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2,463 results on '"Chanock, Stephen J"'

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1. Heterogeneous genetic architectures of prostate cancer susceptibility in sub-Saharan Africa

2. Genetic drivers and cellular selection of female mosaic X chromosome loss

4. Geographic variation of mutagenic exposures in kidney cancer genomes

5. Multi-ancestry genome-wide association study of kidney cancer identifies 63 susceptibility regions

7. Genome-wide analyses characterize shared heritability among cancers and identify novel cancer susceptibility regions

8. Genetically adjusted PSA levels for prostate cancer screening.

9. Observational and genetic associations between cardiorespiratory fitness and cancer: a UK Biobank and international consortia study

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

11. Moving towards FAIR practices in epidemiological research

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

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

14. Inflated expectations: Rare-variant association analysis using public controls

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

16. Genetically inferred birthweight, height, and puberty timing and risk of osteosarcoma

17. Transcriptome- and proteome-wide association studies identify genes associated with renal cell carcinoma

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

19. Cross-ancestry genome-wide meta-analysis of 61,047 cases and 947,237 controls identifies new susceptibility loci contributing to lung cancer.

20. Transcriptome-wide association analysis identifies candidate susceptibility genes for prostate-specific antigen levels in men without prostate cancer

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

22. Mosaic chromosomal alterations in peripheral blood leukocytes of children in sub-Saharan Africa

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

25. Genome-wide association study of lung adenocarcinoma in East Asia and comparison with a European population

26. GWAS Explorer: an open-source tool to explore, visualize, and access GWAS summary statistics in the PLCO Atlas

27. Correction: Polygenic risk modeling for prediction of epithelial ovarian cancer risk

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

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

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

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

32. 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

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

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

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

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

37. Genetic insights into biological mechanisms governing human ovarian ageing

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

39. Functional annotation of the 2q35 breast cancer risk locus implicates a structural variant in influencing activity of a long-range enhancer element

41. Health diplomacy in action: The cancer legacy of the Good Friday Agreement

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

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

44. Discovery and fine-mapping of height loci via high-density imputation of GWASs in individuals of African ancestry

45. 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

46. Combined Associations of a Polygenic Risk Score and Classical Risk Factors With Breast Cancer Risk.

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

48. CYP3A7*1C allele: linking premenopausal oestrone and progesterone levels with risk of hormone receptor-positive breast cancers

49. Breast Cancer Risk Genes — Association Analysis in More than 113,000 Women

50. Cross-Cancer Genome-Wide Association Study of Endometrial Cancer and Epithelial Ovarian Cancer Identifies Genetic Risk Regions Associated with Risk of Both Cancers

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