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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. Genetic risk impacts the association of menopausal hormone therapy with colorectal cancer risk

7. Fine-mapping analysis including over 254,000 East Asian and European descendants identifies 136 putative colorectal cancer susceptibility genes

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

9. Identification of novel genetic loci for risk of multiple myeloma by functional annotation

10. Probing the diabetes and colorectal cancer relationship using gene – environment interaction analyses

11. Integrative multi-omics analyses to identify the genetic and functional mechanisms underlying ovarian cancer risk regions

13. Combining Asian and European genome-wide association studies of colorectal cancer improves risk prediction across racial and ethnic populations

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

17. A cross-sectional study of inflammatory markers as determinants of circulating kynurenines in the Lung Cancer Cohort Consortium

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

19. Association between circulating inflammatory markers and adult cancer risk: a Mendelian randomization analysis

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

23. Genome-wide interaction analysis of folate for colorectal cancer risk

24. Role of Polyunsaturated Fat in Modifying Cardiovascular Risk Associated With Family History of Cardiovascular Disease: Pooled De Novo Results From 15 Observational Studies

25. Elucidating the Risk of Colorectal Cancer for Variants in Hereditary Colorectal Cancer Genes

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

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

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

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

36. Epigenetic mechanisms of lung carcinogenesis involve differentially methylated CpG sites beyond those associated with smoking

38. Association of allergic diseases and epilepsy with risk of glioma, meningioma and acoustic neuroma: results from the INTERPHONE international case–control study

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

40. Associations between early-life growth pattern and body size and follicular lymphoma risk and survival: a family-based case-control study

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

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

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

44. Identifying colorectal cancer caused by biallelic MUTYH pathogenic variants using tumor mutational signatures

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

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

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

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

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

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