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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. Ovarian cancer pathology characteristics as predictors of variant pathogenicity in BRCA1 and BRCA2

4. Exome sequencing identifies breast cancer susceptibility genes and defines the contribution of coding variants to breast cancer risk

5. Associations of height, body mass index, and weight gain with breast cancer risk in carriers of a pathogenic variant in BRCA1 or BRCA2: the BRCA1 and BRCA2 Cohort Consortium

6. PREDICT validity for prognosis of breast cancer patients with pathogenic BRCA1/2 variants

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

8. Cancer Risks Associated With BRCA1 and BRCA2 Pathogenic Variants

9. Rare germline copy number variants (CNVs) and breast cancer risk

10. Germline variants and breast cancer survival in patients with distant metastases at primary breast cancer diagnosis.

11. The predictive ability of the 313 variant-based polygenic risk score for contralateral breast cancer risk prediction in women of European ancestry with a heterozygous BRCA1 or BRCA2 pathogenic variant.

12. Clinical implications of incorporating genetic and non-genetic risk factors in CanRisk-based breast cancer risk prediction

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

14. The impact of coding germline variants on contralateral breast cancer risk and survival

15. Author Correction: Exome sequencing identifies breast cancer susceptibility genes and defines the contribution of coding variants to breast cancer risk

16. Polygenic risk modeling for prediction of epithelial ovarian cancer risk

17. Breast cancer risks associated with missense variants in breast cancer susceptibility genes

18. Copy number variants as modifiers of breast cancer risk for BRCA1/BRCA2 pathogenic variant carriers

19. Polygenic risk scores indicate extreme ages at onset of breast cancer in female BRCA1/2 pathogenic variant carriers

20. Common variants in breast cancer risk loci predispose to distinct tumor subtypes

22. The BRCA2 c.68‐7T > A variant is not pathogenic: A model for clinical calibration of spliceogenicity

23. Olaparib Addition to Maintenance Bevacizumab Therapy in Ovarian Carcinoma With BRCA-Like Genomic Aberrations

24. Generalized Additive Models for the Detection of Copy Number Variations (CNVs) Using Multi-gene Panel Sequencing Data

25. Mendelian randomisation study of smoking exposure in relation to breast cancer risk

26. PHIP - a novel candidate breast cancer susceptibility locus on 6q14.1

27. Genetic modifiers of CHEK2*1100delC-associated breast cancer risk

28. Olaparib Addition to Maintenance Bevacizumab Therapy in Ovarian Carcinoma with BRCA -Like Genomic Aberrations

29. Olaparib Addition to Maintenance Bevacizumab Therapy in Ovarian Carcinoma With BRCA-Like Genomic Aberrations

30. Polygenic risk scores and breast and epithelial ovarian cancer risks for carriers of BRCA1 and BRCA2 pathogenic variants

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

33. Evidence that the 5p12 Variant rs10941679 Confers Susceptibility to Estrogen-Receptor-Positive Breast Cancer through FGF10 and MRPS30 Regulation

34. Fine‐scale mapping of 8q24 locus identifies multiple independent risk variants for breast cancer

35. Fine scale mapping of the 17q22 breast cancer locus using dense SNPs, genotyped within the Collaborative Oncological Gene-Environment Study (COGs).

36. Genetically Predicted Body Mass Index and Breast Cancer Risk: Mendelian Randomization Analyses of Data from 145,000 Women of European Descent.

37. Age- and Tumor Subtype–Specific Breast Cancer Risk Estimates for CHEK2*1100delC Carriers

38. An intergenic risk locus containing an enhancer deletion in 2q35 modulates breast cancer risk by deregulating IGFBP5 expression

39. Association of genetic susceptibility variants for type 2 diabetes with breast cancer risk in women of European ancestry

40. No evidence that protein truncating variants in BRIP1 are associated with breast cancer risk: implications for gene panel testing.

41. Breast cancer risk variants at 6q25 display different phenotype associations and regulate ESR1, RMND1 and CCDC170.

42. Genetic variation in the immunosuppression pathway genes and breast cancer susceptibility: a pooled analysis of 42,510 cases and 40,577 controls from the Breast Cancer Association Consortium

43. Fine-Mapping of the 1p11.2 Breast Cancer Susceptibility Locus.

44. RAD51B in Familial Breast Cancer.

45. An original phylogenetic approach identified mitochondrial haplogroup T1a1 as inversely associated with breast cancer risk in BRCA2 mutation carriers

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

48. Polymorphisms in a Putative Enhancer at the 10q21.2 Breast Cancer Risk Locus Regulate NRBF2 Expression

49. Fine-Scale Mapping of the 5q11.2 Breast Cancer Locus Reveals at Least Three Independent Risk Variants Regulating MAP3K1

50. Candidate Genetic Modifiers for Breast and Ovarian Cancer Risk in BRCA1 and BRCA2 Mutation Carriers

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