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37 results on '"RS: CARIM - R1.06 - Genetic Epidemiology and Genomics of cardiovascular diseases"'

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1. The ESC-EORP EURO-ENDO (European Infective Endocarditis) registry

2. Pressure and flow properties of cannulae for extracorporeal membrane oxygenation II: drainage (venous) cannulae

3. Long-term survival and major outcomes in post-cardiotomy extracorporeal membrane oxygenation for adult patients in cardiogenic shock

4. Protracted aortic valve closure during peripheral veno-arterial extracorporeal life support

5. Targeted resequencing of a locus for heparin-induced thrombocytopenia on chromosome 5 identified in a genome-wide association study

6. Pharmacogenomics study of thiazide diuretics and QT interval in multi-ethnic populations: the cohorts for heart and aging research in genomic epidemiology

7. Association of the IGF1 gene with fasting insulin levels

8. ADAMTS genes and the risk of cerebral aneurysm

9. Meta-analysis of 49 549 individuals imputed with the 1000 Genomes Project reveals an exonic damaging variant in ANGPTL4 determining fasting TG levels

10. Somatic, positive and negative domains of the Center for Epidemiological Studies Depression (CES-D) scale: a meta-analysis of genome-wide association studies

11. Pressure and Flow Properties of Cannulae for Extracorporeal Membrane Oxygenation I: Return (Arterial) Cannulae

12. Clinical presentation, aetiology and outcomes of infective endocarditis. Results of the ESC-EORP EURO-ENDO (European infective endocarditis) registry: a prospective cohort study

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

14. PR interval genome-wide association meta-analysis identifies 50 loci associated with atrial and atrioventricular electrical activity

15. Exome-chip meta-analysis identifies novel loci associated with cardiac conduction, including ADAMTS6

16. Common and Rare Coding Genetic Variation Underlying the Electrocardiographic PR Interval

17. A combined linkage, microarray and exome analysis suggests MAP3K11 as a candidate gene for left ventricular hypertrophy

18. Discriminative Ability of Plasma Branched-Chain Amino Acid Levels for Glucose Intolerance in Families At Risk for Type 2 Diabetes

19. 52 Genetic Loci Influencing Myocardial Mass

20. Multiethnic Exome-Wide Association Study of Subclinical Atherosclerosis

21. Refined mapping of autoimmune disease associated genetic variants with gene expression suggests an important role for non-coding RNAs

22. Revised roles of ISL1 in a hES cell-based model of human heart chamber specification

23. ExomeChip-Wide Analysis of 95 626 Individuals Identifies 10 Novel Loci Associated With QT and JT Intervals

24. Natural genetic variation of the cardiac transcriptome in non-diseased donors and patients with dilated cardiomyopathy

25. A principal component meta-analysis on multiple anthropometric traits identifies novel loci for body shape

26. A Combined Linkage and Exome Sequencing Analysis for Electrocardiogram Parameters in the Erasmus Rucphen Family Study

27. Genetic variants in RBFOX3 are associated with sleep latency

28. Fine-mapping, novel loci identification, and SNP association transferability in a genome-wide association study of QRS duration in African Americans

29. Genome-wide meta-analysis uncovers novel loci influencing circulating leptin levels

30. Genetic associations at 53 loci highlight cell types and biological pathways relevant for kidney function

31. Genomewide meta-analysis identifies loci associated with IGF-I and IGFBP-3 levels with impact on age-related traits

32. DNA methylation in an engineered heart tissue model of cardiac hypertrophy: common signatures and effects of DNA methylation inhibitors

33. Pathway-based variant enrichment analysis on the example of dilated cardiomyopathy

34. Expert consensus document: Defining the major health modifiers causing atrial fibrillation: a roadmap to underpin personalized prevention and treatment

35. CLEC4M and STXBP5 gene variations contribute to vonWillebrand factor level variation in von Willebrand disease

36. Long non-coding RNA Databases in Cardiovascular Research

37. Twenty-eight genetic loci associated with ST-T-wave amplitudes of the electrocardiogram

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