Bourgeron, Thomas
Bourgeron, Thomas, 1965-....
![Sudoc [ABES], France](/viaf/images/flags/SUDOC.png "Sudoc [ABES], France")
Thomas Bourgeron
VIAF ID: 66796677 ( Personal )
Permalink: http://viaf.org/viaf/66796677
Preferred Forms
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200 _ | ‡a Bourgeron ‡b Thomas
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100 1 _
‡a
Bourgeron, Thomas
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100 1 _ ‡a Bourgeron, Thomas
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100 1 _ ‡a Bourgeron, Thomas
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100 1 _
‡a
Bourgeron, Thomas
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100 1 _ ‡a Bourgeron, Thomas
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100 1 _ ‡a Bourgeron, Thomas
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100 1 _
‡a
Bourgeron, Thomas,
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1965-....
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100 0 _
‡a
Thomas Bourgeron
4xx's: Alternate Name Forms (4)
Works
| Title | Sources |
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| 3 minutes pour comprendre les 50 découvertes fondamentales de la génétique |
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| 30-seconds genetics. |
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| Adult male mice emit context-specific ultrasonic vocalizations that are modulated by prior isolation or group rearing environment |
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| [Alterations in synapsis formation and function in autism disorders]. |
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| Analysis of the chromosome X exome in patients with autism spectrum disorders identified novel candidate genes, including TMLHE |
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| Annotation and prioritization of non-coding variants in the context of human diseases. |
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| Annotation et hiérarchisation de variants non-codants dans le contexte de maladies humaines |
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| Autism-associated SHANK3 mutations impair maturation of neuromuscular junctions and striated muscles |
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| [Autism: more evidence of a genetic cause]. |
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| The Autism ProSAP1/Shank2 mouse model displays quantitative and structural abnormalities in ultrasonic vocalisations. |
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| Autistic-like behaviours and hyperactivity in mice lacking ProSAP1/Shank2 |
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| Biochemical and genetic study of the impairements of the serotonin-melatonin pathway as suceptibility factors to autism. |
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| Brain imaging and study of the functional connectivity by ultrafast Doppler imaging in awake and moving rodents. |
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| CNTN6 mutations are risk factors for abnormal auditory sensory perception in autism spectrum disorders |
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| Cntnap4 differentially contributes to GABAergic and dopaminergic synaptic transmission |
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| Convergence of genes and cellular pathways dysregulated in autism spectrum disorders |
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| Copy number variations in autism spectrum disorders : identification and characterization of new candidate genes ( SEZ6L2 ans CNTN3-6) |
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| Current knowledge on the genetics of autism and propositions for future research |
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| A de novo microdeletion of SEMA5A in a boy with autism spectrum disorder and intellectual disability. |
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| Decreased phenol sulfotransferase activities associated with hyperserotonemia in autism spectrum disorders |
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| Development of an autism severity score for mice using Nlgn4 null mutants as a construct-valid model of heritable monogenic autism. |
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| Disentangling the myriad genomics of complex disorders, specifically focusing on autism, epilepsy, and schizophrenia |
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| Dynamics in enzymatic protein complexes offer a novel principle for the regulation of melatonin synthesis in the human pineal gland |
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| Étude biochimique et génétique des anomalies de la voie sérotonine-mélatonine comme facteurs de vulnérabilité à lʼautisme |
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| Etude du gène CADPS dans la vulnérabilité aux formes à début précoce de troubles bipolaires |
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| Etudes des mécanismes à l'origine de l'excès de garçons dans la déficience intellectuelle et les troubles du spectre autistique |
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| Exploration de deux processus associés à l'autisme : la synaptogénèse et la signalisation de la mélatonine |
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| Fragile X syndrome and autism at the intersection of genetic and neural networks |
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| From the genetic architecture to synaptic plasticity in autism spectrum disorder |
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| Functional analysis of the CADPS gene for early-onset form of bipolar disorder vulnerability. |
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| Gene sequence, localization, and evolutionary conservation of DAZLA, a candidate male sterility gene |
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| Genetic analysis of generalized epilepsies in a sudanese cohort and functional validation in the worm C. elegans |
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| Genetic and functional abnormalities of the melatonin biosynthesis pathway in patients with bipolar disorder. |
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| Genetic markers in psychiatric genetics |
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| Genetic studies of synaptic proteins in autism : implication of SHANK3. |
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| The genetics and neurobiology of ESSENCE: The third Birgit Olsson lecture |
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| [Genetics of autism: from genome scans to candidate genes]. |
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| La génétique de l'autisme... : un entretien avec Thomas Bourgeron |
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| Génétique en trente secondes |
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| Génétique etbusiness : défendons la iberté de critique ! |
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| A genome-wide scan for common alleles affecting risk for autism |
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| 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 |
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| Heritability Estimation in High-dimensional Mixed Models : Theory and Applications. |
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| A high frequency of Y chromosome deletions in males with nonidiopathic infertility |
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| Identification of genes that predispose to autism and/or schizophrenia. |
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| Imagerie cérébrale et étude de la connectivité fonctionnelle par échographie Doppler ultrarapide chez le petit animal éveillé et en mouvement |
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| Implementation of high-throughput sequencing for the identification of the molecular basis of intellectual disability. |
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| In vitro and in vivo phenotypic analysis of de novo truncating mutations in SHANK3. |
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| Individual common variants exert weak effects on the risk for autism spectrum disorders |
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| Innate : how the wiring of our brains shapes who we are |
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| Inné : génotype, développement, comportement |
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| Investigation of two ASD-associated processes : synaptogenesis and melatonin pathway. |
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| Le jour où... : le déclic qui a tout changé |
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| Linkage and association of the glutamate receptor 6 gene with autism |
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| The meaning of significant mean group differences for biomarker discovery |
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| Meta-analysis of SHANK Mutations in Autism Spectrum Disorders: a gradient of severity in cognitive impairments |
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| Mitochondrial DNA inheritance in patients with deleted mtDNA. |
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| Mutation screening of ASMT, the last enzyme of the melatonin pathway, in a large sample of patients with intellectual disability |
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| Neuroanatomical Diversity of Corpus Callosum and Brain Volume in Autism: Meta-analysis, Analysis of the Autism Brain Imaging Data Exchange Project, and Simulation |
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| Neurobiology of autism gene products: towards pathogenesis and drug targets. |
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| New prospects in autism, anglais |
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| No human tryptophan hydroxylase-2 gene R441H mutation in a large cohort of psychiatric patients and control subjects |
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| Planète autisme |
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| Progress toward treatments for synaptic defects in autism |
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| Qu'est-ce que l'autisme ? |
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| Recording Mouse Ultrasonic Vocalizations to Evaluate Social Communication |
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| Screening, intervention and outcome in autism and other developmental disorders: the role of randomized controlled trials. |
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| Searching for ways out of the autism maze: genetic, epigenetic and environmental clues |
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| Sequencing ASMT identifies rare mutations in Chinese Han patients with autism |
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| The serotonin-N-acetylserotonin-melatonin pathway as a biomarker for autism spectrum disorders |
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| SHANK2, a novel gene involved in the susceptibility of autism spectrum disorders. |
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| SHANK2 : un nouveau gène impliqué dans la vulnérabilité des troubles du spectre autistique |
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| Significant correlation between a set of genetic polymorphisms and a functional brain network revealed by feature selection and sparse Partial Least Squares. |
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| Social communication in mice--are there optimal cage conditions? |
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| Support for the association between the rare functional variant I425V of the serotonin transporter gene and susceptibility to obsessive compulsive disorder |
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| Transduction of the human gene FAM8A1 by endogenous retrovirus during primate evolution. |
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| Vitamin d in the general population of young adults with autism in the faroe islands |
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| [Y chromosome and spermatogenesis] |
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| Y chromosome haplogroups in autistic subjects |
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