Genome-wide association study identifies five susceptibility loci for glioma

To identify risk variants for glioma, we conducted a meta-analysis of two genome-wide association studies by genotyping 550K tagging SNPs in a total of 1,878 cases and 3,670 controls, with validation in three additional independent series totaling 2,545 cases and 2,953 controls. We identified five r...

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Detalhes bibliográficos
Publicado no:Nat Genet
Main Authors: Shete, Sanjay, Hosking, Fay J, Robertson, Lindsay B, Dobbins, Sara E, Sanson, Marc, Malmer, Beatrice, Simon, Matthias, Marie, Yannick, Boisselier, Blandine, Delattre, Jean-Yves, Hoang-Xuan, Khe, Hallani, Soufiane El, Idbaih, Ahmed, Zelenika, Diana, Andersson, Ulrika, Henriksson, Roger, Bergenheim, A Tommy, Feychting, Maria, Lönn, Stefan, Ahlbom, Anders, Schramm, Johannes, Linnebank, Michael, Hemminki, Kari, Kumar, Rajiv, Hepworth, Sarah J, Price, Amy, Armstrong, Georgina, Liu, Yanhong, Gu, Xiangjun, Yu, Robert, Lau, Ching, Schoemaker, Minouk, Muir, Kenneth, Swerdlow, Anthony, Lathrop, Mark, Bondy, Melissa, Houlston, Richard S
Formato: Artigo
Idioma:Inglês
Publicado em: 2009
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Article
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC4501476/
https://ncbi.nlm.nih.gov/pubmed/19578367
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1038/ng.407
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