Distinct genetic risk based on association of MET in families with co-occurring autism and gastrointestinal conditions.
Research Articles
Mouse neurexin-1alpha deletion causes correlated electrophysiological and behavioral changes consistent with cognitive impairments.
Neuroligin-2 deletion selectively decreases inhibitory synaptic transmission originating from fast-spiking but not from somatostatin-positive interneurons.
Common circuit defect of excitatory-inhibitory balance in mouse models of autism.
Differential gene expression in the developing lateral geniculate nucleus and medial geniculate nucleus reveals novel roles for ZIC4 and FOXP2 in visual and auditory pathway development.
Personal space regulation by the human amygdala.
LRRTM2 functions as a neurexin ligand in promoting excitatory synapse formation.
Neuroligin-1 performs neurexin-dependent and neurexin-independent functions in synapse validation.
Inactivation of primate superior colliculus impairs covert selection of signals for perceptual judgments.
Friendship and internalizing symptoms among children and adolescents with ASD.
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