The timing of response onset and offset in macaque visual neurons
Open accessAbstract
We used fast, pseudorandom temporal sequences of preferred and antipreferred stimuli to drive neuronal firing rates rapidly between minimal and maximal across the visual system. Stimuli were tailored to the preferences of cells recorded in the lateral geniculate nucleus (magnocellular and parvocellular), primary visual cortex (simple and complex), and the extrastriate motion area MT. We found that cells took longer to turn on (to increase their firing rate) than to turn off (to reduce their rate). The latency difference (onset minus offset) varied from several to tens of milliseconds across cell type and stimulus class and was correlated with spontaneous or driven firing rates for most cell classes. The delay for response onset depended on the nature of the stimulus present before the preferred stimulus appeared, and may result from persistent inhibition caused by antipreferred stimuli or from suppression that followed the offset of the preferred stimulus. The onset delay showed three distinct types of dependence on the temporal sequence of stimuli across classes of cells, implying that suppression may accumulate or wear off with time. Onset latency is generally longer, can be more variable, and has marked stimulus dependence compared with offset latency. This suggests an important role for offset latency in assessing the speed of information transmission in the visual system and raises the possibility that signal offsets provide a timing reference for visual processing. We discuss the origin of the delay in onset latency compared with offset latency and consider how it may limit the utility of certain feedforward circuits.
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The representation of accumulated evidence in LIP is delayed by at least 100 ms compared with the activity of direction-selective neurons in the middle temporal area (MT).
“First, the representation of accumulated evidence in LIP is delayed by at least 100 ms compared with the activity of direction-selective neurons in the middle temporal area (MT) (Britten et al., 1996;Bair et al., 2002;Roitman and Shadlen, 2002;Osborne et al., 2004;Huk and Shadlen, 2005).”
From Bounded Integration in Parietal Cortex Underlies Decisions Even When Viewing Duration Is Dictated by the Environment (2008) · cites this paper as Bair et al., 2002
The latency of decision-related activity in LIP is at least 100 ms longer than the emergence of directional responses from MT and V1, and it exceeds simple saccadic latencies.
“The latency of decision-related activity is at least 100 ms longer than the emergence of directional responses from neurons in areas MT and V1 (Britten et al., 1996;Bair et al., 2002;Osborne et al., 2004), and it exceeds simple saccadic latencies (Carpenter, 1988).”
From Bounded Integration in Parietal Cortex Underlies Decisions Even When Viewing Duration Is Dictated by the Environment (2008) · cites this paper as Bair et al., 2002
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Numerical recipes in C: the art of scientific computing
(1993) · Choice Reviews Online · doi:10.5860/choice.30-5638 · Cited by 17,933 · see citing works
Receptive fields of single neurones in the cat's striate cortex
Hubel, D. H., & Wiesel, T. N. (1959) · The Journal of Physiology · doi:10.1113/jphysiol.1959.sp006308 · Cited by 4,653 · see citing works
Spatiotemporal energy models for the perception of motion
Adelson, E. H., & Bergen, J. R. (1985) · Journal of the Optical Society of America A · doi:10.1364/josaa.2.000284 · Cited by 3,442 · see citing works
The contrast sensitivity of retinal ganglion cells of the cat
Enroth-Cugell, C., & Robson, J. G. (1966) · The Journal of Physiology · doi:10.1113/jphysiol.1966.sp008107 · Cited by 2,625 · see citing works
DISCHARGE PATTERNS AND FUNCTIONAL ORGANIZATION OF MAMMALIAN RETINA
Kuffler, S. W. (1953) · Journal of Neurophysiology · doi:10.1152/jn.1953.16.1.37 · Cited by 2,609 · see citing works
Discharge Patterns of Single Fibers in the Cat's Auditory Nerve
Nelson, S. B., Watanabe, T., c., T. E., et al. (1966) · Defense Technical Information Center (DTIC) · Cited by 1,546 · see citing works
Maunsell, J. H. R., & Essen, D. C. V. (1983) · Journal of Neurophysiology · doi:10.1152/jn.1983.49.5.1127 · Cited by 1,462 · see citing works
Pattern recognition computation using action potential timing for stimulus representation
Hopfield, J. J. (1995) · Nature · doi:10.1038/376033a0 · Cited by 1,163 · see citing works
Sustained and transient neurones in the cat's retina and lateral geniculate nucleus
Cleland, B. G., Dubin, M. W., & Levick, W. R. (1971) · The Journal of Physiology · doi:10.1113/jphysiol.1971.sp009581 · Cited by 1,039 · see citing works
Signal timing across the macaque visual system
Schmolesky, M. T., Wang, Y., Hanes, D. P., Thompson, K. G., Leutgeb, S., Schall, J. D., & Leventhal, A. G. (1998) · Journal of Neurophysiology · doi:10.1152/jn.1998.79.6.3272 · Cited by 1,032 · see citing works
Zeki, S. (1974) · The Journal of Physiology · doi:10.1113/jphysiol.1974.sp010452 · Cited by 982 · see citing works
The Analysis of Moving Visual Patterns
Movshon, J. A., Adelson, E. H., Gizzi, M. S., & Newsome, W. T. (1985) · Experimental brain research. Supplementum · doi:10.1007/978-3-662-09224-8_7 · Cited by 968 · see citing works
Self-citationTHE RESPONSE OF SINGLE OPTIC NERVE FIBERS OF THE VERTEBRATE EYE TO ILLUMINATION OF THE RETINA
Hartline, H. K. (1938) · American Journal of Physiology-Legacy Content · doi:10.1152/ajplegacy.1938.121.2.400 · Cited by 966 · see citing works
Linearity and Normalization in Simple Cells of the Macaque Primary Visual Cortex
Carandini, M., Heeger, D. J., & Movshon, J. A. (1997) · Journal of Neuroscience · doi:10.1523/jneurosci.17-21-08621.1997 · Cited by 926 · see citing works
Self-citationSummation and inhibition in the frog's retina
Barlow, H. B. (1953) · The Journal of Physiology · doi:10.1113/jphysiol.1953.sp004829 · Cited by 892 · see citing works
Spatial summation in the receptive fields of simple cells in the cat's striate cortex.
Movshon, J. A., Thompson, I. D., & Tolhurst, D. J. (1978) · The Journal of Physiology · doi:10.1113/jphysiol.1978.sp012488 · Cited by 890 · see citing works
Self-citationIntegrative action in the cat's lateral geniculate body
Hubel, D. H., & Wiesel, T. N. (1961) · The Journal of Physiology · doi:10.1113/jphysiol.1961.sp006635 · Cited by 789 · see citing works
Sillito, A. M. (1975) · The Journal of Physiology · doi:10.1113/jphysiol.1975.sp011056 · Cited by 742 · see citing works
Specificity of monosynaptic connections from thalamus to visual cortex
Reid, R. C., & Alonso, J. (1995) · Nature · doi:10.1038/378281a0 · Cited by 732 · see citing works
Visual input evokes transient and strong shunting inhibition in visual cortical neurons
Graham, L. J., Monier, C., & Frégnac, Y. (1998) · Nature · doi:10.1038/30735 · Cited by 669 · see citing works
Neural Mechanisms of Orientation Selectivity in the Visual Cortex
Ferster, D., & Miller, K. D. (2000) · Annual Review of Neuroscience · doi:10.1146/annurev.neuro.23.1.441 · Cited by 665 · see citing works
Visual Response Properties of Striate Cortical Neurons Projecting to Area MT in Macaque Monkeys
Movshon, J. A., & Newsome, W. T. (1996) · The Journal of Neuroscience · doi:10.1523/jneurosci.16-23-07733.1996 · Cited by 651 · see citing works
Self-citationClassifying simple and complex cells on the basis of response modulation
SKOTTUN, B. C., Valois, R. L. D., Grosof, D. H., Movshon, J. A., Albrecht, D. G., & Bonds, A. B. (1991) · Vision Research · doi:10.1016/0042-6989(91)90033-2 · Cited by 608 · see citing works
Self-citationGlass-coated platinum-plated tungsten microelectrodes
Merrill, E. G., & Ainsworth, A. (1972) · Medical & Biological Engineering & Computing · doi:10.1007/bf02476084 · Cited by 597 · see citing works
Columnar organization of directionally selective cells in visual area MT of the macaque
Albright, T. D., Desimone, R., & Gross, C. G. (1984) · Journal of Neurophysiology · doi:10.1152/jn.1984.51.1.16 · Cited by 564 · see citing works
Visual response latencies in striate cortex of the macaque monkey
Maunsell, J. H. R., & Gibson, J. R. (1992) · Journal of Neurophysiology · doi:10.1152/jn.1992.68.4.1332 · Cited by 557 · see citing works
Recherches quantitatives sur l' excitation electrique des nerfs traitee comme une polarization.
Lapique, L. (1907) · Medical Entomology and Zoology · Cited by 557 · see citing works
The effect of contrast on the transfer properties of cat retinal ganglion cells.
Shapley, R. M., & Victor, J. D. (1978) · The Journal of Physiology · doi:10.1113/jphysiol.1978.sp012571 · Cited by 528 · see citing works
The control of retinogeniculate transmission in the mammalian lateral geniculate nucleus
Sherman, S. M., & Christof Koch, A. (1986) · Experimental Brain Research · doi:10.1007/bf00235642 · Cited by 513 · see citing works
Evidence for a Physiological Explanation of the Waterfall Phenomenon and Figural After-effects
Barlow, H. B., & Hill, R. (1963) · Nature · doi:10.1038/2001345a0 · Cited by 461 · see citing works
The timing of information transfer in the visual system
Nowak, L. G., & Bullier, J. (1997) · Cerebral cortex · doi:10.1007/978-1-4757-9625-4_5 · Cited by 444 · see citing works
Troyer, T. W., Krukowski, A. E., Priebe, N. J., & Miller, K. D. (1998) · Journal of Neuroscience · doi:10.1523/jneurosci.18-15-05908.1998 · Cited by 429 · see citing works
Membrane Potential and Firing Rate in Cat Primary Visual Cortex
Carandini, M., & Ferster, D. (2000) · Journal of Neuroscience · doi:10.1523/jneurosci.20-01-00470.2000 · Cited by 413 · see citing works
Cellular Mechanisms Contributing to Response Variability of Cortical NeuronsIn Vivo
Azouz, R., & Gray, C. M. (1999) · Journal of Neuroscience · doi:10.1523/jneurosci.19-06-02209.1999 · Cited by 408 · see citing works
Transformation from temporal to rate coding in a somatosensory thalamocortical pathway
Ahissar, E., Sosnik, R., & Haidarliu, S. (2000) · Nature · doi:10.1038/35018568 · Cited by 393 · see citing works
A Tonic Hyperpolarization Underlying Contrast Adaptation in Cat Visual Cortex
Carandini, M., & Ferster, D. (1997) · Science · doi:10.1126/science.276.5314.949 · Cited by 372 · see citing works
Temporal Precision of Spike Trains in Extrastriate Cortex of the Behaving Macaque Monkey
Bair, W., & Christof Koch, A. (1996) · Neural Computation · doi:10.1162/neco.1996.8.6.1185 · Cited by 368 · see citing works
Self-citationThe ON and OFF channels of the visual system
Schiller, P. H. (1992) · Trends in Neurosciences · doi:10.1016/0166-2236(92)90017-3 · Cited by 365 · see citing works
Latency: another potential code for feature binding in striate cortex
Gawne, T. J., Kjær, T. W., & Richmond, B. J. (1996) · Journal of Neurophysiology · doi:10.1152/jn.1996.76.2.1356 · Cited by 363 · see citing works
Responses to moving slits by single units in cat striate cortex
Pettigrew, J. D., Nikara, T., & Bishop, P. O. (1968) · Experimental Brain Research · doi:10.1007/bf00233185 · Cited by 359 · see citing works
Visual latencies in areas V1 and V2 of the macaque monkey
Nowak, L. G., Munk, M., Girard, P., & Bullier, J. (1995) · Visual Neuroscience · doi:10.1017/s095252380000804x · Cited by 353 · see citing works
A Panoramic Code for Sound Location by Cortical Neurons
Middlebrooks, J. C., Eddins, A. C., Xu, L., & Green, D. M. (1994) · Science · doi:10.1126/science.8171339 · Cited by 351 · see citing works
Agmon, A., & Connors, B. W. (1992) · Journal of Neuroscience · doi:10.1523/jneurosci.12-01-00319.1992 · Cited by 345 · see citing works
Porter, J. T., Johnson, C. K., & Agmon, A. (2001) · Journal of Neuroscience · doi:10.1523/jneurosci.21-08-02699.2001 · Cited by 344 · see citing works
Synaptic Integration in Striate Cortical Simple Cells
Hirsch, J. A., Alonso, J., Reid, R. C., & Martı́nez, L. M. (1998) · Journal of Neuroscience · doi:10.1523/jneurosci.18-22-09517.1998 · Cited by 326 · see citing works
Visual Motion Analysis for Pursuit Eye Movements in Area MT of Macaque Monkeys
Lisberger, S. G., & Movshon, J. A. (1999) · Journal of Neuroscience · doi:10.1523/jneurosci.19-06-02224.1999 · Cited by 322 · see citing works
Self-citationMembrane Mechanisms Underlying Contrast Adaptation in Cat Area 17In Vivo
Sanchez-Vives, M. V., Nowak, L. G., & McCormick, D. A. (2000) · Journal of Neuroscience · doi:10.1523/jneurosci.20-11-04267.2000 · Cited by 315 · see citing works
The action of light on the eye
Adrian, E. D., & Matthews, R. (1927) · The Journal of Physiology · doi:10.1113/jphysiol.1927.sp002410 · Cited by 303 · see citing works
Neural activity in cortical area MST of alert monkey during ocular following responses
Kawano, K., Shidara, M., Watanabe, Y., & Yamane, S. (1994) · Journal of Neurophysiology · doi:10.1152/jn.1994.71.6.2305 · Cited by 302 · see citing works
Transparent motion perception as detection of unbalanced motion signals. II. Physiology
Qian, N., & Andersen, R. (1994) · Journal of Neuroscience · doi:10.1523/jneurosci.14-12-07367.1994 · Cited by 302 · see citing works
Visual response latencies of magnocellular and parvocellular LGN neurons in macaque monkeys
Maunsell, J. H. R., Ghose, G. M., Assad, J. A., McAdams, C. J., Boudreau, C. E., & Noerager, B. D. (1999) · Visual Neuroscience · doi:10.1017/s0952523899156177 · Cited by 298 · see citing works
Motion Opponency in Visual Cortex
Heeger, D. J., Boynton, G. M., Demb, J. B., Seidemann, E., & Newsome, W. T. (1999) · Journal of Neuroscience · doi:10.1523/jneurosci.19-16-07162.1999 · Cited by 283 · see citing works
Tamás, G., Buhl, E. H., & Somogyi, P. (1997) · The Journal of Physiology · doi:10.1113/jphysiol.1997.sp022054 · Cited by 278 · see citing works
Influence of low and high frequency inputs on spike timing in visual cortical neurons
Nowak, L. G. (1997) · Cerebral Cortex · doi:10.1093/cercor/7.6.487 · Cited by 272 · see citing works
Dynamics of orientation coding in area V1 of the awake primate
Celebrini, S., Thorpe, S. J., Trotter, Y., & Imbert, M. (1993) · Visual Neuroscience · doi:10.1017/s0952523800006052 · Cited by 270 · see citing works
SAUL, A. B., & Humphrey, A. L. (1990) · Journal of Neurophysiology · doi:10.1152/jn.1990.64.1.206 · Cited by 269 · see citing works
Paired-spike interactions and synaptic efficacy of retinal inputs to the thalamus
Usrey, W. M., Reppas, J. B., & Reid, R. C. (1998) · Nature · doi:10.1038/26487 · Cited by 246 · see citing works
Spatially opponent excitation and inhibition in simple cells of the cat visual cortex
Ferster, D. (1988) · Journal of Neuroscience · doi:10.1523/jneurosci.08-04-01172.1988 · Cited by 240 · see citing works
Receptive field structure in the primate retina
Lee, B. B. (1996) · Vision Research · doi:10.1016/0042-6989(95)00167-0 · Cited by 238 · see citing works
Mastronarde, D. N. (1987) · Journal of Neurophysiology · doi:10.1152/jn.1987.57.2.381 · Cited by 237 · see citing works
Rate coding versus temporal order coding: a theoretical approach
Gautrais, J., & Thorpe, S. J. (1998) · Biosystems · doi:10.1016/s0303-2647(98)00050-1 · Cited by 236 · see citing works
Figural After-Effects and Apparent Size
Sutherland, N. (1961) · Quarterly Journal of Experimental Psychology · doi:10.1080/17470216108416498 · Cited by 233 · see citing works
Auditory-Nerve Activity in Cats Exposed to Ototoxic Drugs and High-Intensity Sounds
Kiang, N. Y. S., Liberman, M. C., & Levine, R. A. (1976) · Annals of Otology Rhinology & Laryngology · doi:10.1177/000348947608500605 · Cited by 230 · see citing works
The use of m-sequences in the analysis of visual neurons: Linear receptive field properties
Reid, R. C., Victor, J. D., & Shapley, R. M. (1997) · Visual Neuroscience · doi:10.1017/s0952523800011743 · Cited by 224 · see citing works
Contrast gain control in the primate retina: P cells are not X-like, some M cells are
Benardete, E. A., Kaplan, E., & Knight, B. W. (1992) · Visual Neuroscience · doi:10.1017/s0952523800004995 · Cited by 216 · see citing works
Speed and direction selectivity of macaque middle temporal neurons
Lagae, L. G., Raiguel, S. E., & Orban, G. A. (1993) · Journal of Neurophysiology · doi:10.1152/jn.1993.69.1.19 · Cited by 212 · see citing works
Singer, W., & Creutzfeldt, O. D. (1970) · Experimental Brain Research · doi:10.1007/bf00235054 · Cited by 209 · see citing works
Response latencies of visual cells in macaque areas V1, V2 and V5
Raiguel, S. E., Lagae, L., Gulyàs, B., & Orban, G. A. (1989) · Brain Research · doi:10.1016/0006-8993(89)91010-x · Cited by 206 · see citing works
Levitt, J. B., Schumer, R. A., Sherman, S. M., Spear, P. D., & Movshon, J. A. (2001) · Journal of Neurophysiology · doi:10.1152/jn.2001.85.5.2111 · Cited by 200 · see citing works
Self-citationReceptive-field structure in cat striate cortex.
Palmer, L. A., & Davis, T. L. (1981) · Journal of Neurophysiology · doi:10.1152/jn.1981.46.2.260 · Cited by 192 · see citing works
Coenen, A. M. L., & Vendrik, A. J. H. (1972) · Experimental Brain Research · doi:10.1007/bf00816160 · Cited by 191 · see citing works
Functional synaptic organization of primary visual cortex neurones in the cat
Creutzfeldt, O. D., & Ito, M. (1968) · Experimental Brain Research · doi:10.1007/bf00233183 · Cited by 185 · see citing works
The dynamics of primate M retinal ganglion cells
Benardete, E. A., & Kaplan, E. (1999) · Visual Neuroscience · doi:10.1017/s0952523899162151 · Cited by 184 · see citing works
Vautin, R. G., & Berkley, M. A. (1977) · Journal of Neurophysiology · doi:10.1152/jn.1977.40.5.1051 · Cited by 183 · see citing works
Mastronarde, D. N. (1987) · Journal of Neurophysiology · doi:10.1152/jn.1987.57.2.357 · Cited by 173 · see citing works
On the relationship between synaptic input and spike output jitter in individual neurons
Maršálek, P., Christof Koch, A., & Maunsell, J. H. R. (1997) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.94.2.735 · Cited by 167 · see citing works
Freund, T. F., Martin, K. A. C., Somogyi, P., & Whitteridge, D. (1985) · The Journal of Comparative Neurology · doi:10.1002/cne.902420209 · Cited by 165 · see citing works
Responses to pulses and sinusoids in macaque ganglion cells
Lee, B. B., Pokorny, J., Smith, V. C., et al. (1994) · Vision Research · doi:10.1016/0042-6989(94)90074-4 · Cited by 164 · see citing works
Snodderly, D. M., & Gur, M. (1995) · Journal of Neurophysiology · doi:10.1152/jn.1995.74.5.2100 · Cited by 156 · see citing works
Processing of first- and second-order motion signals by neurons in area MT of the macaque monkey
O’Keefe, L. P., & Movshon, J. A. (1998) · Visual Neuroscience · doi:10.1017/s0952523898152094 · Cited by 155 · see citing works
Self-citationMitzdorf, U., & Singer, W. (1979) · The Journal of Comparative Neurology · doi:10.1002/cne.901870105 · Cited by 143 · see citing works
McIlwain, J. T., & Creutzfeldt, O. D. (1967) · Journal of Neurophysiology · doi:10.1152/jn.1967.30.1.1 · Cited by 141 · see citing works
Latency changes in the human visual evoked response to sinusoidal gratings
PARKER, D. M., & Salzen, E. A. (1977) · Vision Research · doi:10.1016/0042-6989(77)90154-7 · Cited by 139 · see citing works
Inhibitory interaction in the cat's lateral geniculate nucleus
Singer, W., Pöppel, E., & Creutzfeldt, O. D. (1972) · Experimental Brain Research · doi:10.1007/bf00234800 · Cited by 130 · see citing works
Response Latency of Macaque Area MT/V5 Neurons and Its Relationship to Stimulus Parameters
Raiguel, S. E., Xiao, D. K., Marcar, V. L., & Orban, G. A. (1999) · Journal of Neurophysiology · doi:10.1152/jn.1999.82.4.1944 · Cited by 128 · see citing works
Response of units in striate cortex of squirrel monkeys to visual and electrical stimuli.
Bartlett, J. R., & Doty, R. W. (1974) · Journal of Neurophysiology · doi:10.1152/jn.1974.37.4.621 · Cited by 123 · see citing works
The receptive field of the primate P retinal ganglion cell, I: Linear dynamics
Benardete, E. A., & Kaplan, E. (1997) · Visual Neuroscience · doi:10.1017/s0952523800008853 · Cited by 122 · see citing works
The Design of Chromatically Opponent Receptive Fields
Lennie, P., Haake, P. W., & Williams, D. R. (1991) · The MIT Press eBooks · doi:10.7551/mitpress/2002.003.0010 · Cited by 121 · see citing works
Swadlow, H. A. (1995) · Journal of Neurophysiology · doi:10.1152/jn.1995.73.4.1584 · Cited by 120 · see citing works
Variation in the response latency of cat retinal ganglion cells
Levick, W. R. (1973) · Vision Research · doi:10.1016/0042-6989(73)90047-3 · Cited by 118 · see citing works
How Simple Cells Are Made in a Nonlinear Network Model of the Visual Cortex
Wielaard, D. J., Shelley, M., McLaughlin, D. W., & Shapley, R. M. (2001) · Journal of Neuroscience · doi:10.1523/jneurosci.21-14-05203.2001 · Cited by 113 · see citing works
Visual evoked response as a function of grating spatial frequency.
Jones, R. D., & Keck, M. J. (1978) · PubMed · Cited by 103 · see citing works
Functionally distinct groups of X‐cells in the lateral geniculate nucleus of the cat
Humphrey, A. L., & Weller, R. E. (1988) · The Journal of Comparative Neurology · doi:10.1002/cne.902680311 · Cited by 103 · see citing works
Spike train encoding by regular-spiking cells of the visual cortex
Carandini, M., Mechler, F., Leonard, C. S., et al. (1996) · Journal of Neurophysiology · doi:10.1152/jn.1996.76.5.3425 · Cited by 93 · see citing works
Statistische Eigenschaften der Neuronaktivität im ascendierenden visuellen System
Herz, V. A., Creutzfeldt, O. D., & Fuster, J. M. (1964) · Kybernetik · doi:10.1007/bf00288559 · Cited by 86 · see citing works
Broadband temporal stimuli decrease the integration time of neurons in cat striate cortex
Reid, R. C., Victor, J. D., & Shapley, R. M. (1992) · Visual Neuroscience · doi:10.1017/s0952523800006350 · Cited by 86 · see citing works
Eysel, U. T., Shevelev, I. A., Лазарева, Н. А., & Sharaev, G. A. (1998) · Neuroscience · doi:10.1016/s0306-4522(97)00378-3 · Cited by 68 · see citing works
Morphology of individual axons projecting from area V2 to MT in the macaque
Rockland, K. S. (1995) · The Journal of Comparative Neurology · doi:10.1002/cne.903550105 · Cited by 66 · see citing works
Tolhurst, D. J., & Dean, A. F. (1990) · Experimental Brain Research · doi:10.1007/bf00229326 · Cited by 62 · see citing works
Visual response latency of X- and Y-cells in the dorsal lateral geniculate nucleus of the cat
Sestokas, A. K., & Lehmkuhle, S. W. (1986) · Vision Research · doi:10.1016/0042-6989(86)90038-6 · Cited by 62 · see citing works
Dynamics of the orientation tuning of postsynaptic potentials in the cat visual cortex
Volgushev, M., Vidyasagar, T. R., & Pei, X. (1995) · Visual Neuroscience · doi:10.1017/s0952523800008919 · Cited by 61 · see citing works
Microelectrode studies on the visual cortex.
Von Baumgarten, R., & Jung, R. (1952) · PubMed · Cited by 50 · see citing works
Creutzfeldt, O. D., & Sakmann, B. (1969) · Annual Review of Physiology · doi:10.1146/annurev.ph.31.030169.002435 · Cited by 41 · see citing works
Heggelund, P. (1986) · The Journal of Physiology · doi:10.1113/jphysiol.1986.sp016048 · Cited by 40 · see citing works
Color vision: Putting it together
Lennie, P. (2000) · Current Biology · doi:10.1016/s0960-9822(00)00632-1 · Cited by 36 · see citing works
Visual Cortical Signals Supporting Smooth Pursuit Eye MovementsPreprint
Movshon, J. A., Lisberger, S. G., & Krauzlis, R. J. (1990) · Cold Spring Harbor Symposia on Quantitative Biology · doi:10.1101/sqb.1990.055.01.066 · Cited by 32 · see citing works
Self-citationInformation filtering in the lateral geniculate nucleus
Kaplan, E., Mukherjee, P., & Shapley, R. M. (1993) · Cited by 30 · see citing works
Responses to Opposed Directions of Motion:
Raymond, J. E., & Braddick, O. (1996) · Vision Research · doi:10.1016/0042-6989(95)00241-3 · Cited by 24 · see citing works
Reconstructing Stimulus Velocity from Neuronal Responses in Area MT
Bair, W., Cavanaugh, J. R., & Movshon, J. A. (1996) · Cited by 20 · see citing works
Self-citationON and OFF channels of the visual system
Schiller, P. H. (1990) · Optical Society of America Annual Meeting · doi:10.1364/oam.1990.thf2 · Cited by 20 · see citing works
SAUL, A. B. (1995) · Visual Neuroscience · doi:10.1017/s0952523800007872 · Cited by 18 · see citing works
Synaptic delay in the lateral geniculate nucleus of the cat
Wang, C., Cleland, B. G., & Burke, W. J. (1985) · Brain Research · doi:10.1016/0006-8993(85)90740-1 · Cited by 17 · see citing works
Coenen, A. M. L., Gerrits, H. J. M., & Vendrik, A. J. H. (1972) · Experimental Brain Research · doi:10.1007/bf00236402 · Cited by 17 · see citing works
Switching between off and on in the macaque visual system
Bair, W., Cavanaugh, J. R., Smith, M. A., et al. (2010) · Journal of Vision · doi:10.1167/1.3.202 · Cited by 1 · see citing works
Self-citation
Flagged first, then by citations
Research works printed but not linked: 2
- Casagrande VA, Norton TT (1991) Lateral geniculate nucleus: a review of its physiology and function. In: Vision and visual dysfunction: the neural basis of visual function, Vol 4, (Leventhal AG, ed), pp 41-84. London: Macmillan.
- Sutter EE (1987) A practical non-stochastic approach to nonlinear time- domain analysis. In: Advanced methods of physiological systems mod- eling, Vol 1 (Marmaerelis V, ed), pp 303-315. Los Angeles, CA: University of Southern California.
Cited by
Sorted by citations
Kiani, R., Hanks, T. D., & Shadlen, M. N. (2008) · The Journal of Neuroscience · doi:10.1523/jneurosci.4761-07.2008 · Cited by 500 · see citing works
Predictive feedback can account for biphasic responses in the lateral geniculate nucleus
Jehee, J. F. M., & Ballard, D. H. (2009) · PLoS Computational Biology · doi:10.1371/journal.pcbi.1000373 · Cited by 75 · see citing works
- Authors
- Bair, W., Cavanaugh, J. R., Smith, M. A., & Movshon, J. A.
- Affiliations
- Howard Hughes Medical Institute (US)
- New York University (US)
- Venue
- The Journal of Neuroscience
- Publisher
- Society for Neuroscience
- Published
- 2002-04-15
- Volume
- 22
- Issue
- 8
- Pages
- 3189-3205
- ISSN
- 0270-6474 (ISSN-L)
- 1529-2401
- PMC
- PMC6757536
- OpenAlex
- W2124621238
- Cited by
- 170
- References
- 114
- Citations by year
- 2026: 6 · 2025: 7 · 2024: 3 · 2023: 5 · 2022: 4 · 2021: 6 · 2020: 10 · 2019: 3 · 2018: 2 · 2017: 7 · 2016: 4 · 2015: 4 · 2014: 8 · 2013: 12 · 2012: 4
- FWCI
- 5.17
- Type
- journal article
- Language
- en
- Open access
- bronze
- doi.org
- Locations
- Journal of Neuroscience (publishedVersion)
- PubMed Central (publishedVersion)
- PubMed (publishedVersion)
- Funders
- National Institutes of Health
- National Eye Institute (R01EY002017)
- Topics
- Life Sciences › Neuroscience › Cognitive Neuroscience › Visual perception and processing mechanisms
- Life Sciences › Neuroscience › Cognitive Neuroscience › Neural dynamics and brain function
- Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Neuroscience and Neuropharmacology Research
- Keywords
- visual neurons, lateral geniculate nucleus, primary visual cortex, spontaneous firing rate, feedforward circuits, macaque visual system
- MeSH terms
- Action Potentials, Animals, Geniculate Bodies, Macaca fascicularis, Motion Perception, Neural Inhibition, Synaptic Transmission, Neurons, Photic Stimulation, Reaction Time, Signal Processing, Computer-Assisted, Visual Cortex, Visual Pathways
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.
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