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226 results on '"Christopher S, Carlson"'

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1. Minority-centric meta-analyses of blood lipid levels identify novel loci in the Population Architecture using Genomics and Epidemiology (PAGE) study.

2. Imputation-Aware Tag SNP Selection To Improve Power for Large-Scale, Multi-ethnic Association Studies

3. High-throughput sequencing of the B-cell receptor in African Burkitt lymphoma reveals clues to pathogenesis

4. Genetics of Chronic Kidney Disease Stages Across Ancestries: The PAGE Study

5. Predicted gene expression in ancestrally diverse populations leads to discovery of susceptibility loci for lifestyle and cardiometabolic traits

6. New insights into the genetic etiology of Alzheimer's disease and related dementias

7. Data from Genetic Variation in Prostaglandin E2 Synthesis and Signaling, Prostaglandin Dehydrogenase, and the Risk of Colorectal Adenoma

8. Supplementary Tables 1-9, Supplementary Figure 1 from Genetic Variation in Prostaglandin E2 Synthesis and Signaling, Prostaglandin Dehydrogenase, and the Risk of Colorectal Adenoma

9. Data from Vitamin D Related Genes, CYP24A1 and CYP27B1, and Colon Cancer Risk

10. Data Supplement from Gene–Environment Interaction Involving Recently Identified Colorectal Cancer Susceptibility Loci

12. Data from Gene–Environment Interaction Involving Recently Identified Colorectal Cancer Susceptibility Loci

13. Multi-ethnic GWAS and fine-mapping of glycaemic traits identify novel loci in the PAGE Study

14. Enrichment of colorectal cancer associations in functional regions: Insight for using epigenomics data in the analysis of whole genome sequence-imputed GWAS data.

16. Use of diverse electronic medical record systems to identify genetic risk for type 2 diabetes within a genome-wide association study.

19. Variant Discovery and Fine Mapping of Genetic Loci Associated with Blood Pressure Traits in Hispanics and African Americans.

20. Strategies for Enriching Variant Coverage in Candidate Disease Loci on a Multiethnic Genotyping Array.

21. A Public Database of Memory and Naive B-Cell Receptor Sequences.

22. Fine-Mapping of Common Genetic Variants Associated with Colorectal Tumor Risk Identified Potential Functional Variants.

24. TagSNP analyses of the PON gene cluster: effects on PON1 activity, LDL oxidative susceptibility, and vascular disease

25. Genome-wide diet-gene interaction analyses for risk of colorectal cancer.

26. Trials and Tribulations with VH Replacement

27. Pleiotropy of cancer susceptibility variants on the risk of non-Hodgkin lymphoma: the PAGE consortium.

28. Genetic discovery and risk characterization in type 2 diabetes across diverse populations

29. Generalization and dilution of association results from European GWAS in populations of non-European ancestry: the PAGE study.

30. Genome-wide association of body fat distribution in African ancestry populations suggests new loci.

31. Genetic variation and reproductive timing: African American women from the Population Architecture using Genomics and Epidemiology (PAGE) Study.

32. Confirmation of the reported association of clonal chromosomal mosaicism with an increased risk of incident hematologic cancer.

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

34. Genome-wide search for gene-gene interactions in colorectal cancer.

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

36. Imputation-Aware Tag SNP Selection To Improve Power for Large-Scale, Multi-ethnic Association Studies

37. Genetic determinants of lipid traits in diverse populations from the population architecture using genomics and epidemiology (PAGE) study.

38. Population history and natural selection shape patterns of genetic variation in 132 genes.

39. Immunosequencing identifies signatures of cytomegalovirus exposure history and HLA-mediated effects on the T cell repertoire

40. High-throughput sequencing of the B-cell receptor in African Burkitt lymphoma reveals clues to pathogenesis

41. Genetic variant predictors of gene expression provide new insight into risk of colorectal cancer

42. Correction to: Genetic variant predictors of gene expression provide new insight into risk of colorectal cancer

43. CYP24A1 variant modifies the association between use of oestrogen plus progestogen therapy and colorectal cancer risk

45. Minority-centric meta-analyses of blood lipid levels identify novel loci in the Population Architecture using Genomics and Epidemiology (PAGE) study

46. CYP2D6-inhibiting medication use and inherited CYP2D6 variation in relation to adverse breast cancer outcomes after tamoxifen therapy

47. Discovery, fine-mapping, and conditional analyses of genetic variants associated with C-reactive protein in multiethnic populations using the Metabochip in the Population Architecture using Genomics and Epidemiology (PAGE) study

48. The mutational landscape of recurrent versus nonrecurrent human papillomavirus–related oropharyngeal cancer

49. Trans-ethnic analysis of metabochip data identifies two new loci associated with BMI

50. IgH-V(D)J NGS-MRD measurement pre- and early post-allotransplant defines very low- and very high-risk ALL patients

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