Evidence map›Paper›PMID 28889005›Full record

ArticleNeuroImage2017

A flexible graphical model for multi-modal parcellation of the cortex.

Sarah Parisot, Ben Glocker, Sofia Ira Ktena, Salim Arslan, Markus D Schirmer, Daniel Rueckert

Abstract read
In one paragraph

Article in NeuroImage, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing 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

5 citing papers in PubMed.

  1. Review
  2. Review
  3. Article
  4. Article
  5. Review
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.

Sarah ParisotBiomedical Image Analysis Group, Department of Computing, Imperial College London, 180 Queens Gate, London, SW7 2AZ, UK. Electronic address: s.parisot@imperial.ac.uk.
Ben GlockerBiomedical Image Analysis Group, Department of Computing, Imperial College London, 180 Queens Gate, London, SW7 2AZ, UK.
Sofia Ira KtenaBiomedical Image Analysis Group, Department of Computing, Imperial College London, 180 Queens Gate, London, SW7 2AZ, UK.
Salim ArslanBiomedical Image Analysis Group, Department of Computing, Imperial College London, 180 Queens Gate, London, SW7 2AZ, UK.
Markus D SchirmerDepartment of Neurology, Massachusetts General Hospital, Harvard Medical School, Boston, MA, USA; Computer Science and Artificial Intelligence Lab, Massachusetts Institute of Technology, Boston, MA, USA.
Daniel RueckertBiomedical Image Analysis Group, Department of Computing, Imperial College London, 180 Queens Gate, London, SW7 2AZ, UK.

Funding

Mapping the Human Connectome: Structure, Function, and HeritabilityU54MH091657 · NIMH · WASHINGTON UNIVERSITY · PI UGURBIL, KAMIL, VAN ESSEN, DAVID C · 2010 to 2014
$34.7M
Training and DisseminationP41EB015902 · NIBIB · BRIGHAM AND WOMEN'S HOSPITAL · PI KIKINIS, RON, WESTIN, CARL-FREDRIK · 2012 to 2022
$20.9M
NIBIB NIH HHS P41 EB015902NIMH NIH HHS U54 MH091657
6 · The paper itself

Abstract

Advances in neuroimaging have provided a tremendous amount of in-vivo information on the brain's organisation. Its anatomy and cortical organisation can be investigated from the point of view of several imaging modalities, many of which have been studied for mapping functionally specialised cortical areas. There is strong evidence that a single modality is not sufficient to fully identify the brain's cortical organisation. Combining multiple modalities in the same parcellation task has the potential to provide more accurate and robust subdivisions of the cortex. Nonetheless, existing brain parcellation methods are typically developed and tested on single modalities using a specific type of information. In this paper, we propose Graph-based Multi-modal Parcellation (GraMPa), an iterative framework designed to handle the large variety of available input modalities to tackle the multi-modal parcellation task. At each iteration, we compute a set of parcellations from different modalities and fuse them based on their local reliabilities. The fused parcellation is used to initialise the next iteration, forcing the parcellations to converge towards a set of mutually informed modality specific parcellations, where correspondences are established. We explore two different multi-modal configurations for group-wise parcellation using resting-state fMRI, diffusion MRI tractography, myelin maps and task fMRI. Quantitative and qualitative results on the Human Connectome Project database show that integrating multi-modal information yields a stronger agreement with well established atlases and more robust connectivity networks that provide a better representation of the population.

Indexed as

Brain MappingCerebral CortexHumansImage Processing, Computer-AssistedBrain connectivityConnectomicsCortex parcellationdiffusion Magnetic Resonance Imagingfunctional Magnetic Resonance ImagingMarkov random fields

Identifiers

PMID28889005
PMCPMC6440540

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Registered trials

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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.