Autism Rat Models Consortium: Publications
From ARC
Results
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Development of the emotion dysregulation inventory: A PROMIS®ing method for creating sensitive and unbiased questionnaires for autism spectrum disorder.
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Behavioral symptoms of reported abuse in children and adolescents with autism spectrum disorder in inpatient settings.
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Characterization of medication use in a multicenter sample of pediatric inpatients with autism spectrum disorder.
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Predictors of inpatient psychiatric hospitalization for children and adolescents with autism spectrum disorder.
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The severe end of the spectrum: Insights and opportunities from the Autism Inpatient Collection (AIC).
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Verbal ability and psychiatric symptoms in clinically referred inpatient and outpatient youth with ASD.
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Sleep problems and their relationship to maladaptive behavior severity in psychiatrically hospitalized children with autism spectrum disorder (ASD).
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Risk factors for self-injurious behavior in an inpatient psychiatric sample of children with autism spectrum disorder: A naturalistic observation study.
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Behavioral outcomes of specialized psychiatric hospitalization in the autism inpatient collection (AIC): A multisite comparison.
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Mouse Cntnap2 and human CNTNAP2 ASD alleles cell autonomously regulate PV+ cortical interneurons.
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Talking about death or suicide: Prevalence and clinical correlates in youth with autism spectrum disorder in the psychiatric inpatient setting.
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Lost in translation: Traversing the complex path from genomics to therapeutics in autism spectrum disorder.
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A reference haplotype panel for genome-wide imputation of short tandem repeats.
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p38α MAPK signaling drives pharmacologically reversible brain and gastrointestinal phenotypes in the SERT Ala56 mouse.
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Calculating the effects of autism risk gene variants on dysfunction of biological processes identifies clinically-useful information.
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Language delay aggregates in toddler siblings of children with autism spectrum disorder.
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Gastrointestinal and psychiatric symptoms among children and adolescents with autism spectrum disorder.
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Early adolescent Rai1 reactivation reverses transcriptional and social interaction deficits in a mouse model of Smith-Magenis syndrome.
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Functional equivalence of genome sequencing analysis pipelines enables harmonized variant calling across human genetics projects.
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Impaired perceptual learning in a mouse model of fragile X syndrome is mediated by parvalbumin neuron dysfunction and is reversible.
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Biallelic variants in VARS in a family with two siblings with intellectual disability and microcephaly: Case report and review of the literature.
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Maturational trajectories of local and long-range functional connectivity in autism during face processing.
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Identifying specific prefrontal neurons that contribute to autism-associated abnormalities in physiology and social behavior.
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TiSAn: Estimating tissue specific effects of coding and non-coding variants.
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Adult Ube3a gene reinstatement restores the electrophysiological deficits of prefrontal cortex layer 5 neurons in a mouse model of Angelman syndrome.
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Characteristics of sleep in children with autism spectrum disorders from the Simons Simplex Collection.
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Insistence on sameness and broader autism phenotype in simplex families with autism spectrum disorder.
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Modified penetrance of coding variants by cis-regulatory variation contributes to disease risk.
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5-hydroxymethylcytosine alterations in the human postmortem brains of autism spectrum disorder.
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Deficits in mesolimbic reward pathway underlie social interaction impairments in children with autism.
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Zebrafish models of neurodevelopmental disorders: Past, present, and future.
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MAP1B mutations cause intellectual disability and extensive white matter deficit.
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Smartphone measures of day-to-day behavior changes in children with autism.
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Quantifying the effects of 16p11.2 copy number variants on brain structure: A multisite genetic-first study.
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Increased axonal bouton stability during learning in the mouse model of MECP2 duplication syndrome.
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5-HT release in nucleus accumbens rescues social deficits in mouse autism model.
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Autism-like phenotype and risk gene mRNA deadenylation by CPEB4 mis-splicing.
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Connectivity dynamics in typical development and its relationship to autistic traits and autism spectrum disorder.
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Patient-derived iPSCs show premature neural differentiation and neuron type-specific phenotypes relevant to neurodevelopment.
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Radial glial lineage progression and differential intermediate progenitor amplification underlie striatal compartments and circuit organization.
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Luminance changes drive directional startle through a thalamic pathway.
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Pharmacological inhibition of ERK signaling rescues pathophysiology and behavioral phenotype associated with 16p11.2 chromosomal deletion in mice.
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A versatile method for viral transfection of calcium indicators in the neonatal mouse brain.
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Focal cortical anomalies and language impairment in 16p11.2 deletion and duplication syndrome.
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Simple, transparent, and flexible automated quality assessment procedures for ambulatory electrodermal activity data.
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Insights into clonal haematopoiesis from 8,342 mosaic chromosomal alterations.
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An interactome perturbation framework prioritizes damaging missense mutations for developmental disorders.
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Autism-associated 16p11.2 microdeletion impairs prefrontal functional connectivity in mouse and human.