Search

Your search keyword '"Trégouët, David-Alexandre"' showing total 187 results

Search Constraints

Start Over You searched for: Author "Trégouët, David-Alexandre" Remove constraint Author: "Trégouët, David-Alexandre" Search Limiters Peer Reviewed Remove constraint Search Limiters: Peer Reviewed
187 results on '"Trégouët, David-Alexandre"'

Search Results

1. Genome-wide association study reveals mechanisms underlying dilated cardiomyopathy and myocardial resilience

2. Genome-wide association analysis provides insights into the molecular etiology of dilated cardiomyopathy

4. Assessment of a next generation sequencing gene panel strategy in 133 patients with negative thrombophilia screening

5. High risk of long-term recurrence after a first episode of venous thromboembolism during pregnancy or postpartum: the REcurrence after a PrEgnAncy related Thrombosis (REPEAT) Study

7. Integrative Multiomics in the Lung Reveals a Protective Role of Asporin in Pulmonary Arterial Hypertension

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

11. Transcriptome-wide association study and Mendelian randomization in pancreatic cancer identifies susceptibility genes and causal relationships with type 2 diabetes and venous thromboembolism

12. Genome-wide investigation of exogenous female hormones, genetic variation, and venous thromboembolism risk

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

15. Genomics of perivascular space burden unravels early mechanisms of cerebral small vessel disease

16. Elevated plasma complement factor H related 5 protein is associated with venous thromboembolism

19. Polygenic risk of major depressive disorder as a risk factor for venous thromboembolism

20. DNA methylation analysis is used to identify novel genetic loci associated with circulating fibrinogen levels in blood

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

22. Two SERPINC1 variants affecting N-glycosylation of Asn224 cause severe thrombophilia not detected by functional assays

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

24. FGL1 as a modulator of plasma D‐dimer levels: Exome‐wide marker analysis of plasma tPA, PAI‐1, and D‐dimer

25. Association between ABO haplotypes and the risk of venous thrombosis: impact on disease risk estimation

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

32. An artificial neural network approach integrating plasma proteomics and genetic data identifies PLXNA4 as a new susceptibility locus for pulmonary embolism

33. Genetic determinants of risk in pulmonary arterial hypertension: international genome-wide association studies and meta-analysis

35. DNA methylation age is associated with an altered hemostatic profile in a multiethnic meta-analysis

37. Anti-integrin αv therapy improves cardiac fibrosis after myocardial infarction by blunting cardiac PW1+ stromal cells

38. Association of LIfestyle for BRAin health risk score (LIBRA) and genetic susceptibility with incident dementia and cognitive decline.

39. PDGFB, a new candidate plasma biomarker for venous thromboembolism: results from the VEREMA affinity proteomics study

42. DNA‐pools targeted‐sequencing as a robust cost‐effective method to detect rare variants: Application to dilated cardiomyopathy genetic diagnosis.

43. Causal relationships between risk of venous thromboembolism and 18 cancers: a bidirectional Mendelian randomization analysis.

44. Addressing unmeasured confounders in cohort studies: Instrumental variable method for a time‐fixed exposure on an outcome trajectory.

45. Runs of Homozygosity: Association with Coronary Artery Disease and Gene Expression in Monocytes and Macrophages

46. Meta-analysis of 65,734 Individuals Identifies TSPAN15 and SLC44A2 as Two Susceptibility Loci for Venous Thromboembolism

47. Four missense genetic variants in CUBN are associated with higher levels of eGFR in non-diabetes but not in diabetes mellitus or its subtypes: A genetic association study in Europeans

50. DNA methylation and body-mass index: a genome-wide analysis

Catalog

Books, media, physical & digital resources