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Works matching AU Duncanson, Audrey

Results: 5
    1

    A genome-wide association study identifies new psoriasis susceptibility loci and an interaction between HLA-C and ERAP1.

    Published in:
    Nature Genetics, 2010, v. 42, n. 11, p. 985, doi. 10.1038/ng.694
    By:
    • Strange, Amy;
    • Capon, Francesca;
    • Spencer, Chris C. A.;
    • Knight, Jo;
    • Weale, Michael E.;
    • Allen, Michael H.;
    • Barton, Anne;
    • Band, Gavin;
    • Bellenguez, Céline;
    • Bergboer, Judith G. M.;
    • Blackwell, Jenefer M.;
    • Bramon, Elvira;
    • Bumpstead, Suzannah J.;
    • Casas, Juan P.;
    • Cork, Michael J.;
    • Corvin, Aiden;
    • Deloukas, Panos;
    • Dilthey, Alexander;
    • Duncanson, Audrey;
    • Edkins, Sarah
    Publication type:
    Article
    2

    Association scan of 14,500 nonsynonymous SNPs in four diseases identifies autoimmunity variants.

    Published in:
    Nature Genetics, 2007, v. 39, n. 11, p. 1329, doi. 10.1038/ng.2007.17
    By:
    • Burton, Paul R;
    • Clayton, David G;
    • Cardon, Lon R;
    • Craddock, Nick;
    • Deloukas, Panos;
    • Duncanson, Audrey;
    • Kwiatkowski, Dominic P;
    • McCarthy, Mark I;
    • Ouwehand, Willem H;
    • Samani, Nilesh J;
    • Todd, John A;
    • Donnelly (Chair), Peter;
    • Barrett, Jeffrey C;
    • Davison, Dan;
    • Donnelly, Peter;
    • Easton, Doug;
    • Evans, David M;
    • Leung, Hin-Tak;
    • Marchini, Jonathan L;
    • Morris, Andrew P
    Publication type:
    Article
    3

    Characterizing genetic variants for clinical action.

    Published in:
    American Journal of Medical Genetics. Part C: Seminars in Medical Genetics, 2014, v. 166C, n. 1, p. 93, doi. 10.1002/ajmg.c.31386
    By:
    • Ramos, Erin M.;
    • Din‐Lovinescu, Corina;
    • Berg, Jonathan S.;
    • Brooks, Lisa D.;
    • Duncanson, Audrey;
    • Dunn, Michael;
    • Good, Peter;
    • Hubbard, Tim J.P.;
    • Jarvik, Gail P.;
    • O'Donnell, Christopher;
    • Sherry, Stephen T.;
    • Aronson, Naomi;
    • Biesecker, Leslie G.;
    • Blumberg, Bruce;
    • Calonge, Ned;
    • Colhoun, Helen M.;
    • Epstein, Robert S.;
    • Flicek, Paul;
    • Gordon, Erynn S.;
    • Green, Eric D.
    Publication type:
    Article
    4

    Population‐based identity‐by‐descent mapping combined with exome sequencing to detect rare risk variants for schizophrenia.

    Published in:
    American Journal of Medical Genetics. Part B: Neuropsychiatric Genetics, 2019, v. 180, n. 3, p. 223, doi. 10.1002/ajmg.b.32716
    By:
    • Harold, Denise;
    • Connolly, Siobhan;
    • Riley, Brien P.;
    • Kendler, Kenneth S.;
    • McCarthy, Shane E.;
    • McCombie, William R.;
    • Richards, Alex;
    • Owen, Michael J.;
    • O'Donovan, Michael C.;
    • Walters, James;
    • Donnelly, Peter;
    • Bates, Lesley;
    • Barroso, Ines;
    • Blackwell, Jenefer M.;
    • Bramon, Elvira;
    • Brown, Matthew A.;
    • Casas, Juan P.;
    • Corvin, Aiden;
    • Deloukas, Panos;
    • Duncanson, Audrey
    Publication type:
    Article
    5

    Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls.

    Published in:
    Nature, 2007, v. 447, n. 7145, p. 661, doi. 10.1038/nature05911
    By:
    • Burton, Paul R.;
    • Clayton, David G.;
    • Cardon, Lon R.;
    • Craddock, Nick;
    • Deloukas, Panos;
    • Duncanson, Audrey;
    • Kwiatkowski, Dominic P.;
    • McCarthy, Mark I.;
    • Ouwehand, Willem H.;
    • Samani, Nilesh J.;
    • Todd, John A.;
    • Donnelly, Peter;
    • Barrett, Jeffrey C.;
    • Davison, Dan;
    • Easton, Doug;
    • Evans, David;
    • Leung, Hin-Tak;
    • Marchini, Jonathan L.;
    • Morris, Andrew P.;
    • Spencer, Chris C. A.
    Publication type:
    Article