22q11.2 microdeletions: linking DNA structural variation to brain dysfunction and schizophrenia.
Review and Opinion Articles
Neurobiology of obsessive-compulsive disorder: Insights into neural circuitry dysfunction through mouse genetics.
Synaptic microcircuit dysfunction in genetic models of neurodevelopmental disorders: Focus on MeCP2 and MET.
The conundrums of understanding genetic risks for autism spectrum disorders.
Mechanisms of inhibition within the telencephalon: “where the wild things are.”
Translating glutamate: from pathophysiology to treatment.
Analysis of a purported SHANK3 mutation in a boy with autism: clinical impact of rare variant research in neurodevelopmental disabilities.
Toward fulfilling the promise of molecular medicine in fragile X syndrome.
The von Economo neurons in the frontoinsular and anterior cingulate cortex.
Functional consequences of mutations in postsynaptic scaffolding proteins and relevance to psychiatric disorders.
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