De novo PHIP-predicted deleterious variants are associated with developmental delay, intellectual disability, obesity, and dysmorphic features.
Research Articles
De novo loss of function mutations in KIAA2022 are associated with epilepsy and neurodevelopmental delay in females.
Thalamic reticular impairment underlies attention deficit in PTCHD1Y/- mice.
The role of mGluR copy number variation in genetic and environmental forms of syndromic autism spectrum disorder.
22q11.2 duplication syndrome: Elevated rate of autism spectrum disorder and need for medical screening.
Layer specific and general requirements for ERK/MAPK signaling in the developing neocortex.
Brain responses to biological motion predict treatment outcome in young children with autism.
Central amygdala somatostatin neurons gate passive and active defensive behaviors.
A search for blood biomarkers for autism: Peptoids.
Mice with Shank3 mutations associated with ASD and schizophrenia display both shared and distinct defects.
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