Insight in glioma susceptibility through an analysis of 6p22.3, 12p13.33-12.1, 17q22-23.2 and 18q23 SNP genotypes in familial and non-familial glioma

BACKGROUND: The risk of glioma has consistently been shown to be increased two-fold in relatives of patients with primary brain tumors (PBT). A recent genome-wide linkage study of glioma families provided evidence for a disease locus on 17q12-21.32, with the possibility of four additional risk loci...

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Main Authors: Liu, Yanhong, Melin, Beatrice S, Rajaraman, Preetha, Wang, Zhaoming, Linet, Martha, Shete, Sanjay, Amos, Christopher I, Lau, Ching C, Scheurer, Michael E, Tsavachidis, Spiridon, Armstrong, Georgina N, Houlston, Richard S, Hosking, Fay J, Claus, Elizabeth B, Barnholtz-Sloan, Jill, Lai, Rose, Il’yasova, Dora, Schildkraut, Joellen, Sadetzki, Siegal, Johansen, Christoffer, Bernstein, Jonine L, Olson, Sara H, Jenkins, Robert B, LaChance, Daniel, Vick, Nicholas A, Wrensch, Margaret, Davis, Faith, McCarthy, Bridget J, Andersson, Ulrika, Thompson, Patricia A, Chanock, Stephen, Bondy, Melissa L
Formato: Artigo
Idioma:Inglês
Publicado em: 2012
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Article
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC3604903/
https://ncbi.nlm.nih.gov/pubmed/22688887
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1007/s00439-012-1187-x
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