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4. Protein-Truncating Variants at the Cholesteryl Ester Transfer Protein Gene and Risk for Coronary Heart Disease

5. Cumulative effects of common genetic variants on risk of sudden cardiac death

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

8. Novel loci associated with increased risk of sudden cardiac death in the context of coronary artery disease.

15. Secretory Phospholipase A2-IIA and Cardiovascular Disease: A Mendelian Randomization Study

16. Variant ASGR1 Associated with a Reduced Risk of Coronary Artery Disease

17. Supplement to: Myocardial Infarction Genetics and CARDIoGRAM Exome Consortia Investigators. Coding variation in ANGPTL4, LPL, and SVEP1 and the risk of coronary disease.

18. Association of Rare and Common Variation in the Lipoprotein Lipase Gene With Coronary Artery Disease

19. Inheritance of coronary artery disease in men: an analysis of the role of the Y chromosome

21. Identification of ADAMTS7 as a novel locus for coronary atherosclerosis and association of ABO with myocardial infarction in the presence of coronary atherosclerosis: two genome-wide association studies

24. Supplement to: Loss-of-function mutations in APOC3, triglycerides, and coronary disease.

29. Age- and Sex-Specific Causal Effects of Adiposity on Cardiovascular Risk Factors

30. Genetically Determined Height and Coronary Artery Disease

31. Adiposity as a cause of cardiovascular disease: a Mendelian randomization study

32. Mendelian randomization of blood lipids for coronary heart disease

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

37. Shared Genetic Susceptibility to Ischemic Stroke and Coronary Artery Disease: A Genome-Wide Analysis of Common Variants

39. Genetic loci associated with C-reactive protein levels and risk of coronary heart disease

40. Lack of association of genetic variants in the LRP8 gene with familial and sporadic myocardial infarction

41. Dysfunctional nitric oxide signalling increases risk of myocardial infarction

42. Ensuring that COVID-19 research is inclusive: guidance from the NIHR INCLUDE project

43. Additional file 3 of Developing a roadmap to improve trial delivery for under-served groups: results from a UK multi-stakeholder process

44. Additional file 1 of Developing a roadmap to improve trial delivery for under-served groups: results from a UK multi-stakeholder process

45. Additional file 2 of Developing a roadmap to improve trial delivery for under-served groups: results from a UK multi-stakeholder process

47. Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls

50. Ensuring that COVID-19 research is inclusive: guidance from the NIHR INCLUDE project

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