Timeline
Richard Delorme
Permanent Researcher
06 Feb 2019
publication
Morning Plasma Melatonin Differences in Autism: Beyond the Impact of Pineal Gland Volume
Read more14 Jan 2019
publication
Altered spinogenesis in iPSC-derived cortical neurons from patients with autism carrying de novo SHANK3 mutations
Read more09 Jan 2019
publication
Synesthesia & Autistic Features in a Large Family:evidence for spatial imagery as a common factor
Read more27 Feb 2018
18 Dec 2017
publication
Heritability of the melatonin synthesis variability in autism spectrum disorders
Read more23 Oct 2017
publication
A framework to identify contributing genes in patients with Phelan-McDermid syndrome
Read more21 Nov 2016
14 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
23 Sep 2015
publication
A de novo microdeletion of SEMA5A in a boy with autism spectrum disorder and intellectual disability
Read more03 Sep 2015
publication
11q24.2-25 micro-rearrangements in autism spectrum disorders: Relation to brain structures
Read more16 Jul 2015
01 Dec 2014
04 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
06 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 more26 May 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