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1. Assessment of differentially methylated loci in individuals with end-stage kidney disease attributed to diabetic kidney disease: an exploratory study

2. Loci for insulin processing and secretion provide insight into type 2 diabetes risk

3. A global initiative to deliver precision health in diabetes

4. Strong Association of Socioeconomic Status and Genetic Ancestry in Latinos: Implications for Admixture Studies of Type 2 Diabetes

8. The trans-ancestral genomic architecture of glycemic traits

9. Sex-dimorphic genetic effects and novel loci for fasting glucose and insulin variability

10. The trans-ancestral genomic architecture of glycemic traits

11. Transferability and fine-mapping of glucose and insulin quantitative trait loci across populations: CARe, the Candidate Gene Association Resource

18. Publisher Correction: Protein-altering variants associated with body mass index implicate pathways that control energy intake and expenditure in obesity (Nature Genetics, (2018), 50, 1, (26-41), 10.1038/s41588-017-0011-x)

26. Genome-Wide Association Study of Diabetic Kidney Disease Highlights Biology Involved in Glomerular Basement Membrane Collagen

28. Dietary fat quality and genetic risk of type 2 diabetes

29. The presence of two reduced function variants in CYP2C9 influences the acute response to glipizide.

32. Genetic studies of body mass index yield new insights for obesity biology

33. Metabolite profiles and the risk of developing diabetes

34. Genome-wide association identifies nine common variants associated with fasting proinsulin levels and provides new insights into the pathophysiology of type 2 diabetes

35. Association testing of TCF7L2 polymorphisms with type 2 diabetes in multi-ethnic youth

36. Strong Association of Socioeconomic Status and Genetic Ancestry in Latinos

37. The SH2B1 obesity locus and abnormal glucose homeostasis:Lack of evidence for association from a meta-analysis in individuals of European ancestry

38. Common genetic variants differentially influence the transition from clinically defined states of fasting glucose metabolism

39. Metabolite profiles and the risk of developing diabetes

41. 42 HAPLOTYPE STRUCTURE AND ASSOCIATION OF COMMON VARIANTS IN THE GENE ENCODING THE ISLET ATP-SENSITIVE POTASSIUM CHANNEL WITH TYPE 2 DIABETES.

42. HAPLOTYPE STRUCTURE AND ASSOCIATION OF COMMON VARIANTS IN THE GENE ENCODING THE ISLET ATP-SENSITIVE POTASSIUM CHANNEL WITH TYPE 2 DIABETES.

44. Additional file 2 of Assessment of differentially methylated loci in individuals with end-stage kidney disease attributed to diabetic kidney disease: an exploratory study

45. Additional file 2 of Assessment of differentially methylated loci in individuals with end-stage kidney disease attributed to diabetic kidney disease: an exploratory study

46. Common variants at 10 genomic loci influence hemoglobin A1C levels via glycemic and nonglycemic pathways (Diabetes (2010) 59, (3229-3239))

47. Consistent Directions of Effect for Established Type 2 Diabetes Risk Variants Across Populations: The Population Architecture using Genomics and Epidemiology (PAGE) Consortium

48. Common variants at 10 genomic loci influence hemoglobin A1C levels via glycemic and nonglycemic pathways (Diabetes (2010) 59, (3229-3239))

49. Common variants at 10 genomic loci influence hemoglobin A1Clevels via glycemic and nonglycemic pathways (Diabetes (2010) 59, (3229-3239))

50. The SH2B1 obesity locus and abnormal glucose homeostasis: lack of evidence for association from a meta-analysis in individuals of European ancestry.

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