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1. X-chromosome and kidney function: evidence from a multi-trait genetic analysis of 908,697 individuals reveals sex-specific and sex-differential findings in genes regulated by androgen response elements.

2. A methylation risk score for chronic kidney disease: a HyperGEN study

3. Genome-wide study investigating effector genes and polygenic prediction for kidney function in persons with ancestry from Africa and the Americas

4. Lac-Phe mediates the effects of metformin on food intake and body weight

5. Whole-genome sequencing uncovers two loci for coronary artery calcification and identifies ARSE as a regulator of vascular calcification.

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

7. Genetic insights into resting heart rate and its role in cardiovascular disease.

10. Genetic drivers of heterogeneity in type 2 diabetes pathophysiology

11. Investigating Gene-Diet Interactions Impacting the Association Between Macronutrient Intake and Glycemic Traits.

12. Causal effects on complex traits are similar for common variants across segments of different continental ancestries within admixed individuals.

13. The Type 2 Diabetes Knowledge Portal: An open access genetic resource dedicated to type 2 diabetes and related traits

14. A genetic association study of circulating coagulation factor VIII and von Willebrand factor levels

15. Whole-exome sequencing study identifies four novel gene loci associated with diabetic kidney disease.

16. Gene expression associations with body mass index in the Multi-Ethnic Study of Atherosclerosis

17. Powerful, scalable and resource-efficient meta-analysis of rare variant associations in large whole genome sequencing studies

18. Whole genome sequence analysis of apparent treatment resistant hypertension status in participants from the Trans-Omics for Precision Medicine program.

19. Canonical correlation analysis for multi-omics: Application to cross-cohort analysis

20. Large scale proteomic studies create novel privacy considerations

21. A framework for detecting noncoding rare-variant associations of large-scale whole-genome sequencing studies

22. Assessing the contribution of rare genetic variants to phenotypes of chronic obstructive pulmonary disease using whole-genome sequence data

23. Understanding the complex genetic architecture connecting rheumatoid arthritis, osteoporosis and inflammation: discovering causal pathways

24. Polygenic transcriptome risk scores for COPD and lung function improve cross-ethnic portability of prediction in the NHLBI TOPMed program

25. Strong protective effect of the APOL1 p.N264K variant against G2-associated focal segmental glomerulosclerosis and kidney disease

26. Whole-Genome Sequencing Association Analyses of Stroke and Its Subtypes in Ancestrally Diverse Populations From Trans-Omics for Precision Medicine Project

27. Assessing the contribution of rare variants to complex trait heritability from whole-genome sequence data

28. Obesity Partially Mediates the Diabetogenic Effect of Lowering LDL Cholesterol.

29. The Value of Rare Genetic Variation in the Prediction of Common Obesity in European Ancestry Populations.

30. Whole genome sequence analysis of blood lipid levels in >66,000 individuals

31. Non-linear machine learning models incorporating SNPs and PRS improve polygenic prediction in diverse human populations

32. Whole genome sequence association analysis of fasting glucose and fasting insulin levels in diverse cohorts from the NHLBI TOPMed program

33. Protein prediction for trait mapping in diverse populations

34. Causal effects on complex traits are similar for common variants across segments of different continental ancestries within admixed individuals

35. Whole-genome analysis of plasma fibrinogen reveals population-differentiated genetic regulators with putative liver roles

36. Associations between DNA methylation and BMI vary by metabolic health status: a potential link to disparate cardiovascular outcomes

37. Epigenome-wide association study of kidney function identifies trans-ethnic and ethnic-specific loci

38. Whole-genome sequencing in diverse subjects identifies genetic correlates of leukocyte traits: The NHLBI TOPMed program

39. Multiethnic Genome-Wide Association Study of Subclinical Atherosclerosis in Individuals With Type 2 Diabetes

40. Determinants of penetrance and variable expressivity in monogenic metabolic conditions across 77,184 exomes.

41. Whole-genome sequencing association analysis of quantitative red blood cell phenotypes: The NHLBI TOPMed program

42. Chromosome Xq23 is associated with lower atherogenic lipid concentrations and favorable cardiometabolic indices.

43. Meta-analysis uncovers genome-wide significant variants for rapid kidney function decline

44. Sequencing of 53,831 diverse genomes from the NHLBI TOPMed Program

45. Whole genome sequence analyses of eGFR in 23,732 people representing multiple ancestries in the NHLBI trans-omics for precision medicine (TOPMed) consortium

46. Epigenome-wide DNA methylation association study of circulating IgE levels identifies novel targets for asthma

47. Genetic Studies of Leptin Concentrations Implicate Leptin in the Regulation of Early Adiposity

48. Whole genome sequence analysis of pulmonary function and COPD in 19,996 multi-ethnic participants.

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

50. The Type 2 Diabetes Knowledge Portal: An open access genetic resource dedicated to type 2 diabetes and related traits

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