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Matthew W State

Showing results (51-60 of 123) with videos related to

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Nature Reviews. Disease Primers|January 18, 2020
Autism spectrum disorderCatherine Lord, Traolach S Brugha, Tony Charman, et al.
Nature Reviews. Disease Primers|April 28, 2026
Author Correction: Autism spectrum disorderCatherine Lord, Traolach S Brugha, Tony Charman, et al.
Cell Reports|June 8, 2024
Five autism-associated transcriptional regulators target shared loci proximal to brain-expressed genesSiavash Fazel Darbandi, Joon-Yong An, Kenneth Lim, et al.
Neurogenetics|March 7, 2008
Novel NTRK1 mutations cause hereditary sensory and autonomic neuropathy type IV: demonstration of a founder mutation in the Turkish populationBeyhan Tüysüz, Fatih Bayrakli, Michael L DiLuna, et al.
American Journal of Medical Genetics. Part A|October 31, 2009
The syndrome of pachygyria, mental retardation, and arachnoid cysts maps to 11p15Kaya Bilguvar, Ali K Ozturk, Fatih Bayrakli, et al.
Cell Reports|April 16, 2020
Enhancing WNT Signaling Restores Cortical Neuronal Spine Maturation and Synaptogenesis in Tbr1 MutantsSiavash Fazel Darbandi, Sarah E Robinson Schwartz, Emily Ling-Lin Pai, et al.
American Journal of Human Genetics|June 26, 2012
Genome-wide transcriptome profiling reveals the functional impact of rare de novo and recurrent CNVs in autism spectrum disordersRui Luo, Stephan J Sanders, Yuan Tian, et al.
Neurogenetics|January 19, 2010
Novel VLDLR microdeletion identified in two Turkish siblings with pachygyria and pontocerebellar atrophyLuis E Kolb, Zulfikar Arlier, Cengiz Yalcinkaya, et al.
Brain & Development|December 20, 2011
Searching for Potocki-Lupski syndrome phenotype: a patient with language impairment and no autismA Gulhan Ercan-Sencicek, Nicole R Davis Wright, Stephen J Frost, et al.
Plos Genetics|August 23, 2013
Integrated model of de novo and inherited genetic variants yields greater power to identify risk genesXin He, Stephan J Sanders, Li Liu, et al.
Pageof 13

Showing results (51-60 of 123) with videos related to

Sort By:
Pageof 13
Nature Reviews. Disease Primers|January 18, 2020
Autism spectrum disorderCatherine Lord, Traolach S Brugha, Tony Charman, et al.
Nature Reviews. Disease Primers|April 28, 2026
Author Correction: Autism spectrum disorderCatherine Lord, Traolach S Brugha, Tony Charman, et al.
Cell Reports|June 8, 2024
Five autism-associated transcriptional regulators target shared loci proximal to brain-expressed genesSiavash Fazel Darbandi, Joon-Yong An, Kenneth Lim, et al.
Neurogenetics|March 7, 2008
Novel NTRK1 mutations cause hereditary sensory and autonomic neuropathy type IV: demonstration of a founder mutation in the Turkish populationBeyhan Tüysüz, Fatih Bayrakli, Michael L DiLuna, et al.
American Journal of Medical Genetics. Part A|October 31, 2009
The syndrome of pachygyria, mental retardation, and arachnoid cysts maps to 11p15Kaya Bilguvar, Ali K Ozturk, Fatih Bayrakli, et al.
Cell Reports|April 16, 2020
Enhancing WNT Signaling Restores Cortical Neuronal Spine Maturation and Synaptogenesis in Tbr1 MutantsSiavash Fazel Darbandi, Sarah E Robinson Schwartz, Emily Ling-Lin Pai, et al.
American Journal of Human Genetics|June 26, 2012
Genome-wide transcriptome profiling reveals the functional impact of rare de novo and recurrent CNVs in autism spectrum disordersRui Luo, Stephan J Sanders, Yuan Tian, et al.
Neurogenetics|January 19, 2010
Novel VLDLR microdeletion identified in two Turkish siblings with pachygyria and pontocerebellar atrophyLuis E Kolb, Zulfikar Arlier, Cengiz Yalcinkaya, et al.
Brain & Development|December 20, 2011
Searching for Potocki-Lupski syndrome phenotype: a patient with language impairment and no autismA Gulhan Ercan-Sencicek, Nicole R Davis Wright, Stephen J Frost, et al.
Plos Genetics|August 23, 2013
Integrated model of de novo and inherited genetic variants yields greater power to identify risk genesXin He, Stephan J Sanders, Li Liu, et al.
Pageof 13