ArticleImaging neuroscience (Cambridge, Mass.)2024
Generative AI for rapid diffusion MRI with improved image quality, reliability, and generalizability.
Article in Imaging neuroscience (Cambridge, Mass.), 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.
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
3 citing papers in PubMed.
- Gray Matter Morphological Networks are Associated with Neurobiological Features, Cognitive Status and Clinical Recovery in Traumatic Brain Injury.medRxiv : the preprint server for health sciences · 2026Article
- Deep Learning Empowered Microstructure Codebook: New Paradigm for Multi-Parameter Tissue Characterization Estimation.Human brain mapping · 2026Article
- Mapping the microstructure of human cerebral cortex in vivo with diffusion MRI.Communications biology · 2025Article
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
5 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
We use generative AI to enable rapid diffusion MRI (dMRI) with high fidelity, reproducibility, and generalizability across clinical and research settings. We employ a Swin UNEt Transformers (SWIN) model, trained on Human Connectome Project (HCP) data (n = 1021) and conditioned on registered T1 scans, to perform generalized dMRI denoising. We also qualitatively demonstrate super-resolution with artificially downsampled HCP data. Remarkably, SWIN can be fine-tuned for an out-of-domain dataset with a single example scan, as we demonstrate on dMRI of children with neurodevelopmental disorders (n = 40), adults with acute traumatic brain injury (n = 40), and adolescents with intracerebral hemorrhage due to vascular malformations undergoing resection (n = 8), each cohort scanned on different scanner models with different imaging protocols at different sites. This robustness to scan acquisition parameters, patient populations, scanner types, and sites eliminates the advantages of self-supervised methods over our fully supervised generative AI approach. We exceed current state-of-the-art denoising methods in accuracy and test-retest reliability of rapid diffusion tensor imaging (DTI) requiring only 90 seconds of scan time. SWIN denoising also achieves dramatic improvements over the state-of-the-art for test-retest reliability of intracellular volume fraction and free water fraction measurements and can remove heavy-tail noise, improving biophysical modeling fidelity. SWIN enables rapid diffusion MRI with unprecedented accuracy and reliability, especially at high diffusion weighting for probing biological tissues at microscopic spatial scales. The code and model are publicly available athttps://github.com/ucsfncl/dmri-swin.
Indexed as
Identifiers
What OpenQuestion holds
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.