Compensation between FOXP transcription factors maintains proper striatal function.
Research Articles
Elevated levels of FMRP-target MAP1B impair human and mouse neuronal development and mouse social behaviors via autophagy pathway.
Genetic control of mRNA splicing as a potential mechanism for incomplete penetrance of rare coding variants.
Benchmarking of local genetic correlation estimation methods using summary statistics from genome-wide association studies
Three generation families: Analysis of de novo variants in autism.
Quantitative genome-wide association study of six phenotypic subdomains identifies novel genome-wide significant variants in autism spectrum disorder.
Dissecting autism and schizophrenia through neuroimaging genomics.
Scn2a severe hypomorphic mutation decreases excitatory synaptic input and causes autism-associated behaviors
A genome-wide investigation into parent-of-origin effects in autism spectrum disorder identifies previously associated genes including SHANK3.
Mechanism of KMT5B haploinsufficiency in neurodevelopment in humans and mice.
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