Exome and Genome Analysis to Elucidate Genetic Etiologies and Population Characteristics in the Plain Community
NCT02927158
This study is recruiting at 1 US site in 1 state, according to its ClinicalTrials.gov record last updated .
Summary
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.
Shortened from the sponsor's brief summary. View official record on ClinicalTrials.gov
Conditions studied
- Undiagnosed Disease
Eligibility basics and study details
- Study type
- Observational
- Phase
- Not applicable
- Ages
- Up to 100 years
- Sex
- All
- Healthy volunteers
- Accepted
- Sponsor
- University of Pittsburgh
- Last updated on ClinicalTrials.gov
- March 10, 2026
These are the basic criteria only. The full inclusion and exclusion criteria are on the official record, and the study team decides who can take part.
US recruiting sites
Pennsylvania · 1
- Children's Hospital of Pittsburgh of UPMC · Pittsburgh, PA
Source: ClinicalTrials.gov, data processed . Recruiting US sites filtered by distance and site status; summaries shortened.