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197 results on '"Weitzel, Jn"'

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

2. Use of risk-reducing surgeries in a prospective cohort of 1,499 BRCA1 and BRCA2 mutation carriers

3. A KRAS variant is a biomarker of poor outcome, platinum chemotherapy resistance and a potential target for therapy in ovarian cancer

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

5. Correction: Polygenic risk modeling for prediction of epithelial ovarian cancer risk.

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

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

8. Weight Gain and the Risk of Ovarian Cancer in BRCA1 and BRCA2 Mutation Carriers

9. Germline Pathogenic Variants in Cancer Predisposition Genes Among Women With Invasive Lobular Carcinoma of the Breast

10. A case-only study to identify genetic modifiers of breast cancer risk for BRCA1/BRCA2 mutation carriers (vol 12, 1078, 2021)

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

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

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

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

15. Cancer Risks Associated With Germline PALB2 Pathogenic Variants: An International Study of 524 Families

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

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

18. Association of germline variation with the survival of women with BRCA1/2 pathogenic variants and breast cancer

19. Transcriptome-wide association study of breast cancer risk by estrogen-receptor status

20. Suggested application of HER2+breast tumor phenotype for germline TP53 variant classification within ACMG/AMP guidelines

22. Shared heritability and functional enrichment across six solid cancers

23. The FANCM:p.Arg658* truncating variant is associated with risk of triple-negative breast cancer

24. Genome-wide association and transcriptome studies identify target genes and risk loci for breast cancer

25. Shared heritability and functional enrichment across six solid cancers (vol 10, 431, 2019)

26. Oophorectomy and risk of contralateral breast cancer among BRCA1 and BRCA2 mutation carriers

27. The association between smoking and cancer incidence in BRCA1 and BRCA2 mutation carriers

28. Abstract GS2-01: Age-related breast cancer risk estimates for the general population based on sequencing of cancer predisposition genes in 19,228 breast cancer patients and 20,211 matched unaffected controls from US based cohorts in the CARRIERS study

29. Mutational spectrum in a worldwide study of 29,700 families with BRCA1 or BRCA2 mutations

30. Evaluation of Polygenic Risk Scores for Breast and Ovarian Cancer Risk Prediction in BRCA1 and BRCA2 Mutation Carriers

31. Prediction of Breast and Prostate Cancer Risks in Male BRCA1 and BRCA2 Mutation Carriers Using Polygenic Risk Scores

32. BRCA2 Polymorphic Stop Codon K3326X and the Risk of Breast, Prostate, and Ovarian Cancers

33. Fine-Scale Mapping at 9p22.2 Identifies Candidate Causal Variants That Modify Ovarian Cancer Risk in BRCA1 and BRCA2 Mutation Carriers

34. Candidate genetic modifiers for breast and ovarian cancer risk inBRCA1andBRCA2 mutation carriers

35. Association of type and location of BRCA1 and BRCA2 mutations with risk of breast and ovarian cancer

36. Associations of common breast cancer susceptibility alleles with risk of breast cancer subtypes in BRCA1 and BRCA2 mutation carriers

37. Male breast cancer in BRCA1 and BRCA2 mutation carriers: pathology data from the Consortium of Investigators of Modifiers of BRCA1/2

38. Identification of four novel susceptibility loci for oestrogen receptor negative breast cancer

39. Functional mechanisms underlying pleiotropic risk alleles at the 19p13.1 breast-ovarian cancer susceptibility locus

40. Identification of independent association signals and putative functional variants for breast cancer risk through fine-scale mapping of the 12p11 locus

41. Inheritance of deleterious mutations at both BRCA1 and BRCA2 in an international sample of 32,295 women

42. PMS2 monoallelic mutation carriers: the known unknown

43. DNA Glycosylases Involved in Base Excision Repair May Be Associated with Cancer Risk in BRCA1 and BRCA2 Mutation Carriers

45. Identification of six new susceptibility loci for invasive epithelial ovarian cancer

46. Assessing Associations between the AURKA-HMMR-TPX2-TUBG1 Functional Module and Breast Cancer Risk in BRCA1/2 Mutation Carriers

47. Genome-Wide Association Study in BRCA1 Mutation Carriers Identifies Novel Loci Associated with Breast and Ovarian Cancer Risk

48. Associations of common breast cancer susceptibility alleles with risk of breast cancer subtypes in BRCA1 and BRCA2 mutation carriers

49. Identification of a BRCA2-Specific Modifier Locus at 6p24 Related to Breast Cancer Risk

50. Genome-Wide Association Study in BRCA1 Mutation Carriers Identifies Novel Loci Associated with Breast and Ovarian Cancer Risk

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