Autism Rat Models Consortium: Publications
From ARC
Results
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Distinct roles of putative excitatory and inhibitory neurons in the macaque inferior temporal cortex in core object recognition behavior.
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The contributions of rare inherited and polygenic risk to ASD in multiplex families.
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Landscape of mSWI/SNF chromatin remodeling complex perturbations in neurodevelopmental disorders.
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The Autism Symptom Dimensions Questionnaire: Development and psychometric evaluation of a new, open-source measure of autism symptomatology.
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Large-scale whole genome sequence analysis of 22,000 subjects provides no evidence of FMR1 premutation allele involvement in autism spectrum disorder.
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VBASS enables integration of single cell gene expression data in Bayesian association analysis of rare variants.
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Autism-linked UBE3A gain-of-function mutation causes interneuron and behavioral phenotypes when inherited maternally or paternally in mice.
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Rhesus macaque social functioning is paternally, but not maternally, inherited by sons: Potential implications for autism.
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Reprogramming method does not impact the neuronal differentiation potential of 16p11.2 deletion patient iPSCs.
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ANK2 loss-of-function variants are associated with epilepsy, and lead to impaired axon initial segment plasticity and hyperactive network activity in hiPSC-derived neuronal networks.
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A mixed methods study of autistic adults' mental health therapy experiences.
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Changes in social behavior with MAPK2 and KCTD13/CUL3 pathways alterations in two new outbred rat models for the 16p11.2 syndromes with autism spectrum disorders.
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A qualitative exploration of autistic mothers' experiences I: Pregnancy experiences.
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Are autistic people disadvantaged by the criminal justice system? A case comparison.
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Phenotypically driven subgroups of ASD display distinct metabolomic profiles.
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Relationship between childhood obesity and autism spectrum disorder varies by child's age and parents' weight status in a sample of sibling dyads.
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Autistic people's perinatal experiences II: A survey of childbirth and postnatal experiences.
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Validity of the SNAP-IV for ADHD assessment in South African children with neurodevelopmental disorders.
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Autism spectrum disorders and brain volume link through a set of mTOR-related genes.
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Multi-omic analysis along the gut-brain axis points to a functional architecture of autism.
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Phenotypic effects of genetic variants associated with autism.
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Developmental molecular controls over arealization of descending cortical motor pathways.
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Elevated levels of FMRP-target MAP1B impair human and mouse neuronal development and mouse social behaviors via autophagy pathway.
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Structural neuroplasticity after sleep loss modifies behavior and requires neurexin and neuroligin.
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Environmental adversity moderates polygenic score effects on childhood behavioral problems in the United States.
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Glial dysregulation in the human brain in fragile X-associated tremor/ataxia syndrome.
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Immersive and maladaptive daydreaming and divergent thinking in autism spectrum disorders.
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Agreement of parent-reported cognitive level with standardized measures among children with autism spectrum disorder.
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Agreement of parent-reported cognitive level with standardized measures among children with autism spectrum disorder.
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A PROMIS®ing new measure for quantifying emotion dysregulation in toddlers and preschoolers: Development of the Emotion Dysregulation Inventory-Young Child.
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Reliability of the Motor Optimality Score-Revised: A study of infants at elevated likelihood for adverse neurological outcomes.
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Data-driven dissection of the fever effect in autism spectrum disorder.
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Rubella virus tropism and single cell responses in human primary tissue and microglia-containing organoids.
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Repetitive and restricted behaviors and interests in autism spectrum disorder: relation to individual characteristics and mental health problems.
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Challenges in screening for de novo noncoding variants contributing to genetically complex phenotypes.
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CERT1 mutations perturb human development by disrupting sphingolipid homeostasis.
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Examining indicators of psychosocial risk and resilience in parents of autistic children.
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Sharing parental genomes by siblings concordant or discordant for autism.
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Cross-replicating findings on unique motor impairments of children with ASD using confirmatory factor analysis and a novel SPARK study sample.
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Clinical, neuroimaging and molecular characteristics of PPP2R5D-related neurodevelopmental disorders: An expanded series with functional characterisation and genotype-phenotype analysis.
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Identifying rare genetic variants in 21 highly multiplex autism families: The role of diagnosis and autistic traits.
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Dimensional assessment of restricted and repetitive behaviors: Development and preliminary validation of a new measure.
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Effect of children’s autism spectrum disorder severity on family strain and sleep quality: A cross-sectional online survey in the U.S.
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Synaptic boutons are smaller in chandelier cell cartridges in autism.
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Functional brain networks reflect spatial and temporal autocorrelation.
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Pyramidal neurons form active, transient, multilayered circuits perturbed by autism-associated mutations at the inception of neocortex.
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Using brain cell-type-specific protein interactomes to interpret genetic data in schizophrenia.
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Ventral striatal dopamine encodes unique properties of visual stimuli in mice.