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208 results on '"Chanock, Stephen J"'

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

2. Geographic variation of mutagenic exposures in kidney cancer genomes

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

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

5. Polygenic risk scores, radiation treatment exposures and subsequent cancer risk in childhood cancer survivors

6. JAK2V617Fmutation and associated chromosomal alterations in primary and secondary myelofibrosis and post-HCT outcomes

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

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

9. Harnessing cancer genomes for precision oncology

10. Genetically adjusted PSA levels for prostate cancer screening

11. FANCMmissense variants and breast cancer risk: a case-control association study of 75,156 European women

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

13. Anthropometric measures, body mass index, and pancreatic cancer: a pooled analysis from the Pancreatic Cancer Cohort Consortium (PanScan)

14. ABO blood group and the risk of pancreatic cancer

15. Common variants in immune and DNA repair genes and risk for human papillomavirus persistence and progression to cervical cancer

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

17. Genetic regulation of OAS1nonsense-mediated decay underlies association with COVID-19 hospitalization in patients of European and African ancestries

18. Genetic basis for adverse events after smallpox vaccination

19. Lung cancer survival and functional polymorphisms in MBL2, an innate-immunity gene

20. Serum selenium and risk of prostate cancer--nested case-control study

21. Polymorphisms in folate metabolizing genes and risk for spontaneous preterm and small-for-gestational age birth

22. Association of breast cancer outcome with status of p53 and MDM2 SNP309

23. Host immunogenetics and control of human herpesvirus-8 infection

24. Immunogenetic risk and protective factors for the idiopathic inflammatory myopathies: distinct HLA-A, -B, -Cw, -DRB1, and-DQA1 allelic profiles distinguish European American patients with different myositis autoantibodies

25. Immunogenetic risk and protective factors for the idiopathic inflammatory myopathies: distinct HLA-A, -B, -Cw, -DRB1 and-DQA1 allelic profiles and motifs define clinicopathologic groups in Caucasians

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

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

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

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

33. HBB rs334, ABO Rs8176703and Plasmodium FalciparumPositivity at Enrollment Are Independently Associated with Lower Risk for Endemic Burkitt Lymphoma in Uganda, Tanzania, Kenya, and Malawi

34. Human Leukocyte Antigen Contributes to Childhood Endemic Burkitt Lymphoma in Eastern Africa: A Case-Control Association Study

37. HBB rs334, ABO Rs8176703 and Plasmodium Falciparum Positivity at Enrollment Are Independently Associated with Lower Risk for Endemic Burkitt Lymphoma in Uganda, Tanzania, Kenya, and Malawi

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

40. Genetic insights into biological mechanisms governing human ovarian ageing

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

42. Trans-ancestry genome-wide association meta-analysis of prostate cancer identifies new susceptibility loci and informs genetic risk prediction

43. Genetic architectures of proximal and distal colorectal cancer are partly distinct

44. Common variants in signaling transcription-factor-binding sites drive phenotypic variability in red blood cell traits

45. Coinherited genetics of multiple myeloma and its precursor, monoclonal gammopathy of undetermined significance

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

47. Genome-wide association meta-analyses combining multiple risk phenotypes provide insights into the genetic architecture of cutaneous melanoma susceptibility

48. Frequency of Pathogenic Germline Variants in Cancer-Susceptibility Genes in Patients With Osteosarcoma

49. A meta-analysis of genome-wide association studies of multiple myeloma among men and women of African ancestry

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