Evidence map›Paper›PMID 42527301›Full record

ArticleeNeuro2026

Pretraining for Large-Scale Functional Connectome Fingerprinting Supports Generalization and Transfer Learning in Functional Neuroimaging.

Mattson Ogg, Lindsey Kitchell

Abstract read
In one paragraph

Article in eNeuro, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

2 authors.

Mattson OggResearch and Exploratory Development Department, Johns Hopkins Applied Physics Laboratory, Laurel, Maryland 20723 mattson.ogg@jhuapl.edu.ORCID https://orcid.org/0009-0004-5583-0586
Lindsey KitchellResearch and Exploratory Development Department, Johns Hopkins Applied Physics Laboratory, Laurel, Maryland 20723.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Functional MRI (fMRI) currently supports a limited application space stemming from modest dataset sizes, large interindividual variability, and heterogeneity among scanning protocols. These constraints have made it difficult for fMRI researchers to take full advantage of modern deep-learning tools that have revolutionized other fields such as NLP, speech transcription, and image recognition. To help address these issues, we scaled up functional connectome fingerprinting as a neural network pretraining task, drawing inspiration from speaker recognition research, to learn a generalizable representation of brain function. This approach achieves strong performance for neural fingerprinting on a previously unseen scale, across multiple public fMRI datasets (individual recognition from held-out scan sessions, 93% on MPI-Leipzig, 94% on NKI-Rockland, 73% on OASIS-3, and 99% on HCP). Performance is maintained even when evaluation scan duration is truncated to <2 min. We show that this representation can also generalize to support accurate neural fingerprinting for completely new datasets and participants of either sex not used in training. Finally, we demonstrate that the representation learned by the network encodes features related to individual variability that partially transfers to new tasks. These results support the development of scalable transfer-learning approaches for future clinical and cognitive neuroimaging applications.

Indexed as

BrainConnectomeDeep LearningFunctional NeuroimagingMagnetic Resonance ImagingFemaleHumansMaledeep learningfMRIfunctional connectometransfer learning

Identifiers

PMID42527301
PMCPMC13505883

What OpenQuestion holds

Textmetadata
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.