Biophysical modeling of anatomically realistic prenatal cortical folding development

J Jixin Hou Z Zhengwang Wu K Kun Jiang (Shanghai Key Laboratory of Molecular Catalysis and Innovative Materials, State Key Laboratory of Porous Materials for Separation and Conversion, iChEM (Collaborative Innovation Center of Chemistry for Energy Materials), Department of Chemistry) T Taotao Wu L Lu Zhang D Dajiang Zhu W Wei Gao M Mir Jalil Razavi T Tianming Liu E Ellen Kuhl G Gang Li (State Key Laboratory of Molecular Reaction Dynamics and Dalian Coherent Light Source Dalian Institute of Chemical Physics, Chinese Academy of Sciences, 457 Zhongshan Road, Dalian 116023, China) X Xianqiao Wang

Abstract

Abstract Cortical folds encode the architecture of human cognition, yet the mechanisms that transform the smooth fetal cortex into its convoluted geometry remain elusive. Biophysical modeling enables mechanistic insight into cortical morphogenesis, but existing models often lack anatomical realism and fail to capture key hallmarks and morphometrics of dynamic cortical folding in the developing human brain. Here, we introduce a whole-brain developmental framework that integrates region-specific, data-driven growth laws with anatomically realistic cortical geometry to enable biologically interpretable modeling of cortical morphogenesis during gestation. Growth fields derived from large-scale prenatal magnetic resonance imaging data capture spatiotemporal variations in cortical expansion and thickness across parcellated regions. Incorporating heterogeneous growth yields folding patterns that match key anatomical landmarks and quantitative morphometrics from human imaging. Systematic perturbations of geometry and growth attributes delineate control parameters that produce realistic morphological variability and replicate clinically atypical brain phenotypes consistent with lissencephaly, pachygyria, and polymicrogyria. This framework provides a quantitative foundation for elucidating the mechanisms of typical and atypical fetal brain development.

Article Details

Volume / Issue Vol. 1, Issue 1
Published July 16, 2026
ISSN 2041-1723
Publisher Nature Portfolio

Journal Info

Nature Communications

Nature Portfolio

ISSN: 2041-1723 Open Access Life Sciences

Authors (12)

J

Jixin Hou

Z

Zhengwang Wu

K

Kun Jiang

Shanghai Key Laboratory of Molecular Catalysis and Innovative Materials, State Key Laboratory of Porous Materials for Separation and Conversion, iChEM (Collaborative Innovation Center of Chemistry for Energy Materials), Department of Chemistry

T

Taotao Wu

L

Lu Zhang

D

Dajiang Zhu

W

Wei Gao

M

Mir Jalil Razavi

T

Tianming Liu

E

Ellen Kuhl

G

Gang Li

State Key Laboratory of Molecular Reaction Dynamics and Dalian Coherent Light Source Dalian Institute of Chemical Physics, Chinese Academy of Sciences, 457 Zhongshan Road, Dalian 116023, China

X

Xianqiao Wang