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1. Multi-phenotype analyses of hemostatic traits with cardiovascular events reveal novel genetic associations

2. Elucidating mechanisms of genetic cross-disease associations at the PROCR vascular disease locus (vol 13, 1222, 2022)

3. Discovery and systematic characterization of risk variants and genes for coronary artery disease in over a million participants

4. Mendelian Randomization Analysis of Hemostatic Factors and Their Contribution to Peripheral Artery Disease-Brief Report

5. Genetic loci associated with prevalent and incident myocardial infarction and coronary heart disease in the Cohorts for Heart and Aging Research in Genomic Epidemiology (CHARGE) Consortium

6. A genome-wide association study identifies new loci for factor VII and implicates factor VII in ischemic stroke etiology

7. Genomic and transcriptomic association studies identify 16 novel susceptibility loci for venous thromboembolism

8. GWAS and colocalization analyses implicate carotid intima-media thickness and carotid plaque loci in cardiovascular outcomes

9. Serum metabolic signatures of coronary and carotid atherosclerosis and subsequent cardiovascular disease

10. Mendelian randomization evaluation of causal effects of fibrinogen on incident coronary heart disease

11. Multi-ancestry study of blood lipid levels identifies four loci interacting with physical activity

12. Exome sequencing of 20,791 cases of type 2 diabetes and 24,440 controls.

13. Serum metabolic signatures of coronary and carotid atherosclerosis and subsequent cardiovascular disease

14. Multi-ancestry study of blood lipid levels identifies four loci interacting with physical activity

15. Genetic discovery and translational decision support from exome sequencing of 20,791 type 2 diabetes cases and 24,440 controls from five ancestries

17. Rare and low-frequency variants and their association with plasma levels of fibrinogen, FVII, FVIII, and vWF

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

19. Rare variant contribution to the heritability of coronary artery disease.

20. Regulation of fibrinogen synthesis.

21. Bivariate genome-wide association study of circulating fibrinogen and C-reactive protein levels.

22. A Large-Scale Genome-Wide Gene-Sleep Interaction Study in 732,564 Participants Identifies Lipid Loci Explaining Sleep-Associated Lipid Disturbances.

23. Whole-genome analysis of plasma fibrinogen reveals population-differentiated genetic regulators with putative liver roles.

24. Rare damaging CCR2 variants are associated with lower lifetime cardiovascular risk.

25. Time-to-Event Genome-Wide Association Study for Incident Cardiovascular Disease in People With Type 2 Diabetes.

27. A genetic association study of circulating coagulation factor VIII and von Willebrand factor levels.

28. An approach to identify gene-environment interactions and reveal new biological insight in complex traits.

29. Genomic and phenotypic correlates of mosaic loss of chromosome Y in blood.

30. A multitrait genetic study of hemostatic factors and hemorrhagic transformation after stroke treatment.

31. A Large-Scale Genome-Wide Study of Gene-Sleep Duration Interactions for Blood Pressure in 811,405 Individuals from Diverse Populations.

32. Genome-Wide Interaction Analysis With DASH Diet Score Identified Novel Loci for Systolic Blood Pressure.

34. Whole genome sequence analysis of apparent treatment resistant hypertension status in participants from the Trans-Omics for Precision Medicine program.

35. Whole-genome sequencing uncovers two loci for coronary artery calcification and identifies ARSE as a regulator of vascular calcification.

36. Type 2 Diabetes Modifies the Association of CAD Genomic Risk Variants With Subclinical Atherosclerosis.

38. Genome-Wide Interaction Analysis with DASH Diet Score Identified Novel Loci for Systolic Blood Pressure.

39. Gene-educational attainment interactions in a multi-population genome-wide meta-analysis identify novel lipid loci.

40. A statistical framework for powerful multi-trait rare variant analysis in large-scale whole-genome sequencing studies.

41. A new Approach to Identify Gene-Environment Interactions and Reveal New Biological Insight in Complex traits.

42. Rare variants in long non-coding RNAs are associated with blood lipid levels in the TOPMed whole-genome sequencing study.

43. Multi-ancestry genome-wide study identifies effector genes and druggable pathways for coronary artery calcification.

44. Lowering of Circulating Sclerostin May Increase Risk of Atherosclerosis and Its Risk Factors: Evidence From a Genome-Wide Association Meta-Analysis Followed by Mendelian Randomization.

45. Genetic insights into resting heart rate and its role in cardiovascular disease.

46. Ancestral diversity in lipoprotein(a) studies helps address evidence gaps.

47. Time-to-Event Genome-Wide Association Study for Incident Cardiovascular Disease in People with Type 2 Diabetes Mellitus.

48. Antithrombin, Protein C, and Protein S: Genome and Transcriptome-Wide Association Studies Identify 7 Novel Loci Regulating Plasma Levels.

49. Coronary heart disease and ischemic stroke polygenic risk scores and atherosclerotic cardiovascular disease in a diverse, population-based cohort study.

50. Whole genome analysis of plasma fibrinogen reveals population-differentiated genetic regulators with putative liver roles.

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