ArticleScientific data2026
A dense longitudinal multimodal single-subject rs-fMRI dataset acquired by self-administered scanning.
Article in Scientific data, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.
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.
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.
Who cites it
1 citing paper in PubMed.
- A dense longitudinal multimodal single-subject rs-fMRI dataset acquired by self-administered scanning.Scientific data · 2026Article
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PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
1 author.
Funding
No grant is acknowledged in the PubMed record.
Abstract
Dense longitudinal neuroimaging usually requires substantial institutional resources, yet can also be achieved by an individual using standard clinical MRI infrastructure. This work presents a multimodal single-subject dataset comprising 85 hours of resting-state fMRI acquired over 11 months, including 51.6 hours under a standardized protocol (paired eyes-open/-closed runs, 128 sessions over 7.5 months). Additional data include 195 T1-weighted structural scans, 54 diffusion MRI sessions, physiological recordings, pre-session behavioral assessments, and detailed medication and lifestyle logs. Scans were collected primarily via self-administered acquisition on a clinical 3 T system, with sub-3 mm between-session positioning reproducibility observed in later sessions. Quality control identified 58 hours of low-motion data (mean framewise displacement <0.2 mm), with higher-motion runs occurring predominantly during sleep. The acquisition period included antidepressant dose changes and seasonal variation, forming a single-subject naturalistic context with collinear factors that preclude causal inference. The dataset follows the BIDS standard and is intended for methodological development, reliability analyses, preprocessing benchmarking, and educational use.
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Registered trials
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.