Autism Rat Models Consortium: Publications
From ARC
Results
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The AAA(+) ATPase thorase regulates AMPA receptor-dependent synaptic plasticity and behavior.
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Circuit-specific intracortical hyperconnectivity in mice with deletion of the autism-associated Met receptor tyrosine kinase.
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Next-generation sequencing strategies enable routine detection of balanced chromosome rearrangements for clinical diagnostics and genetic research.
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Mechanisms of inhibition within the telencephalon: “where the wild things are.”
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The von Economo neurons in the frontoinsular and anterior cingulate cortex.
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Analysis of a purported SHANK3 mutation in a boy with autism: clinical impact of rare variant research in neurodevelopmental disabilities.
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Using induced pluripotent stem cells to investigate cardiac phenotypes in Timothy syndrome.
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Early developmental regression in autism spectrum disorder: evidence from an international multiplex sample.
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Model' or 'tool'? New definitions for translational research.
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Intra-family phenotypic heterogeneity of 16p11.2 deletion carriers in a three-generation Chinese family.
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EEG complexity as a biomarker for autism spectrum disorder risk.
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Toward fulfilling the promise of molecular medicine in fragile X syndrome.
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Impaired theory of mind for moral judgment in high-functioning autism.
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Cognitive dysfunction and prefrontal synaptic abnormalities in a mouse model of fragile X syndrome.
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Dissociable brain mechanisms for processing social exclusion and rule violation.
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Rare familial 16q21 microdeletions under a linkage peak implicate cadherin 8 (CDH8) in susceptibility to autism and learning disability.
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People watching: visual, motor, and social processes in the perception of human movement.
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Facilitating the iterative design of informatics tools to advance the science of autism.
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A presynaptic role for FMRP during protein synthesis-dependent long-term plasticity in Aplysia.
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Haploinsufficiency of the autism-associated SHANK3 gene leads to deficits in synaptic function, social interaction, and social communication.
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A homozygous mutation in the tight-junction protein JAM3 causes hemorrhagic destruction of the brain, subependymal calcification, and congenital cataracts.
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Neural signatures of autism.
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Face processing abilities in relatives of individuals with ASD.
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Prenatal polycyclic aromatic hydrocarbon exposure leads to behavioral deficits and downregulation of receptor tyrosine kinase, MET.
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Hypersensitivity to mGluR5 and ERK1/2 leads to excessive protein synthesis in the hippocampus of a mouse model of fragile X syndrome.
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Deletion 17q12 is a recurrent copy number variant that confers high risk of autism and schizophrenia.
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De novo rates and selection of large copy number variation.
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Allelic diversity in human developmental neurogenetics: insights into biology and disease.
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The Simons Simplex Collection: a resource for identification of autism genetic risk factors.
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I can see you better if I can hear you coming: action-consistent sounds facilitate the visual detection of human gait.
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The origins of social impairments in autism spectrum disorder: studies of infants at risk.
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Impaired fixation to eyes following amygdala damage arises from abnormal bottom-up attention.
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Disruption at the PTCHD1 Locus on Xp22.11 in Autism spectrum disorder and intellectual disability.
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High-density SNP association study and copy number variation analysis of the AUTS1 and AUTS5 loci implicate the IMMP2L-DOCK4 gene region in autism susceptibility.
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Does bilateral damage to the human amygdala produce autistic symptoms?
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Activation of mGluR5 induces rapid and long-lasting protein kinase D phosphorylation in hippocampal neurons.
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Distinct subclasses of medium spiny neurons differentially regulate striatal motor behaviors.
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Characterization of a family with rare deletions in CNTNAP5 and DOCK4 suggests novel risk loci for autism and dyslexia.
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Microglial activation and increased microglial density observed in the dorsolateral prefrontal cortex in autism.
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Centrosome motility is essential for initial axon formation in the neocortex.
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Comparison of visual sensitivity to human and object motion in autism spectrum disorder.
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MicroRNAs in psychiatric and neurodevelopmental disorders.
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Deletions of NRXN1 (neurexin-1) predispose to a wide spectrum of developmental disorders.
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22q11.2 microdeletions: linking DNA structural variation to brain dysfunction and schizophrenia.
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The von Economo neurons in frontoinsular and anterior cingulate cortex in great apes and humans.
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Neurexins physically and functionally interact with GABAA receptors.
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Live face-to-face interaction during fMRI : A new tool for social cognitive neuroscience.
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Fragile X mental retardation protein is required for synapse elimination by the activity-dependent transcription factor MEF2.