Selected publications
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Factors Associated with Deciding between Risk-Reducing Salpingo-oophorectomy and Ovarian Cancer Screening among High-Risk Women Enrolled in GOG-0199: An NRG Oncology/Gynecologic Oncology Group Study.
Obstetrical and Gynecological Survey.
2017
Comment
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Times cited: 1 -
Factors associated with deciding between risk-reducing salpingo-oophorectomy and ovarian cancer screening among high-risk women enrolled in GOG-0199: An NRG Oncology/Gynecologic Oncology Group study.
Gynecologic Oncology.
2017
Academic Article
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Times cited: 5 -
Association of breast cancer risk in BRCA1 and BRCA2 mutation carriers with genetic variants showing differential allelic expression: identification of a modifier of breast cancer risk at locus 11q22.3.
Breast Cancer Research and Treatment.
2017
Academic Article
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Times cited: 9 -
Inheritance of deleterious mutations at both BRCA1 and BRCA2 in an international sample of 32,295 women.
Breast Cancer Research.
2016
Academic Article
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Times cited: 13 -
Functional mechanisms underlying pleiotropic risk alleles at the 19p13.1 breast-ovarian cancer susceptibility locus.
Nature Communications.
2016
Academic Article
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Times cited: 24 -
Identification of independent association signals and putative functional variants for breast cancer risk through fine-scale mapping of the 12p11 locus.
Breast Cancer Research.
2016
Academic Article
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Times cited: 13 -
No clinical utility of KRAS variant rs61764370 for ovarian or breast cancer.
Gynecologic Oncology.
2016
Review
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Times cited: 8 -
Identification of four novel susceptibility loci for oestrogen receptor negative breast cancer.
Nature Communications.
2016
Academic Article
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Times cited: 38 -
Breast cancer risk variants at 6q25 display different phenotype associations and regulate ESR1, RMND1 and CCDC170.
Nature Genetics.
2016
Review
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Times cited: 53 -
Male breast cancer in BRCA1 and BRCA2 mutation carriers: Pathology data from the Consortium of Investigators of Modifiers of BRCA1/2.
Breast Cancer Research.
2016
Academic Article
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Times cited: 33 -
BRCA2 Polymorphic Stop Codon K3326X and the Risk of Breast, Prostate, and Ovarian Cancers.
Journal of the National Cancer Institute.
2016
Academic Article
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Times cited: 43 -
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: 13 -
Assessing associations between the AURKAHMMR-TPX2-TUBG1 functional module and breast cancer risk in BRCA1/2 mutation carriers.
PLoS ONE.
2015
Academic Article
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Times cited: 11 -
Association of type and location of BRCA1 and BRCA2 mutations with risk of breast and ovarian cancer.
JAMA - Journal of the American Medical Association.
2015
Academic Article
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Times cited: 179 -
Candidate genetic modifiers for breast and ovarian cancer risk inBRCA1andBRCA2 mutation carriers.
Cancer Epidemiology Biomarkers and Prevention.
2015
Academic Article
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Times cited: 14 -
Characterization of large structural genetic mosaicism in human autosomes.
American Journal of Human Genetics.
2015
Review
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Times cited: 44 -
Identification of six new susceptibility loci for invasive epithelial ovarian cancer.
Nature Genetics.
2015
Review
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Times cited: 133 -
Associations of common breast cancer susceptibility alleles with risk of breast cancer subtypes in BRCA1 and BRCA2 mutation carriers.
Breast Cancer Research.
2014
Academic Article
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Times cited: 25 -
Imputation and subset-based association analysis across different cancer types identifies multiple independent risk loci in the TERT-CLPTM1L region on chromosome 5p15.33.
Human Molecular Genetics.
2014
Academic Article
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Times cited: 60 -
DNA Glycosylases Involved in Base Excision Repair May Be Associated with Cancer Risk in BRCA1 and BRCA2 Mutation Carriers.
PLoS Genetics.
2014
Academic Article
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Times cited: 22 -
Quantifying cancer absolute risk and cancer mortality in the presence of competing events after a myotonic dystrophy diagnosis.
PLoS ONE.
2013
Academic Article
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Times cited: 15 -
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: 169 -
Identification of a BRCA2-Specific Modifier Locus at 6p24 Related to Breast Cancer Risk.
PLoS Genetics.
2013
Academic Article
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Times cited: 75 -
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 -
Detectable clonal mosaicism and its relationship to aging and cancer.
Nature Genetics.
2012
Academic Article
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Times cited: 303 -
Pathology of breast and ovarian cancers among BRCA1 and BRCA2 mutation carriers: Results from the consortium of investigators of modifiers of BRCA1/2 (CIMBA).
Cancer Epidemiology Biomarkers and Prevention.
2012
Academic Article
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Times cited: 259 -
Cancer risk among patients with myotonic muscular dystrophy.
JAMA - Journal of the American Medical Association.
2011
Academic Article
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Times cited: 64 -
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.
Breast Cancer Research.
2011
Academic Article
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Times cited: 50 -
Haplotype structure in Ashkenazi Jewish BRCA1 and BRCA2 mutation carriers.
Human Genetics.
2011
Academic Article
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Times cited: 12 -
Genetic variation at 9p22.2 and ovarian cancer risk for BRCA1 and BRCA2 mutation carriers.
Journal of the National Cancer Institute.
2011
Academic Article
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Times cited: 31 -
The scientific foundation for personal genomics: Recommendations from a national institutes of health-centers for disease control and prevention multidisciplinary workshop.
Genetics in Medicine.
2009
Conference Paper
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Times cited: 161