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1. Insights, opportunities and challenges provided by large cell atlases

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. Atherosclerotic Plaque Epigenetic Age Acceleration Predicts a Poor Prognosis and Is Associated With Endothelial-to-Mesenchymal Transition in Humans

6. Genetic and clinical determinants of abdominal aortic diameter: genome-wide association studies, exome array data and Mendelian randomization study

7. Atherosclerotic Plaque Epigenetic Age Acceleration Predicts a Poor Prognosis and Is Associated With Endothelial-to-Mesenchymal Transition in Humans

8. The accumulation of erythrocytes quantified and visualized by Glycophorin C in carotid atherosclerotic plaque reflects intraplaque hemorrhage and pre-procedural neurological symptoms

13. Multi-ancestry genetic analysis of gene regulation in coronary arteries prioritizes disease risk loci

14. Proteogenomic Data Integration Reveals CXCL10 as a Potentially Downstream Causal Mediator for IL-6 Signaling on Atherosclerosis

15. Integrative single-cell meta-analysis reveals disease-relevant vascular cell states and markers in human atherosclerosis

16. Transcriptomic-based clustering of human atherosclerotic plaques identifies subgroups with different underlying biology and clinical presentation

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

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

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

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

23. Atherosclerotic Plaque Epigenetic Age Acceleration Predicts a Poor Prognosis and Is Associated With Endothelial-to-Mesenchymal Transition in Humans

24. Proteogenomic Data Integration Reveals CXCL10 as a Potentially Downstream Causal Mediator for IL-6 Signaling on Atherosclerosis

25. Enhanced single-cell RNA-seq workflow reveals coronary artery disease cellular cross-talk and candidate drug targets

26. Evidence of survival bias in the association between APOE-Є4 and age at ischemic stroke onset.

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

28. Multiancestry genome-wide association study of 520,000 subjects identifies 32 loci associated with stroke and stroke subtypes

29. Proteogenomic Data Integration Reveals CXCL10 as a Potentially Downstream Causal Mediator for IL-6 Signaling on Atherosclerosis

30. Association between BMD and coronary artery calcification: an observational and Mendelian randomization study

32. Genetic loci associated with heart rate variability and their effects on cardiac disease risk.

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

35. Genetic variants associated with subjective well-being, depressive symptoms, and neuroticism identified through genome-wide analyses

37. Evidence of survival bias in the association betweenAPOE-Є4and age of ischemic stroke onset

40. Directional dominance on stature and cognition in diverse human populations

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

42. Fine mapping the CETP region reveals a common intronic insertion associated to HDL-C

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

44. Circulating CD14+CD16− classical monocytes do not associate with a vulnerable plaque phenotype, and do not predict secondary events in severe atherosclerotic patients

45. Proteomic Atlas of Atherosclerosis: The Contribution of Proteoglycans to Sex Differences, Plaque Phenotypes, and Outcomes

46. 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

47. Functional investigation of the coronary artery disease gene SVEP1

49. Common coding variant in SERPINA1 increases the risk for large artery stroke

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