Exome sequencing

GENETIC5 trials

Sponsors

University Hospital, Montpellier, University of California, San Francisco, Hospices Civils de Lyon, Helix, Inc

Conditions

Birth DefectFetal AnomalyGenetic Predisposition to DiseaseGenetics DiseaseHearing ImpairmentHydrops FetalisHypospadiasIntellectual Disability

Unknown Phase

Hypospadias and Exome: Identification of New Genes for Familial Hypospadias

CompletedNCT02495090

University Hospital, MontpellierHypospadias

Start: 2014-11-13End: 2024-04-24Updated: 2025-09-25

Hydrops: Diagnosing & Redefining Outcomes With Precision Study

Active, not recruitingNCT03412760

University of California, San FranciscoBirth Defect, Fetal Anomaly, Hydrops Fetalis

Start: 2018-10-11End: 2027-02-01Target: 500Updated: 2026-04-17

Exome Analysis in Hearing Impaired Patients

University Hospital, MontpellierHearing Impairment

Start: 2018-06-04End: 2019-06-01Updated: 2018-06-15

Second Molecular Event Identification by Exome Sequencing for Intellectually Disabled Patients Carrying 16p13.11 CNVs

Hospices Civils de LyonIntellectual Disability

Start: 2018-09-30End: 2019-03-31Target: 18Updated: 2018-08-23

Helix Research Network

RecruitingNCT06057181

Helix, IncGenetic Predisposition to Disease, Genetics Disease

Start: 2021-09-13End: 2036-09-13Target: 2000000Updated: 2026-03-23

Related Papers

Exome Sequencing for Prenatal Diagnosis in Nonimmune Hydrops Fetalis

New England Journal of Medicine2020-10-07183 citations