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2011 Journal Article GWAS findings for human iris patterns: Associations with variants in genes that influence normal neuronal pattern developmentLarsson, Mats, Duffy, David L., Zhu, Gu, Liu, Jimmy Z., Macgregor, Stuart, McRae, Allan F., Wright, Margaret J., Sturm, Richard A., Mackey, David A., Montgomery, Grant W., Martin, Nicholas G. and Medland, Sarah E. (2011). GWAS findings for human iris patterns: Associations with variants in genes that influence normal neuronal pattern development. American Journal of Human Genetics, 89 (2), 334-343. doi: 10.1016/j.ajhg.2011.07.011 |
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2011 Journal Article Risk for suicidal thoughts and behavior after childhood sexual abuse in women and menBedi, Saaniya, Nelson, Elliot C., Lynskey, Michael T., McCutcheon, Vivia V., Heath, Andrew C., Madden, Pamela A. F. and Martin, Nicholas G. (2011). Risk for suicidal thoughts and behavior after childhood sexual abuse in women and men. Suicide and Life-Threatening Behavior, 41 (4), 406-415. doi: 10.1111/j.1943-278X.2011.00040.x |
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2011 Journal Article LPAR1 and ITGA4 Regulate Peripheral Blood Monocyte CountsMaugeri, Narelle, Powell, Joseph E., 't Hoen, Peter A. C., de Geus, Eco J. C., Willemsen, Gonneke, Kattenberg, Mathijs, Henders, Anjali K., Wallace, Leanne, Penninx, Brenda, Hottenga, Jouke-Jan, Medland, Sarah E., Saviouk, Viatcheslav, Martin, Nicholas G., Visscher, Peter M., van Ommen, Gert-Jan B., Frazer, Ian H., Boomsma, Dorret I., Montgomery, Grant W. and Ferreira, Manuel A. R (2011). LPAR1 and ITGA4 Regulate Peripheral Blood Monocyte Counts. Human Mutation, 32 (8), 873-876. doi: 10.1002/humu.21536 |
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2011 Journal Article Genome-wide association analysis of coffee drinking suggests association with CYP1A1/CYP1A2 and NRCAMAmin, N., Byrne, E., Johnson, J., Chenevix-Trench, G., Walter, S., Nolte, I. M., kConFab Investigators, Vink, J.M., Rawal, R., Mangino, M., Teumer, A., Keers, J. C., Verwoert, G., Baumeister, S., Biffar, R., Petersmann, A., Dahmen, N., Doering, A., Isaacs, A., Broer, L., Wray, N. R., Montgomery, G. W., Levy, D., Psaty, B. M., Gudnason, V., Chakravarti, A., Sulem, P., Gudbjartsson, D. F., Kiemeney, L. A. ... van Duijn, C. M. (2011). Genome-wide association analysis of coffee drinking suggests association with CYP1A1/CYP1A2 and NRCAM. Molecular Psychiatry, 17 (11), 1116-1129. doi: 10.1038/mp.2011.101 |
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2011 Journal Article Heritability of working memory brain activationBlokland, Gabriella A. M., McMahon, Katie L., Thompson, Paul M., Martin, Nicholas G., de Zubicaray, Greig I. and Wright, Margaret J. (2011). Heritability of working memory brain activation. Journal of Neuroscience, 31 (30), 10882-10890. doi: 10.1523/JNEUROSCI.5334-10.2011 |
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2011 Journal Article Ophthalmic phenotypes and the representativeness of twin data for the general populationSanfilippo, Paul G., Medland, Sarah E., Hewitt, Alex W., Kearns, Lisa S., Ruddle, Jonathan B., Sun, Cong, Hammond, Christopher J., Young, Terri L., Martin, Nicholas G. and Mackey, David A. (2011). Ophthalmic phenotypes and the representativeness of twin data for the general population. Investigative Ophthalmology & Visual Science, 52 (8), 5565-5572. doi: 10.1167/iovs.11-7258 |
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2011 Journal Article Sensation seeking in females from opposite-versus same-sex twin pairs: hormone transfer or sibling imitation?Slutske, Wendy S., Bascom, Elise N., Meier, Madeline H., Medland, Sarah E. and Martin, Nicholas G. (2011). Sensation seeking in females from opposite-versus same-sex twin pairs: hormone transfer or sibling imitation?. Behavior Genetics, 41 (4), 533-542. doi: 10.1007/s10519-010-9416-3 |
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2011 Journal Article Genomic inflation factors under polygenic inheritanceYang, Jian, Weedon, Michael N., Purcell, Shaun, Lettre, Guillaume, Estrada, Karol, Willer, Cristen J., Smith, Albert V., Ingelsson, Erik, O'Connell, Jeffrey R., Mangino, Massimo, Maegi, Reedik, Madden, Pamela A., Heath, Andrew C., Nyholt, Dale R., Martin, Nicholas G., Montgomery, Grant W., Frayling, Timothy M., Hirschhorn, Joel N., McCarthy, Mark I., Goddard, Michael E. and Visscher, Peter M. (2011). Genomic inflation factors under polygenic inheritance. European Journal of Human Genetics, 19 (7), 807-812. doi: 10.1038/ejhg.2011.39 |
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2011 Journal Article Parental depression and offspring psychopathology: a Children of Twins studySingh, A. L., D'Onofrio, B. M., Slutske, W. S., Turkheimer, E., Emery, R. E., Harden, K. P., Heath, A. C., Madden, P. A. F., Statham, D. J. and Martin, N. G. (2011). Parental depression and offspring psychopathology: a Children of Twins study. Psychological Medicine, 41 (7), 1385-1395. doi: 10.1017/S0033291710002059 |
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2011 Journal Article Genetic architecture of circulating lipid levelsDemirkan, Ayse, Amin, Najaf, Isaacs, Aaron, Jarvelin, Marjo-Riitta, Whitfield, John B., Wichmann, Heinz-Erich, Kyvik, Kirsten Ohm, Rudan, Igor, Gieger, Christian, Hicks, Andrew A., Johansson, Asa, Hottenga, Jouke-Jan, Smith, Johannes J., Wild, Sarah H., Pedersen, Nancy L., Willemsen, Gonneke, Mangino, Massimo, Hayward, Caroline, Uitterlinden, Andre G., Hofman, Albert, Witteman, Jacqueline, Montgomery, Grant W., Pietilainen, Kirsi H., Rantanen, Taina, Kaprio, Jaakko, Doering, Angela, Pramstaller, Peter P., Gyllensten, Ulf, de Geus, Eco J. C. ... van Duijn, Cornelia M. (2011). Genetic architecture of circulating lipid levels. European Journal of Human Genetics, 19 (7), 813-819. doi: 10.1038/ejhg.2011.21 |
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2011 Journal Article Performance of a third-generation TSH-receptor antibody in a UK clinicTheodoraki, A., Jones, G., Parker, J., Woolman, E., Martin, N., Perera, S., Thomas, M., Bunn, C., Khoo, B., Bouloux, P. M. and Vanderpump, M. P. J. (2011). Performance of a third-generation TSH-receptor antibody in a UK clinic. Clinical Endocrinology, 75 (1), 127-133. doi: 10.1111/j.1365-2265.2011.04022.x |
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2011 Journal Article High-density fine-mapping of a chromosome 10q26 linkage peak suggests association between endometriosis and variants close to CYP2C19Painter, Jodie N., Nyholt, Dale R., Morris, Andrew, Zhao, Zhen Z., Henders, Anjali K., Lambert, Ann, Wallace, Leanne, Martin, Nicholas G., Kennedy, Stephen H., Treloar, Susan A., Zondervan, Krina T. and Montgomery, Grant W. (2011). High-density fine-mapping of a chromosome 10q26 linkage peak suggests association between endometriosis and variants close to CYP2C19. Fertility and Sterility, 95 (7), 2236-2240. doi: 10.1016/j.fertnstert.2011.03.062 |
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2011 Journal Article Genetics of insomniaGehrman, Philip R., Byrne, Enda, Gillespie, Nathan and Martin, Nicholas G. (2011). Genetics of insomnia. Sleep Medicine Clinics, 6 (2), 191-202. doi: 10.1016/j.jsmc.2011.03.003 |
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2011 Journal Article Genome-wide association study identifies susceptibility loci for open angle glaucoma at TMCO1 and CDKN2B-AS1Burdon, Kathryn P., Macgregor, Stuart, Hewitt, Alex W., Sharma, Shiwani, Chidlow, Glyn, Mills, Richard A., Danoy, Patrick, Casson, Robert, Viswanathan, Ananth C., Liu, Jimmy Z., Landers, John, Henders, Anjali K., Wood, John, Souzeau, Emmanuelle, Crawford, April, Leo, Paul, Wang, Jie Jin, Rochtchina, Elena, Nyholt, Dale R., Martin, Nicholas G., Montgomery, Grant W., Mitchell, Paul, Brown, Matthew A., Mackey, David A. and Craig, Jamie E. (2011). Genome-wide association study identifies susceptibility loci for open angle glaucoma at TMCO1 and CDKN2B-AS1. Nature Genetics, 43 (6), 574-578. doi: 10.1038/ng.824 |
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2011 Journal Article Transferrin saturation and mortalityBenyamin, Beben, Montgomery, Grant W., Martin, Nicholas G. and Whitfield, John B. (2011). Transferrin saturation and mortality. Clinical Chemistry, 57 (6), 921-923. doi: 10.1373/clinchem.2011.162784 |
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2011 Journal Article SNP sets and reading ability: testing confirmation of a 10-SNP set in a population sampleLuciano, Michelle, Montgomery, Grant W., Martin, Nicholas G., Wright, Margaret J. and Bates, Timothy C. (2011). SNP sets and reading ability: testing confirmation of a 10-SNP set in a population sample. Twin Research and Human Genetics, 14 (3), 228-232. doi: 10.1375/twin.14.3.228 |
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2011 Journal Article Educational Attainment: A Genome Wide Association Study in 9538 AustraliansMartin, Nicolas W., Medland, Sarah E., Verweij, Karin J. H., Lee, S. Hong, Nyholt, Dale R., Madden, Pamela A., Heath, Andrew C., Montgomery, Grant W., Wright, Margaret J. and Martin, Nicholas G. (2011). Educational Attainment: A Genome Wide Association Study in 9538 Australians. PLoS One, 6 (6) e20128, e20128.1-e20128.8. doi: 10.1371/journal.pone.0020128 |
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2011 Journal Article Revisiting the effect of marital support on depressive symptoms in mothers and fathers: a genetically informed studyBeam, Christopher R., Horn, Erin E., Hunt, Stacy Karagis, Emery, Robert E., Turkheimer, Eric and Martin, Nick (2011). Revisiting the effect of marital support on depressive symptoms in mothers and fathers: a genetically informed study. Journal of Family Psychology, 25 (3), 336-344. doi: 10.1037/a0023758 |
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2011 Journal Article Genome-wide association and genetic functional studies identify autism susceptibility candidate 2 gene (AUTS2) in the regulation of alcohol consumption (vol 108, pg 7119, 2011)Schumann, Gunter, Coin, Lachlan J., Lourdusamy, Anbarasu, Charoen, Pimphen, Berger, Karen H., Stacey, David, Desrivieres, Sylvane, Aliev, Fazil A., Khan, Anokhi A., Amin, Najaf, Aulchenko, Yurii S., Bakalkin, Georgy, Bakker, Stephan J., Balkau, Beverley, Beulens, Joline W., Bilbao, Ainhoa, de Boer, Rudolf A., Beury, Delphine, Bots, Michiel L., Breetvelt, Elemi J., Cauchi, Stephane, Cavalcanti-Proenca, Christine, Chambers, John C., Clarke, Toni-Kim, Dahmen, Norbert, de Geus, Eco J., Dick, Danielle, Ducci, Francesca, Easton, Alanna ... Elliott, Paul (2011). Genome-wide association and genetic functional studies identify autism susceptibility candidate 2 gene (AUTS2) in the regulation of alcohol consumption (vol 108, pg 7119, 2011). Proceedings of the National Academy of Sciences of the United States of America, 108 (22), 9316-9316. doi: 10.1073/pnas.1106917108 |
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2011 Journal Article Common Alzheimer's disease risk variant within the CLU gene affects white matter microstructure in young adultsBraskie, Meredith N., Jahanshad, Neda, Stein, Jason L., Barysheva, Marina, McMahon, Katie L., de Zubicaray, Greig I., Martin, Nicholas G., Wright, Margaret J., Ringman, John M., Toga, Arthur W. and Thompson, Paul M. (2011). Common Alzheimer's disease risk variant within the CLU gene affects white matter microstructure in young adults. The Journal of Neuroscience, 31 (18), 6764-6770. doi: 10.1523/JNEUROSCI.5794-10.2011 |
