Disrupted neural synchronization in toddlers with autism.
Research Articles
Autism-linked neuroligin-3 R451C mutation differentially alters hippocampal and cortical synaptic function.
An autism-associated point mutation in the neuroligin cytoplasmic tail selectively impairs AMPA receptor-mediated synaptic transmission in hippocampus.
Genetics of autism spectrum disorders.
Rare de novo variants associated with autism implicate a large functional network of genes involved in formation and function of synapses.
Dosage-dependent phenotypes in models of 16p11.2 lesions found in autism.
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.
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