White matter microstructure and atypical visual orienting in 7-month-olds at risk for autism.
Repetitive behavior in 12-month-olds later classified with autism spectrum disorder.
Genome sequencing identifies multiple deleterious variants in autism patients with more severe phenotypes.
Calculating the effects of autism risk gene variants on dysfunction of biological processes identifies clinically-useful information.
Diminished respiratory sinus arrhythmia response in infants later diagnosed with autism spectrum disorder.
Male-specific deficits in natural reward learning in a mouse model of neurodevelopmental disorders.
De novo rates and selection of large copy number variation.
Sporadic autism exomes reveal a highly interconnected protein network of de novo mutations.
Denovo-db: A compendium of human de novo variants.
Association of rare missense variants in the second intracellular loop of NaV1.7 sodium channels with familial autism.
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