Vascular contributions to 16p11.2 deletion autism syndrome modeled in mice.
Research Articles
Evaluating heterogeneity in ASD symptomatology, cognitive ability, and adaptive functioning among 16p11.2 CNV carriers.
Cortical neurons derived from human pluripotent stem cells lacking FMRP display altered spontaneous firing patterns.
DeepND: Deep multitask learning of gene risk for comorbid neurodevelopmental disorders.
Parallel RNA and DNA analysis after deep-sequencing (PRDD-seq) reveals cell type specific lineage patterns in human brain.
A large population-based investigation into the genetics of susceptibility to gastrointestinal infections and the link between gastrointestinal infections and mental illness.
Neuronal inactivity co-opts LTP machinery to drive potassium channel splicing and homeostatic spike widening.
Identification of amygdala-expressed genes associated with autism spectrum disorder.
Gene discoveries in autism are biased towards comorbidity with intellectual disability.
Saccade dysmetria indicates attenuated visual exploration in autism spectrum disorder.
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