Virtual International Authority File


Bourgeron, Thomas Library and Archives Canada Library of Congress/NACO RERO - Library Network of Western Switzerland ISNI National Library of France National Library of the Netherlands National Library and Archives of Québec

Thomas Bourgeron Wikidata

Bourgeron, Thomas, 1965-.... Sudoc [ABES], France

VIAF ID: 66796677 (Personal)


Open Section Close Section Preferred Forms





Open Section Close Section 4xx's: Alternate Name Forms (4)

Open Section Close SectionWorks

Title Sources
3 minutes pour comprendre les 50 découvertes fondamentales de la génétique RERO - Library Network of Western Switzerland Sudoc [ABES], France
30-seconds genetics. Library of Congress/NACO National Library of the Netherlands National Library and Archives of Québec
Adult male mice emit context-specific ultrasonic vocalizations that are modulated by prior isolation or group rearing environment. Wikidata
[Alterations in synapsis formation and function in autism disorders]. Wikidata
Analysis of the chromosome X exome in patients with autism spectrum disorders identified novel candidate genes, including TMLHE Wikidata
Annotation and prioritization of non-coding variants in the context of human diseases. Sudoc [ABES], France
Annotation et hiérarchisation de variants non-codants dans le contexte de maladies humaines Sudoc [ABES], France
Autism-associated SHANK3 mutations impair maturation of neuromuscular junctions and striated muscles Wikidata
[Autism: more evidence of a genetic cause]. Wikidata
The Autism ProSAP1/Shank2 mouse model displays quantitative and structural abnormalities in ultrasonic vocalisations. Wikidata
Autistic-like behaviours and hyperactivity in mice lacking ProSAP1/Shank2 Wikidata
Biochemical and genetic study of the impairements of the serotonin-melatonin pathway as suceptibility factors to autism. Sudoc [ABES], France
Brain imaging and study of the functional connectivity by ultrafast Doppler imaging in awake and moving rodents. Sudoc [ABES], France
CNTN6 mutations are risk factors for abnormal auditory sensory perception in autism spectrum disorders Wikidata
Cntnap4 differentially contributes to GABAergic and dopaminergic synaptic transmission Wikidata
Current knowledge on the genetics of autism and propositions for future research. Wikidata
A de novo microdeletion of SEMA5A in a boy with autism spectrum disorder and intellectual disability. Wikidata
Development of an autism severity score for mice using Nlgn4 null mutants as a construct-valid model of heritable monogenic autism. Wikidata
Disentangling the myriad genomics of complex disorders, specifically focusing on autism, epilepsy, and schizophrenia. Wikidata
Dynamics in enzymatic protein complexes offer a novel principle for the regulation of melatonin synthesis in the human pineal gland Wikidata
The emerging role of SHANK genes in neuropsychiatric disorders. Wikidata
Étude biochimique et génétique des anomalies de la voie sérotonine-mélatonine comme facteurs de vulnérabilité à lʼautisme Sudoc [ABES], France
Etude du gène CADPS dans la vulnérabilité aux formes à début précoce de troubles bipolaires Sudoc [ABES], France
Etudes des mécanismes à l'origine de l'excès de garçons dans la déficience intellectuelle et les troubles du spectre autistique Sudoc [ABES], France
Exploration de deux processus associés à l'autisme : la synaptogénèse et la signalisation de la mélatonine Sudoc [ABES], France
Fragile X syndrome and autism at the intersection of genetic and neural networks. Wikidata
Functional analysis of the CADPS gene for early-onset form of bipolar disorder vulnerability. Sudoc [ABES], France
Functional impact of global rare copy number variation in autism spectrum disorders Wikidata
Gene sequence, localization, and evolutionary conservation of DAZLA, a candidate male sterility gene. Wikidata
Genetic markers in psychiatric genetics. Wikidata
Genetic studies of synaptic proteins in autism : implication of SHANK3. Sudoc [ABES], France
Genetic variants of FOXP2 and KIAA0319/TTRAP/THEM2 locus are associated with altered brain activation in distinct language-related regions. Wikidata
The genetics and neurobiology of ESSENCE: The third Birgit Olsson lecture Wikidata
[Genetics of autism: from genome scans to candidate genes]. Wikidata
La génétique de l'autisme... : un entretien avec Thomas Bourgeron RERO - Library Network of Western Switzerland Sudoc [ABES], France Library and Archives Canada National Library of France
Génétique en trente secondes National Library and Archives of Québec
Génétique etbusiness : défendons la iberté de critique ! Wikidata
A genome-wide scan for common alleles affecting risk for autism Wikidata
Genome-wide scan for genes involved in bipolar affective disorder in 70 European families ascertained through a bipolar type I early-onset proband: supportive evidence for linkage at 3p14 Wikidata
Genomic architecture of human neuroanatomical diversity. Wikidata
Heritability Estimation in High-dimensional Mixed Models : Theory and Applications. Sudoc [ABES], France
A high frequency of Y chromosome deletions in males with nonidiopathic infertility Wikidata
Identification de gènes de prédisposition à l'autisme et la schizophrénie Sudoc [ABES], France
Identification of the human KIF13A gene homologous to Drosophila kinesin-73 and candidate for schizophrenia Sudoc [ABES], France Wikidata
Imagerie cérébrale et étude de la connectivité fonctionnelle par échographie Doppler ultrarapide chez le petit animal éveillé et en mouvement Sudoc [ABES], France
Implementation of high-throughput sequencing for the identification of the molecular basis of intellectual disability. Sudoc [ABES], France
Individual common variants exert weak effects on the risk for autism spectrum disorders Wikidata
Lack of replication of previous autism spectrum disorder GWAS hits in European populations. Wikidata
Mapping autism risk loci using genetic linkage and chromosomal rearrangements. Wikidata
Meta-analysis of SHANK Mutations in Autism Spectrum Disorders: a gradient of severity in cognitive impairments Wikidata
Mitochondrial DNA inheritance in patients with deleted mtDNA. Wikidata
Mitochondrial function and male infertility. Wikidata
Mutation screening of ASMT, the last enzyme of the melatonin pathway, in a large sample of patients with intellectual disability Wikidata
Mutations of the X-linked genes encoding neuroligins NLGN3 and NLGN4 are associated with autism Wikidata
Neuroanatomical Diversity of Corpus Callosum and Brain Volume in Autism: Meta-analysis, Analysis of the Autism Brain Imaging Data Exchange Project, and Simulation. Wikidata
Neurobiology of autism gene products: towards pathogenesis and drug targets. Wikidata
New prospects in autism, anglais Sudoc [ABES], France
No human tryptophan hydroxylase-2 gene R441H mutation in a large cohort of psychiatric patients and control subjects. Wikidata
Planète autisme Sudoc [ABES], France National Library of France
The possible interplay of synaptic and clock genes in autism spectrum disorders. Sudoc [ABES], France Wikidata
Progress toward treatments for synaptic defects in autism. Wikidata
Qu'est-ce que l'autisme ? Sudoc [ABES], France National Library of France
Recording Mouse Ultrasonic Vocalizations to Evaluate Social Communication. Wikidata
Screening, intervention and outcome in autism and other developmental disorders: the role of randomized controlled trials. Wikidata
Searching for ways out of the autism maze: genetic, epigenetic and environmental clues Wikidata
Sequencing ASMT identifies rare mutations in Chinese Han patients with autism Wikidata
The serotonin-N-acetylserotonin-melatonin pathway as a biomarker for autism spectrum disorders. Wikidata
SHANK2, a novel gene involved in the susceptibility of autism spectrum disorders. Sudoc [ABES], France Wikidata
SHANK2 : un nouveau gène impliqué dans la vulnérabilité des troubles du spectre autistique Sudoc [ABES], France
Significant correlation between a set of genetic polymorphisms and a functional brain network revealed by feature selection and sparse Partial Least Squares. Wikidata
Social communication in mice--are there optimal cage conditions? Wikidata
Support for the association between the rare functional variant I425V of the serotonin transporter gene and susceptibility to obsessive compulsive disorder Wikidata
Three-dimensional Quantification of Dendritic Spines from Pyramidal Neurons Derived from Human Induced Pluripotent Stem Cells. Wikidata
Transduction of the human gene FAM8A1 by endogenous retrovirus during primate evolution. Wikidata
Vitamin d in the general population of young adults with autism in the faroe islands. Wikidata
[Y chromosome and spermatogenesis] Wikidata
Y chromosome haplogroups in autistic subjects Wikidata

Open Section Close Section Selected Co-authors

Open Section Close Section Countries and Regions of Publication (4)

Open Section Close Section Publication Statistics

Open Section Close Section Selected Publishers (9)

Open Section Close Section About

Open Section Close Section History of VIAF ID:66796677 (12)