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Thomas Bourgeron

Showing results (151-160 of 166) with videos related to

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Biorxiv : the Preprint Server for Biology|December 11, 2023
A foundational atlas of autism protein interactions reveals molecular convergenceBelinda Wang, Rasika Vartak, Yefim Zaltsman, et al.
Molecular Psychiatry|October 15, 2020
Genome-wide association study reveals new insights into the heritability and genetic correlates of developmental dyslexiaAlessandro Gialluisi, Till F M Andlauer, Nazanin Mirza-Schreiber, et al.
NPJ Genomic Medicine|July 10, 2019
Erratum: Author Correction: A framework to identify contributing genes in patients with Phelan-McDermid syndromeAnne-Claude Tabet, Thomas Rolland, Marie Ducloy, et al.
Plos Genetics|February 21, 2012
Genetic and functional analyses of SHANK2 mutations suggest a multiple hit model of autism spectrum disordersClaire S Leblond, Jutta Heinrich, Richard Delorme, et al.
Plos Genetics|September 5, 2014
Meta-analysis of SHANK Mutations in Autism Spectrum Disorders: a gradient of severity in cognitive impairmentsClaire S Leblond, Caroline Nava, Anne Polge, et al.
NPJ Genomic Medicine|December 22, 2017
A framework to identify contributing genes in patients with Phelan-McDermid syndromeAnne-Claude Tabet, Thomas Rolland, Marie Ducloy, et al.
Molecular Autism|June 27, 2017
The EU-AIMS Longitudinal European Autism Project (LEAP): design and methodologies to identify and validate stratification biomarkers for autism spectrum disordersEva Loth, Tony Charman, Luke Mason, et al.
Molecular Autism|June 27, 2017
The EU-AIMS Longitudinal European Autism Project (LEAP): clinical characterisationTony Charman, Eva Loth, Julian Tillmann, et al.
American Journal of Human Genetics|April 30, 2019
Mutations in ACTL6B Cause Neurodevelopmental Deficits and Epilepsy and Lead to Loss of Dendrites in Human NeuronsScott Bell, Justine Rousseau, Huashan Peng, et al.
Proceedings of the National Academy of Sciences of the United States of America|August 23, 2022
Genome-wide analyses of individual differences in quantitatively assessed reading- and language-related skills in up to 34,000 peopleElse Eising, Nazanin Mirza-Schreiber, Eveline L de Zeeuw, et al.
Pageof 17

Showing results (151-160 of 166) with videos related to

Sort By:
Pageof 17
Biorxiv : the Preprint Server for Biology|December 11, 2023
A foundational atlas of autism protein interactions reveals molecular convergenceBelinda Wang, Rasika Vartak, Yefim Zaltsman, et al.
Molecular Psychiatry|October 15, 2020
Genome-wide association study reveals new insights into the heritability and genetic correlates of developmental dyslexiaAlessandro Gialluisi, Till F M Andlauer, Nazanin Mirza-Schreiber, et al.
NPJ Genomic Medicine|July 10, 2019
Erratum: Author Correction: A framework to identify contributing genes in patients with Phelan-McDermid syndromeAnne-Claude Tabet, Thomas Rolland, Marie Ducloy, et al.
Plos Genetics|February 21, 2012
Genetic and functional analyses of SHANK2 mutations suggest a multiple hit model of autism spectrum disordersClaire S Leblond, Jutta Heinrich, Richard Delorme, et al.
Plos Genetics|September 5, 2014
Meta-analysis of SHANK Mutations in Autism Spectrum Disorders: a gradient of severity in cognitive impairmentsClaire S Leblond, Caroline Nava, Anne Polge, et al.
NPJ Genomic Medicine|December 22, 2017
A framework to identify contributing genes in patients with Phelan-McDermid syndromeAnne-Claude Tabet, Thomas Rolland, Marie Ducloy, et al.
Molecular Autism|June 27, 2017
The EU-AIMS Longitudinal European Autism Project (LEAP): design and methodologies to identify and validate stratification biomarkers for autism spectrum disordersEva Loth, Tony Charman, Luke Mason, et al.
Molecular Autism|June 27, 2017
The EU-AIMS Longitudinal European Autism Project (LEAP): clinical characterisationTony Charman, Eva Loth, Julian Tillmann, et al.
American Journal of Human Genetics|April 30, 2019
Mutations in ACTL6B Cause Neurodevelopmental Deficits and Epilepsy and Lead to Loss of Dendrites in Human NeuronsScott Bell, Justine Rousseau, Huashan Peng, et al.
Proceedings of the National Academy of Sciences of the United States of America|August 23, 2022
Genome-wide analyses of individual differences in quantitatively assessed reading- and language-related skills in up to 34,000 peopleElse Eising, Nazanin Mirza-Schreiber, Eveline L de Zeeuw, et al.
Pageof 17