Evidence map›Paper›PMID 42079056›Full record

ArticlebioRxiv : the preprint server for biology2026

Robustness of NeuroMark-Derived Functional Networks to fMRI Spatial Normalization Across the Human Lifespan.

Zening Fu, Sarah Shultz, Armin Iraji, Vince D Calhoun

Abstract readPreprint
In one paragraph

Article in bioRxiv : the preprint server for biology, 2026. 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

Who cites it

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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

4 authors.

Zening FuTri-Institutional Center for Translational Research in Neuroimaging and Data Science (TReNDS), Georgia State University, Georgia Institute of Technology, Emory University, Atlanta, Georgia, United States.
Sarah ShultzDepartment of Pediatrics, Emory University School of Medicine, Atlanta, Georgia, United States.
Armin IrajiTri-Institutional Center for Translational Research in Neuroimaging and Data Science (TReNDS), Georgia State University, Georgia Institute of Technology, Emory University, Atlanta, Georgia, United States.
Vince D CalhounTri-Institutional Center for Translational Research in Neuroimaging and Data Science (TReNDS), Georgia State University, Georgia Institute of Technology, Emory University, Atlanta, Georgia, United States.

Funding

Male/Female differences in psychosis and mood disorders:Dynamic imaging-genomic models for characterizing and predicting psychosis and mood dR01MH118695 · NIMH · GEORGIA STATE UNIVERSITY · PI ADALI, TULAY, CALHOUN, VINCE D · 2019 to 2023
$3.8M
Unified multivariate data-driven solutions for static and dynamic brain connectivityR01EB020407 · NIBIB · THE MIND RESEARCH NETWORK · PI ADALI, TULAY, CALHOUN, VINCE D · 2015 to 2018
$2.7M
Data-driven approaches to identify biomarkers from multimodal imaging big dataR01MH117107 · NIMH · GEORGIA STATE UNIVERSITY · PI CALHOUN, VINCE D · 2019 to 2022
$1.6M
Mapping the Infant Brain Developmental Connectome: Temporally Precise Growth Trajectories of Changing Infant Brain TopologyR01MH119251 · NIMH · EMORY UNIVERSITY · PI IRAJI, ARMIN, SHULTZ, SARAH · 2020 to 2023
$1.0M
NIBIB NIH HHS R01 EB020407NIMH NIH HHS R01 MH117107NIMH NIH HHS R01 MH118695NIMH NIH HHS R01 MH119251
6 · The paper itself

Abstract

NeuroMark is a fully automated hybrid independent component analysis (ICA) framework designed to extract functional network features that are individually resolved and comparable across different cohorts. By integrating a reliable spatial template with spatially constrained ICA that adapts to each scan, NeuroMark retains the advantages of data-driven decomposition while avoiding limitations of fixed region-of-interest approaches. NeuroMark typically employs direct spatial normalization of fMRI data to a standardized adult EPI template; it remains unclear whether this approach is optimal for populations whose anatomy differs substantially from that of adults. We evaluated two normalization strategies in three large datasets spanning infancy, development, and aging: (1) direct normalization to the adult EPI template (EPInorm), and (2) normalization using an age-specific anatomical T1 template followed by transformation to the adult EPI template (T1toEPInorm). Across all cohorts, average intrinsic connectivity networks derived from EPInorm and T1toEPInorm exhibited very high spatial correspondence (mean ± SD: 0.9966 ± 0.0012 in infants; 0.9947 ± 0.0019 in development; 0.9963 ± 0.0012 in aging). The individual level also showed high similarity, though time courses showed slightly higher consistency than spatial maps (average correlations for time courses: 0.7990-0.9931; average correlations for spatial maps: 0.6879-0.9131). Functional network connectivity (FNC) measures were extremely well preserved across scans (95% of FNC with r > 0.9374 in infants; r > 0.8670 in developmental cohorts; r > 0.9219 in aging), demonstrating the robustness of NeuroMark features to different normalization strategies. Together, these results indicate that NeuroMark yields highly stable functional network features irrespective of whether an age-specific intermediate registration step is incorporated. NeuroMark, along with direct normalization to the adult EPI template, thus provides a robust, efficient, and harmonizable approach for large-scale, multisite, and lifespan neuroimaging studies, facilitating broad comparability across datasets while avoiding potential biases introduced by using multiple age-specific templates within a single study.

Identifiers

PMID42079056
PMCPMC13131602

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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.