Subventricular zone cytoarchitecture changes in autism.
Research Articles
Biallelic truncating mutations in FMN2, encoding the actin-regulatory protein formin 2, cause nonsyndromic autosomal-recessive intellectual disability.
Cryptic and complex chromosomal aberrations in early-onset neuropsychiatric disorders.
Facial emotion recognition in agenesis of the corpus callosum.
A novel ribosomopathy caused by dysfunction of RPL10 disrupts neurodevelopment and causes X-linked microcephaly in humans.
Maturation of cortical circuits requires semaphorin 7A.
Dosage changes of a segment at 17p13.1 lead to intellectual disability and microcephaly as a result of complex genetic interaction of multiple genes.
Functional recovery with recombinant human IGF1 treatment in a mouse model of Rett Syndrome.
Protein interaction network of alternatively spliced isoforms from brain links genetic risk factors for autism.
Loss of Tet enzymes compromises proper differentiation of embryonic stem cells.
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