Multiplex targeted sequencing identifies recurrently mutated genes in autism spectrum disorders.
Research Articles
Sporadic autism exomes reveal a highly interconnected protein network of de novo mutations.
The behavioral phenotype in MeCP2 duplication syndrome: A comparison to idiopathic autism.
Neurocognitive and behavioral outcomes of younger siblings of children with autism spectrum disorder at age five.
Accuracy of phenotyping children with autism based on parent report: What specifically do we gain phenotyping ‘rapidly’?
A common X-linked inborn error of carnitine biosynthesis may be a risk factor for nondysmorphic autism.
Simons Variation in Individuals Project (Simons VIP): A genetics-first approach to studying autism spectrum and related neurodevelopmental disorders.
Neurobiology meets genomic science: The promise of human-induced pluripotent stem cells.
A 600 kb deletion syndrome at 16p11.2 leads to energy imbalance and neuropsychiatric disorders.
Axon selection: from a polarized cytoplasm to a migrating neuron.
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