This work proposes a cross-attention-guided subject-adaptive graph network (CAS-GNN) model that integrates structural MRI and resting-state functional connectivity data, effectively fusing complementary multimodal information and provides a promising tool for interpretable and robust ASD diagnosis, accelerating biomarker discovery and development.
Abstract
Autism spectrum disorder (ASD) is a complex neurodevelopmental condition marked by structural atypicality and abnormal functional connectivity. It remains challenging to accurately delineate an ASD-associated neural marker due to individual heterogeneity and multi-site data variability. To address these issues, we propose a cross-attention-guided subject-adaptive graph network (CAS-GNN) model that integrates structural MRI and resting-state functional connectivity data, effectively fusing complementary multimodal information. By modeling individualized brain network topologies and incorporating a site-invariant learning strategy, our approach enhances discriminability and cross-site generalization. On the ABIDE-I dataset, CAS-GNN significantly outperformed machine learning baselines and achieved an accuracy of 79.25% ± 4.71% on independent test data and an average accuracy of 78.75% ± 1.56% on five-fold cross-validation. Exploratory analyses identified key ASD-related brain regions and connections, revealing a notable right-hemisphere dominance consistent with atypical asymmetry in ASD. Our framework offers valuable neurobiological insights and provides a promising tool for interpretable and robust ASD diagnosis, accelerating biomarker discovery and development.
The Collaborative Graph Attention Multi-Task Network (CoGA-MTN), a deep learning framework that integrates multi-scale structural features to jointly predict task-based functional connectivity (FC) and identify potential disease-related network alterations, is introduced.
Findings indicate that anatomically grounded node-level multimodal fusion can improve classification performance while preserving neurobiological interpretability, thereby providing a principled framework for multimodal schizophrenia classification and biomarker discovery.
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Findings indicate that the learned brain network representations capture distinct and quantifiable abnormalities in ASD-related neural dynamics, establishing the proposed framework as a robust, interpretable, and measurement-aligned tool for objective ASD assessment.
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The proposed framework demonstrates robust diagnostic performance and provides reliable biomarkers for neurological assessment, and the identified regions and connectivity patterns offer insights into ASD neural mechanisms and potential diagnostic biomarkers.
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