The DOI matches its Crossref record; 26 of the 26 references it cites were found in a registry or an index.
Neural Mechanisms of Saccadic Suppression
Open accessAbstract
In normal vision our gaze leaps from detail to detail, resulting in rapid image motion across the retina. Yet we are unaware of such motion, a phenomenon known as saccadic suppression. We recorded neural activity in the middle temporal and middle superior temporal cortical areas during saccades and identical image motion under passive viewing conditions. Some neurons were selectively silenced during saccadic image motion, but responded well to identical external image motion. In addition, a subpopulation of neurons reversed their preferred direction of motion during saccades. Consequently, oppositely directed motion signals annul one another, and motion percepts are suppressed.
Overview
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Integrity signals
Registry
Cites
Statistics
Verification
Claims the paper makes
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Claims other papers make about this one
Each is checked against this paper’s own text: does it say what the citing paper says it does?
The source backs part of the claim, not all of it — or backs it for a different population, condition or comparison.
In the citing paper
“For example, during a saccade there is neither visual nor proprioceptive sensory feedback (Keller and Robinson, 1971; Guthrie et al., 1983; Thiele et al., 2002).”
From Cerebellum, Predictions and Errors (2019) · cites this paper as Thiele et al., 2002
Experimental — accuracy not yet measuredIn the citing paper
“Saccadic suppression mechanisms have been identified in a host of different species, such as pigeons, chickens, locusts, monkeys and cats34–38.”
From Corollary discharge across the animal kingdom (2008) · cites this paper as [36]
Self-check
Percentages, sums and reported differences re-computed from the paper’s own numbers.
The self-check needs the paper’s full text.
Citations
Cites
Das Reafferenzprinzip: Wechselwirkungen zwischen Zentralnervensystem und Peripherie
von Holst, E., & Mittelstaedt, H. (1950) · Naturwissenschaften · doi:10.1007/bf00622503 · Cited by 2,655
The analysis of visual motion: a comparison of neuronal and psychophysical performance
Britten, K., Shadlen, M., Newsome, W., & Movshon, J. (1992) · The Journal of Neuroscience · doi:10.1523/jneurosci.12-12-04745.1992 · Cited by 1,958
Attentional modulation of visual motion processing in cortical areas MT and MST
Treue, S., & Maunsell, J. H. R. (1996) · Nature · doi:10.1038/382539a0 · Cited by 1,025
Failure to detect displacement of the visual world during saccadic eye movements
Bridgeman, B., Hendry, D. P., & STARK, L. W. (1975) · Vision Research · doi:10.1016/0042-6989(75)90290-4 · Cited by 881
Saccadic suppression: A review and an analysis.
Matin, E. (1974) · Psychological Bulletin · doi:10.1037/h0037368 · Cited by 793
Selective suppression of the magnocellular visual pathway during saccadic eye movements
Burr, D. C., Morrone, M. C., & Ross, J. (1994) · Nature · doi:10.1038/371511a0 · Cited by 685
Contrast sensitivity at high velocities
Burr, D. C., & Ross, J. (1982) · Vision Research · doi:10.1016/0042-6989(82)90196-1 · Cited by 349
Saccadic omission: Why we do not see a grey-out during a saccadic eye movement
Campbell, F. W., & Wurtz, R. H. (1978) · Vision Research · doi:10.1016/0042-6989(78)90219-5 · Cited by 346
Extraretinal Control of Saccadic Suppression
Diamond, M. R., Ross, J., & Morrone, M. C. (2000) · Journal of Neuroscience · doi:10.1523/jneurosci.20-09-03449.2000 · Cited by 307
Celebrini, S., & Newsome, W. (1994) · The Journal of Neuroscience · doi:10.1523/jneurosci.14-07-04109.1994 · Cited by 232
Microsaccades differentially modulate neural activity in the striate and extrastriate visual cortex
Leopold, D. A., & Logothetis, N. K. (1998) · Experimental Brain Research · doi:10.1007/s002210050577 · Cited by 226
Elevation of Visual Threshold by Displacement of Retinal Image
Dm, M. (1970) · Nature · doi:10.1038/225090a0 · Cited by 197
Selective depression of motion sensitivity during saccades.
Burr, D. C., Holt, J., Johnstone, J. R., & Ross, J. (1982) · The Journal of Physiology · doi:10.1113/jphysiol.1982.sp014434 · Cited by 180
The influence of fixational eye movements on the response of neurons in area MT of the macaque
Bair, W., & O’Keefe, L. P. (1998) · Visual Neuroscience · doi:10.1017/s0952523898154160 · Cited by 178
Vision during saccadic eye movements. I. Visual interactions in striate cortex
Judge, S. J., Wurtz, R. H., & Richmond, B. J. (1980) · Journal of Neurophysiology · doi:10.1152/jn.1980.43.4.1133 · Cited by 139
Saccadic suppression of image displacement
STARK, L. W., Robert, K., Susan, S., Derek, H., & Bridgeman, B. (1976) · Vision Research · doi:10.1016/0042-6989(76)90262-5 · Cited by 129
Metacontrast and Saccadic Suppression
Matin, E., Clymer, A. B., & Matin, L. (1972) · Science · doi:10.1126/science.178.4057.179 · Cited by 124
Suppression of the magnocellular pathway during saccades
Ross, J., Burr, D. C., & Morrone, M. C. (1996) · Behavioural Brain Research · doi:10.1016/0166-4328(96)00012-5 · Cited by 107
Motion perception during saccades
Ilg, U. J., & Hoffmann, K. (1993) · Vision Research · doi:10.1016/0042-6989(93)90159-t · Cited by 84
Self-citationThe analysis of neuronal discharge sequences: Change‐point estimation and comparison of variances
Commenges, D., & Seal, J. (1985) · Statistics in Medicine · doi:10.1002/sim.4780040113 · Cited by 42
Decision‐related activity in the macaque dorsal visual pathway
Thiele, A., Distler, C., & Hoffmann, K. (1999) · European Journal of Neuroscience · doi:10.1046/j.1460-9568.1999.00630.x · Cited by 34
Self-citationNoda, H. (1975) · The Journal of Physiology · doi:10.1113/jphysiol.1975.sp011071 · Cited by 33
Fischer, W. H., Schmidt, M., Stuphorn, V., & Hoffmann, K. ‐. (1996) · Experimental Brain Research · doi:10.1007/bf00229143 · Cited by 28
Self-citationNon-veridical visual motion perception immediately after saccades
Park, J., Lee, J., & Lee, C. (2001) · Vision Research · doi:10.1016/s0042-6989(01)00211-5 · Cited by 16
A program for analysing single neuron activity by methods based on estimation of a change-point
Commenges, D., Pinatel, F., & Seal, J. (1986) · Computer Methods and Programs in Biomedicine · doi:10.1016/0169-2607(86)90107-0 · Cited by 14
Peripheral shift reduces visual sensitivity in cat geniculate neurones
Derrington, A. M., & Felisberti, F. M. (1998) · Visual Neuroscience · doi:10.1017/s0952523898155128 · Cited by 11
Research works printed but not linked: 3
- Holt E., Harvard Psychol. Stud. 1, 3 (1903).
- Sperry R. W., Vision Res. 16, 1185 (1950).
- Supplementary Web material is available on Science Online at www.sciencemag.org/cgi/content/full/295/5564/2460/DC1.
Cited by
Sorted by citations
Human gaze control during real-world scene perception
Henderson, J. (2003) · Trends in Cognitive Sciences · doi:10.1016/j.tics.2003.09.006 · Cited by 1,409
A computational neuroanatomy for motor control
Shadmehr, R., & Krakauer, J. W. (2008) · Experimental Brain Research · doi:10.1007/s00221-008-1280-5 · Cited by 1,187
STRUCTURE AND FUNCTION OF VISUAL AREA MT
Born, R. T., & Bradley, D. C. (2005) · Annual Review of Neuroscience · doi:10.1146/annurev.neuro.26.041002.131052 · Cited by 1,023
Corollary discharge across the animal kingdom
Crapse, T. B., & Sommer, M. A. (2008) · Nature Reviews Neuroscience · doi:10.1038/nrn2457 · Cited by 789
Neuronal mechanisms of visual stability
Wurtz, R. H. (2008) · Vision Research · doi:10.1016/j.visres.2008.03.021 · Cited by 619
Metadata
- Authors
- Thiele, A., Henning, P., Kubischik, M., & Hoffmann, K.-P.
- Affiliations
- Ruhr University Bochum (DE)
- Corresponding author
- Thiele, A.
- Hoffmann, K.-P.
- ORCID
- Thiele, A.
- Venue
- Science
- Published
- 2002-03-29
- Volume
- 295
- Issue
- 5564
- Pages
- 2460-2462
- ISSN
- 0036-8075 (ISSN-L)
- 1095-9203
- OpenAlex
- W1995699966
- Cited by
- 278
- References
- 26
- Citations by year
- 2026: 6 · 2025: 11 · 2024: 9 · 2023: 8 · 2022: 13 · 2021: 19 · 2020: 10 · 2019: 11 · 2018: 4 · 2017: 14 · 2016: 12 · 2015: 10 · 2014: 10 · 2013: 6 · 2012: 13
- FWCI
- 7.07
- Type
- journal article
- Language
- en
- Open access
- green
- doi.org
- Locations
- Science (publishedVersion)
- PubMed (publishedVersion)
- Newcastle University ePrints (Newcastle Univesity)
- Topics
- Life Sciences › Neuroscience › Cognitive Neuroscience › Visual perception and processing mechanisms
- Life Sciences › Neuroscience › Cognitive Neuroscience › Motor Control and Adaptation
- Social Sciences › Psychology › Experimental and Cognitive Psychology › Multisensory perception and integration
- Keywords
- saccadic suppression, saccades, middle temporal cortex, visual motion perception, neuronal silencing, direction-selective neurons
- MeSH terms
- Animals, Macaca mulatta, Motion Perception, Neurons, Perceptual Masking, Retina, Saccades, Temporal Lobe, Visual Pathways, Visual Perception
About these checks
Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.
Statistics and arithmetic are recomputed, not judged.
Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.
What counts as a claim ›How we measure confidence ›How we check this ›
Are you an author, or do you see a problem with this page? Request a review