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    Genome-wide meta-analysis identifies five new susceptibility loci for cutaneous malignant melanoma

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    Fulltext not available
    Authors
    Law, M.
    Bishop, D.
    Lee, J.
    Brossard, M.
    Martin, N.
    Moses, Eric
    Song, F.
    Barrett, J.
    Kumar, R.
    Easton, D.
    Pharoah, P.
    Swerdlow, A.
    Kypreou, K.
    Taylor, J.
    Harland, M.
    Randerson-Moor, J.
    Akslen, L.
    Andresen, P.
    Avril, M.
    Azizi, E.
    Scarrà, G.
    Brown, K.
    Debniak, T.
    Duffy, D.
    Elder, D.
    Fang, S.
    Friedman, E.
    Galan, P.
    Ghiorzo, P.
    Gillanders, E.
    Goldstein, A.
    Gruis, N.
    Hansson, J.
    Helsing, P.
    Hocevar, M.
    Höiom, V.
    Ingvar, C.
    Kanetsky, P.
    Chen, W.
    Landi, M.
    Lang, J.
    Lathrop, G.
    Lubinski, J.
    MacKie, R.
    Mann, G.
    Molven, A.
    Montgomery, G.
    Novakovic, S.
    Olsson, H.
    Puig, S.
    Puig-Butille, J.
    Qureshi, A.
    Radford-Smith, G.
    Van Der Stoep, N.
    Van Doorn, R.
    Whiteman, D.
    Craig, J.
    Schadendorf, D.
    Simms, L.
    Burdon, K.
    Nyholt, D.
    Pooley, K.
    Orr, N.
    Stratigos, A.
    Cust, A.
    Ward, S.
    Hayward, N.
    Han, J.
    Schulze, H.
    Dunning, A.
    Bishop, J.
    Demenais, F.
    Amos, C.
    MacGregor, S.
    Iles, M.
    Date
    2015
    Type
    Journal Article
    
    Metadata
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    Citation
    Law, M. and Bishop, D. and Lee, J. and Brossard, M. and Martin, N. and Moses, E. and Song, F. et al. 2015. Genome-wide meta-analysis identifies five new susceptibility loci for cutaneous malignant melanoma. Nature Genetics. 47 (9): pp. 987-995.
    Source Title
    Nature Genetics
    DOI
    10.1038/ng.3373
    ISSN
    1061-4036
    School
    School of Biomedical Sciences
    URI
    http://hdl.handle.net/20.500.11937/11908
    Collection
    • Curtin Research Publications
    Abstract

    Thirteen common susceptibility loci have been reproducibly associated with cutaneous malignant melanoma (CMM). We report the results of an international 2-stage meta-analysis of CMM genome-wide association studies (GWAS). This meta-analysis combines 11 GWAS (5 previously unpublished) and a further three stage 2 data sets, totaling 15,990 CMM cases and 26,409 controls. Five loci not previously associated with CMM risk reached genome-wide significance (P < 5 × 10−8), as did 2 previously reported but unreplicated loci and all 13 established loci. Newly associated SNPs fall within putative melanocyte regulatory elements, and bioinformatic and expression quantitative trait locus (eQTL) data highlight candidate genes in the associated regions, including one involved in telomere biology.

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