Associated Papers
A Survey of BRCA1, BRCA2, and PALB2 mutations in women with breast cancer in Trinidad and Tobago.
Donenberg T et al.
Breast Cancer Research and Treatment, 2016
Inherited predisposition to breast cancer among African American women.
Churpek JE et al.
Breast Cancer Research and Treatment, 2015
Hereditary breast and ovarian cancer syndrome : the impact of race on uptake of genetic counseling and testing.
Simon MS et al.
Methods in Molecular Biology (clifton, N.j.), 2009
Application of embryonic lethal or other obvious phenotypes to characterize the clinical significance of genetic variants found in trans with known deleterious mutations.
Judkins T et al.
Cancer Research, 2005
Genetic testing in an ethnically diverse cohort of high-risk women: a comparative analysis of BRCA1 and BRCA2 mutations in American families of European and African ancestry.
Nanda R et al.
Jama, 2005
Single nucleotide polymorphisms in clinical genetic testing: the characterization of the clinical significance of genetic variants and their application in clinical research for BRCA1.
Judkins T et al.
Mutation Research, 2005
Racial differences in genetic factors associated with breast cancer.
Ademuyiwa FO et al.
Cancer Metastasis Reviews, 2003
Prevalence of BRCA1 and BRCA2 mutations among clinic-based African American families with breast cancer.
Gao Q et al.
Human Genetics, 2000
Mutation analysis of BRCA1 gene in African-American patients with breast cancer.
Shen D et al.
Journal of the National Medical Association, 2000
Recurrent germ-line BRCA1 mutations in extended African American families with early-onset breast cancer.
Gao Q et al.
American Journal of Human Genetics, 1997
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