Targeted massively parallel sequencing of autism spectrum disorder-associated genes in a case control cohort reveals rare loss-of-function risk variants.
Protein interaction network of alternatively spliced isoforms from brain links genetic risk factors for autism.
Natural neural projection dynamics underlying social behavior.
Targeting the mitochondrial electron transport chain in autism, a systematic review and synthesis of a novel therapeutic approach.
A common X-linked inborn error of carnitine biosynthesis may be a risk factor for nondysmorphic autism.
A 600 kb deletion syndrome at 16p11.2 leads to energy imbalance and neuropsychiatric disorders.
Cognitive consilience: primate non-primary neuroanatomical circuits underlying cognition.
Disruption at the PTCHD1 Locus on Xp22.11 in Autism spectrum disorder and intellectual disability.
Rare familial 16q21 microdeletions under a linkage peak implicate cadherin 8 (CDH8) in susceptibility to autism and learning disability.
Ten_m3 regulates eye-specific patterning in the mammalian visual pathway and is required for binocular vision.
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