Neural Mechanisms of Saccadic Suppression

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

Neuronal and psychophysical sensitivity to motion signals in extrastriate area MST of the macaque monkey

Celebrini, S., & Newsome, W. (1994) · The Journal of Neuroscience · doi:10.1523/jneurosci.14-07-04109.1994 · Cited by 232

Corrections in saccade endpoints scale to the amplitude of target displacements in a double-step paradigm

Kiernan, D., Manson, G. A., Heath, M. D., Tremblay, L., & Welsh, T. N. (2015) · Neuroscience Letters · doi:10.1016/j.neulet.2015.11.022 · Cited by 6

Distinct roles of prefrontal subregion feedback to the primary visual cortex across behavioral states

Ährlund‐Richter, S., Osako, Y., Jenks, K. R., Odom, E., Huang, H., Arnold, D. B., & Sur, M. (2025) · Neuron · doi:10.1016/j.neuron.2025.10.037 · Cited by 12

Microsaccadic suppression of peripheral perceptual detection performance as a function of foveated visual image appearance

Greilich, J., Baumann, M. P., & Hafed, Z. M. (2024) · Journal of Vision · doi:10.1167/jov.24.11.3 · Cited by 5

Gaze behavior during 3-D face identification is depth cue invariant

Akhavein, H., & Farivar, R. (2017) · Journal of Vision · doi:10.1167/17.2.9 · Cited by 5

Macaques preferentially attend to visual patterns with higher fractal dimension contours

Finn, K. R., Crutchfield, J. P., & Bliss‐Moreau, E. (2019) · Scientific Reports · doi:10.1038/s41598-019-46799-0 · Cited by 5

Visual Perception and Eye Movements

Greenlee, M. W., & Kimmig, H. (2019) · Studies in neuroscience, psychology and behavioral economics · doi:10.1007/978-3-030-20085-5_5 · Cited by 5

Seeing changes: How familiarity alters our perception of change

Tovey, M., & Herdman, C. M. (2014) · Visual Cognition · doi:10.1080/13506285.2014.894167 · Cited by 5

Both Lexical and Non-Lexical Characters Are Processed during Saccadic Eye Movements

Zhang, H., Yan, H., Kendrick, K. M., & Li, C. (2012) · PLoS ONE · doi:10.1371/journal.pone.0046383 · Cited by 5

Bayesian and Discriminative Models for Active Visual Perception across Saccades

Subramanian, D., Pearson, J., & Sommer, M. A. (2023) · eNeuro · doi:10.1523/eneuro.0403-22.2023 · Cited by 4

A Brief History of Eye Movement Research

Fletcher, A., Dunne, S., & Butler, J. (2022) · Neuromethods · doi:10.1007/978-1-0716-2391-6_2 · Cited by 6

Pupil dynamics: A potential proxy of neural preparation for goal‐directed eye movement

Pandey, P., & Ray, S. (2021) · European Journal of Neuroscience · doi:10.1111/ejn.15453 · Cited by 4

Eye movements and visual word recognition

Shillcock, R. C. (2012) · Oxford University Press eBooks · doi:10.1093/oxfordhb/9780198568971.013.0006 · Cited by 4

Erasing motion: Scrambling direction selectivity in visual cortex during saccadesPreprint

Miura, S. K., & Scanziani, M. (2021) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2021.03.30.437338 · Cited by 4

The geometry of working memory in action: Uncovering the latent structure of systematic and unsystematic errors with and without saccadic eye movements

Moussaoui, S., Frost, A., & Niemeier, M. (2025) · Acta Psychologica · doi:10.1016/j.actpsy.2025.105633 · Cited by 3

Action-dependent processing of self-motion in parietal cortex of macaque monkeys

Churan, J., Kaminiarz, A., Schwenk, J. C. B., & Bremmer, F. (2021) · Journal of Neurophysiology · doi:10.1152/jn.00049.2021 · Cited by 3

Rehabilitation Support System for Attentional Deficits Based on Trail-Making Test

Tonomura, R., Tadamitsu, T., Manji, A., Kubota, N., & Obo, T. (2018) · Joint International Conference on Soft Computing and Intelligent Systems and International Symposium on Advanced Intelligent Systems (SCIS&ISIS) · doi:10.1109/scis-isis.2018.00177 · Cited by 3

Saccade-induced image motion cannot account for post-saccadic enhancement of visual processing in primate MST

Cloherty, S. L., Crowder, N. A., Mustari, M. J., & Ibbotson, M. R. (2015) · Frontiers in Systems Neuroscience · doi:10.3389/fnsys.2015.00122 · Cited by 3

Statistical regularities and the sensory consequences of self-action: A multi-species, multi-modal perspective

Hafed, Z. M., Arrenberg, A. B., Schwarz, C., Benda, J., & Grewe, J. (2025) · Current Opinion in Neurobiology · doi:10.1016/j.conb.2025.103087 · Cited by 2

Perisaccadic encoding of temporal information in macaque area V4

Schwenk, J. C. B., Klingenhoefer, S., Werner, B.-O., Dowiasch, S., & Bremmer, F. (2021) · Journal of Neurophysiology · doi:10.1152/jn.00387.2020 · Cited by 2

Vision: Neuronal mechanisms enabling stable perception

Burr, D. C., & Morrone, M. C. (2022) · Current Biology · doi:10.1016/j.cub.2022.11.003 · Cited by 2

Veridical stimulus localization is linked to human area V5/MT+ activity

Bonkhoff, A. K., Zimmermann, E., & Fink, G. R. (2017) · NeuroImage · doi:10.1016/j.neuroimage.2017.05.010 · Cited by 3

Identifying High-resolution Spatiotemporal Components Contributing to the Fast Spiking Response Dynamics of Visual Neurons

Zamani, Y., & Nategh, N. (2019) · IEEE Global Conference on Signal and Information Processing · doi:10.1109/globalsip45357.2019.8969435 · Cited by 2

Insect Flight: Navigating with Smooth Turns and Quick Saccades

Theobald, J. C. (2017) · Current Biology · doi:10.1016/j.cub.2017.09.002 · Cited by 2

Translation invariance in a network of oscillatory units

Rao, A. R., Cecchi, G., Peck, C., & Kozloski, J. (2006) · Proceedings of SPIE, the International Society for Optical Engineering/Proceedings of SPIE · doi:10.1117/12.648229 · Cited by 2

Ethnography Through the Digital Eye: What Do We See When We Look?

Sumartojo, S., Dyer, A. G., García, J. E., & Cruz, E. G. (2017) · Springer eBooks · doi:10.1007/978-3-319-61222-5_6 · Cited by 1

Diverse and dynamic influences of saccades on visual representations in the mouse superior colliculus

Hunt, J. B., Buteau, A., Barreto, J., Hanson, S., Scholl, B., Poleg-Polsky, A., & Felsen, G. (2025) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.2425788122 · Cited by 1

Cortical mechanisms for transsaccadic vision: Extrinsic and intrinsic feature updating

Baltaretu, B. R., & Crawford, J. D. (2026) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2026.106644 · Cited by 1

How a neuron perceives visual motion during self-motion

Shimegi, S., Soma, S., Suematsu, N., Mizuyama, R., Tanaka, Y., & Fujie, H. (2014) · The Journal of Physical Fitness and Sports Medicine · doi:10.7600/jpfsm.3.235 · Cited by 1

Illusory Motion Produced by Dichoptic Stimuli during Saccades

Mitsudo, H., & Nakamizo, S. (2010) · Perception · doi:10.1068/p6739 · Cited by 1

Circuit mechanisms of spatial perception and visuomotor integration

Takeuchi, R. F., & Osakada, F. (2020) · Folia Pharmacologica Japonica · doi:10.1254/fpj.19132 · Cited by 1

Spontaneous modulations of high frequency cortical activity

Ono, H., Sonoda, M., Silverstein, B. H., Sonoda, K., Kubota, T., Luat, A. F., Rothermel, R., Sood, S., & Asano, E. (2021) · Clinical Neurophysiology · doi:10.1016/j.clinph.2021.06.020 · Cited by 1

Decoding Neural Activity to Anticipate Eye Movements

Nategh, N. (2020) · Asilomar Conference on Signals, Systems and Computers (ACSSC) · doi:10.1109/ieeeconf51394.2020.9443415 · Cited by 1

Insect vision: Head saccades to reset the view

Theobald, J. C. (2021) · Current Biology · doi:10.1016/j.cub.2021.07.056 · Cited by 1

Intrasaccadic Motion: Neural Evidence for Saccadic Suppression and Postsaccadic Enhancement

Ibbotson, M. R. (2009) · Springer eBooks · doi:10.1007/978-1-4419-0781-3_11 · Cited by 1

Switching sides

Jones, R. (2002) · Nature reviews. Neuroscience · doi:10.1038/nrn815 · Cited by 1

Laminar Mechanisms of Saccadic Suppression in Primate Visual CortexPreprint

Denagamage, S., Morton, M. P., Reynolds, J. H., Jadi, M. P., & Nandy, A. S. (2021) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2021.01.09.426063 · Cited by 1

A Brief History of Eye Movement ResearchPreprint

Fletcher, A., Dunne, S., & Butler, J. (2021) · doi:10.31234/osf.io/yb4zq · Cited by 1

Seeing changes : how familiarity alters our perception of change

Tovey, M. (2011) · doi:10.22215/etd/2011-09489 · Cited by 1

De la prise d'information visuelle à la formation d'impressions : apports de l'oculométrie pour l'étude des processus de la perception et de la cognition visuelle des objets manufacturés

Couronné, T. (2007) · OpenGrey (Institut de l'Information Scientifique et Technique) · Cited by 1

Vectorial efference copy and visuomotor transformation through gap junctionsPreprint

Falt, T., Ammer, G., Serbe-Kamp, E., Kroell, L. M., Friedrich, A. B., Mota, S. G., Simsova, E., & Fenk, L. M. (2026) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.64898/2026.08.11.744090 · Cited by 2

Learning mechanisms to account for the speed, selectivity and invariance of responses in the visual cortex

Masquelier, T. (2008) · Thèses en ligne de l'Université Toulouse III (Université Toulouse III) · Cited by 1

The Influence of Spatial Attention on Neuronal Receptive Field Structure within Macaque Area MT

Womelsdorf, T. (2005) · doi:10.53846/goediss-190

Influences of voluntary eye movements on object perception in peripheral vision

Harrison, W. J. (2012)

Cognitive Physiology: Moving the Mind's Eye Before the Head's Eye Dispatch

Treue, S., & Martínez-Trujillo, J. (2003)

Vision: A Brake on the Speed of Sight

Thiele, A. (2005) · Current Biology · doi:10.1016/j.cub.2005.10.057

Cortical Dynamics in Behaving Monkeys Long-Term Voltage-Sensitive Dye Imaging Reveals

Arieli, A., Hildesheim, R., Sato, H., Shimegi, S., Ishikawa, A. W., Kida, H., Sakamoto, H., Hara, S.-I., Zurawel, G., Ayzenshtat, I., et al. (2015)

MST Neurons During Pursuit Eye Movement Modulation of Visual Signals in Macaque MT and

NeurophysiolChukoskie, J., Movshon, J. A., Leclercq, G., Blohm, G., Lefèvre, P., Brostek, L., Büttner, U., Mustari, M. J., Glasauer, S., & Murdison, T. S. (2015)

SaccadicModulationofNeuralResponses:PossibleRolesin SaccadicSuppression,Enhancement,andTimeCompression

Ibbotson, M. R., Cloherty, S. L., & Price, N. S. C. (2008)

Integración de información en tareas secuenciales

Kamienkowski, J. E. (2011) · Repositorio Digital Institucional de la Universidad de Buenos Aires (Universidad de Buenos Aires)

White noise analysis of visual selectivity in area MT during fixation and eye movements

Hartmann, T. S. (2012) · Rutgers University Community Repository (Rutgers University) · doi:10.7282/t3nv9h98

Neural mechanisms and functional signficance of peri-saccadic response modulation

Guez, J. (2015) · doi:10.7282/t3ww7kps

Perspectives and Challenges for Future Research in Bat Hearing

Wiegrebe, L., Grinnell, A. D., & Fenton, M. B. (2016) · Springer handbook of auditory research · doi:10.1007/978-1-4939-3527-7_11

Direct inhibition of histamine receptors in the antennal lobe of Manduca sexta: Putative evidence for an olfactory corollary discharge circuit

Burkland, R. (2016) · doi:10.33915/etd.5283

Objective (Real-world) Motion Responses in Scene Responsive RegionsPreprint

Stark, D., & Bartels, A. (2017) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/145573

The role of attention and adaptation in shaping cortical representations and the perception of abrupt changes in the visual environment

Mehrpour, V. (2017) · eDiss (Georg-August-Universität Göttingen) · doi:10.53846/goediss-6599

Effects of Social and Non-Social Interpretations of Complex Images on Human Eye Movement and Brain Activation

Prostko, A. L. (2012) · The Research Repository @ WVU (West Virginia University) · doi:10.33915/etd.626

Modulation of free viewing and saccades on visual cortex

Cao, S. (2008)

Pupillary aperture is a potential biomarker of movement preparationPreprint

Pandey, P., & Ray, S. (2021) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2021.01.30.428981

Peer Review #1 of "Intrasaccadic perception triggers pupillary constriction (v0.2)"

(2015) · PeerJ · doi:10.7287/peerj.1150v0.2/reviews/1

Peer Review #1 of "Intrasaccadic perception triggers pupillary constriction (v0.1)"

(2015) · PeerJ · doi:10.7287/peerj.1150v0.1/reviews/1

Contributions of Bayesian and Discriminative Models to Active Visual Perception across SaccadesPreprint

Subramanian, D., Pearson, J., & Sommer, M. A. (2022) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2022.06.22.497244

Oculomotor Thalamus and Efference Copy

Sommer, M. A. (2023) · Oxford University Press eBooks · doi:10.1093/med/9780197676158.003.0036

A thalamic hub-and-spoke circuit enables visual perception during action by coordinating visuomotor dynamicsPreprint

Vega‐Zuniga, T., Sumser, A., Symonova, O., Koppensteiner, P., Schmidt, F. H., & Joesch, M. (2023) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2023.12.23.573221

Behavioral Aspects of Migraine: A Focus on the Response to Visual Phenomenon

Kalita, J., Gutti, N. B., & Kalita, J. (2024) · Springer eBooks · doi:10.1007/978-3-031-32046-0_50-1

Neural substrates for saccadic modulation of visual representations in mouse superior colliculusPreprint

Hunt, J. B., Buteau, A., Hanson, S., Poleg-Polsky, A., & Felsen, G. (2024) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2024.09.21.613770

Contributions of temporal and spatial masking signals in perception of sequential visual eventsPreprint

Buonocore, A., Cuomo, M., Maresca, M., & Fracasso, A. (2024) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2024.12.20.629621

Selective Encoding of Priors for Flexible Categorization But Not Bayesian Inference in the Frontal Eye Field

Subramanian, D., Pearson, J. M., & Sommer, M. A. (2026) · Journal of Neuroscience · doi:10.1523/jneurosci.2271-25.2026

WITHDRAWNPreprint

Moussaoui, S. (2025) · doi:10.31234/osf.io/z7p2d_v1

Behavioral Aspects of Migraine: A Focus on the Response to Visual Phenomenon

Kalita, J., Gutti, N. B., & Kalita, J. (2025) · Springer eBooks · doi:10.1007/978-3-031-73363-5_50

The interaction between human vision and eye movements in health and disease

Sylvester, R. J. (2010) · UCL Discovery (University College London)

Gaze-Contingent Rendering in VR

Zhu, Y. (2026) · Synthesis lectures on computer architecture · doi:10.1007/978-3-032-05018-2_10

Contributions of temporal and spatial masking signals in the perception of sequential visual events

Buonocore, A., Cuomo, M., Maresca, M., Cafaro, C., & Fracasso, A. (2025) · Visual Cognition · doi:10.1080/13506285.2026.2647350

Reaction time perception and plasticity

Vencato, V. (2019) · theses.fr (ABES) · doi:10.70675/8b7276b4z24f7z44f4zaef2z240b492e62aa

L'impact des troubles du champ visuel sur les dynamiques spatio-temporelles de l'observation de scènes naturelles : analyses et modélisation

David, E. J. (2019) · theses.fr (ABES) · doi:10.70675/8cd5db3fzdec6z4180z91ddzd9b9c00e18c2

Couplage entre adaptation saccadique et perception visuo-spatiale : études neurophysiologiques chez l’homme

Cheviet, A. (2021) · theses.fr (ABES) · doi:10.70675/66ee7d58zb3d6z49fdz8463z9a5b3612db6f

Psychophysical studies on Monte Carlo rendering-noise visual perception

Myrodia, V. (2021) · doi:10.70675/335b1d35z1c05z44e6za989zdbffd0b7ef5a

Memory Guides Attention: Evidence from Eye Movements and Encoding StrengthPreprint

Whitlock, J., Ding, H., & Sahakyan, L. (2026) · SSRN Electronic Journal · doi:10.2139/ssrn.6555794

A population readout of extrastriate activity reveals biased and smoothed temporal representations across saccadesPreprint

Poursadegh, A., Zekri, M., Weng, G., Aghdam, A. A., Clark, K., Rabbani, H., Noudoost, B., & Nategh, N. (2026) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.64898/2026.06.16.732385

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

Direction and Contrast Tuning of Macaque MSTd Neurons During Saccades

Crowder, N. A., Price, N. S. C., Mustari, M. J., & Ibbotson, M. R. (2009) · Journal of Neurophysiology · doi:10.1152/jn.91254.2008 · Cited by 16

Behavioral/Systems/Cognitive Neural Dynamics of Saccadic Suppression

Bremmer, F., Kubischik, M., Hoffmann, K.-P., & Krekelberg, B. (2009)

A neural locus for spatial-frequency specific saccadic suppression in visual-motor neurons of the primate superior colliculus

Chen, C.-Y., & Hafed, Z. M. (2017) · Journal of Neurophysiology · doi:10.1152/jn.00911.2016 · Cited by 63

Suppression and reversal of motion perception around the time of the saccade

Frost, A., & Niemeier, M. (2015) · Frontiers in Systems Neuroscience · doi:10.3389/fnsys.2015.00143 · Cited by 16