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S Abrahams

Showing results (91-100 of 109) with videos related to

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Journal of Neurology|July 2, 2010
Right hemisphere dysfunction and emotional processing in ALS: an fMRI studyA Palmieri, M Naccarato, S Abrahams, et al.
The New England Journal of Medicine|November 7, 2008
A functional genetic link between distinct developmental language disordersSonja C Vernes, Dianne F Newbury, Brett S Abrahams, et al.
Epilepsia|September 12, 2021
Soticlestat, a novel cholesterol 24-hydroxylase inhibitor, reduces seizures and premature death in Dravet syndrome miceNicole A Hawkins, Manuel Jurado, Tyler T Thaxton, et al.
Plos One|June 29, 2016
A Common CYFIP1 Variant at the 15q11.2 Disease Locus Is Associated with Structural Variation at the Language-Related Left Supramarginal GyrusYoung Jae Woo, Tao Wang, Tulio Guadalupe, et al.
Science Translational Medicine|November 5, 2010
Altered functional connectivity in frontal lobe circuits is associated with variation in the autism risk gene CNTNAP2Ashley A Scott-Van Zeeland, Brett S Abrahams, Ana I Alvarez-Retuerto, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|February 15, 2013
The disruption of Celf6, a gene identified by translational profiling of serotonergic neurons, results in autism-related behaviorsJoseph D Dougherty, Susan E Maloney, David F Wozniak, et al.
Cell|October 4, 2011
Absence of CNTNAP2 leads to epilepsy, neuronal migration abnormalities, and core autism-related deficitsOlga Peñagarikano, Brett S Abrahams, Edward I Herman, et al.
Cell|March 24, 2020
Aralar Sequesters GABA into Hyperactive Mitochondria, Causing Social Behavior DeficitsAlexandros K Kanellopoulos, Vittoria Mariano, Marco Spinazzi, et al.
American Journal of Human Genetics|January 9, 2008
Linkage, association, and gene-expression analyses identify CNTNAP2 as an autism-susceptibility geneMaricela Alarcón, Brett S Abrahams, Jennifer L Stone, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|January 22, 2008
Initial association of NR2E1 with bipolar disorder and identification of candidate mutations in bipolar disorder, schizophrenia, and aggression through resequencingRavinesh A Kumar, Kevin A McGhee, Stephen Leach, et al.
Pageof 11

Showing results (91-100 of 109) with videos related to

Sort By:
Pageof 11
Journal of Neurology|July 2, 2010
Right hemisphere dysfunction and emotional processing in ALS: an fMRI studyA Palmieri, M Naccarato, S Abrahams, et al.
The New England Journal of Medicine|November 7, 2008
A functional genetic link between distinct developmental language disordersSonja C Vernes, Dianne F Newbury, Brett S Abrahams, et al.
Epilepsia|September 12, 2021
Soticlestat, a novel cholesterol 24-hydroxylase inhibitor, reduces seizures and premature death in Dravet syndrome miceNicole A Hawkins, Manuel Jurado, Tyler T Thaxton, et al.
Plos One|June 29, 2016
A Common CYFIP1 Variant at the 15q11.2 Disease Locus Is Associated with Structural Variation at the Language-Related Left Supramarginal GyrusYoung Jae Woo, Tao Wang, Tulio Guadalupe, et al.
Science Translational Medicine|November 5, 2010
Altered functional connectivity in frontal lobe circuits is associated with variation in the autism risk gene CNTNAP2Ashley A Scott-Van Zeeland, Brett S Abrahams, Ana I Alvarez-Retuerto, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|February 15, 2013
The disruption of Celf6, a gene identified by translational profiling of serotonergic neurons, results in autism-related behaviorsJoseph D Dougherty, Susan E Maloney, David F Wozniak, et al.
Cell|October 4, 2011
Absence of CNTNAP2 leads to epilepsy, neuronal migration abnormalities, and core autism-related deficitsOlga Peñagarikano, Brett S Abrahams, Edward I Herman, et al.
Cell|March 24, 2020
Aralar Sequesters GABA into Hyperactive Mitochondria, Causing Social Behavior DeficitsAlexandros K Kanellopoulos, Vittoria Mariano, Marco Spinazzi, et al.
American Journal of Human Genetics|January 9, 2008
Linkage, association, and gene-expression analyses identify CNTNAP2 as an autism-susceptibility geneMaricela Alarcón, Brett S Abrahams, Jennifer L Stone, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|January 22, 2008
Initial association of NR2E1 with bipolar disorder and identification of candidate mutations in bipolar disorder, schizophrenia, and aggression through resequencingRavinesh A Kumar, Kevin A McGhee, Stephen Leach, et al.
Pageof 11