Autism Rat Models Consortium: Publications
From ARC
Results
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Can mouse imaging studies bring order to autism connectivity chaos?
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De novo genic mutations among a Chinese autism spectrum disorder cohort.
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The central nervous system and the gut microbiome.
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Identification of a RAI1-associated disease network through integration of exome sequencing, transcriptomics, and 3D genomics.
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16p11.2 deletion and duplication: Characterizing neurologic phenotypes in a large clinically ascertained cohort.
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De novo PHIP-predicted deleterious variants are associated with developmental delay, intellectual disability, obesity, and dysmorphic features.
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Developmental timing and critical windows for the treatment of psychiatric disorders.
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Genome-wide prediction and functional characterization of the genetic basis of autism spectrum disorder.
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Multisensory perceptual learning is dependent upon task difficulty.
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TSHZ3 deletion causes an autism syndrome and defects in cortical projection neurons.
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Genetic evidence for elevated pathogenicity of mitochondrial DNA heteroplasmy in autism spectrum disorder.
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Early predictors of impaired social functioning in male rhesus macaques (Macaca mulatta).
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MEF2C regulates cortical inhibitory and excitatory synapses and behaviors relevant to neurodevelopmental disorders.
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Molecular and neural functions of RAI1, the causal gene for Smith-Magenis syndrome.
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Development and psychometric evaluation of the Hansen Research Services Matrix Adaptive Test: A measure of nonverbal IQ.
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Mutations in human accelerated regions disrupt cognition and social behavior.
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Mutations in MBOAT7, encoding lysophosphatidylinositol acyltransferase I, lead to intellectual disability accompanied by epilepsy and autistic features.
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A systematic variant annotation approach for ranking genes associated with autism spectrum disorders.
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Thalamic inhibition: Diverse sources, diverse scales.
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Live interaction distinctively shapes social gaze dynamics in rhesus macaques.
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Stability and change in autism spectrum disorder diagnosis from age 3 to middle childhood in a high-risk sibling cohort.
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Prenatal beta-catenin/BRN2/TBR2 transcriptional cascade regulates adult social and stereotypic behaviors.
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LTD-like molecular pathways in developmental synaptic pruning.
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Greater pupil size in response to emotional faces as an early marker of social-communicative difficulties in infants at high risk for autism.
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Characterizing cognitive control abilities in children with 16p11.2 deletion using adaptive 'video game' technology: A pilot study.
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Normal evoked response to rapid sequences of tactile pulses in autism spectrum disorders.
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The contribution of mosaic variants to autism spectrum disorder.
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Cortical feedback regulates feedforward retinogeniculate refinement.
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Zebrafish: A translational model system for studying neuropsychiatric disorders.
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Dysfunction of sensory oscillations in autism spectrum disorder.
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Characterization of Greater Middle Eastern genetic variation for enhanced disease gene discovery.
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Variants in HNRNPH2 on the X chromosome are associated with a neurodevelopmental disorder in females.
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Maternal immune activation: Implications for neuropsychiatric disorders.
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Loss and gain of MeCP2 cause similar hippocampal circuit dysfunction that is rescued by deep brain stimulation in a Rett syndrome mouse model.
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Emergence of a Homo sapiens-specific gene family and chromosome 16p11.2 CNV susceptibility.
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Subdimensions of social-communication impairment in autism spectrum disorder.
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Autism spectrum disorder, developmental and psychiatric features in 16p11.2 duplication.
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Reciprocal white matter alterations due to 16p11.2 chromosomal deletions versus duplications.
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Multisensory processes: A balancing act across the lifespan.
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Differential sensory fMRI signatures in autism and schizophrenia: Analysis of amplitude and trial-to-trial variability.
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Complementary contributions of striatal projection pathways to action initiation and execution.
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Microglia contribute to circuit defects in Mecp2 null mice independent of microglia-specific loss of Mecp2 expression.
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Neural connectivity evidence for a categorical-dimensional hybrid model of autism spectrum disorder.
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The number of genomic copies at the 16p11.2 locus modulates language, verbal memory, and inhibition.
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Peripheral mechanosensory neuron dysfunction underlies tactile and behavioral deficits in mouse models of ASDs.
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Autosomal-recessive mutations in the tRNA splicing endonuclease subunit TSEN15 cause pontocerebellar hypoplasia and progressive microcephaly.
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Emerging executive functioning and motor development in infants at high and low risk for autism spectrum disorder.
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Ligation-free ribosome profiling of cell type-specific translation in the brain.