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

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

4. Genome-wide association meta-analysis identifies risk loci for abdominal aortic aneurysm and highlights PCSK9 as a therapeutic target

5. Identification of novel genetic risk factors of dilated cardiomyopathy: from canine to human

8. Pharmacogenomics in kidney transplant recipients and potential for integration into practice.

9. Genetic Determinants of Electrocardiographic P-Wave Duration and Relation to Atrial Fibrillation

10. Genome-wide association and Mendelian randomisation analysis provide insights into the pathogenesis of heart failure.

11. A saturated map of common genetic variants associated with human height

12. Tacrolimus troughs and genetic determinants of metabolism in kidney transplant recipients: A comparison of four ancestry groups.

13. Allele-specific NKX2-5 binding underlies multiple genetic associations with human electrocardiographic traits

14. Genetic Variants Associated With Immunosuppressant Pharmacokinetics and Adverse Effects in the DeKAF Genomics Genome-wide Association Studies.

15. A multi-layer functional genomic analysis to understand noncoding genetic variation in lipids

17. Functionally distinct ERAP1 and ERAP2 are a hallmark of HLA-A29-(Birdshot) Uveitis

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

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

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

21. Implicating genes, pleiotropy, and sexual dimorphism at blood lipid loci through multi-ancestry meta-analysis

22. The power of genetic diversity in genome-wide association studies of lipids

24. Discovery of novel heart rate-associated loci using the Exome Chip

26. Multiethnic Exome-Wide Association Study of Subclinical Atherosclerosis

27. 52 Genetic Loci Influencing Myocardial Mass

29. Concept and design of a genome-wide association genotyping array tailored for transplantation-specific studies.

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

31. The impact of donor and recipient common clinical and genetic variation on estimated glomerular filtration rate in a European renal transplant population

33. A genome-wide association study identifies a functional ERAP2 haplotype associated with birdshot chorioretinopathy

34. Defining the role of common variation in the genomic and biological architecture of adult human height

35. No evidence for shared genetic basis of common variants in multiple sclerosis and amyotrophic lateral sclerosis

37. Loci influencing blood pressure identified using a cardiovascular gene-centric array.

38. Genome-wide association meta-analysis of 30,000 samples identifies seven novel loci for quantitative ECG traits

39. Large-Scale Gene-Centric Meta-analysis across 32 Studies Identifies Multiple Lipid Loci

41. Association of Factor V Leiden With Subsequent Atherothrombotic Events: A GENIUS-CHD Study of Individual Participant Data

44. Protein-altering variants associated with body mass index implicate pathways that control energy intake and expenditure in obesity

45. Druggable proteins influencing cardiac structure and function: Implications for heart failure therapies and cancer cardiotoxicity

46. Identification of novel genetic risk factors of dilated cardiomyopathy: from canine to human

47. Identification of novel genetic risk factors of dilated cardiomyopathy: from canine to human

48. Druggable proteins influencing cardiac structure and function: Implications for heart failure therapies and cancer cardiotoxicity

49. Effect of tissue-grouped regulatory variants associated to type 2 diabetes in related secondary outcomes

50. The association between a genetic variant in the SULF2 gene, metabolic parameters and vascular disease in patients at high cardiovascular risk.

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