Thomas Bourgeron - Concepedia

Author

Thomas Bourgeron

Also Known As

Ahmed Bouras, Alzheimer’s Disease Neuroimaging Initiative, Amber Ruigrok, Anita Beggiato, Bourgeron Thomas, Bourgeron, Thibault, Bourgeron, Thomas, Brody, David L., Catalina Betancur , Christian Beckmann

815

Publications

31.4K

Citations

H-Index

267

Concepts

All Affiliations

Institut Pasteur Université Paris Cité Centre National de la Recherche Scientifique Inserm Délégation Paris 7

About

Thomas Bourgeron is an author at Institut Pasteur specializing in medicine, neuroscience, and genetics.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Engineering	6	6	523
2	Health Sciences	6	6	233
3	Arts	4	4	222
4	Education	4	4	91
5	Language Studies	2	2	85

Thomas Bourgeron

158

Publications

20.6K

Citations

H-Index

Page 1

	Year	Citations
Functional impact of global rare copy number variation in autism spectrum disorders Dalila Pinto, Alistair T. Pagnamenta, Lambertus Klei, Nature Autism Spectrum DisordersSyndromic AutismGeneticsPsychiatric GeneticsAutism	2010	2K
Mutations of the X-linked genes encoding neuroligins NLGN3 and NLGN4 are associated with autism Stéphane Jamain, Hélène Quach, Catalina Betancur, Nature Genetics Neurodevelopmental DisordersMolecular NeuroscienceSyndromic AutismGenetic DisorderGenetics	2003	1.8K
Mutations in the gene encoding the synaptic scaffolding protein SHANK3 are associated with autism spectrum disorders Christelle M. Durand, Catalina Betancur, Tobias M. Boeckers, Nature Genetics Neurodevelopmental DisordersSynaptic PlasticityMolecular NeuroscienceAutism Spectrum DisordersSyndromic Autism	2006	1.6K
Convergence of Genes and Cellular Pathways Dysregulated in Autism Spectrum Disorders Dalila Pinto, Elsa Delaby, Daniele Merico, The American Journal of Human Genetics	2014	1K
Mutation of a nuclear succinate dehydrogenase gene results in mitochondrial respiratory chain deficiency Thomas Bourgeron, Pierre Rustin, Dominique Chrétien, Nature Genetics Mitochondrial FunctionBiochemistryNatural SciencesGeneticsMitochondrial Structure	1995	723
Autistic-like behaviours and hyperactivity in mice lacking ProSAP1/Shank2 Michael J. Schmeißer, Elodie Ey, S Wegener, Nature Mice Lacking Prosap1/shank2Behavioral NeuroscienceSyndromic AutismAutismNeuroscience	2012	647
A genome-wide scan for common alleles affecting risk for autism Richard Anney, Lambertus Klei, Dalila Pinto, Human Molecular Genetics	2010	585
Reduced social interaction and ultrasonic communication in a mouse model of monogenic heritable autism Stéphane Jamain, Konstantin Radyushkin, Kurt Hammerschmidt, Proceedings of the National Academy of Sciences GeneticsSocial SciencesSynapse FunctionNeurodiversitySocial Communication Disorder	2008	558
Abnormal melatonin synthesis in autism spectrum disorders Jonas Melke, Hany Goubran Botros, Pauline Chaste, Molecular Psychiatry Syndromic AutismNeuropharmacologyAutismNeuroscienceMedicine	2007	517
Genetic and Functional Analyses of SHANK2 Mutations Suggest a Multiple Hit Model of Autism Spectrum Disorders Claire S. Leblond, Jutta Heinrich, Richard Delorme, PLoS Genetics	2012	437

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