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1. Pre-diagnosis tea and coffee consumption and survival after a diagnosis of ovarian cancer: results from the Ovarian Cancer Association Consortium

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

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

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

8. Intratumoral presence of the genotoxic gut bacteria pks+E. coli, Enterotoxigenic Bacteroides fragilis, and Fusobacterium nucleatum and their association with clinicopathological and molecular features of colorectal cancer

9. Lifetime ovulatory years and risk of epithelial ovarian cancer: a multinational pooled analysis

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

11. Epigenome-wide meta-analysis of BMI in nine cohorts: Examining the utility of epigenetically predicted BMI.

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

13. Does a Multiple Myeloma Polygenic Risk Score Predict Overall Survival of Patients with Myeloma?

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

15. Genome-Wide Interaction Analysis of Genetic Variants With Menopausal Hormone Therapy for Colorectal Cancer Risk.

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

17. 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

19. Hypertensive conditions of pregnancy, preterm birth, and premenopausal breast cancer risk: a premenopausal breast cancer collaborative group analysis

20. BMI and breast cancer risk around age at menopause

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

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

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

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

26. Association of germline genetic variants with breast cancer-specific survival in patient subgroups defined by clinic-pathological variables related to tumor biology and type of systemic treatment

27. Genome-wide association studies identify 137 genetic loci for DNA methylation biomarkers of aging

28. Dietary Fiber Intake and Risk of Advanced and Aggressive Forms of Prostate Cancer: A Pooled Analysis of 15 Prospective Cohort Studies

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

30. Prognostic role of detailed colorectal location and tumor molecular features: analyses of 13,101 colorectal cancer patients including 2994 early-onset cases

32. Cancer Risks Associated With TP53 Pathogenic Variants: Maximum Likelihood Analysis of Extended Pedigrees for Diagnosis of First Cancers Beyond the Li-Fraumeni Syndrome Spectrum

34. Distinct germline genetic susceptibility profiles identified for common non-Hodgkin lymphoma subtypes

36. Genome-wide Association Study of Bladder Cancer Reveals New Biological and Translational Insights

38. Design and methodological considerations for biomarker discovery and validation in the Integrative Analysis of Lung Cancer Etiology and Risk (INTEGRAL) Program

39. Correction: Distinct germline genetic susceptibility profiles identified for common non-Hodgkin lymphoma subtypes

40. Segregation analysis of 17,425 population-based breast cancer families: Evidence for genetic susceptibility and risk prediction

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

43. Methylation-based markers of aging and lifestyle-related factors and risk of breast cancer: a pooled analysis of four prospective studies

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

45. Interactions between folate intake and genetic predictors of gene expression levels associated with colorectal cancer risk

46. Genome-wide and transcriptome-wide association studies of mammographic density phenotypes reveal novel loci

48. Association of neighbourhood disadvantage and individual socioeconomic position with all-cause mortality: a longitudinal multicohort analysis

49. Prevalence of Germline Pathogenic Variants in Renal Cancer Predisposition Genes in a Population-Based Study of Renal Cell Carcinoma.

50. Time to Diagnosis and Treatment for Ovarian Cancer and Associations with Outcomes: A Systematic Review.

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