Excess of rare, inherited truncating mutations in autism.
Research Articles
FOXG1-dependent dysregulation of GABA/glutamate neuron differentiation in autism spectrum disorders.
Epigenetics of autism-related impairment: Copy number variation and maternal infection.
Regulatory domain or CpG site variation in SLC12A5, encoding the chloride transporter KCC2, in human autism and schizophrenia.
No evidence for association of autism with rare heterozygous point mutations in contactin-associated protein-like 2 (CNTNAP2), or in other contactin-associated proteins or contactins.
Insights into autism spectrum disorder genomic architecture and biology from 71 risk loci.
Symmetrical dose-dependent DNA-methylation profiles in children with deletion or duplication of 7q11.23.
Sex differences in structural organization of motor systems and their dissociable links with repetitive/restricted behaviors in children with autism.
In vivo interrogation of gene function in the mammalian brain using CRISPR-Cas9.
Maternal gesture use and language development in infant siblings of children with autism spectrum disorder.
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