Opposing brain differences in 16p11.2 deletion and duplication carriers.
Research Articles
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.
Alternative splicing of the pituitary adenylate cyclase-activating polypeptide receptor PAC1: Mechanisms of fine tuning of brain activity.
Brain-reactive lgG correlates with autoimmunity in mothers of a child with an autism spectrum disorder.
Optogenetic stimulation of lateral orbitofronto-striatal pathway suppresses compulsive behaviors.
Stereotypical alterations in cortical patterning are associated with maternal illness-induced placental dysfunction.
Fast association tests for genes with FAST.
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