Selected publications
- A network analysis to identify mediators of germline-driven differences in breast cancer prognosis. Nature Communications. 2020 Academic Article GET IT
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A transcriptome-wide association study of 229,000 women identifies new candidate susceptibility genes for breast cancer.
Nature Genetics.
2018
Academic Article
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Times cited: 24 -
Identification of ten variants associated with risk of estrogen-receptor-negative breast cancer.
Nature Genetics.
2017
Academic Article
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Times cited: 73 -
Association analysis identifies 65 new breast cancer risk loci.
Nature.
2017
Academic Article
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Times cited: 236 -
Identification of 12 new susceptibility loci for different histotypes of epithelial ovarian cancer.
Nature Genetics.
2017
Academic Article
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Times cited: 73 -
An original phylogenetic approach identified mitochondrial haplogroup T1a1 as inversely associated with breast cancer risk in BRCA2 mutation carriers.
Breast Cancer Research.
2015
Academic Article
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Times cited: 14 -
Genome-Wide Association Study in BRCA1 Mutation Carriers Identifies Novel Loci Associated with Breast and Ovarian Cancer Risk.
PLoS Genetics.
2013
Academic Article
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Times cited: 172 -
A nonsynonymous polymorphism in IRS1 modifies risk of developing breast and ovarian cancers in BRCA1 and ovarian cancer in BRCA2 mutation carriers.
Cancer Epidemiology Biomarkers and Prevention.
2012
Academic Article
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Times cited: 14 -
Oral contraceptives and the risk of breast cancer in BRCA1 and BRCA2 mutation carriers.
Journal of the National Cancer Institute.
2002
Academic Article
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Times cited: 290 -
A Collaborative Survey of 80 Mutations in the BRCA1 Breast and Ovarian Cancer Susceptibility Gene: Implications for Presymptomatic Testing and Screening.
JAMA - Journal of the American Medical Association.
1995
Academic Article
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Times cited: 403