A low frequency variant at 8q24.21 is strongly associated with risk of oligodendroglial tumors and IDH1 or IDH2 mutated astrocytomas

SNPs mapped to 8q24.21 have been shown to be associated with glioma development. By means of tag SNP genotyping/imputation, pooled next-generation sequencing (NGS) using long-range PCR, and subsequent validation SNP genotyping we identified seven low-frequency SNPs that were consistently and highly...

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Detalhes bibliográficos
Main Authors: Jenkins, Robert B., Xiao, Yuanyuan, Sicotte, Hugues, Decker, Paul A., Kollmeyer, Thomas M., Hansen, Helen M., Kosel, Matthew L., Zheng, Shichun, Walsh, Kyle M., Rice, Terri, Bracci, Paige, McCoy, Lucie S., Smirnov, Ivan, Patoka, Joseph S., Hsuang, George, Wiemels, Joe L., Tihan, Tarik, Pico, Alexander R., Prados, Michael D., Chang, Susan M., Berger, Mitchel S., Caron, Alissa A., Fink, Stephanie R., Halder, Chandralekha, Rynearson, Amanda L., Fridley, Brooke L., Buckner, Jan C., O’Neill, Brian P., Giannini, Caterina, Lachance, Daniel H., Wiencke, John K., Eckel-Passow, Jeanette E., Wrensch, Margaret R.
Formato: Artigo
Idioma:Inglês
Publicado em: 2012
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Article
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC3600846/
https://ncbi.nlm.nih.gov/pubmed/22922872
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1038/ng.2388
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