Timeline

Richard Delorme
Permanent Researcher
26 Jun 2023
publication

Phenotypic effects of genetic variants associated with autism.

Read more
08 Dec 2022
event

Troubles du spectre de l’autisme, troubles du neurodéveloppement : vulnérabilités et inégalités au sein des parcours de vie

Read more
15 Jul 2022
publication

Insights from an autism imaging biomarker challenge: Promises and threats to biomarker discovery.

Read more
13 Jun 2022
project

Étude des facteurs génétiques impliqués dans l’autisme et les troubles apparentés (projet “C07/C16”)

Read more
19 Jul 2021
publication

Discriminant value of repetitive behaviors in families with autism spectrum disorder and obsessional compulsive disorder probands.

Read more
01 Jun 2021
publication

Operative list of genes associated with autism and neurodevelopmental disorders based on database review.

Read more
08 Oct 2020
publication

HyPyP: a Hyperscanning Python Pipeline for inter-brain connectivity analysis.

Read more
11 Jun 2020
project

PARIS: Paris Autism Research International Sib-Pair Study

Read more
10 Jun 2020
publication

Autism-associated SHANK3 mutations impair maturation of neuromuscular junctions and striated muscles.

Read more
09 Jan 2019
publication

Synesthesia & Autistic Features in a Large Family:evidence for spatial imagery as a common factor

Read more
01 Jan 2019
publication

Morning Plasma Melatonin Differences in Autism: Beyond the Impact of Pineal Gland Volume.

Read more
01 Apr 2018
publication

Cerebellar Volume in Autism: Literature Meta-analysis and Analysis of the Autism Brain Imaging Data Exchange Cohort.

Read more
27 Feb 2018
project

EU-AIMS

Read more
01 Jan 2017
publication

A framework to identify contributing genes in patients with Phelan-McDermid syndrome.

Read more
14 Nov 2016
software

GRAVITY

Read more
05 Nov 2016
project

SoNeTAA

Read more
10 May 2016
publication

CNTN6 mutations are risk factors for abnormal auditory sensory perception in autism spectrum disorders

Read more
22 Feb 2016
project

Phelan-McDermid Syndrome: from mechanisms to treatments

Read more
01 Dec 2015
publication

11q24.2-25 micro-rearrangements in autism spectrum disorders: Relation to brain structures.

Read more
23 Sep 2015
publication

A de novo microdeletion of SEMA5A in a boy with autism spectrum disorder and intellectual disability

Read more
01 Dec 2014
team

Human Genetics and Cognitive Functions

Read more
01 Sep 2014
publication

Meta-analysis of SHANK Mutations in Autism Spectrum Disorders: a gradient of severity in cognitive impairments.

Read more
10 Jul 2014
publication

Cntnap4 differentially contributes to GABAergic and dopaminergic synaptic transmission

Read more
24 Apr 2014
publication

Convergence of genes and cellular pathways dysregulated in autism spectrum disorders

Read more
03 Mar 2014
publication

Heterogeneous pattern of selective pressure for PRRT2 in human populations, but no association with autism spectrum disorders

Read more
03 Dec 2013
publication

Heterozygous FA2H mutations in autism spectrum disorders

Read more
07 Oct 2013
publication

The emerging role of SHANK genes in neuropsychiatric disorders

Read more
01 Jun 2013
publication

Progress toward treatments for synaptic defects in autism.

Read more
27 Jun 2012
publication

High-functioning autism spectrum disorder and fragile X syndrome: report of two affected sisters

Read more
09 Feb 2012
publication

Genetic and functional analyses of SHANK2 mutations suggest a multiple hit model of autism spectrum disorders.

Read more
01 Nov 2011
publication

Genetic variations of the melatonin pathway in patients with attention-deficit and hyperactivity disorders.

Read more
04 Mar 2011
publication

Variations of the candidate SEZ6L2 gene on Chromosome 16p11.2 in patients with autism spectrum disorders and in human populations.

Read more
20 Jan 2011
publication

Mutation screening of ASMT, the last enzyme of the melatonin pathway, in a large sample of patients with intellectual disability

Read more
15 Jul 2010
publication

Identification of pathway-biased and deleterious melatonin receptor mutants in autism spectrum disorders and in the general population

Read more
06 Jul 2010
publication

Key role for gene dosage and synaptic homeostasis in autism spectrum disorders.

Read more
05 Jul 2010
publication

Mutation screening of NOS1AP gene in a large sample of psychiatric patients and controls

Read more
01 Feb 2009
publication

[Autism: more evidence of a genetic cause]

Read more
23 Jan 2009
publication

An investigation of ribosomal protein L10 gene in autism spectrum disorders

Read more
01 Sep 2008
publication

Analysis of X chromosome inactivation in autism spectrum disorders

Read more
17 Dec 2006
publication

Mutations in the gene encoding the synaptic scaffolding protein SHANK3 are associated with autism spectrum disorders

Read more
01 Jan 2006
publication

Expression and genetic variability of PCDH11Y, a gene specific to Homo sapiens and candidate for susceptibility to psychiatric disorders

Read more