Evidence map›Paper›PMID 33226978›Full record

ArticlePLoS biology2020

Cortical morphology at birth reflects spatiotemporal patterns of gene expression in the fetal human brain.

Gareth Ball, Jakob Seidlitz, Jonathan O'Muircheartaigh, Ralica Dimitrova, Daphna Fenchel, Antonios Makropoulos, Daan Christiaens, Andreas Schuh, Jonathan Passerat-Palmbach, Jana Hutter and 7 more

Open access · goldAbstract read
In one paragraph

Article in PLoS biology, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 33 papers.

0numbers the graph read from it
0cells of the map it votes in
33citing papers in PubMed
12.4field-weighted citation impact, top 1% of its field
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

33 citing papers in PubMed, 62 citations in OpenAlex.

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  10. Maturation of Neuronal Activity in the Human Cortex Exhibits Robust Spatial Gradients across the Birth Transition.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2025
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  15. Deciphering the functional specialization of whole-brain spatiomolecular gradients in the adult brain.Proceedings of the National Academy of Sciences of the United States of America · 2024
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

17 authors at 4 institutions in 4 countries.

Gareth BallDevelopmental Imaging, Murdoch Children's Research Institute, Melbourne, Australia.ORCID 0000-0003-3509-1435
Jakob SeidlitzDevelopmental Neurogenomics Unit, National Institute of Mental Health, Bethesda, United States of America.ORCID 0000-0002-8164-7476
Jonathan O'MuircheartaighCentre for the Developing Brain, Department of Perinatal Imaging & Health, King's College London, United Kingdom.
Ralica DimitrovaCentre for the Developing Brain, Department of Perinatal Imaging & Health, King's College London, United Kingdom.ORCID 0000-0002-6903-7990
Daphna FenchelCentre for the Developing Brain, Department of Perinatal Imaging & Health, King's College London, United Kingdom.
Antonios MakropoulosCentre for the Developing Brain, Department of Perinatal Imaging & Health, King's College London, United Kingdom.
Daan ChristiaensCentre for the Developing Brain, Department of Perinatal Imaging & Health, King's College London, United Kingdom.ORCID 0000-0001-8323-5451
Andreas SchuhBiomedical Image Analysis Group, Department of Computing, Imperial College London, United Kingdom.ORCID 0000-0002-8214-116X
Jonathan Passerat-PalmbachBiomedical Image Analysis Group, Department of Computing, Imperial College London, United Kingdom.
Jana HutterCentre for the Developing Brain, Department of Perinatal Imaging & Health, King's College London, United Kingdom.
Lucilio Cordero-GrandeCentre for the Developing Brain, Department of Perinatal Imaging & Health, King's College London, United Kingdom.
Emer HughesCentre for the Developing Brain, Department of Perinatal Imaging & Health, King's College London, United Kingdom.
Anthony PriceCentre for the Developing Brain, Department of Perinatal Imaging & Health, King's College London, United Kingdom.
Jo V HajnalCentre for the Developing Brain, Department of Perinatal Imaging & Health, King's College London, United Kingdom.
Daniel RueckertBiomedical Image Analysis Group, Department of Computing, Imperial College London, United Kingdom.ORCID 0000-0002-5683-5889
Emma C RobinsonCentre for the Developing Brain, Department of Perinatal Imaging & Health, King's College London, United Kingdom.
A David EdwardsCentre for the Developing Brain, Department of Perinatal Imaging & Health, King's College London, United Kingdom.ORCID 0000-0003-4801-7066
King's College London · GBInstitute of Group Analysis · GBThe University of Melbourne · AUUniversity of Cambridge · GB

Funding

Medical Research Council MR/N026063/1Wellcome Trust 201374/Z/16/Z
6 · The paper itself

Abstract

Interruption to gestation through preterm birth can significantly impact cortical development and have long-lasting adverse effects on neurodevelopmental outcome. We compared cortical morphology captured by high-resolution, multimodal magnetic resonance imaging (MRI) in n = 292 healthy newborn infants (mean age at birth = 39.9 weeks) with regional patterns of gene expression in the fetal cortex across gestation (n = 156 samples from 16 brains, aged 12 to 37 postconceptional weeks [pcw]). We tested the hypothesis that noninvasive measures of cortical structure at birth mirror areal differences in cortical gene expression across gestation, and in a cohort of n = 64 preterm infants (mean age at birth = 32.0 weeks), we tested whether cortical alterations observed after preterm birth were associated with altered gene expression in specific developmental cell populations. Neonatal cortical structure was aligned to differential patterns of cell-specific gene expression in the fetal cortex. Principal component analysis (PCA) of 6 measures of cortical morphology and microstructure showed that cortical regions were ordered along a principal axis, with primary cortex clearly separated from heteromodal cortex. This axis was correlated with estimated tissue maturity, indexed by differential expression of genes expressed by progenitor cells and neurons, and engaged in stem cell differentiation, neuron migration, and forebrain development. Preterm birth was associated with altered regional MRI metrics and patterns of differential gene expression in glial cell populations. The spatial patterning of gene expression in the developing cortex was thus mirrored by regional variation in cortical morphology and microstructure at term, and this was disrupted by preterm birth. This work provides a framework to link molecular mechanisms to noninvasive measures of cortical development in early life and highlights novel pathways to injury in neonatal populations at increased risk of neurodevelopmental disorder.

Indexed as

BrainCerebral CortexFemaleFetal Organ MaturityFetusFunctional NeuroimagingGene Expression ProfilingGene Expression Regulation, DevelopmentalGestational AgeHumansInfant, NewbornInfant, PrematureMaleMultiparametric Magnetic Resonance ImagingNeurogenesisPregnancy

Identifiers

PMID33226978
PMCPMC7721147
OpenAlexW3107351341

What OpenQuestion holds

Textmetadata
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.