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1. A Likelihood Ratio Approach for Utilizing Case-Control Data in the Clinical Classification of Rare Sequence Variants: Application to BRCA1 and BRCA2

2. Cancer Risks Associated With BRCA1 and BRCA2 Pathogenic Variants

3. Aggregation tests identify new gene associations with breast cancer in populations with diverse ancestry

4. FANCM missense variants and breast cancer risk: a case-control association study of 75,156 European women

5. Breast Cancer Risk Factors and Survival by Tumor Subtype: Pooled Analyses from the Breast Cancer Association ConsortiumBreast Cancer Risk Factors and Survival By Tumor Subtype

7. Differences in polygenic score distributions in European ancestry populations: implications for breast cancer risk prediction

8. A case-only study to identify genetic modifiers of breast cancer risk for BRCA1/BRCA2 mutation carriers

9. Co-observation of germline pathogenic variants in breast cancer predisposition genes: Results from analysis of the BRIDGES sequencing dataset

10. Spectrum and Frequency of Germline FANCM Protein-Truncating Variants in 44,803 European Female Breast Cancer Cases

11. Association of the CHEK2 c.1100delC variant, radiotherapy, and systemic treatment with contralateral breast cancer risk and breast cancer-specific survival

12. Interplay between BRCA1 and RHAMM regulates epithelial apicobasal polarization and may influence risk of breast cancer.

13. FANCM missense variants and breast cancer risk: a case-control association study of 75,156 European women

14. Supplementary Tables 1-9 from Pathology of Breast and Ovarian Cancers among BRCA1 and BRCA2 Mutation Carriers: Results from the Consortium of Investigators of Modifiers of BRCA1/2 (CIMBA)

15. Association of the CHEK2 c.1100delC variant, radiotherapy, and systemic treatment with contralateral breast cancer risk and breast cancer-specific survival

16. Aggregation tests identify new gene associations with breast cancer in populations with diverse ancestry

17. Two truncating variants in FANCC and breast cancer risk

20. FANCMmissense variants and breast cancer risk: a case-control association study of 75,156 European women

21. Breast Cancer Risk Factors and Survival by Tumor Subtype: Pooled Analyses from the Breast Cancer Association Consortium

24. Characterization of the Cancer Spectrum in Men With Germline BRCA1 and BRCA2 Pathogenic Variants: Results From the Consortium of Investigators of Modifiers of BRCA1/2 (CIMBA)

25. Genome-wide association study identifies 32 novel breast cancer susceptibility loci from overall and subtype-specific analyses

26. Characterization of the cancer spectrum in men with germline BRCA1 and BRCA2 pathogenic variants

27. Association of Genomic Domains in BRCA1 and BRCA2 with Prostate Cancer Risk and Aggressiveness

32. A novel deleterious c.2656G>T MSH2 germline mutation in a Pakistani family with a phenotypic overlap of hereditary breast and ovarian cancer and Lynch syndrome

40. Pathology of Breast and Ovarian Cancers among BRCA1 and BRCA2 Mutation Carriers: Results from the Consortium of Investigators of Modifiers of BRCA1/2 (CIMBA)

42. Family History, Genetic Testing, and Clinical Risk Prediction: Pooled Analysis of CHEK2*1100delC in 1,828 Bilateral Breast Cancers and 7,030 Controls

46. German populations with infrequent CHEK2*1100delC and minor associations with early-onset and familial breast cancer

47. Constitutional CHEK2 mutations are infrequent in early-onset and familial breast/ovarian cancer patients from Pakistan.

48. Two truncating variants in FANCC and breast cancer risk

49. Breast Cancer Risk Genes - Association Analysis in More than 113,000 Women

50. Association of Genomic Domains in BRCA1 and BRCA2 with Prostate Cancer Risk and Aggressiveness

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