ArticleResearch square2026
A neuro-computational framework for modeling the development of cross-sensory interactions in Autism: from mechanistic understanding to targeted intervention.
Article in Research square, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.
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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
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4 authors.
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Abstract
Recent studies have shown that multisensory processing in children shifts from a competitive to a facilitative state as development progresses, and this transition appears delayed in children with autism spectrum diagnosis (ASD). The neural mechanisms underlying this developmental change, and its alteration in ASD, remain largely unknown. To address this gap, we investigated how sensory modalities interact in the developing brain using a biologically plausible neurocomputational model governed by Hebbian learning rules. We also explored the neural substrates that may underlie atypical multisensory development in ASD. Our results suggest that inhibitory cross-modal projections gradually become excitatory during development, mediating the observed shift from competition to facilitation in typical children. Furthermore, our simulations show that the delayed transition in ASD may stem either from reduced neural plasticity or diminished multisensory experience. Our model informs the potential benefits that a multisensory rehabilitation strategy may have on the development of perceptual abilities of ASD children, and possibly on the core social symptoms characterizing Autism as well. By linking computational modelling with behavioural findings, our work provides a framework for understanding atypical sensory development. We anticipate that this model could inform future neurophysiological studies and guide the design of multisensory-based therapeutic interventions for ASD.
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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.