Research Articles

A common X-linked inborn error of carnitine biosynthesis may be a risk factor for nondysmorphic autism.

Simons Variation in Individuals Project (Simons VIP): A genetics-first approach to studying autism spectrum and related neurodevelopmental disorders.

Neurobiology meets genomic science: The promise of human-induced pluripotent stem cells.

A 600 kb deletion syndrome at 16p11.2 leads to energy imbalance and neuropsychiatric disorders.

Axon selection: from a polarized cytoplasm to a migrating neuron.

Differences between neural activity in prefrontal cortex and striatum during learning of novel abstract categories.

Mutations causing syndromic autism define an axis of synaptic pathophysiology.

Mouse model of Timothy syndrome recapitulates triad of autistic traits.

Pathway-specific dopaminergic deficits in a mouse model of Angelman syndrome.

Activity-dependent phosphorylation of GABA A receptors regulates receptor insertion and tonic current.