Search

Your search keyword '"Hixson JE"' showing total 220 results

Search Constraints

Start Over You searched for: Author "Hixson JE" Remove constraint Author: "Hixson JE"
220 results on '"Hixson JE"'

Search Results

1. Meta-analysis identifies multiple loci associated with kidney function-related traits in east Asian populations

2. Genetic associations at 53 loci highlight cell types and biological pathways relevant for kidney function.

3. Variation in the Maternal Corticotrophin Releasing Hormone-Binding Protein (CRH-BP) Gene and Birth Weight in Blacks, Hispanics and Whites

14. Association of common C-reactive protein (CRP) gene polymorphisms with baseline plasma CRP levels and fenofibrate response: the GOLDN study.

17. Multi-ancestry genome-wide gene-smoking interaction study of 387,272 individuals identifies new loci associated with serum lipids

18. Genetic associations at 53 loci highlight cell types and biological pathways relevant for kidney function

19. Clonal hematopoiesis of indeterminate potential is associated with reduced risk of cognitive impairment in patients with chronic kidney disease.

20. Clonal hematopoiesis of indeterminate potential contributes to accelerated chronic kidney disease progression.

21. WHOLE GENOME SEQUENCING ANALYSIS OF BODY MASS INDEX IDENTIFIES NOVEL AFRICAN ANCESTRY-SPECIFIC RISK ALLELE.

22. Whole-exome sequencing study identifies four novel gene loci associated with diabetic kidney disease.

23. Insights From a Large-Scale Whole-Genome Sequencing Study of Systolic Blood Pressure, Diastolic Blood Pressure, and Hypertension.

24. Host diversity and behavior determine patterns of interspecies transmission and geographic diffusion of avian influenza A subtypes among North American wild reservoir species.

25. Mendelian randomization supports bidirectional causality between telomere length and clonal hematopoiesis of indeterminate potential.

26. Author Correction: Inherited causes of clonal haematopoiesis in 97,691 whole genomes.

27. Human myelomeningocele risk and ultra-rare deleterious variants in genes associated with cilium, WNT-signaling, ECM, cytoskeleton and cell migration.

28. Inherited causes of clonal haematopoiesis in 97,691 whole genomes.

29. Burden of rare deleterious variants in WNT signaling genes among 511 myelomeningocele patients.

30. Multi-ancestry sleep-by-SNP interaction analysis in 126,926 individuals reveals lipid loci stratified by sleep duration.

31. Multiancestry Genome-Wide Association Study of Lipid Levels Incorporating Gene-Alcohol Interactions.

32. Proteomic Architecture of Human Coronary and Aortic Atherosclerosis.

33. Associations of NADPH oxidase-related genes with blood pressure changes and incident hypertension: The GenSalt Study.

34. Resequencing Epithelial Sodium Channel Genes Identifies Rare Variants Associated With Blood Pressure Salt-Sensitivity: The GenSalt Study.

35. Blood Pressure Genetic Risk Score Predicts Blood Pressure Responses to Dietary Sodium and Potassium: The GenSalt Study (Genetic Epidemiology Network of Salt Sensitivity).

36. Genome-Wide Gene-Potassium Interaction Analyses on Blood Pressure: The GenSalt Study (Genetic Epidemiology Network of Salt Sensitivity).

37. Mutations in folate transporter genes and risk for human myelomeningocele.

38. Uncovering the DNA methylation landscape in key regulatory regions within the FADS cluster.

39. Whole Exome Sequencing to Identify Genetic Variants Associated with Raised Atherosclerotic Lesions in Young Persons.

40. Resequencing Study Identifies Rare Renin-Angiotensin-Aldosterone System Variants Associated With Blood Pressure Salt-Sensitivity: The GenSalt Study.

41. Associations Between Genetic Variants of NADPH Oxidase-Related Genes and Blood Pressure Responses to Dietary Sodium Intervention: The GenSalt Study.

42. Genome-Wide Association Study Meta-Analysis of Long-Term Average Blood Pressure in East Asians.

43. Associations of the Serum/Glucocorticoid Regulated Kinase Genes With BP Changes and Hypertension Incidence: The Gensalt Study.

44. Associations of Variants in the CACNA1A and CACNA1C Genes With Longitudinal Blood Pressure Changes and Hypertension Incidence: The GenSalt Study.

45. Human epithelial Na+ channel missense variants identified in the GenSalt study alter channel activity.

46. Genetic association of the glycine cleavage system genes and myelomeningocele.

47. Assessment of postprandial triglycerides in clinical practice: Validation in a general population and coronary heart disease patients.

48. Common variants in the Na(+)-coupled bicarbonate transporter genes and salt sensitivity of blood pressure: the GenSalt study.

49. Genome-Wide Gene-Sodium Interaction Analyses on Blood Pressure: The Genetic Epidemiology Network of Salt-Sensitivity Study.

50. Associations Between Genetic Variants of the Natriuretic Peptide System and Blood Pressure Response to Dietary Sodium Intervention: The GenSalt Study.

Catalog

Books, media, physical & digital resources