H., Ruigrok, Ynte M., Hege Aamodt, Anne, Heidi Skogholt, Anne, Brumpton, Ben M., Willer, Cristen J., Sandset, Else C., Kristoffersen, Espen S., Ellekjær, Hanne ... International Stroke Genetics Consortium (ISGC) Intracranial Aneurysm Working Group (2023). Genetic risk score for intracranial aneurysms: prediction of subarachnoid hemorrhage and role in clinical heterogeneity. Stroke, 54 (3), 810-818. doi: 10.1161/STROKEAHA.122.040715 |
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2023 Journal Article Discovery of genomic loci associated with sleep apnoea risk through multi-trait GWAS analysis with snoringCampos, Adrian I., Ingold, Nathan, Huang, Yunru, Mitchell, Brittany L., Kho, Pik-Fang, Han, Xikun, García-Marín, Luis M., Ong, Jue-Sheng, 23andMe Research Team, Law, Matthew H., Yokoyama, Jennifer S., Martin, Nicholas G., Dong, Xianjun, Cuellar-Partida, Gabriel, MacGregor, Stuart, Aslibekyan, Stella and Rentería, Miguel E. (2023). Discovery of genomic loci associated with sleep apnoea risk through multi-trait GWAS analysis with snoring. Sleep, 46 (3) zsac308, 1-14. doi: 10.1093/sleep/zsac308 |
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2023 Journal Article Author Correction: Discovery of 42 genome-wide significant loci associated with dyslexiaDoust, Catherine, Fontanillas, Pierre, Eising, Else, Gordon, Scott D., Wang, Zhengjun, Alagöz, Gökberk, Molz, Barbara, Aslibekyan, Stella, Auton, Adam, Babalola, Elizabeth, Bell, Robert K., Bielenberg, Jessica, Bryc, Katarzyna, Bullis, Emily, Coker, Daniella, Partida, Gabriel Cuellar, Dhamija, Devika, Das, Sayantan, Elson, Sarah L., Filshtein, Teresa, Fletez-Brant, Kipper, Freyman, Will, Gandhi, Pooja M., Heilbron, Karl, Hicks, Barry, Hinds, David A., Jewett, Ethan M., Jiang, Yunxuan, Kukar, Katelyn ... Quantitative Trait Working Group of the GenLang Consortium (2023). Author Correction: Discovery of 42 genome-wide significant loci associated with dyslexia. Nature Genetics, 55 (3), 520-520. doi: 10.1038/s41588-023-01336-8 |
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2023 Journal Article Epigenome-wide association study reveals CpG sites associated with thyroid function and regulatory effects on KLF9Weihs, Antoine, Chaker, Layal, Martin, Tiphaine Christiane, Braun, Kim V.E., Campbell, Purdey J, Cox, Simon R, Fornage, Myriam, Gieger, Christian, Grabe, Hans J, Grallert, Harald, Harris, Sarah E, Kühnel, Brigitte, Marioni, Riccardo E, Martin, Nicholas G, McCartney, Daniel L, McRae, Allan F, Meisinger, Christa, Meurs, Joyce van, Nano, Jana, Nauck, Matthias, Peters, Annette, Prokisch, Holger, Roden, Michael, Selvin, Elizabeth, Beekman, Marian, van Heemst, Diana, Slagboom, Eline P, Swenson, Brenton R, Tin, Adrienne ... Teumer, Alexander (2023). Epigenome-wide association study reveals CpG sites associated with thyroid function and regulatory effects on KLF9. Thyroid (ja), 301-311. doi: 10.1089/thy.2022.0373 |
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2023 Journal Article Polygenic risk scores and the prediction of onset of mood and psychotic disorders in adolescents and young adultsScott, Jan, Crouse, Jacob J., Medland, Sarah, Byrne, Enda, Iorfino, Frank, Mitchell, Brittany, Gillespie, Nathan A., Martin, Nicholas, Wray, Naomi and Hickie, Ian B. (2023). Polygenic risk scores and the prediction of onset of mood and psychotic disorders in adolescents and young adults. Early Intervention in Psychiatry, 18 (6), 397-405. doi: 10.1111/eip.13472 |
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2023 Journal Article Adolescent substance use and high school noncompletion: exploring the nature of the relationship using a discordant twin designDavis, Christal N., Gizer, Ian R., Lynskey, Michael T., Statham, Dixie J., Heath, Andrew C., Martin, Nicholas G. and Slutske, Wendy S. (2023). Adolescent substance use and high school noncompletion: exploring the nature of the relationship using a discordant twin design. Addiction, 118 (1), 167-176. doi: 10.1111/add.15996 |
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2023 Journal Article Genome-wide analysis identifies genetic effects on reproductive success and ongoing natural selection at the FADS locusMathieson, Iain, Day, Felix R., Barban, Nicola, Tropf, Felix C., Brazel, David M., van Heemst, Diana, Vaez, Ahmad, van Zuydam, Natalie, Bitarello, Bárbara D., Gardner, Eugene J., Akimova, Evelina T., Azad, Ajuna, Bergmann, Sven, Bielak, Lawrence F., Boomsma, Dorret I., Bosak, Kristina, Brumat, Marco, Buring, Julie E., Cesarini, David, Chasman, Daniel I., Chavarro, Jorge E., Cocca, Massimiliano, Concas, Maria Pina, Davey Smith, George, Davies, Gail, Deary, Ian J., Esko, Tõnu, Faul, Jessica D., Franco, Oscar ... Perry, John R. B. (2023). Genome-wide analysis identifies genetic effects on reproductive success and ongoing natural selection at the FADS locus. Nature Human Behaviour, 7 (5), 790-801. doi: 10.1038/s41562-023-01528-6 |
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2022 Journal Article Implicating genes, pleiotropy, and sexual dimorphism at blood lipid loci through multi-ancestry meta-analysisKanoni, Stavroula, Graham, Sarah E., Wang, Yuxuan, Surakka, Ida, Ramdas, Shweta, Zhu, Xiang, Clarke, Shoa L., Bhatti, Konain Fatima, Vedantam, Sailaja, Winkler, Thomas W., Locke, Adam E., Marouli, Eirini, Zajac, Greg J. M., Wu, Kuan-Han H., Ntalla, Ioanna, Hui, Qin, Klarin, Derek, Hilliard, Austin T., Wang, Zeyuan, Xue, Chao, Thorleifsson, Gudmar, Helgadottir, Anna, Gudbjartsson, Daniel F., Holm, Hilma, Olafsson, Isleifur, Hwang, Mi Yeong, Han, Sohee, Akiyama, Masato, Sakaue, Saori ... Peloso, Gina M. (2022). Implicating genes, pleiotropy, and sexual dimorphism at blood lipid loci through multi-ancestry meta-analysis. Genome Biology, 23 (1) 268, 1-42. doi: 10.1186/s13059-022-02837-1 |
