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You searched for: Author Buys, Saundra Remove constraint Author: Buys, Saundra Academic Unit Epidemiology Remove constraint Academic Unit: Epidemiology Subject Genetics Remove constraint Subject: Genetics Type Articles Remove constraint Type: Articles Start Over

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1. Common variants at 12p11, 12q24, 9p21, 9q31.2 and in ZNF365 are associated with breast cancer risk for BRCA1 and/or BRCA2 mutation carriers

2. Common breast cancer susceptibility alleles are associated with tumour subtypes in BRCA1 and BRCA2 mutation carriers: results from the Consortium of Investigators of Modifiers of BRCA1/2

3. Contribution of large genomic BRCA1 alterations to early-onset breast cancer selected for family history and tumour morphology: a report from The Breast Cancer Family Registry

4. Rare variants in the ATM gene and risk of breast cancer

5. The Breast Cancer Family Registry: an infrastructure for cooperative multinational, interdisciplinary and translational studies of the genetic epidemiology of breast cancer