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2016 Journal Article Cohort profile: Nausea and vomiting during pregnancy genetics consortium (NVP Genetics Consortium)Colodro-Conde, Lucıa, Cross, Simone M., Lind, Penelope A., Painter, Jodie N., Gunst, Annika, Jern, Patrick, Johansson, Ada, Lund Maegbaek, Merete, Munk-Olsen, Trine, Nyholt, Dale R., Ordonana, Juan R., Paternoster, Lavinia, Sanchez-Romera, Juan F., Wright, Margaret J. and Medland, Sarah E. (2016). Cohort profile: Nausea and vomiting during pregnancy genetics consortium (NVP Genetics Consortium). International Journal of Epidemiology, 46 (2) e17, e17. doi: 10.1093/ije/dyv360 |
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2016 Journal Article Impact of a cis-associated gene expression SNP on chromosome 20q11.22 on bipolar disorder susceptibility, hippocampal structure and cognitive performanceLi, Ming, Luo, Xiong-Jian, Landén, Mikael, Bergen, Sarah E., Hultman, Christina M., Li, Xiao, Zhang, Wen, Yao, Yong-Gang, Zhang, Chen, Liu, Jiewei, Mattheisen, Manuel, Cichon, Sven, Mühleisen, Thomas W., Degenhardt, Franziska A., Nöthen, Markus M., Schulze, Thomas G., Grigoroiu-Serbanescu, Maria, Li, Hao, Fuller, Chris K., Chen, Chunhui, Dong, Qi, Chen, Chuansheng, Jamain, Stéphane, Leboyer, Marion, Bellivier, Frank, Etain, Bruno, Kahn, Jean-Pierre, Henry, Chantal, Preisig, Martin ... The Swedish Bipolar Study Group (2016). Impact of a cis-associated gene expression SNP on chromosome 20q11.22 on bipolar disorder susceptibility, hippocampal structure and cognitive performance. British Journal of Psychiatry, 208 (2), 128-137. doi: 10.1192/bjp.bp.114.156976 |
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2016 Journal Article Head motion and inattention/hyperactivity share common genetic influences: Implications for fMRI studies of ADHDCouvy-Duchesne, Baptiste, Ebejer, Jane L., Gillespie, Nathan A., Duffy, David L., Hickie, Ian B., Thompson, Paul M., Martin, Nicholas G., de Zubicaray, Greig I., McMahon, Katie L., Medland, Sarah E. and Wright, Margaret J. (2016). Head motion and inattention/hyperactivity share common genetic influences: Implications for fMRI studies of ADHD. PLoS One, 11 (1) e0146271, 1-19. doi: 10.1371/journal.pone.0146271 |
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2016 Journal Article Subcortical brain alterations in major depressive disorder: findings from the ENIGMA Major Depressive Disorder working groupSchmaal, L., Veltman, D. J., van Erp, T. G. M., Sämann, P. G., Frodl, T., Jahanshad, N., Loehrer, E., Tiemeier, H., Hofman, A., Niessen, W. J., Vernooij, M. W., Ikram, M. A., Wittfeld, K., Grabe, H. J., Block, A., Hegenscheid, K., Völzke, H., Hoehn, D., Czisch, M., Lagopoulos, J., Hatton, S. N., Hickie, I. B., Goya-Maldonado, R., Krämer, B., Gruber, O., Couvy-Duchesne, B., Rentería, M. E., Strike, L. T., Mills, N. T. ... Hibar, D. P. (2016). Subcortical brain alterations in major depressive disorder: findings from the ENIGMA Major Depressive Disorder working group. Molecular Psychiatry, 21 (6), 806-812. doi: 10.1038/mp.2015.69 |
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2016 Conference Publication Heritability of different aggression phenotypes in an Australian and a Dutch cohortConde, Lucia Colodro, Martin, Nicholas, Hatemi, Peter, Boomsma, Dorret, Middeldorp, Christel, van Beijsterveldt, Toos, Bartels, Meike and Medland, Sarah (2016). Heritability of different aggression phenotypes in an Australian and a Dutch cohort. 46th Annual Meeting of the Behavior-Genetics-Association, Brisbane, Australia, Jun 20-23, 2016. NEW YORK: SPRINGER. |
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2016 Journal Article Examining non-syndromic autosomal recessive intellectual disability (NS-ARID) genes for an enriched association with intelligence differencesHill, W. D., Davies, G., Liewald, D. C., Payton, A., McNeil, C. J., Whalley, L. J., Horan, M., Ollier, W., Starr, J. M., Pendleton, N., Hansel, N. K., Montgomery, G. W., Medland, S. E., Martin, N. G., Wright, M. J., Bates, T. C. and Deary, I. J. (2016). Examining non-syndromic autosomal recessive intellectual disability (NS-ARID) genes for an enriched association with intelligence differences. Intelligence, 54, 80-89. doi: 10.1016/j.intell.2015.11.005 |
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2015 Other Outputs Genome-wide association study of offspring birth weight in 86,577 women highlights maternal genetic effects that are independent of fetal geneticsBeaumont, Robin N, Warrington, Nicole M, Cavadino, Alana, Tyrrell, Jessica, Nodzenski, Michael, Horikoshi, Momoko, Geller, Frank, Myhre, Ronny, Richmond, Rebecca C., Paternoster, Lavinia, Bradfield, Jonathan P., Kreiner-Møller, Eskil, Huikari, Ville, Metrustry, Sarah, Lunetta, Kathryn L., Painter, Jodie N., Hottenga, Jouke-Jan, Allard, Catherine, Barton, Sheila J., Espinosa, Ana, Marsh, Julie A., Potter, Catherine, Zhang, Ge, Ang, Wei, Berry, Diane J., Bouchard, Luigi, Das, Shikta, Consortium, Early Growth Genetics, Hakonarson, Hakon ... Freathy, Rachel M. (2015). Genome-wide association study of offspring birth weight in 86,577 women highlights maternal genetic effects that are independent of fetal genetics. doi: 10.1101/034207 |
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2015 Journal Article Genetic fine mapping and genomic annotation defines causal mechanisms at type 2 diabetes susceptibility lociGaulton, Kyle J., Ferreira, Teresa, Lee, Yeji, Raimondo, Anne, Maegi, Reedik, Reschen, Michael E., Mahajan, Anubha, Locke, Adam, Rayner, N. William, Robertson, Neil, Scott, Robert A., Prokopenko, Inga, Scott, Laura J., Green, Todd, Sparso, Thomas, Thuillier, Dorothee, Yengo, Loic, Grallert, Harald, Wahl, Simone, Franberg, Mattias, Strawbridge, Rona J., Kestler, Hans, Chheda, Himanshu, Eisele, Lewin, Gustafsson, Stefan, Steinthorsdottir, Valgerdur, Thorleifsson, Gudmar, Qi, Lu, Karssen, Lennart C. ... Morris, Andrew P. (2015). Genetic fine mapping and genomic annotation defines causal mechanisms at type 2 diabetes susceptibility loci. Nature Genetics, 47 (12), 1415-1425. doi: 10.1038/ng.3437 |
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2015 Journal Article Genome-wide analysis implicates microRNAs and their target genes in the development of bipolar disorderForstner, A. J., Hofmann, A., Maaser, A., Sumer, S., Khudayberdiev, S., Muehleisen, T. W., Leber, M., Schulze, T. G., Strohmaier, J., Degenhardt, F., Treutlein, J., Mattheisen, M., Schumacher, J., Breuer, R., Meier, S., Herms, S., Hoffmann, P., Lacour, A., Witt, S. H., Reif, A., Mueller-Myhsok, B., Lucae, S., Maier, W., Schwarz, M., Vedder, H., Kammerer-Ciernioch, J., Pfennig, A., Bauer, M., Hautzinger, M. ... Noethen, M. M. (2015). Genome-wide analysis implicates microRNAs and their target genes in the development of bipolar disorder. Translational psychiatry, 5 (11) e678, e678-e678. doi: 10.1038/tp.2015.159 |
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2015 Journal Article Zygosity differences in height and body mass index of twins from infancy to old age: a study of the CODATwins projectJelenkovic, Aline, Yokoyama, Yoshie, Sund, Reijo, Honda, Chika, Bogl, Leonie H., Aaltonen, Sari, Ji, Fuling, Ning, Feng, Pang, Zengchang, Ordonana, Juan R., Sanchez-Romera, Juan F., Colodro-Conde, Lucia, Burt, S. Alexandra, Klump, Kelly L., Medland, Sarah E., Montgomery, Grant W., Kandler, Christian, McAdams, Tom A., Eley, Thalia C., Gregory, Alice M., Saudino, Kimberly J., Dubois, Lise, Boivin, Michel, Tarnoki, Adam D., Tarnoki, David L., Haworth, Claire M. A., Plomin, Robert, Oncel, Sevgi Y., Aliev, Fazil ... Silventoinen, Karri (2015). Zygosity differences in height and body mass index of twins from infancy to old age: a study of the CODATwins project. Twin Research and Human Genetics, 18 (5), 557-570. doi: 10.1017/thg.2015.57 |
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2015 Journal Article Meta-analysis of Genome-Wide Association Studies for Extraversion: Findings from the Genetics of Personality Consortiumvan Den Berg, Stephanie M., de Moor, Marleen H.M., Verweij, Karin J.H., Krueger, Robert F., Luciano, Michelle, Arias Vasquez, Alejandro, Matteson, Lindsay K., Derringer, Jaime, Esko, Tonu, Amin, Najaf, Gordon, Scott D., Hansell, Narelle K., Hart, Amy B., Seppala, Ilkka, Huffman, Jennifer, Konte, Bettina, Lahti, Jari, Lee, Minyoung, Miller, Mike, Nutile, Teresa, Tanaka, Toshiko, Teumer, Alexander, Viktorin, Alexander, Wedenoja, Juho, Abdellaoui, Abdel, Abecasis, Goncalo R., Adkins, Daniel E., Agrawal, Arpana, Allik, Juri ... Boomsma, Dorret I. (2015). Meta-analysis of Genome-Wide Association Studies for Extraversion: Findings from the Genetics of Personality Consortium. Behavior Genetics, 46 (2), 170-182. doi: 10.1007/s10519-015-9735-5 |
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2015 Journal Article Converging evidence does not support GIT1 as an ADHD risk geneKlein, Marieke, van der Voet, Monique, Harich, Benjamin, van Hulzen, Kimm J. E., Onnink, A. Marten H., Hoogman, Martine, Guadalupe, Tulio, Zwiers, Marcel, Groothuismink, Johanne M., Verberkt, Alicia, Nijhof, Bonnie, Castells-Nobau, Anna, Faraone, Stephen V., Buitelaar, Jan K., Schenck, Annette, Arias-Vasquez, Alejandro, Franke, Barbara, Anney, Richard J.L., Vasquez, Alejandro Arias, Asherson, Philip, Banaschewski, Tobias, Bayés, Mònica, Biederman, Joseph, Buitelaar, Jan K., Casas, Miguel, Charach, Alice, Cormand, Bru, Crosbie, Jennifer, Daly, Mark J. ... Yang, Li (2015). Converging evidence does not support GIT1 as an ADHD risk gene. American Journal of Medical Genetics, Part B: Neuropsychiatric Genetics, 168 (6), 492-507. doi: 10.1002/ajmg.b.32327 |
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2015 Journal Article The CODATwins project: the cohort description of collaborative project of development of anthropometrical measures in twins to study macro-environmental variation in genetic and environmental effects on anthropometric traitsSilventoinen, Karri, Jelenkovic, Aline, Sund, Reijo, Honda, Chika, Aaltonen, Sari, Yokoyama, Yoshie, Tarnoki, Adam D., Tarnoki, David L., Ning, Feng, Ji, Fuling, Pang, Zengchang, Ordonana, Juan R., Sanchez-Romera, Juan F., Colodro-Conde, Lucia, Burt, S. Alexandra, Klump, Kelly L., Medland, Sarah E., Montgomery, Grant W., Kandler, Christian, McAdams, Tom A., Eley, Thalia C., Gregory, Alice M., Saudino, Kimberly J., Dubois, Lise, Boivin, Michel, Haworth, Claire M. A., Plomin, Robert, Oncel, Sevgi Y., Aliev, Fazil ... Kaprio, Jaakko (2015). The CODATwins project: the cohort description of collaborative project of development of anthropometrical measures in twins to study macro-environmental variation in genetic and environmental effects on anthropometric traits. Twin Research and Human Genetics, 18 (4), 348-360. doi: 10.1017/thg.2015.29 |
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2015 Journal Article Meta-analysis of genome-wide association studies for neuroticism, and the polygenic association with major depressive disorderDe Moor, Marleen H.M, Van Den Berg, Stephanie M, Verweij, Karin J.H, Krueger, Robert F, Luciano, Michelle, Arias Vasquez, Alejandro, Matteson, Lindsay K, Derringer, Jaime, Esko, Tonu, Amin, Najaf, Gordon, Scott D, Hansell, Narelle K, Hart, Amy B, Seppala, Ilkka, Huffman, Jennifer E, Konte, Bettina, Lahti, Jari, Lee, Minyoung, Miller, Mike, Nutile, Teresa, Tanaka, Toshiko, Teumer, Alexander, Viktorin, Alexander, Wedenoja, Juho, Abecasis, Goncalo R, Adkins, Daniel E, Agrawal, Arpana, Allik, Juri, Appel, Katja ... Boomsma, Dorret I (2015). Meta-analysis of genome-wide association studies for neuroticism, and the polygenic association with major depressive disorder. JAMA Psychiatry, 72 (7), 642-650. doi: 10.1001/jamapsychiatry.2015.0554 |
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2015 Journal Article Directional dominance on stature and cognition in diverse human populationsJoshi, Peter K., Esko, Tonu, Mattsson, Hannele, Eklund, Niina, Gandin, Ilaria, Nutile, Teresa, Jackson, Anne U., Schurmann, Claudia, Smith, Albert V., Zhang, Weihua, Okada, Yukinori, Stancakova, Alena, Faul, Jessica D., Zhao, Wei, Bartz, Traci M., Concas, Maria Pina, Franceschini, Nora, Enroth, Stefan, Vitart, Veronique, Trompet, Stella, Guo, Xiuqing, Chasman, Daniel I., O'Connel, Jeffrey R., Corre, Tanguy, Nongmaithem, Suraj S., Chen, Yuning, Mangino, Massimo, Ruggiero, Daniela, Traglia, Michela ... Wilson, James F. (2015). Directional dominance on stature and cognition in diverse human populations. Nature, 523 (7561), 459-462. doi: 10.1038/nature14618 |
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2015 Journal Article Retinal microvessels reflect familial vulnerability to psychotic symptoms: A comparison of twins discordant for psychotic symptoms and controlsMeier, Madeline H., Gillespie, Nathan A., Hansell, Narelle K., Hewitt, Alex W., Hickie, Ian B., Lu, Yi, McGrath, John, MacGregor, Stuart, Medland, Sarah E., Sun, Cong, Wong, Tien Y., Wright, Margaret J., Zhu, Gu, Martin, Nicholas G. and Mackey, David A. (2015). Retinal microvessels reflect familial vulnerability to psychotic symptoms: A comparison of twins discordant for psychotic symptoms and controls. Schizophrenia Research, 164 (1-3), 47-52. doi: 10.1016/j.schres.2015.01.045 |
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2015 Journal Article Common genetic variants influence human subcortical brain structuresHibar, Derrek P, Stein, Jason L, Renteria, Miguel E, Arias-Vasquez, Alejandro, Desrivieres, Sylvane, Jahanshad, Neda, Toro, Roberto, Wittfeld, Katharina, Abramovic, Lucija, Andersson, Micael, Aribisala, Benjamin S, Armstrong, Nicola J, Bernard, Manon, Bohlken, Marc M, Boks, Marco P, Bralten, Janita, Brown, Andrew A, Mallar Chakravarty M., Chen, Qiang, Ching, Christopher R.K., Cuellar-Partida, Gabriel, Den Braber, Anouk, Giddaluru, Sudheer, Goldman, Aaron L, Grimm, Oliver, Guadalupe, Tulio, Hass, Johanna, Woldehawariat, Girma, Holmes, Avram J ... Medland, Sarah E (2015). Common genetic variants influence human subcortical brain structures. Nature, 520 (7546), 224-229. doi: 10.1038/nature14101 |
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2015 Journal Article Genetic basis of a cognitive complexity metricHansell, Narelle K., Halford, Graeme S., Andrews, Glenda, Shum, David H. K., Harris, Sarah E., Davies, Gail, Franic, Sanja, Christoforou, Andrea, Zietsch, Brendan, Painter, Jodie, Medland, Sarah E., Ehli, Erik A., Davies, Gareth E., Steen, Vidar M., Lundervold, Astri J., Reinvang, Ivar, Montgomery, Grant W., Espeseth, Thomas, Pol, Hilleke E. Hulshoff, Starr, John M., Martin, Nicholas G., Le Hellard, Stephanie, Boomsma, Dorret I., Deary, Ian J. and Wright, Margaret J. (2015). Genetic basis of a cognitive complexity metric. PLoS One, 10 (4) e0123886, 1-19. doi: 10.1371/journal.pone.0123886 |
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2015 Journal Article Genetics and brain morphologyStrike, Lachlan T, Couvy-Duchesne, Baptiste, Hansell, Narelle K, Cuellar-Partida, Gabriel, Medland, Sarah E and Wright, Margaret J (2015). Genetics and brain morphology. Neuropsychology Review, 25 (1), 63-96. doi: 10.1007/s11065-015-9281-1 |
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2015 Journal Article Large-scale discovery of novel genetic causes of developmental disordersFitzgerald, T. W., Gerety, S. S., Jones, W. D., van Kogelenberg, M., King, D. A., McRae, J., Morley, K. I., Parthiban, V., Al-Turki, S., Ambridge, K., Barrett, D. M., Bayzetinova, T., Clayton, S., Coomber, E. L., Gribble, S., Jones, P., Krishnappa, N., Mason, L. E., Middleton, A., Miller, R., Prigmore, E., Rajan, D., Sifrim, A., Tivey, A. R., Ahmed, M., Akawi, N., Andrews, R., Anjum, U., Archer, H. ... Hurles, M. E. (2015). Large-scale discovery of novel genetic causes of developmental disorders. Nature, 519 (7542), 223-+. doi: 10.1038/nature14135 |
