The DOI matches its Crossref record; 23 of the 23 references it cites were found in a registry or an index.
The Contribution of Noise to Contrast Invariance of Orientation Tuning in Cat Visual Cortex
Abstract
Feedforward models of visual cortex appear to be inconsistent with a well-known property of cortical cells: contrast invariance of orientation tuning. The models' fixed threshold broadens orientation tuning as contrast increases, whereas in real cells tuning width is invariant with contrast. We have compared the orientation tuning of spike and membrane potential responses in single cells. Both are contrast invariant, yet a threshold-linear relation applied to the membrane potential accurately predicts the orientation tuning of spike responses. The key to this apparent paradox lies in the noisiness of the membrane potential. Responses that are subthreshold on average are still capable of generating spikes on individual trials. Unlike the iceberg effect, contrast invariance remains intact even as threshold narrows orientation selectivity. Noise may, by extension, smooth the average relation between membrane potential and spike rate throughout the brain.
Overview
Integrity signals
Registry
Cites
Statistics
Verification
Claims the paper makes
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?
In the citing paper
“Neurons in many cortical and subcortical brain areas exhibit robust gain modulation that may contribute to multiple cognitive functions, including attention, learning, sensory processing and multimodal integration1–3,7,8,13–17.”
From Mechanisms underlying gain modulation in the cortex (2020) · cites this paper as [13]
In the citing paper
“These fluctuations may contribute to contrast-invariant tuning in neurons of the visual cortex of cats and rodents10,13,63,64.”
From Mechanisms underlying gain modulation in the cortex (2020) · cites this paper as [13]
In the citing paper
“Synaptically driven fluctuations in the Vm smooth the transformation from Vm depolarization to spike output, creating a power-law relationship between the mean Vm and the mean firing rate13,63.”
From Mechanisms underlying gain modulation in the cortex (2020) · cites this paper as [13]
In the citing paper
“Similarly, background synaptic noise that is uncorrelated with ongoing visual stimulation contributes to maintaining stable orientation tuning in visual cortex neurons across varying levels of visual contrast13.”
From Mechanisms underlying gain modulation in the cortex (2020) · cites this paper as [13]
Citations
Cites
Brainard, D. H. (1997) · Spatial Vision · doi:10.1163/156856897x00357 · Cited by 19,308
Receptive fields, binocular interaction and functional architecture in the cat’s visual cortex
Hubel, D. H., & Wiesel, T. N. (1962) · The Journal of Physiology · doi:10.1113/jphysiol.1962.sp006837 · Cited by 13,680
The VideoToolbox software for visual psychophysics: transforming numbers into movies
Pelli, D. G. (1997) · Spatial Vision · doi:10.1163/156856897x00366 · Cited by 11,110
Stochastic resonance and the benefits of noise: from ice ages to crayfish and SQUIDs
Wiesenfeld, K., & Moss, F. (1995) · Nature · doi:10.1038/373033a0 · Cited by 1,830
Theory of orientation tuning in visual cortex.
Ben-Yishai, R., Bar‐Or, R. L., & Sompolinsky, H. (1995) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.92.9.3844 · Cited by 1,091
An emergent model of orientation selectivity in cat visual cortical simple cells
Somers, D., Nelson, S., & Sur, M. (1995) · The Journal of Neuroscience · doi:10.1523/jneurosci.15-08-05448.1995 · Cited by 860
Dynamics of Encoding in a Population of Neurons
Knight, B. W. (1972) · The Journal of General Physiology · doi:10.1085/jgp.59.6.734 · Cited by 720
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
Self-citationPrecisely correlated firing in cells of the lateral geniculate nucleus
Alonso, J., Usrey, W. M., & Reid, R. C. (1996) · Nature · doi:10.1038/383815a0 · Cited by 514
Synchronous Membrane Potential Fluctuations in Neurons of the Cat Visual Cortex
Lampl, I., Reichova, I., & Ferster, D. (1999) · Neuron · doi:10.1016/s0896-6273(00)81096-x · Cited by 435
Self-citation
Flagged first, then by citations
Cited by
Sorted by citations
Faisal, A. A., Selen, L. P. J., & Wolpert, D. M. (2008) · Nature Reviews Neuroscience · doi:10.1038/nrn2258 · Cited by 2,883
Bayesian inference with probabilistic population codes
Ma, W. J., Beck, J. M., Latham, P. E., & Pouget, A. (2006) · Nature Neuroscience · doi:10.1038/nn1790 · Cited by 1,457
The Normalization Model of Attention
Reynolds, J. H., & Heeger, D. J. (2009) · Neuron · doi:10.1016/j.neuron.2009.01.002 · Cited by 1,457
Turning on and off recurrent balanced cortical activity
Shu, Y., Hasenstaub, A., & McCormick, D. A. (2003) · Nature · doi:10.1038/nature01616 · Cited by 1,054
Stochastic resonance and sensory information processing: A tutorial and review of application
Moss, F., Ward, L. M., & Sannita, W. G. (2004) · Clinical Neurophysiology · doi:10.1016/j.clinph.2003.09.014 · Cited by 994
Gain Modulation from Background Synaptic Input
Chance, F. S., Abbott, L. F., & Reyes, A. D. (2002) · Neuron · doi:10.1016/s0896-6273(02)00820-6 · Cited by 1,012
Cellular mechanisms of brain state-dependent gain modulation in visual cortex
Polack, P.-O., Friedman, J., & Golshani, P. (2013) · Nature Neuroscience · doi:10.1038/nn.3464 · Cited by 628
Probabilistic population codes for Bayesian decision making
Beck, J. M., Ma, W. J., Kiani, R., Hanks, T., Churchland, A. K., Roitman, J., Shadlen, M. N., Latham, P. E., & Pouget, A. (2008) · Neuron · doi:10.1016/j.neuron.2008.09.021 · Cited by 645
Statistically optimal perception and learning: from behavior to neural representations
Fiser, J., Berkes, P., Orbán, G., & Lengyel, M. (2010) · Trends in Cognitive Sciences · doi:10.1016/j.tics.2010.01.003 · Cited by 672
Orientation Selectivity in Macaque V1: Diversity and Laminar Dependence
Ringach, D. L., Shapley, R. M., & Hawken, M. J. (2002) · Journal of Neuroscience · doi:10.1523/jneurosci.22-13-05639.2002 · Cited by 653
Probabilistic brains: knowns and unknowns
Pouget, A., Beck, J. M., Ma, W. J., & Latham, P. E. (2013) · Nature Neuroscience · doi:10.1038/nn.3495 · Cited by 615
“This is inconsistent with what is seen in primary visual cortex, where the widths of orientation tuning curves are independent of contrast 65 , even though lower contrast implies higher uncertainty, that is, wider probability distributions (see Table 1 ).”
Shunting Inhibition Modulates Neuronal Gain during Synaptic Excitation
Mitchell, S. J., & Silver, R. A. (2003) · Neuron · doi:10.1016/s0896-6273(03)00200-9 · Cited by 602
Conjunctive input processing drives feature selectivity in hippocampal CA1 neurons
Bittner, K. C., Grienberger, C., Vaidya, S. P., Milstein, A. D., Macklin, J. J., Suh, J., Tonegawa, S., & Magee, J. C. (2015) · Nature Neuroscience · doi:10.1038/nn.4062 · Cited by 540
Vogels, T. P., Rajan, K., & Abbott, L. F. (2005) · Annual Review of Neuroscience · doi:10.1146/annurev.neuro.28.061604.135637 · Cited by 497
Maximum likelihood estimation of cascade point-process neural encoding models
Paninski, L. (2004) · Network Computation in Neural Systems · doi:10.1088/0954-898x/15/4/002 · Cited by 481
Silver, R. A. (2010) · Nature Reviews Neuroscience · doi:10.1038/nrn2864 · Cited by 481
Inhibitory Stabilization of the Cortical Network Underlies Visual Surround Suppression
Ozeki, H., Finn, I. M., Schaffer, E., Miller, K. D., & Ferster, D. (2009) · Neuron · doi:10.1016/j.neuron.2009.03.028 · Cited by 470
Self-citationSignal Propagation and Logic Gating in Networks of Integrate-and-Fire Neurons
Vogels, T. P., & Abbott, L. F. (2005) · Journal of Neuroscience · doi:10.1523/jneurosci.3508-05.2005 · Cited by 461
Rapid Neocortical Dynamics: Cellular and Network Mechanisms
Haider, B., & McCormick, D. A. (2009) · Neuron · doi:10.1016/j.neuron.2009.04.008 · Cited by 441
Wang, X.-J., Tegner, J. N., Constantinidis, C., & Goldman‐Rakic, P. S. (2004) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0305337101 · Cited by 405
Discrete attractor dynamics underlies persistent activity in the frontal cortex
Inagaki, H. K., Fontolan, L., Romani, S., & Svoboda, K. (2019) · Nature · doi:10.1038/s41586-019-0919-7 · Cited by 334
Internal Dynamics Determine the Cortical Response to Thalamic Stimulation
MacLean, J. N., Watson, B. O., Aaron, G. B., & Yuste, R. (2005) · Neuron · doi:10.1016/j.neuron.2005.09.035 · Cited by 373
Inhibition, Spike Threshold, and Stimulus Selectivity in Primary Visual Cortex
Priebe, N. J., & Ferster, D. (2008) · Neuron · doi:10.1016/j.neuron.2008.02.005 · Cited by 359
Self-citationOrientation and Direction Selectivity of Synaptic Inputs in Visual Cortical Neurons
Monier, C., Chavane, F., Baudot, P., Graham, L. J., & Frégnac, Y. (2003) · Neuron · doi:10.1016/s0896-6273(03)00064-3 · Cited by 356
Balanced Amplification: A New Mechanism of Selective Amplification of Neural Activity Patterns
Murphy, B. K., & Miller, K. D. (2009) · Neuron · doi:10.1016/j.neuron.2009.02.005 · Cited by 338
The organization of two new cortical interneuronal circuits
Jiang, X., Wang, G., Lee, A. J., Stornetta, R. L., & Zhu, J. J. (2013) · Nature Neuroscience · doi:10.1038/nn.3305 · Cited by 338
Mechanisms underlying gain modulation in the cortex
Ferguson, K. A., & Cardin, J. A. (2020) · Nature Reviews Neuroscience · doi:10.1038/s41583-019-0253-y · Cited by 327
Barrages of Synaptic Activity Control the Gain and Sensitivity of Cortical Neurons
Shu, Y., Hasenstaub, A., Badoual, M., Bal, T., & McCormick, D. A. (2003) · The Journal of Neuroscience · doi:10.1523/jneurosci.23-32-10388.2003 · Cited by 298
From Subthreshold to Firing-Rate Resonance
Richardson, M. J. E., Brunel, N., & Hakim, V. (2003) · Journal of Neurophysiology · doi:10.1152/jn.00955.2002 · Cited by 285
Adaptive Coincidence Detection and Dynamic Gain Control in Visual Cortical Neurons In Vivo
Azouz, R., & Gray, C. M. (2003) · Neuron · doi:10.1016/s0896-6273(02)01186-8 · Cited by 277
Haider, B., Krause, M. R., Duque, A., Yu, Y., Touryan, J., Mazer, J. A., & McCormick, D. A. (2010) · Neuron · doi:10.1016/j.neuron.2009.12.005 · Cited by 263
The Emergence of Contrast-Invariant Orientation Tuning in Simple Cells of Cat Visual Cortex
Finn, I. M., Priebe, N. J., & Ferster, D. (2007) · Neuron · doi:10.1016/j.neuron.2007.02.029 · Cited by 248
Self-citationThe Emergence of Up and Down States in Cortical Networks
Holcman, D., & Tsodyks, M. V. (2005) · PLoS Computational Biology · doi:10.1371/journal.pcbi.0020023 · Cited by 249
Direction Selectivity of Excitation and Inhibition in Simple Cells of the Cat Primary Visual Cortex
Priebe, N. J., & Ferster, D. (2005) · Neuron · doi:10.1016/j.neuron.2004.12.024 · Cited by 250
Self-citationOn the Distribution of Firing Rates in Networks of Cortical Neurons
Roxin, A., Brunel, N., Hansel, D., Mongillo, G., & van Vreeswijk, C. (2011) · Journal of Neuroscience · doi:10.1523/jneurosci.1677-11.2011 · Cited by 252
Synaptic depression enables neuronal gain control
Rothman, J. S., Cathala, L., Steuber, V., & Silver, R. A. (2009) · Nature · doi:10.1038/nature07604 · Cited by 249
Ostojic, S., Brunel, N., & Hakim, V. (2009) · Journal of Neuroscience · doi:10.1523/jneurosci.1275-09.2009 · Cited by 234
From Spiking Neuron Models to Linear-Nonlinear Models
Ostojic, S., & Brunel, N. (2011) · PLoS Computational Biology · doi:10.1371/journal.pcbi.1001056 · Cited by 227
Gain control of firing rate by shunting inhibition: Roles of synaptic noise and dendritic saturation
Prescott, S. A., & De Koninck, Y. (2003) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0337591100 · Cited by 226
A Synaptic Explanation of Suppression in Visual Cortex
Carandini, M., Heeger, D. J., & Senn, W. (2002) · Journal of Neuroscience · doi:10.1523/jneurosci.22-22-10053.2002 · Cited by 219
The contribution of spike threshold to the dichotomy of cortical simple and complex cells
Priebe, N. J., Mechler, F., Carandini, M., & Ferster, D. (2004) · Nature Neuroscience · doi:10.1038/nn1310 · Cited by 217
Self-citationFast Propagation of Firing Rates through Layered Networks of Noisy Neurons
van Rossum, M. C. W., Turrigiano, G. G., & Nelson, S. B. (2002) · Journal of Neuroscience · doi:10.1523/jneurosci.22-05-01956.2002 · Cited by 207
Amplification of Trial-to-Trial Response Variability by Neurons in Visual Cortex
Carandini, M. (2004) · PLoS Biology · doi:10.1371/journal.pbio.0020264 · Cited by 210
Neural Noise Can Explain Expansive, Power-Law Nonlinearities in Neural Response Functions
Miller, K. D., & Troyer, T. W. (2002) · Journal of Neurophysiology · doi:10.1152/jn.00425.2001 · Cited by 207
Egner (2005) · doi:10.1038/nn1591 · Cited by 207
Visual Cortex Neurons of Monkeys and Cats: Temporal Dynamics of the Contrast Response Function
Albrecht, D. G., Geisler, W. S., Frazor, R. A., & Crane, A. M. (2002) · Journal of Neurophysiology · doi:10.1152/jn.2002.88.2.888 · Cited by 207
Neuronal Integration of Synaptic Input in the Fluctuation-Driven Regime
Kuhn, A., Aertsen, A., & Rotter, S. (2004) · Journal of Neuroscience · doi:10.1523/jneurosci.3349-03.2004 · Cited by 200
Yu, Y., Shu, Y., & McCormick, D. A. (2008) · Journal of Neuroscience · doi:10.1523/jneurosci.1613-08.2008 · Cited by 199
Noise as a Resource for Computation and Learning in Networks of Spiking Neurons
Maass, W. (2014) · Proceedings of the IEEE · doi:10.1109/jproc.2014.2310593 · Cited by 194
Persistent Cortical Activity: Mechanisms of Generation and Effects on Neuronal Excitability
McCormick, D. A. (2003) · Cerebral Cortex · doi:10.1093/cercor/bhg104 · Cited by 200
Stimulus feature selectivity in excitatory and inhibitory neurons in primary visual cortex
Cardin, J. A., Palmer, L. A., & Contreras, D. (2007) · The Journal of Neuroscience · doi:10.1523/jneurosci.1692-07.2007 · Cited by 185
Neural tuning and representational geometry
Kriegeskorte, N., & Wei, X.-X. (2021) · Nature Reviews Neuroscience · doi:10.1038/s41583-021-00502-3 · Cited by 187
Mechanisms underlying cross-orientation suppression in cat visual cortex
Priebe, N. J., & Ferster, D. (2006) · Nature Neuroscience · doi:10.1038/nn1660 · Cited by 184
Self-citationMetastability of Active CA3 Networks
Sasaki, T., Matsuki, N., & Ikegaya, Y. (2007) · Journal of Neuroscience · doi:10.1523/jneurosci.4514-06.2007 · Cited by 177
Processing in layer 4 of the neocortical circuit: new insights from visual and somatosensory cortex
Miller, K. (2001) · Current Opinion in Neurobiology · doi:10.1016/s0959-4388(00)00239-7 · Cited by 170
How Noise Affects the Synchronization Properties of Recurrent Networks of Inhibitory Neurons
Brunel, N., & Hansel, D. (2006) · Neural Computation · doi:10.1162/neco.2006.18.5.1066 · Cited by 164
A Canonical Neural Circuit for Cortical Nonlinear Operations
Kouh, M., & Poggio, T. (2008) · Neural Computation · doi:10.1162/neco.2008.02-07-466 · Cited by 165
Grienberger, C., Milstein, A. D., Bittner, K. C., Romani, S., & Magee, J. C. (2017) · Nature Neuroscience · doi:10.1038/nn.4486 · Cited by 165
Pyramidal Neurons Switch From Integrators In Vitro to Resonators Under In Vivo-Like Conditions
Prescott, S. A., Ratté, S., Koninck, Y. D., & B, T. J. S. A. (2008) · Journal of Neurophysiology · doi:10.1152/jn.90634.2008 · Cited by 159
UP-DOWN cortical dynamics reflect state transitions in a bistable network
Jercog, D., Roxin, A., Barthó, P., Luczak, A., Compte, A., & de la Rocha, J. (2017) · eLife · doi:10.7554/elife.22425 · Cited by 166
Drivers and modulators from push-pull and balanced synaptic input
Abbott, L. F., & Chance, F. S. (2005) · Progress in brain research · doi:10.1016/s0079-6123(05)49011-1 · Cited by 153
How Noise Contributes to Contrast Invariance of Orientation Tuning in Cat Visual Cortex
Hansel, D., & van Vreeswijk, C. (2002) · The Journal of Neuroscience · doi:10.1523/jneurosci.22-12-05118.2002 · Cited by 157
Inhibitory synchrony as a mechanism for attentional gain modulation
Tiesinga, P. H. E., Fellous, J., Salinas, E., José, J. V., & B, T. J. S. A. (2004) · Journal of Physiology-Paris · doi:10.1016/j.jphysparis.2005.09.002 · Cited by 161
Orientation-selective Responses in the Mouse Lateral Geniculate Nucleus
Zhao, X., Chen, H., Liu, X., & Cang, J. (2013) · Journal of Neuroscience · doi:10.1523/jneurosci.0095-13.2013 · Cited by 156
Coding of color and form in the geniculostriate visual pathway (invited review)
Lennie, P., & Movshon, J. A. (2005) · Journal of the Optical Society of America A · doi:10.1364/josaa.22.002013 · Cited by 154
Firing Rate of the Noisy Quadratic Integrate-and-Fire Neuron
Brunel, N., & Latham, P. E. (2003) · Neural Computation · doi:10.1162/089976603322362365 · Cited by 152
The Mechanism of Orientation Selectivity in Primary Visual Cortex without a Functional Map
Hansel, D., & van Vreeswijk, C. (2012) · Journal of Neuroscience · doi:10.1523/jneurosci.6284-11.2012 · Cited by 147
de Almeida, L., Idiart, M., & Lisman, J. E. (2009) · Journal of Neuroscience · doi:10.1523/jneurosci.6044-08.2009 · Cited by 154
Wall, M., Woodward, K. R., Doyle, C. K., & Artes, P. H. (2009) · Investigative Ophthalmology & Visual Science · doi:10.1167/iovs.08-1789 · Cited by 148
Multiplicative Gain Changes Are Induced by Excitation or Inhibition Alone
Murphy, B. K., & Miller, K. D. (2003) · Journal of Neuroscience · doi:10.1523/jneurosci.23-31-10040.2003 · Cited by 144
Interpreting Neural Response Variability as Monte Carlo Sampling of the Posterior
Hoyer, P. O., & Hyvärinen, A. (2002) · Cited by 144
Influence of Contrast on Orientation and Temporal Frequency Tuning in Ferret Primary Visual Cortex
Alitto, H. J., & Usrey, W. M. (2004) · Journal of Neurophysiology · doi:10.1152/jn.00943.2003 · Cited by 143
Analysis of the Stabilized Supralinear Network
Ahmadian, Y., Rubin, D. B., & Miller, K. D. (2013) · Neural Computation · doi:10.1162/neco_a_00472 · Cited by 142
An egalitarian network model for the emergence of simple and complex cells in visual cortex
Tao, L., Shelley, M., McLaughlin, D. W., & Shapley, R. M. (2003) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.2036460100 · Cited by 142
Subthreshold voltage noise of rat neocortical pyramidal neurones
Jacobson, G. A., Diba, K., Yaron‐Jakoubovitch, A., Oz, Y., Christof Koch, A., Segev, I., & Yarom, Y. (2005) · The Journal of Physiology · doi:10.1113/jphysiol.2004.080903 · Cited by 140
Marginalization in Neural Circuits with Divisive Normalization
Beck, J. M., Latham, P. E., & Pouget, A. (2011) · Journal of Neuroscience · doi:10.1523/jneurosci.1706-11.2011 · Cited by 135
Synaptic Integration by V1 Neurons Depends on Location within the Orientation Map
Schummers, J., Mariño, J., & Sur, M. (2002) · Neuron · doi:10.1016/s0896-6273(02)01012-7 · Cited by 136
Enhancement of visual responsiveness by spontaneous local network activity in vivo
Haider, B., Duque, A., Hasenstaub, A. R., Yu, Y., & McCormick, D. A. (2007) · Journal of Neurophysiology · doi:10.1152/jn.01114.2006 · Cited by 130
Cortical gamma oscillations: the functional key is activation, not cognition
Merker, B. H. (2013) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2013.01.013 · Cited by 136
Canonical computations of cerebral cortex
Miller, K. D. (2016) · Current Opinion in Neurobiology · doi:10.1016/j.conb.2016.01.008 · Cited by 136
The dynamical stability of reverberatory neural circuits
Tegnér, J., Compte, A., & Wang, X.-J. (2002) · Biological Cybernetics · doi:10.1007/s00422-002-0363-9 · Cited by 150
Mechanisms of Orientation Selectivity in the Primary Visual Cortex
Priebe, N. J. (2016) · Annual Review of Vision Science · doi:10.1146/annurev-vision-111815-114456 · Cited by 134
Cai, D., Tao, L., Shelley, M., & McLaughlin, D. W. (2004) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0401906101 · Cited by 120
In Vivo Analysis of Inhibitory Synaptic Inputs and Rebounds in Deep Cerebellar Nuclear Neurons
Bengtsson, F., Ekerot, C. ‐., & Jörntell, H. (2011) · PLoS ONE · doi:10.1371/journal.pone.0018822 · Cited by 118
How mechanisms of perceptual decision-making affect the psychometric function
Gold, J. I., & Ding, L. (2012) · Progress in Neurobiology · doi:10.1016/j.pneurobio.2012.05.008 · Cited by 120
Interstitial ions: A key regulator of state-dependent neural activity?
Rasmussen, R. N., O’Donnell, J., Ding, F., & Nedergaard, M. (2020) · Progress in Neurobiology · doi:10.1016/j.pneurobio.2020.101802 · Cited by 119
Inferring learning rules from distributions of firing rates in cortical neurons
Lim, S., McKee, J. L., Woloszyn, L., Amit, Y., Freedman, D. J., Sheinberg, D. L., & Brunel, N. (2015) · Nature Neuroscience · doi:10.1038/nn.4158 · Cited by 110
Schüz, A. (2002) · CRC Press eBooks · doi:10.1201/9780203299296 · Cited by 112
Intrinsic Noise in Cultured Hippocampal Neurons: Experiment and Modeling
Diba, K., Lester, H. A., & Christof Koch, A. (2004) · Journal of Neuroscience · doi:10.1523/jneurosci.1721-04.2004 · Cited by 103
Grady, C. L., & Garrett, D. D. (2017) · NeuroImage · doi:10.1016/j.neuroimage.2017.12.031 · Cited by 103
Lee, A. J., Wang, G., Jiang, X., Johnson, S. M., Hoang, E. T., Lanté, F., Stornetta, R. L., Beenhakker, M. P., Shen, Y., & Julius Zhu, J. (2015) · Cerebral Cortex · doi:10.1093/cercor/bhu020 · Cited by 94
O’Brien, S. J., Johnson, W. E., Driscoll, C. A., Pontius, J. U., Pecon‐Slattery, J., & Menotti-Raymond, M. A. (2008) · Trends in Genetics · doi:10.1016/j.tig.2008.03.004 · Cited by 94
Cross-frequency coupling of brain oscillations indicates the success in visual motion discrimination
Händel, B., & Haarmeier, T. (2008) · NeuroImage · doi:10.1016/j.neuroimage.2008.12.013 · Cited by 96
Nowak, L. G., Sanchez-Vives, M. V., & McCormick, D. A. (2007) · Cerebral Cortex · doi:10.1093/cercor/bhm137 · Cited by 96
Different Roles for Simple-Cell and Complex-Cell Inhibition in V1
Lauritzen, T. Z., & Miller, K. D. (2003) · Journal of Neuroscience · doi:10.1523/jneurosci.23-32-10201.2003 · Cited by 94
Kemkemer, R., Schrank, S., Vogel, W., Gruler, H., & Kaufmann, D. (2002) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.212386999 · Cited by 93
Cardin, J. A., Palmer, L. A., & Contreras, D. (2008) · Neuron · doi:10.1016/j.neuron.2008.05.002 · Cited by 90
Unbalanced synaptic inhibition can create intensity-tuned auditory cortex neurons
Tan, A. Y. Y., Atencio, C. A., Polley, D. B., Merzenich, M. M., & Schreiner, C. E. (2007) · Neuroscience · doi:10.1016/j.neuroscience.2007.01.019 · Cited by 90
Attractor Dynamics in Networks with Learning Rules Inferred from In Vivo Data
Pereira, U., & Brunel, N. (2018) · Neuron · doi:10.1016/j.neuron.2018.05.038 · Cited by 87
Neural Correlation Is Stimulus Modulated by Feedforward Inhibitory Circuitry
Middleton, J. W., Omar, C., Doiron, B., & Simons, D. J. (2012) · Journal of Neuroscience · doi:10.1523/jneurosci.3474-11.2012 · Cited by 85
Metadata
- Authors
- Anderson, J. S., Lampl, I., Gillespie, D. C., & Ferster, D.
- Affiliations
- Northwestern University (US)
- Corresponding author
- Ferster, David
- Venue
- Science
- Published
- 2000-12-08
- Volume
- 290
- Issue
- 5498
- Pages
- 1968-1972
- ISSN
- 0036-8075 (ISSN-L)
- 1095-9203
- OpenAlex
- W2028546686
- Cited by
- 422
- References
- 23
- Citations by year
- 2026: 3 · 2025: 8 · 2024: 10 · 2023: 7 · 2022: 7 · 2021: 10 · 2020: 16 · 2019: 10 · 2018: 10 · 2017: 11 · 2016: 9 · 2015: 13 · 2014: 18 · 2013: 20 · 2012: 19
- FWCI
- 10.35
- Type
- journal article
- Language
- en
- Open access
- closed
- Locations
- Science (publishedVersion)
- PubMed (publishedVersion)
- Funders
- National Eye Institute (R01 EY-04726, R01EY004726)
- 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
- contrast invariance, orientation tuning, visual cortex, noise, membrane potential, spike responses, feedforward models, cats, orientation selectivity, subthreshold responses
- MeSH terms
- Action Potentials, Animals, Cats, Membrane Potentials, Microelectrodes, Models, Neurological, Nerve Net, Neurons, Orientation, Photic Stimulation, Visual Cortex, Visual Perception, Contrast Sensitivity, Patch-Clamp Techniques
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