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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Gorde:
Xehetasun bibliografikoak
Argitaratua izan da:Neuro Oncol
Egile Nagusiak: 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
Formatua: Artigo
Hizkuntza:Inglês
Argitaratua: Oxford University Press 2019
Gaiak:
Basic and Translational Investigations
Sarrera elektronikoa: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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