Area of research
Genetics · Reproductive Medicine
Research interest
Research interests include BRCA gene mutations in cancer, Genetic Associations and Epidemiology, Nutrition, Genetics, and Disease, and Genomic variations and chromosomal abnormalities.
Polygenic risk modeling for prediction of epithelial ovarian cancer risk
Correction: Polygenic risk modeling for prediction of epithelial ovarian cancer risk
Oral contraceptive use and ovarian cancer risk for BRCA1/2 mutation carriers: an international cohort study
Breast and Prostate Cancer Risks for Male<i>BRCA1</i>and<i>BRCA2</i>Pathogenic Variant Carriers Using Polygenic Risk Scores
A case-only study to identify genetic modifiers of breast cancer risk for BRCA1/BRCA2 mutation carriers
The predictive ability of the 313 variant–based polygenic risk score for contralateral breast cancer risk prediction in women of European ancestry with a heterozygous BRCA1 or BRCA2 pathogenic variant
Author Correction: A case-only study to identify genetic modifiers of breast cancer risk for BRCA1/BRCA2 mutation carriers
Genome-wide association study identifies 32 novel breast cancer susceptibility loci from overall and subtype-specific analyses
Fine-mapping of 150 breast cancer risk regions identifies 191 likely target genes
Polygenic risk scores and breast and epithelial ovarian cancer risks for carriers of BRCA1 and BRCA2 pathogenic variants
Risk-reducing salpingo-oophorectomy, natural menopause, and breast cancer risk: an international prospective cohort of BRCA1 and BRCA2 mutation carriers
Characterization of the Cancer Spectrum in Men With Germline<i>BRCA1</i>and<i>BRCA2</i>Pathogenic Variants
Transcriptome‐wide association study of breast cancer risk by estrogen‐receptor status
Correction to: Risk-reducing salpingo-oophorectomy, natural menopause, and breast cancer risk: an international prospective cohort of BRCA1 and BRCA2 mutation carriers
Polygenic Risk Modelling for Prediction of Epithelial Ovarian Cancer Risk
Prostate Cancer Risks for Male BRCA1 and BRCA2 Mutation Carriers: A Prospective Cohort Study
Genome-wide association and transcriptome studies identify target genes and risk loci for breast cancer
Association of Genomic Domains in <i>BRCA1</i> and <i>BRCA2</i> with Prostate Cancer Risk and Aggressiveness
Genome-wide association study identifies 32 novel breast cancer susceptibility loci from overall and subtype-specific analyses
The FANCM:p.Arg658* truncating variant is associated with risk of triple-negative breast cancer
Alcohol Consumption, Cigarette Smoking, and Risk of Breast Cancer for <i>BRCA1</i> and <i>BRCA2</i> Mutation Carriers: Results from The BRCA1 and BRCA2 Cohort Consortium
Mendelian randomisation study of height and body mass index as modifiers of ovarian cancer risk in 22,588 BRCA1 and BRCA2 mutation carriers
Fine-mapping of 150 breast cancer risk regions identifies 178 high confidence target genes
Mutational spectrum in a worldwide study of 29,700 families with<i>BRCA1</i>or<i>BRCA2</i>mutations
Height and Body Mass Index as Modifiers of Breast Cancer Risk in <i>BRCA1</i>/<i>2</i> Mutation Carriers: A Mendelian Randomization Study
Oral Contraceptive Use and Breast Cancer Risk: Retrospective and Prospective Analyses From a BRCA1 and BRCA2 Mutation Carrier Cohort Study
The Influence of Number and Timing of Pregnancies on Breast Cancer Risk for Women With BRCA1 or BRCA2 Mutations
Risks of Breast, Ovarian, and Contralateral Breast Cancer for <i>BRCA1</i> and <i>BRCA2</i> Mutation Carriers
Identification of 12 new susceptibility loci for different histotypes of epithelial ovarian cancer
Identification of ten variants associated with risk of estrogen-receptor-negative breast cancer