ArticleNeuroImage2023
Identifying cortical areas that underlie the transformation from 2D retinal to 3D head-centric motion signals.
Article in NeuroImage, 2023. 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.
- A large-scale heterogeneous 3D magnetic resonance brain imaging dataset for self-supervised learning.Scientific data · 2026Article
- Single-Trial fMRI Decoding of 3D Motion with Stereoscopic and Perspective Cues.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2025Article
- Functional Localization of Visual Motion Area FST in Humans.Imaging neuroscience (Cambridge, Mass.) · 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
3 authors.
Funding
Abstract
Accurate motion perception requires that the visual system integrate the 2D retinal motion signals received by the two eyes into a single representation of 3D motion. However, most experimental paradigms present the same stimulus to the two eyes, signaling motion limited to a 2D fronto-parallel plane. Such paradigms are unable to dissociate the representation of 3D head-centric motion signals (i.e., 3D object motion relative to the observer) from the associated 2D retinal motion signals. Here, we used stereoscopic displays to present separate motion signals to the two eyes and examined their representation in visual cortex using fMRI. Specifically, we presented random-dot motion stimuli that specified various 3D head-centric motion directions. We also presented control stimuli, which matched the motion energy of the retinal signals, but were inconsistent with any 3D motion direction. We decoded motion direction from BOLD activity using a probabilistic decoding algorithm. We found that 3D motion direction signals can be reliably decoded in three major clusters in the human visual system. Critically, in early visual cortex (V1-V3), we found no significant difference in decoding performance between stimuli specifying 3D motion directions and the control stimuli, suggesting that these areas represent the 2D retinal motion signals, rather than 3D head-centric motion itself. In voxels in and surrounding hMT and IPS0 however, decoding performance was consistently superior for stimuli that specified 3D motion directions compared to control stimuli. Our results reveal the parts of the visual processing hierarchy that are critical for the transformation of retinal into 3D head-centric motion signals and suggest a role for IPS0 in their representation, in addition to its sensitivity to 3D object structure and static depth.
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.