Autism Rat Models Consortium: Publications
From ARC
Results
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Multimodal pathways to joint attention in infants with a familial history of autism.
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Characterizing subdomains of insistence on sameness in autistic youth.
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Endogenous noise of neocortical neurons correlates with atypical sensory response variability in the Fmr1-/y mouse model of autism
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Copy-number variants and polygenic risk for intelligence confer risk for autism spectrum disorder irrespective of their effects on cognitive ability.
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Single-cell long-read sequencing in human cerebral organoids uncovers cell-type-specific and autism-associated exons.
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The phenotypic variability of 16p11.2 distal BP2-BP3 deletion in a transgenerational family and in neurodevelopmentally ascertained samples.
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Genetically predicted causal associations between periodontitis and psychiatric disorders.
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Genomic data resources of the Brain Somatic Mosaicism Network for neuropsychiatric diseases.
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Hyperthermia elevates brain temperature and improves behavioural signs in animal models of autism spectrum disorder.
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Genetic ablation of GIGYF1, associated with autism, causes behavioral and neurodevelopmental defects in zebrafish and mice.
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Cre-dependent massively parallel reporter assay allows for cell-type specific assessment of the functional effects of genetic variants in vivo.
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Peripheral temperature dysregulation associated with functionally altered NaV1.8 channels.
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Remote vs. In-person Schooling during the COVID-19 Pandemic and Internalizing Symptoms among Children on the Autism Spectrum.
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Examining treatment outcomes across contexts: How do child baseline characteristics impact measurement of treatment response?
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DeepGAMI: deep biologically guided auxiliary learning for multimodal integration and imputation to improve genotype-phenotype prediction.
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Deficits in integrative NMDA receptors caused by Grin1 disruption can be rescued in adulthood.
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Robust hierarchically organized whole-brain patterns of dysconnectivity in schizophrenia spectrum disorders observed after personalized intrinsic network topography.
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Long COVID-19 syndrome associated with Omicron XBB.1.5 infection: a case report.
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Age-related changes in neural responses to sensory stimulation in autism: a cross-sectional study.
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Primary complex motor stereotypies are associated with de novo damaging DNA coding mutations that identify KDM5B as a risk gene.
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Identifying crossovers and shared genetic material in whole genome sequencing data from families.
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Epilepsy-associated SCN2A (NAV1.2) variants exhibit diverse and complex functional properties.
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Mutations in genes related to myocyte contraction and ventricular septum development in non-syndromic tetralogy of Fallot.
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Mutations in genes related to myocyte contraction and ventricular septum development in non-syndromic tetralogy of Fallot.
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Developing a measure of key adult outcomes in adults with developmental disabilities: Conceptual model and item generation of the REALS (Relationships, Employment, Autonomy, and Life Satisfaction).
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Parental tuning of language input to autistic and nonspectrum children.
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Rare variation in noncoding regions with evolutionary signatures contributes to autism spectrum disorder risk.
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Single cell analysis of dup15q syndrome reveals developmental and postnatal molecular changes in autism.
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Benchmarking of local genetic correlation estimation methods using summary statistics from genome-wide association studies
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Increased rates of chronic physical health conditions across all organ systems in autistic adolescents and adults.
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Phenotype and genetic analysis of data collected within the first year of NeuroDev.
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Community providers' reported use of treatment practices in the United States.
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Accelerated longitudinal weight gain among infants with in utero COVID-19 exposure.
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Classification of missense variants in the N-methyl-d-aspartate receptor GRIN gene family as gain- or loss-of-function.
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Single-cell brain organoid screening identifies developmental defects in autism.
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SnapShot: Reporting practices for publishing results with human PSCs and tissue stem cells.
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The relationship between augmentative and alternative communication use by pediatric psychiatric inpatients with autism spectrum disorder and interfering behaviors.
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Subcortical brain alterations in carriers of genomic copy number variants.
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Three generation families: Analysis of de novo variants in autism.
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Discovery of eQTL alleles associated with autism spectrum disorder: A case-control study.
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The autism impact measure (AIM): Meaningful change thresholds and core symptom changes over one year from an online survey in the U.S.
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Examining the latent structure and correlates of sensory reactivity in autism: a multi-site integrative data analysis by the autism sensory research consortium.
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Behavioral parent training engagement among young children with autism spectrum disorder.
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Protocol for the development of joint attention-based subclassification of autism spectrum disorder and validation using multi-modal data.
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Modeling idiopathic autism in forebrain organoids reveals an imbalance of excitatory cortical neuron subtypes during early neurogenesis.
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Genetic control of mRNA splicing as a potential mechanism for incomplete penetrance of rare coding variants.
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Genetic control of mRNA splicing as a potential mechanism for incomplete penetrance of rare coding variants.
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FOXP1 orchestrates neurogenesis in human cortical basal radial glial cells.