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2,039 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. Genomic characterization of cervical lymph node metastases in papillary thyroid carcinoma following the Chornobyl accident

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

6. Geographic variation of mutagenic exposures in kidney cancer genomes

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

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

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

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

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

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

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

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

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

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

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

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

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

24. Genetically adjusted PSA levels for prostate cancer screening

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

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

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

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

31. Evidence of Novel Susceptibility Variants for Prostate Cancer and a Multiancestry Polygenic Risk Score Associated with Aggressive Disease in Men of African Ancestry

32. Targeted long-read sequencing of the Ewing sarcoma 6p25.1 susceptibility locus identifies germline-somatic interactions with EWSR1-FLI1 binding

33. A saturated map of common genetic variants associated with human height

34. A Multimedia Strategy to Integrate Introductory Broad-Based Radiation Science Education in US Medical Schools

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

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

37. Genetic regulation of OAS1 nonsense-mediated decay underlies association with COVID-19 hospitalization in patients of European and African ancestries

38. The renal lineage factor PAX8 controls oncogenic signalling in kidney cancer

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

42. Germline-somatic JAK2 interactions are associated with clonal expansion in myelofibrosis

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

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

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

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

48. Genomic and evolutionary classification of lung cancer in never smokers

49. Identifying Novel Susceptibility Genes for Colorectal Cancer Risk From a Transcriptome-Wide Association Study of 125,478 Subjects

50. Pre-HCT mosaicism increases relapse risk and lowers survival in acute lymphoblastic leukemia patients post–unrelated HCT

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