Autism Rat Models Consortium: Publications
From ARC
Results
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Noncoding variants and sulcal patterns in congenital heart disease: Machine learning to predict functional impact.
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Comparative profiling of white matter development in the human and mouse brain reveals volumetric deficits and delayed myelination in Angelman syndrome.
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A normative model representing autistic individuals amidst autism spectrum phenotypic heterogeneity.
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Effects of gene dosage on cognitive ability: A function-based association study across brain and non-brain processes.
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Genetic architecture of postpartum psychosis: From common to rare genetic variation.
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Using deep learning to classify developmental differences in reaching and placing movements in children with and without autism spectrum disorder.
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Using deep learning to classify developmental differences in reaching and placing movements in children with and without autism spectrum disorder.
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Patterns and correlates of two-year changes in depressive symptoms for autistic adults.
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An examination of psychological flexibility as a mediator between mental health concerns and satisfaction with life among autistic adults.
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Inner experiences, mental health, and well-being in autistic and non-autistic adults.
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Motor phenotypes associated with genetic neurodevelopmental disorders.
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How auditory processing influences the autistic profile: A review.
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Parental experiences and perspectives of healthcare providers' genetic testing recommendations for their children diagnosed with autism spectrum disorder in the United States.
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Sequential replacement of PSD95 subunits in postsynaptic supercomplexes is slowest in the cortex.
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Large-scale metagenomic analysis of oral microbiomes reveals markers for autism spectrum disorders.
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A deep learning model for prediction of autism status using whole-exome sequencing data.
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Maternal dietary patterns during pregnancy and child autism-related traits in the environmental influences on child health outcomes consortium.
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Machine learning differentiation of autism spectrum sub-classifications.
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Temporally distinct 3D multi-omic dynamics in the developing human brain.
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Examining sociodemographic variability in the amount and type of interventions for children with autism.
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Enrichment of a subset of Neanderthal polymorphisms in autistic probands and siblings.
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Developing forebrain synapses are uniquely vulnerable to sleep loss.
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Sex differences in sleep deficits in mice with an autism-linked Shank3 mutation.
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Transgenerational transmission of post-zygotic mutations suggests symmetric contribution of first two blastomeres to human germline.
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Genetically modified animals as models of neurodevelopmental conditions: A review of systematic review reporting quality.
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Sex differences in human brain structure at birth.
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Copy-number variants differ in frequency across genetic ancestry groups.
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SETBP1 haploinsufficiency and related disorders clinical and neurobehavioral phenotype study.
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Application of multiple mosaic callers improves post-zygotic mutation detection from exome sequencing data.
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Return of genetic research results in 21,532 individuals with autism.
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Validating motor delays across the developmental coordination disorder-questionnaire and the Vineland adaptive behavior scales (VABS) in children with autism spectrum disorderASD: A SPARK dataset analysis.
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Barriers, motivators and strategies to increase participation in genetic research among Asian and Black families of autistic individuals.
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Unveiling the role of IGF1R in autism spectrum disorder: a multi-omics approach to decipher common pathogenic mechanisms in the IGF signaling pathway.
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An examination of perceived stress and emotion regulation challenges as mediators of associations between camouflaging and internalizing symptomatology.
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Specific EEG resting state biomarkers in FXS and ASD.
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Impact of interaction between individual genomes and preeclampsia on the severity of autism spectrum disorder symptoms.
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Genetic modifiers and ascertainment drive variable expressivity of complex disorders.
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MED13L-related disorder characterized by severe motor speech impairment.
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Reference-informed prediction of alternative splicing and splicing-altering mutations from sequences.
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Decomposition of phenotypic heterogeneity in autism reveals distinct and coherent genetic programs.
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Rare variation in non-coding regions with evolutionary signatures contributes to autism spectrum disorder risk.
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Cell-type-specific effects of autism-associated 15q duplication syndrome in the human brain.
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Astrocyte mitochondria are a sensitive target of PCB52 and its human-relevant metabolites.
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Molecular and cellular dynamics of the developing human neocortex at single-cell resolution.
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Association of behavioural and social-communicative profiles in children with 16p11.2 copy number variants: a multi-site study.
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De novo variants in the RNU4-2 snRNA cause a frequent neurodevelopmental syndrome
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Expanded clinical phenotype spectrum correlates with variant function in SCN2A-related disorders.
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Machine learning prediction of autism spectrum disorder from a minimal set of medical and background information.