Area of research
Genetics · Cancer Research
Research interest
Research interests include BRCA gene mutations in cancer, Breast Cancer Treatment Studies, Digital Radiography and Breast Imaging, and Cancer Risks and Factors.
Mammographic density, pathogenic breast cancer susceptibility gene variants and breast cancer risk
Differences in polygenic score distributions in European ancestry populations: implications for breast cancer risk prediction
Co-observation of germline pathogenic variants in breast cancer predisposition genes: Results from analysis of the BRIDGES sequencing dataset
Publisher Correction: Understanding the genetic complexity of puberty timing across the allele frequency spectrum
Analysis of more than 400,000 women provides case-control evidence for BRCA1 and BRCA2 variant classification
Germline copy number variants and endometrial cancer risk
Analysis of variants in untranslated and promoter regions and breast cancer risk using whole genome sequencing data
Clinical biomarker-based biological aging and risk of cancer in the UK Biobank
Evaluation of circulating plasma proteins in breast cancer using Mendelian randomisation
Long-Term Performance of an Image-Based Short-Term Risk Model for Breast Cancer
Side effects of low-dose tamoxifen: results from a six-armed randomised controlled trial in healthy women
The impact of coding germline variants on contralateral breast cancer risk and survival
Associations of a Breast Cancer Polygenic Risk Score With Tumor Characteristics and Survival
Breast Cancer Incidence After a False-Positive Mammography Result
FANCM missense variants and breast cancer risk: a case-control association study of 75,156 European women
A genome-wide gene-environment interaction study of breast cancer risk for women of European 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
PREDICT validity for prognosis of breast cancer patients with pathogenic BRCA1/2 variants
A Likelihood Ratio Approach for Utilizing Case-Control Data in the Clinical Classification of Rare Sequence Variants: Application to BRCA1 and BRCA2
Polymorphisms in genes of melatonin biosynthesis and signaling support the light-at-night hypothesis for breast cancer
Evaluation of European-based polygenic risk score for breast cancer in Ashkenazi Jewish women in Israel
Understanding the genetic complexity of puberty timing across the allele frequency spectrum
Prediction of breast cancer risk for sisters of women attending screening
Spectrum and Frequency of Germline FANCM Protein-Truncating Variants in 44,803 European Female Breast Cancer Cases
Pathology of Tumors Associated With Pathogenic Germline Variants in 9 Breast Cancer Susceptibility Genes
Physical activity, sedentary time and breast cancer risk: a Mendelian randomisation study
Prospective validation of the BOADICEA multifactorial breast cancer risk prediction model in a large prospective cohort study
Breast cancer risks associated with missense variants in breast cancer susceptibility genes
Distinct Reproductive Risk Profiles for Intrinsic-Like Breast Cancer Subtypes: Pooled Analysis of Population-Based Studies
A risk model for digital breast tomosynthesis to predict breast cancer and guide clinical care