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BMC Neuroscience
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September 16, 2021
NRXN1α<sup>+/-</sup> is associated with increased excitability in ASD iPSC-derived neurons
Sahar Avazzadeh, Leo R Quinlan, Jamie Reilly, et al.
Cell
|
September 1, 2023
Bridge-building between communities: Imagining the future of biomedical autism research
Síofra Heraty, Alexandra Lautarescu, David Belton, et al.
Translational Psychiatry
|
June 24, 2020
The role of rare compound heterozygous events in autism spectrum disorder
Bochao Danae Lin, Fabrice Colas, Isaac J Nijman, et al.
Molecular Autism
|
November 14, 2014
The Autism Simplex Collection: an international, expertly phenotyped autism sample for genetic and phenotypic analyses
Joseph D Buxbaum, Nadia Bolshakova, Jessica M Brownfeld, et al.
Nature Reviews. Genetics
|
April 23, 2020
A framework for an evidence-based gene list relevant to autism spectrum disorder
Christian P Schaaf, Catalina Betancur, Ryan K C Yuen, et al.
Journal of Medical Genetics
|
June 14, 2012
Intragenic CAMTA1 rearrangements cause non-progressive congenital ataxia with or without intellectual disability
Julien Thevenon, Estelle Lopez, Boris Keren, et al.
Autism : the International Journal of Research and Practice
|
April 29, 2015
Use of early intervention for young children with autism spectrum disorder across Europe
Erica Salomone, Štěpánka Beranová, Frédérique Bonnet-Brilhault, et al.
The American Journal of Psychiatry
|
January 1, 2021
A Genetics-First Approach to Dissecting the Heterogeneity of Autism: Phenotypic Comparison of Autism Risk Copy Number Variants
Samuel J R A Chawner, Joanne L Doherty, Richard J L Anney, et al.
Cell
|
January 26, 2020
Large-Scale Exome Sequencing Study Implicates Both Developmental and Functional Changes in the Neurobiology of Autism
F Kyle Satterstrom, Jack A Kosmicki, Jiebiao Wang, et al.
Scientific Data
|
March 15, 2017
Enhancing studies of the connectome in autism using the autism brain imaging data exchange II
Adriana Di Martino, David O'Connor, Bosi Chen, et al.
Page
of 14
Search research articles
Search
Showing results (111-120 of 140) with videos related to
Sort By:
Page
of 14
BMC Neuroscience
|
September 16, 2021
NRXN1α<sup>+/-</sup> is associated with increased excitability in ASD iPSC-derived neurons
Sahar Avazzadeh, Leo R Quinlan, Jamie Reilly, et al.
Cell
|
September 1, 2023
Bridge-building between communities: Imagining the future of biomedical autism research
Síofra Heraty, Alexandra Lautarescu, David Belton, et al.
Translational Psychiatry
|
June 24, 2020
The role of rare compound heterozygous events in autism spectrum disorder
Bochao Danae Lin, Fabrice Colas, Isaac J Nijman, et al.
Molecular Autism
|
November 14, 2014
The Autism Simplex Collection: an international, expertly phenotyped autism sample for genetic and phenotypic analyses
Joseph D Buxbaum, Nadia Bolshakova, Jessica M Brownfeld, et al.
Nature Reviews. Genetics
|
April 23, 2020
A framework for an evidence-based gene list relevant to autism spectrum disorder
Christian P Schaaf, Catalina Betancur, Ryan K C Yuen, et al.
Journal of Medical Genetics
|
June 14, 2012
Intragenic CAMTA1 rearrangements cause non-progressive congenital ataxia with or without intellectual disability
Julien Thevenon, Estelle Lopez, Boris Keren, et al.
Autism : the International Journal of Research and Practice
|
April 29, 2015
Use of early intervention for young children with autism spectrum disorder across Europe
Erica Salomone, Štěpánka Beranová, Frédérique Bonnet-Brilhault, et al.
The American Journal of Psychiatry
|
January 1, 2021
A Genetics-First Approach to Dissecting the Heterogeneity of Autism: Phenotypic Comparison of Autism Risk Copy Number Variants
Samuel J R A Chawner, Joanne L Doherty, Richard J L Anney, et al.
Cell
|
January 26, 2020
Large-Scale Exome Sequencing Study Implicates Both Developmental and Functional Changes in the Neurobiology of Autism
F Kyle Satterstrom, Jack A Kosmicki, Jiebiao Wang, et al.
Scientific Data
|
March 15, 2017
Enhancing studies of the connectome in autism using the autism brain imaging data exchange II
Adriana Di Martino, David O'Connor, Bosi Chen, et al.
Page
of 14