arXiv subjects

Dengyi Zhao

Publications and source records attributed to Dengyi Zhao.

5 recordsLinked to original sources

arXiv2026

From Diffusion to Reaction-Diffusion: A Dynamical-Systems View of Oversmoothing in Hypergraph Neural Networks

Higher-order couplings enhance the expressive power of hypergraph neural networks (HGNNs), but they also intensify representation collapse in deep propagation due to strong multi-way feature mixing. This work investigates hypergraph oversmoothing from a dynamical-systems perspective and develops a reaction--diffusion framework for depth-resistant hypergraph learning. By defining hypergraph gradient and divergence operators, we interpret message passing as an incidence-level diffusion process. The analysis of pure diffusion shows that its continuous semiflow exponentially contracts the null-mode-free component of node representations and drives the Dirichlet energy to zero, revealing hypergraph oversmoothing as an intrinsic transverse-energy dissipation phenomenon. Motivated by this analysis, we propose Hypergraph Neural Reaction--Diffusion (HNRD), which introduces a reaction mechanism acting on the transverse component to compensate diffusion-induced dissipation and stabilize discriminative variations. We establish global well-posedness of the proposed dynamics and prove that the null-mode-free Dirichlet energy remains bounded away from zero. A forward-Euler discretization provides a practical HNRD layer with a stability condition for deep propagation. Experiments on benchmark and synthetic heterophilic hypergraphs demonstrate that HNRD consistently improves over representative hypergraph baselines. Depth, robustness, and efficiency analyses further show that HNRD preserves stable performance and nonzero Dirichlet energy under deep propagation and perturbations. These results provide a principled dynamical framework for designing deep hypergraph architectures that maintain higher-order expressiveness without representation collapse.

cs.LG↗

arXiv2026

Hypergraph Neural Stochastic Diffusion: An SDE Framework for Uncertainty Estimation

Hypergraph neural networks have shown powerful capability in modeling higher-order relations, yet their predictive uncertainty remains underexplored. Unlike pairwise graphs, uncertainty in hypergraphs arises not only from noisy attributes and ambiguous labels, but also from variations in node-hyperedge incidence structures and complex higher-order dependencies. Existing approaches mainly estimate uncertainty from final predictions or rely on computationally expensive ensembles and Bayesian inference, limiting their ability to capture uncertainty evolution during representation learning. In this paper, we propose Hypergraph Neural Stochastic Diffusion(HyperNSD), a stochastic differential equation framework for uncertainty estimation on hypergraphs. HyperNSD models hypergraph representations as stochastic processes evolving over node-hyperedge incidence structures. A learnable drift function captures deterministic higher-order diffusion dynamics, while a learnable stochastic forcing function characterizes structural ambiguity and representation noise. Predictive uncertainty is directly quantified through the variability of stochastic representation trajectories, providing an intrinsic uncertainty measure beyond post-hoc confidence scores. We formulate HyperNSD with neural drift and diffusion networks, enabling joint learning of prediction and uncertainty propagation. Theoretical analyses establish well posedness, perturbation stability,permutation equivariance, and numerical convergence of the proposed stochastic dynamics. Experiments on multiple hypergraph benchmarks demonstrate that HyperNSD achieves reliable uncertainty estimation for out-of-distribution and misclassification detection while preserving competitive prediction accuracy. These results provide a principled stochastic-dynamical framework for trustworthy higher-order representation learning.

cs.LG↗

arXiv2026

Interpretable Information-Decomposed Brain Graph Learning for fMRI-based Disease Diagnosis

Resting-state functional magnetic resonance imaging (rs-fMRI) has enabled non-invasive mapping of functional brain interactions for computer-aided diagnosis, yet most existing approaches reduce inter-regional relationships to correlation-based edge weights. Such representations capture co-fluctuation strength but obscure how information is shared across brain regions. Because brain disorders may disrupt not only connectivity strength but also the organization of redundancy, uniqueness and synergy, traditional functional connectivity may miss disease-relevant information structures. Here we introduce IID-GCN, an interpretable graph learning framework that decomposes rs-fMRI interactions into redundancy, uniqueness and synergy graphs using partial entropy decomposition. These information-specific graphs separately characterize shared, region-specific and jointly emergent components of brain activity. A multi-channel graph convolutional network then integrates the decomposed graphs through edge recalibration, cross-information interaction, ROI-attention readout and channel-attentive fusion. Across three datasets, IID-GCN consistently captures complementary diagnostic information beyond traditional functional connectivity. The learned information profiles reveal disorder-specific patterns of altered redundancy, uniqueness and synergy, suggesting that brain diseases reshape functional information organization rather than merely changing connection strength. These results establish information-decomposed brain graphs as an interpretable representation for rs-fMRI-based diagnosis. Our code is available at https://github.com/Zdy12/IID-GCN.

q-bio.NC↗

arXiv2026

HOI-Brain: a novel multi-channel transformers framework for brain disorder diagnosis by accurately extracting signed higher-order interactions from fMRI

Accurately characterizing higher-order interactions of brain regions and extracting interpretable organizational patterns from Functional Magnetic Resonance Imaging data is crucial for brain disease diagnosis. Current graph-based deep learning models primarily focus on pairwise or triadic patterns while neglecting signed higher-order interactions, limiting comprehensive understanding of brain-wide communication. We propose HOI-Brain, a novel computational framework leveraging signed higher-order interactions and organizational patterns in fMRI data for brain disease diagnosis. First, we introduce a co-fluctuation measure based on Multiplication of Temporal Derivatives to detect higher-order interactions with temporal resolution. We then distinguish positive and negative synergistic interactions, encoding them in signed weighted simplicial complexes to reveal brain communication insights. Using Persistent Homology theory, we apply two filtration processes to these complexes to extract signed higher-dimensional neural organizations spatiotemporally. Finally, we propose a multi-channel brain Transformer to integrate heterogeneous topological features. Experiments on Alzheimer' s disease, Parkinson' s syndrome, and autism spectrum disorder datasets demonstrate our framework' s superiority, effectiveness, and interpretability. The identified key brain regions and higher-order patterns align with neuroscience literature, providing meaningful biological insights.

q-bio.NC↗

arXiv2025

Extracting Interpretable Higher-Order Topological Features across Multiple Scales for Alzheimer's Disease Classification

Brain network topology, derived from functional magnetic resonance imaging (fMRI), holds promise for improving Alzheimer's disease (AD) diagnosis. Current methods primarily focus on lower-order topological features, often overlooking the significance of higher-order features such as connected components, cycles, and cavities. These higher-order features are critical for understanding normal brain function and have been increasingly linked to the pathological mechanisms of AD. However, their quantification for diagnosing AD is hindered by their inherent nonlinearity and stochasticity in the brain. This paper introduces a novel framework for diagnosing Alzheimer's disease that uses persistent homology to extract higher-order topological features from fMRI data. It also introduces four quantitative methods that capture subtle, multiscale geometric variations in functional brain networks associated with AD. Our experimental results demonstrate that this framework significantly outperforms existing methods in AD classification. Extensive ablation studies and interpretability analysis confirm the effectiveness of our framework. Our study also reveals that the number of cycles or cavities significantly decrease in AD patients. The extracted key brain regions derived from cycles and cavities align with domain knowledge in neuroscience literature and provide direct and insightful findings. This study highlights the potential of higher-order topological features for early AD detection and significantly advances the field of brain topology analysis in neurodegenerative disease research.

math.GT↗