Disruptive variants of CSDE1 associate with autism and interfere with neuronal development and synaptic transmission.
Research Articles
Aberrant somatosensory processing and connectivity in mice lacking Engrailed-2.
The knockout of Synapsin II in mice impairs social behavior and functional connectivity generating an ASD-like phenotype.
A GluN2B mutation identified in autism prevents NMDA receptor trafficking and interferes with dendrite growth.
Systematic phenomics analysis of ASD-associated genes reveals shared functions and parallel networks underlying reversible impairments in habituation learning.
Pathogenicity and functional impact of non-frameshifting insertion/deletion variation in the human genome.
Sensitivity and specificity of early screening for autism.
Developmental trajectories of neuroanatomical alterations associated with the 16p11.2 copy number variations.
Mania- and anxiety-like behavior and impaired maternal care in female diacylglycerol kinase eta and iota double knockout mice.
Altered neural connectivity in females, but not males with autism: Preliminary evidence for the female protective effect from a quality-controlled diffusion tensor imaging study.
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