Autism Rat Models Consortium: Publications
From ARC
Results
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Oligogenic effects of 16p11.2 copy number variation on craniofacial development.
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ST-Steiner: A spatio-temporal gene discovery algorithm.
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Enhanced population coding for rewarded choices in the medial frontal cortex of the mouse.
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FMRP binding to a ranked subset of long genes is revealed by coupled CLIP and TRAP in specific neuronal cell types.
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Sensorimotor cortical oscillations during movement preparation in 16p11.2 deletion carriers.
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Slower binocular rivalry in the autistic brain.
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Getting to the cores of autism.
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Shared risk alleles with discordant polygenic effects: Disentangling the genetic overlap between ASD and ADHD.
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Thalamocortical circuit motifs: A general framework.
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Memo1-mediated tiling of radial glial cells facilitates cerebral cortical development.
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Social and non-social autism symptoms and trait domains are genetically dissociable.
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Profiling allele-specific gene expression in brains from individuals with autism spectrum disorder reveals preferential minor allele usage.
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Atypical neural variability in carriers of 16p11.2 copy number variants.
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Differences in profiles of emotional behavioral problems across instruments in verbal versus minimally verbal children with autism spectrum disorder.
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Excitation-inhibition balance as a framework for investigating mechanisms in neuropsychiatric disorders.
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Immunity and mental illness: Findings from a Danish population-based immunogenetic study of seven psychiatric and neurodevelopmental disorders.
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Exome sequencing of 457 autism families recruited online provides evidence for novel ASD genes.
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The autism-associated gene Scn2a contributes to dendritic excitability and synaptic function in the prefrontal cortex.
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In vivo functional study of disease-associated rare human variants using Drosophila.
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Habituation learning is a widely affected mechanism in Drosophila models of intellectual disability and autism spectrum disorders.
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Evidence of assortative mating in autism spectrum disorder.
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Primary complex motor stereotypies are associated with de novo damaging DNA coding mutations that identify candidate risk genes and biological pathways.
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Placental neurosteroids shape cerebellar development and social behaviour.
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Reduced frontal gamma power at 24 months is associated with better expressive language in toddlers at risk for autism.
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Inherited and de novo genetic risk for autism impacts shared networks.
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Targeting peripheral somatosensory neurons to improve tactile-related phenotypes in ASD models.
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Exosomes regulate neurogenesis and circuit assembly.
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Investigating potential biomarkers in autism spectrum disorder.
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A third linear association between Olduvai (DUF1220) copy number and severity of the classic symptoms of inherited autism.
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Predicting aggression to others in youth with autism using a wearable biosensor.
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Clinical and genetic characterization of individuals with predicted deleterious PHIP variants.
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Epilepsy and autism severity: A study of 6,975 children.
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A pathogenic CtBP1 missense mutation causes altered cofactor binding and transcriptional activity.
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Placental programming of neuropsychiatric disease.
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Linking social motivation with social skill: The role of emotion dysregulation in autism spectrum disorder.
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Next-Generation Sequencing in Autism Spectrum Disorder.
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Pharmacological enhancement of KCC2 gene expression exerts therapeutic effects on human Rett syndrome neurons and Mecp2 mutant mice
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Leveraging biobank-scale rare and common variant analyses to identify ASPHD1 as the main driver of reproductive traits in the 16p11.2 locus.
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FMRP modulates neural differentiation through m6A-dependent mRNA nuclear export.
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AGO CLIP reveals an activated network for acute regulation of brain glutamate homeostasis in ischemic stroke.
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Infraslow state fluctuations govern spontaneous fMRI network dynamics.
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Antigenic targets of patient and maternal autoantibodies in autism spectrum disorder.
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Enhancing rigor and reproducibility in maternal immune activation models: Practical considerations and predicting resilience and susceptibility using baseline immune responsiveness before pregnancy.
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Paternal-age-related de novo mutations and risk for five disorders.
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A genome-wide scan statistic framework for whole-genome sequence data analysis.
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The effect of the genetic liability to autism spectrum disorder on emotion recognition in young unaffected probands from a population-based cohort.
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Deletion of autism risk gene Shank3 disrupts prefrontal connectivity.
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Genome-wide DNA methylation profiling identifies convergent molecular signatures associated with idiopathic and syndromic autism in post-mortem human brain tissue.