Denovo-db: A compendium of human de novo variants.
Association of rare missense variants in the second intracellular loop of NaV1.7 sodium channels with familial autism.
Genome sequencing of autism-affected families reveals disruption of putative noncoding regulatory DNA.
Maternal modifiers and parent-of-origin bias of the autism-associated 16p11.2 CNV.
Closed-loop and activity-guided optogenetic control.
Natural neural projection dynamics underlying social behavior.
Rare-variant extensions of the transmission disequilibrium test: Application to autism exome sequence data.
The contribution of de novo coding mutations to autism spectrum disorder.
Recurrent de novo mutations implicate novel genes underlying simplex autism risk.
AMPD2 regulates GTP synthesis and is mutated in a potentially treatable neurodegenerative brainstem disorder.
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