Reciprocal effects on neurocognitive and metabolic phenotypes in mouse models of 16p11.2 deletion and duplication syndromes.
Research Articles
Variants in HNRNPH2 on the X chromosome are associated with a neurodevelopmental disorder in females.
Jointly reduced inhibition and excitation underlies circuit-wide changes in cortical processing in Rett syndrome.
SHANK3 controls maturation of social reward circuits in the VTA.
Prenatal beta-catenin/BRN2/TBR2 transcriptional cascade regulates adult social and stereotypic behaviors.
Loss of UBE3A from TH-expressing neurons suppresses GABA co-release and enhances VTA-NAc optical self-stimulation.
BONLAC: A combinatorial proteomic technique to measure stimulus-induced translational profiles in brain slices.
Frequency and complexity of de novo structural mutation in autism.
Autosomal-recessive mutations in the tRNA splicing endonuclease subunit TSEN15 cause pontocerebellar hypoplasia and progressive microcephaly.
Stability and change in autism spectrum disorder diagnosis from age 3 to middle childhood in a high-risk sibling cohort.
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