ArticleBiomedical optics express2023
Unobtrusive biometric data de-identification of fundus images using latent space disentanglement.
Article in Biomedical optics express, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 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
2 citing papers in PubMed.
- Optic Disc Fundus Images Retain Biometric Identity Signals Under Deep Learning.Research square · 2026Article
- AI-based fully automatic analysis of retinal vascular morphology in pediatric high myopia.BMC ophthalmology · 2024Article
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
7 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
With the incremental popularity of ophthalmic imaging techniques, anonymization of the clinical image datasets is becoming a critical issue, especially the fundus images, which would have unique patient-specific biometric content. Towards achieving a framework to anonymize ophthalmic images, we propose an image-specific de-identification method on the vascular structure of retinal fundus images while preserving important clinical features such as hard exudates. Our method calculates the contribution of latent code in latent space to the vascular structure by computing the gradient map of the generated image with respect to latent space and then by computing the overlap between the vascular mask and the gradient map. The proposed method is designed to specifically target and effectively manipulate the latent code with the highest contribution score in vascular structures. Extensive experimental results show that our proposed method is competitive with other state-of-the-art approaches in terms of identity similarity and lesion similarity, respectively. Additionally, our approach allows for a better balance between identity similarity and lesion similarity, thus ensuring optimal performance in a trade-off manner.
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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.