Evidence map›Paper›PMID 26037235›Full record

ArticleScientific reports2015

A novel brain partition highlights the modular skeleton shared by structure and function.

Ibai Diez, Paolo Bonifazi, Iñaki Escudero, Beatriz Mateos, Miguel A Muñoz, Sebastiano Stramaglia, Jesus M Cortes

Abstract read
In one paragraph

Article in Scientific reports, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 49 papers.

0numbers the graph read from it
0cells of the map it votes in
49citing 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

49 citing papers in PubMed.

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  14. Amyloid-β and tau pathologies relate to distinctive brain dysconnectomics in preclinical autosomal-dominant Alzheimer's disease.Proceedings of the National Academy of Sciences of the United States of America · 2022
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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

7 authors.

Ibai DiezBiocruces Health Research Institute, Cruces University Hospital, Barakaldo, Spain.
Paolo BonifaziSchool of Physics and Astronomy, George S. Wise Faculty of Life Sciences, Sagol School of Neuroscience, Tel Aviv University, Tel Aviv, Israel.
Iñaki Escudero1] Biocruces Health Research Institute, Cruces University Hospital, Barakaldo, Spain [2] Radiology Service, Cruces University Hospital, Barakaldo, Spain.
Beatriz Mateos1] Biocruces Health Research Institute, Cruces University Hospital, Barakaldo, Spain [2] Radiology Service, Cruces University Hospital, Barakaldo, Spain.
Miguel A MuñozDepartamento de Electromagnetismo y Física de la Materia and Instituto Carlos I de Física Teórica y Computacional, Universidad de Granada, Spain.
Sebastiano Stramaglia1] Biocruces Health Research Institute, Cruces University Hospital, Barakaldo, Spain [2] Dipartimento di Fisica, Universita degli Studi di Bari and INFN, Bari, Italy [3] Ikerbasque: The Basque Foundation for Science, Bilbao, Spain.
Jesus M Cortes1] Biocruces Health Research Institute, Cruces University Hospital, Barakaldo, Spain [2] Ikerbasque: The Basque Foundation for Science, Bilbao, Spain [3] Department of Cell Biology and Histology. University of the Basque Country. Leioa, Spain.

Funding

Mapping the Human Connectome: Structure, Function, and HeritabilityU54MH091657 · NIMH · WASHINGTON UNIVERSITY · PI UGURBIL, KAMIL, VAN ESSEN, DAVID C · 2010 to 2014
$34.7M
NIMH NIH HHS U54 MH091657
6 · The paper itself

Abstract

Elucidating the intricate relationship between brain structure and function, both in healthy and pathological conditions, is a key challenge for modern neuroscience. Recent progress in neuroimaging has helped advance our understanding of this important issue, with diffusion images providing information about structural connectivity (SC) and functional magnetic resonance imaging shedding light on resting state functional connectivity (rsFC). Here, we adopt a systems approach, relying on modular hierarchical clustering, to study together SC and rsFC datasets gathered independently from healthy human subjects. Our novel approach allows us to find a common skeleton shared by structure and function from which a new, optimal, brain partition can be extracted. We describe the emerging common structure-function modules (SFMs) in detail and compare them with commonly employed anatomical or functional parcellations. Our results underline the strong correspondence between brain structure and resting-state dynamics as well as the emerging coherent organization of the human brain.

Indexed as

Brain MappingAdultBrainCluster AnalysisConnectomeFemaleHumansMagnetic Resonance ImagingMaleMiddle AgedModels, BiologicalYoung Adult

Identifiers

PMID26037235
PMCPMC4453230

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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.