Evidence map›Paper›PMID 40539077›Full record

ArticleProceedings. IEEE International Symposium on Biomedical Imaging2025

DUAL MULTI-ATLAS REPRESENTATION ALIGNMENT FOR BRAIN DISORDER DIAGNOSIS USING MORPHOLOGICAL CONNECTOME.

Kangfu Han, Dan Hu, Jiale Cheng, Tianming Liu, Andrea Bozoki, Dajiang Zhu, Gang Li

Abstract read
In one paragraph

Article in Proceedings. IEEE International Symposium on Biomedical Imaging, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0citing papers in PubMed
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1 · What the graph read from it

What it found

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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

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3 · Its place in the literature

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0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

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5 · Who and what money

Authors and funding

7 authors.

Kangfu HanDepartment of Radiology and Biomedical Research Imaging Center, University of North Carolina at Chapel Hill, Chapel Hill, NC, USA.
Dan HuDepartment of Radiology and Biomedical Research Imaging Center, University of North Carolina at Chapel Hill, Chapel Hill, NC, USA.
Jiale ChengDepartment of Radiology and Biomedical Research Imaging Center, University of North Carolina at Chapel Hill, Chapel Hill, NC, USA.
Tianming LiuSchool of Computing, University of Georgia, Athens, GA, USA.
Andrea BozokiDepartment of Neurology, University of North Carolina at Chapel Hill, Chapel Hill, NC, USA.
Dajiang ZhuDepartment of Computer Science and Engineering, University of Texas at Arlington, Arlington, TX, USA.
Gang LiDepartment of Radiology and Biomedical Research Imaging Center, University of North Carolina at Chapel Hill, Chapel Hill, NC, USA.

Funding

Mapping Trajectories of Alzheimer's Progression via Personalized Brain Anchor-nodesR01AG075582 · NIA · UNIVERSITY OF TEXAS ARLINGTON · PI Gang Li, Dajiang Zhu · 2022 to 2026
$2.7M
Developing an Individualized Deep Connectome Framework for ADRD AnalysisRF1NS128534 · NINDS · UNIVERSITY OF TEXAS ARLINGTON · PI LI, GANG, LIU, TIANMING · 2022 to 2022
$1.7M
SCH: Using Data-Driven Computational Biomechanics to Disentangle Brain Structural Commonality, Variability, and Abnormality in ASDR01NS135574 · NINDS · UNIVERSITY OF GEORGIA · PI Xianqiao Wang · 2023 to 2026
$1.1M
Harmonizing and Archiving of Large-scale Infant Neuroimaging DataRF1MH123202 · NIMH · UNIV OF NORTH CAROLINA CHAPEL HILL · PI LI, GANG · 2021 to 2021
$627k
NIA NIH HHS R01 AG075582NIMH NIH HHS RF1 MH123202NINDS NIH HHS R01 NS135574NINDS NIH HHS RF1 NS128534
6 · The paper itself

Abstract

In structural magnetic resonance imaging (MRI), morphological connectome plays an important role in capturing coordinated patterns of region-wise morphological features for brain disorder diagnosis. However, significant challenges remain in aggregating diverse representations from multiple brain atlases, stemming from variations in the definition of regions of interest. To effectively integrate complementary information from multiple atlases while mitigating possible biases, we propose a novel dual multi-atlas representation alignment approach (DMAA) for brain disorder diagnosis. Specifically, we first minimize the maximum mean discrepancy of multi-atlas representations to align them into a unified distribution, reducing inter-atlas variability and enhancing effective feature fusion. Then, to further manage the anatomical variability, we apply optimal transport to capture and harmonize region-wise differences, preserving plausible relationships across atlases. Extensive experiments on ADNI, PPMI, ADHD200, and SchizConnect datasets demonstrate the effectiveness of our proposed DMAA on brain disorder diagnosis using multi-atlas morphological connectome.

Indexed as

Brain DisorderMaximum Mean DiscrepancyMorphological ConnectomeOptimal Transport

Identifiers

PMID40539077
PMCPMC12178661

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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.