Global transcriptional and translational repression in human-embryonic-stem-cell-derived Rett syndrome neurons.
Research Articles
Reduced neural sensitivity to social stimuli in infants at risk for autism.
Co-expression profiling of autism genes in the mouse brain.
A higher mutational burden in females supports a “female protective model” in neurodevelopmental disorders.
Aberrant white matter microstructure in children with 16p11.2 deletions.
Opposing brain differences in 16p11.2 deletion and duplication carriers.
SFARI Gene 2. A community-driven knowledgebase for the autism spectrum disorders (ASDs).
AMPD2 regulates GTP synthesis and is mutated in a potentially treatable neurodegenerative brainstem disorder.
Whole-exome sequencing identifies mutated C12ORF57 in recessive corpus callosum hypoplasia.
Presynaptic neurexin-3 alternative splicing trans-synaptically controls postsynaptic AMPA receptor trafficking.
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