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1. Germline copy number variants and endometrial cancer risk

4. Polygenic score distribution differences across European ancestry populations: implications for breast cancer risk prediction

6. Understanding the genetic complexity of puberty timing across the allele frequency spectrum

7. Disentangling the relationships of body mass index and circulating sex hormone concentrations in mammographic density using Mendelian randomization

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

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

10. Associations of a Breast Cancer Polygenic Risk Score With Tumor Characteristics and Survival

12. Distinct Reproductive Risk Profiles for Intrinsic-Like Breast Cancer Subtypes: Pooled Analysis of Population-Based Studies

13. Characterizing prostate cancer risk through multi-ancestry genome-wide discovery of 187 novel risk variants

14. Publisher Correction: Understanding the genetic complexity of puberty timing across the allele frequency spectrum

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

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

17. Polymorphisms in genes of melatonin biosynthesis and signaling support the light-at-night hypothesis for breast cancer

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

20. Cancer Risks Associated With BRCA1 and BRCA2 Pathogenic Variants

21. PredictCBC-2.0: a contralateral breast cancer risk prediction model developed and validated in ~ 200,000 patients

22. Genome-wide interaction analysis of menopausal hormone therapy use and breast cancer risk among 62,370 women

23. Age-specific breast and ovarian cancer risks associated with germline BRCA1 or BRCA2 pathogenic variants – an Asian study of 572 families

24. A genome-wide gene-environment interaction study of breast cancer risk for women of European ancestry

25. 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

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

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

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

29. Cross-ancestry GWAS meta-analysis identifies six breast cancer loci in African and European ancestry women.

30. Genome-Wide Interaction Analysis of Menopausal Hormone Therapy Use and Breast Cancer Risk Among 62,370 Women

31. 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

32. Improving reporting standards for polygenic scores in risk prediction studies

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

35. Gene-Environment Interactions Relevant to Estrogen and Risk of Breast Cancer: Can Gene-Environment Interactions Be Detected Only among Candidate SNPs from Genome-Wide Association Studies?

36. Personalized early detection and prevention of breast cancer: ENVISION consensus statement

37. Publisher Correction: Personalized early detection and prevention of breast cancer: ENVISION consensus statement

38. The effect of sample size on polygenic hazard models for prostate cancer

39. A Genetic Risk Score to Personalize Prostate Cancer Screening, Applied to Population Data

40. Assessment of polygenic architecture and risk prediction based on common variants across fourteen cancers.

41. Evidence of Novel Susceptibility Variants for Prostate Cancer and a Multiancestry Polygenic Risk Score Associated with Aggressive Disease in Men of African Ancestry

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

44. A saturated map of common genetic variants associated with human height

45. Relevance of the MHC region for breast cancer susceptibility in Asians

46. Assessment of interactions between 205 breast cancer susceptibility loci and 13 established risk factors in relation to breast cancer risk, in the Breast Cancer Association Consortium

47. Identification of 31 loci for mammographic density phenotypes and their associations with breast cancer risk

48. BRCA1 and BRCA2 pathogenic sequence variants in women of African origin or ancestry

49. Mendelian randomisation study of height and body mass index as modifiers of ovarian cancer risk in 22,588 BRCA1 and BRCA2 mutation carriers

50. Associations of obesity and circulating insulin and glucose with breast cancer risk: a Mendelian randomization analysis.

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