Ken Wiley - Concepedia

Author

Ken Wiley

National Human Genome Research Institute

Also Known As

K Wiley, Ken L. Wiley, Ken Wiley, Ken Wiley, Jr., Kenneth Wiley, Polygenic Risk Methods in Diverse Populations Consortium, Wiley, Ken

Publications

793

Citations

H-Index

Concepts

All Affiliations

National Human Genome Research Institute Vanderbilt University Medical Center National Institutes of Health Children's Hospital of Philadelphia Northwestern University

About

Ken Wiley is an author at National Human Genome Research Institute specializing in medicine, genomics, and genetics.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	6	6	410
2	Public Health	5	5	202
3	Engineering	3	3	272
4	Biostatistics	2	2	128
5	Management	1	1	29

Ken Wiley

Publications

731

Citations

H-Index

Page 1

	Year	Citations
Inverting the model of genomics data sharing with the NHGRI Genomic Data Science Analysis, Visualization, and Informatics Lab-space Michael C. Schatz, Anthony Philippakis, Enis Afgan, Cell Genomics EngineeringBiological DatabaseData ScienceInformatics Lab-spaceBioinformatics Database	2022	126
Harmonizing Clinical Sequencing and Interpretation for the eMERGE III Network Hana Zouk, Eric Venner, Niall J. Lennon, The American Journal of Human Genetics BioinformaticsFunctional GenomicsEngineeringClinical SequencingTranslational Bioinformatics	2019	114
Returning integrated genomic risk and clinical recommendations: The eMERGE study Jodell E. Linder, Aimee Allworth, Harris T. Bland, Genetics in Medicine Emerge StudyGenome-wide Association StudyPolygenic RiskGenetic EpidemiologyGenomics	2023	104
Regional Patterns and Association Between Obesity and Hypertension in Africa Onoja Akpa, Felix Made, Akinlolu Ojo, Hypertension	2020	81
Facilitating phenotype transfer using a common data model George Hripcsak, Ning Shang, Peggy Peissig, Journal of Biomedical Informatics PhenomicsBiomedical Data IntegrationGenotype-phenotype AssociationGeneticsGenetic Epidemiology	2019	72
Workshop proceedings: GWAS summary statistics standards and sharing Jacqueline A. L. MacArthur, Annalisa Buniello, Laura W. Harris, Cell Genomics	2021	45
Making work visible for electronic phenotype implementation: Lessons learned from the eMERGE network Ning Shang, Cong Liu, Luke V. Rasmussen, Journal of Biomedical Informatics Electronic Phenotype ImplementationTechnologyEngineeringSystem MedicineEhealth	2019	32
Data Resource Profile: Cardiovascular H3Africa Innovation Resource (CHAIR) Mayowa Owolabi, Onoja Akpa, Felix Made, International Journal of Epidemiology Cardiovascular DiseaseData Resource ProfilePublic HealthHealth InformaticsCardiovascular Translational Research	2018	29
The PRIMED Consortium: Reducing disparities in polygenic risk assessment Iftikhar J. Kullo, Matthew P. Conomos, Sarah C. Nelson, The American Journal of Human Genetics Primed ConsortiumDisease Risk AssessmentPolygenic RiskRisk ManagementManagement	2024	29
Empowering genomic medicine by establishing critical sequencing result data flows: the eMERGE example Samuel Aronson, Lawrence Babb, Darren C. Ames, Journal of the American Medical Informatics Association Genetic TestingGeneticsGenetic EpidemiologyGenomicsHigh Throughput Sequencing	2018	26

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