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1. Publisher Correction: Sex-dimorphic genetic effects and novel loci for fasting glucose and insulin variability (Nature Communications, (2021), 12, 1, (24), 10.1038/s41467-020-19366-9)

2. Sex-dimorphic genetic effects and novel loci for fasting glucose and insulin variability

3. Cross-ancestry genome-wide association analysis of corneal thickness strengthens link between complex and Mendelian eye diseases

4. Genome-wide association meta-analysis of fish and EPA+DHA consumption in 17 US and European cohorts

5. Association of the IGF1 gene with fasting insulin levels

6. Genome-Wide Association Study for Incident Myocardial Infarction and Coronary Heart Disease in Prospective Cohort Studies: The CHARGE Consortium

7. Pleiotropy among common genetic loci identified for cardiometabolic disorders and C-reactive protein

8. Pleiotropy among common genetic loci identified for cardiometabolic disorders and C-reactive protein

9. Low-frequency and rare exome chip variants associate with fasting glucose and type 2 diabetes susceptibility

10. Fetuin-A and risk of coronary heart disease: A Mendelian randomization analysis and a pooled analysis of AHSG genetic variants in 7 prospective studies

11. Consumption of meat is associated with higher fasting glucose and insulin concentrations regardless of glucose and insulin genetic risk scores: A meta-analysis of 50,345 Caucasians

12. Genome-wide association study of kidney function decline in individuals of European descent

13. Parent-of-Origin Effects of the APOB Gene on Adiposity in Young Adults

14. Gene × dietary pattern interactions in obesity: Analysis of up to 68 317 adults of European ancestry

15. Genome-wide meta-analysis identifies six novel loci associated with habitual coffee consumption

16. Association between alcohol and cardiovascular disease: Mendelian randomisation analysis based on individual participant data

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

18. Whole-exome sequencing identifies rare and low-frequency coding variants associated with LDL cholesterol

19. Common variation in fatty acid metabolic genes and risk of incident sudden cardiac arrest

20. Effects of long-term averaging of quantitative blood pressure traits on the detection of genetic associations

21. Association of low-frequency and rare coding-sequence variants with blood lipids and coronary heart disease in 56,000 whites and blacks

22. Genetic association study of QT interval highlights role for calcium signaling pathways in myocardial repolarization

23. Gene-age interactions in blood pressure regulation: A large-scale investigation with the CHARGE, global BPgen, and ICBP consortia

24. Meta-Analysis of Genome-Wide Association Studies Identifies Six New Loci for Serum Calcium Concentrations

25. Are C-Reactive Protein Associated Genetic Variants Associated with Serum Levels and Retinal Markers of Microvascular Pathology in Asian Populations from Singapore?

26. Insights into the Genetic Architecture of Early Stage Age-Related Macular Degeneration: A Genome-Wide Association Study Meta-Analysis

27. Best Practices and Joint Calling of the HumanExome BeadChip: The CHARGE Consortium

28. Genome-Wide Association Study of Retinopathy in Individuals without Diabetes

29. Common variants in mendelian kidney disease genes and their association with renal function

30. Genetic Loci for Retinal Arteriolar Microcirculation

31. A genome-wide association meta-analysis of circulating sex hormone-binding globulin reveals multiple loci implicated in s

32. A genome-wide association meta-analysis of circulating sex hormone-binding globulin reveals multiple loci implicated in s

33. Novel loci for adiponectin levels and their influence on type 2 diabetes and metabolic traits: A multi-ethnic meta-analysis of 45,891 individuals

34. Genome-wide association and functional follow-up reveals new loci for kidney function

35. Genome-wide association study identifies six new loci influencing pulse pressure and mean arterial pressure

36. RANTES/CCL5 and risk for coronary events: Results from the MONICA/KORA Augsburg case-cohort, Athero-express and CARDIoGRAM studies

37. Identification of a sudden cardiac death susceptibility locus at 2q24.2 through genome-wide association in european ancestry individuals

38. Association of eGFR-related loci identified by GWAS with incident CKD and ESRD

39. Large-scale association analysis identifies 13 new susceptibility loci for coronary artery disease

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

41. Hundreds of variants clustered in genomic loci and biological pathways affect human height

42. New genetic loci implicated in fasting glucose homeostasis and their impact on type 2 diabetes risk

43. Genome-wide association analysis identifies multiple loci related to resting heart rate

44. Common variants in the calcium-sensing receptor gene are associated with total serum calcium levels

45. Association analyses of 249,796 individuals reveal 18 new loci associated with body mass index

46. Genome-wide association studies of serum magnesium, potassium, and sodium concentrations identify six loci influencing serum magnesium levels

47. From vulnerable plaque to vulnerable patient: a call for new definitions and risk assessment strategies: Part I.

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