Evidence map›Paper›PMID 42890481›Full record

ArticleNeurophotonics2026

Multiscale neural signatures of long-lag repetition learning: a simultaneous fNIRS-EEG study.

Jinglei Ren, Adam Noah, Xian Zhang, Vincent Gracco, Marc Joanisse, Aahana Bajracharya, Jay G Rueckl, Augusto Buchweitz, Nabin Koirala, Joy Hirsch and 1 more

Abstract read
In one paragraph

Article in Neurophotonics, 2026. 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
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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

11 authors.

Jinglei RenYale School of Medicine, Yale Child Study Center, New Haven, Connecticut, United States.
Adam NoahYale School of Medicine, Brain Function Laboratory, New Haven, Connecticut, United States.ORCID https://orcid.org/0000-0001-9773-2790
Xian ZhangYale School of Medicine, Brain Function Laboratory, New Haven, Connecticut, United States.
Vincent GraccoYale School of Medicine, Yale Child Study Center, New Haven, Connecticut, United States.
Marc JoanisseThe University of Western Ontario, Department of Psychology, London, Ontario, Canada.ORCID https://orcid.org/0000-0002-6352-291X
Aahana BajracharyaYale School of Medicine, Yale Child Study Center, New Haven, Connecticut, United States.ORCID https://orcid.org/0000-0002-7361-6020
Jay G RuecklUniversity of Connecticut, Department of Psychological Sciences, Storrs, Connecticut, United States.
Augusto BuchweitzUniversity of Connecticut, Department of Psychological Sciences, Storrs, Connecticut, United States.ORCID https://orcid.org/0000-0003-3791-7472
Nabin KoiralaYale School of Medicine, Yale Child Study Center, New Haven, Connecticut, United States.ORCID https://orcid.org/0000-0002-8261-8271
Joy HirschYale School of Medicine, Brain Function Laboratory, New Haven, Connecticut, United States.ORCID https://orcid.org/0000-0002-1418-6489
Ken PughYale School of Medicine, Yale Child Study Center, New Haven, Connecticut, United States.

Funding

Tracking neurocognitive changes during evidence-based reading instruction in typically and atypically developing childrenR37HD090153 · NICHD · UNIVERSITY OF CONNECTICUT STORRS · PI Kenneth R. Pugh · 2017 to 2026
$6.0M
Sensorimotor Basis of Speech Motor Learning and RetentionR01DC022097 · NIDCD · YALE UNIVERSITY · PI DAVID J OSTRY · 2024 to 2026
$2.1M
NICHD NIH HHS R37 HD090153NIDCD NIH HHS R01 DC022097
6 · The paper itself

Abstract

Significance: Repetition-based learning supports word recognition and reading fluency, yet its neural mechanisms remain poorly understood, particularly where deficits in consolidating repeated linguistic input may underlie reading and language difficulties. Establishing reliable neural markers of repetition-based learning is a critical first step toward characterizing the phenotypes of these difficulties in children. Aim: We developed a whole-brain simultaneous functional near-infrared spectroscopy-electroencephalography (fNIRS-EEG) approach to capture fast temporal electrophysiological and spatially accurate hemodynamic signals during long-lag repetition learning. Approach: Thirty participants performed a semantic judgment task with words repeated across four runs with intervening items, modeling repetition demands central to reading instruction. A multimodal decoding framework integrating electrophysiological, hemodynamic, and cross-modal fNIRS-EEG correlation features was used to classify repetition-based learning. Results: Repeated words showed response time reductions. EEG captured a frontal N400-range repetition-related negativity and attenuation of alpha-beta suppression, reflecting changes in recognition-related and post-recognition processing. fNIRS revealed left inferior frontal and superior temporal efficiency increases alongside right supramarginal activation, suggesting integrative processing. Multimodal classifiers outperformed unimodal classifiers, indicating that each modality captured complementary aspects of learning. Conclusions: Combining fNIRS and EEG with multimodal machine learning provides a richer characterization of repetition-based learning than either modality alone, establishing a framework for phenotyping language learning capacity and identifying neural markers of reading difficulties in pediatric populations.

Indexed as

electroencephalographyfunctional near-infrared spectroscopylong-lag repetition learningmultimodal neuroimagingmultiscale neural adaptation

Identifiers

PMID42890481
PMCPMC13673251

What OpenQuestion holds

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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.