Dosage-dependent phenotypes in models of 16p11.2 lesions found in autism.
Research Articles
Gene‐based tests of association
Facilitating the iterative design of informatics tools to advance the science of autism.
Neuroligins/LRRTMs prevent activity- and Ca2+/calmodulin-dependent synapse elimination in cultured neurons.
De novo gene disruptions in children on the autistic spectrum.
Common genetic variants, acting additively, are a major source of risk for autism.
Characteristics and predictive value of blood transcriptome signature in males with autism spectrum disorders.
A multisite study of the clinical diagnosis of different autism spectrum disorders.
Genome-wide transcriptome profiling reveals the functional impact of rare de novo and recurrent CNVs in autism spectrum disorder.
Predicting improvement in social-communication symptoms of autism spectrum disorders using retrospective treatment data.
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