The 16p11.2 deletion mouse model of autism exhibits altered cortical progenitor proliferation and brain cytoarchitecture linked to the ERK MAPK pathway.
Research Articles
Reduced GABAergic action in the autistic brain.
Functional genome-wide siRNA screen identifies KIAA0586 as mutated in Joubert syndrome.
A computational perspective on autism.
Genetic background modulates impaired excitability of inhibitory neurons in a mouse model of Dravet syndrome.
Sex differences in cortical volume and gyrification in autism.
DUF1220 copy number is associated with schizophrenia risk and severity: Implications for understanding autism and schizophrenia as related diseases.
The autism inpatient collection: Methods and preliminary sample description.
UBE3A reinstatement identifies distinct developmental windows in a murine Angelman syndrome model.
Mutations in DDX3X are a common cause of unexplained intellectual disability with gender-specific effects on Wnt signaling.
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