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1. Cerebral small vessel disease genomics and its implications across the lifespan

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

3. Genome-wide meta-analysis of 158,000 individuals of European ancestry identifies three loci associated with chronic back pain

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

5. Association between telomere length and risk of cancer and non-neoplastic diseases a mendelian randomization study

6. Gene Set Enrichment Analyses: Lessons learned from the heart failure phenotype

7. Comparison of HapMap and 1000 genomes reference panels in a large-scale genome-wide association study

8. Genome-wide association studies identify genetic loci for low von Willebrand factor levels

9. Genome-Wide Association Study for Incident Myocardial Infarction and Coronary Heart Disease in Prospective Cohort Studies: The CHARGE Consortium

10. A meta-analysis of 120 246 individuals identifies 18 new loci for fibrinogen concentration

11. Pleiotropy among common genetic loci identified for cardiometabolic disorders and C-reactive protein

12. Pleiotropy among common genetic loci identified for cardiometabolic disorders and C-reactive protein

13. Rare and low-frequency variants and their association with plasma levels of fibrinogen, FVII, FVIII, and vWF

14. Drug-gene interactions of antihypertensive medications and risk of incident cardiovascular disease: A pharmacogenomics study from the CHARGE consortium

15. Pharmacogenetic meta-analysis of genome-wide association studies of LDL cholesterol response to statins

16. Genetic Loci for Retinal Arteriolar Microcirculation

17. Genome-wide association study for circulating levels of PAI-1 provides novel insights into its regulation

18. Genetic variation associated with plasma vonWillebrand factor levels and the risk of incident venous thrombosis

19. RANTES/CCL5 and risk for coronary events: Results from the MONICA/KORA Augsburg case-cohort, Athero-express and CARDIoGRAM studies

20. Genetic predictors of fibrin D-dimer levels in healthy adults

21. Effect of genetic variations in syntaxin-binding protein-5 and syntaxin-2 on von willebrand factor concentration and cardiovascular risk

22. New genetic loci implicated in fasting glucose homeostasis and their impact on type 2 diabetes risk

23. Large-scale genomic studies reveal central role of ABO in sP-selectin and sICAM-1 levels

24. Genomic variation associated with mortality among adults of European and African ancestry with heart failure: The cohorts for heart and aging research in genomic epidemiology consortium

25. Common variants in KCNN3 are associated with lone atrial fibrillation

26. Genetic variants associated with cardiac structure and function: A meta-analysis and replication of genome-wide association data

27. Genomewide association studies of stroke

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