Search research articles
Contact Us
Filters
Showing results (81-90 of 376) with videos related to
Page
of 38
Sort By:
Journal of Autism and Developmental Disorders
|
March 29, 2011
The effect of an autism-associated polymorphism in the STK39 gene on the autism symptom domains
Rick D Vavolizza, James Schmeidler, Nicolas Ramoz, et al.
Molecular Autism
|
February 22, 2012
Optimizing the phenotyping of rodent ASD models: enrichment analysis of mouse and human neurobiological phenotypes associated with high-risk autism genes identifies morphological, electrophysiological, neurological, and behavioral features
Joseph D Buxbaum, Catalina Betancur, Ozlem Bozdagi, et al.
Journal of Immunology (Baltimore, Md. : 1950)
|
June 1, 2014
A critical role for human caspase-4 in endotoxin sensitivity
Yuji Kajiwara, Tamar Schiff, Georgios Voloudakis, et al.
Archives of Neurology
|
March 11, 2009
PGC-1alpha expression decreases in the Alzheimer disease brain as a function of dementia
Weiping Qin, Vahram Haroutunian, Pavel Katsel, et al.
Autism Research : Official Journal of the International Society for Autism Research
|
April 11, 2009
A large-scale screen for coding variants in SERT/SLC6A4 in autism spectrum disorders
Takeshi Sakurai, Jennifer Reichert, Ellen J Hoffman, et al.
Autism Research : Official Journal of the International Society for Autism Research
|
April 15, 2011
No evidence for IL1RAPL1 involvement in selected high-risk autism pedigrees from the AGRE data set
Kristina Allen-Brady, Guiqing Cai, Dale Cannon, et al.
Nature Genetics
|
November 3, 2025
Liability threshold model-based disease risk prediction based on electronic health record phenotypes
Cue Hyunkyu Lee, Atlas Khan, Chen Wang, et al.
Molecular Autism
|
June 21, 2020
Transcriptional signatures of participant-derived neural progenitor cells and neurons implicate altered Wnt signaling in Phelan-McDermid syndrome and autism
Michael S Breen, Andrew Browne, Gabriel E Hoffman, et al.
The American Journal of Psychiatry
|
June 25, 2025
Significant Role for Maternal Genetic Nurture in the Risk Architecture of Attention Deficit Hyperactivity Disorder
Behrang Mahjani, Adrianna P Kępińska, Shelby Smout, et al.
Journal of Chemical Information and Modeling
|
April 17, 2026
Examining Genetic Variants Associated with FOXP1 Syndrome through Molecular Dynamics of Its DNA-Binding Domain and Self-Organizing Maps
Stefano Motta, Nunzio Perta, Alice Romagnoli, et al.
Page
of 38
Search research articles
Search
Showing results (81-90 of 376) with videos related to
Sort By:
Page
of 38
Journal of Autism and Developmental Disorders
|
March 29, 2011
The effect of an autism-associated polymorphism in the STK39 gene on the autism symptom domains
Rick D Vavolizza, James Schmeidler, Nicolas Ramoz, et al.
Molecular Autism
|
February 22, 2012
Optimizing the phenotyping of rodent ASD models: enrichment analysis of mouse and human neurobiological phenotypes associated with high-risk autism genes identifies morphological, electrophysiological, neurological, and behavioral features
Joseph D Buxbaum, Catalina Betancur, Ozlem Bozdagi, et al.
Journal of Immunology (Baltimore, Md. : 1950)
|
June 1, 2014
A critical role for human caspase-4 in endotoxin sensitivity
Yuji Kajiwara, Tamar Schiff, Georgios Voloudakis, et al.
Archives of Neurology
|
March 11, 2009
PGC-1alpha expression decreases in the Alzheimer disease brain as a function of dementia
Weiping Qin, Vahram Haroutunian, Pavel Katsel, et al.
Autism Research : Official Journal of the International Society for Autism Research
|
April 11, 2009
A large-scale screen for coding variants in SERT/SLC6A4 in autism spectrum disorders
Takeshi Sakurai, Jennifer Reichert, Ellen J Hoffman, et al.
Autism Research : Official Journal of the International Society for Autism Research
|
April 15, 2011
No evidence for IL1RAPL1 involvement in selected high-risk autism pedigrees from the AGRE data set
Kristina Allen-Brady, Guiqing Cai, Dale Cannon, et al.
Nature Genetics
|
November 3, 2025
Liability threshold model-based disease risk prediction based on electronic health record phenotypes
Cue Hyunkyu Lee, Atlas Khan, Chen Wang, et al.
Molecular Autism
|
June 21, 2020
Transcriptional signatures of participant-derived neural progenitor cells and neurons implicate altered Wnt signaling in Phelan-McDermid syndrome and autism
Michael S Breen, Andrew Browne, Gabriel E Hoffman, et al.
The American Journal of Psychiatry
|
June 25, 2025
Significant Role for Maternal Genetic Nurture in the Risk Architecture of Attention Deficit Hyperactivity Disorder
Behrang Mahjani, Adrianna P Kępińska, Shelby Smout, et al.
Journal of Chemical Information and Modeling
|
April 17, 2026
Examining Genetic Variants Associated with FOXP1 Syndrome through Molecular Dynamics of Its DNA-Binding Domain and Self-Organizing Maps
Stefano Motta, Nunzio Perta, Alice Romagnoli, et al.
Page
of 38