Evidence map›Paper›PMID 41459648›Full record

ArticleeLife2025

Biophysical basis for brain folding and misfolding patterns in ferrets and humans.

Gary P T Choi, Chunzi Liu, Sifan Yin, Gabrielle Séjourné, Richard S Smith, Christopher A Walsh, L Mahadevan

Abstract read
In one paragraph

Article in eLife, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

2 citing papers in PubMed.

  1. Article
  2. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

7 authors.

Gary P T ChoiDepartment of Mathematics, The Chinese University of Hong Kong, Hong Kong, China.ORCID https://orcid.org/0000-0001-5407-9111
Chunzi LiuSchool of Engineering and Applied Sciences, Harvard University, Cambridge, United States.
Sifan YinSchool of Engineering and Applied Sciences, Harvard University, Cambridge, United States.ORCID https://orcid.org/0000-0002-0296-3981
Gabrielle SéjournéSchool of Engineering and Applied Sciences, Harvard University, Cambridge, United States.
Richard S SmithDepartment of Pharmacology, Feinberg School of Medicine, Northwestern University, Chicago, United States.
Christopher A WalshDivision of Genetics and Genomics, Manton Center for Orphan Disease, and Howard Hughes Medical Institute, Chevy Chase, United States.
L MahadevanSchool of Engineering and Applied Sciences, Harvard University, Cambridge, United States.ORCID https://orcid.org/0000-0002-5114-0519

Funding

Cell Identity Determination In Human Brain: Somatic Mutation and Cell LineageR01NS032457 · NINDS · BOSTON CHILDREN'S HOSPITAL · PI Alice Eunjung Lee, Christopher A. Walsh · 1995 to 2026
$12.7M
Medical Scientist Training Program Training GrantT32GM145449 · NIGMS · DUKE UNIVERSITY · PI Christopher D Kontos · 2022 to 2026
$6.6M
Human Epilepsy Genetics Neuronal Migration DisordersR37NS035129 · NINDS · BOSTON CHILDREN'S HOSPITAL · PI Christopher A. Walsh · 2002 to 2026
$6.5M
Sodium Channel Dysfunction in Altered Brain DevelopmentR01NS140046 · NINDS · NORTHWESTERN UNIVERSITY · PI Richard S Smith · 2025 to 2026
$1.3M
Role for ion conducting proteins in cortical malformation diseasesR00NS112604 · NINDS · NORTHWESTERN UNIVERSITY · PI SMITH, RICHARD S · 2023 to 2025
$715k
CUHK Faculty of Science Direct Grant for Research 4053650Harvard Quantitative Biology Initiative and the NSF-Simons Center for Mathematical and Statistical Analysis of Biology at Harvard 1764269John Templeton Foundation 62587NIGMS NIH HHS T32 GM145449NINDS NIH HHS R00 NS112604NINDS NIH HHS R00NS112604NINDS NIH HHS R01 NS032457NINDS NIH HHS R01NS032457NINDS NIH HHS R01 NS140046NINDS NIH HHS R01NS140046NINDS NIH HHS R37 NS035129NINDS NIH HHS R37NS035129
6 · The paper itself

Abstract

A mechanistic understanding of neurodevelopment requires us to follow the multiscale processes that connect molecular genetic processes to macroscopic cerebral cortical formations and thence to neurological function. Using MRI of the brain of the ferret, a model organism for studying cortical morphogenesis, we create in vitro physical gel models and in silico numerical simulations of normal brain gyrification. Using observations of genetically manipulated animal models, we identify cerebral cortical thickness and cortical expansion rate as the primary drivers of dysmorphogenesis and demonstrate that in silico models allow us to examine the causes of aberrations in morphology and developmental processes at various stages of cortical ontogenesis. Finally, we explain analogous cortical malformations in human brains, with comparisons with human phenotypes induced by the same genetic defects, providing a unified perspective on brain morphogenesis that is driven proximally by genetic causes and affected mechanically via variations in the geometry of the brain and differential growth of the cortex.

Indexed as

BrainCerebral CortexFerretsAnimalsComputer SimulationHumansMagnetic Resonance Imagingbraindevelopmental biologyferrethumanneuroscience

Identifiers

PMID41459648
PMCPMC12747519

What OpenQuestion holds

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LicenceCC BY
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.