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1. An Ethical Framework for Research Using Genetic Ancestry

2. Epigenetic and proteomic signatures associate with clonal hematopoiesis expansion rate

3. Epigenetic and proteomic signatures associate with clonal hematopoiesis expansion rate

5. Validation of human telomere length multi-ancestry meta-analysis association signals identifies POP5 and KBTBD6 as human telomere length regulation genes

6. Rare variant contribution to the heritability of coronary artery disease

7. Disease risk and healthcare utilization among ancestrally diverse groups in the Los Angeles region

8. A draft human pangenome reference

9. The genetic determinants of recurrent somatic mutations in 43,693 blood genomes

10. Gaps and complex structurally variant loci in phased genome assemblies

11. Selection, optimization and validation of ten chronic disease polygenic risk scores for clinical implementation in diverse US populations

13. Rare coding variants in RCN3 are associated with blood pressure

14. Assessing efficiency of fine-mapping obesity-associated variants through leveraging ancestry architecture and functional annotation using PAGE and UKBB cohorts

15. Insights From a Large-Scale Whole-Genome Sequencing Study of Systolic Blood Pressure, Diastolic Blood Pressure, and Hypertension

16. TOP-LD: A tool to explore linkage disequilibrium with TOPMed whole-genome sequence data

17. Getting Genetic Ancestry Right for Science and Society

18. Evaluating parental personal utility of pediatric genetic and genomic testing in a diverse, multilingual population

19. Managing differential performance of polygenic risk scores across groups: Real-world experience of the eMERGE Network

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

21. Multi-population genome-wide association study implicates immune and non-immune factors in pediatric steroid-sensitive nephrotic syndrome

22. The TeleKidSeq pilot study: incorporating telehealth into clinical care of children from diverse backgrounds undergoing whole genome sequencing

23. The Human Pangenome Project: a global resource to map genomic diversity

24. Mendelian randomization supports bidirectional causality between telomere length and clonal hematopoiesis of indeterminate potential

25. Genome-wide association analyses define pathogenic signaling pathways and prioritize drug targets for IgA nephropathy

26. MUSSEL: Enhanced Bayesian polygenic risk prediction leveraging information across multiple ancestry groups

27. Genetic determinants of telomere length from 109,122 ancestrally diverse whole-genome sequences in TOPMed

28. Physician services and costs after disclosure of diagnostic sequencing results in the NYCKidSeq program

29. Aberrant activation of TCL1A promotes stem cell expansion in clonal haematopoiesis

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

31. The NYCKidSeq randomized controlled trial: Impact of GUÍA digitally enhanced genetic results disclosure in diverse families

32. Estimating heritability explained by local ancestry and evaluating stratification bias in admixture mapping from summary statistics

33. Molecular diagnostic yield of genome sequencing versus targeted gene panel testing in racially and ethnically diverse pediatric patients

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

36. Poison exon annotations improve the yield of clinically relevant variants in genomic diagnostic testing

37. Inherited causes of clonal haematopoiesis in 97,691 whole genomes

38. Multi-Ethnic Genome-Wide Association Study of Decomposed Cardioelectric Phenotypes Illustrates Strategies to Identify and Characterize Evidence of Shared Genetic Effects for Complex Traits

39. Global Biobank analyses provide lessons for developing polygenic risk scores across diverse cohorts

40. Returning integrated genomic risk and clinical recommendations: The eMERGE study

41. Genome-wide polygenic score to predict chronic kidney disease across ancestries

42. Meta-analysis fine-mapping is often miscalibrated at single-variant resolution

43. Author Correction: Association study in African-admixed populations across the Americas recapitulates asthma risk loci in non-African populations.

44. Genetic analyses of diverse populations improves discovery for complex traits.

45. The Genomic Medicine Integrative Research Framework: A Conceptual Framework for Conducting Genomic Medicine Research

46. Association study in African-admixed populations across the Americas recapitulates asthma risk loci in non-African populations.

47. Global Biobank Meta-analysis Initiative: Powering genetic discovery across human disease

49. Development and validation of a trans-ancestry polygenic risk score for type 2 diabetes in diverse populations

50. Genomic Disorders in CKD across the Lifespan

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