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Evaluation of European-based polygenic risk score for breast cancer in Ashkenazi Jewish women in Israel
Spectrum and frequency of germline FANCM protein-truncating variants in 44,803 European female breast cancer cases
The impact of coding germline variants on contralateral breast cancer risk and survival
FANCM missense variants and breast cancer riskn
Aggregation tests identify new gene associations with breast cancer in populations with diverse ancestry
Physical activity, sedentary time and breast cancer risk
Breast cancer risks associated with missense variants in breast cancer susceptibility genes
Rare germline copy number variants (CNVs) and breast cancer risk
Common variants in breast cancer risk loci predispose to distinct tumor subtypes
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
Mendelian randomisation study of smoking exposure in relation to breast cancer risk
Gene-environment interactions relevant to estrogen and risk of breast cancer
CYP3A7*1C allele
Breast Cancer Polygenic Risk Score and Contralateral Breast Cancer Risk
Germline HOXB13 mutations p.G84E and p.R217C do not confer an increased breast cancer risk
Two truncating variants in FANCC and breast cancer risk
Associations of obesity and circulating insulin and glucose with breast cancer risk: a Mendelian randomization analysis
Genome-wide association study of germline variants and breast cancer-specific mortality
A transcriptome-wide association study of 229,000 women identifies new candidate susceptibility genes for breast cancer
PHIP - a novel candidate breast cancer susceptibility locus on 6q14.1
BRCA2 Hypomorphic Missense Variants Confer Moderate Risks of Breast Cancer
BRCA2 Hypomorphic Missense Variants Confer Moderate Risks of Breast Cancer
Association of breast cancer risk with genetic variants showing differential allelic expression: Identification of a novel breast cancer susceptibility locus at 4q21
Evidence that the 5p12 Variant rs10941679 Confers Susceptibility to Estrogen-Receptor-Positive Breast Cancer through FGF10 and MRPS30 Regulation