Autism Rat Models Consortium: Publications
From ARC
Results
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Interval timing is altered in male Nrxn1+/- mice: A model of autism spectrum disorder.
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Temporal and cell-specific regulation of synaptic homeostasis by the chromatin remodeler Chd1.
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Increasing power in language genetics with Lingo: A web-based digital phenotyping platform.
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The choice-wide behavioral association study: Data-driven identification of interpretable behavioral components.
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Delayed milestones and demographic factors relate to the accuracy of autism screening in females using spoken language.
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Single-cell proteomic landscape of the developing human brain.
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Evaluating Computerised Assessment of Motor Imitation (CAMI) for identifying autism-specific difficulties not observed for attention-deficit hyperactivity disorder or neurotypical development.
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Sex differences and parent-teacher discrepancies in reports of autism traits: Evidence for camouflaging in a school setting.
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Autistic characteristics, cognitive impairment, and sex as predictors of anxiety and depression among autistic youth.
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Transcriptomic convergence and the female protective effect in autism.
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MED13L-related disorder characterized by severe motor speech impairment.
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Cortical versus hippocampal network dysfunction in a human brain assembloid model of epilepsy and intellectual disability.
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Tunable, proteolytic dosage control of CRISPR-Cas systems enables precise gene therapy for dosage sensitive disorders.
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Human-specific gene expansions contribute to brain evolution.
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CRISPR activation for SCN2A-related neurodevelopmental disorders.
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The neural bases of language processing during social and non-social contexts: A fNIRS study of autistic and neurotypical preschool-aged children.
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Multimodal analyses reveal genes driving electrophysiological maturation of neurons in the primate prefrontal cortex.
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Prematurity and genetic liability for autism spectrum disorder.
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Polygenic and developmental profiles of autism differ by age at diagnosis.
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Early developmental origins of cortical disorders modeled in human neural stem cells.
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Decomposition of phenotypic heterogeneity in autism reveals distinct and coherent genetic programs.
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Single-cell analysis of dup15q syndrome reveals developmental and postnatal molecular changes in autism.
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Human-specific gene expansions contribute to brain evolution.
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Cholinergic modulation of dopamine release drives effortful behavior.
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Estimation of direct and indirect polygenic effects and gene-environment interactions using polygenic scores in case-parent trio studies.
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Analysis of variant interactions in families with autism points to genes involved in the development of the central nervous system.
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Noncoding de novo mutations in SCN2A are associated with autism spectrum disorders.
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m6A-mRNA reader YTHDF2 identified as a potential risk gene in autism with disproportionate megalencephaly.
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Quantifying neurobehavioral profiles across neurodevelopmental genetic syndromes and idiopathic neurodevelopmental disorders.
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Mapping the landscape of social behavior.
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Cell-type-specific roles of FOXP1 in the excitatory neuronal lineage during early neocortical murine development.
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SINEUP RNA rescues molecular phenotypes associated with CHD8 suppression in autism spectrum disorder model systems
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Reports of echolalia and related behaviors in autism from parents, teachers, and clinicians: Evidence from the Simon Simplex Collection.
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The Relationships, Employment, Autonomy, and Life Satisfaction (REALS) measures for autistic adults and adults with other intellectual and developmental disabilities: Psychometric testing of the self-report and proxy versions.
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Cell type-specific roles of FOXP1 in the excitatory neuronal lineage during early neocortical murine development.
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Paving the way toward treatment solutions for CTNNB1 syndrome: A patient organization perspective.
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Comparison of autism domains across thirty rare variant genotypes.
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Remote monitoring of social attention in neurogenetic syndromes and idiopathic neurodevelopmental disability.
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De novo missense variants in the PP2A regulatory subunit PPP2R2B in a neurodevelopmental syndrome: Potential links to mitochondrial dynamics and spinocerebellar ataxias.
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Rare variant analyses in ancestrally diverse cohorts reveal novel ADHD risk genes.
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Molecular and cellular dynamics of the developing human neocortex at single-cell resolution.
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Deleterious coding variation associated with autism is consistent across populations, as exemplified by admixed Latin American populations.
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Relationship between service receipt during the COVID-19 pandemic and autistic children's multisystem outcomes and autism severity: A SPARK dataset analysis.
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Children's social preference for teachers versus peers in autism inclusion classrooms: An objective perspective.
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Demographic factors relate to autism diagnostic certainty: Implications for enhancing equitable diagnosis among youth.
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Impact of receiving genetic diagnoses on parents' perceptions of their children with autism and intellectual disability.
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Genetic variants in DDX53 contribute to autism spectrum disorder associated with the Xp22.11 locus.
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Chromosome X-wide common variant association study in autism spectrum disorder.