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2014 Journal Article Genetic and environmental influences on the ages of drinking and gambling initiation: evidence for distinct aetiologies and sex differencesRichmond-Rakerd, Leah S., Slutske, Wendy S., Heath, Andrew C. and Martin, Nicholas G. (2014). Genetic and environmental influences on the ages of drinking and gambling initiation: evidence for distinct aetiologies and sex differences. Addiction, 109 (2), 323-331. doi: 10.1111/add.12310 |
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2014 Journal Article Genetic effects on the cerebellar role in working memory: same brain, different genes?Blokland, Gabriëlla A. M., McMahon, Katie L., Thompson, Paul M., Hickie, Ian B., Martin, Nicholas G., de Zubicaray, Greig I. and Wright, Margaret J. (2014). Genetic effects on the cerebellar role in working memory: same brain, different genes?. NeuroImage, 86, 392-403. doi: 10.1016/j.neuroimage.2013.10.006 |
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2014 Journal Article Genetic risk score analysis indicates migraine with and without comorbid depression are genetically different disordersLigthart, Lannie, Hottenga, Jouke-Jan, Lewis, Cathryn M., Farmer, Anne E., Craig, Ian W., Breen, Gerome, Willemsen, Gonneke, Vink, Jacqueline M., Middeldorp, Christel M., Byrne, Enda M., Heath, Andrew C., Madden, Pamela A. F., Pergadia, Michele L., Montgomery, Grant W., Martin, Nicholas G., Penninx, Brenda W. J. H., McGuffin, Peter, Boomsma, Dorret I. and Nyholt, Dale R. (2014). Genetic risk score analysis indicates migraine with and without comorbid depression are genetically different disorders. Human Genetics, 133 (2), 173-186. doi: 10.1007/s00439-013-1370-8 |
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2014 Journal Article Multi-site genetic analysis of diffusion images and voxelwise heritability analysis: A pilot project of the ENIGMA-DTI working group (vol 81, pg 455, 2013)Jahanshad, Neda, Kochunov, Peter V., Sprooten, Emma, Mandl, Rene C., Nichols, Thomas E., Almasy, Laura, Blangero, John, Brouwer, Rachel M., Curran, Joanne E., de Zubicaray, Greig I., Duggirala, Ravi, Fox, Peter T., Hong, L. Elliot, Landman, Bennett A., Martin, Nicholas G., McMahon, Katie L., Medland, Sarah E., Mitchell, Braxton D., Olvera, Rene L., Peterson, Charles P., Starr, John M., Sussmann, Jessika E., Toga, Arthur W., Wardlaw, Joanna M., Wright, Margaret J., Pol, Hilleke E. Hulshoff, Bastin, Mark E., McIntosh, Andrew M., Deary, Ian J. ... Glahn, David C. (2014). Multi-site genetic analysis of diffusion images and voxelwise heritability analysis: A pilot project of the ENIGMA-DTI working group (vol 81, pg 455, 2013). Neuroimage, 90, 470-471. doi: 10.1016/j.neuroimage.2013.12.053 |
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2014 Journal Article Human cognitive ability is influenced by genetic variation in components of postsynaptic signalling complexes assembled by NMDA receptors and MAGUK proteinsHill, W. D., Davies, G., Van De Lagemaat, L. N., Christoforou, A., Marioni, R. E., Fernandes, C. P. D., Liewald, D. C., Croning, M. D. R., Payton, A., Craig, L. C. A., Whalley, L. J., Horan, M., Ollier, W., Hansell, N. K., Wright, M. J., Martin, N. G., Montgomery, G. W., Steen, V. M., Le Hellard, S., Espeseth, T., Lundervold, A. J., Reinvang, I., Starr, J. M., Pendleton, N., Grant, S. G. N., Bates, T. C. and Deary, I. J. (2014). Human cognitive ability is influenced by genetic variation in components of postsynaptic signalling complexes assembled by NMDA receptors and MAGUK proteins. Translational Psychiatry, 4 (1) e341, 1-8. doi: 10.1038/tp.2013.114 |
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2014 Journal Article DNA modification study of major depressive disorder: beyond locus-by-locus comparisonsOh, Gabriel, Wang, Sun-Chong, Pal, Mrinal, Chen, Zheng Fei, Khare, Tarang, Tochigi, Mamoru, Ng, Catherine, Yang, Yeqing A., Kwan, Andrew, Kaminsky, Zachary A., Mill, Jonathan, Gunasinghe, Cerisse, Tackett, Jennifer L., Gottesman, Irving I., Willemsen, Gonneke, de Geus, Eco J. C., Vink, Jacqueline M., Slagboom, P. Eline, Wray, Naomi R., Heath, Andrew C., Montgomery, Grant W., Turecki, Gustavo, Martin, Nicholas G., Boomsma, Dorret I., McGuffin, Peter, Kustra, Rafal and Petronis, Art (2014). DNA modification study of major depressive disorder: beyond locus-by-locus comparisons. Biological Psychiatry, 77 (3), 246-255. doi: 10.1016/j.biopsych.2014.06.016 |
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2014 Journal Article POT1 loss-of-function variants predispose to familial melanomaRobles-Espinoza, Carla Daniela, Harland, Mark, Ramsay, Andrew J, Aoude, Lauren G, Quesada, Víctor, Ding, Zhihao, Pooley, Karen A, Pritchard, Antonia L, Tiffen, Jessamy C, Petljak, Mia, Palmer, Jane M, Symmons, Judith, Johansson, Peter, Stark, Mitchell S., Gartside, Michael G, Snowden, Helen, Montgomery, Grant W, Martin, Nicholas G, Liu, Jimmy Z, Choi, Jiyeon, Makowski, Matthew, Brown, Kevin M, Dunning, Alison M, Keane, Thomas M, Lopez-Otin, Carlos, Gruis, Nelleke A, Hayward, Nicholas K, Bishop, D Timothy, Newton-Bishop, Julia A and Adams, David J (2014). POT1 loss-of-function variants predispose to familial melanoma. Nature Genetics, 46 (5), 478-481. doi: 10.1038/ng.2947 |
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2014 Journal Article Substance use and sexual intercourse onsets in adolescence: A genetically informative discordant twin designDeutsch, Arielle R., Slutske, Wendy S., Heath, Andrew C., Madden, Pamela A. F. and Martin, Nicholas G. (2014). Substance use and sexual intercourse onsets in adolescence: A genetically informative discordant twin design. Journal of Adolescent Health, 54 (1), 114-116. doi: 10.1016/j.jadohealth.2013.07.013 |
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2014 Journal Article Sexual orientation, prejudice, and segregationPlug, Erik, Webbink, Dinand and Martin, Nick (2014). Sexual orientation, prejudice, and segregation. Journal of Labor Economics, 32 (1), 123-159. doi: 10.1086/673315 |
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2014 Journal Article Genome-wide association study on detailed profiles of smoking behavior and nicotine dependence in a twin sampleLoukola, A., Wedenoja, J., Keskitalo-Vuokko, K., Broms, U., Korhonen, T., Ripatti, S., Sarin, A-P, Pitkaniemi, J., He, L., Happola, A., Heikkila, K., Chou, Y-L, Pergadia, M. L., Heath, A. C., Montgomery, G. W., Martin, N. G., Madden, P. A. F. and Kaprio, J. (2014). Genome-wide association study on detailed profiles of smoking behavior and nicotine dependence in a twin sample. Molecular Psychiatry, 19 (5), 615-624. doi: 10.1038/mp.2013.72 |
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2014 Journal Article Novel Approach Identifies SNPs in SLC2A10 and KCNK9 with Evidence for Parent-of-Origin Effect on Body Mass IndexHoggart, C. J., Venturini, G., Mangino, M., Gomez, F., Ascari, G., Zhao, J.H., Teumer, A., Winkler, T. W., Tsernikova, N., Luan, J., Mihailov, E., Ehret, G. B., Zhang, W., Lamparter, D., Esko, T., Mace, A., Rueger, S., Bochud, P.-Y., Barcella, M., Dauvilliers, Y., Benyamin, B., Evans, D. M., Hayward, C., Lopez, M. F., Franke, L., Russo, A., Heid, I. M., Salvi, E., Vendantam, S. ... Kutalik Z. (2014). Novel Approach Identifies SNPs in SLC2A10 and KCNK9 with Evidence for Parent-of-Origin Effect on Body Mass Index. PLoS Genetics, 10 (7) e1004508, 1-12. doi: 10.1371/journal.pgen.1004508 |
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2014 Journal Article Common variants in the CYP2C19 gene are associated with susceptibility to endometriosisPainter, Jodie N., Nyholt, Dale R, Krause, Lutz, Zhao, Zhen Z., Chapman, Brett, Zhang, Christine, Medland, Sarah, Martin, Nicholas G., Kennedy, Stephen, Treloar, Susan, Zondervan, Krina and Montgomery, Grant W. (2014). Common variants in the CYP2C19 gene are associated with susceptibility to endometriosis. Fertility and Sterility, 102 (2), 496-502.e5. doi: 10.1016/j.fertnstert.2014.04.015 |
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2014 Journal Article Allelic differences between Europeans and Chinese for CREB1 SNPs and their implications in gene expression regulation, hippocampal structure and function, and bipolar disorder susceptibilityLi, M., Luo, X-j, Rietschel, M., Lewis, C. M., Mattheisen, M., Mueller-Myhsok, B., Jamain, S., Leboyer, M., Landen, M., Thompson, P. M., Cichon, S., Noethen, M. M., Schulze, T. G., Sullivan, P. F., Bergen, S. E., Donohoe, G., Morris, D. W., Hargreaves, A., Gill, M., Corvin, A., Hultman, C., Toga, A. W., Shi, L., Lin, Q., Shi, H., Gan, L., Meyer-Lindenberg, A., Czamara, D., Henry, C. ... Su, B. (2014). Allelic differences between Europeans and Chinese for CREB1 SNPs and their implications in gene expression regulation, hippocampal structure and function, and bipolar disorder susceptibility. Molecular Psychiatry, 19 (4), 452-461. doi: 10.1038/mp.2013.37 |
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2014 Journal Article Automatic clustering and population analysis of white matter tracts using maximum density pathsPrasad, Gautam, Joshi, Shantanu H., Jahanshad, Neda, Villalon-Reina, Julio, Aganj, Iman, Lenglet, Christophe, Guillermo Sapiro, McMahon, Katie L., de Zubicaray, Greig I., Martin, Nicholas G., Wright, Margaret J., Toga, Arthur W. and Thompson, Paul M. (2014). Automatic clustering and population analysis of white matter tracts using maximum density paths. NeuroImage, 97, 284-295. doi: 10.1016/j.neuroimage.2014.04.033 |
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2014 Journal Article Genetic factors that increase male facial masculinity decrease facial attractiveness of female relativesLee, Anthony J., Mitchem, Dorian G., Wright, Margaret J., Martin, Nicholas G., Keller, Matthew C. and Zietsch, Brendan P. (2014). Genetic factors that increase male facial masculinity decrease facial attractiveness of female relatives. Psychological Science, 25 (2), 476-484. doi: 10.1177/0956797613510724 |
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2014 Journal Article Association of OPRD1 polymorphisms with heroin dependence in a large case-control seriesNelson, Elliot C., Lynskey, Michael T., Heath, Andrew C., Wray, Naomi, Agrawal, Arpana, Shand, Fiona L., Henders, Anjali K., Wallace, Leanne, Todorov, Alexandre A., Schrage, Andrew J., Madden, Pamela A. F., Degenhardt, Louisa, Martin, Nicholas G. and Montgomery, Grant W. (2014). Association of OPRD1 polymorphisms with heroin dependence in a large case-control series. Addiction Biology, 19 (1), 111-121. doi: 10.1111/j.1369-1600.2012.00445.x |
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2014 Journal Article Heritability of head motion during resting state functional MRI in 462 healthy twinsCouvy-Duchesne, Baptiste, Blokland, Gabriëlla A.M., Hickie, Ian B., Thompson, Paul M., Martin, Nicholas G., de Zubicaray, Greig I., McMahon, Katie L. and Wright, Margaret J. (2014). Heritability of head motion during resting state functional MRI in 462 healthy twins. Neuroimage, 102 (2), 424-434. doi: 10.1016/j.neuroimage.2014.08.010 |
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2014 Journal Article Testing the role of circadian genes in conferring risk for psychiatric disordersByrne, Enda M., Heath, Andrew C., Madden, Pamela A. F., Pergadia, Michele L., Hickie, Ian B., Montgomery, Grant W., Martin, Nicholas G. and Wray, Naomi R. (2014). Testing the role of circadian genes in conferring risk for psychiatric disorders. American Journal of Medical Genetics, Part B: Neuropsychiatric Genetics, 165 (3), 254-260. doi: 10.1002/ajmg.b.32230 |
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2014 Journal Article Genetic predisposition to schizophrenia associated with increased use of cannabisPower, R. A., Verweij, K. J. H., Zuhair, M., Montgomery, G. W., Henders, A. K., Heath, A. C., Madden, P. A. F., Medland, S. E., Wray, N. R. and Martin, N. G. (2014). Genetic predisposition to schizophrenia associated with increased use of cannabis. Molecular Psychiatry, 19 (11), 1201-1204. doi: 10.1038/mp.2014.51 |
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2014 Journal Article Common variant at 16p11.2 conferring risk of psychosisSteinberg, S., de Jong, S., Mattheisen, M., Costas, J., Demontis, D., Jamain, S., Pietilainen, O. P. H., Lin, K., Papiol, S., Huttenlocher, J., Sigurdsson, E., Vassos, E., Giegling, I., Breuer, R., Fraser, G., Walker, N., Melle, I., Djurovic, S., Agartz, I., Tuulio-Henriksson, A., Suvisaari, J., Lonnqvist, J., Paunio, T., Olsen, L., Hansen, T., Ingason, A., Pirinen, M., Strengman, E., Hougaard, D. M. ... Stefansson, K. (2014). Common variant at 16p11.2 conferring risk of psychosis. Molecular Psychiatry, 19 (1), 108-114. doi: 10.1038/mp.2012.157 |
