Language impairment and dyslexia genes influence language skills in children with autism spectrum disorders.
Research Articles
CRISPR-CAS9 knockin mice for genome editing and cancer modeling.
Behavioral abnormalities and circuit defects in the basal ganglia of a mouse model of 16p11.2 deletion syndrome.
Intracellular mGluR5 can mediate synaptic plasticity in the hippocampus.
MET receptor tyrosine kinase controls dendritic complexity, spine morphogenesis, and glutamatergic synapse maturation in the hippocampus.
16p11.2 600 kb duplications confer risk for typical and atypical rolandic epilepsy.
EphB receptor forward signaling regulates area-specific reciprocal thalamic and cortical axonpathfinding.
Autism-associated neuroligin-3 mutations commonly impair striatal circuits to boost repetitive behaviors.
CLP1 founder mutation links tRNA splicing and maturation to cerebellar development and neurodegeneration.
Genes for endosomal NHE6 and NHE9 are misregulated in autism brains.
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