Researcher profile

Mario Senden

Mario Senden contributes to research discovery and scholarly infrastructure.

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Published work

2 published item(s)

preprint2026arXiv

Functional Whole-Brain Models: A New Framework for Unifying Brain Structure and Cognitive Function

Contemporary computational neuroscience features two prominent modeling traditions. Bottom-up whole-brain modeling (WBM) builds biophysically detailed simulations of brain structure and dynamics, whereas top-down neuroconnectionism optimizes deep neural networks for functional performance. Each has achieved remarkable success yet remains incomplete with WBMs lacking functional competence and neuroconnectionist models showing limited biological grounding. Here we propose functional whole-brain models (fWBMs) as a unified modeling paradigm that integrates structural and dynamical realism with task-performing capacity. fWBMs are defined by four minimal criteria: structural grounding in empirical connectomes and regional biology, continuous-time dynamical realism, functional competence across cognitive domains, and mappable observables to neuroimaging, electrophysiologcal and behavioral data. To formalize this integration, we establish a three-pillar roadmap across short-, mid-, and long-term horizons, and outline the scientific and clinical opportunities this paradigm enables. We argue that the disciplined pursuit of this integrative vision will generate the tools, common language, and cross-scale hypotheses needed to advance our understanding of the brain.

preprint2019arXiv

Effects of Synaptic and Myelin Plasticity on Learning in a Network of Kuramoto Phase Oscillators

Models of learning typically focus on synaptic plasticity. However, learning is the result of both synaptic and myelin plasticity. Specifically, synaptic changes often co-occur and interact with myelin changes, leading to complex dynamic interactions between these processes. Here, we investigate the implications of these interactions for the coupling behavior of a system of Kuramoto oscillators. To that end, we construct a fully connected, one-dimensional ring network of phase oscillators whose coupling strength (reflecting synaptic strength) as well as conduction velocity (reflecting myelination) are each regulated by a Hebbian learning rule. We evaluate the behavior of the system in terms of structural (pairwise connection strength and conduction velocity) and functional connectivity (local and global synchronization behavior). We find that for conditions in which a system limited to synaptic plasticity develops two distinct clusters both structurally and functionally, additional adaptive myelination allows for functional communication across these structural clusters. Hence, dynamic conduction velocity permits the functional integration of structurally segregated clusters. Our results confirm that network states following learning may be different when myelin plasticity is considered in addition to synaptic plasticity, pointing towards the relevance of integrating both factors in computational models of learning.