Timeline
Richard Delorme
Permanent Researcher
08 Dec 2022
event
Troubles du spectre de l’autisme, troubles du neurodéveloppement : vulnérabilités et inégalités au sein des parcours de vie
Read more15 Jul 2022
publication
Insights from an autism imaging biomarker challenge: Promises and threats to biomarker discovery.
Read more13 Jun 2022
project
(FR) Étude des facteurs génétiques impliqués dans l’autisme et les troubles apparentés (projet “C07/C16”)
Read more19 Jul 2021
publication
Discriminant value of repetitive behaviors in families with autism spectrum disorder and obsessional compulsive disorder probands.
Read more08 Oct 2020
11 Jun 2020
10 Jun 2020
publication
Autism-associated SHANK3 mutations impair maturation of neuromuscular junctions and striated muscles.
Read more09 Jan 2019
publication
Synesthesia & Autistic Features in a Large Family:evidence for spatial imagery as a common factor
Read more01 Jan 2019
publication
Morning Plasma Melatonin Differences in Autism: Beyond the Impact of Pineal Gland Volume.
Read more01 Apr 2018
publication
Cerebellar Volume in Autism: Literature Meta-analysis and Analysis of the Autism Brain Imaging Data Exchange Cohort.
Read more27 Feb 2018
01 Jan 2017
publication
A framework to identify contributing genes in patients with Phelan-McDermid syndrome.
Read more14 Nov 2016
05 Nov 2016
10 May 2016
publication
CNTN6 mutations are risk factors for abnormal auditory sensory perception in autism spectrum disorders
Read more22 Feb 2016
01 Dec 2015
publication
11q24.2-25 micro-rearrangements in autism spectrum disorders: Relation to brain structures.
Read more23 Sep 2015
publication
A de novo microdeletion of SEMA5A in a boy with autism spectrum disorder and intellectual disability
Read more01 Dec 2014
01 Sep 2014
publication
Meta-analysis of SHANK Mutations in Autism Spectrum Disorders: a gradient of severity in cognitive impairments.
Read more10 Jul 2014
publication
Cntnap4 differentially contributes to GABAergic and dopaminergic synaptic transmission
Read more24 Apr 2014
publication
Convergence of genes and cellular pathways dysregulated in autism spectrum disorders
Read more03 Mar 2014
publication
Heterogeneous pattern of selective pressure for PRRT2 in human populations, but no association with autism spectrum disorders
Read more03 Dec 2013
07 Oct 2013
01 Jun 2013
27 Jun 2012
publication
High-functioning autism spectrum disorder and fragile X syndrome: report of two affected sisters
Read more09 Feb 2012
publication
Genetic and functional analyses of SHANK2 mutations suggest a multiple hit model of autism spectrum disorders.
Read more01 Nov 2011
publication
Genetic variations of the melatonin pathway in patients with attention-deficit and hyperactivity disorders.
Read more04 Mar 2011
publication
Variations of the candidate SEZ6L2 gene on Chromosome 16p11.2 in patients with autism spectrum disorders and in human populations.
Read more20 Jan 2011
publication
Mutation screening of ASMT, the last enzyme of the melatonin pathway, in a large sample of patients with intellectual disability
Read more15 Jul 2010
publication
Identification of pathway-biased and deleterious melatonin receptor mutants in autism spectrum disorders and in the general population
Read more06 Jul 2010
publication
Key role for gene dosage and synaptic homeostasis in autism spectrum disorders.
Read more05 Jul 2010
publication
Mutation screening of NOS1AP gene in a large sample of psychiatric patients and controls
Read more01 Feb 2009
23 Jan 2009
01 Sep 2008
17 Dec 2006
publication
Mutations in the gene encoding the synaptic scaffolding protein SHANK3 are associated with autism spectrum disorders
Read more01 Jan 2006
publication