Common variation at 3q26.2, 6p21.33, 17p11.2 and 22q13.1 influences multiple myeloma risk

To identify variants for multiple myeloma risk, we conducted a genome-wide association study with validation in additional series totaling 4,692 cases and 10,990 controls. We identified four risk loci at 3q26.2 (rs10936599, P=8.70x10(-14)), 6p21.33 (rs2285803, PSORS1C2; P= 9.67x10(-11)), 17p11.2 (rs...

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書誌詳細
出版年:Nat Genet
主要な著者: Chubb, Daniel, Weinhold, Niels, Broderick, Peter, Chen, Bowang, Johnson, David C, Försti, Asta, Vijayakrishnan, Jayaram, Migliorini, Gabriele, Dobbins, Sara E, Holroyd, Amy, Hose, Dirk, Walker, Brian A, Davies, Faith E, Gregory, Walter A, Jackson, Graham H, Irving, Julie A, Pratt, Guy, Fegan, Chris, Fenton, James AL, Neben, Kai, Hoffmann, Per, Nöthen, Markus M, Mühleisen, Thomas W, Eisele, Lewin, Ross, Fiona M, Straka, Christian, Einsele, Hermann, Langer, Christian, Dörner, Elisabeth, Allan, James M, Jauch, Anna, Morgan, Gareth J, Hemminki, Kari, Houlston, Richard S, Goldschmidt, Hartmut
フォーマット: Artigo
言語:Inglês
出版事項: 2013
主題:
Article
オンライン･アクセス:https://ncbi.nlm.nih.gov/pmc/articles/PMC5053356/
https://ncbi.nlm.nih.gov/pubmed/23955597
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1038/ng.2733
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