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Matthew W State

Showing results (71-80 of 123) with videos related to

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Molecular Autism|March 8, 2014
DAWN: a framework to identify autism genes and subnetworks using gene expression and geneticsLi Liu, Jing Lei, Stephan J Sanders, et al.
Neuron|October 16, 2018
Neonatal Tbr1 Dosage Controls Cortical Layer 6 ConnectivitySiavash Fazel Darbandi, Sarah E Robinson Schwartz, Qihao Qi, et al.
European Journal of Human Genetics : EJHG|May 1, 2014
Homozygous loss of DIAPH1 is a novel cause of microcephaly in humansA Gulhan Ercan-Sencicek, Samira Jambi, Daniel Franjic, et al.
Biorxiv : the Preprint Server for Biology|December 16, 2024
Convergence of autism proteins at the ciliumElina Kostyanovskaya, Micaela C Lasser, Belinda Wang, et al.
American Journal of Human Genetics|January 9, 2008
Molecular cytogenetic analysis and resequencing of contactin associated protein-like 2 in autism spectrum disordersBetul Bakkaloglu, Brian J O'Roak, Angeliki Louvi, et al.
Molecular Autism|May 27, 2014
Rare deleterious mutations of the gene EFR3A in autism spectrum disordersAbha R Gupta, Michelle Pirruccello, Feng Cheng, et al.
Human Molecular Genetics|August 26, 2011
Use of array CGH to detect exonic copy number variants throughout the genome in autism families detects a novel deletion in TMLHEPatricia B S Celestino-Soper, Chad A Shaw, Stephan J Sanders, et al.
American Journal of Medical Genetics. Part A|October 7, 2008
Molecular characterization of a patient with 3p deletion syndrome and a review of the literatureThomas V Fernandez, I J García-González, Christopher E Mason, et al.
Neuron|May 5, 2017
De Novo Coding Variants Are Strongly Associated with Tourette DisorderA Jeremy Willsey, Thomas V Fernandez, Dongmei Yu, et al.
Nature Communications|December 6, 2023
Rare X-linked variants carry predominantly male risk in autism, Tourette syndrome, and ADHDSheng Wang, Belinda Wang, Vanessa Drury, et al.
Pageof 13

Showing results (71-80 of 123) with videos related to

Sort By:
Pageof 13
Molecular Autism|March 8, 2014
DAWN: a framework to identify autism genes and subnetworks using gene expression and geneticsLi Liu, Jing Lei, Stephan J Sanders, et al.
Neuron|October 16, 2018
Neonatal Tbr1 Dosage Controls Cortical Layer 6 ConnectivitySiavash Fazel Darbandi, Sarah E Robinson Schwartz, Qihao Qi, et al.
European Journal of Human Genetics : EJHG|May 1, 2014
Homozygous loss of DIAPH1 is a novel cause of microcephaly in humansA Gulhan Ercan-Sencicek, Samira Jambi, Daniel Franjic, et al.
Biorxiv : the Preprint Server for Biology|December 16, 2024
Convergence of autism proteins at the ciliumElina Kostyanovskaya, Micaela C Lasser, Belinda Wang, et al.
American Journal of Human Genetics|January 9, 2008
Molecular cytogenetic analysis and resequencing of contactin associated protein-like 2 in autism spectrum disordersBetul Bakkaloglu, Brian J O'Roak, Angeliki Louvi, et al.
Molecular Autism|May 27, 2014
Rare deleterious mutations of the gene EFR3A in autism spectrum disordersAbha R Gupta, Michelle Pirruccello, Feng Cheng, et al.
Human Molecular Genetics|August 26, 2011
Use of array CGH to detect exonic copy number variants throughout the genome in autism families detects a novel deletion in TMLHEPatricia B S Celestino-Soper, Chad A Shaw, Stephan J Sanders, et al.
American Journal of Medical Genetics. Part A|October 7, 2008
Molecular characterization of a patient with 3p deletion syndrome and a review of the literatureThomas V Fernandez, I J García-González, Christopher E Mason, et al.
Neuron|May 5, 2017
De Novo Coding Variants Are Strongly Associated with Tourette DisorderA Jeremy Willsey, Thomas V Fernandez, Dongmei Yu, et al.
Nature Communications|December 6, 2023
Rare X-linked variants carry predominantly male risk in autism, Tourette syndrome, and ADHDSheng Wang, Belinda Wang, Vanessa Drury, et al.
Pageof 13