Evidence map›Paper›PMID 41292797›Full record

ArticlebioRxiv : the preprint server for biology2025

Precision functional imaging in infants using multi-echo fMRI at 7T.

Julia Moser, Alireza Sadeghi-Tarakameh, Julian S B Ramirez, Thomas J Madison, Lana Hantzsch, Kimberly B Weldon, Han H N Pham, Jacob T Lundquist, Sooyeon Sung, Inyene Ukpong and 10 more

Abstract readPreprint
In one paragraph

Article in bioRxiv : the preprint server for biology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

20 authors.

Julia MoserMasonic Institute for the Developing Brain, University of Minnesota, Minneapolis, MN, USA.ORCID 0000-0002-6219-415X
Alireza Sadeghi-TarakamehCenter for Magnetic Resonance Research (CMRR), University of Minnesota, Minneapolis, MN, USA.ORCID 0000-0001-5718-6553
Julian S B RamirezMasonic Institute for the Developing Brain, University of Minnesota, Minneapolis, MN, USA.ORCID 0000-0002-5284-6863
Thomas J MadisonMasonic Institute for the Developing Brain, University of Minnesota, Minneapolis, MN, USA.ORCID 0000-0003-3030-6580
Lana HantzschMasonic Institute for the Developing Brain, University of Minnesota, Minneapolis, MN, USA.ORCID 0000-0001-9420-0174
Kimberly B WeldonMasonic Institute for the Developing Brain, University of Minnesota, Minneapolis, MN, USA.ORCID 0000-0003-4349-9916
Han H N PhamMasonic Institute for the Developing Brain, University of Minnesota, Minneapolis, MN, USA.
Jacob T LundquistMasonic Institute for the Developing Brain, University of Minnesota, Minneapolis, MN, USA.ORCID 0000-0001-9573-1954
Sooyeon SungMasonic Institute for the Developing Brain, University of Minnesota, Minneapolis, MN, USA.ORCID 0000-0001-8557-1168
Inyene UkpongMasonic Institute for the Developing Brain, University of Minnesota, Minneapolis, MN, USA.
Emily DrexlerMasonic Institute for the Developing Brain, University of Minnesota, Minneapolis, MN, USA.
Alyssa K LabonteDepartment of Psychiatry, Washington University in St. Louis, St. Louis, MO, USA.ORCID 0000-0001-9660-9280
Edward J AuerbachCenter for Magnetic Resonance Research (CMRR), University of Minnesota, Minneapolis, MN, USA.ORCID 0000-0003-4553-1545
Gregor AdrianyCenter for Magnetic Resonance Research (CMRR), University of Minnesota, Minneapolis, MN, USA.ORCID 0000-0002-6428-9005
Chad M SylvesterDepartment of Psychiatry, Washington University in St. Louis, St. Louis, MO, USA.ORCID 0000-0003-2154-0826
Steven M NelsonMasonic Institute for the Developing Brain, University of Minnesota, Minneapolis, MN, USA.
Yigitcan EryamanCenter for Magnetic Resonance Research (CMRR), University of Minnesota, Minneapolis, MN, USA.ORCID 0009-0006-7880-9872
Jed T ElisonMasonic Institute for the Developing Brain, University of Minnesota, Minneapolis, MN, USA.ORCID 0000-0002-6246-1000
Damien A FairMasonic Institute for the Developing Brain, University of Minnesota, Minneapolis, MN, USA.ORCID 0000-0001-8602-393X
Essa YacoubCenter for Magnetic Resonance Research (CMRR), University of Minnesota, Minneapolis, MN, USA.ORCID 0009-0000-1007-9056

Funding

TRD4 - Ultrahigh Field Engineering and SafetyP41EB027061 · NIBIB · UNIVERSITY OF MINNESOTA · PI Gregory John Metzger · 2019 to 2026
$11.7M
NEUROSCIENCE TRAINING IN DRUG ABUSE RESEARCHT32DA007234 · NIDA · UNIVERSITY OF MINNESOTA TWIN CITIES · PI Paul G Mermelstein, Jocelyn M Richard · 1986 to 2026
$10.9M
Individualized Mechanisms of Neural Plasticity and Response to Interventions in NeonatesR01MH134966 · NIMH · WASHINGTON UNIVERSITY · PI Chad Michael Sylvester · 2024 to 2026
$4.2M
Safe Magnetic Resonance Imaging of Patients with Deep Brain Stimulation SystemsR01NS115180 · NINDS · UNIVERSITY OF MINNESOTA · PI ERYAMAN, YIGITCAN · 2020 to 2024
$1.9M
NIBIB NIH HHS P41 EB027061NIDA NIH HHS T32 DA007234NIMH NIH HHS R01 MH134966NINDS NIH HHS R01 NS115180
6 · The paper itself

Abstract

Personalized functional brain developmental trajectories can be studied with Precision Functional Mapping (PFM). Our previous work has demonstrated that PFM can be achieved in infants despite rapid brain growth. However, even with extensive data collection (up to 1 hour of fMRI), the reliability and precision of these maps remain lower than those observed in youth and adults - particularly within subcortical structures. In this work we demonstrate the utility of high-field 7T MRI compared to 3T MRI for facilitating PFM in infants. We showcase data from multi-echo fMRI acquisitions in the same infants at both 7T and 3T and demonstrate that 7T imaging in infants is safe and feasible with our subject-specific safety workflow. Moreover, we demonstrate that the use of a higher magnetic field strength affords a spatial resolution more appropriately matched to infants' smaller head and brain sizes, yielding notable improvements in data quality, especially for PFM. The increase in both spatial precision and reliability also suggests that 7T MRI can reduce the amount of data required for PFM. Last, we show how ultra-high field imaging can help us study the development of subcortical-to-cortical connectivity patterns, crucial for understanding brain development during this developmental window. 7T MRI is a promising new avenue for developmental cognitive neuroscience.

Identifiers

PMID41292797
PMCPMC12642582

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.