Evidence map›Paper›PMID 28968835›Full record

ArticleCerebral cortex (New York, N.Y. : 1991)2018

Cell-Specific Gene-Expression Profiles and Cortical Thickness in the Human Brain.

Jean Shin, Leon French, Ting Xu, Gabriel Leonard, Michel Perron, G Bruce Pike, Louis Richer, Suzanne Veillette, Zdenka Pausova, Tomáš Paus

Open access · bronzeAbstract read
In one paragraph

Article in Cerebral cortex (New York, N.Y. : 1991), 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 75 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
75citing papers in PubMed, 1 pooled it
6.0field-weighted citation impact, top 3% 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

75 citing papers in PubMed, 1 synthesis or guideline pooled it, 152 citations in OpenAlex.

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  16. Cells and Molecules Underpinning Cannabis-Related Variations in Cortical Thickness during Adolescence.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2024
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15 more citing papers are in PubMed but not listed here.

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

10 authors at 6 institutions in 2 countries.

Jean ShinThe Hospital for Sick Children, University of Toronto, Toronto, Canada.
Leon FrenchCentre for Addition and Mental Health, Toronto, Canada.
Ting XuCenter for Developing Brain, Child Mind Institute, New York, NY, USA.
Gabriel LeonardMontreal Neurological Institute, McGill University, Montreal, Canada.
Michel PerronCEGEP Jonquiere, Jonquiere, Canada.
G Bruce PikeDepartments of Radiology & Clinical Neuroscience, University of Calgary, Calgary, Canada.
Louis RicherDepartment of Psychology, University of Quebec in Chicoutimi, Chicoutimi, Canada.
Suzanne VeilletteCEGEP Jonquiere, Jonquiere, Canada.
Zdenka PausovaThe Hospital for Sick Children, University of Toronto, Toronto, Canada.
Tomáš PausRotman Research Institute, University of Toronto, Toronto, Canada.
University of Toronto · CACégep de Jonquière · CAChild Mind Institute · USMontreal Neurological Institute and Hospital · CAUniversité du Québec à Chicoutimi · CAUniversity of Calgary · CA

Funding

CRCNS: Linking receptorarchitecture and functional brain networks across speciesR01MH139349 · NIMH · CHILD MIND INSTITUTE, INC. · PI Thomas Funck · 2024 to 2026
$516k
CIHRNIMH NIH HHS R01 MH139349
6 · The paper itself

Abstract

Neurobiological underpinnings of cortical thickness in the human brain are largely unknown. Here we use cell-type-specific gene markers to evaluate the contribution of 9 neural cell-types in explaining inter-regional variations in cortical thickness and age-related cortical thinning in the adolescent brain. Gene-expression data were derived from the Allen Human Brain Atlas (and validated using the BrainSpan Atlas). Values of cortical thickness/thinning were obtained with magnetic resonance imaging in a sample of 987 adolescents. We show that inter-regional profiles in cortical thickness relate to those in the expression of genes marking CA1 pyramidal cells, astrocytes, and microglia; taken together, the 3 cell types explain 70% of regional variation in cortical thickness. We also show that inter-regional profiles in cortical thinning relate to those in the expression of genes marking CA1 and S1 pyramidal cells, astrocytes and microglia. Using Gene Ontology analysis, we demonstrate that the difference in the contribution of CA1 and S1 pyramidal cells may relate to biological processes such as neuronal plasticity and potassium channel activity, respectively. This "virtual histology" approach (scripts provided) can be used to examine neurobiological underpinnings of cortical profiles associated with development, aging, and various disorders.

Indexed as

AdolescentCerebral CortexFemaleHumansMaleNeurogliaNeuronsOrgan SizeTranscriptome

Identifiers

PMID28968835
PMCPMC13017599
OpenAlexW2742494644

What OpenQuestion holds

Textmetadata
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.