Meta-analysis of BRCA1 and BRCA2 penetrance.
By Sining Chen, Giovanni Parmigiani. Journal of Clinical Oncology, 2007
1,823 citations recorded by the source corpus.
Subfields: Genetics, Oncology, Pathology and Forensic Medicine
View Paper: https://www.semanticscholar.org/paper/d6079e7f2325f395e17e267520768c0d5e48eb5c
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In Genetics
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Citations in the corpus
- Association of Risk-Reducing Surgery in BRCA1 or BRCA2 Mutation Carriers with Cancer Risk and Mortality (2010, positive): “The estimated ovarian cancer risks range from 36% to 63% for BRCA1 mutation carriers and 10% to 27% for BRCA2 mutation carriers.(3-6) Women who are mutation carriers have cancer risk–management options that include risk-reducing salpingooophorectomy, risk-reducing mastectomy, annual cancer screening”
- Association of Rad51 polymorphism with DNA repair in BRCA1 mutation carriers and sporadic breast cancer risk (2011, positive): “While BRCA1 and BRCA2 mutations are highly penetrant [1], resulting in higher risk for breast cancer, both of these genes are also highly polymorphic.”
- Risks of Breast, Ovarian, and Contralateral Breast Cancer for BRCA1 and BRCA2 Mutation Carriers (2017, neutral): “05 14 (9-21) 36 (30-43) 56 (49-63) 64 (57-71)”
- Risk Factors and Preventions of Breast Cancer (2017, positive): “A meta-analysis by Chen showed that the breast cancer risk ratio in women older than 70 years carrying BRCA1 or BRCA2 mutations was 57% and 49%, respectively [32].”
- Loss of BRCA1 in the cells of origin of ovarian cancer induces glycolysis: A window of opportunity for ovarian cancer chemoprevention (2017, background): “Carriers of a BRCA1mutation have up to a 46% risk of developing ovarian cancer by age 70 (1); in contrast, the general population lifetime risk of ovarian cancer is only 1.”