Timeline

Richard Delorme
Permanent Researcher
06 Feb 2019
publication

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

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09 Jan 2019
publication

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

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27 Feb 2018
project

EU-AIMS

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18 Dec 2017
publication

Heritability of the melatonin synthesis variability in autism spectrum disorders

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23 Oct 2017
publication

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

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21 Nov 2016
project

Communauté des médecins affiliés de l’Institut Pasteur

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14 Nov 2016
software

GRAVITY

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05 Nov 2016
project

SoNeTAA

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10 May 2016
publication

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

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22 Feb 2016
project

Phelan McDermid Syndrome: from mechanisms to treatments

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23 Sep 2015
publication

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

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03 Sep 2015
publication

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

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16 Jul 2015
project

Establishment of cohorts of patients with ASD

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01 Dec 2014
team

Human Genetics and Cognitive Functions

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04 Sep 2014
publication

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

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10 Jul 2014
publication

Cntnap4 differentially contributes to GABAergic and dopaminergic synaptic transmission

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24 Apr 2014
publication

Convergence of genes and cellular pathways dysregulated in autism spectrum disorders

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03 Mar 2014
publication

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

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03 Dec 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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06 Jun 2013
publication

Progress toward treatments for synaptic defects in autism

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27 Jun 2012
publication

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

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09 Feb 2012
publication

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

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26 May 2011
publication

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

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04 Mar 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 Jan 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 Jul 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 Jul 2010
publication

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

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05 Jul 2010
publication

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

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01 Feb 2009
publication

[Autism: more evidence of a genetic cause]

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23 Jan 2009
publication

An investigation of ribosomal protein L10 gene in autism spectrum disorders

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01 Sep 2008
publication

Analysis of X chromosome inactivation in autism spectrum disorders

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17 Dec 2006
publication

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

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01 Jan 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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