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Prediction of BRCA Mutations Using the BRCAPRO Model in Clinic-Based African American, Hispanic, and Other Minority Families in the United States.
c-Myc activates BRCA1 gene expression through distal promoter elements in breast cancer cells.
Novel germline PALB2 truncating mutations in African American breast cancer patients.
Basal-like Breast cancer DNA copy number losses identify genes involved in genomic instability, response to therapy, and patient survival.
Evidence for an ancient BRCA1 mutation in breast cancer patients of Yoruban ancestry.
CpG island methylation affects accessibility of the proximal BRCA1 promoter to transcription factors.
Searching for large genomic rearrangements of the BRCA1 gene in a Nigerian population.
Genetic testing in diverse populations: are researchers doing enough to get out the correct message?
Association of type and location of BRCA1 and BRCA2 mutations with risk of breast and ovarian cancer.
Inherited mutations in cancer susceptibility genes are common among survivors of breast cancer who develop therapy-related leukemia.
Genetic anticipation in BRCA1/BRCA2 families after controlling for ascertainment bias and cohort effect.
Effect of BRCA germline mutations on breast cancer prognosis: A systematic review and meta-analysis.
Mendelian randomisation study of height and body mass index as modifiers of ovarian cancer risk in 22,588 BRCA1 and BRCA2 mutation carriers.
Prediction of Breast and Prostate Cancer Risks in Male BRCA1 and BRCA2 Mutation Carriers Using Polygenic Risk Scores.