Absence of familiarity triggers hallmarks of autism in mouse model through aberrant tail-of-striatum and prelimbic cortex signaling

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Familial long-read sequencing increases yield of de novo mutations

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Single-Cell Analysis of Foxp1-Driven Mechanisms Essential for Striatal Development

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ASH1L haploinsufficiency results in autistic-like phenotypes in mice and links Eph receptor gene to autism spectrum disorder

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FMRP Control of Ribosome Translocation Promotes Chromatin Modifications and Alternative Splicing of Neuronal Genes Linked to Autism

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Chromatin and gene-regulatory dynamics of the developing human cerebral cortex at single-cell resolution

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Continuous Whole-Body 3D Kinematic Recordings across the Rodent Behavioral Repertoire

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Large neutral amino acid levels tune perinatal neuronal excitability and survival

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Mouse population genetics phenocopies heterogeneity of human Chd8 haploinsufficiency

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Taok1 haploinsufficiency leads to autistic-like behaviors in mice via the dorsal raphe nucleus

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Anterior thalamic dysfunction underlies cognitive deficits in a subset of neuropsychiatric disease models

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Distinct Pathogenic Genes Causing Intellectual Disability and Autism Exhibit a Common Neuronal Network Hyperactivity Phenotype

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Developmental and temporal characteristics of clonal sperm mosaicism

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Monoallelic intragenic POU3F2 variants lead to neurodevelopmental delay and hyperphagic obesity,confirming the gene’s candidacy in 6q16.1 deletions

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Genomic architecture of autism from comprehensive whole-genome sequence annotation

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Oxytocin normalizes altered circuit connectivity for social rescue of the Cntnap2 knockout mouse

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Parallel in vivo analysis of large-effect autism genes implicates cortical neurogenesis and estrogen in risk and resilience

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The Protein Tyrosine Phosphatase Receptor Delta Regulates Developmental Neurogenesis

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A brain atlas of synapse protein lifetime across the mouse lifespan

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Upregulation of SYNGAP1 expression in mice and human neurons by redirecting alternative splicing

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