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Your search keyword '"Lind, L."' showing total 54 results

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54 results on '"Lind, L."'

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

2. Erratum: New genetic loci implicated in fasting glucose homeostasis and their impact on type 2 diabetes risk (Nature Genetics (2010) 42 (105-116))

3. New genetic loci implicated in fasting glucose homeostasis and their impact on type 2 diabetes risk (vol 42, pg 105, 2010)

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

5. Genetic association study of QT interval highlights role for calcium signaling pathways in myocardial repolarization

6. Common variants associated with plasma triglycerides and risk for coronary artery disease

7. Discovery and refinement of loci associated with lipid levels

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

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

10. Author Correction: New genetic signals for lung function highlight pathways and chronic obstructive pulmonary disease associations across multiple ancestries.

11. Author Correction: Multi-ancestry genome-wide association analyses improve resolution of genes and pathways influencing lung function and chronic obstructive pulmonary disease risk.

12. Genome-wide association study and functional characterization identifies candidate genes for insulin-stimulated glucose uptake.

13. Multi-ancestry genome-wide association analyses improve resolution of genes and pathways influencing lung function and chronic obstructive pulmonary disease risk.

14. Multi-ancestry genetic study of type 2 diabetes highlights the power of diverse populations for discovery and translation.

15. The trans-ancestral genomic architecture of glycemic traits.

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

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

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

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

20. Author Correction: New genetic signals for lung function highlight pathways and chronic obstructive pulmonary disease associations across multiple ancestries.

21. New genetic signals for lung function highlight pathways and chronic obstructive pulmonary disease associations across multiple ancestries.

22. Protein-coding variants implicate novel genes related to lipid homeostasis contributing to body-fat distribution.

23. Mosaic loss of chromosome Y in leukocytes matters.

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

25. Fine-mapping type 2 diabetes loci to single-variant resolution using high-density imputation and islet-specific epigenome maps.

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

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

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

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

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

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

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

33. Multiethnic genome-wide meta-analysis of ectopic fat depots identifies loci associated with adipocyte development and differentiation.

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

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

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

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

38. The impact of low-frequency and rare variants on lipid levels.

39. Genetic association study of QT interval highlights role for calcium signaling pathways in myocardial repolarization.

40. Genome-wide association analysis identifies six new loci associated with forced vital capacity.

41. Mosaic loss of chromosome Y in peripheral blood is associated with shorter survival and higher risk of cancer.

42. Loss-of-function mutations in SLC30A8 protect against type 2 diabetes.

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

44. Discovery and refinement of loci associated with lipid levels.

45. Common variants associated with plasma triglycerides and risk for coronary artery disease.

46. Identification of heart rate-associated loci and their effects on cardiac conduction and rhythm disorders.

47. Genome-wide meta-analysis identifies 11 new loci for anthropometric traits and provides insights into genetic architecture.

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

49. Large-scale association analyses identify new loci influencing glycemic traits and provide insight into the underlying biological pathways.

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

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