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1. Benefits of nature-based walking for breast cancer survivors.

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

3. Mortality by age, gene and gender in carriers of pathogenic mismatch repair gene variants receiving surveillance for early cancer diagnosis and treatment: a report from the prospective Lynch syndrome database

4. Endoscopic History and Provider Characteristics Influence Gastric Cancer Survival in Asian Americans

5. Potential impact of family history–based screening guidelines on the detection of early‐onset colorectal cancer

6. Impaired Immune Health in Survivors of Diffuse Large B-Cell Lymphoma.

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

8. Methylated SEPTIN9 plasma test for colorectal cancer detection may be applicable to Lynch syndrome

9. Continued Increase in Melanoma Incidence across all Socioeconomic Status Groups in California, 1998–2012

10. Variation in the risk of colorectal cancer in families with Lynch syndrome: a retrospective cohort study

11. Risk-reducing hysterectomy and bilateral salpingo-oophorectomy in female heterozygotes of pathogenic mismatch repair variants: a Prospective Lynch Syndrome Database report

12. Meta-analysis of genome-wide association studies identifies common susceptibility polymorphisms for colorectal and endometrial cancer near SH2B3 and TSHZ1.

13. Mutation Spectrum and Risk of Colorectal Cancer in African American Families with Lynch Syndrome

14. Cancer risks by gene, age, and gender in 6350 carriers of pathogenic mismatch repair variants: findings from the Prospective Lynch Syndrome Database

15. Identification of a common variant with potential pleiotropic effect on risk of inflammatory bowel disease and colorectal cancer

16. Type 2 diabetes mellitus, blood cholesterol, triglyceride and colorectal cancer risk in Lynch syndrome

17. Ability of known susceptibility SNPs to predict colorectal cancer risk for persons with and without a family history

19. Discovery of common and rare genetic risk variants for colorectal cancer

24. Perspectives on This Article from Association between Folate Levels and CpG Island Hypermethylation in Normal Colorectal Mucosa

25. Circulating bilirubin levels and risk of colorectal cancer: serological and Mendelian randomization analyses

26. Supplementary Table 1 from Cross-Cancer Genome-Wide Analysis of Lung, Ovary, Breast, Prostate, and Colorectal Cancer Reveals Novel Pleiotropic Associations

27. Data from Cross-Cancer Genome-Wide Analysis of Lung, Ovary, Breast, Prostate, and Colorectal Cancer Reveals Novel Pleiotropic Associations

28. Supplemental Table 1 from Association of the Colorectal CpG Island Methylator Phenotype with Molecular Features, Risk Factors, and Family History

30. Supplementary Tables S1-3 from Mendelian Randomization Study of Body Mass Index and Colorectal Cancer Risk

31. Supplementary Table 2 and Supplemental Figures from Cross-Cancer Genome-Wide Analysis of Lung, Ovary, Breast, Prostate, and Colorectal Cancer Reveals Novel Pleiotropic Associations

33. Data from Mendelian Randomization Study of Body Mass Index and Colorectal Cancer Risk

34. Data from A Randomized Trial to Increase Colonoscopy Screening in Members of High-Risk Families in the Colorectal Cancer Family Registry and Cancer Genetics Network

35. Supplementary Data from Lynch Syndrome–Associated Breast Cancers: Clinicopathologic Characteristics of a Case Series from the Colon Cancer Family Registry

36. Data from Prevalence and Penetrance of Major Genes and Polygenes for Colorectal Cancer

37. Data from Lynch Syndrome–Associated Breast Cancers: Clinicopathologic Characteristics of a Case Series from the Colon Cancer Family Registry

38. Supplementary Tables from Identification of Novel Variants in Colorectal Cancer Families by High-Throughput Exome Sequencing

39. FHPP Baseline Survey from A Randomized Trial to Increase Colonoscopy Screening in Members of High-Risk Families in the Colorectal Cancer Family Registry and Cancer Genetics Network

40. Appendix - clean version from Prevalence and Penetrance of Major Genes and Polygenes for Colorectal Cancer

41. Supplementary Table 2 from A Candidate Gene Study of Folate-Associated One Carbon Metabolism Genes and Colorectal Cancer Risk

42. Supplementary Figure 1 from Identification of Novel Variants in Colorectal Cancer Families by High-Throughput Exome Sequencing

43. Data from Genetic Variation in the Vitamin D Receptor (VDR) and the Vitamin D–Binding Protein (GC) and Risk for Colorectal Cancer: Results from the Colon Cancer Family Registry

44. Supplementary Tables from Prevalence and Penetrance of Major Genes and Polygenes for Colorectal Cancer

45. Supplementary Table 1 from Genetic Variation in the Vitamin D Receptor (VDR) and the Vitamin D–Binding Protein (GC) and Risk for Colorectal Cancer: Results from the Colon Cancer Family Registry

46. Supplementary Figure 2 from Identification of Novel Variants in Colorectal Cancer Families by High-Throughput Exome Sequencing

47. Supplementary Material: Funding, Acknowledgements, Consortia, and Bioinformatics Tools Funding sources from Cross-Cancer Genome-Wide Analysis of Lung, Ovary, Breast, Prostate, and Colorectal Cancer Reveals Novel Pleiotropic Associations

48. Description of supplementary files from Identification of Novel Variants in Colorectal Cancer Families by High-Throughput Exome Sequencing

49. Supplementary Table 1 from A Candidate Gene Study of Folate-Associated One Carbon Metabolism Genes and Colorectal Cancer Risk

50. Combining Asian-European Genome-Wide Association Studies of Colorectal Cancer Improves Risk Prediction Across Race and Ethnicity

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