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1. Incorporating progesterone receptor expression into the PREDICT breast prognostic model

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

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

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

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

11. Prediction of contralateral breast cancer: external validation of risk calculators in 20 international cohorts

12. Genome-wide association study identifies 25 known breast cancer susceptibility loci as risk factors for triple-negative breast cancer.

14. Genome-wide association study of germline variants and breast cancer-specific mortality

15. Recurrent activating STAT5B N642H mutation in myeloid neoplasms with eosinophilia

16. A network analysis to identify mediators of germline-driven differences in breast cancer prognosis

17. Associations of breast cancer risk factors with tumor subtypes: a pooled analysis from the Breast Cancer Association Consortium studies.

19. Prediction and clinical utility of a contralateral breast cancer risk model

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

26. Supplementary Table 1 from Mapping of Chromosome 1p Deletions in Myeloma Identifies FAM46C at 1p12 and CDKN2C at 1p32.3 as Being Genes in Regions Associated with Adverse Survival

27. Supplementary Methods, References, Legends for Table 1 and Figure 1 from Gender Disparities in the Tumor Genetics and Clinical Outcome of Multiple Myeloma

28. Supplementary Table 3 from Mapping of Chromosome 1p Deletions in Myeloma Identifies FAM46C at 1p12 and CDKN2C at 1p32.3 as Being Genes in Regions Associated with Adverse Survival

29. Supplementary Table 2 from Mapping of Chromosome 1p Deletions in Myeloma Identifies FAM46C at 1p12 and CDKN2C at 1p32.3 as Being Genes in Regions Associated with Adverse Survival

30. Data from Common Breast Cancer Susceptibility Loci Are Associated with Triple-Negative Breast Cancer

31. Supplementary Materials and Methods, Tables 1-5 from Common Breast Cancer Susceptibility Loci Are Associated with Triple-Negative Breast Cancer

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

33. A likelihood ratio approach for utilizing case-control data in the clinical classification of rare sequence variants:Application to BRCA1 and BRCA2

34. Age-related loss of chromosome Y is associated with levels of sex hormone binding globulin and clonal hematopoiesis defined by TET2, TP53, and CBL mutations

35. Two truncating variants in FANCC and breast cancer risk

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

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

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

41. Physical activity, sedentary time and breast cancer risk: a Mendelian randomisation study

42. Incorporating progesterone receptor expression into the PREDICT breast prognostic model

43. Physical activity, sedentary time and breast cancer risk : a Mendelian randomisation study

44. Physical activity, sedentary time and breast cancer risk: a Mendelian randomisation study

45. Physical activity, sedentary time and breast cancer risk:a Mendelian randomisation study

46. Additional file 4 of Common variants in breast cancer risk loci predispose to distinct tumor subtypes

47. Prediction of Breast Cancer Risk Based on Profiling With Common Genetic Variants

48. Therapeutic Targeting of Integrin αvβ6 in Breast Cancer

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

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