Evidence map›Paper›PMID 29478144›Full record

ArticleBrain structure & function2018

Integration of transcriptomic and cytoarchitectonic data implicates a role for MAOA and TAC1 in the limbic-cortical network.

Sebastian Bludau, Thomas W Mühleisen, Simon B Eickhoff, Michael J Hawrylycz, Sven Cichon, Katrin Amunts

Open access · hybridAbstract read
In one paragraph

Article in Brain structure & function, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed
1.5field-weighted citation impact, top 19% 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

18 citing papers in PubMed, 32 citations in OpenAlex.

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  5. Transcriptomic gradients of the human cerebellum.Imaging neuroscience (Cambridge, Mass.) · 2025
    Article
  6. Digital tools of analysis and data integration facilitate synergy between mouse and human brain research and enable translation.Mammalian genome : official journal of the International Mammalian Genome Society · 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

6 authors at 2 institutions in 3 countries.

Sebastian BludauResearch Centre Jülich, Institute of Neuroscience and Medicine (INM-1), 52425, Jülich, Germany. s.bludau@fz-juelich.de.ORCID http://orcid.org/0000-0001-6173-9050
Thomas W MühleisenResearch Centre Jülich, Institute of Neuroscience and Medicine (INM-1), 52425, Jülich, Germany.ORCID http://orcid.org/0000-0002-6057-5952
Simon B EickhoffResearch Centre Jülich, Institute of Neuroscience and Medicine (INM-7), 52425, Jülich, Germany.
Michael J HawrylyczAllen Institute for Brain Science, Seattle, WA, 98103, USA.
Sven CichonResearch Centre Jülich, Institute of Neuroscience and Medicine (INM-1), 52425, Jülich, Germany.
Katrin AmuntsResearch Centre Jülich, Institute of Neuroscience and Medicine (INM-1), 52425, Jülich, Germany.
Forschungszentrum Jülich · DEAllen Institute for Brain Science · US

Funding

European Union Seventh Framework program (FP7/2007-2013) grant 604102
6 · The paper itself

Abstract

Decoding the chain from genes to cognition requires detailed insights how areas with specific gene activities and microanatomical architectures contribute to brain function and dysfunction. The Allen Human Brain Atlas contains regional gene expression data, while the JuBrain Atlas offers three-dimensional cytoarchitectonic maps reflecting interindividual variability. To date, an integrated framework that combines the analytical benefits of both scientific platforms towards a multi-level brain atlas of adult humans was not available. We have, therefore, developed JuGEx, a new method for integrating tissue transcriptome and cytoarchitectonic segregation. We investigated differential gene expression in two JuBrain areas of the frontal pole that we have structurally and functionally characterized in previous studies. Our results show a significant upregulation of MAOA and TAC1 in the medial area frontopolaris which is a node in the limbic-cortical network and known to be susceptible for gray matter loss and behavioral dysfunction in patients with depression. The MAOA gene encodes an enzyme which is involved in the catabolism of dopamine, norepinephrine, serotonin, and other monoaminergic neurotransmitters. The TAC1 locus generates hormones that play a role in neuron excitations and behavioral responses. Overall, JuGEx provides a new tool for the scientific community that empowers research from basic, cognitive and clinical neuroscience in brain regions and disease models with regard to gene expression.

Indexed as

Brain MappingAdultAgedAged, 80 and overAnalysis of VarianceAutopsyFemaleFrontal LobeHumansImage Processing, Computer-AssistedLimbic SystemMagnetic Resonance ImagingMaleMiddle AgedMonoamine OxidaseNeural PathwaysMonoamine Oxidasemonoamine oxidase A, humanNKX2-1 protein, humanOxygenThyroid Nuclear Factor 1Adult human brainBrain mapsCytoarchitectureDifferential gene expressionMultimodal analysis

Identifiers

PMID29478144
PMCPMC5968065
OpenAlexW2788474213

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.