Area of research
Genetics · Oncology
Research interest
Research interests include BRCA gene mutations in cancer, Cancer Risks and Factors, Nutrition, Genetics, and Disease, and Nutritional Studies and Diet.
Uptake of Cancer Genetic Services for Chatbot vs Standard-of-Care Delivery Models
Hormonal Contraception and Breast Cancer Risk for Carriers of Germline Mutations in <i>BRCA1</i> and <i>BRCA2</i>
Large-scale genome-wide association study of 398,238 women unveils seven novel loci associated with high-grade serous epithelial ovarian cancer risk
NCCN Guidelines® Insights: Genetic/Familial High-Risk Assessment: Breast, Ovarian, and Pancreatic, Version 2.2024
Real-World Perspectives and Practices for Pneumonitis/Interstitial Lung Disease Associated With Trastuzumab Deruxtecan Use in Human Epidermal Growth Factor Receptor 2–Expressing Metastatic Breast Cancer
Prospective Pilot Study of <sup>18</sup>F-Fluoroestradiol PET/CT in Patients With Invasive Lobular Carcinomas
Associations of a Breast Cancer Polygenic Risk Score With Tumor Characteristics and Survival
Association of Breast Cancer Odds with Background Parenchymal Enhancement Quantified Using a Fully Automated Method at MRI: The IMAGINE Study
Aggregation tests identify new gene associations with breast cancer in populations with diverse ancestry
Association of the <scp> <i>CHEK2</i> </scp> c. <scp>1100delC</scp> variant, radiotherapy, and systemic treatment with contralateral breast cancer risk and breast cancer‐specific survival
A Likelihood Ratio Approach for Utilizing Case-Control Data in the Clinical Classification of Rare Sequence Variants: Application to BRCA1 and BRCA2
Abstract 4176: Timing of pregnancy-related factors and breast cancer risk for women across a range of absolute risk
A human breast cancer-derived xenograft and organoid platform for drug discovery and precision oncology
Physical activity, sedentary time and breast cancer risk: a Mendelian randomisation study
Polygenic risk modeling for prediction of epithelial ovarian cancer risk
Association of Disparities in Family History and Family Cancer History in the Electronic Health Record With Sex, Race, Hispanic or Latino Ethnicity, and Language Preference in 2 Large US Health Care Systems
Common variants in breast cancer risk loci predispose to distinct tumor subtypes
Copy number variants as modifiers of breast cancer risk for BRCA1/BRCA2 pathogenic variant carriers
Correction: Polygenic risk modeling for prediction of epithelial ovarian cancer risk
Genetic/Familial High-Risk Assessment: Breast, Ovarian, and Pancreatic, Version 2.2021, NCCN Clinical Practice Guidelines in Oncology
A prospective prostate cancer screening programme for men with pathogenic variants in mismatch repair genes (IMPACT): initial results from an international prospective study
A Phase 1 dose-escalation study of disulfiram and copper gluconate in patients with advanced solid tumors involving the liver using S-glutathionylation as a biomarker
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
Patient Interactions With an Automated Conversational Agent Delivering Pretest Genetics Education: Descriptive Study
Comparing models of delivery for cancer genetics services among patients receiving primary care who meet criteria for genetic evaluation in two healthcare systems: BRIDGE randomized controlled trial
Association of Risk-Reducing Salpingo-Oophorectomy With Breast Cancer Risk in Women With <i>BRCA1</i> and <i>BRCA2</i> Pathogenic Variants
Association of germline genetic variants with breast cancer-specific survival in patient subgroups defined by clinic-pathological variables related to tumor biology and type of systemic treatment
Common variants in breast cancer risk loci predispose to distinct tumor subtypes.
Author Correction: A case-only study to identify genetic modifiers of breast cancer risk for BRCA1/BRCA2 mutation carriers