Network topologies and convergent aetiologies arising from deletions and duplications observed in individuals with autism.
SFARI Gene: An evolving database for the autism research community.
Impaired fixation to eyes following amygdala damage arises from abnormal bottom-up attention.
SFARI genes and where to find them; classification modelling to identify genes associated with autism spectrum disorder from RNA-seq data.
Chromatin remodeler Arid1a regulates subplate neuron identity and wiring of cortical connectivity.
Patterns of delay in early gross motor and expressive language milestone attainment in probands with genetic conditions versus idiopathic ASD from SFARI registries.
SFARI genes and where to find them; modelling autism spectrum disorder specific gene expression dysregulation with RNA-seq data.
The Genotype and Phenotypes in Families (GPF) platform manages the large and complex data at SFARI.
Opposing effects on Nav1.2 function underlie differences between SCN2A variants observed in individuals with autism spectrum disorder or infantile seizures.
The autism-associated gene Scn2a contributes to dendritic excitability and synaptic function in the prefrontal cortex.
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