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

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

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

6. Identification of new susceptibility loci for type 2 diabetes and shared etiological pathways with coronary heart disease

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

8. 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

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

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

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

14. Stroke genetics informs drug discovery and risk prediction across ancestries

15. Burden of Type 2 Diabetes and Associated Cardiometabolic Traits and Their Heritability Estimates in Endogamous Ethnic Groups of India: Findings From the INDIGENIUS Consortium

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

20. Additional file 1 of 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

21. Additional file 3 of 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

22. Additional file 2 of 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

23. Additional file 1 of APOC3 genetic variation, serum triglycerides, and risk of coronary artery disease in Asian Indians, Europeans, and other ethnic groups

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

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

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

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

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

33. 1639-P: Effect of Educational Status on Fasting Glucose and HbA1c Concentrations Independent of Income and Population Differences in Indian Populations

34. 1717-P: Burden of Type 2 Diabetes and Its Genetic Determinants in Indian Populations: Findings from the INDIGENIUS Consortium

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

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

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

40. Transethnic Evaluation Identifies Low-Frequency Loci Associated With 25-Hydroxyvitamin D Concentrations

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

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

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

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

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

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

47. A comprehensive 1000 Genomes-based genome-wide association meta-analysis of coronary artery disease

48. Trans-ancestry genome-wide association study identifies 12 genetic loci influencing blood pressure and implicates a role for DNA methylation

50. Genome-wide trans-ancestry meta-analysis provides insight into the genetic architecture of type 2 diabetes susceptibility

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