Autism Rat Models Consortium: Publications
From ARC
Results
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Keeping time in the brain: Autism spectrum disorder and audiovisual temporal processing.
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SHANK3 controls maturation of social reward circuits in the VTA.
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Deletion and duplication of 16p11.2 are associated with opposing effects on visual evoked potential amplitude.
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Persistent neuronal UBE3A expression in the suprachiasmatic nucleus of Angelman syndrome model mice.
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Central amygdala somatostatin neurons gate passive and active defensive behaviors.
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SMASH, a fragmentation and sequencing method for genomic copy number analysis.
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Relationship between M100 auditory evoked response and auditory radiation microstructure in 16p11.2 deletion and duplication carriers.
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High frequency stimulation at the subthalamic nucleus suppresses excessive self-grooming in autism-like mouse models.
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Chromosomal contacts connect loci associated with autism, BMI and head circumference phenotypes.
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Neural circuits underlying mother's voice perception predict social communication abilities in children.
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Transcriptome analysis of cortical tissue reveals shared sets of downregulated genes in autism and schizophrenia.
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22q11.2 duplication syndrome: Elevated rate of autism spectrum disorder and need for medical screening.
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Transgenic labeling of parvalbumin-expressing neurons with tdTomato.
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Cellular correlates of selfish spermatogonial selection.
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16p11.2 locus modulates response to satiety before the onset of obesity.
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Auditory evoked M100 response latency is delayed in children with 16p11.2 deletion but not 16p11.2 duplication.
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Genetic risk for autism spectrum disorders and neuropsychiatric variation in the general population.
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Brief report: Further examination of self-injurious behaviors in children and adolescents with autism spectrum disorders.
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Neocortical neurogenesis and the etiology of autism spectrum disorder.
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Maternal loss of UBE3A impairs experience-driven dendritic spine maintenance in the developing visual cortex.
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Neurobiology of social behavior abnormalities in autism and Williams syndrome.
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CNView: a visualization and annotation tool for copy number variation from whole-genome sequencing.
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Putative microcircuit-level substrates for attention are disrupted in mouse models of autism.
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The genetics-driven revival in neuropsychiatric drug development.
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Sex differences in cerebellar synaptic transmission and sex-specific responses to autism-linked GABRB3 mutations in mice.
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Robust classification of protein variation using structural modelling and large-scale data integration.
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Thalamic reticular impairment underlies attention deficit in PTCHD1Y/- mice.
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Frequency and complexity of de novo structural mutation in autism.
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GABAergic neuron-specific loss of UBE3A causes Angelman syndrome-like EEG abnormalities and enhances seizure susceptibility.
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Clinical phenotype of the recurrent 1q21.1 copy-number variant.
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Is there concordance in attitudes and beliefs between parents and scientists about autism spectrum disorder?
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An expanded sequence context model broadly explains variability in polymorphism levels across the human genome.
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No difference in cross-modal attention or sensory discrimination thresholds in autism and matched controls.
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Anatomical abnormalities in autism?
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Feedback modulation of neural network synchrony and seizure susceptibility by Mdm2-p53-Nedd4-2 signaling.
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Unifying views of autism spectrum disorders: A consideration of autoregulatory feedback loops.
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Prenatal neurogenesis in autism spectrum disorders.
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Disruption of POGZ is associated with intellectual disability and autism spectrum disorders.
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Evidence for contribution of common genetic variants within chromosome 8p21.2-8p21.1 to restricted and repetitive behaviors in autism spectrum disorders.
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Altered functional connectivity networks in acallosal and socially impaired BTBR mice.
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Language differences at 12 months in infants who develop autism spectrum disorder.
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Understanding the experience of stigma for parents of children with autism spectrum disorder and the role stigma plays in families' lives.
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Engineering microdeletions and microduplications by targeting segmental duplications with CRISPR.
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Visualization of cortical, subcortical and deep brain neural circuit dynamics during naturalistic mammalian behavior with head-mounted microscopes and chronically implanted lenses.
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Visualizing the origins of selfish de novo mutations in individual seminiferous tubules of human testes.
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Enhanced social attention in female infant siblings at risk for autism.
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The maternal interleukin-17a pathway in mice promotes autism-like phenotypes in offspring.
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Molecular subtyping and improved treatment of neurodevelopmental disease.