ArticleMedical image analysis2022
Quantitative characterization of the human retinotopic map based on quasiconformal mapping.
Article in Medical image analysis, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 10 papers.
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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.
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Who cites it
10 citing papers in PubMed, 20 citations in OpenAlex.
- Uncertainty in population receptive field estimates revealed by variational qPRF.Journal of neuroscience methods · 2026Article
- Quantification of planar cortical magnification with optimal transport and topological smoothing.NeuroImage · 2026Article
- Quantification of retinotopic maps with a Gaussian process modeling.Journal of vision · 2025Article
- qPRF: A system to accelerate population receptive field modeling.NeuroImage · 2025Article
- qPRF: A system to accelerate population receptive field decoding.bioRxiv : the preprint server for biology · 2024Article
- ENHANCING 3T RETINOTOPIC MAPS USING DIFFEOMORPHIC REGISTRATION.Proceedings. IEEE International Symposium on Biomedical Imaging · 2024Article
- A spatial map: a propitious choice for constraining the binding problem.Frontiers in computational neuroscience · 2024Article
- Diffeomorphic registration for retinotopic maps of multiple visual regions.Brain structure & function · 2022Article
- Quantitative characterization of the human retinotopic map based on quasiconformal mapping.Medical image analysis · 2022Article
- Topology-preserving smoothing of retinotopic maps.PLoS computational biology · 2021Article
Corrections and comments
- Erratum issued
Authors and funding
4 authors at 2 institutions in 2 countries.
Funding
Abstract
The retinotopic map depicts the cortical neurons' response to visual stimuli on the retina and has contributed significantly to our understanding of human visual system. Although recent advances in high field functional magnetic resonance imaging (fMRI) have made it possible to generate the in vivo retinotopic map with great detail, quantifying the map remains challenging. Existing quantification methods do not preserve surface topology and often introduce large geometric distortions to the map. In this study, we developed a new framework based on computational conformal geometry and quasiconformal Teichmüller theory to quantify the retinotopic map. Specifically, we introduced a general pipeline, consisting of cortical surface conformal parameterization, surface-spline-based cortical activation signal smoothing, and vertex-wise Beltrami coefficient-based map description. After correcting most of the violations of the topological conditions, the result was a "Beltrami coefficient map" (BCM) that rigorously and completely characterizes the retinotopic map by quantifying the local quasiconformal mapping distortion at each visual field location. The BCM provided topological and fully reconstructable retinotopic maps. We successfully applied the new framework to analyze the V1 retinotopic maps from the Human Connectome Project (n=181), the largest state of the art retinotopy dataset currently available. With unprecedented precision, we found that the V1 retinotopic map was quasiconformal and the local mapping distortions were similar across observers. The new framework can be applied to other visual areas and retinotopic maps of individuals with and without eye diseases, and improve our understanding of visual cortical organization in normal and clinical populations.
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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.