Genomic patterns of de novo mutation in simplex autism.
Modeling the interplay between neurons and astrocytes in autism using human induced pluripotent stem cells.
Recurrent de novo mutations in neurodevelopmental disorders: Properties and clinical implications.
Biallelic variants in KIF14 cause intellectual disability with microcephaly.
Impaired perceptual learning in a mouse model of fragile X syndrome is mediated by parvalbumin neuron dysfunction and is reversible.
In the line-up: Deleted genes associated with DiGeorge/22q11.2 deletion syndrome: Are they all suspects?
Viral manipulation of functionally distinct interneurons in mice, non-human primates and humans.
Neuronal inactivity co-opts LTP machinery to drive potassium channel splicing and homeostatic spike widening.
Genome-wide detection of tandem DNA repeats that are expanded in autism.
Heterozygous deletion of SYNGAP enzymatic domains in rats causes selective learning, social and seizure phenotypes.
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