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...

Descrición completa

Gardado en:
Detalles Bibliográficos
Publicado en: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: Oxford University Press 2019
Assuntos:
Basic and Translational Investigations
Acceso en liña: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
Tags: Engadir etiqueta
Sen Etiquetas, Sexa o primeiro en etiquetar este rexistro!

Títulos similares