Distinct, dosage-sensitive requirements for the autism-associated factor CHD8 during cortical development.
A recurrent SHANK3 frameshift variant in autism spectrum disorder.
A normative model representing autistic individuals amidst autism spectrum disorders phenotypic heterogeneity.
Recent ultra-rare inherited variants implicate new autism candidate risk genes.
Single-cell transcriptome identifies molecular subtype of autism spectrum disorder impacted by de novo loss-of-function variants regulating glial cells.
Memo1-mediated tiling of radial glial cells facilitates cerebral cortical development.
Optimizing intact skull intrinsic signal imaging for subsequent targeted electrophysiology across mouse visual cortex.
Combined omic analyses reveal novel loss-of-function NLGN3 variants in GnRH deficiency and autism.
Opposite expression patterns of Spry3 and p75NTR in cerebellar vermis suggest a male-specific mechanism of autism pathogenesis.
Imbalance of flight-freeze responses and their cellular correlates in the Nlgn3−/y rat model of autism.
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