Ligne de temps

Richard Delorme
Chercheur(euse) Permanent(e)
26 juin 2023
publication

Phenotypic effects of genetic variants associated with autism.

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08 déc. 2022
event

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

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15 juil. 2022
publication

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

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13 juin 2022
project

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

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19 juil. 2021
publication

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

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01 juin 2021
publication

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

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08 oct. 2020
publication

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

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11 juin 2020
project

PARIS: Paris Autism Research International Sib-Pair Study

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10 juin 2020
publication

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

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09 janv. 2019
publication

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

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01 janv. 2019
publication

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

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01 avr. 2018
publication

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

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27 févr. 2018
project

EU-AIMS

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01 janv. 2017
publication

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

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14 nov. 2016
software

GRAVITY

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05 nov. 2016
project

SoNeTAA

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10 mai 2016
publication

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

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22 févr. 2016
project

Le syndrome de Phelan-McDermid : des mécanismes aux traitements

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01 déc. 2015
publication

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

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23 sept. 2015
publication

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

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01 déc. 2014
team

Génétique Humaine et Fonctions Cognitives

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01 sept. 2014
publication

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

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10 juil. 2014
publication

Cntnap4 differentially contributes to GABAergic and dopaminergic synaptic transmission

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24 avr. 2014
publication

Convergence of genes and cellular pathways dysregulated in autism spectrum disorders

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03 mars 2014
publication

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

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03 déc. 2013
publication

Heterozygous FA2H mutations in autism spectrum disorders

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07 oct. 2013
publication

The emerging role of SHANK genes in neuropsychiatric disorders

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01 juin 2013
publication

Progress toward treatments for synaptic defects in autism.

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27 juin 2012
publication

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

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09 févr. 2012
publication

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

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01 nov. 2011
publication

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

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04 mars 2011
publication

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

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20 janv. 2011
publication

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

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15 juil. 2010
publication

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

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06 juil. 2010
publication

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

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05 juil. 2010
publication

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

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01 févr. 2009
publication

[Autism: more evidence of a genetic cause]

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23 janv. 2009
publication

An investigation of ribosomal protein L10 gene in autism spectrum disorders

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01 sept. 2008
publication

Analysis of X chromosome inactivation in autism spectrum disorders

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17 déc. 2006
publication

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

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01 janv. 2006
publication

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

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