Autism Rat Models Consortium: Publications
From ARC
Results
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A framework for the interpretation of de novo mutation in human disease.
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The transcriptional regulator ADNP links the BAF (SWI/SNF) complexes with autism.
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Opposing brain differences in 16p11.2 deletion and duplication carriers.
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Dysfunctional dopaminergic neurotransmission in asocial BTBR mice.
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Plasma oxytocin concentrations and OXTR polymorphisms predict social impairments in children with and without autism spectrum disorder.
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Microglia function during brain development: New insights from animal models.
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Facial emotion recognition in agenesis of the corpus callosum.
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Testing the accuracy of an observation-based classifier for rapid detection of autism risk.
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CC2D1A regulates human intellectual and social function as well as NF-kappaB signaling homeostasis.
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Violations of personal space by individuals with autism spectrum disorder.
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Longitudinal patterns of repetitive behavior in toddlers with autism.
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No increase in autism associated genetic events in children conceived by assisted reproductive technology.
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Neurons in the human amygdala selective for perceived emotion.
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Optogenetic insights on the relationship between anxiety-related behaviors and social deficits.
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Disruptive CHD8 mutations define a subtype of autism early in development.
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CNTNAP4 differentially contributes to GABAergic and dopaminergic synaptic transmission.
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Beta2-adrenergic receptor agonist ameliorates phenotypes and corrects microRNA-mediated IGF1 deficits in a mouse model of Rett syndrome.
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Functional recovery with recombinant human IGF1 treatment in a mouse model of Rett Syndrome.
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Autism-associated neuroligin-3 mutations commonly impair striatal circuits to boost repetitive behaviors.
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Developmental regression among children with autism spectrum disorders: Onset, duration, and effects on functional outcomes.
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Emotion dysregulation and the core features of autism spectrum disorder.
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Largely typical patterns of resting-state functional connectivity in high-functioning adults with autism
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Natural neural projection dynamics underlying social behavior.
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Unlocking epigenetic codes in neurogenesis.
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A role for dendritic mGluR5-mediated local translation of ARC/ARG3.1 in MEF2-dependent synapse elimination.
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Transcriptional consequences of 16p11.2 deletion and duplication in mouse cortex and multiplex autism families.
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Modest impact on risk for autism spectrum disorder of rare copy number variants at 15q11.2, specifically breakpoints 1 to 2.
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Brief report: Arrested development of audiovisual speech perception in autism spectrum disorders.
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The autism brain imaging data exchange: Towards a large-scale evaluation of the intrinsic brain architecture in autism.
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Internet-based, randomized, controlled trial of omega-3 fatty acids for hyperactivity in autism.
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Snx14 regulates neuronal excitability, promotes synaptic transmission, and is imprinted in the brain of mice.
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Behavioral abnormalities and circuit defects in the basal ganglia of a mouse model of 16p11.2 deletion syndrome.
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The impact of multisensory integration deficits on speech perception in children with autism spectrum disorders.
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Dopaminergic dynamics contributing to social behavior.
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Neurosteroids promote phosphorylation and membrane insertion of extrasynaptic GABAA receptors.
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Fragile X mental retardation protein regulates synaptic and behavioral plasticity to repeated cocaine administration.
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De novo truncating mutations in AHDC1 in individuals with syndromic expressive language delay, hypotonia, and sleep apnea.
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The Rhode Island Consortium for Autism Research and Treatment (RI-CART): A new statewide autism collaborative.
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Aberrant white matter microstructure in children with 16p11.2 deletions.
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Rare deleterious mutations of the gene EFR3A in autism spectrum disorders.
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CLP1 founder mutation links tRNA splicing and maturation to cerebellar development and neurodegeneration.
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The potential of accelerating early detection of autism through content analysis of YouTube videos.
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Circuit-selective striatal synaptic dysfunction in the SAPAP3 knockout mouse model of obsessive-compulsive disorder.
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Loss of Tet enzymes compromises proper differentiation of embryonic stem cells.
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Protein interaction network of alternatively spliced isoforms from brain links genetic risk factors for autism.
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Chromatin regulators, phenotypic robustness, and autism risk.
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Equivalent neural responses in children and adolescents with and without autism during judgments of affect.
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Investigation of maternal genotype effects in autism by genome-wide association.