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(1 - 20 of 127)

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Evaluation of European-based polygenic risk score for breast cancer in Ashkenazi Jewish women in Israel
Exome sequencing identifies breast cancer susceptibility genes and defines the contribution of coding variants to breast cancer risk (vol 55, pg 1435, 2023)
a likelihood ratio approach for utilizing case-control data in the clinical classification of rare sequence variants
Exome sequencing identifies breast cancer susceptibility genes and defines the contribution of coding variants to breast cancer risk
Association of the CHEK2 c.1100delC variant, radiotherapy, and systemic treatment with contralateral breast cancer risk and breast cancer-specific survival
Spectrum and frequency of germline FANCM protein-truncating variants in 44,803 European female breast cancer cases
PREDICT validity for prognosis of breast cancer patients with pathogenic BRCA1/2 variants
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
Incorporating progesterone receptor expression into the PREDICT breast prognostic model
Physical activity, sedentary time and breast cancer risk
Uncovering the Contribution of Moderate-Penetrance Susceptibility Genes to Breast Cancer by Whole-Exome Sequencing and Targeted Enrichment Sequencing of Candidate Genes in Women of European Ancestry
Breast cancer risks associated with missense variants in breast cancer susceptibility genes
Pathology of tumors associated with pathogenic germline variants in 9 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
Germline variants and breast cancer survival in patients with distant metastases at primary breast cancer diagnosis
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
Genetic insights into biological mechanisms governing human ovarian ageing

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