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COMPLETED
NCT02628808

Susceptibility Genes in Autism Spectrum Disorders

Sponsor: Institut National de la Santé Et de la Recherche Médicale, France

View on ClinicalTrials.gov

Summary

The main objective of the study is to define, for Autism Spectrum Disorder, the extent of genetic variation in synaptic pathways that may be targeted for therapeutic development. For this purpose the investigators will take advantage of large, well-characterized cohorts of patients with Autism Spectrum Disorder for genetic screenings. Targeted sequencing of selected synaptic genes, previously associated with Autism Spectrum Disorder, will be carried out in these cohorts with deep coverage of coding regions and a strong focus on previously untested regulatory regions. Genomic data from Copy Number Variant, whole genome sequencing and exome sequencing, available for some of these patients, will be integrated in the overall analysis. The investigators will strongly emphasize the establishment of comprehensive genotype/phenotype correlations and set up an induced Pluripotent Stem Cells collection from selected patients with synaptic mutations for functional and expression analysis.

Official title: Search of Susceptibility Genes in Autism Spectrum Disorders

Key Details

Gender

All

Age Range

18 Months - 70 Years

Study Type

OBSERVATIONAL

Enrollment

1616

Start Date

2009-02-04

Completion Date

2021-12-03

Last Updated

2026-06-23

Healthy Volunteers

Yes

Locations (5)

Centre de Ressources Autisme Aquitaine, CHU de Bordeaux

Bordeaux, France

CADIPA Centree hospitalier de Saint Egreve

Grenoble, France

Cic Henri Mondor

Paris, France

Albert Chenevier Hospital

Créteil, Île-de-France Region, France

Robert Debré Hospital

Paris, Île-de-France Region, France