Thomas Bourgeron

Human Genetics and Cognitive Functions, Institut Pasteur

Affiliated withInstitut Pasteur Université Paris Diderot, Sorbonne Paris Cité University Paris Diderot, CNRS UMR 3571, Institut Pasteur

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JoVE Journal Publications

ArticleTotal : 2	Year
Publication title Cited by 7	2015
Publication title Cited by 80	2016

Other Publications

Article	Year
Genetic markers in psychiatric genetics. Methods in molecular medicine\| PubMed ID: 12298376	2003
Mutations of the X-linked genes encoding neuroligins NLGN3 and NLGN4 are associated with autism. Nature genetics\| PubMed ID: 12669065	2003
[Genetics of autism: from genome scans to candidate genes]. Médecine sciences : M/S\| PubMed ID: 14648479	2003
Frequency and transmission of glutamate receptors GRIK2 and GRIK3 polymorphisms in patients with obsessive compulsive disorder. Neuroreport\| PubMed ID: 15094479	2004
Expression and genetic variability of PCDH11Y, a gene specific to Homo sapiens and candidate for susceptibility to psychiatric disorders. American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics\| PubMed ID: 16331680	2006
No human tryptophan hydroxylase-2 gene R441H mutation in a large cohort of psychiatric patients and control subjects. Biological psychiatry\| PubMed ID: 16581035	2006
Searching for ways out of the autism maze: genetic, epigenetic and environmental clues. Trends in neurosciences\| PubMed ID: 16808981	2006
Fragile X syndrome and autism at the intersection of genetic and neural networks. Nature neuroscience\| PubMed ID: 17001341	2006
Mutations in the gene encoding the synaptic scaffolding protein SHANK3 are associated with autism spectrum disorders. Nature genetics\| PubMed ID: 17173049	2007
Mapping autism risk loci using genetic linkage and chromosomal rearrangements. Nature genetics\| PubMed ID: 17322880	2007
[Genetics and business: in defence of free speech!]. MÃ©decine sciences : M/S\| PubMed ID: 17502073	2007
[Alterations in synapsis formation and function in autism disorders]. Médecine sciences : M/S\| PubMed ID: 18198104	2008
Reduced social interaction and ultrasonic communication in a mouse model of monogenic heritable autism. Proceedings of the National Academy of Sciences of the United States of America\| PubMed ID: 18227507	2008
Analysis of X chromosome inactivation in autism spectrum disorders. American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics\| PubMed ID: 18361425	2008
An investigation of ribosomal protein L10 gene in autism spectrum disorders. BMC medical genetics\| PubMed ID: 19166581	2009
A synaptic trek to autism. Current opinion in neurobiology\| PubMed ID: 19545994	2009
Reduced 3-O-methyl-dopa levels in OCD patients and their unaffected parents is associated with the low activity M158 COMT allele. American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics\| PubMed ID: 19676096	2010
[Autism: more evidence of a genetic cause]. Bulletin de l'Académie nationale de médecine\| PubMed ID: 19718887	2009
Functional impact of global rare copy number variation in autism spectrum disorders. Nature\| PubMed ID: 20531469	2010
Mutation screening of NOS1AP gene in a large sample of psychiatric patients and controls. BMC medical genetics\| PubMed ID: 20602773	2010
Key role for gene dosage and synaptic homeostasis in autism spectrum disorders. Trends in genetics : TIG\| PubMed ID: 20609491	2010
Identification of pathway-biased and deleterious melatonin receptor mutants in autism spectrum disorders and in the general population. PloS one\| PubMed ID: 20657642	2010
A genome-wide scan for common alleles affecting risk for autism. Human molecular genetics\| PubMed ID: 20663923	2010
Production of soluble, active acetyl serotonin methyl transferase in Leishmania tarentolae. Protein expression and purification\| PubMed ID: 20688166	2011
Against le packing: a consensus statement. Journal of the American Academy of Child and Adolescent Psychiatry\| PubMed ID: 21241956	2011
Mutation screening of ASMT, the last enzyme of the melatonin pathway, in a large sample of patients with intellectual disability. BMC medical genetics\| PubMed ID: 21251267	2011
Behavioral profiles of mouse models for autism spectrum disorders. Autism research : official journal of the International Society for Autism Research\| PubMed ID: 21328568	2011
Variations of the candidate SEZ6L2 gene on Chromosome 16p11.2 in patients with autism spectrum disorders and in human populations. PloS one\| PubMed ID: 21394203	2011
Dynamics in enzymatic protein complexes offer a novel principle for the regulation of melatonin synthesis in the human pineal gland. Journal of pineal research\| PubMed ID: 21517958	2011
Genetic variations of the melatonin pathway in patients with attention-deficit and hyperactivity disorders. Journal of pineal research\| PubMed ID: 21615493	2011
A novel approach of homozygous haplotype sharing identifies candidate genes in autism spectrum disorder. Human genetics\| PubMed ID: 21996756	2011
Adult male mice emit context-specific ultrasonic vocalizations that are modulated by prior isolation or group rearing environment. PloS one\| PubMed ID: 22238608	2012
Genetic variants of FOXP2 and KIAA0319/TTRAP/THEM2 locus are associated with altered brain activation in distinct language-related regions. The Journal of neuroscience : the official journal of the Society for Neuroscience\| PubMed ID: 22262880	2012
Genetic and functional analyses of SHANK2 mutations suggest a multiple hit model of autism spectrum disorders. PLoS genetics\| PubMed ID: 22346768	2012
SHANK1 Deletions in Males with Autism Spectrum Disorder. American journal of human genetics\| PubMed ID: 22503632	2012
Genetic and functional abnormalities of the melatonin biosynthesis pathway in patients with bipolar disorder. Human molecular genetics\| PubMed ID: 22694957	2012
Autistic-like behaviours and hyperactivity in mice lacking ProSAP1/Shank2. Nature\| PubMed ID: 22699619	2012
High-functioning autism spectrum disorder and fragile X syndrome: report of two affected sisters. Molecular autism\| PubMed ID: 22738402	2012
Crystal structure and functional mapping of human ASMT, the last enzyme of the melatonin synthesis pathway. Journal of pineal research\| PubMed ID: 22775292	2013
Significant correlation between a set of genetic polymorphisms and a functional brain network revealed by feature selection and sparse Partial Least Squares. NeuroImage\| PubMed ID: 22781162	2012
Individual common variants exert weak effects on the risk for autism spectrum disorderspi. Human molecular genetics\| PubMed ID: 22843504	2012
Development of an autism severity score for mice using Nlgn4 null mutants as a construct-valid model of heritable monogenic autism. Behavioural brain research\| PubMed ID: 23183221	2013
Sequencing ASMT identifies rare mutations in Chinese Han patients with autism. PloS one\| PubMed ID: 23349736	2013
Contactin 4, -5 and -6 differentially regulate neuritogenesis while they display identical PTPRG binding sites. Biology open\| PubMed ID: 23519440	2013
Progress toward treatments for synaptic defects in autism. Nature medicine\| PubMed ID: 23744158	2013
The genetic landscapes of autism spectrum disorders. Annual review of genomics and human genetics\| PubMed ID: 23875794	2013
The Autism ProSAP1/Shank2 mouse model displays quantitative and structural abnormalities in ultrasonic vocalisations. Behavioural brain research\| PubMed ID: 23994547	2013
The emerging role of SHANK genes in neuropsychiatric disorders. Developmental neurobiology\| PubMed ID: 24124131	2014
Heterozygous FA2H mutations in autism spectrum disorders. BMC medical genetics\| PubMed ID: 24299421	2013
Neurobiology of autism gene products: towards pathogenesis and drug targets. Psychopharmacology\| PubMed ID: 24419271	2014
Common variants in genes of the postsynaptic FMRP signalling pathway are risk factors for autism spectrum disorders. Human genetics\| PubMed ID: 24442360	2014
Screening, intervention and outcome in autism and other developmental disorders: the role of randomized controlled trials. Journal of autism and developmental disorders\| PubMed ID: 24554162	2014
Heterogeneous pattern of selective pressure for PRRT2 in human populations, but no association with autism spectrum disorders. PloS one\| PubMed ID: 24594579	2014
Convergence of genes and cellular pathways dysregulated in autism spectrum disorders. American journal of human genetics\| PubMed ID: 24768552	2014
Genetic and Environmental Influences on the Visual Word Form and Fusiform Face Areas. Cerebral cortex (New York, N.Y. : 1991)\| PubMed ID: 24825786	2015
Vitamin d in the general population of young adults with autism in the faroe islands. Journal of autism and developmental disorders\| PubMed ID: 24927807	2014
Meta-analysis of SHANK Mutations in Autism Spectrum Disorders: a gradient of severity in cognitive impairments. PLoS genetics\| PubMed ID: 25188300	2014
Social communication in mice--are there optimal cage conditions? PloS one\| PubMed ID: 25806942	2015
Neuroanatomical Diversity of Corpus Callosum and Brain Volume in Autism: Meta-analysis, Analysis of the Autism Brain Imaging Data Exchange Project, and Simulation. Biological psychiatry\| PubMed ID: 25850620	2015
The genetics and neurobiology of ESSENCE: The third Birgit Olsson lecture. Nordic journal of psychiatry\| PubMed ID: 25971862	2015
From the genetic architecture to synaptic plasticity in autism spectrum disorder. Nature reviews. Neuroscience\| PubMed ID: 26289574	2015
11q24.2-25 micro-rearrangements in autism spectrum disorders: Relation to brain structures. American journal of medical genetics. Part A\| PubMed ID: 26334118	2015
A de novo microdeletion of SEMA5A in a boy with autism spectrum disorder and intellectual disability. European journal of human genetics : EJHG\| PubMed ID: 26395558	2015