New England Journal of Medicine · 1996 · 387 citations · 20 references
Background. Mutations in a germ-line allele of the BRCA1 gene contribute to the familial breast cancer syndrome. However, the prevalence of these mutations is unknown in women with breast cancer who do not have the features of this familial syndrome. We sought BRCA1 mutations in women who were given a diagnosis of breast cancer at an early age, because early onset is characteristic of a genetic predisposition to cancer.
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A Strong Candidate for the Breast and Ovarian Cancer Susceptibility Gene <i>BRCA1</i>
Yoshio Miki, Jeffrey Swensen, Donna Shattuck-Eidens et al. · Science · 1994 · 6.1K citations
Linkage of Early-Onset Familial Breast Cancer to Chromosome 17q21
Jeff Hall, Ming K. Lee, Beth Newman et al. · Science · 1990 · 2.5K citations