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Search clinical trials for: Family History Whole Genome Sequencing
Total 324 results
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Brigham and Women's HospitalBaylor College of Medicine; Duke University; National Human Genome Research Institute...CompletedHealthy Adults (Full Study and Extension Phase) | Hypertrophic Cardiomyopathy or Dilated CardiomyopathyUnited States
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Children's Hospital of Fudan UniversityNot yet recruitingDiarrhea, Infantile | Enteropathy
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Thomas Jefferson UniversityRecruitingGenetic Disorders | Nonimmune Fetal Hydrops | Nonimmune Hydrops in NeonateUnited States
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Sydney Children's Hospitals NetworkChildren's Cancer Institute AustraliaRecruitingCancer | Neoplastic Syndromes, Hereditary | Genetic Predisposition to DiseaseAustralia
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Boston Children's HospitalNational Eye Institute (NEI)RecruitingStrabismus | Nystagmus, CongenitalUnited States
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Brigham and Women's HospitalEunice Kennedy Shriver National Institute of Child Health and Human Development... and other collaboratorsCompletedGenetic Predisposition to Disease | Hereditary DiseaseUnited States
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Institut National de la Santé Et de la Recherche...Commissariat A L'energie Atomique; Imagine InstituteCompleted
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Taipei Veterans General Hospital, TaiwanNot yet recruitingInflammation | Sjogren's Syndrome | Dry Eye Syndrome | Healthy ControlTaiwan
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Charite University, Berlin, GermanyGerman Federal Ministry of Education and ResearchCompleted
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Boston Children's HospitalRecruitingEpilepsy | Dravet Syndrome | Infantile Spasms | Epileptic Encephalopathy | Ohtahara Syndrome | Early Myoclonic Epileptic Encephalopathy | PCDH19-related Epilepsy and Related Conditions | KCNQ2-Related Epileptic Encephalopathy | Epilepsy of Infancy With Migrating Focal Seizures (Disorder)United States
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Institut National de la Santé Et de la Recherche...Hospices Civils de Lyon; University Hospital, Rouen; Centre Hospitalier Universitaire... and other collaboratorsActive, not recruitingIntellectual DisabilityFrance
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Nantes University HospitalAXA Assurances VIE MutuelleNot yet recruitingSudden Infant Death | Sudden Unexplained Infant DeathFrance
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University of CambridgeIllumina, Inc.; Rosetrees Trust; Isaac Newton Trust; NIHR Cambridge Biomedical...Recruiting
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Istituto Superiore di SanitàFondazione G.B. Bietti, IRCCS; Ospedale Pediatrico Bambin GesùRecruitingRetinitis Pigmentosa | Macular Dystrophy | Inherited Retinal DystrophyItaly
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Children's Mercy Hospital Kansas CityRecruiting
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Nanfang Hospital of Southern Medical UniversityFerring PharmaceuticalsUnknownDiminished Ovarian ReserveChina
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Massachusetts General HospitalBroad Institute; Laboratory for Molecular MedicineCompletedGenetic Predisposition to Disease | Hereditary DiseaseUnited States
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Seoul National University HospitalUnknownCystic Fibrosis | Bronchiectasis Idiopathic | Primary Ciliary DyskinesiaKorea, Republic of
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Xinhua Hospital, Shanghai Jiao Tong University...UnknownIntellectual Disability | Rare Diseases | Multiple Congenital AnomalyChina
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UMC UtrechtRadboud University Medical Center; University Medical Center Groningen; Maastricht... and other collaboratorsRecruiting
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University of California, San FranciscoJohns Hopkins University; Eunice Kennedy Shriver National Institute of Child... and other collaboratorsEnrolling by invitation
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London School of Hygiene and Tropical MedicineWellcome Sanger InstituteCompleted
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Neuromed IRCCSNot yet recruitingParkinson Disease | REM Sleep Behavior DisorderItaly
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Heinrich-Heine University, DuesseldorfGerman Cancer AidNot yet recruitingProstate Cancer | Familial Prostate Cancer
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Illumina, Inc.CompletedNeurologic Disorder | Neurologic Deficits | Neurologic AbnormalitiesUnited States
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University Health Network, TorontoWestern University, Canada; Public Health Ontario Laboratory, CanadaRecruitingRespiratory Tract Diseases | Mycobacterium Infections | Mycobacterium Infections, Nontuberculous | Nontuberculous Mycobacterial Lung Disease | Mycobacterium AviumCanada
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Baylor College of MedicineCompletedNeurodevelopmental Disorders | Birth Defects | Multiple Congenital AnomalyUnited States
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Blood Donation Service Zurich, SRCUnknownGenetic Blood Group (bg) Polymorphism in U Negativity and St(a) of MNSsSwitzerland
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Munich Leukemia LaboratoryIllumina, Inc.RecruitingLeukemia | Rare Diseases | Refractory Lymphoma | Hematologic Malignancy | Refractory Leukemia | Unknown Primary TumorsGermany
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Peking University First HospitalRecruitingRenal Cell Carcinoma | VHL SyndromeChina
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Nantes University HospitalInserm UMR1087, CNRS UMR6291; Clinique des Données, CIC 1413, CHU Nantes; CIC-FEA...Recruiting
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Nantes University HospitalCompletedStudy of cardiovAscular Contrasted Phenotypes in Patients With FamIliaI hypercholesteRolemia (SAFIR)Homozygous Familial HypercholesterolemiaFrance
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Children's Mercy Hospital Kansas CityCompletedGenetic Disease | Diseases/DiagnosesUnited States
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Peter MacCallum Cancer Centre, AustraliaNational Health and Medical Research Council, Australia; University of MelbourneRecruitingHematologic Diseases | Inherited Platelet Disorder | Inherited BMF SyndromeAustralia
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University Health Network, TorontoRecruitingEsophagogastric AdenocarcinomaCanada
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University of Illinois College of Medicine at PeoriaRady Children's Institute of Genomic MedicineActive, not recruitingGenetic Disease | Genetic SyndromeUnited States
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Illumina, Inc.Children's Hospital of Philadelphia; St. Louis Children's Hospital; Children's... and other collaboratorsCompleted
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Peking Union Medical College HospitalUnknown
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Imperial College London Diabetes CentreUnknownDiabetes Mellitus, Type 2 | Diabetes Mellitus, Type 1 | Maturity-onset Diabetes of the YoungUnited Arab Emirates
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University of North Carolina, Chapel HillEunice Kennedy Shriver National Institute of Child Health and Human Development... and other collaboratorsCompletedMetabolism, Inborn Errors | Hearing Loss | Hereditary DiseaseUnited States
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Steno Diabetes Center GreenlandZealand University Hospital; University of CopenhagenRecruitingDiabetes Mellitus, Type 2 | Diabetic Neuropathies | Diabetic Retinopathy | Obstructive Sleep Apnea | Obesity, Morbid | MODYGreenland
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Geneplus-Beijing Co. Ltd.Beijing Hospital; Emergency General HospitalRecruitingPulmonary Nodule, Solitary | Whole-genome Methylation SequencingChina
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Kaiser PermanenteNational Human Genome Research Institute (NHGRI)CompletedGenetic DisordersUnited States
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Sun Yat-Sen Memorial Hospital of Sun Yat-Sen UniversityNanjing Geneseeq Technology Inc.RecruitingEndometrial CancerChina
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Rady Pediatric Genomics & Systems Medicine InstituteActive, not recruiting
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University of California, San DiegoWithdrawnMajor Fetal AnomalyUnited States
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Scripps Translational Science InstituteRecruitingCongenital Heart DiseaseUnited States
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University of California, San FranciscoNational Human Genome Research Institute (NHGRI)CompletedEpilepsy | Cerebral Palsy | Intellectual Disability | Developmental Delay | Metabolic Disease | Neuro-Degenerative Disease | Encephalopathy | Birth Defect | Multiple Congenital Anomaly | Developmental DefectUnited States
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Copenhagen University Hospital at HerlevRecruiting
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Fondazione IRCCS Ca' Granda, Ospedale Maggiore...RecruitingLow Von Willebrand FactorItaly