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Richard Delorme

Showing results (211-220 of 225) with videos related to

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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|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.
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.
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.
American Journal of Human Genetics|April 29, 2014
Convergence of genes and cellular pathways dysregulated in autism spectrum disordersDalila Pinto, Elsa Delaby, Daniele Merico, et al.
Human Genetics|October 15, 2011
A novel approach of homozygous haplotype sharing identifies candidate genes in autism spectrum disorderJillian P Casey, Tiago Magalhaes, Judith M Conroy, et al.
Journal of the American Academy of Child and Adolescent Psychiatry|July 27, 2014
Copy number variation in obsessive-compulsive disorder and tourette syndrome: a cross-disorder studyLauren M McGrath, Dongmei Yu, Christian Marshall, et al.
Human Molecular Genetics|July 31, 2012
Individual common variants exert weak effects on the risk for autism spectrum disordersRichard Anney, Lambertus Klei, Dalila Pinto, et al.
Plos Genetics|November 9, 2013
Partitioning the heritability of Tourette syndrome and obsessive compulsive disorder reveals differences in genetic architectureLea K Davis, Dongmei Yu, Clare L Keenan, et al.
The American Journal of Psychiatry|August 27, 2014
Cross-disorder genome-wide analyses suggest a complex genetic relationship between Tourette's syndrome and OCDDongmei Yu, Carol A Mathews, Jeremiah M Scharf, et al.
Pageof 23

Showing results (211-220 of 225) with videos related to

Sort By:
Pageof 23
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|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.
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.
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.
American Journal of Human Genetics|April 29, 2014
Convergence of genes and cellular pathways dysregulated in autism spectrum disordersDalila Pinto, Elsa Delaby, Daniele Merico, et al.
Human Genetics|October 15, 2011
A novel approach of homozygous haplotype sharing identifies candidate genes in autism spectrum disorderJillian P Casey, Tiago Magalhaes, Judith M Conroy, et al.
Journal of the American Academy of Child and Adolescent Psychiatry|July 27, 2014
Copy number variation in obsessive-compulsive disorder and tourette syndrome: a cross-disorder studyLauren M McGrath, Dongmei Yu, Christian Marshall, et al.
Human Molecular Genetics|July 31, 2012
Individual common variants exert weak effects on the risk for autism spectrum disordersRichard Anney, Lambertus Klei, Dalila Pinto, et al.
Plos Genetics|November 9, 2013
Partitioning the heritability of Tourette syndrome and obsessive compulsive disorder reveals differences in genetic architectureLea K Davis, Dongmei Yu, Clare L Keenan, et al.
The American Journal of Psychiatry|August 27, 2014
Cross-disorder genome-wide analyses suggest a complex genetic relationship between Tourette's syndrome and OCDDongmei Yu, Carol A Mathews, Jeremiah M Scharf, et al.
Pageof 23