Search clinical trials for: Exome Sequencing

Total 1094 results

Fondazione IRCCS Ca' Granda, Ospedale Maggiore...

Recruiting

Genetic Diagnosis and Personalized Medicine for Patients With Epilepsy

Epilepsy

Italy
Centre Hospitalier Universitaire Dijon

Recruiting

Evaluation of Rapid First-line Genome Sequencing for Prenatal Diagnosis of Congenital Malformations in Comparison With Chromosomal Microarray and Exome Sequencing (PRENATOMEultra)

Congenital Malformation

France
ASST Fatebenefratelli Sacco

Not yet recruiting

Clonal Hematopoiesis in Giant Cell Arteritis (CH-GCA)

Giant Cell Arteritis | Temporal Arteritis | Clonal Hematopoiesis of Indeterminate Potential | Horton Disease | Systemic Vasculitis Primary
Cancer Institute and Hospital, Chinese Academy...

Not yet recruiting

Multi-omics Analysis to Characterize the Invasive Evolution of Pulmonary Subsolid Nodules

Adenocarcinoma of Lung
Karolinska Institutet

Recruiting

Prognostic Markers for a Better Follow-up in Head and Neck Cancer.

Head and Neck Cancer

Sweden
Fondazione Policlinico Universitario Agostino Gemelli...

Recruiting

Analysis of Molecular Biomarkers in Periocular Adnexal Tumours

Sebaceous Cell Tumor of Eyelid

Italy
University Hospital, Montpellier
IntegraGen SA

Not yet recruiting

Genomic Study of Cutis Tricolor (Cutis Tricolor)

Pigmentary; Dermatosis
Helix, Inc
Medical University of South Carolina; HealthPartners Institute; WellSpan Health; St. Luke's Hospital and Health Network, Pennsylvania and other collaborators

Recruiting

Helix Research Network (HRN)

Genetic Predisposition to Disease | Genetics Disease

United States
Mayo Clinic

Recruiting

INTERogating Cancer for Etiology, Prevention and Therapy Navigation (INTERCEPTioN)

Cancer | Cancer Gene Mutation | PAN Gene Mutation

United States
Mario Negri Institute for Pharmacological Research

Recruiting

Developing a Pipeline to Employ RNA-Seq as a Complementary Diagnostic Tool in Rare Diseases (ANTHEM)

Healthy | Autosomal Dominant Polycystic Kidney | Atypical Hemolytic Uremic Syndrome | Membranoproliferative Glomerulonephritis

Italy
Centre Hospitalier Universitaire Dijon

Recruiting

Study of the Value of Trio Exome Sequencing in the Etiological Assessment of Specific Non-syndromic Language and Learning Disorders (TSLA ES)

Specific Language and Learning Disorders (SLLD)

France
Regina Elena Cancer Institute

Recruiting

Single-cell RNAseq Breast Cancer (SCRBC)

Breast Neoplasms

Italy
Imperial College London
Royal Brompton & Harefield NHS Foundation Trust; St George's, University of... and other collaborators

Recruiting

Low QRS Voltages in Young Healthy Individuals and Athletes

Dilated Cardiomyopathy | Sudden Cardiac Death | Sudden Cardiac Death Due to Cardiac Arrhythmia | Sudden Cardiac Arrest | Arrhythmogenic Right Ventricular Cardiomyopathy | Arrhythmogenic Left Ventricular Cardiomyopathy

United Kingdom
Copenhagen University Hospital at Herlev

Recruiting

Identification and Verification of Candidate Genes Responsible for Optic Disc Drusen Development (GENODD)

Optic Disk Drusen

Denmark
Number 2 Children's Hospital, Ho Chi Minh City
University Hospital, Geneva; Swiss National Science Foundation; University of... and other collaborators

Recruiting

Genetic Investigations in Children With Developmental and Epileptic Encephalopathies in Ho Chi Minh City, Vietnam

Epileptic Encephalopathy | Whole Exome Sequencing

Vietnam
Heinrich-Heine University, Duesseldorf
German Cancer Aid

Not yet recruiting

Prostate Cancer Prevention Clinic for Men With Risk of Familial Prostate Cancer (ProFam-Risk)

Prostate Cancer | Familial Prostate Cancer
Guangdong Provincial People's Hospital

Recruiting

Liquid Biopsy in Advanced Oligometastatic NSCLC Receiving Surgery

Non-small Cell Lung Cancer | Oligometastatic Disease

China
Buddhist Tzu Chi General Hospital

Not yet recruiting

The Use of Molecular Radiogenomics in Non-small Cell Lung Cancer (NSCLC)

Lung Cancer
Chang Gung Memorial Hospital
Ministry of Science and Technology, Taiwan

Recruiting

Genetic Biomarkers of Child Language Development in Taiwan: an Identification and Validation Study

Child Language

Taiwan
Far Eastern Memorial Hospital
Ministry of Science and Technology, Taiwan

Recruiting

Polygenic Risk Score to Predict Weight Loss Intervention in Children With Obesity

Obesity | Children

Taiwan
Sohag University
Assiut University; Kyoto University

Recruiting

Mutations and Phenotypes of Unclassifiable Inherited Bone Marrow Failure Syndromes

Inherited BMF Syndrome

Egypt
Hospices Civils de Lyon

Recruiting

Genetic Predisposition in Cerebral Palsy (PREGENE PC)

Cerebral Palsy

France
Hospital Moinhos de Vento
Ministry of Health, Brazil

Recruiting

Onco-Genomas Brasil: Mapping Breast and Prostate Cancer in the Brazilian Public Health System

Breast Cancer | Prostate Cancer

Brazil
HaEmek Medical Center, Israel

Recruiting

The Pathogenesis of Depression - Possible Autoimmune Mechanisms

Depression | Autoimmune Diseases

Israel
LMU Klinikum

Recruiting

Pompe & Pain - Study to Assess Nociceptive Pain in Adult Patients With Pompe Disease

Pompe Disease (Late-onset) | FSHD | Spinal Muscular Atrophy Type 3 | Inclusion Body Myositis

Germany
Universitair Ziekenhuis Brussel
Marguerite - Marie Delacroix Foundation

Not yet recruiting

Combining Exome and Transcriptome Data to Unravel the Genetic Basis of the Lissencephalies

Classical Lissencephalies and Subcortical Band Heterotopias

Belgium
Centre Hospitalier Universitaire Dijon

Recruiting

Comparison of the Non-invasive Approach and Fetal Exome Sequencing in Prenatal Diagnosis When Fetal Ultrasound Signs Are Discovered (DPNI-Exome)

Antenatal Congenital Malformations

France
YULISU
Ono Pharmaceutical Co. Ltd

Recruiting

Neoadjuvant Nivolumab for Upper Tract Urothelial Carcinoma

Upper Urinary Tract Urothelial Carcinoma

Taiwan
Fondazione IRCCS Ca' Granda, Ospedale Maggiore...

Recruiting

Genetic Background of Patients With Low Von Willebrand Factor Levels (LOVMIC)

Low Von Willebrand Factor

Italy
Yonsei University

Not yet recruiting

Pembrolizumab and Paclitaxel in Hormone Receptor-positive, hyperMUTATted Metastatic Breast Cancer Identified by Whole exOme sequeNcing ('MUTATION2')

Breast Cancer

Korea, Republic of
Boston Children's Hospital
National Eye Institute (NEI)

Recruiting

Genetic Studies of Strabismus, Nystagmus, and Associated Disorders

Strabismus | Nystagmus, Congenital

United States
University Hospital Tuebingen

Recruiting

Genome-based Management of Patients in Precision Medicine (Ge-Med) Towards a Genomic Health Program (GE-MED)

Genetic Predisposition to Disease | Rare Diseases

Germany
University Hospital Tuebingen

Recruiting

Diagnostic Value of Exome/ Genome Sequencing, Conventional Methods in Rare Diseases and Familial Tumor Syndromes (EXGEFATU)

Rare Diseases | Genetic Predisposition

Germany
Children's Hospital of Fudan University

Not yet recruiting

Whole Genome Sequencing Versus Whole Exome Sequencing for Congenital Diarrhea and Enteropahty

Diarrhea, Infantile | Enteropathy
Chang Gung Memorial Hospital
Ministry of Science and Technology, Taiwan

Recruiting

Genetic Biomarkers Associated With Child Language Development in Taiwan

Child Language

Taiwan
RenJi Hospital

Recruiting

Heterogeneity and Evolution of hepatoceLlular Carcinoma in Post-transplant HCC Recurrence (HELP-2020)

Liver Transplant; Complications | Hepatocellular Carcinoma Recurrent

China
Medical College of Wisconsin

Recruiting

Assessment of the TGF-beta Pathway and Micro-RNA in Pediatric Pulmonary Arterial Hypertension

Pulmonary Arterial Hypertension

United States
University Hospital, Montpellier
Soroptimist association of Monaco

Recruiting

Analyse of Tumour and Constitutional DNA for the Study of the Determinism in Child Neoplasia (ALADIN)

Solid Tumor, Childhood | Pediatric Tumor | Familial Cancer | Hematological Tumor

France
University Hospital, Strasbourg, France

Recruiting

Realization of Sequencing of All Known Human Genes in Case of Detection of Cerebral, Renal or Ophthalmological Fetal Malformations During Pregnancy in Order to Make an Etiological Diagnosis and to Precise the Fetal Prognosis (PRENATEX)

Pregnancy Related | Rare Genetic Disease | Fetal Malformation

France
University Hospital Tuebingen

Recruiting

Identification of the Genetic Causes of Rare Diseases With Negative Exome Findings

Genetic Predisposition to Disease | Rare Diseases

Germany
Centre Georges Francois Leclerc

Recruiting

EXOME Analysis Position in the Strategy of Genetic Predisposition Factors Identification in Early-onset Cancer (EX²TRICAN)

Cancer | Genetic Predisposition

France
Yinghao Sun

Not yet recruiting

Precise Therapy for mCRPC Patients Through Whole Exome Sequencing(PTtWES) (PTtWES)

Castration-Resistant Prostatic Cancer
University Hospital, Rouen

Recruiting

Diagnostic Performance of Exome Sequencing in Autism Spectrum Disorders (REDIA)

Autism Spectrum Disorder

France
Benjamin Terrier

Recruiting

Whole Exome Sequencing of Familial and Pediatric Forms of Vasculitis (FAMILYVASC)

Vasculitis

France
Taipei Veterans General Hospital, Taiwan

Not yet recruiting

Dry Eye Syndrome, Healthy Control, Sjögren's Syndrome and Other Inflammation Disease in Taiwan Biobank

Inflammation | Sjogren's Syndrome | Dry Eye Syndrome | Healthy Control

Taiwan
Children's Hospital of Fudan University

Recruiting

The China Neonatal Genomes Project (CNGP)

Genetic Predisposition to Disease | Newborn | Defect, Congenital | Hereditary Disease

China
Thomas Jefferson University

Recruiting

Whole Exome Sequencing and Whole Genome Sequencing for Nonimmune Fetal/Neonatal Hydrops

Genetic Disorders | Nonimmune Fetal Hydrops | Nonimmune Hydrops in Neonate

United States
Institute of Child Health
University College, London; Great Ormond Street Hospital for Children NHS Foundation...

Recruiting

Natural History Study of ATP1A3-related Disease

Alternating Hemiplegia of Childhood | ATP1A3-related Disease | Rapid Onset Dystonia Parkinsonism | CAPOS

United Kingdom
Tongji Hospital

Recruiting

Exome Sequencing Study in Cardiomyopathy to Identify New Risk Variants

Cardiomyopathy

China
Central Hospital, Nancy, France
Institut National de la Santé Et de la Recherche Médicale, France; French Innovative...

Recruiting

Genomic and Proteomic Study of Richter Syndrome (CGPSR) (CGPSR)

Richter Syndrome

France

Search clinical trials for: Exome Sequencing

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