Research: Funded Publications
Explore publications and preprints from SFARI-funded investigators and researchers using SFARI-supported data and resources.
Results
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Genomic selection signatures in autism spectrum disorder identifies cognitive genomic tradeoff and its relevance in paradoxical phenotypes of deficits versus potentialities.
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Imbalanced social-communicative and restricted repetitive behavior subtypes of autism spectrum disorder exhibit different neural circuitry.
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Bayonet-shaped language development in autism with regression: A retrospective study.
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Individuals with autism spectrum disorder have altered visual encoding capacity.
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A unified resource and configurable model of the synapse proteome and its role in disease.
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Broad frequency sensitivity and complex neural coding in the larval zebrafish auditory system.
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Chandelier cartridge density is reduced in the prefrontal cortex in autism.
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Genoppi is an open-source software for robust and standardized integration of proteomic and genetic data.
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Optimising a simple fully convolutional network for accurate brain age prediction in the PAC 2019 challenge.
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Rare variant analysis of 4241 pulmonary arterial hypertension cases from an international consortium implicates FBLN2, PDGFD, and rare de novo variants in PAH.
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Integrating barcoded neuroanatomy with spatial transcriptional profiling enables identification of gene correlates of projections.
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An investigation of the diet, exercise, sleep, BMI, and health outcomes of autistic adults.
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Gene-environment correlations and causal effects of childhood maltreatment on physical and mental health: A genetically informed approach.
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Discovery of autism/intellectual disability somatic mutations in Alzheimer's brains: mutated ADNP cytoskeletal impairments and repair as a case study
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Assessing child postural variability: Development, feasibility, and reliability of a video coding system.
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Generation of fate patterns via intercellular forces.
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Delayed motor learning in a 16p11.2 deletion mouse model of autism is rescued by locus coeruleus activation.
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The role of GABAergic signalling in neurodevelopmental disorders.
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The factor structure of the macaque social responsiveness scale-revised predicts social behavior and personality dimensions.
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Exons as units of phenotypic impact for truncating mutations in autism.
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Geometric deep learning enables 3D kinematic profiling across species and environments.
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CaMKII activation persistently segregates postsynaptic proteins via liquid phase separation.
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Deletion of a non-canonical regulatory sequence causes loss of Scn1a expression and epileptic phenotypes in mice.
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A normative model representing autistic individuals amidst autism spectrum disorders phenotypic heterogeneity.
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Tissue-specific enhancer functional networks for associating distal regulatory regions to disease.
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Coordinated postnatal maturation of striatal cholinergic interneurons and dopamine release dynamics in mice.
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Genetic vulnerability of exposures to antenatal maternal treatments in 1- to 2-month-old infants.
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Rare deleterious mutations of HNRNP genes result in shared neurodevelopmental disorders.
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An epigenetically distinct subset of children with autism spectrum disorder resulting from differences in blood cell composition.
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Social cognition in 22q11.2 deletion syndrome and idiopathic developmental neuropsychiatric disorders.
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Female-specific synaptic dysfunction and cognitive impairment in a mouse model of PCHD19 disorder.
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fmr1 mutation interacts with sensory experience to alter the early development of behavior and sensory coding in zebrafish.
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The gut-brain-microbiome axis and its link to autism: Emerging insights and the potential of zebrafish models.
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The relationship between developmental coordination disorder and concurrent deficits in social communication and repetitive behaviors among children with autism spectrum disorder.
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Perceived helpfulness of depression treatments among young adults with autism.
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Differences in subcortico-cortical interactions identified from connectome and microcircuit models in autism.
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Overexpression of CD47 is associated with brain overgrowth and 16p11.2 deletion syndrome.
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Assessment of medical morbidities in a rhesus monkey model of naturally occurring low sociality.
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Genotype and defects in microtubule-based motility correlate with clinical severity in KIF1A-associated neurological disorder.
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Diagnostic classification and prognostic prediction using common genetic variants in autism spectrum disorder: Genotype-based deep learning.
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Autism spectrum disorders classification using genotype data: A deep learning-based predictive classifier.
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Microglia complement signaling promotes neuronal elimination and normal brain functional connectivity.
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Measuring depression in autistic adults: Psychometric validation of the Beck Depression Inventory-II.
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Spontaneous neural activity relates to psychiatric traits in 16p11.2 CNV carriers: An analysis of EEG spectral power and multiscale entropy.
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Computation of the electroencephalogram (EEG) from network models of point neurons.
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Multivariate genome-wide analysis of education, socioeconomic status and brain phenome.
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De novo structural mutation rates and gamete-of-origin biases revealed through genome sequencing of 2,396 families.
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Autism BrainNet.