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Matthew W State

Showing results (91-100 of 123) with videos related to

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Nature Neuroscience|March 18, 2018
Publisher Correction: Whole genome sequencing in psychiatric disorders: the WGSPD consortiumStephan J Sanders, Benjamin M Neale, Hailiang Huang, et al.
The New England Journal of Medicine|May 7, 2010
L-histidine decarboxylase and Tourette's syndromeA Gulhan Ercan-Sencicek, Althea A Stillman, Ananda K Ghosh, et al.
Nature|August 24, 2010
Whole-exome sequencing identifies recessive WDR62 mutations in severe brain malformationsKaya Bilgüvar, Ali Kemal Oztürk, Angeliki Louvi, et al.
Nature Neuroscience|November 30, 2017
Whole genome sequencing in psychiatric disorders: the WGSPD consortiumStephan J Sanders, Benjamin M Neale, Hailiang Huang, et al.
Autism Research : Official Journal of the International Society for Autism Research|May 14, 2014
Modest impact on risk for autism spectrum disorder of rare copy number variants at 15q11.2, specifically breakpoints 1 to 2Pauline Chaste, Stephan J Sanders, Kommu N Mohan, et al.
Cell Reports|October 7, 2014
De novo insertions and deletions of predominantly paternal origin are associated with autism spectrum disorderShan Dong, Michael F Walker, Nicholas J Carriero, et al.
Cell Reports|December 20, 2018
De Novo Sequence and Copy Number Variants Are Strongly Associated with Tourette Disorder and Implicate Cell Polarity in PathogenesisSheng Wang, Jeffrey D Mandell, Yogesh Kumar, et al.
Cell Reports|September 27, 2018
De Novo Sequence and Copy Number Variants Are Strongly Associated with Tourette Disorder and Implicate Cell Polarity in PathogenesisSheng Wang, Jeffrey D Mandell, Yogesh Kumar, et al.
Nature Genetics|November 11, 2008
Susceptibility loci for intracranial aneurysm in European and Japanese populationsKaya Bilguvar, Katsuhito Yasuno, Mika Niemelä, et al.
Cell|November 26, 2013
Coexpression networks implicate human midfetal deep cortical projection neurons in the pathogenesis of autismA Jeremy Willsey, Stephan J Sanders, Mingfeng Li, et al.
Pageof 13

Showing results (91-100 of 123) with videos related to

Sort By:
Pageof 13
Nature Neuroscience|March 18, 2018
Publisher Correction: Whole genome sequencing in psychiatric disorders: the WGSPD consortiumStephan J Sanders, Benjamin M Neale, Hailiang Huang, et al.
The New England Journal of Medicine|May 7, 2010
L-histidine decarboxylase and Tourette's syndromeA Gulhan Ercan-Sencicek, Althea A Stillman, Ananda K Ghosh, et al.
Nature|August 24, 2010
Whole-exome sequencing identifies recessive WDR62 mutations in severe brain malformationsKaya Bilgüvar, Ali Kemal Oztürk, Angeliki Louvi, et al.
Nature Neuroscience|November 30, 2017
Whole genome sequencing in psychiatric disorders: the WGSPD consortiumStephan J Sanders, Benjamin M Neale, Hailiang Huang, et al.
Autism Research : Official Journal of the International Society for Autism Research|May 14, 2014
Modest impact on risk for autism spectrum disorder of rare copy number variants at 15q11.2, specifically breakpoints 1 to 2Pauline Chaste, Stephan J Sanders, Kommu N Mohan, et al.
Cell Reports|October 7, 2014
De novo insertions and deletions of predominantly paternal origin are associated with autism spectrum disorderShan Dong, Michael F Walker, Nicholas J Carriero, et al.
Cell Reports|December 20, 2018
De Novo Sequence and Copy Number Variants Are Strongly Associated with Tourette Disorder and Implicate Cell Polarity in PathogenesisSheng Wang, Jeffrey D Mandell, Yogesh Kumar, et al.
Cell Reports|September 27, 2018
De Novo Sequence and Copy Number Variants Are Strongly Associated with Tourette Disorder and Implicate Cell Polarity in PathogenesisSheng Wang, Jeffrey D Mandell, Yogesh Kumar, et al.
Nature Genetics|November 11, 2008
Susceptibility loci for intracranial aneurysm in European and Japanese populationsKaya Bilguvar, Katsuhito Yasuno, Mika Niemelä, et al.
Cell|November 26, 2013
Coexpression networks implicate human midfetal deep cortical projection neurons in the pathogenesis of autismA Jeremy Willsey, Stephan J Sanders, Mingfeng Li, et al.
Pageof 13