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Exome and Genome Analysis to Elucidate Genetic Etiologies and Population Characteristics in the Plain Community
RecruitingObservational studyHealthy volunteers welcome
Use of Whole Exome Sequencing/Whole Genome Sequencing in the Plain Communities
Who can join
Up to age 100 · All sexes · Healthy volunteers welcome
Full eligibility criteria
Inclusion Criteria: * Any person of Amish or Mennonite descent Exclusion Criteria: * Individuals who are not of Amish or Mennonite descent
About the study
This study is designed to utilize whole exome and whole genome sequencing techniques to identify underlying genetic causes for undiagnosed disorders in the Plain Communities, and to do population genetic studies looking at genetic drift and founder mutations in this unique population.
Sponsor: University of Pittsburgh · Participants: 300 · Started: 2016-08
Contact the study team
- Cate Walsh Vockley, MS, LCGC · Phone: 412-692-7349
- Jenifer Baker, MA · Phone: 412-6926378
Official record on ClinicalTrials.gov — NCT02927158
Locations in the U.S.
| Pennsylvania | Children's Hospital of Pittsburgh of UPMC, Pittsburgh |
From ClinicalTrials.gov, data retrieved Sep 30, 2026. Each study sets its own eligibility; the study team decides who can join.