Ligne de temps
Thomas Bourgeron
Responsable de Structure
27 nov. 2025
publication
The influence of CHRNA5 and D398N missense variation onsocial and emotional behaviors in rodents and humans
Lire plus27 nov. 2025
publication
The influence of CHRNA5 and D398N missense variation on social and emotional behaviors in rodents and humans.
Lire plus18 oct. 2025
publication
Female C57BL/6J mice perform distinctive urination behaviour accompanied by ultrasonic vocalisation sequences with a stereotyped temporal organisation.
Lire plus01 oct. 2025
publication
Decomposing the Brain in Autism: Linking Behavioral Domains to Neuroanatomical Variation and Genomic Underpinnings.
Lire plus30 sept. 2025
01 août 2025
publication
Genetic Architecture and Risk of Childhood Maltreatment Across 5 Psychiatric Diagnoses.
Lire plus22 juil. 2025
publication
Transcriptomic decoding of surface-based imaging phenotypes and its application to pharmacotranscriptomics.
Lire plus10 juil. 2025
publication
Parsing Autism Heterogeneity: Transcriptomic Subgrouping of Imaging-Derived Phenotypes in Autism.
Lire plus15 mai 2025
03 mars 2025
01 janv. 2025
publication
Neuroimaging insights into brain mechanisms of early-onset restrictive eating disorders.
Lire plus01 janv. 2025
publication
From Symptomatology to Functioning – Applying the ICF to Autism Measures to Facilitate Neurodiversity-Affirmative Data Harmonization.
Lire plus01 janv. 2025
publication
A multimodal neural signature of face processing in autism within the fusiform gyrus.
Lire plus01 déc. 2024
28 nov. 2024
publication
Conceptual framework for data harmonisation in mental health using the International Classification of Functioning, Disability and Health: an example with the R2D2-MH consortium.
Lire plus28 oct. 2024
26 juin 2024
publication
Effectiveness of a positive psychology and mindfulness-based app on mental health for parents of children with a neurodevelopmental disorder: study protocol of a pragmatic international randomized controlled trial.
Lire plus04 juin 2024
publication
European Autism GEnomics Registry (EAGER): protocol for a multicentre cohort study and registry.
Lire plus15 janv. 2024
publication
Differences in Intrinsic Gray Matter Connectivity and Their Genomic Underpinnings in Autism Spectrum Disorder.
Lire plus27 nov. 2023
publication
Exploring the multidimensional nature of repetitive and restricted behaviors and interests (RRBI) in autism: neuroanatomical correlates and clinical implications.
Lire plus07 nov. 2023
31 oct. 2023
26 oct. 2023
event
Neuroscience Seminar Series | Varun Warrier “Using genetics to investigate the structure of the human cortex and links to psychiatric diagnoses.”
Lire plus04 oct. 2023
publication
The neuroanatomical substrates of autism and ADHD and their link to putative genomic underpinnings.
Lire plus31 août 2023
publication
Bridge-building between communities: Imagining the future of biomedical autism research.
Lire plus27 juil. 2023
publication
Fine-grained topographic organization within somatosensory cortex during resting-state and emotional face-matching task and its association with ASD traits.
Lire plus01 juil. 2023
publication
Definition and clinical variability of SHANK3-related Phelan-McDermid syndrome.
Lire plus26 juin 2023
01 juin 2023
01 mai 2023
publication
Dissecting the 22q13 region to explore the genetic and phenotypic diversity of patients with Phelan-McDermid syndrome.
Lire plus01 mai 2023
publication
Cross-sectional and longitudinal neuroanatomical profiles of distinct clinical (adaptive) outcomes in autism.
Lire plus19 avr. 2023
publication
Brain functional connectivity mirrors genetic pleiotropy in psychiatric conditions.
Lire plus03 avr. 2023
news
Semaine du cerveau 2023 – A quoi pensent les bébés ? Conférence du 18 mars à l’Institut Pasteur.
Lire plus01 mars 2023
01 févr. 2023
publication
Tackling hypo and hyper sensory processing heterogeneity in autism: From clinical stratification to genetic pathways.
Lire plus21 janv. 2023
publication
Excitatory/inhibitory imbalance in autism: the role of glutamate and GABA gene-sets in symptoms and cortical brain structure.
Lire plus01 janv. 2023
publication
The Link Between Autism and Sex-Related Neuroanatomy, and Associated Cognition and Gene Expression.
Lire plus01 janv. 2023
publication
Excessive self-grooming, gene dysregulation and imbalance between the striosome and matrix compartments in the striatum of Shank3 mutant mice.
Lire plus01 janv. 2023
publication
Cortico-Cerebellar neurodynamics during social interaction in Autism Spectrum Disorders.
Lire plus08 déc. 2022
event
Troubles du spectre de l’autisme, troubles du neurodéveloppement : vulnérabilités et inégalités au sein des parcours de vie
Lire plus01 sept. 2022
30 août 2022
publication
Genome-wide analyses of individual differences in quantitatively assessed reading- and language-related skills in up to 34,000 people.
Lire plus26 août 2022
news
INCEPTION 2022 meeting: Integrative Biology, Social and Data Sciences to understand the Emergence of Diseases in Populations and in Individuals
Lire plus25 août 2022
event
INCEPTION 2022 meeting: Integrative Biology, Social and Data Sciences to understand the Emergence of Diseases in Populations and in Individuals
Lire plus17 août 2022
publication
Stratifying the autistic phenotype using electrophysiological indices of social perception.
Lire plus15 juil. 2022
publication
Insights from an autism imaging biomarker challenge: Promises and threats to biomarker discovery.
Lire plus13 juin 2022
project
Étude des facteurs génétiques impliqués dans l’autisme et les troubles apparentés (projet “Gènes et Autisme”)
Lire plus18 mai 2022
publication
Resting state EEG power spectrum and functional connectivity in autism: a cross-sectional analysis.
Lire plus01 mai 2022
25 mars 2022
01 mars 2022
publication
Interindividual Differences in Cortical Thickness and Their Genomic Underpinnings in Autism Spectrum Disorder.
Lire plus29 janv. 2022
publication
Phelan-McDermid syndrome: a classification system after 30 years of experience.
Lire plus01 janv. 2022
publication
The Synaptic Gene Study: Design and Methodology to Identify Neurocognitive Markers in Phelan-McDermid Syndrome and NRXN1 Deletions.
Lire plus04 nov. 2021
01 nov. 2021
11 oct. 2021
news
INCEPTION 2021 meeting. A joint event: 5th annual meeting & Symposium « Social Sciences and Biology for Understanding Emerging Diseases »
Lire plus11 oct. 2021
event
INCEPTION 2021 meeting. A joint event: 5th annual meeting & Symposium « Social Sciences and Biology for Understanding Emerging Diseases »
Lire plus19 juil. 2021
publication
Discriminant value of repetitive behaviors in families with autism spectrum disorder and obsessional compulsive disorder probands.
Lire plus01 juin 2021
publication
Genome-wide analysis of gene dosage in 24,092 individuals estimates that 10,000 genes modulate cognitive ability.
Lire plus01 juin 2021
publication
Operative list of genes associated with autism and neurodevelopmental disorders based on database review.
Lire plus14 mai 2021
publication
Imbalanced social-communicative and restricted repetitive behavior subtypes of autism spectrum disorder exhibit different neural circuitry.
Lire plus10 mai 2021
event
Call for abstracts – INCEPTION Symposium: Social Sciences and Biology for Understanding Emerging Diseases
Lire plus03 mars 2021
event
INCEPTION annual meeting 2020 – Integrative Biology, Social and Data Sciences to understand the Emergence of Diseases in Populations and in Individuals: Insights into COVID 19
Lire plus01 mars 2021
publication
Systematic detection of brain protein-coding genes under positive selection during primate evolution and their roles in cognition.
Lire plus07 janv. 2021
publication
Decreased phenol sulfotransferase activities associated with hyperserotonemia in autism spectrum disorders.
Lire plus01 janv. 2021
publication
Testosterone Increases the Emission of Ultrasonic Vocalizations With Different Acoustic Characteristics in Mice.
Lire plus01 janv. 2021
publication
SHANK2 Mutations Result in Dysregulation of the ERK1/2 Pathway in Human Induced Pluripotent Stem Cells-Derived Neurons and Shank2(-/-) Mice.
Lire plus01 janv. 2021
publication
LMT USV Toolbox, a Novel Methodological Approach to Place Mouse Ultrasonic Vocalizations in Their Behavioral Contexts-A Study in Female and Male C57BL/6J Mice and in Shank3 Mutant Females.
Lire plus23 déc. 2020
publication
Mass-spectrometry analysis of the human pineal proteome during night and day and in autism.
Lire plus06 nov. 2020
19 oct. 2020
publication
Mutations associated with neuropsychiatric conditions delineate functional brain connectivity dimensions contributing to autism and schizophrenia.
Lire plus14 oct. 2020
publication
Genome-wide association study reveals new insights into the heritability and genetic correlates of developmental dyslexia.
Lire plus08 oct. 2020
11 sept. 2020
31 août 2020
publication
Dissecting the phenotypic heterogeneity in sensory features in autism spectrum disorder: a factor mixture modelling approach.
Lire plus25 août 2020
publication
Atypical Brain Asymmetry in Autism-A Candidate for Clinically Meaningful Stratification.
Lire plus07 août 2020
publication
A chimeric mouse model to study human iPSC-derived neurons: the case of a truncating SHANK3 mutation.
Lire plus22 juin 2020
11 juin 2020
10 juin 2020
publication
Autism-associated SHANK3 mutations impair maturation of neuromuscular junctions and striated muscles.
Lire plus07 mai 2020
14 avr. 2020
01 janv. 2020
19 juil. 2019
01 juil. 2019
20 mai 2019
publication
Real-time analysis of the behaviour of groups of mice via a depth-sensing camera and machine learning.
Lire plus04 mai 2019
02 mai 2019
publication
Mutations in ACTL6B Cause Neurodevelopmental Deficits and Epilepsy and Lead to Loss of Dendrites in Human Neurons
Lire plus11 févr. 2019
publication
Genome-wide association scan identifies new variants associated with a cognitive predictor of dyslexia
Lire plus25 janv. 2019
21 janv. 2019
publication
Both rare and common genetic variants contribute to autism in the Faroe Islands.
Lire plus09 janv. 2019
publication
Synesthesia & Autistic Features in a Large Family:evidence for spatial imagery as a common factor
Lire plus01 janv. 2019
publication
Morning Plasma Melatonin Differences in Autism: Beyond the Impact of Pineal Gland Volume.
Lire plus07 nov. 2018
04 oct. 2018
publication
Homozygous 2p11.2 deletion supports the implication of ELMOD3 in hearing loss and reveals the potential association of CAPG with ASD/ID etiology
Lire plus03 mai 2018
01 mai 2018
publication
Measuring and Estimating the Effect Sizes of Copy Number Variants on General Intelligence in Community-Based Samples.
Lire plus01 avr. 2018
publication
Cerebellar Volume in Autism: Literature Meta-analysis and Analysis of the Autism Brain Imaging Data Exchange Cohort.
Lire plus12 mars 2018
publication
Genome-wide analyses of self-reported empathy: correlations with autism, schizophrenia, and anorexia nervosa.
Lire plus27 févr. 2018
27 févr. 2018
06 juin 2017
publication
Genome-wide meta-analysis of cognitive empathy: heritability, and correlates with sex, neuropsychiatric conditions and cognition
Lire plus01 janv. 2017
publication
A framework to identify contributing genes in patients with Phelan-McDermid syndrome.
Lire plus19 déc. 2016
14 nov. 2016
14 nov. 2016
28 oct. 2016
program_project
INCEPTION – INstitut Convergences pour l’étude de l’Émergence des Pathologies au Travers des Individus et des populatiONs
Lire plus16 sept. 2016
publication
mouseTube – a database to collaboratively unravel mouse ultrasonic communication
Lire plus05 juin 2016
10 mai 2016
publication
CNTN6 mutations are risk factors for abnormal auditory sensory perception in autism spectrum disorders
Lire plus22 févr. 2016
18 févr. 2016
31 déc. 2015
01 déc. 2015
publication
11q24.2-25 micro-rearrangements in autism spectrum disorders: Relation to brain structures.
Lire plus23 sept. 2015
publication
A de novo microdeletion of SEMA5A in a boy with autism spectrum disorder and intellectual disability
Lire plus20 août 2015
publication
From the genetic architecture to synaptic plasticity in autism spectrum disorder
Lire plus16 juil. 2015
16 juil. 2015
16 juil. 2015
16 juil. 2015
15 juil. 2015
publication
Neuroanatomical Diversity of Corpus Callosum and Brain Volume in Autism: Meta-analysis, Analysis of the Autism Brain Imaging Data Exchange Project, and Simulation.
Lire plus14 mai 2015
25 mars 2015
01 déc. 2014
01 déc. 2014
publication
Vitamin d in the general population of young adults with autism in the faroe islands
Lire plus01 déc. 2014
publication
Influencing circadian and sleep-wake regulation for prevention and intervention in mood and anxiety disorders: what makes a good homeostat?
Lire plus01 sept. 2014
publication
Meta-analysis of SHANK Mutations in Autism Spectrum Disorders: a gradient of severity in cognitive impairments.
Lire plus01 août 2014
publication
Screening, intervention and outcome in autism and other developmental disorders: the role of randomized controlled trials
Lire plus10 juil. 2014
publication
Cntnap4 differentially contributes to GABAergic and dopaminergic synaptic transmission
Lire plus13 mai 2014
publication
Genetic and Environmental Influences on the Visual Word Form and Fusiform Face Areas
Lire plus24 avr. 2014
publication
Convergence of genes and cellular pathways dysregulated in autism spectrum disorders
Lire plus03 mars 2014
publication
Heterogeneous pattern of selective pressure for PRRT2 in human populations, but no association with autism spectrum disorders
Lire plus19 janv. 2014
publication
Common variants in genes of the postsynaptic FMRP signalling pathway are risk factors for autism spectrum disorders
Lire plus03 déc. 2013
07 oct. 2013
28 août 2013
publication
The Autism ProSAP1/Shank2 mouse model displays quantitative and structural abnormalities in ultrasonic vocalisations
Lire plus22 juil. 2013
01 juin 2013
09 juil. 2012
publication
Crystal structure and functional mapping of human ASMT, the last enzyme of the melatonin synthesis pathway
Lire plus27 juin 2012
publication
High-functioning autism spectrum disorder and fragile X syndrome: report of two affected sisters
Lire plus29 avr. 2012
09 févr. 2012
publication
Genetic and functional analyses of SHANK2 mutations suggest a multiple hit model of autism spectrum disorders.
Lire plus06 janv. 2012
publication
Adult male mice emit context-specific ultrasonic vocalizations that are modulated by prior isolation or group rearing environment
Lire plus01 nov. 2011
publication
Genetic variations of the melatonin pathway in patients with attention-deficit and hyperactivity disorders.
Lire plus04 mars 2011
publication
Variations of the candidate SEZ6L2 gene on Chromosome 16p11.2 in patients with autism spectrum disorders and in human populations.
Lire plus20 janv. 2011
publication
Mutation screening of ASMT, the last enzyme of the melatonin pathway, in a large sample of patients with intellectual disability
Lire plus05 janv. 2011
03 août 2010
publication
Production of soluble, active acetyl serotonin methyl transferase in Leishmania tarentolae
Lire plus15 juil. 2010
publication
Identification of pathway-biased and deleterious melatonin receptor mutants in autism spectrum disorders and in the general population
Lire plus06 juil. 2010
publication
Key role for gene dosage and synaptic homeostasis in autism spectrum disorders.
Lire plus05 juil. 2010
publication
Mutation screening of NOS1AP gene in a large sample of psychiatric patients and controls
Lire plus21 juin 2009
01 févr. 2009
23 janv. 2009
01 sept. 2008
01 janv. 2008
17 déc. 2006
publication
Mutations in the gene encoding the synaptic scaffolding protein SHANK3 are associated with autism spectrum disorders
Lire plus01 janv. 2006
publication
Expression and genetic variability of PCDH11Y, a gene specific to Homo sapiens and candidate for susceptibility to psychiatric disorders
Lire plus01 nov. 2003
01 janv. 2003