Autism Rat Models Consortium: Publications
From ARC
Results
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Sentinel interaction mapping — a generic approach for the functional analysis of human disease gene variants using yeast.
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Autism-associated biomarkers: Test–retest reliability and relationship to quantitative social trait variation in rhesus monkeys.
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Maternal steroid levels and the autistic traits of the mother and infant.
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Atypical gaze patterns in autism are heterogeneous across subjects but reliable within individuals.
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Autism-linked Cullin3 germline haploinsufficiency impacts cytoskeletal dynamics and cortical neurogenesis through RhoA signaling.
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Innate immunity at the crossroads of healthy brain maturation and neurodevelopmental disorders.
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Cell-type-specific synaptic imbalance and disrupted homeostatic plasticity in cortical circuits of ASD-associated Chd8 haploinsufficient mice
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Modulation of striatal functional connectivity differences in adults with and without autism spectrum disorder in a single-dose randomized trial of cannabidivarin.
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Closing the species gap: Translational approaches to studying sensory processing differences relevant for autism spectrum disorder.
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Autism symptoms in anorexia nervosa: A comparative study with females with autism spectrum disorder.
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Novel epigenetic clock for fetal brain development predicts prenatal age for cellular stem cell models and derived neurons.
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Identifying developing interneurons as a potential target for multiple genetic autism risk factors in human and rodent forebrain.
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Estimating genetic nurture with summary statistics of multi-generational genome-wide association studies.
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Reflections on the genetics-first approach to advancements in molecular genetic and neurobiological research on neurodevelopmental disorders.
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Computational neuroimaging of cognition-emotion interactions: Affective and task-similar interference differentially impact working memory.
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Diminished cortical excitation and elevated inhibition during perceptual impairments in a mouse model of autism.
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Genetic and morphological estimates of androgen exposure predict social deficits in multiple neurodevelopmental disorder cohorts.
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Estimating the prevalence and genetic risk mechanisms of ARFID in a large autism cohort.
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Neural basis of opioid-induced respiratory depression and its rescue.
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The ciliary gene INPP5E confers dorsal telencephalic identity to human cortical organoids by negatively regulating sonic hedgehog signalling.
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The tectum/superior colliculus as the vertebrate solution for spatial sensory integration and action.
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Genetic subtypes, allelic effects, and convergent neurodevelopmental mechanisms.
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Psychometric validation and refinement of the Interoception Sensory Questionnaire (ISQ) in adolescents and adults on the autism spectrum.
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The CHD8 CHD7/Kismet family links blood-brain barrier glia and serotonin to ASD-associated sleep defects
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Truncating SRCAP variants outside the Floating-Harbor syndrome locus cause a distinct neurodevelopmental disorder with a specific DNA methylation signature.
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16p11.2 deletion syndrome.
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Patterns and correlates of two-year changes in depressive symptoms for autistic adults.
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Structural and functional brain alterations revealed by neuroimaging in CNV carriers.
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Prevalence of returnable genetic results based on recognizable phenotypes among children with autism spectrum disorder.
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CNVxplorer: A web tool to assist clinical interpretation of CNVs in rare disease patients.
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Sex-specific stress-related behavioral phenotypes and central amygdala dysfunction in a mouse model of 16p11.2 microdeletion.
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FOXP1 negatively regulates intrinsic excitability in D2 striatal projection neurons by promoting inwardly rectifying and leak potassium currents.
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Robust and replicable measurement for prepulse inhibition of the acoustic startle response.
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Genome-wide analysis of gene dosage in 24,092 individuals estimates that 10,000 genes modulate cognitive ability.
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Disruption of RFX family transcription factors causes autism, attention-deficit/hyperactivity disorder, intellectual disability, and dysregulated behavior.
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Resting and functional pupil response metrics indicate features of reward sensitivity and ASD in children.
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Adaptive behavior profiles of intellectually gifted children with autism spectrum disorder.
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Brain gene co-expression networks link complement signaling with convergent synaptic pathology in schizophrenia.
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A large-scale investigation into the role of classical HLA loci in multiple types of severe infections, with a focus on overlaps with autoimmune and mental disorders.
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Differences in social brain function in autism spectrum disorder are linked to the serotonin transporter.
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Using the big data approach to clarify the structure of restricted and repetitive behaviors across the most commonly used autism spectrum disorder measures.
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Atlas of functional connectivity relationships across rare and common genetic variants, traits, and psychiatric conditions.
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Relationship between social motivation in children with autism spectrum disorder and their parents.
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Chromatin remodeler Arid1a regulates subplate neuron identity and wiring of cortical connectivity.
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Association of CDH11 with ASD revealed by matched-gene co-expression analysis and mouse behavioral studies.
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Altered maturation and atypical cortical processing of spoken sentences in autism spectrum disorder.
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A method to delineate de novo missense variants across pathways prioritizes genes linked to autism.
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COVID-19 health and social care access for autistic people: European policy review.