The pathogenic p.N1662D SCN2A mutation reveals an essential molecular interaction for Nav1.2 channel inactivation.
Preprints
Disruption of cell-type-specific molecular programs of medium spiny neurons in autism.
Genomic dissection of sleep archetypes in a large autism cohort.
Cholinergic modulation of dopamine release drives effortful behavior.
Transcriptomic convergence and the female protective effect in autism.
Rare variant analyses in ancestrally diverse cohorts reveal novel ADHD risk genes.
Genetic architecture of postpartum psychosis: From common to rare genetic variation.
Genetic modifiers and ascertainment drive variable expressivity of complex disorders.
The choice-wide behavioral association study: Data-driven identification of interpretable behavioral components.
Proteome-wide assessment of clustering of missense variants in neurodevelopmental disorders versus cancer.
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