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Chromosome 7p11.2 (EGFR) variation influences glioma risk

While gliomas are the most common primary brain tumors, their etiology is largely unknown. To identify novel risk loci for glioma, we conducted genome-wide association (GWA) analysis of two case–control series from France and Germany (2269 cases and 2500 controls). Pooling these data with previously...

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Autors principals: Sanson, Marc, Hosking, Fay J., Shete, Sanjay, Zelenika, Diana, Dobbins, Sara E., Ma, Yussanne, Enciso-Mora, Victor, Idbaih, Ahmed, Delattre, Jean-Yves, Hoang-Xuan, Khe, Marie, Yannick, Boisselier, Blandine, Carpentier, Catherine, Wang, Xiao-Wei, Di Stefano, Anna Luisa, Labussière, Marianne, Gousias, Konstantinos, Schramm, Johannes, Boland, Anne, Lechner, Doris, Gut, Ivo, Armstrong, Georgina, Liu, Yanhong, Yu, Robert, Lau, Ching, Di Bernardo, Maria Chiara, Robertson, Lindsay B., Muir, Kenneth, Hepworth, Sarah, Swerdlow, Anthony, Schoemaker, Minouk J, Wichmann, H.-Erich, Müller, Martina, Schreiber, Stefan, Franke, Andre, Moebus, Susanne, Eisele, Lewin, Försti, Asta, Hemminki, Kari, Lathrop, Mark, Bondy, Melissa, Houlston, Richard S., Simon, Matthias
Format: Artigo
Idioma:Inglês
Publicat: Oxford University Press 2011
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Accés en línia:https://ncbi.nlm.nih.gov/pmc/articles/PMC3118762/
https://ncbi.nlm.nih.gov/pubmed/21531791
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/hmg/ddr192
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