Works matching AU St Clair, David


Results: 57
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    Rare chromosomal deletions and duplications increase risk of schizophrenia.

    Published in:
    Nature, 2008, v. 455, n. 7210, p. 237, doi. 10.1038/nature07239
    By:
    • Stone, Jennifer L.;
    • O’Donovan, Michael C.;
    • Gurling, Hugh;
    • Kirov, George K.;
    • Blackwood, Douglas H. R.;
    • Corvin, Aiden;
    • Craddock, Nick J.;
    • Gill, Michael;
    • Hultman, Christina M.;
    • Lichtenstein, Paul;
    • McQuillin, Andrew;
    • Pato, Carlos N.;
    • Ruderfer, Douglas M.;
    • Owen, Michael J.;
    • St Clair, David;
    • Sullivan, Patrick F.;
    • Sklar, Pamela;
    • Purcell (Leader), Shaun M.;
    • Korn, Joshua;
    • Macgregor, Stuart
    Publication type:
    Article
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    Mosaic copy number variation in schizophrenia.

    Published in:
    European Journal of Human Genetics, 2013, v. 21, n. 9, p. 1007, doi. 10.1038/ejhg.2012.287
    By:
    • Ruderfer, Douglas M;
    • Chambert, Kim;
    • Moran, Jennifer;
    • Talkowski, Michael;
    • Chen, Elizabeth S;
    • Gigek, Carolina;
    • Gusella, James F;
    • Blackwood, Douglas H;
    • Corvin, Aiden;
    • Gurling, Hugh M;
    • Hultman, Christina M;
    • Kirov, George;
    • Magnusson, Patrick;
    • O'Donovan, Michael C;
    • Owen, Michael J;
    • Pato, Carlos;
    • St Clair, David;
    • Sullivan, Patrick F;
    • Purcell, Shaun M;
    • Sklar, Pamela
    Publication type:
    Article
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    Confirmation of the genetic association between the U2AF homology motif (UHM) kinase 1 (UHMK1) gene and schizophrenia on chromosome 1q23.3.

    Published in:
    European Journal of Human Genetics, 2008, v. 16, n. 10, p. 1275, doi. 10.1038/ejhg.2008.76
    By:
    • Puri, Vinay;
    • McQuillin, Andrew;
    • Datta, Susmita;
    • Choudhury, Khalid;
    • Pimm, Jonathan;
    • Thirumalai, Srinivasa;
    • Krasucki, Robert;
    • Lawrence, Jacob;
    • Quested, Digby;
    • Bass, Nicholas;
    • Crombie, Caroline;
    • Fraser, Gillian;
    • Walker, Nicholas;
    • Moorey, Helen;
    • Ray, Manaan Kar;
    • Sule, Akeem;
    • Curtis, David;
    • St Clair, David;
    • Gurling, Hugh
    Publication type:
    Article
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    Genome-wide association study identifies five new schizophrenia loci.

    Published in:
    Nature Genetics, 2011, v. 43, n. 10, p. 969, doi. 10.1038/ng.940
    By:
    • Ripke, Stephan;
    • Sanders, Alan R;
    • Kendler, Kenneth S;
    • Levinson, Douglas F;
    • Sklar, Pamela;
    • Holmans, Peter A;
    • Lin, Dan-Yu;
    • Duan, Jubao;
    • Ophoff, Roel A;
    • Andreassen, Ole A;
    • Scolnick, Edward;
    • Cichon, Sven;
    • St. Clair, David;
    • Corvin, Aiden;
    • Gurling, Hugh;
    • Werge, Thomas;
    • Rujescu, Dan;
    • Blackwood, Douglas H R;
    • Pato, Carlos N;
    • Malhotra, Anil K
    Publication type:
    Article
    11

    Common variants near CAV1 and CAV2 are associated with primary open-angle glaucoma.

    Published in:
    Nature Genetics, 2010, v. 42, n. 10, p. 906, doi. 10.1038/ng.661
    By:
    • Thorleifsson, Gudmar;
    • Walters, G. Bragi;
    • Hewitt, Alex W.;
    • Masson, Gisli;
    • Helgason, Agnar;
    • DeWan, Andrew;
    • Sigurdsson, Asgeir;
    • Jonasdottir, Adalbjorg;
    • Gudjonsson, Sigurjon A.;
    • Magnusson, Kristinn P.;
    • Stefansson, Hreinn;
    • Lam, Dennis S. C.;
    • Tam, Pancy O. S.;
    • Gudmundsdottir, Gudrun J.;
    • Southgate, Laura;
    • Burdon, Kathryn P.;
    • Gottfredsdottir, Maria Soffia;
    • Aldred, Micheala A.;
    • Mitchell, Paul;
    • Clair, David St.
    Publication type:
    Article
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    Study of Novel Autoantibodies in Schizophrenia.

    Published in:
    Schizophrenia Bulletin, 2018, v. 44, n. 6, p. 1341, doi. 10.1093/schbul/sbx175
    By:
    • Whelan, Ruth;
    • Clair, David St;
    • Mustard, Colette J;
    • Hallford, Philomena;
    • Wei, Jun
    Publication type:
    Article
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    Genome-wide association study reveals greater polygenic loading for schizophrenia in cases with a family history of illness.

    Published in:
    American Journal of Medical Genetics. Part B: Neuropsychiatric Genetics, 2016, v. 171B, n. 2, p. 276, doi. 10.1002/ajmg.b.32402
    By:
    • Bigdeli, Tim B.;
    • Ripke, Stephan;
    • Bacanu, Silviu‐Alin;
    • Lee, Sang Hong;
    • Wray, Naomi R.;
    • Gejman, Pablo V.;
    • Rietschel, Marcella;
    • Cichon, Sven;
    • St Clair, David;
    • Corvin, Aiden;
    • Kirov, George;
    • McQuillin, Andrew;
    • Gurling, Hugh;
    • Rujescu, Dan;
    • Andreassen, Ole A.;
    • Werge, Thomas;
    • Blackwood, Douglas H. R.;
    • Pato, Carlos N.;
    • Pato, Michele T.;
    • Malhotra, Anil K.
    Publication type:
    Article
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    Association between Alzheimer's disease and the NOS3 gene.

    Published in:
    1999
    By:
    • Dahiyat, Mohammed;
    • Cumming, Alastair;
    • Harrington, Charles;
    • Wischik, Claude;
    • Xuereb, John;
    • Corrigan, Frank;
    • Breen, Gerome;
    • Shaw, Duncan;
    • St Clair, David;
    • Dahiyat, M;
    • Cumming, A;
    • Harrington, C;
    • Wischik, C;
    • Xuereb, J;
    • Corrigan, F;
    • Breen, G;
    • Shaw, D;
    • St Clair, D
    Publication type:
    journal article
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    PYRROLOQUINOLINES.

    Published in:
    Organic Preparations & Procedures International, 1991, v. 23, n. 1, p. 67, doi. 10.1080/00304949109458287
    By:
    • Black, David St. Clair;
    • Kumar, Naresh
    Publication type:
    Article
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    An integrated genetic-epigenetic analysis of schizophrenia: evidence for co-localization of genetic associations and differential DNA methylation.

    Published in:
    Genome Biology, 2016, v. 17, p. 1, doi. 10.1186/s13059-016-1041-x
    By:
    • Hannon, Eilis;
    • Dempster, Emma;
    • Viana, Joana;
    • Burrage, Joe;
    • Smith, Adam R.;
    • Macdonald, Ruby;
    • Clair, David St;
    • Mustard, Colette;
    • Breen, Gerome;
    • Therman, Sebastian;
    • Kaprio, Jaakko;
    • Timothea Toulopoulou;
    • Hulshoff Pol, Hilleke E.;
    • Bohlken, Marc M.;
    • Kahn, Rene S.;
    • Nenadic, Igor;
    • Hultman, Christina M.;
    • Murray, Robin M.;
    • Collier, David A.;
    • Bass, Nick
    Publication type:
    Article
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    Generation Scotland: the Scottish Family Health Study; a new resource for researching genes and heritability.

    Published in:
    BMC Medical Genetics, 2006, v. 7, p. 74, doi. 10.1186/1471-2350-7-74
    By:
    • Smith, Blair H;
    • Campbell, Harry;
    • Blackwood, Douglas;
    • Connell, John;
    • Connor, Mike;
    • Deary, Ian J;
    • Dominiczak, Anna F;
    • Fitzpatrick, Bridie;
    • Ford, Ian;
    • Jackson, Cathy;
    • Haddow, Gillian;
    • Kerr, Shona;
    • Lindsay, Robert;
    • McGilchrist, Mark;
    • Morton, Robin;
    • Murray, Graeme;
    • Palmer, Colin NA;
    • Pell, Jill P;
    • Ralston, Stuart H;
    • St Clair, David
    Publication type:
    Article
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