Thomas Bourgeron Human Genetics and Cognitive Functions University Paris Diderot, CNRS UMR 3571, Institut Pasteur Biography Publications Institution JoVE Articles Thomas Bourgeron has not added a biography. If you are Thomas Bourgeron and would like to personalize this page please email our Author Liaison for assistance. Publications A De Novo Microdeletion of SEMA5A in a Boy with Autism Spectrum Disorder and Intellectual Disability European Journal of Human Genetics : EJHG. Sep, 2015 | Pubmed ID: 26395558 11q24.2-25 Micro-rearrangements in Autism Spectrum Disorders: Relation to Brain Structures American Journal of Medical Genetics. Part A. Sep, 2015 | Pubmed ID: 26334118 From the Genetic Architecture to Synaptic Plasticity in Autism Spectrum Disorder Nature Reviews. Neuroscience. Aug, 2015 | Pubmed ID: 26289574 The Genetics and Neurobiology of ESSENCE: The Third Birgit Olsson Lecture Nordic Journal of Psychiatry. May, 2015 | Pubmed ID: 25971862 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. Jul, 2015 | Pubmed ID: 25850620 Social Communication in Mice--are There Optimal Cage Conditions? PloS One. 2015 | Pubmed ID: 25806942 Genetic and Environmental Influences on the Visual Word Form and Fusiform Face Areas Cerebral Cortex (New York, N.Y. : 1991). Sep, 2015 | Pubmed ID: 24825786 Meta-analysis of SHANK Mutations in Autism Spectrum Disorders: a Gradient of Severity in Cognitive Impairments PLoS Genetics. Sep, 2014 | Pubmed ID: 25188300 Vitamin D in the General Population of Young Adults with Autism in the Faroe Islands Journal of Autism and Developmental Disorders. Dec, 2014 | Pubmed ID: 24927807 Convergence of Genes and Cellular Pathways Dysregulated in Autism Spectrum Disorders American Journal of Human Genetics. May, 2014 | Pubmed ID: 24768552 Heterogeneous Pattern of Selective Pressure for PRRT2 in Human Populations, but No Association with Autism Spectrum Disorders PloS One. 2014 | Pubmed ID: 24594579 Screening, Intervention and Outcome in Autism and Other Developmental Disorders: the Role of Randomized Controlled Trials Journal of Autism and Developmental Disorders. Aug, 2014 | Pubmed ID: 24554162 Common Variants in Genes of the Postsynaptic FMRP Signalling Pathway Are Risk Factors for Autism Spectrum Disorders Human Genetics. Jun, 2014 | Pubmed ID: 24442360 Neurobiology of Autism Gene Products: Towards Pathogenesis and Drug Targets Psychopharmacology. Mar, 2014 | Pubmed ID: 24419271 The Emerging Role of SHANK Genes in Neuropsychiatric Disorders Developmental Neurobiology. Feb, 2014 | Pubmed ID: 24124131 Heterozygous FA2H Mutations in Autism Spectrum Disorders BMC Medical Genetics. 2013 | Pubmed ID: 24299421 The Autism ProSAP1/Shank2 Mouse Model Displays Quantitative and Structural Abnormalities in Ultrasonic Vocalisations Behavioural Brain Research. Nov, 2013 | Pubmed ID: 23994547 The Genetic Landscapes of Autism Spectrum Disorders Annual Review of Genomics and Human Genetics. 2013 | Pubmed ID: 23875794 Progress Toward Treatments for Synaptic Defects in Autism Nature Medicine. Jun, 2013 | Pubmed ID: 23744158 Contactin 4, -5 Et -6 Différentiellement Réglementent Neuritogenesis Alors Qu'ils Affichent Des Sites Identiques De Liaison PTPRG Biology Open. Mar, 2013 | Pubmed ID: 23519440 Sequencing ASMT Identifies Rare Mutations in Chinese Han Patients with Autism PloS One. 2013 | Pubmed ID: 23349736 Development of an Autism Severity Score for Mice Using Nlgn4 Null Mutants As a Construct-valid Model of Heritable Monogenic Autism Behavioural Brain Research. Aug, 2013 | Pubmed ID: 23183221 Crystal Structure and Functional Mapping of Human ASMT, the Last Enzyme of the Melatonin Synthesis Pathway Journal of Pineal Research. Jan, 2013 | Pubmed ID: 22775292 Individual Common Variants Exert Weak Effects on the Risk for Autism Spectrum Disorderspi Human Molecular Genetics. Jul, 2012 | Pubmed ID: 22843504 Significant Correlation Between a Set of Genetic Polymorphisms and a Functional Brain Network Revealed by Feature Selection and Sparse Partial Least Squares NeuroImage. Oct, 2012 | Pubmed ID: 22781162 High-functioning Autism Spectrum Disorder and Fragile X Syndrome: Report of Two Affected Sisters Molecular Autism. 2012 | Pubmed ID: 22738402 Autistic-like Behaviours and Hyperactivity in Mice Lacking ProSAP1/Shank2 Nature. Jun, 2012 | Pubmed ID: 22699619 Genetic and Functional Abnormalities of the Melatonin Biosynthesis Pathway in Patients with Bipolar Disorder Human Molecular Genetics. Sep, 2012 | Pubmed ID: 22694957 SHANK1 Deletions in Males with Autism Spectrum Disorder American Journal of Human Genetics. May, 2012 | Pubmed ID: 22503632 Genetic and Functional Analyses of SHANK2 Mutations Suggest a Multiple Hit Model of Autism Spectrum Disorders PLoS Genetics. Feb, 2012 | Pubmed ID: 22346768 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. Jan, 2012 | Pubmed ID: 22262880 Des Souris Mâles Adultes émettent Contextuelle Vocalisations Ultrasoniques Qui Sont Modulées Par Isolement Préalable Ou Le Groupe Environnement De L'élevage PloS One. 2012 | Pubmed ID: 22238608 Une Nouvelle Approche Du Haplotype Homozygote Partage Identifie Les Gènes Candidats Dans Les Troubles Du Spectre Autistique Human Genetics. Oct, 2011 | Pubmed ID: 21996756 Genetic Variations of the Melatonin Pathway in Patients with Attention-deficit and Hyperactivity Disorders Journal of Pineal Research. Nov, 2011 | Pubmed ID: 21615493 Dynamics in Enzymatic Protein Complexes Offer a Novel Principle for the Regulation of Melatonin Synthesis in the Human Pineal Gland Journal of Pineal Research. Aug, 2011 | Pubmed ID: 21517958 Variations of the Candidate SEZ6L2 Gene on Chromosome 16p11.2 in Patients with Autism Spectrum Disorders and in Human Populations PloS One. 2011 | Pubmed ID: 21394203 Behavioral Profiles of Mouse Models for Autism Spectrum Disorders Autism Research : Official Journal of the International Society for Autism Research. Feb, 2011 | Pubmed ID: 21328568 Mutation Screening of ASMT, the Last Enzyme of the Melatonin Pathway, in a Large Sample of Patients with Intellectual Disability BMC Medical Genetics. 2011 | Pubmed ID: 21251267 Against Le Packing: a Consensus Statement Journal of the American Academy of Child and Adolescent Psychiatry. Feb, 2011 | Pubmed ID: 21241956 Production of Soluble, Active Acetyl Serotonin Methyl Transferase in Leishmania Tarentolae Protein Expression and Purification. Jan, 2011 | Pubmed ID: 20688166 Un Balayage De Génome-large D'allèles Communs Qui Affectent Le Risque De L'autisme Human Molecular Genetics. Oct, 2010 | Pubmed ID: 20663923 Identification of Pathway-biased and Deleterious Melatonin Receptor Mutants in Autism Spectrum Disorders and in the General Population PloS One. 2010 | Pubmed ID: 20657642 Key Role for Gene Dosage and Synaptic Homeostasis in Autism Spectrum Disorders Trends in Genetics : TIG. Aug, 2010 | Pubmed ID: 20609491 Mutation Screening of NOS1AP Gene in a Large Sample of Psychiatric Patients and Controls BMC Medical Genetics. 2010 | Pubmed ID: 20602773 Impact Fonctionnel De Variation Numéro Mondial Exemplaire Rare Des Troubles Du Spectre Autistique Nature. Jul, 2010 | Pubmed ID: 20531469 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. Mar, 2010 | Pubmed ID: 19676096 [Autism: More Evidence of a Genetic Cause] Bulletin De L'Académie Nationale De Médecine. Feb, 2009 | Pubmed ID: 19718887 A Synaptic Trek to Autism Current Opinion in Neurobiology. Apr, 2009 | Pubmed ID: 19545994 An Investigation of Ribosomal Protein L10 Gene in Autism Spectrum Disorders BMC Medical Genetics. 2009 | Pubmed ID: 19166581 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. Sep, 2008 | Pubmed ID: 18361425 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. Feb, 2008 | Pubmed ID: 18227507 [Alterations in Synapsis Formation and Function in Autism Disorders] Médecine Sciences : M/S. Jan, 2008 | Pubmed ID: 18198104 [Génétique Et Affaires : Pour La Défense De La Liberté D'expression!] Médecine Sciences : M/S. May, 2007 | Pubmed ID: 17502073 Cartographie De Locus De Risque De L'autisme à L'aide De La Génétique Et Des Réarrangements Chromosomiques Nature Genetics. Mar, 2007 | Pubmed ID: 17322880 Mutations in the Gene Encoding the Synaptic Scaffolding Protein SHANK3 Are Associated with Autism Spectrum Disorders Nature Genetics. Jan, 2007 | Pubmed ID: 17173049 Syndrome Du X Fragile Et Autisme à L'intersection Des Réseaux Génétiques Et Neural Nature Neuroscience. Oct, 2006 | Pubmed ID: 17001341 Searching for Ways out of the Autism Maze: Genetic, Epigenetic and Environmental Clues Trends in Neurosciences. Jul, 2006 | Pubmed ID: 16808981 No Human Tryptophan Hydroxylase-2 Gene R441H Mutation in a Large Cohort of Psychiatric Patients and Control Subjects Biological Psychiatry. Jul, 2006 | Pubmed ID: 16581035 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. Jan, 2006 | Pubmed ID: 16331680 Frequency and Transmission of Glutamate Receptors GRIK2 and GRIK3 Polymorphisms in Patients with Obsessive Compulsive Disorder Neuroreport. Mar, 2004 | Pubmed ID: 15094479 [Genetics of Autism: from Genome Scans to Candidate Genes] Médecine Sciences : M/S. Nov, 2003 | Pubmed ID: 14648479 Mutations of the X-linked Genes Encoding Neuroligins NLGN3 and NLGN4 Are Associated with Autism Nature Genetics. May, 2003 | Pubmed ID: 12669065 Genetic Markers in Psychiatric Genetics Methods in Molecular Medicine. 2003 | Pubmed ID: 12298376 Enregistrement souris vocalisations ultrasoniques pour évaluer la Communication Sociale Allain-Thibeault Ferhat1, Nicolas Torquet2, Anne-Marie Le Sourd1, Fabrice de Chaumont3, Jean-Christophe Olivo-Marin3, Philippe Faure2, Thomas Bourgeron1, Elodie Ey1 1Human Genetics and Cognitive Functions, University Paris Diderot, CNRS UMR 3571, Institut Pasteur, 2Neurophysiology and Behavior, University Pierre et Marie Curie Paris 6, CNRS UMR 7102, 3Bio Image Analysis, CNRS URA 2582, Institut Pasteur Behavior Quantification tridimensionnelle d'épines dendritiques de Pyramidal neurones humains induits Dérivé de cellules souches pluripotentes Laura Gouder1,2,3, Jean-Yves Tinevez4, Hany Goubran-Botros1,2,3, Alexandra Benchoua5, Thomas Bourgeron1,2,3, Isabelle Cloëz-Tayarani1,2,3 1Human Genetics and Cognitive Functions, Institut Pasteur, 2CNRS URA 2182 'Genes, synapses and cognition', Institut Pasteur, 3Human Genetics and Cognitive Functions, Université Paris Diderot, Sorbonne Paris Cité, 4Plateforme d' Imagerie Dynamique, Imagopole, CiTech, Institut Pasteur, 5Neuroplasticity and Therapeutics, CECS, I-STEM, AFM, Evry JoVE 53197 Developmental Biology
Enregistrement souris vocalisations ultrasoniques pour évaluer la Communication Sociale Allain-Thibeault Ferhat1, Nicolas Torquet2, Anne-Marie Le Sourd1, Fabrice de Chaumont3, Jean-Christophe Olivo-Marin3, Philippe Faure2, Thomas Bourgeron1, Elodie Ey1 1Human Genetics and Cognitive Functions, University Paris Diderot, CNRS UMR 3571, Institut Pasteur, 2Neurophysiology and Behavior, University Pierre et Marie Curie Paris 6, CNRS UMR 7102, 3Bio Image Analysis, CNRS URA 2582, Institut Pasteur Behavior
Quantification tridimensionnelle d'épines dendritiques de Pyramidal neurones humains induits Dérivé de cellules souches pluripotentes Laura Gouder1,2,3, Jean-Yves Tinevez4, Hany Goubran-Botros1,2,3, Alexandra Benchoua5, Thomas Bourgeron1,2,3, Isabelle Cloëz-Tayarani1,2,3 1Human Genetics and Cognitive Functions, Institut Pasteur, 2CNRS URA 2182 'Genes, synapses and cognition', Institut Pasteur, 3Human Genetics and Cognitive Functions, Université Paris Diderot, Sorbonne Paris Cité, 4Plateforme d' Imagerie Dynamique, Imagopole, CiTech, Institut Pasteur, 5Neuroplasticity and Therapeutics, CECS, I-STEM, AFM, Evry JoVE 53197 Developmental Biology
