Neural Dynamics-Informed Pre-trained Framework for Personalized Brain Functional Network Construction

We propose the Neural Functional Alignment Space (NFAS), a brain-referenced representational framework for characterizing artificial neural networks on equal functional grounds. NFAS departs from conventional alignment approaches that rely on layer-wise features or task-specific activations by modeling the intrinsic dynamical evolution of stimulus representations across network depth. Specifically, we model layer-wise embeddings as a depth-wise dynamical trajectory and apply Dynamic Mode Decomposition (DMD) to extract the stable mode. This representation is then projected into a biologically anchored coordinate system defined by distributed neural responses. We also introduce the Signal-to-Noise Consistency Index (SNCI) to quantify cross-model consistency at the modality level. Across 45 pretrained models spanning vision, audio, and language, NFAS reveals structured organization within this brain-referenced space, including modality-specific clustering and cross-modal convergence in integrative cortical systems. Our findings suggest that representation dynamics provide a principled basis for

Masked autoencoders (MAEs) have recently shown promise for self-supervised representation learning of resting-state brain functional connectivity (FC). However, a fundamental question remains unresolved: how should FC matrices be tokenized to align with the intrinsic modular organization of large-scale brain networks? Existing approaches typically adopt region-centric or graph-based schemes that treat FC as structurally homogeneous elements and overlook the large-scale network brain organization. We introduce NERVE (Network-Aware Representations of Brain Functional Connectivity via Bilinear Tokenization), a self-supervised learning framework that redefines FC tokenization by partitioning FC matrices into patches of intra- and inter-network connectivity blocks. Unlike image-based MAE, where fixed-size patches share a common tokenizer, FC patches defined by network pairs are heterogeneous in size and correspond to distinct functional roles. To resolve this problem, NERVE embeds FC patches through a novel structured bilinear factorization. This formulation preserves network identity and reduces parameter complexity from quadratic to linear scaling in the number of networks. We evaluate NERVE across three large-scale developmental cohorts (ABCD, PNC, and CCNP) for behavior and psychopathology prediction. Compared to structurally agnostic MAE variants and graph-based self-supervised baselines, the proposed network-aware formulation yields more stable and transferable representations, particularly in cross-cohort evaluation. Ablation studies confirm that the proposed bilinear network embedding and anatomically grounded parcellation are critical for performance. These findings highlight the importance of incorporating domain-specific structural priors into self-supervised learning for functional connectomics. Code is available at: https://github.com/leomlck/NERVE.

Brain activity unfolds as coordinated patterns across regions over time, and modeling these dynamics is a central goal in computational neuroscience. Because activity is distributed over connected brain regions, it is naturally represented on a graph whose nodes are brain regions or recording electrodes and whose edges capture relationships between these nodes, with message-passing modeling regional communication. However, standard message-passing networks place every node in a single shared feature space and typically aggregate messages from neighbors by scalar summation, which does not align with neurobiological evidence of brain communication. In order to model the heterogeneous nature of the brain, we introduce BrainDyn, a graph ordinary differential equation (ODE) network built on a cellular sheaf with dynamic restriction maps, recomputed from the forecasting context window rather than fixed once, mediating region-to-region communication through learned linear transformations that drive the time evolution of neural activity. We evaluate BrainDyn on resting-state fMRI, EEG, and simulated activity from the NEST simulator. Across these modalities, we test multi-region forecasting and autoregressive generation of brain transients, and, using NEST, prediction of altered transients following controlled perturbations. BrainDyn outperforms competing models across modalities, while analysis of the learned features shows that they are expressive, interpretable, and biologically aligned.