Search

Your search keyword '"Kenny, Eimear E"' showing total 26 results

Search Constraints

Start Over You searched for: Author "Kenny, Eimear E" Remove constraint Author: "Kenny, Eimear E" Topic humans Remove constraint Topic: humans
26 results on '"Kenny, Eimear E"'

Search Results

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

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

3. A draft human pangenome reference

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

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

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

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

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

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

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

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

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

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

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

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

16. Genome-wide association study of primary open-angle glaucoma in continental and admixed African populations.

17. The Clinical Sequencing Evidence-Generating Research Consortium: Integrating Genomic Sequencing in Diverse and Medically Underserved Populations

18. A multi-stage genome-wide association study of uterine fibroids in African Americans

19. GBStools: A Statistical Method for Estimating Allelic Dropout in Reduced Representation Sequencing Data

20. The genetics of Mexico recapitulates Native American substructure and affects biomedical traits

21. Evolution and Functional Impact of Rare Coding Variation from Deep Sequencing of Human Exomes

22. Worldwide Frequencies of Apolipoprotein L1 Renal Risk Variants

23. Reconstructing Native American Migrations from Whole-Genome and Whole-Exome Data

24. A first update on mapping the human genetic architecture of COVID-19

25. Mapping the human genetic architecture of COVID-19

26. The genetic architecture of membranous nephropathy and its potential to improve non-invasive diagnosis

Catalog

Books, media, physical & digital resources