Search

Your search keyword '"Newton Cheh, C"' showing total 396 results

Search Constraints

Start Over You searched for: Author "Newton Cheh, C" Remove constraint Author: "Newton Cheh, C"
396 results on '"Newton Cheh, C"'

Search Results

1. Pharmacogenomics study of thiazide diuretics and QT interval in multi-ethnic populations: the cohorts for heart and aging research in genomic epidemiology

2. A Blood Conservation Approach to Peri-Transplant Care Informed by Successful Heart Transplantation in a Jehovah’s Witness

3. Drug–gene interactions and the search for missing heritability: a cross-sectional pharmacogenomics study of the QT interval

4. Common genetic variation near the connexin-43 gene is associated with resting heart rate in African Americans: A genome-wide association study of 13,372 participants

5. (275) Early Renal Outcomes Following Cardiac Transplantation Using Organs Procured after Circulatory Death

6. Transethnic genome-wide association study provides insights in the genetic architecture and heritability of long QT syndrome

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

9. Publisher Correction:Discovery of rare variants associated with blood pressure regulation through meta-analysis of 1.3 million individuals

11. Discovery of rare variants associated with blood pressure regulation through meta-analysis of 1.3 million individuals

12. Transethnic Genome-Wide Association Study Provides Insights in the Genetic Architecture and Heritability of Long QT Syndrome .

13. Multi-ancestry GWAS of the electrocardiographic PR interval identifies 202 loci underlying cardiac conduction

14. Genome-wide association and Mendelian randomisation analysis provide insights into the pathogenesis of heart failure

15. Discovery of rare variants associated with blood pressure regulation through meta-analysis of 1.3 million individuals

16. Discovery of rare variants associated with blood pressure regulation through meta-analysis of 1.3 million individuals

18. Erratum to: Genetic analysis of over 1 million people identifies 535 new loci associated with blood pressure traits (Nature Genetics, (2018), 50, 10, (1412-1425), 10.1038/s41588-018-0205-x)

21. Association of Chromosome 9p21 With Subsequent Coronary Heart Disease Events

22. Subsequent Event Risk in Individuals With Established Coronary Heart Disease

23. Publisher Correction: Genetic analysis of over 1 million people identifies 535 new loci associated with blood pressure traits (vol 50, pg 1412, 2018)

24. Publisher Correction: Genetic analysis of over 1 million people identifies 535 new loci associated with blood pressure traits

25. Evaluation of Early Allograft Function in Donor HCV-Positive to Recipient HCV-Negative Cardiac Transplantation Managed with Preemptive Direct Acting Antiviral Therapy

26. Preemptive Pan-Genotypic Direct Acting Antiviral Therapy in Donor HCV-Positive to Recipient HCV-Negative Cardiac Transplantation Produces Viral Clearance and is Associated with Favorable Outcomes

27. Erratum to: Genetic analysis of over 1 million people identifies 535 new loci associated with blood pressure traits

28. ExomeChip-Wide Analysis of 95 626 Individuals Identifies 10 Novel Loci Associated With QT and JT Intervals

29. Exome-chip meta-analysis identifies novel loci associated with cardiac conduction, including ADAMTS6

30. Atrial fibrillation genetic risk differentiates cardioembolic stroke from other stroke subtypes

31. New genetic loci link adipose and insulin biology to body fat distribution

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

33. New Blood Pressure-Associated Loci Identified in Meta-Analyses of 475,000 Individuals

34. Erratum: Plasma HDL cholesterol and risk of myocardial infarction: A mendelian randomisation study (The Lancet (2012) DOI:10.1016/S0140-6736(12) 60312-2)

35. The genetics of blood pressure regulation and its target organs from association studies in 342,415 individuals

36. Common Variants in the ATP2B1 Gene Are Associated With Susceptibility to Hypertension

37. Pharmacogenomics study of thiazide diuretics and QT interval in multi-ethnic populations: the cohorts for heart and aging research in genomic epidemiology

38. Fine-mapping, novel loci identification, and SNP association transferability in a genome-wide association study of QRS duration in African Americans

39. The genetics of blood pressure regulation and its target organs from association studies in 342,415 individuals

40. Meta-analysis identifies common and rare variants influencing blood pressure and overlapping with metabolic trait loci

41. Trans-ancestry meta-analyses identify rare and common variants associated with blood pressure and hypertension

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

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

44. The genetics of blood pressure regulation and its target organs from association studies in 342,415 individuals

45. Discovery of Genetic Variation on Chromosome 5q22 Associated with Mortality in Heart Failure

46. blood pressure loci identified with a gene-centricarray

47. Four novel loci (19q13, 6q24, 12q24, and 5q14) influence the microcirculation In vivo

48. Common variants in the ATP2B1 gene are associated with susceptibility to hypertension: the Japanese Millennium GenomeProject

49. Genome-wide association study identifies eight loci associated with blood pressure

50. Drug–gene interactions and the search for missing heritability: a cross-sectional pharmacogenomics study of the QT interval

Catalog

Books, media, physical & digital resources