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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 |
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2015 Journal Article A twin study of breastfeeding with a preliminary genome-wide association scanColodro-Conde, Lucia, Zhu, Gu, Power, Robert A., Henders, Anjali, Heath, Andrew C., Madden, Pamela A. F., Montgomery, Grant W., Medland, Sarah, Ordonana, Juan R. and Martin, Nicholas G. (2015). A twin study of breastfeeding with a preliminary genome-wide association scan. Twin Research and Human Genetics, 18 (1), 61-72. doi: 10.1017/thg.2014.74 |
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2015 Journal Article Psychiatric genome-wide association study analyses implicate neuronal, immune and histone pathwaysO'Dushlaine, Colm, Rossin, Lizzy, Lee, Phil H., Duncan, Laramie, Parikshak, Neelroop N., Newhouse, Stephen, Ripke, Stephan, Neale, Benjamin M., Purcell, Shaun M., Posthuma, Danielle, Nurnberger, John I., Lee, S. Hong, Faraone, Stephen V., Perlis, Roy H., Mowry, Bryan J, Thapar, Anita, Goddard, Michael E., Witte, John S., Absher, Devin, Agartz, Ingrid, Akil, Huda, Amin, Farooq, Andreassen, Ole A., Anjorin, Adebayo, Anney, Richard, Anttila, Verneri, Arking, Dan E., Asherson, Philip, Azevedo, Maria H. ... Breen, Gerome (2015). Psychiatric genome-wide association study analyses implicate neuronal, immune and histone pathways. Nature Neuroscience, 18 (2), 199-209. doi: 10.1038/nn.3922 |
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2014 Journal Article Replicability and robustness of genome-wide-association studies for behavioral traitsRietveld, Cornelius A., Conley, Dalton, Eriksson, Nicholas, Esko, Tonu, Medland, Sarah E., Vinkhuyzen, Anna A. E., Yang, Jian, Boardman, Jason D., Chabris, Christopher F., Dawes, Christopher T., Domingue, Benjamin W., Hinds, David A., Johannesson, Magnus, Kiefer, Amy K., Laibson, David, Magnusson, Patrik K. E., Mountain, Joanna L., Oskarsson, Sven, Rostapshova, Olga, Teumer, Alexander, Tung, Joyce Y., Visscher, Peter M., Benjamin, Daniel J., Cesarini, David and Koellinger, Philipp D. (2014). Replicability and robustness of genome-wide-association studies for behavioral traits. Psychological Science, 25 (11), 1975-1986. doi: 10.1177/0956797614545132 |
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2014 Journal Article Genetic architecture of subcortical brain regions: common and region-specific genetic contributionsRentería, M. E., Hansell, N. K., Strike, L. T., McMahon, K. L., de Zubicaray, G. I., Hickie, Ian B., Thompson, Paul M., Martin, N. G., Medland, S. E. and Wright, M. J. (2014). Genetic architecture of subcortical brain regions: common and region-specific genetic contributions. Genes, Brain and Behavior, 13 (8), 821-830. doi: 10.1111/gbb.12177 |
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2014 Journal Article Joint genetic analysis of hippocampal size in mouse and human identifies a novel gene linked to neurodegenerative diseaseAshbrook, David G., Williams, Robert W., Lu, Lu, Stein, Jason L., Hibar, Derrek P., Nichols, Thomas E., Medland, Sarah E., Thompson, Paul M. and Hager, Reinmar (2014). Joint genetic analysis of hippocampal size in mouse and human identifies a novel gene linked to neurodegenerative disease. BMC Genomics, 15 (1) 850. doi: 10.1186/1471-2164-15-850 |
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2014 Journal Article Common genetic variants associated with cognitive performance identified using the proxy-phenotype methodRietveld, Cornelius A., Esko, Tonu, Davies, Gail, Pers, Tune H., Turley, Patrick, Benyamin, Beben, Chabris, Christopher F., Emilsson, Valur, Johnson, Andrew D., Lee, James J., De Leeuw, Christiaan, Marioni, Riccardo E., Medland, Sarah E., Miller, Michael B., Rostapshova, Olga, Van Der Lee, Sven J., Vinkhuyzen, Anna A. E., Amin, Najaf, Conley, Dalton, Derringer, Jaime, Van Duijn, Cornelia M., Fehrmann, Rudolf, Franke, Lude, Glaeser, Edward L., Hansell, Narelle K., Hayward, Caroline, Iacono, William G., Ibrahim-Verbaas, Carla, Jaddoe, Vincent ... Koellinger, Philipp D. (2014). Common genetic variants associated with cognitive performance identified using the proxy-phenotype method. Proceedings of the National Academy of Sciences of the United States of America, 111 (38), 13790-13794. doi: 10.1073/pnas.1404623111 |
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2014 Journal Article Common genetic variants associated with cognitive performance identified using the proxy-phenotype method (vol 111, pg 13790, 2014)Rietveld, Cornelius A., Esko, Tonu, Davies, Gail, Pers, Tune H., Turley, Patrick, Benyamin, Beben, Chabris, Christopher F., Emilsson, Valur, Johnson, Andrew D., Lee, James J., de Leeuw, Christiaan, Marioni, Riccardo E., Medland, Sarah E., Miller, Michael B., Rostapshova, Olga, van der Lee, Sven J., Vinkhuyzen, Anna A. E., Amin, Najaf, Conley, Dalton, Derringer, Jaime, van Duijn, Cornelia M., Fehrmann, Rudolf, Franke, Lude, Glaeser, Edward L., Hansell, Narelle K., Hayward, Caroline, Iacono, William G., Ibrahim-Verbaas, Carla, Jaddoe, Vincent ... Koellinger, Philipp D. (2014). Common genetic variants associated with cognitive performance identified using the proxy-phenotype method (vol 111, pg 13790, 2014). Proceedings of the National Academy of Sciences of the United States of America, 112 (4), E380-E380. doi: 10.1073/pnas.1424631112 |
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2014 Journal Article Variants close to NTRK2 gene are associated with birth weight in female twinsMetrustry, Sarah J., Edwards, Mark H., Medland, Sarah E., Holloway, John W., Montgomery, Grant W., Martin, Nicholas G., Spector, Tim D., Cooper, Cyrus and Valdes, Ana M. (2014). Variants close to NTRK2 gene are associated with birth weight in female twins. Twin Research and Human Genetics, 17 (4), 254-261. doi: 10.1017/thg.2014.34 |
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2014 Journal Article The ENIGMA Consortium: large-scale collaborative analyses of neuroimaging and genetic dataThompson, Paul M., Stein, Jason L., Medland, Sarah E., Hibar, Derrek P., Arias Vasquez, Alejandro, Renteria, Miguel E., Toro, Roberto, Jahanshad, Neda, Schumann, Gunter, Franke, Barbara, Wright, Margaret J., Martin, Nicholas G., Agartz, Ingrid, Alda, Martin, Alhusaini, Saud, Almasy, Laura, Almeida, Jorge, Alpert, Kathryn, Andreasen, Nancy C., Andreassen, Ole A., Apostolova, Liana G., Appel, Katja, Armstrong, Nicola J., Aribisala, Benjamin, Bastin, Mark E., Bauer, Michael, Bearden, Carrie E., Bergmann, Ørjan, Binder, Elisabeth B. ... Saguenay Youth Study (SYS) Group (2014). The ENIGMA Consortium: large-scale collaborative analyses of neuroimaging and genetic data. Brain Imaging and Behavior, 8 (2), 153-182. doi: 10.1007/s11682-013-9269-5 |
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2014 Journal Article Genetic influences on political ideologies: Twin analyses of 19 measures of political ideologies from five democracies and genome-wide findings from three populationsHatemi, Peter K., Medland, Sarah E., Klemmensen, Robert, Oskarsson, Sven, Littvay, Levente, Dawes, Christopher T., Verhulst, Brad, McDermott, Rose, Norgaard, Asbjorn Sonne, Klofstad, Casey A., Christensen, Kaare, Johannesson, Magnus, Magnusson, Patrik K. E., Eaves, Lindon J. and Martin, Nicholas G. (2014). Genetic influences on political ideologies: Twin analyses of 19 measures of political ideologies from five democracies and genome-wide findings from three populations. Behavior Genetics, 44 (3), 282-294. doi: 10.1007/s10519-014-9648-8 |
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2014 Journal Article Genome-wide association study reveals two new risk loci for bipolar disorderMuehleisen, Thomas W., Leber, Markus, Schulze, Thomas G., Strohmaier, Jana, Degenhardt, Franziska, Treutlein, Jens, Mattheisen, Manuel, Forstner, Andreas J., Schumacher, Johannes, Breuer, Rene, Meier, Sandra, Herms, Stefan, Hoffmann, Per, Lacour, Andre, Witt, Stephanie H., Reif, Andreas, Mueller-Myhsok, Bertram, Lucae, Susanne, Maier, Wolfgang, Schwarz, Markus, Vedder, Helmut, Kammerer-Ciernioch, Jutta, Pfennig, Andrea, Bauer, Michael, Hautzinger, Martin, Moebus, Susanne, Priebe, Lutz, Czerski, Piotr M., Hauser, Joanna ... Cichon, Sven (2014). Genome-wide association study reveals two new risk loci for bipolar disorder. Nature Communications, 5 (3339) 3339, 1-8. doi: 10.1038/ncomms4339 |
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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 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 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 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 Whole-genome analyses of whole-brain data: working within an expanded search spaceMedland, Sarah E., Jahanshad, Neda, Neale, Benjamin M. and Thompson, Paul M. (2014). Whole-genome analyses of whole-brain data: working within an expanded search space. Nature Neuroscience, 17 (6), 791-800. doi: 10.1038/nn.3718 |
