Autism Rat Models Consortium: Publications
From ARC
Results
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Perception of cry characteristics in 1-month-old infants later diagnosed with autism spectrum disorder.
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A longitudinal study of parent-reported sensory responsiveness in toddlers at-risk for autism.
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Impaired voice processing in reward and salience circuits predicts social communication in children with autism.
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Modeling autism-related disorders in mice with maternal immune activation (MIA).
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Aberrant somatosensory processing and connectivity in mice lacking Engrailed-2.
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Differential NOVA2-mediated splicing in excitatory and inhibitory neurons regulates cortical development and cerebellar function.
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Increased excitation-inhibition ratio stabilizes synapse and circuit excitability in four autism mouse models.
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Clinical presentation of a complex neurodevelopmental disorder caused by mutations in ADNP.
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Recessive rare variants in deoxyhypusine synthase, an enzyme involved in the synthesis of hypusine, are associated with a neurodevelopmental disorder.
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Establishing cerebral organoids as models of human-specific brain evolution.
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mTOR suppresses macroautophagy during postnatal development of the striatum.
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Predicting splicing from primary sequence with deep learning.
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Disentangling polygenic associations between attention-deficit/hyperactivity disorder, educational attainment, literacy and language.
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Both rare and common genetic variants contribute to autism in the Faroe Islands.
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An interaction-based model for neuropsychiatric features of copy-number variants.
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Psychiatric disorders in children with 16p11.2 deletion and duplication.
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Dendritic spines in early postnatal fragile X mice are insensitive to novel sensory experience.
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Single-cell RNA sequencing of microglia throughout the mouse lifespan and in the injured brain reveals complex cell-state changes.
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Single-cell transcriptomic analysis of mouse neocortical development.
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Customized head molds reduce motion during resting state fMRI scans.
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Nucleosome turnover regulates histone methylation patterns over the genome.
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The NeuroDev study: Phenotypic and genetic characterization of neurodevelopmental disorders in Kenya and South Africa.
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Spectrum or subtypes? A latent profile analysis of restricted and repetitive behaviours in autism.
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Outgroup machine learning approach identifies single nucleotide variants in noncoding DNA associated with autism spectrum disorder.
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Early motor abilities in infants at heightened versus low risk for ASD: A Baby Siblings Research Consortium (BSRC) study.
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Interacting neural ensembles in orbitofrontal cortex for social and feeding behaviour.
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Neurodevelopmental disease genes implicated by de novo mutation and copy number variation morbidity.
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The ASD living biology: From cell proliferation to clinical phenotype.
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Deregulation of synaptic plasticity in autism.
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Integrative functional genomic analysis of human brain development and neuropsychiatric risks.
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Transcriptome-wide isoform-level dysregulation in ASD, schizophrenia, and bipolar disorder.
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Genome-wide de novo risk score implicates promoter variation in autism spectrum disorder.
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Inherited and multiple de novo mutations in autism/developmental delay risk genes suggest a multifactorial model.
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Cellular-resolution imaging of vestibular processing across the larval zebrafish brain.
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Diffuse light-sheet microscopy for stripe-free calcium imaging of neural populations.
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Selfish mutations dysregulating RAS-MAPK signaling are pervasive in aged human testes.
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Neural coding of sex-specific social information in the mouse brain.
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Psychometric properties of the Simons Simplex Collection sleep interview.
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Brain organoids and the study of neurodevelopment.
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Thalamic regulation of switching between cortical representations enables cognitive flexibility.
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Large-scale associations between the leukocyte transcriptome and BOLD responses to speech differ in autism early language outcome subtypes.
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Haploinsufficiency of the intellectual disability gene SETD5 disturbs developmental gene expression and cognition.
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Partial loss of psychiatric risk gene Mir137 in mice causes repetitive behavior and impairs sociability and learning via increased Pde10a.
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Regulation of cell-type-specific transcriptomes by microRNA networks during human brain development.
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Rbfox1 mediates cell-type-specific splicing in cortical interneurons.
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Problem behaviors in autism spectrum disorder: Association with verbal ability and adapting/coping skills.
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Genome-wide CRISPR-Cas9 interrogation of splicing networks reveals a mechanism for recognition of autism-misregulated neuronal microexons.
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m6A facilitates hippocampus-dependent learning and memory through YTHDF1.