Search arXivSearch

arXiv · 2607.08534

Open-source MRI-informed computational model of human cortical folding

Abstract

The human cerebral cortex, initially smooth, progressively folds during fetal brain development in utero, giving rise to cortical convolutions. Atypical cortical folding patterns can be associated with neurodevelopmental and neurological disorders. To better understand these conditions, it is crucial to first examine the factors governing healthy cortical folding. Computational modeling provides a powerful way for this purpose and has already helped understanding the influence of key biomechanical parameters on the folding pattern. However, most existing models use simplified geometries, limiting calibration and validation with fetal and neonatal brain Magnetic Resonance Imaging (MRI) and neglecting the influence of initial geometry on fold development. On the other hand, simulations on realistic brain geometries introduce additional challenges, including collision handling, fold characterization, and additional computational cost. Furthermore, model parameters are often difficult to interpret, complicating comparison, clinical translation, and calibration. Finally, computational models of cortical folding also remain rarely accessible. In this work, we introduce a novel computational model of cortical folding, developed using the open-source code FEniCS to simulate folding on a whole-brain geometry generated from fetal MRI data. We also propose a modular, interpretable, and scalable simulation framework built around this computational model and openly available to the community. It uses fetal MRI data to generate realistic input brain meshes and estimate key biomechanical parameters such as cortical growth rate. The framework also integrates a spectral metric for cortical surface analysis to optimize folding pattern predictions from an healthy fetal MRI dataset.

Explore related subjects

Keep this discovery

Explore connections, maps & timelines

BibTeXRIS

Anne Kerachni, Thomas Lavigne, Stéphane Urcun, Mireia Alenya, Oscar Camara, Julien Lefèvre François Rousseau. 2026-07-09. Open-source MRI-informed computational model of human cortical folding. https://arxiv.org/abs/2607.08534

Cite the original work for its findings. Save a collection to share your selection of sources.

KEEP EXPLORING

Related papers

Signature of mechanically induced cell extrusions in cell size distribution

How a growing tissue organizes its own homeostatic state is a central question in the physics of living matter. We show that when a growing epithelial sheet counteracts increasing cell density by mechanically squeezing cells out of its plane, a homeostatic in-plane pressure emerges as a generalization of a yield stress. We find that in the quasistatic growth limit the homeostatic state is marginally stable, with a pseudogap in the distribution of local distances to the extrusion threshold pressure. Because such mechanically induced extrusions arise from an instability of individual cells, the pseudogap is imprinted in the distribution of cell areas. This provides an image-based way to test for presence of mechanically induced extrusions and we identify this signature in the developing wing epithelium of \textit{D.~melanogaster}. We expect the same principles to apply to confined three-dimensional tissues.

physics.bio-ph

Towards Accurate Prediction of Mutation-Induced Changes in Protein Structure

Proteins can possess numerous mutations relative to their wild-type amino acid sequences with minimal impact to their structure and function. However, in other cases, even a single amino acid mutation relative to the wild-type sequence can lead to a large change in structure or even a disease phenotype. While the accuracy of wild-type protein structure prediction has improved significantly in recent years, it remains difficult to accurately predict the structure of mutant proteins. Here, we characterize the local mutation-induced structural changes in proteins for a dataset of wildtype and the corresponding single-amino acid mutant x-ray crystal structures from the Protein Data Bank (PDB). We find that mutation-induced structural changes in these proteins are localized at the site of the mutation, decaying rapidly with increasing spatial distance from the mutation site. In addition, we evaluate how well AlphaFold3 can recapitulate the observed mutation-induced structural deformations in the x-ray crystal structures. We find that the accuracy of the AlphaFold3 predictions decreases strongly with increasing mutation-induced deformation. In contrast to the results for AlphaFold3, the Pearson correlation between a single physical feature, i.e. the change in solvent accessibility, and the mutation-induced deformation does not depend on the magnitude of the deformation. Our results and analyses provide a framework for further studies aimed at predicting the structural changes in proteins caused by single amino acid mutations.

physics.bio-ph

Biology and Physics

This article frames the relation between biology and physics by characterizing the former as a subdiscipline rather than a special case of the latter. To do this, we posit biological physics as the science of living matter in contrast to classic biophysics, the study of organismal properties by physical techniques. At the scale of the individual cell, living matter is nonunitary, i.e., not composed of aggregated subunits, and has features (e.g., intracellular organizational arrangements and biomolecular condensates) that are unlike any materials of the nonliving world. In transiently or constitutively multicellular forms (social microorganisms, animals, plants), living matter sustains physical processes that are generic (shared with nonliving matter, e.g., subunit communication by molecular diffusion in cellular slime molds), biogeneric (analogous to nonliving matter but realized through cellular activities, e.g., subunit demixing in animal embryos) or nongeneric (pertaining to sui generis materials, e.g., budding of active solids in plants). This "forms of matter" perspective is philosophically situated in the dialectical materialism of Engels and Hessen and the multilevel physicalism of Neurath and the logical empiricists. We counterpose this view to informationism and to genetic and other hierarchically reductionist physical theories of biological systems and highlight open questions regarding incompletely characterized and enigmatic forms of living matter.

physics.bio-ph