Repetitive behavior in 12-month-olds later classified with autism spectrum disorder.
Multiplex targeted sequencing identifies recurrently mutated genes in autism spectrum disorders.
Sporadic autism exomes reveal a highly interconnected protein network of de novo mutations.
Exome sequencing in sporadic autism spectrum disorders identifies severe de novo mutations.
De novo rates and selection of large copy number variation.
Male-specific deficits in natural reward learning in a mouse model of neurodevelopmental disorders.
Diminished respiratory sinus arrhythmia response in infants later diagnosed with autism spectrum disorder.
Calculating the effects of autism risk gene variants on dysfunction of biological processes identifies clinically-useful information.
Genome sequencing identifies multiple deleterious variants in autism patients with more severe phenotypes.
Whole exome sequencing identifies a splicing mutation in NSUN2 as a cause of a Dubowitz-like syndrome.
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