Using germline variants to estimate glioma and subtype risks

BACKGROUND: Twenty-five single nucleotide polymorphisms (SNPs) are associated with adult diffuse glioma risk. We hypothesized that the inclusion of these 25 SNPs with age at diagnosis and sex could estimate risk of glioma as well as identify glioma subtypes. METHODS: Case-control design and multinom...

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Detalhes bibliográficos
Publicado no:Neuro Oncol
Main Authors: Eckel-Passow, Jeanette E, Decker, Paul A, Kosel, Matt L, Kollmeyer, Thomas M, Molinaro, Annette M, Rice, Terri, Caron, Alissa A, Drucker, Kristen L, Praska, Corinne E, Pekmezci, Melike, Hansen, Helen M, McCoy, Lucie S, Bracci, Paige M, Erickson, Bradley J, Lucchinetti, Claudia F, Wiemels, Joseph L, Wiencke, John K, Bondy, Melissa L, Melin, Beatrice, Burns, Terry C, Giannini, Caterina, Lachance, Daniel H, Wrensch, Margaret R, Jenkins, Robert B
Formato: Artigo
Idioma:Inglês
Publicado em: Oxford University Press 2019
Assuntos:
Basic and Translational Investigations
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC6422428/
https://ncbi.nlm.nih.gov/pubmed/30624711
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/neuonc/noz009
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