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Your search keyword '"O. Melander"' showing total 42 results

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42 results on '"O. Melander"'

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1. A genome-wide association analysis reveals new pathogenic pathways in gout.

2. Publisher Correction: A genome-wide association analysis reveals new pathogenic pathways in gout.

3. Genome-wide analysis in over 1 million individuals of European ancestry yields improved polygenic risk scores for blood pressure traits.

4. Discovery and systematic characterization of risk variants and genes for coronary artery disease in over a million participants.

5. Cross-ancestry genome-wide meta-analysis of 61,047 cases and 947,237 controls identifies new susceptibility loci contributing to lung cancer.

6. Genome-wide association analyses highlight etiological differences underlying newly defined subtypes of diabetes.

7. Publisher Correction: Discovery of rare variants associated with blood pressure regulation through meta-analysis of 1.3 million individuals.

8. Discovery of rare variants associated with blood pressure regulation through meta-analysis of 1.3 million individuals.

9. Discovery of 318 new risk loci for type 2 diabetes and related vascular outcomes among 1.4 million participants in a multi-ancestry meta-analysis.

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

11. A catalog of genetic loci associated with kidney function from analyses of a million individuals.

12. Trans-ethnic association study of blood pressure determinants in over 750,000 individuals.

13. Publisher Correction: Genetic analysis of over 1 million people identifies 535 new loci associated with blood pressure traits.

14. Genetic analysis of over 1 million people identifies 535 new loci associated with blood pressure traits.

15. Multi-ethnic genome-wide association study for atrial fibrillation.

16. Refining the accuracy of validated target identification through coding variant fine-mapping in type 2 diabetes.

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

18. Exome-wide association study of plasma lipids in >300,000 individuals.

19. Identification of new susceptibility loci for type 2 diabetes and shared etiological pathways with coronary heart disease.

20. Erratum: Large-scale analyses of common and rare variants identify 12 new loci associated with atrial fibrillation.

21. Large-scale association analysis identifies new lung cancer susceptibility loci and heterogeneity in genetic susceptibility across histological subtypes.

22. Large-scale analyses of common and rare variants identify 12 new loci associated with atrial fibrillation.

23. Trans-ancestry meta-analyses identify rare and common variants associated with blood pressure and hypertension.

24. The genetics of blood pressure regulation and its target organs from association studies in 342,415 individuals.

25. Genetic fine mapping and genomic annotation defines causal mechanisms at type 2 diabetes susceptibility loci.

26. A comprehensive 1,000 Genomes-based genome-wide association meta-analysis of coronary artery disease.

27. Genome-wide trans-ancestry meta-analysis provides insight into the genetic architecture of type 2 diabetes susceptibility.

28. Meta-analysis of gene-level tests for rare variant association.

29. Large-scale association analysis identifies new risk loci for coronary artery disease.

30. Large-scale association analysis provides insights into the genetic architecture and pathophysiology of type 2 diabetes.

31. Meta-analysis identifies six new susceptibility loci for atrial fibrillation.

32. Genome-wide association study identifies six new loci influencing pulse pressure and mean arterial pressure.

33. Large-scale association analysis identifies 13 new susceptibility loci for coronary artery disease.

34. Association analyses of 249,796 individuals reveal 18 new loci associated with body mass index.

35. Genetic loci influencing kidney function and chronic kidney disease.

36. A genome-wide meta-analysis identifies 22 loci associated with eight hematological parameters in the HaemGen consortium.

37. Genome-wide association study identifies eight loci associated with blood pressure.

38. New susceptibility locus for coronary artery disease on chromosome 3q22.3.

39. Association of common variants in NPPA and NPPB with circulating natriuretic peptides and blood pressure.

40. Genome-wide association of early-onset myocardial infarction with single nucleotide polymorphisms and copy number variants.

41. Common variants at 30 loci contribute to polygenic dyslipidemia.

42. Six new loci associated with blood low-density lipoprotein cholesterol, high-density lipoprotein cholesterol or triglycerides in humans.

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