Ligne de temps
Richard Delorme
Chercheur(euse) Permanent(e)
26 juin 2023
08 déc. 2022
event
Troubles du spectre de l’autisme, troubles du neurodéveloppement : vulnérabilités et inégalités au sein des parcours de vie
Lire plus15 juil. 2022
publication
Insights from an autism imaging biomarker challenge: Promises and threats to biomarker discovery.
Lire plus13 juin 2022
project
Étude des facteurs génétiques impliqués dans l’autisme et les troubles apparentés (projet “C07/C16”)
Lire plus19 juil. 2021
publication
Discriminant value of repetitive behaviors in families with autism spectrum disorder and obsessional compulsive disorder probands.
Lire plus01 juin 2021
publication
Operative list of genes associated with autism and neurodevelopmental disorders based on database review.
Lire plus08 oct. 2020
11 juin 2020
10 juin 2020
publication
Autism-associated SHANK3 mutations impair maturation of neuromuscular junctions and striated muscles.
Lire plus09 janv. 2019
publication
Synesthesia & Autistic Features in a Large Family:evidence for spatial imagery as a common factor
Lire plus01 janv. 2019
publication
Morning Plasma Melatonin Differences in Autism: Beyond the Impact of Pineal Gland Volume.
Lire plus01 avr. 2018
publication
Cerebellar Volume in Autism: Literature Meta-analysis and Analysis of the Autism Brain Imaging Data Exchange Cohort.
Lire plus27 févr. 2018
01 janv. 2017
publication
A framework to identify contributing genes in patients with Phelan-McDermid syndrome.
Lire plus14 nov. 2016
05 nov. 2016
10 mai 2016
publication
CNTN6 mutations are risk factors for abnormal auditory sensory perception in autism spectrum disorders
Lire plus22 févr. 2016
01 déc. 2015
publication
11q24.2-25 micro-rearrangements in autism spectrum disorders: Relation to brain structures.
Lire plus23 sept. 2015
publication
A de novo microdeletion of SEMA5A in a boy with autism spectrum disorder and intellectual disability
Lire plus01 déc. 2014
01 sept. 2014
publication
Meta-analysis of SHANK Mutations in Autism Spectrum Disorders: a gradient of severity in cognitive impairments.
Lire plus10 juil. 2014
publication
Cntnap4 differentially contributes to GABAergic and dopaminergic synaptic transmission
Lire plus24 avr. 2014
publication
Convergence of genes and cellular pathways dysregulated in autism spectrum disorders
Lire plus03 mars 2014
publication
Heterogeneous pattern of selective pressure for PRRT2 in human populations, but no association with autism spectrum disorders
Lire plus03 déc. 2013
07 oct. 2013
01 juin 2013
27 juin 2012
publication
High-functioning autism spectrum disorder and fragile X syndrome: report of two affected sisters
Lire plus09 févr. 2012
publication
Genetic and functional analyses of SHANK2 mutations suggest a multiple hit model of autism spectrum disorders.
Lire plus01 nov. 2011
publication
Genetic variations of the melatonin pathway in patients with attention-deficit and hyperactivity disorders.
Lire plus04 mars 2011
publication
Variations of the candidate SEZ6L2 gene on Chromosome 16p11.2 in patients with autism spectrum disorders and in human populations.
Lire plus20 janv. 2011
publication
Mutation screening of ASMT, the last enzyme of the melatonin pathway, in a large sample of patients with intellectual disability
Lire plus15 juil. 2010
publication
Identification of pathway-biased and deleterious melatonin receptor mutants in autism spectrum disorders and in the general population
Lire plus06 juil. 2010
publication
Key role for gene dosage and synaptic homeostasis in autism spectrum disorders.
Lire plus05 juil. 2010
publication
Mutation screening of NOS1AP gene in a large sample of psychiatric patients and controls
Lire plus01 févr. 2009
23 janv. 2009
01 sept. 2008
17 déc. 2006
publication
Mutations in the gene encoding the synaptic scaffolding protein SHANK3 are associated with autism spectrum disorders
Lire plus01 janv. 2006
publication