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1. Identification of genetic effects underlying type 2 diabetes in South Asian and European populations.

2. Author Correction: Identification of genetic effects underlying type 2 diabetes in South Asian and European populations.

3. Mapping the human genetic architecture of COVID-19

4. A Large-Scale Genome-Wide Gene-Sleep Interaction Study in 732,564 Participants Identifies Lipid Loci Explaining Sleep-Associated Lipid Disturbances.

5. Integrating Genetic and Transcriptomic Data to Identify Genes Underlying Obesity Risk Loci.

6. A Large-Scale Genome-Wide Study of Gene-Sleep Duration Interactions for Blood Pressure in 811,405 Individuals from Diverse Populations.

7. Genetic drivers of heterogeneity in type 2 diabetes pathophysiology.

8. Genetic risk converges on regulatory networks mediating early type 2 diabetes.

9. Genome-wide Association Study Identifies Novel Risk Loci for Apical Periodontitis.

10. Multi-ancestry genome-wide study in >2.5 million individuals reveals heterogeneity in mechanistic pathways of type 2 diabetes and complications.

11. Exploring the genetics of rhythmic perception and musical engagement in the Vanderbilt Online Musicality Study.

12. IMMerge: merging imputation data at scale.

13. Genetic variants associated with circulating liver injury markers in Mexican Americans, a population at risk for non-alcoholic fatty liver disease.

14. Novel diabetes gene discovery through comprehensive characterization and integrative analysis of longitudinal gene expression changes.

15. Genetic pleiotropy underpinning adiposity and inflammation in self-identified Hispanic/Latino populations.

16. Polygenic risk impacts PDGFRA mutation penetrance in non-syndromic cleft lip and palate.

17. Gut Microbiome Alterations Associated with Diabetes in Mexican Americans in South Texas.

18. Author Correction: Identification of genetic effects underlying type 2 diabetes in South Asian and European populations.

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

20. Identification of genetic effects underlying type 2 diabetes in South Asian and European populations.

21. Gut microbiome features associated with liver fibrosis in Hispanics, a population at high risk for fatty liver disease.

22. Associations of carotid intima media thickness with gene expression in whole blood and genetically predicted gene expression across 48 tissues.

23. Genetically regulated expression in late-onset Alzheimer's disease implicates risk genes within known and novel loci.

24. Population-based genetic effects for developmental stuttering.

25. Phenome risk classification enables phenotypic imputation and gene discovery in developmental stuttering.

26. Improving End of Life Cancer Outcomes Through Development and Implementation of a Spiritual Care Advocate Program.

27. Identifying developmental stuttering and associated comorbidities in electronic health records and creating a phenome risk classifier.

28. Pedigree reconstruction and distant pairwise relatedness estimation from genome sequence data: A demonstration in a population of rhesus macaques (Macaca mulatta).

29. Host genetic effects in pneumonia.

30. Optimizing Genetic Analyses of Serum Lipids in Longitudinal Data.

31. Importance of Genetic Studies of Cardiometabolic Disease in Diverse Populations.

32. Identification of type 2 diabetes loci in 433,540 East Asian individuals.

33. Minority-centric meta-analyses of blood lipid levels identify novel loci in the Population Architecture using Genomics and Epidemiology (PAGE) study.

34. A diagnostic ceiling for exome sequencing in cerebellar ataxia and related neurological disorders.

35. A Genome-Wide Association Study Identifies Blood Disorder-Related Variants Influencing Hemoglobin A 1c With Implications for Glycemic Status in U.S. Hispanics/Latinos.

36. GWAS of QRS duration identifies new loci specific to Hispanic/Latino populations.

37. Functionally oriented analysis of cardiometabolic traits in a trans-ethnic sample.

38. GWAS and Beyond: Using Omics Approaches to Interpret SNP Associations.

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

40. Identification of likely pathogenic and known variants in TSPEAR, LAMB3, BCOR, and WNT10A in four Turkish families with tooth agenesis.

42. Whole-Exome Sequencing Identifies Novel Variants for Tooth Agenesis.

43. GWAS of the electrocardiographic QT interval in Hispanics/Latinos generalizes previously identified loci and identifies population-specific signals.

44. Prevalence of spinocerebellar ataxia 36 in a US population.

45. Admixture mapping in two Mexican samples identifies significant associations of locus ancestry with triglyceride levels in the BUD13/ZNF259/APOA5 region and fine mapping points to rs964184 as the main driver of the association signal.

46. Variants in angiopoietin-2 (ANGPT2) contribute to variation in nocturnal oxyhaemoglobin saturation level.

47. Genome-Wide Association Study of Staphylococcus aureus Carriage in a Community-Based Sample of Mexican-Americans in Starr County, Texas.

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