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Journal of the National Cancer Institute|January 24, 2018
Cost-effectiveness of Population-Based BRCA1, BRCA2, RAD51C, RAD51D, BRIP1, PALB2 Mutation Testing in Unselected General Population WomenRanjit Manchanda, Shreeya Patel, Vladimir S Gordeev, et al.
Cancer Research|January 25, 2003
BRCA1/2 mutation status influences somatic genetic progression in inherited and sporadic epithelial ovarian cancer casesSusan J Ramus, Paul D P Pharoah, Patricia Harrington, et al.
Journal of Medical Genetics|May 7, 2018
Evaluation of polygenic risk scores for ovarian cancer risk prediction in a prospective cohort studyXin Yang, Goska Leslie, Aleksandra Gentry-Maharaj, et al.
Cancer Epidemiology, Biomarkers & Prevention : a Publication of the American Association for Cancer Research, Cosponsored by the American Society of Preventive Oncology|December 19, 2007
Association between single-nucleotide polymorphisms in hormone metabolism and DNA repair genes and epithelial ovarian cancer: results from two Australian studies and an additional validation setJonathan Beesley, Susan J Jordan, Amanda B Spurdle, et al.
British Journal of Cancer|February 24, 2011
Morphological predictors of BRCA1 germline mutations in young women with breast cancerM C Southey, S J Ramus, J G Dowty, et al.
Plos One|March 8, 2007
Tagging single nucleotide polymorphisms in the BRIP1 gene and susceptibility to breast and ovarian cancerHonglin Song, Susan J Ramus, Susanne Krüger Kjaer, et al.
Human Molecular Genetics|March 10, 2009
Functional complementation studies identify candidate genes and common genetic variants associated with ovarian cancer survivalLydia Quaye, Dimitra Dafou, Susan J Ramus, et al.
Carcinogenesis|June 16, 2006
Common variants in mismatch repair genes and risk of invasive ovarian cancerHonglin Song, Susan J Ramus, Lydia Quaye, et al.
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