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.
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
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?
During a saccade there is neither visual nor proprioceptive sensory feedback.
“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
The introduction (p. 1) says people are usually unaware of image motion during saccades, and the report (p. 2) describes suppression of motion perception. That supports reduced visual awareness, not the categorical absence of visual sensory feedback: the paper also reports retinal image motion and neuronal responses during saccades. It does not address proprioceptive feedback. (LLM, conf=0.85)
Experimental — accuracy not yet measuredSaccadic suppression mechanisms have been identified in pigeons, chickens, locusts, monkeys and cats.
“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.
Cites
Das Reafferenzprinzip: Wechselwirkungen zwischen Zentralnervensystem und Peripherie
von Holst, E., & Mittelstaedt, H. (1950) · Naturwissenschaften · doi:10.1007/bf00622503 · Cited by 2,655 · see citing works
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 · see citing works
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 · see citing works
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 · see citing works
Saccadic suppression: A review and an analysis.
Matin, E. (1974) · Psychological Bulletin · doi:10.1037/h0037368 · Cited by 793 · see citing works
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 · see citing works
Contrast sensitivity at high velocities
Burr, D. C., & Ross, J. (1982) · Vision Research · doi:10.1016/0042-6989(82)90196-1 · Cited by 349 · see citing works
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 · see citing works
Celebrini, S., & Newsome, W. (1994) · Journal of Neuroscience · doi:10.1523/jneurosci.14-07-04109.1994 · Cited by 323 · see citing works
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 · see citing works
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 224 · see citing works
Elevation of Visual Threshold by Displacement of Retinal Image
Dm, M. (1970) · Nature · doi:10.1038/225090a0 · Cited by 197 · see citing works
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 · see citing works
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 179 · see citing works
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 · see citing works
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 · see citing works
Metacontrast and Saccadic Suppression
Matin, E., Clymer, A. B., & Matin, L. (1972) · Science · doi:10.1126/science.178.4057.179 · Cited by 124 · see citing works
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 · see citing works
Motion perception during saccades
Ilg, U. J., & Hoffmann, K. (1993) · Vision Research · doi:10.1016/0042-6989(93)90159-t · Cited by 84 · see citing works
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 · see citing works
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 · see citing works
Self-citationNoda, H. (1975) · The Journal of Physiology · doi:10.1113/jphysiol.1975.sp011071 · Cited by 33 · see citing works
Fischer, W. H., Schmidt, M., Stuphorn, V., & Hoffmann, K. ‐. (1996) · Experimental Brain Research · doi:10.1007/bf00229143 · Cited by 28 · see citing works
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 · see citing works
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 · see citing works
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 · see citing works
Flagged first, then by citations
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 · see citing works
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 · see citing works
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 · see citing works
Corollary discharge across the animal kingdom
Crapse, T. B., & Sommer, M. A. (2008) · Nature Reviews Neuroscience · doi:10.1038/nrn2457 · Cited by 789 · see citing works
Neuronal mechanisms of visual stability
Wurtz, R. H. (2008) · Vision Research · doi:10.1016/j.visres.2008.03.021 · Cited by 587 · see citing works
Brain Circuits for the Internal Monitoring of Movements
Sommer, M. A., & Wurtz, R. H. (2008) · Annual Review of Neuroscience · doi:10.1146/annurev.neuro.31.060407.125627 · Cited by 508 · see citing works
Visual saliency does not account for eye movements during visual search in real-world scenes
Henderson, J. M., Brockmole, J. R., Castelhano, M. S., & Mack, M. L. (2007) · Elsevier eBooks · doi:10.1016/b978-008044980-7/50027-6 · Cited by 429 · see citing works
Saliency-Guided Quality Assessment of Screen Content Images
Gu, K., Wang, S., Yang, H., Lin, W., Zhai, G., Yang, X., & Zhang, W. (2016) · IEEE Transactions on Multimedia · doi:10.1109/tmm.2016.2547343 · Cited by 303 · see citing works
Realistic avatar eye and head animation using a neurobiological model of visual attention
Itti, L., Dhavale, N., & Pighin, F. P. (2004) · Proceedings of SPIE, the International Society for Optical Engineering/Proceedings of SPIE · doi:10.1117/12.512618 · Cited by 296 · see citing works
Sensory signals during active versus passive movement
Cullen, K. E. (2004) · Current Opinion in Neurobiology · doi:10.1016/j.conb.2004.10.002 · Cited by 262 · see citing works
Sommer, M. A., & Wurtz, R. H. (2004) · Journal of Neurophysiology · doi:10.1152/jn.00740.2003 · Cited by 254 · see citing works
Long-Term Voltage-Sensitive Dye Imaging Reveals Cortical Dynamics in Behaving Monkeys
Slovin, H., Arieli, A., Hildesheim, R., & Grinvald, A. (2002) · Journal of Neurophysiology · doi:10.1152/jn.00194.2002 · Cited by 216 · see citing works
Neural Dynamics of Saccadic Suppression
Bremmer, F., Kubischik, M., Hoffmann, K., & Krekelberg, B. (2009) · Journal of Neuroscience · doi:10.1523/jneurosci.2908-09.2009 · Cited by 213 · see citing works
Self-citationCerebellum, Predictions and Errors
Popa, L. S., & Ebner, T. J. (2019) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2018.00524 · Cited by 191 · see citing works
Transient Cortical Excitation at the Onset of Visual Fixation
Rajkai, C., Lakatos, P., Chen, C. A., Pincze, Z., Karmos, G., & Schroeder, C. E. (2007) · Cerebral Cortex · doi:10.1093/cercor/bhm046 · Cited by 202 · see citing works
Saccadic Eye Movements Modulate Visual Responses in the Lateral Geniculate Nucleus
Reppas, J. B., Usrey, W. M., & Reid, R. C. (2002) · Neuron · doi:10.1016/s0896-6273(02)00823-1 · Cited by 202 · see citing works
Perceptual Issues in the Use of Head-Mounted Visual Displays
Patterson, R., Winterbottom, M., & Pierce, B. J. (2006) · Human Factors The Journal of the Human Factors and Ergonomics Society · doi:10.1518/001872006778606877 · Cited by 200 · see citing works
The primate working memory networks
Constantinidis, C., & Procyk, E. (2004) · Cognitive Affective & Behavioral Neuroscience · doi:10.3758/cabn.4.4.444 · Cited by 185 · see citing works
Hout, M. C., & Goldinger, S. D. (2014) · Attention Perception & Psychophysics · doi:10.3758/s13414-014-0764-6 · Cited by 175 · see citing works
The significance of microsaccades for vision and oculomotor control
Collewijn, H., & Kowler, E. (2008) · Journal of Vision · doi:10.1167/8.14.20 · Cited by 173 · see citing works
Predicting Cognitive State from Eye Movements
Henderson, J. M., Shinkareva, S. V., Wang, J., Luke, S. G., & Olejarczyk, J. (2013) · PLoS ONE · doi:10.1371/journal.pone.0064937 · Cited by 166 · see citing works
The dorsal visual stream revisited: Stable circuits or dynamic pathways?
Galletti, C., & Fattori, P. (2017) · Cortex · doi:10.1016/j.cortex.2017.01.009 · Cited by 162 · see citing works
Microsaccadic Suppression of Visual Bursts in the Primate Superior Colliculus
Hafed, Z. M., & Krauzlis, R. J. (2010) · Journal of Neuroscience · doi:10.1523/jneurosci.1137-10.2010 · Cited by 152 · see citing works
Bartels, A., Zeki, S., & Logothetis, N. K. (2007) · Cerebral Cortex · doi:10.1093/cercor/bhm107 · Cited by 148 · see citing works
Signals Conveyed in the Pulvinar Pathway from Superior Colliculus to Cortical Area MT
Berman, R. A., & Wurtz, R. H. (2011) · Journal of Neuroscience · doi:10.1523/jneurosci.4738-10.2011 · Cited by 149 · see citing works
Kagan, I., Gur, M., & Snodderly, D. M. (2008) · Journal of Vision · doi:10.1167/8.14.19 · Cited by 136 · see citing works
Neuronal mechanisms for visual stability: progress and problems
Wurtz, R. H., Joiner, W. M., & Berman, R. A. (2011) · Philosophical Transactions of the Royal Society B Biological Sciences · doi:10.1098/rstb.2010.0186 · Cited by 140 · see citing works
Thalamic pathways for active vision
Wurtz, R. H., McAlonan, K., Cavanaugh, J., & Berman, R. A. (2011) · Trends in Cognitive Sciences · doi:10.1016/j.tics.2011.02.004 · Cited by 127 · see citing works
Saccades during visual exploration align hippocampal 3–8 Hz rhythms in human and non-human primates
Hoffman, K. L., Dragan, M. C., Leonard, T. K., Micheli, C., Montefusco‐Siegmund, R., & Valiante, T. A. (2013) · Frontiers in Systems Neuroscience · doi:10.3389/fnsys.2013.00043 · Cited by 128 · see citing works
Sylvester, R. J., Haynes, J., & Rees, G. E. (2005) · Current Biology · doi:10.1016/j.cub.2004.12.061 · Cited by 117 · see citing works
Perisaccadic Mislocalization Orthogonal to Saccade Direction
Kaiser, M., & Lappe, M. (2004) · Neuron · doi:10.1016/s0896-6273(03)00849-3 · Cited by 115 · see citing works
Reduced-Reference Quality Assessment of Screen Content Images
Wang, S., Gu, K., Zhang, X., Lin, W., Ma, S., & Gao, W. (2016) · IEEE Transactions on Circuits and Systems for Video Technology · doi:10.1109/tcsvt.2016.2602764 · Cited by 110 · see citing works
Identifying corollary discharges for movement in the primate brain
Wurtz, R. H., & Sommer, M. A. (2004) · Progress in brain research · doi:10.1016/s0079-6123(03)14403-2 · Cited by 106 · see citing works
The site of saccadic suppression
Thilo, K. V., Santoro, L., Walsh, V., & Blakemore, C. B. (2003) · Nature Neuroscience · doi:10.1038/nn1171 · Cited by 108 · see citing works
The role of the human thalamus in processing corollary discharge
Bellebaum, C., Daum, I., Koch, B., Schwarz, M., & Hoffmann, K.-P. (2005) · Brain · doi:10.1093/brain/awh474 · Cited by 105 · see citing works
Self-citationThe maturation of eye movement behavior: Scene viewing characteristics in children and adults
Helo, A., Pannasch, S., Sirri, L., & Pia Rämä, A. (2014) · Vision Research · doi:10.1016/j.visres.2014.08.006 · Cited by 106 · see citing works
Predictive Sensing: The Role of Motor Signals in Sensory Processing
Brooks, J. X., & Cullen, K. E. (2019) · Biological Psychiatry Cognitive Neuroscience and Neuroimaging · doi:10.1016/j.bpsc.2019.06.003 · Cited by 101 · see citing works
Palinopsia revamped: A systematic review of the literature
Gersztenkorn, D., & Lee, A. G. (2014) · Survey of Ophthalmology · doi:10.1016/j.survophthal.2014.06.003 · Cited by 103 · see citing works
(Micro)Saccades, corollary activity and cortical oscillations
Melloni, L., Schwiedrzik, C. M., Rodríguez, E., & Singer, W. (2009) · Trends in Cognitive Sciences · doi:10.1016/j.tics.2009.03.007 · Cited by 101 · see citing works
Neuronal mechanisms for detection of motion in the field of view
Galletti, C., & Fattori, P. (2003) · Neuropsychologia · doi:10.1016/s0028-3932(03)00174-x · Cited by 101 · see citing works
Quantitative modelling of perceptual salience at human eye position
Itti, L. (2006) · Visual Cognition · doi:10.1080/13506280500195672 · Cited by 99 · see citing works
Global Transsaccadic Change Blindness During Scene Perception
Henderson, J. M., & Hollingworth, A. (2003) · Psychological Science · doi:10.1111/1467-9280.02459 · Cited by 99 · see citing works
Neural Correlates of Saccadic Suppression in Humans
Kleiser, R., Seitz, R. J., & Krekelberg, B. (2004) · Current Biology · doi:10.1016/j.cub.2004.02.036 · Cited by 97 · see citing works
Ibbotson, M. R., Crowder, N. A., Cloherty, S. L., Price, N. S. C., & Mustari, M. J. (2008) · Journal of Neuroscience · doi:10.1523/jneurosci.3950-08.2008 · Cited by 94 · see citing works
Eye movements in the wild: Oculomotor control, gaze behavior & frames of reference
Lappi, O. (2016) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2016.06.006 · Cited by 112 · see citing works
Perceptual saccadic suppression starts in the retina
Idrees, S., Baumann, M. P., Franke, F., Münch, T. A., & Hafed, Z. M. (2020) · Nature Communications · doi:10.1038/s41467-020-15890-w · Cited by 92 · see citing works
Human thalamus contributes to perceptual stability across eye movements
Ostendorf, F., Liebermann, D., & Ploner, C. J. (2009) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0910742107 · Cited by 92 · see citing works
Motion perception of saccade-induced retinal translation
Castet, É., Jeanjean, S., & Masson, G. S. (2002) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.232377199 · Cited by 91 · see citing works
Baker, J. T., Patel, G. H., Corbetta, M., & Snyder, L. H. (2005) · Cerebral Cortex · doi:10.1093/cercor/bhi124 · Cited by 91 · see citing works
Neural Correlates of Visual Localization and Perisaccadic Mislocalization
Krekelberg, B., Kubischik, M., Hoffmann, K., & Bremmer, F. (2003) · Neuron · doi:10.1016/s0896-6273(03)00003-5 · Cited by 89 · see citing works
Self-citationMST Neurons Code for Visual Motion in Space Independent of Pursuit Eye Movements
Inaba, N., Shinomoto, S., Yamane, S., Takemura, A., & Kawano, K. (2007) · Journal of Neurophysiology · doi:10.1152/jn.01054.2006 · Cited by 88 · see citing works
The corollary discharge in humans is related to synchronous neural oscillations
Chen, C.-M. A., Mathalon, D. H., Roach, B. J., Cavus, I., Spencer, D. D., & Ford, J. M. (2011) · Journal of Cognitive Neuroscience · doi:10.1162/jocn.2010.21589 · Cited by 86 · see citing works
Visual Motion Responses in the Posterior Cingulate Sulcus: A Comparison to V5/MT and MST
Fischer, E., Bülthoff, H., Logothetis, N. K., & Bartels, A. (2011) · Cerebral Cortex · doi:10.1093/cercor/bhr154 · Cited by 79 · see citing works
Distinguishing externally from saccade-induced motion in visual cortex
Miura, S. K., & Scanziani, M. (2022) · Nature · doi:10.1038/s41586-022-05196-w · Cited by 74 · see citing works
Encoding of Naturalistic Optic Flow by a Population of Blowfly Motion-Sensitive Neurons
Karmeier, K., van Hateren, J. H., Kern, R., & Egelhaaf, M. (2006) · Journal of Neurophysiology · doi:10.1152/jn.00023.2006 · Cited by 77 · see citing works
Ibbotson, M. R., Price, N. S. C., Crowder, N. A., Ono, S., & Mustari, M. J. (2006) · Cerebral Cortex · doi:10.1093/cercor/bhl022 · Cited by 76 · see citing works
Flicker can be perceived during saccades at frequencies in excess of 1 kHz
Je, R., & Wilkins, A. J. (2012) · Lighting Research & Technology · doi:10.1177/1477153512436367 · Cited by 76 · see citing works
A Circuit Model for Saccadic Suppression in the Superior Colliculus
Phongphanphanee, P., Mizuno, F., Lee, P. H., Yanagawa, Y., Isa, T., & Hall, W. C. (2011) · Journal of Neuroscience · doi:10.1523/jneurosci.2305-10.2011 · Cited by 75 · see citing works
Encoding of 3D Head Orienting Movements in the Primary Visual Cortex
Guitchounts, G., Masis, J. A., Wolff, S. B. E., & Cox, D. (2020) · Neuron · doi:10.1016/j.neuron.2020.07.014 · Cited by 72 · see citing works
Encoding visual information in retinal ganglion cells with prosthetic stimulation
Freeman, D. K., Rizzo, J. F., & Fried, S. I. (2011) · Journal of Neural Engineering · doi:10.1088/1741-2560/8/3/035005 · Cited by 71 · see citing works
Attaining higher resolution visual prosthetics: a review of the factors and limitations
Eiber, C. D., Lovell, N. H., & Suaning, G. J. (2013) · Journal of Neural Engineering · doi:10.1088/1741-2560/10/1/011002 · Cited by 71 · see citing works
Modulation of Visual Signals in Macaque MT and MST Neurons During Pursuit Eye Movement
Chukoskie, L., & Movshon, J. A. (2009) · Journal of Neurophysiology · doi:10.1152/jn.90692.2008 · Cited by 70 · see citing works
Identity of a pathway for saccadic suppression
Lee, P. H., Sooksawate, T., Yanagawa, Y., Isa, K., Isa, T., & Hall, W. C. (2007) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0701934104 · Cited by 70 · see citing works
Coupling perception to action through incidental sensory consequences of motor behaviour
Rolfs, M., & Schweitzer, R. (2022) · Nature Reviews Psychology · doi:10.1038/s44159-021-00015-x · Cited by 65 · see citing works
Chen, C.-Y., & Hafed, Z. M. (2017) · Journal of Neurophysiology · doi:10.1152/jn.00911.2016 · Cited by 63 · see citing works
Analysis of Perisaccadic Field Potentials in the Occipitotemporal Pathway During Active Vision
Purpura, K. P., Kalik, S. F., & Schiff, N. D. (2003) · Journal of Neurophysiology · doi:10.1152/jn.00011.2003 · Cited by 60 · see citing works
The Relationship between Saccadic Suppression and Perceptual Stability
Watson, T., & Krekelberg, B. (2009) · Current Biology · doi:10.1016/j.cub.2009.04.052 · Cited by 62 · see citing works
A model of active visual search with object-based attention guiding scan paths
Lanyon, L., & Denham, S. L. (2004) · Neural Networks · doi:10.1016/j.neunet.2004.03.012 · Cited by 57 · see citing works
Macaque V1 Activity During Natural Vision: Effects of Natural Scenes and Saccades
MacEvoy, S. P., Hanks, T. D., & Paradiso, M. A. (2007) · Journal of Neurophysiology · doi:10.1152/jn.00612.2007 · Cited by 56 · see citing works
Different gaze strategies during eye versus hand tracking of a moving target
Danion, F., & Flanagan, J. R. (2018) · Scientific Reports · doi:10.1038/s41598-018-28434-6 · Cited by 57 · see citing works
Optimal Sensorimotor Control in Eye Movement Sequences
Munuera, J., Morel, P., Duhamel, J., & Denève, S. (2009) · Journal of Neuroscience · doi:10.1523/jneurosci.1169-08.2009 · Cited by 60 · see citing works
Eye Tracking: Characteristics And Methods
Richardson, D. C., & Spivey, M. (2008) · CRC Press eBooks · doi:10.1081/e-ebbe2-120013920 · Cited by 79 · see citing works
Vallines, I., & Greenlee, M. (2006) · Journal of Neuroscience · doi:10.1523/jneurosci.0817-06.2006 · Cited by 58 · see citing works
Danelli, L., Berlingeri, M., Bottini, G., Ferri, F., Vacchi, L., Sberna, M., & Paulesu, E. (2012) · Human Brain Mapping · doi:10.1002/hbm.22098 · Cited by 52 · see citing works
Throwing a glance at the neural code: Rapid information transmission in the visual system
Gollisch, T. (2008) · HFSP journal · doi:10.2976/1.3027089 · Cited by 51 · see citing works
Transsaccadic processing: stability, integration, and the potential role of remapping
Higgins, E. C., & Rayner, K. (2014) · Attention Perception & Psychophysics · doi:10.3758/s13414-014-0751-y · Cited by 53 · see citing works
A circuit for saccadic suppression in the primate brain
Berman, R. A., Cavanaugh, J. R., McAlonan, K., & Wurtz, R. H. (2016) · Journal of Neurophysiology · doi:10.1152/jn.00679.2016 · Cited by 49 · see citing works
Macaque Middle Temporal Neurons Signal Depth in the Absence of Motion
Palanca, B. J. A., & DeAngelis, G. C. (2003) · Journal of Neuroscience · doi:10.1523/jneurosci.23-20-07647.2003 · Cited by 49 · see citing works
Saccadic suppression as a perceptual consequence of efficient sensorimotor estimation
Crevecoeur, F., & Kording, K. P. (2017) · eLife · doi:10.7554/elife.25073 · Cited by 46 · see citing works
Contrast dependency of saccadic compression and suppression
Michels, L., & Lappe, M. (2004) · Vision Research · doi:10.1016/j.visres.2004.05.008 · Cited by 48 · see citing works
Intrasaccadic motion streaks jump-start gaze correction
Schweitzer, R., & Rolfs, M. (2021) · Science Advances · doi:10.1126/sciadv.abf2218 · Cited by 47 · see citing works
Post-saccadic updating of visual space in the posterior parietal cortex in humans
Bellebaum, C., Hoffmann, K., & Daum, I. (2005) · Behavioural Brain Research · doi:10.1016/j.bbr.2005.05.007 · Cited by 46 · see citing works
Self-citationV1 neurons respond differently to object motion versus motion from eye movements
Troncoso, X. G., McCamy, M. B., Jazi, A. N., Cui, J., Otero‐Millan, J., Macknik, S. L., Costela, F. M., & Martínez‐Conde, S. (2015) · Nature Communications · doi:10.1038/ncomms9114 · Cited by 45 · see citing works
Zhang, W.-H., Wang, H., Chen, A., Gu, Y., Lee, T. S., Wong, K. M., & Wu, S. (2019) · eLife · doi:10.7554/elife.43753 · Cited by 45 · see citing works
Visual Perception: Saccadic Omission — Suppression or Temporal Masking?
Ibbotson, M. R., & Cloherty, S. L. (2009) · Current Biology · doi:10.1016/j.cub.2009.05.010 · Cited by 45 · see citing works
Hafed, Z. M., Yoshida, M., Tian, X., Buonocore, A., & Malevich, T. (2021) · Frontiers in Neural Circuits · doi:10.3389/fncir.2021.638429 · Cited by 44 · see citing works
Saccades actively maintain perceptual continuity
Ross, J., & Ma-Wyatt, A. (2003) · Nature Neuroscience · doi:10.1038/nn1163 · Cited by 44 · see citing works
On the Fight Between Excitation and Inhibition: Location Is Everything
Mel, B. W., & Schiller, J. (2004) · Science s STKE · doi:10.1126/stke.2502004pe44 · Cited by 43 · see citing works
Saccades during Object Viewing Modulate Oscillatory Phase in the Superior Temporal Sulcus
Bartlett, A. M., Ovaysikia, S., Logothetis, N. K., & Hoffman, K. L. (2011) · Journal of Neuroscience · doi:10.1523/jneurosci.4102-11.2011 · Cited by 40 · see citing works
Eye-tracking for human-centered mixed reality: promises and challenges
Gardony, A. L., Lindeman, R. W., & Brunyé, T. T. (2020) · Optical Architectures for Displays and Sensing in Augmented, Virtual, and Mixed Reality (AR, VR, MR) · doi:10.1117/12.2542699 · Cited by 43 · see citing works
Turner, M. H., Krieger, A., Pang, M. M., & Clandinin, T. R. (2022) · eLife · doi:10.7554/elife.82587 · Cited by 42 · see citing works
Eye Tracking: Research Areas And Applications
Richardson, D., & Spivey, M. (2008) · CRC Press eBooks · doi:10.1081/e-ebbe2-120034143 · Cited by 45 · see citing works
Corollary discharge circuits for saccadic modulation of the pigeon visual system
Yang, Y., Cao, P., Yang, Y., & Wang, S.-R. (2008) · Nature Neuroscience · doi:10.1038/nn.2107 · Cited by 41 · see citing works
Contrast sensitivity during the initiation of smooth pursuit eye movements
Schütz, A. C., Braun, D. I., & Gegenfurtner, K. R. (2007) · Vision Research · doi:10.1016/j.visres.2007.07.006 · Cited by 41 · see citing works
The effect of blinks and saccadic eye movements on visual reaction times
Johns, M. W., Crowley, K. E., Chapman, R. J., Tucker, A., & Hocking, C. (2009) · Attention Perception & Psychophysics · doi:10.3758/app.71.4.783 · Cited by 43 · see citing works
Fast and nonuniform dynamics of perisaccadic vision in the central fovea
Intoy, J., Mostofi, N., & Rucci, M. (2021) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.2101259118 · Cited by 40 · see citing works
Funke, K., Kerscher, N., & Wörgötter, F. (2007) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.2007.05735.x · Cited by 40 · see citing works
Rapid Processing of Retinal Slip During Saccades in Macaque Area MT
Price, N. S. C., Ibbotson, M. R., Ono, S., & Mustari, M. J. (2005) · Journal of Neurophysiology · doi:10.1152/jn.00041.2005 · Cited by 39 · see citing works
Embodied cognition and the perception–action link
Bridgeman, B., & Tseng, P. H. (2011) · Physics of Life Reviews · doi:10.1016/j.plrev.2011.01.002 · Cited by 40 · see citing works
Corrigan, B. W., Gulli, R. A., Doucet, G., & Martínez-Trujillo, J. (2017) · Journal of Vision · doi:10.1167/17.12.15 · Cited by 37 · see citing works
- 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
