Mouse models of MeCP2 disorders share gene expression changes in the cerebellum and hypothalamus.
Characterization of a family with rare deletions in CNTNAP5 and DOCK4 suggests novel risk loci for autism and dyslexia.
Networks of neuronal genes affected by common and rare variants in autism spectrum disorders.
Pathway-specific dopaminergic deficits in a mouse model of Angelman syndrome.
Maternal loss of Ube3a produces an excitatory/inhibitory imbalance through neuron type-specific synaptic defects.
Exome sequencing can improve diagnosis and alter patient management.
Evolutionarily assembled cis-regulatory module at a human ciliopathy locus.
Mutations in BCKD-kinase lead to a potentially treatable form of autism with epilepsy.
Using whole-exome sequencing to identify inherited causes of autism.
Synapse adhesion: A dynamic equilibrium conferring stability and flexibility.
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