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Thomas Bourgeron

Showing results (71-80 of 166) with videos related to

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American Journal of Medical Genetics. Part A|September 4, 2015
11q24.2-25 micro-rearrangements in autism spectrum disorders: Relation to brain structuresAnna Maruani, Guillaume Huguet, Anita Beggiato, et al.
Journal of Applied Genetics|October 5, 2018
Homozygous 2p11.2 deletion supports the implication of ELMOD3 in hearing loss and reveals the potential association of CAPG with ASD/ID etiologySaida Lahbib, Claire S Leblond, Mariem Hamza, et al.
Proceedings of the National Academy of Sciences of the United States of America|January 30, 2008
Reduced social interaction and ultrasonic communication in a mouse model of monogenic heritable autismStephane Jamain, Konstantin Radyushkin, Kurt Hammerschmidt, et al.
Autism Research : Official Journal of the International Society for Autism Research|July 19, 2021
Discriminant value of repetitive behaviors in families with autism spectrum disorder and obsessional compulsive disorder probandsAline Lefebvre, Alicia Cohen, Anna Maruani, et al.
Journal of Pineal Research|July 11, 2012
Crystal structure and functional mapping of human ASMT, the last enzyme of the melatonin synthesis pathwayHany Goubran Botros, Pierre Legrand, Cecile Pagan, et al.
Neuroimage|July 12, 2012
Significant correlation between a set of genetic polymorphisms and a functional brain network revealed by feature selection and sparse Partial Least SquaresEdith Le Floch, Vincent Guillemot, Vincent Frouin, et al.
European Journal of Medical Genetics|February 23, 2023
Dissecting the 22q13 region to explore the genetic and phenotypic diversity of patients with Phelan-McDermid syndromeAline Vitrac, Claire S Leblond, Thomas Rolland, et al.
Annual Review of Genetics|November 25, 2024
A Genetic Bridge Between Medicine and Neurodiversity for AutismClaire S Leblond, Thomas Rolland, Eli Barthome, et al.
BMC Medical Genetics|July 7, 2010
Mutation screening of NOS1AP gene in a large sample of psychiatric patients and controlsRichard Delorme, Catalina Betancur, Isabelle Scheid, et al.
BMJ Mental Health|November 28, 2024
Conceptual framework for data harmonisation in mental health using the International Classification of Functioning, Disability and Health: an example with the R2D2-MH consortiumMelissa H Black, Jan Buitelaar, Tony Charman, et al.
Pageof 17

Showing results (71-80 of 166) with videos related to

Sort By:
Pageof 17
American Journal of Medical Genetics. Part A|September 4, 2015
11q24.2-25 micro-rearrangements in autism spectrum disorders: Relation to brain structuresAnna Maruani, Guillaume Huguet, Anita Beggiato, et al.
Journal of Applied Genetics|October 5, 2018
Homozygous 2p11.2 deletion supports the implication of ELMOD3 in hearing loss and reveals the potential association of CAPG with ASD/ID etiologySaida Lahbib, Claire S Leblond, Mariem Hamza, et al.
Proceedings of the National Academy of Sciences of the United States of America|January 30, 2008
Reduced social interaction and ultrasonic communication in a mouse model of monogenic heritable autismStephane Jamain, Konstantin Radyushkin, Kurt Hammerschmidt, et al.
Autism Research : Official Journal of the International Society for Autism Research|July 19, 2021
Discriminant value of repetitive behaviors in families with autism spectrum disorder and obsessional compulsive disorder probandsAline Lefebvre, Alicia Cohen, Anna Maruani, et al.
Journal of Pineal Research|July 11, 2012
Crystal structure and functional mapping of human ASMT, the last enzyme of the melatonin synthesis pathwayHany Goubran Botros, Pierre Legrand, Cecile Pagan, et al.
Neuroimage|July 12, 2012
Significant correlation between a set of genetic polymorphisms and a functional brain network revealed by feature selection and sparse Partial Least SquaresEdith Le Floch, Vincent Guillemot, Vincent Frouin, et al.
European Journal of Medical Genetics|February 23, 2023
Dissecting the 22q13 region to explore the genetic and phenotypic diversity of patients with Phelan-McDermid syndromeAline Vitrac, Claire S Leblond, Thomas Rolland, et al.
Annual Review of Genetics|November 25, 2024
A Genetic Bridge Between Medicine and Neurodiversity for AutismClaire S Leblond, Thomas Rolland, Eli Barthome, et al.
BMC Medical Genetics|July 7, 2010
Mutation screening of NOS1AP gene in a large sample of psychiatric patients and controlsRichard Delorme, Catalina Betancur, Isabelle Scheid, et al.
BMJ Mental Health|November 28, 2024
Conceptual framework for data harmonisation in mental health using the International Classification of Functioning, Disability and Health: an example with the R2D2-MH consortiumMelissa H Black, Jan Buitelaar, Tony Charman, et al.
Pageof 17