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

2. Genomic characterization of cervical lymph node metastases in papillary thyroid carcinoma following the Chornobyl accident

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

4. Geographic variation of mutagenic exposures in kidney cancer genomes

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

7. Genetically adjusted PSA levels for prostate cancer screening.

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

9. Moving towards FAIR practices in epidemiological research

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

28. 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

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

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

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

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

33. Genetic insights into biological mechanisms governing human ovarian ageing

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

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

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

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

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

40. 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

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

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

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

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

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

46. Breast Cancer Polygenic Risk Score and Contralateral Breast Cancer Risk

47. Pathway Analysis of Renal Cell Carcinoma Genome-Wide Association Studies Identifies Novel Associations

48. Transcriptome‐wide association study of breast cancer risk by estrogen‐receptor status

49. Germline HOXB13 mutations p.G84E and p.R217C do not confer an increased breast cancer risk.

50. Genome-wide association study identifies 32 novel breast cancer susceptibility loci from overall and subtype-specific analyses.

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