Variation in CDKN2A at 9p21.3 influences childhood acute lymphoblastic leukemia risk

Using data from a genome-wide association study of 907 individuals with childhood acute lymphoblastic leukemia (cases) and 2,398 controls and with validation in samples totaling 2,386 cases and 2,419 controls, we have shown that common variation at 9p21.3 (rs3731217, intron 1 of CDKN2A) influences a...

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Main Authors: Sherborne, Amy L, Hosking, Fay J, Prasad, Rashmi B, Kumar, Rajiv, Koehler, Rolf, Vijayakrishnan, Jayaram, Papaemmanuil, Elli, Bartram, Claus R, Stanulla, Martin, Schrappe, Martin, Gast, Andreas, Dobbins, Sara E, Ma, Yussanne, Sheridan, Eamonn, Taylor, Malcolm, Kinsey, Sally E, Lightfoot, Tracey, Roman, Eve, Irving, Julie A E, Allan, James M, Moorman, Anthony V, Harrison, Christine J, Tomlinson, Ian P, Richards, Sue, Zimmermann, Martin, Szalai, Csaba, Semsei, Ágnes F, Erdelyi, Daniel J, Krajinovic, Maja, Sinnett, Daniel, Healy, Jasmine, Neira, Anna Gonzalez, Kawamata, Norihiko, Ogawa, Seishi, Koeffler, H Phillip, Hemminki, Kari, Greaves, Mel, Houlston, Richard S
Formato: Artigo
Idioma:Inglês
Publicado em: 2010
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Article
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC3434228/
https://ncbi.nlm.nih.gov/pubmed/20453839
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1038/ng.585
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