Mutations in SPATA5 are associated with microcephaly, intellectual disability, seizures, and hearing loss.
Research Articles
Contribution of mGluR5 to pathophysiology in a mouse model of human chromosome 16p11.2 microdeletion.
Cognitive decline preceding the onset of psychosis in patients with 22q11.2 deletion syndrome.
Correspondence between resting-state activity and brain gene expression.
Atypical visual saliency in autism spectrum disorder quantified through model-based eye tracking.
Preliminary evidence of neuropathology in nonhuman primates prenatally exposed to maternal immune activation.
Autism spectrum disorders: From genes to neurobiology.
Systematic discovery of regulated and conserved alternative exons in the mammalian brain reveals nmd modulating chromatin regulators.
Mapping sub-second structure in mouse behavior.
Thalamic control of sensory selection in divided attention.
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