Cited by 1,789Vestibular and auditory disordersVisual perception and processing mechanismsMotor Control and Adaptation

The DOI matches its Crossref record; 10 of the 10 references it cites were found in a registry or an index.

Neural basis of the spontaneous optokinetic response produced by visual inversion

Sperry, R. W.·1950·Journal of Comparative and Physiological Psychology

Open this paper in CoChat — free account

Abstract

One of the most conspicuous behavioral effects produced by surgical rotation of the eyeball through 180 degrees is the forced circling or spontaneous optokinetic reaction. Animals with inverted vision caused by eye rotation tend to turn continuously in circles (4, 6, 8). In fishes and amphibians this circling may persist indefinitely with little or no correction by reeducation. Similar circus movement is caused by contralateral transplantation of the eyeball with inversion on only one axis and also by cross-connection of the optic nerves to the wrong side of the brain (7). In all these situations movement on the part of the animal causes the visual image to pass over the retinal field or its central projection in a direction opposite to normal. The forced circling phenomenon of inverted vision is an illustration of the importance of kinesthetic effects in visual perception. Under normal conditions the image of the visual field, whether it be stationary or moving across the retina, can be perceived as being either in motion or at rest depending upon whether the perceiving animal is moving or at rest. The apparent position and direction of motion of the visual field depend upon the posture

Integrity signals

Registry

Crossref · 10.1037/h0055479

Cites

10 of 10 references verified0 citation errors · 0 not checkable

Statistics

Recomputing p-values needs the paper’s full text.

Claims the paper makes

This paper’s full text isn’t openly available, so its claims and self-check weren’t run. The registry and citation checks still apply.

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?

RECEIVING AREAS OF THE TACTILE, AUDITORY, AND VISUAL SYSTEMS IN THE CEREBELLUM
Snider, R. S., & Stowell, A. (1944) · Journal of Neurophysiology · doi:10.1152/jn.1944.7.6.331 · Cited by 579
Vision without inversion of the retinal image.
Stratton, G. M. (1897) · Psychological Review · doi:10.1037/h0071173 · Cited by 403
Visuomotor coordination in the newt (triturus viridescens) after regeneration of the optic nerve
Sperry, R. W. (1943) · The Journal of Comparative Neurology · doi:10.1002/cne.900790104 · Cited by 395
Self-citation
OPTIC NERVE REGENERATION WITH RETURN OF VISION IN ANURANS
Sperry, R. W. (1944) · Journal of Neurophysiology · doi:10.1152/jn.1944.7.1.57 · Cited by 366
Self-citation
Some preliminary experiments on vision without inversion of the retinal image.
Stratton, G. M. (1896) · Psychological Review · doi:10.1037/h0072918 · Cited by 342
Effect of 180 degree rotation of the retinal field on visuomotor coordination
Sperry, R. W. (1943) · Journal of Experimental Zoology · doi:10.1002/jez.1400920303 · Cited by 298
Self-citation
RESTORATION OF VISION AFTER CROSSING OF OPTIC NERVES AND AFTER CONTRALATERAL TRANSPLANTATION OF EYE
Sperry, R. W. (1945) · Journal of Neurophysiology · doi:10.1152/jn.1945.8.1.15 · Cited by 200
Self-citation
The central gustatory paths in the brains of bony fishes. Studies from the Neurological Laboratory of Denison University. No. XVIII
Herrick, C. J. (1905) · Journal of Comparative Neurology and Psychology · doi:10.1002/cne.920150503 · Cited by 155
Patterning of Central Synapses in Regeneration of the Optic Nerve in Teleosts
Sperry, R. W. (1948) · Physiological Zoology · doi:10.1086/physzool.21.4.30152014 · Cited by 129
Self-citation
Interocular Transfer of Visual Discrimination Habits in a Teleost Fish
Sperry, R. W., & Clark, E. (1949) · Physiological Zoology · doi:10.1086/physzool.22.4.30152062 · Cited by 47
Self-citation

Show all 10 references

Sorted by citations

Items 701–800 of 1,000

Attention and suppression affect tactile perception in reach-to-grasp movements
Juravle, G., Deubel, H., & Spence, C. J. (2011) · Acta Psychologica · doi:10.1016/j.actpsy.2011.08.001 · Cited by 31
Predictability of visual perturbation during locomotion: implications for corrective efference copy signaling
Chagnaud, B. P., Simmers, J., & Straka, H. (2012) · Biological Cybernetics · doi:10.1007/s00422-012-0528-0 · Cited by 32
Multisensory decisions from self to world
Zaidel, A., & Salomon, R. (2023) · Philosophical Transactions of the Royal Society B Biological Sciences · doi:10.1098/rstb.2022.0335 · Cited by 32
Cerebellar Motor Function in Spina Bifida Meningomyelocele
Dennis, M., Salman, M. S., Juranek, J. J., & Fletcher, J. M. (2010) · The Cerebellum · doi:10.1007/s12311-010-0191-8 · Cited by 31
Attenuation of auditory ERPs to action‐sound coincidences is not explained by voluntary allocation of attention
Horváth, J. (2013) · Psychophysiology · doi:10.1111/psyp.12009 · Cited by 34
Control of Rapid Arm Movements When Target Position is Altered during Saccadic Suppression
Blouin, J., Teasdale, N., Bard, C., & Fleury, M. (1995) · Journal of Motor Behavior · doi:10.1080/00222895.1995.9941704 · Cited by 31
Time course of cross-hemispheric spatial updating in the human parietal cortex
Bellebaum, C., & Daum, I. (2006) · Behavioural Brain Research · doi:10.1016/j.bbr.2006.01.001 · Cited by 32
A localist evaluation solution for visual stability across saccades
Irwin, D. E., McConkie, G. W., Carlson-Radvansky, L. A., & Currie, C. B. (1994) · Behavioral and Brain Sciences · doi:10.1017/s0140525x00034439 · Cited by 32
Medullary electrosensory processing in the little skate
New, J. G., & Bodznick, D. (1990) · Journal of Comparative Physiology A · doi:10.1007/bf00188121 · Cited by 31
Interactions between eye movements and the visually evoked response in the cat
MICHAEL, J. A., & STARK, L. W. (1966) · Electroencephalography and Clinical Neurophysiology · doi:10.1016/0013-4694(66)90196-9 · Cited by 31
Mirroring avatars: dissociation of action and intention in human motor resonance
BORRONI, P. F., Gorini, A., Riva, G., Bouchard, S., & Cerri, G. (2011) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.2011.07779.x · Cited by 32
Representation of Bodily Self in the Multimodal Parieto-Premotor Network
Murata, A., & Ishida, H. (2007) · Springer eBooks · doi:10.1007/978-4-431-73021-7_6 · Cited by 30
Effects of voice harmonic complexity on ERP responses to pitch-shifted auditory feedback
Behroozmand, R., Korzyukov, O. A., & Larson, C. R. (2011) · Clinical Neurophysiology · doi:10.1016/j.clinph.2011.04.019 · Cited by 33
Neuroplasticity subserving the operation of brain–machine interfaces
Oweiss, K. G., & Badreldin, I. S. (2015) · Neurobiology of Disease · doi:10.1016/j.nbd.2015.05.001 · Cited by 33
Motor learning
Halsband, U., & Freund, H. (1993) · Current Opinion in Neurobiology · doi:10.1016/0959-4388(93)90166-v · Cited by 30
Duration of plastic change in a modifiable efference copy
Bell, C. C. (1986) · Brain Research · doi:10.1016/0006-8993(86)90510-x · Cited by 30
Brain mechanisms for 'having a theory of mind'
Frith, C. (1996) · Journal of Psychopharmacology · doi:10.1177/026988119601000103 · Cited by 30
Visuomotor learning from postdictive motor error
Masselink, J., & Lappe, M. (2021) · eLife · doi:10.7554/elife.64278 · Cited by 31
Multisensory and Sensorimotor Integration in the Embodied Self: Relationship between Self-Body Recognition and the Mirror Neuron System
Shimada, S. (2022) · Sensors · doi:10.3390/s22135059 · Cited by 30
Effects of saccades on visual processing in primate MSTd
Cloherty, S. L., Mustari, M. J., Rosa, M. G. P., & Ibbotson, M. R. (2010) · Vision Research · doi:10.1016/j.visres.2010.08.020 · Cited by 29
Neural oscillations as a translational tool in schizophrenia research: Rationale, paradigms and challenges
Phillips, K. G., & Uhlhaas, P. J. (2015) · Journal of Psychopharmacology · doi:10.1177/0269881114562093 · Cited by 30
Imaging in electrosensory systems
Pereira, A. C., & Caputi, A. A. (2010) · Interdisciplinary Sciences Computational Life Sciences · doi:10.1007/s12539-010-0049-2 · Cited by 29
A match does not make a sense: on the sufficiency of the comparator model for explaining the sense of agency
Zaadnoordijk, L., Besold, T. R., & Hunnius, S. (2019) · Neuroscience of Consciousness · doi:10.1093/nc/niz006 · Cited by 33
Characteristics of sensori-motor interaction in the primary and secondary somatosensory cortices in humans: A magnetoencephalography study
Wasaka, T., Kida, T., Nakata, H., Akatsuka, K., & Kakigi, R. (2007) · Neuroscience · doi:10.1016/j.neuroscience.2007.07.040 · Cited by 29
Electrosensory systems in fish
Heiligenberg, W. (1990) · Synapse · doi:10.1002/syn.890060212 · Cited by 29
A pre-reflective indicator of an impaired sense of agency in patients with Schizophrenia
Bulot, V., Thomas, P., & Delevoye, Y. (2007) · Experimental Brain Research · doi:10.1007/s00221-007-1027-8 · Cited by 35
Responses of cerebellar cortical neurons to dynamic proprioceptive inputs from forelimb muscles.
Murphy, J. T., MacKay, W. A., & Johnson, F. (1973) · Journal of Neurophysiology · doi:10.1152/jn.1973.36.4.711 · Cited by 29
Alterations of Perception After Brain Injury
Teuber, H. (1965) · Springer eBooks · doi:10.1007/978-3-642-49168-9_8 · Cited by 30
Excitability Changes in Cat Lateral Geniculate Cells during Saccadic Eye Movements
Noda, H., & ADEY, W. R. (1974) · Science · doi:10.1126/science.183.4124.543 · Cited by 29
Spatial Representation of Predictive Motor Learning
Witney, A. G., & Wolpert, D. M. (2003) · Journal of Neurophysiology · doi:10.1152/jn.00929.2002 · Cited by 29
On the relation between motor imagery and visual imagery
Klatzky, R. L. (1994) · Behavioral and Brain Sciences · doi:10.1017/s0140525x00034178 · Cited by 29
Mechanisms of Space Constancy
Bridgeman, B. (1983) · Springer eBooks · doi:10.1007/978-1-4612-5488-1_15 · Cited by 29
Learning Motor Synergies Makes Use of Information on Muscular LoadPreprint
Fernández-Ruíz, J., Hall‐Haro, C., Díaz, R., Mischner, J., Aragón, P. V., & López, J. C. (2000) · Learning & Memory · doi:10.1101/lm.7.4.193 · Cited by 29
Understanding and Synergy: A Single Concept at Different Levels of Analysis?
Latash, M. L. (2021) · Frontiers in Systems Neuroscience · doi:10.3389/fnsys.2021.735406 · Cited by 29
Speech preparation in adults with persistent developmental stuttering
Mock, J. R., Foundas, A. L., & Golob, E. J. (2015) · Brain and Language · doi:10.1016/j.bandl.2015.05.009 · Cited by 28
What Might Interoceptive Inference Reveal about Consciousness?
Nikolova, N. E., Waade, P. T., Friston, K. J., & Allen, M. (2021) · Review of Philosophy and Psychology · doi:10.1007/s13164-021-00580-3 · Cited by 30
Functional and ultrastructural analysis of reafferent mechanosensation in larval zebrafish
Odstrcil, I., Petkova, M. D., Haesemeyer, M., Boulanger-Weill, J., Nikitchenko, M., Gagnon, J. A., Oteíza, P., Schalek, R. L., Peleg, A., Portugues, R., et al. (2021) · Current Biology · doi:10.1016/j.cub.2021.11.007 · Cited by 28
Perisaccadic Remapping and Rescaling of Visual Responses in Macaque Superior Colliculus
Churan, J., Guitton, D., & Pack, C. C. (2012) · PLoS ONE · doi:10.1371/journal.pone.0052195 · Cited by 28
Parallel processing streams for motor output and sensory prediction during action preparation
Stenner, M., Bauer, M., Heinze, H., Haggard, P., & Dolan, R. J. (2014) · Journal of Neurophysiology · doi:10.1152/jn.00616.2014 · Cited by 31
Memory as Prediction
Vecchi, T., & Gatti, D. (2020) · The MIT Press eBooks · doi:10.7551/mitpress/13543.001.0001 · Cited by 31
Perceptual stability and postsaccadic visual information: Can man bridge a gap?
Deubel, H., & Schneider, W. X. (1994) · Behavioral and Brain Sciences · doi:10.1017/s0140525x00034397 · Cited by 29
A simple translation in cortical log-coordinates may account for the pattern of saccadic localization errors
VanRullen, R. (2004) · Biological Cybernetics · doi:10.1007/s00422-004-0514-2 · Cited by 28
Retinally-generated saccadic suppression of a locust looming-detector neuron: investigations using a robot locust
Santer, R. D., Stafford, R., & Rind, F. C. (2004) · Journal of The Royal Society Interface · doi:10.1098/rsif.2004.0007 · Cited by 28
Parkinson's disease: A conceptualization of neuropsychological deficits within an information-processing framework
Karayanidis, F. (1989) · Biological Psychology · doi:10.1016/0301-0511(89)90035-5 · Cited by 28
A puzzle about visualization
Langland‐Hassan, P. (2011) · Phenomenology and the Cognitive Sciences · doi:10.1007/s11097-011-9197-z · Cited by 27
Rhesus monkeys mislocalize saccade targets flashed for 100ms around the time of a saccade
Jeffries, S. M., Kusunoki, M., Bisley, J. W., Cohen, I. S., & Goldberg, M. E. (2007) · Vision Research · doi:10.1016/j.visres.2007.02.021 · Cited by 27
Perisaccadic remapping: What? How? Why?
Neupane, S., Guitton, D., & Pack, C. C. (2020) · Reviews in the Neurosciences · doi:10.1515/revneuro-2019-0097 · Cited by 29
Brain circuits underlying visual stability across eye movements—converging evidence for a neuro-computational model of area LIP
Ziesche, A., & Hamker, F. H. (2014) · Frontiers in Computational Neuroscience · doi:10.3389/fncom.2014.00025 · Cited by 31
Toward an Integrated Approach to Perception and Action: Conference Report and Future Directions
Gordon, G., Kaplan, D. M., Lankow, B. S., Little, D. Y.-J., Sherwin, J. S., Suter, B. A., & Thaler, L. (2011) · Frontiers in Systems Neuroscience · doi:10.3389/fnsys.2011.00020 · Cited by 27
Behavioral evidence of delayed prediction signals during agency attribution in patients with schizophrenia
Koreki, A., Maeda, T., Fukushima, H., Umeda, S., Takahata, K., Okimura, T., Funayama, M., Iwashita, S., Mimura, M., & Kato, M. (2015) · Psychiatry Research · doi:10.1016/j.psychres.2015.08.023 · Cited by 27
Efference copies in neural control of dynamic biped walking
Manoonpong, P., & Wörgötter, F. (2009) · Robotics and Autonomous Systems · doi:10.1016/j.robot.2009.06.007 · Cited by 27
Exercise-Induced Central Fatigue
Batson, G. (2013) · Journal of Dance Medicine & Science · doi:10.12678/1089-313x.17.2.53 · Cited by 27
Suppression of optokinesis during smooth pursuit eye movements revisited: The role of extra-retinal information
Lindner, A., & Ilg, U. J. (2005) · Vision Research · doi:10.1016/j.visres.2005.09.033 · Cited by 27
Is there a role for extraretinal factors in the maintenance of stability in a structured environment?
Chekaluk, E. (1994) · Behavioral and Brain Sciences · doi:10.1017/s0140525x00034373 · Cited by 27
Optic and Static Contributions to Ocular Counter-Rotation in Carp
Traill, A. B., & Mark, R. F. (1970) · Journal of Experimental Biology · doi:10.1242/jeb.52.1.109 · Cited by 27
Some Mechanisms Underlying Sensory and Postural Stability in Man
Lackner, J. R. (1978) · Springer eBooks · doi:10.1007/978-3-642-46354-9_26 · Cited by 27
Consciousness Is Motor
Klein, A. M. (2025) · doi:10.1093/9780190085872.001.0001 · Cited by 26
An internal model for canceling self-generated sensory input in freely behaving electric fish
Wallach, A., & Sawtell, N. B. (2023) · Neuron · doi:10.1016/j.neuron.2023.05.019 · Cited by 26
Using insects to drive mobile robots — hybrid robots bridge the gap between biological and artificial systems
Ando, N., & Kanzaki, R. (2017) · Arthropod Structure & Development · doi:10.1016/j.asd.2017.02.003 · Cited by 26
Projection Neuron Axon Collaterals in the Dorsal Horn: Placing a New Player in Spinal Cord Pain Processing
Browne, T. J., Hughes, D. I., Dayas, C. V., Callister, R. J., & Graham, B. A. (2020) · Frontiers in Physiology · doi:10.3389/fphys.2020.560802 · Cited by 26
Developmental emergence of self-referential and inhibition mechanisms of body movements underling felicitous behaviors.
Watanabe, H., Homae, F., & Taga, G. (2011) · Journal of Experimental Psychology Human Perception & Performance · doi:10.1037/a0021936 · Cited by 26
Illusory Sensation of Movement Induced by Repetitive Transcranial Magnetic Stimulation
Christensen, M. S., Lundbye‐Jensen, J., Grey, M. J., Vejlby, A. D., Belhage, B., & Nielsen, J. B. (2010) · PLoS ONE · doi:10.1371/journal.pone.0013301 · Cited by 28
Neurophysiology of preparation, movement and imagery
Sanes, J. N. (1994) · Behavioral and Brain Sciences · doi:10.1017/s0140525x00034270 · Cited by 26
A note on the reafference principle
Varjú, D. (1990) · Biological Cybernetics · doi:10.1007/bf00203455 · Cited by 25
Where is the mind within the brain? Transient selection of subnetworks by metabotropic receptors and G protein-gated ion channels
Nikolić, D. (2023) · Computational Biology and Chemistry · doi:10.1016/j.compbiolchem.2023.107820 · Cited by 27
The bioinspiring potential of weakly electric fish
Caputi, A. A. (2017) · Bioinspiration & Biomimetics · doi:10.1088/1748-3190/12/2/025004 · Cited by 25
The Linguistic Determination of Conscious Thought Contents
Vicente, A., & Jorba, M. (2017) · Noûs · doi:10.1111/nous.12239 · Cited by 27
Neuronal representation of saccadic error in macaque posterior parietal cortex (PPC)
Zhou, Y., Liu, Y., Lu, H. D., Wu, S., & Zhang, M. (2016) · eLife · doi:10.7554/elife.10912 · Cited by 26
Rapid Eye Movements in Sleep Furnish a Unique Probe Into Consciousness
Hong, C. C.-H., Fallon, J. H., Friston, K. J., & Harris, J. C. (2018) · Frontiers in Psychology · doi:10.3389/fpsyg.2018.02087 · Cited by 29
Visual Direction Constancy: Perceiving the Visual Direction of Perisaccadic Flashes
Hershberger, W. A., & Jordan, J. S. (1992) · Advances in psychology · doi:10.1016/s0166-4115(08)61741-0 · Cited by 25
Visual signals contribute to the coding of gaze direction
Blouin, J., Amade, N., Vercher, J., Teasdale, N., & Gauthier, G. M. (2002) · Experimental Brain Research · doi:10.1007/s00221-002-1029-5 · Cited by 25
Biodynamic Structures, Cognitive Correlates of Motive Sets and the Development of Motives in Infants
Trevarthen, C. (1984) · Springer eBooks · doi:10.1007/978-3-642-69382-3_20 · Cited by 25
Evidence for efference copy for eye movements in fish
Johnstone, J. R., & Mark, R. F. (1969) · Comparative Biochemistry and Physiology · doi:10.1016/0010-406x(69)90048-6 · Cited by 25
Transfer of Predictive Signals Across Saccades
Vetter, P., Edwards, G., & Muckli, L. (2012) · Frontiers in Psychology · doi:10.3389/fpsyg.2012.00176 · Cited by 24
“An internal copy of the motor command, called efference copy, is used to update these internal predictions (Sperry, 1950).”
Method
Neurobiology of Speech Production
Tremblay, P., Deschamps, I., & Gracco, V. L. (2015) · Elsevier eBooks · doi:10.1016/b978-0-12-407794-2.00059-6 · Cited by 29
Self Beyond the Body: Action-Driven and Task-Relevant Purely Distal Cues Modulate Performance and Body Ownership
Grechuta, K., Ulysse, L., Ballester, B. R., & Verschure, P. F. M. J. (2019) · Frontiers in Human Neuroscience · doi:10.3389/fnhum.2019.00091 · Cited by 27
Action-locked Neural Responses in Auditory Cortex to Self-generated Sounds
Reznik, D., Guttman, N., Buaron, B., Golumbic, E. Z., & Mukamel, R. (2021) · Cerebral Cortex · doi:10.1093/cercor/bhab179 · Cited by 25
Inferring visual space from ultra-fine extra-retinal knowledge of gaze position
Zhao, Z., Ahissar, E., Victor, J. D., & Rucci, M. (2023) · Nature Communications · doi:10.1038/s41467-023-35834-4 · Cited by 24
On theory of motor synergies
Neilson, P. D., & Neilson, M. D. (2010) · Human Movement Science · doi:10.1016/j.humov.2009.10.005 · Cited by 24
Does optic flow parsing depend on prior estimation of heading?
Warren, P. A., Rushton, S. K., & Foulkes, A. J. (2012) · Journal of Vision · doi:10.1167/12.11.8 · Cited by 24
Perception of Time and Causation Through the Kinesthesia of Intentional Action
Freeman, W. (2008) · Integrative Psychological and Behavioral Science · doi:10.1007/s12124-007-9049-0 · Cited by 24
Effect of TMS on Oculomotor Behavior but not Perceptual Stability during Smooth Pursuit Eye Movements
Haarmeier, T., & Kammer, T. (2010) · Cerebral Cortex · doi:10.1093/cercor/bhp285 · Cited by 24
Sensorimotor Incongruence in People with Musculoskeletal Pain: A Systematic Review
Don, S., Voogt, L. P., Meeus, M., Kooning, M. D., & Nijs, J. (2016) · Pain Practice · doi:10.1111/papr.12456 · Cited by 24
Perisaccadic Occipital EEG Changes Quantified with Wavelet Analysis
Bodis-Wollner, I. G., von Gizycki, H., Avitable, M., HUSSAIN, Z., JAVEID, A., HABIB, A., RAZA, A., & SABET, M. (2002) · Annals of the New York Academy of Sciences · doi:10.1111/j.1749-6632.2002.tb02856.x · Cited by 24
Proprioception in Extraocular Muscles
Weir, C. R. (2006) · Journal of Neuro-Ophthalmology · doi:10.1097/01.wno.0000223272.86565.74 · Cited by 24
Awareness of Agency: Three Levels of Analysis
Proust, J. (2000) · The MIT Press eBooks · doi:10.7551/mitpress/4928.003.0027 · Cited by 24
Space perception and its disturbances after brain injury in man
Teuber, H. (1963) · Neuropsychologia · doi:10.1016/0028-3932(63)90012-5 · Cited by 24
The effect of ablation of frontal eye-fields and superior colliculi on visual stability and movement discrimination in rhesus monkeys
Collin, N. G., & Cowey, A. (1980) · Experimental Brain Research · doi:10.1007/bf00237789 · Cited by 24
The neuronal dark discharge during eye movements in awake ‘encéphale isolécats
Corazza, R., & LOMBROSO, C. T. (1971) · Brain Research · doi:10.1016/0006-8993(71)90286-1 · Cited by 24
SIGMA‐MOVEMENT AND SIGMA‐NYSTAGMUS: A NEW TOOL TO INVESTIGATE THE GAZE‐PURSUIT SYSTEM AND VISUAL‐MOVEMENT PERCEPTION IN MAN AND MONKEY*
Adler, B., Collewijn, H., Curio, G., Grüsser, O. ‐., Pause, M., Schreiter, U., & Weiss, L.-R. (1981) · Annals of the New York Academy of Sciences · doi:10.1111/j.1749-6632.1981.tb30877.x · Cited by 24
Self-generation and sound intensity interactively modulate perceptual bias, but not perceptual sensitivity
Paraskevoudi, N., & SanMiguel, I. (2021) · Scientific Reports · doi:10.1038/s41598-021-96346-z · Cited by 26
Corollary Discharge Dysfunction as a Possible Substrate of Anomalous Self-experiences in Schizophrenia
Beño‐Ruiz‐de‐la‐Sierra, R. M., Arjona, A., Hernández-García, M., Fernández‐Linsenbarth, I., Díez, Á., Fondevila, S., Castaño, C., Muñoz, F., Sanz-Fuentenebro, J., Roig-Herrero, A., et al. (2023) · Schizophrenia Bulletin · doi:10.1093/schbul/sbad157 · Cited by 23
The effect of gender on the N1–P2 auditory complex while listening and speaking with altered auditory feedback
Swink, S., & Stuart, A. (2012) · Brain and Language · doi:10.1016/j.bandl.2012.04.007 · Cited by 24
Comparison of brain models for active vs. passive perception
Freeman, W. (1999) · Information Sciences · doi:10.1016/s0020-0255(98)10100-7 · Cited by 23
A simple behaviour provides accuracy and flexibility in odour plume tracking—the robotic control of sensory-motor coupling in silkmoths
Ando, N., & Kanzaki, R. (2015) · Journal of Experimental Biology · doi:10.1242/jeb.124834 · Cited by 23
The Motor Cortex Is Involved in the Generation of Classically Conditioned Eyelid Responses in Behaving Rabbits
Ammann, C., Márquez‐Ruiz, J., Gómez‐Climent, M. Á., Delgado-García, J. M., & Gruart, A. (2016) · Journal of Neuroscience · doi:10.1523/jneurosci.4190-15.2016 · Cited by 23
Decoding Target Distance and Saccade Amplitude from Population Activity in the Macaque Lateral Intraparietal Area (LIP)
Bremmer, F., Kaminiarz, A., Klingenhoefer, S., & Churan, J. (2016) · Frontiers in Integrative Neuroscience · doi:10.3389/fnint.2016.00030 · Cited by 26
Visuomotor Velocity Transformations for Smooth Pursuit Eye Movements
Blohm, G., & Lefèvre, P. (2010) · Journal of Neurophysiology · doi:10.1152/jn.00728.2009 · Cited by 23
3 Vision: The Experimental Analysis of Visual Behavior
Ingle, D. (1971) · Fish physiology · doi:10.1016/s1546-5098(08)60044-8 · Cited by 23
Oculomotor and skeletal motor systems share one map of visual space
Nemire, K. E., & Bridgeman, B. (1987) · Vision Research · doi:10.1016/0042-6989(87)90088-5 · Cited by 23

Authors: Sperry, R. W.
Affiliations: University of Chicago (US)
Corresponding author: Sperry, R. W.
Venue: Journal of Comparative and Physiological Psychology
Publisher: American Psychological Association (APA)
Published: 1950
Volume: 43
Issue: 6
Pages: 482-489
ISSN: 0021-9940 (ISSN-L)
DOI: 10.1037/h0055479
OpenAlex: W2051811141
Cited by: 1,789
References: 10
Citations by year: 2026: 35 · 2025: 85 · 2024: 51 · 2023: 49 · 2022: 41 · 2021: 71 · 2020: 52 · 2019: 58 · 2018: 59 · 2017: 44 · 2016: 55 · 2015: 59 · 2014: 54 · 2013: 53 · 2012: 67
FWCI: 2.61
Type: journal article
Language: en
Open access: closed
Locations: Journal of Comparative and Physiological Psychology (publishedVersion)
PubMed (publishedVersion)
Topics: Life Sciences › Neuroscience › Neurology › Vestibular and auditory disorders
Life Sciences › Neuroscience › Cognitive Neuroscience › Visual perception and processing mechanisms
Life Sciences › Neuroscience › Cognitive Neuroscience › Motor Control and Adaptation
Keywords: eye rotation, inverted vision, retinal image motion
MeSH terms: Humans, Vision, Ocular, Nystagmus, Optokinetic

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

Neural basis of the spontaneous optokinetic response produced by visual inversion

Abstract

Overview

Integrity signals

Verification

Claims the paper makes

Claims other papers make about this one

Citations

Cites

Cited by

Related

Metadata

Record

About these checks