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1. Blood pressure and risk of venous thromboembolism: a cohort analysis of 5.5 million UK adults and Mendelian randomization studies

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

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

5. Multiancestry genome-wide association study of 520,000 subjects identifies 32 loci associated with stroke and stroke subtypes (vol 50, pg 524, 2018)

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

7. Quality control and conduct of genome-wide association meta-analyses

8. Homocysteine levels associate with subtle changes in leukocyte DNA methylation: an epigenome-wide analysis

9. Genetically defined elevated homocysteine levels do not result in widespread changes of DNA methylation in leukocytes

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

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

12. No Evidence for Genome-Wide Interactions on Plasma Fibrinogen by Smoking, Alcohol Consumption and Body Mass Index:Results from Meta-Analyses of 80,607 Subjects

13. The role of adiposity in cardiometabolic traits: a mendelian randomization analysis

14. Genome-wide haplotype association study identifies the FRMD4A gene as a risk locus for Alzheimer's disease

15. Genome-wide meta-analysis identifies 11 new loci for anthropometric traits and provides insights into genetic architecture

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

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

24. Genome-wide meta-analysis identifies 11 new loci for anthropometric traits and provides insights into genetic architecture

25. Genetic variations at the endocannabinoid type 1 receptor gene (CNR1) are associated with obesity phenotypes in men

26. Association of plasminogen activator inhibitor (PAI)-1 (SERPINE1) SNPs with myocardial infarction, plasma PAI-1, and metabolic parameters: the HIFMECH study

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

28. Blood pressure and risk of venous thromboembolism: a cohort analysis of 5.5 million UK adults and Mendelian randomization studies.

29. Association of Coding Variants in Hydroxysteroid 17-beta Dehydrogenase 14 ( HSD17B14 ) with Reduced Progression to End Stage Kidney Disease in Type 1 Diabetes.

30. Whole-exome sequencing identifies rare variants in STAB2 associated with venous thromboembolic disease.

31. Erratum. Multiethnic Genome-Wide Association Study of Diabetic Retinopathy Using Liability Threshold Modeling of Duration of Diabetes and Glycemic Control. Diabetes 2019;68:441-456.

32. Reactivation of the Epicardium at the Origin of Myocardial Fibro-Fatty Infiltration During the Atrial Cardiomyopathy.

33. Design and Rationale of the ERA-CVD Consortium PREMED-CAD-Precision Medicine in Coronary Artery Disease.

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

35. A novel rare CUBN variant and three additional genes identified in Europeans with and without diabetes: results from an exome-wide association study of albuminuria.

36. Multiethnic Genome-Wide Association Study of Diabetic Retinopathy Using Liability Threshold Modeling of Duration of Diabetes and Glycemic Control.

37. Variations in Risk of End-Stage Renal Disease and Risk of Mortality in an International Study of Patients With Type 1 Diabetes and Advanced Nephropathy.

38. Transcriptome-Wide Analysis Identifies Novel Associations With Blood Pressure.

39. GENomE wide analysis of sotalol-induced IKr inhibition during ventricular REPOLarization, "GENEREPOL study": Lack of common variants with large effect sizes.

40. Age- and sex-specific causal effects of adiposity on cardiovascular risk factors.

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

42. SORBS1 gene, a new candidate for diabetic nephropathy: results from a multi-stage genome-wide association study in patients with type 1 diabetes.

43. Human CalDAG-GEFI gene (RASGRP2) mutation affects platelet function and causes severe bleeding.

44. Genome-wide meta-analysis identifies 11 new loci for anthropometric traits and provides insights into genetic architecture.

45. Small platelet microparticle levels are increased in pulmonary arterial hypertension.

46. The role of adiposity in cardiometabolic traits: a Mendelian randomization analysis.

47. Association of soluble endothelial protein C receptor plasma levels and PROCR rs867186 with cardiovascular risk factors and cardiovascular events in coronary artery disease patients: the Athero Gene study.

48. New susceptibility loci associated with kidney disease in type 1 diabetes.

49. Apolipoprotein(a) genetic sequence variants associated with systemic atherosclerosis and coronary atherosclerotic burden but not with venous thromboembolism.

50. ABO blood group and von Willebrand factor levels partially explained the incomplete penetrance of congenital thrombophilia.

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