Výsledky vyhledávání - Thomas Bourgeron
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The Possible Interplay of Synaptic and Clock Genes in Autism Spectrum Disorders Autor Thomas Bourgeron
Vydáno 2007Revisão -
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The Genetics of Autism Spectrum Disorders Autor Guillaume Huguet, Marion Benabou, Thomas Bourgeron
Vydáno 2016Capítulo de Livro -
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SHANK3 mutations identified in autism lead to modification of dendritic spine morphology via an actin-dependent mechanism Autor Christelle M. Durand, Julie Perroy, François Loll, David Perrais, Laurent Fagni, Thomas Bourgeron, Mireille Montcouquiol, Nathalie Sans
Vydáno 2011Artigo -
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Differentiation from human pluripotent stem cells of cortical neurons of the superficial layers amenable to psychiatric disease modeling and high-throughput drug screening Autor Claire Boissart, Aurélie Poulet, Pauline Georges, Hélène Darville, E Julita, Richard Delorme, Thomas Bourgeron, Marc Peschanski, Alexandra Benchoua
Vydáno 2013Artigo -
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Alpha Waves as a Neuromarker of Autism Spectrum Disorder: The Challenge of Reproducibility and Heterogeneity Autor Aline Lefebvre, Richard Delorme, Catherine Delanöe, Frédérique Amsellem, Anita Beggiato, David Germanaud, Thomas Bourgeron, Roberto Toro, Guillaume Dumas
Vydáno 2018Artigo -
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Genome-wide analyses of self-reported empathy: correlations with autism, schizophrenia, and anorexia nervosa Autor Varun Warrier, Roberto Toro, Bhismadev Chakrabarti, Anders D. Børglum, Jakob Grove, David A. Hinds, Thomas Bourgeron, Simon Baron‐Cohen
Vydáno 2018Artigo -
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Genetic and Environmental Influences on the Visual Word Form and Fusiform Face Areas Autor Philippe Pinel, Christophe Lalanne, Thomas Bourgeron, Fabien Fauchereau, Cyril Poupon, Éric Artiges, Denis Le Bihan, Ghislaine Dehaene‐Lambertz, Stanislas Dehaene
Vydáno 2014Artigo
Vyhledávací nástroje:
Související témata
Biology
Autism
Genetics
Psychology
Gene
Medicine
Psychiatry
Neuroscience
Autism spectrum disorder
Developmental psychology
Phenotype
Cognition
Computer science
Internal medicine
Genome
Genotype
Receptor
Mutation
Single-nucleotide polymorphism
Copy-number variation
Cell biology
Clinical psychology
Population
Computational biology
Environmental health
Genome-wide association study
Intellectual disability
Audiology
Endocrinology
Bioinformatics