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Genomic sequencing

GENETIC9 trials

Sponsors

Brigham and Women's Hospital, The Cleveland Clinic, Children's Hospital of Fudan University, Robert Jones and Agnes Hunt Orthopaedic and District NHS Trust, Sixth Affiliated Hospital, Sun Yat-sen University

Conditions

Bone InfectionBone TumoursDefect, CongenitalGene Product Sequence VariationGenetic DiseaseGenetic Predisposition to DiseaseHereditary DiseaseHereditary Diseases

Unknown Phase

Genomic Sequencing for Childhood Risk and Newborn Illness
CompletedNCT02422511
Brigham and Women's HospitalGenetic Predisposition to Disease, Hereditary Disease
Start: 2015-05-31End: 2021-08-05Updated: 2024-04-03
Genomic Sequencing in Patients With HCM Undergoing Septal Myectomy
CompletedNCT03043209
The Cleveland ClinicGene Product Sequence Variation, Genetic Disease, Hypertrophic Cardiomyopathy
Start: 2018-08-30End: 2022-12-28Updated: 2023-01-06
The China Neonatal Genomes Project
RecruitingNCT03931707
Children's Hospital of Fudan UniversityDefect, Congenital, Genetic Predisposition to Disease, Hereditary Disease +1
Start: 2016-08-08End: 2026-12-30Target: 100000Updated: 2026-03-16
Return of Genomic Results and Aggregate Penetrance in Population-Based Cohorts
CompletedNCT04196374
Brigham and Women's HospitalGenetic Predisposition to Disease, Seemingly Healthy
Start: 2021-06-09End: 2025-05-30Updated: 2026-08-03
Artificial Intelligence in the Diagnosis of Orthopaedic Conditions, Particularly Bone Tumours and Infection
NCT04746001
Robert Jones and Agnes Hunt Orthopaedic and District NHS TrustBone Infection, Bone Tumours, Prosthetic Infection +1
Start: 2021-06-28End: 2024-07-01Target: 100Updated: 2021-11-11
Multicenter Analysis of Genomic and Metabolic Data of Neonatal Genetic Diseases
NCT06183138
Sixth Affiliated Hospital, Sun Yat-sen UniversityHereditary Diseases
Start: 2022-09-01End: 2025-12-31Target: 40000Updated: 2024-01-02
The Effect and Mechanism of Gene Variation on Neonatal Hyperbilirubinemia
NCT06186349
Sixth Affiliated Hospital, Sun Yat-sen UniversityNeonatal Hyperbilirubinemia
Start: 2023-09-01End: 2024-12-31Target: 2000Updated: 2024-01-02
Genomic Sequencing in Anatomically Normal Fetuses
RecruitingNCT06211348
University of California, San FranciscoPregnant Individuals Requesting Standard Microarray
Start: 2024-01-01End: 2030-01-01Target: 1000Updated: 2026-04-08
Molecular Genetic Mechanisms of Infantile Epilepsies and the Impact of Genetic Diagnosis
RecruitingNCT06701084
Boston Children's HospitalInfantile Epilepsy, Neonatal Epilepsy
Start: 2021-09-02End: 2029-11-01Target: 600Updated: 2026-04-27

Related Papers

Using metabolic abnormalities of carriers in the neonatal period to evaluate the pathogenicity of variants of uncertain significance in methylmalonic acidemia
Frontiers in Genetics2024-07-15
Rare-variant collapsing analyses identified risk genes for neonatal acute respiratory distress syndrome.
2022-09-011 citations
Parental Attitudes Toward Standard Newborn Screening and Newborn Genomic Sequencing: Findings From the BabySeq Study
Frontiers in Genetics2022-04-2762 citations
CYP2C9*3 Increases the Ibuprofen Response of Hemodynamically Significant Patent Ductus Arteriosus in the Infants with Gestational Age of More Than 30 Weeks.
2021-11-11
Psychosocial Effect of Newborn Genomic Sequencing on Families in the BabySeq Project
JAMA Pediatrics2021-08-2375 citations
Protocol of the China Neonatal Genomes Project: an observational study about genetic testing on 100,000 neonates
Pediatric Medicine2021-07-0916 citations
The BabySeq project: implementing genomic sequencing in newborns.
2018-07-09131 citations