OSCR

The Cerebellar Connectome.

Overview

Authors: Oliver Schmitt1,2, Paulina Morawska2, Vishnu Prathapan1, Peter Eipert1
ORCID iDs: Oliver Schmitt
  1. MSH Medical School Hamburg – University of Applied Sciences and Medical University, Hamburg, Germany
  2. University Medical Center Rostock, Rostock, Germany
Journal: Cerebellum (London, England), volume 25, issue 4, article 110
Dates: received 14 July 2025; accepted 22 June 2026; published online 16 July 2026; in print 2026
Type: Research article · Language: English
License: CC BY
Identifiers: DOI 10.1007/s12311-026-02042-x · PMID 42458125 · PMCID PMC13372957 · OpenAlex W7168359170
Open access: hybrid, a free copy (OpenAlex)
Status: data only
Categories: rat (organism)
Methods: Graphs, fMRI & imaging
Keywords: Cerebellum, Connectome, Network neuroscience, Rat brain, Graph theory, Dynamic modeling
MeSH: Cerebellum*, Connectome*, Nerve Net*, Animals, Models, Neurological, Neural Pathways, Rats (* major topic)
Topic: Functional Brain Connectivity Studies (Cognitive Neuroscience, Neuroscience), according to OpenAlex
Funding: MSH Medical School Hamburg - University of Applied Sciences and Medical University
Citations: not cited yet (Europe PMC); 156 references in the paper

Abstract

The cerebellum, long known for its role in motor control, has increasingly been implicated in cognitive and affective functions. Despite this broadened perspective, its connectivity remains undercharacterized relative to the cerebral cortex. Here, we present the first comprehensive cerebellar connectome analysis derived from a large-scale, meta-analytic database of over 7,800 high-resolution tract-tracing studies in the rat brain. Leveraging the neuroVIISAS framework, we constructed a directionally weighted, hierarchically organized cerebellar subnetwork integrating both intrinsic and extrinsic connections, including lateralization and interhemispheric projections. Our methodological pipeline involved region expansion, graph-theoretical filtering, and systematic edge weighting by anatomical significance. The resulting network, encompassing 862 regions and over 21,000 edges, was analyzed across multiple topological scales. Mesoscale analysis revealed hallmark properties of small-world and scale-free networks, while motif and modularity analyses identified non-random, functionally coherent microcircuits and subsystems. Local connectome metrics uncovered key integrative hubs–especially within brainstem-cerebellar loops–and exposed gradients of modularity, controllability, and vulnerability. A novel vulnerability analysis showed that the removal of high-significance edges leads to rapid and irregular degradation of clustering in the empirical network, in contrast to the robustness of rewired surrogate models. This indicates the presence of structurally privileged bottlenecks essential for cerebellar integration. Our results collectively highlight the cerebellum’s dual design: functionally specialized yet structurally efficient, with both local modularity and long-range integration. This study establishes a robust foundation for future multimodal, dynamic, and cross-species connectomic research. Integrating empirical data on neuronal dynamics, synaptic plasticity, and gene expression will be essential to fully realize the translational potential of cerebellar network models in both health and disease.

Reproduced under the paper's license (CC BY), from the paper cited above.

Code

The paper links to its data, not to its authors' code: see the Data section.

Tracing map

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Data

Datasets cited

Data Availability Statement

https://figshare.com/articles/dataset/Cerebellar_connectome/29528057, 10.6084/m9.figshare.29528057

https://neuroviisas.med.uni-rostock.de/neuroviisas.shtml

Reproduced under the paper's license (CC BY), from the paper cited above.

Versions

The history of this record: each version stored by the harvester or made by a correction of its authors or of the maintainers of its code, and what changed in its facts. The texts of the paper (its abstract, its availability statements) are not part of it; versions that changed only those are not listed.

Version 2, 28 September 2026

  • Publisher: n/a → Springer Science+Business Media

Version 1, 27 September 2026: the first record

Recorded: type, language, journal, volume, issue, pages, dates, 4 authors, 6 keywords, 7 MeSH terms, 1 funder, 144 references.

Cite

This paper

Schmitt, O., Morawska, P., Prathapan, V., & Eipert, P. (2026). The Cerebellar Connectome. Cerebellum (London, England), 25(4), 110. https://doi.org/10.1007/s12311-026-02042-x

BibTeX

@article{schmitt2026cerebellar,
author = {Schmitt, Oliver and Morawska, Paulina and Prathapan, Vishnu and Eipert, Peter},
title = {{The Cerebellar Connectome}},
journal = {Cerebellum (London, England)},
year = {2026},
month = jul,
volume = {25},
number = {4},
pages = {110},
publisher = {Springer Science+Business Media},
issn = {1473-4222},
doi = {10.1007/s12311-026-02042-x},
url = {https://doi.org/10.1007/s12311-026-02042-x},
pmid = {42458125},
pmcid = {PMC13372957}
}

RIS

TY - JOUR
AU - Schmitt, Oliver
AU - Morawska, Paulina
AU - Prathapan, Vishnu
AU - Eipert, Peter
TI - The Cerebellar Connectome
T2 - Cerebellum (London, England)
J2 - Cerebellum
PY - 2026
DA - 2026/07/16
VL - 25
IS - 4
SP - 110
SN - 1473-4222
PB - Springer Science+Business Media
DO - 10.1007/s12311-026-02042-x
UR - https://doi.org/10.1007/s12311-026-02042-x
LA - en
ER -

CSL-JSON

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