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

7. Multi‐phenotype analyses of hemostatic traits with cardiovascular events reveal novel genetic associations

9. Improving Stroke Outcome Prediction Using Molecular and Machine Learning Approaches in Large Vessel Occlusion.

12. APOC3 genetic variation, serum triglycerides, and risk of coronary artery disease in Asian Indians, Europeans, and other ethnic groups

13. A Bidirectional Mendelian Randomization Study to evaluate the causal role of reduced blood vitamin D levels with type 2 diabetes risk in South Asians and Europeans

15. Association of the PHACTR1/EDN1 Genetic Locus With Spontaneous Coronary Artery Dissection

18. Multiancestry genome-wide association study of 520,000 subjects identifies 32 loci associated with stroke and stroke subtypes

19. Associations of autozygosity with a broad range of human phenotypes

25. Directional dominance on stature and cognition in diverse human populations

28. Genome-Wide Association Study Identifies a Novel Locus Contributing to Type 2 Diabetes Susceptibility in Sikhs of Punjabi Origin From India

31. DNA polymorphisms in two paraoxonase genes (PON1 and PON2) are associated with the risk of coronary heart disease

33. Variants in KCNQ1 increase type II diabetes susceptibility in South Asians: A study of 3,310 subjects from India and the US

34. Impact of nine common type 2 diabetes risk polymorphisms in Asian Indian Sikhs: PPARG2 (Pro12Ala), IGF2BP2, TCF7L2 and FTO variants confer a significant risk

36. Targeted sequencing of candidate genes of dyslipidemia in Punjabi Sikhs: Population-specific rare variants in GCKR promote ectopic fat deposition.

37. Obesity genetics and cardiometabolic health: Potential for risk prediction.

38. Investigation of Genetic Variation Underlying Central Obesity amongst South Asians.

39. Genetic and Cultural Reconstruction of the Migration of an Ancient Lineage.

40. PhenX RISING: real world implementation and sharing of PhenX measures.

41. No Association of Coronary Artery Disease with X-Chromosomal Variants in Comprehensive International Meta-Analysis

42. Carriers of a novel frame-shift insertion in WNT16a possess elevated pancreatic expression of TCF7L2.

43. A Replication Study of GWAS-Derived Lipid Genes in Asian Indians: The Chromosomal Region 11q23.3 Harbors Loci Contributing to Triglycerides.

44. Genome-Wide Linkage Scan to Identify Loci Associated with Type 2 Diabetes and Blood Lipid Phenotypes in the Sikh Diabetes Study.

45. Variants in KCNQ1 increase type II diabetes susceptibility in South Asians: A study of 3,310 subjects from India and the US.

46. Replication of Association Between a Common Variant Near Melanocortin-4 Receptor Gene and Obesity-related Traits in Asian Sikhs.

47. Testing the association of novel meta-analysis-derived diabetes risk genes with type II diabetes and related metabolic traits in Asian Indian Sikhs.

48. Impact of nine common type 2 diabetes risk polymorphisms in Asian Indian Sikhs: PPARG2 (Pro12Ala), IGF2BP2, TCF7L2 and FTO variants confer a significant risk.

49. Single Nucleotide Polymorphisms in the Coding Region of the Apolipoprotein H (β2-Glycoprotein I) Gene and their Correlation with the Protein Polymorphism, Anti-β2Glycoprotein I Antibodies and Cardiolipin Binding: Description of Novel Haplotypes and Their Evolution

50. Structure of the human β2‐glycoprotein I (apolipoprotein H) gene*.

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