Neural Noise Can Explain Expansive, Power-Law Nonlinearities in Neural Response Functions
Abstract
Many phenomenological models of the responses of simple cells in primary visual cortex have concluded that a cell's firing rate should be given by its input raised to a power greater than one. This is known as an expansive power-law nonlinearity. However, intracellular recordings have shown that a different nonlinearity, a linear-threshold function, appears to give a good prediction of firing rate from a cell's low-pass-filtered voltage response. Using a model based on a linear-threshold function, Anderson et al. showed that voltage noise was critical to converting voltage responses with contrast-invariant orientation tuning into spiking responses with contrast-invariant tuning. We present two separate results clarifying the connection between noise-smoothed linear-threshold functions and power-law nonlinearities. First, we prove analytically that a power-law nonlinearity is the only input-output function that converts contrast-invariant input tuning into contrast-invariant spike tuning. Second, we examine simulations of a simple model that assumes instantaneous spike rate is given by a linear-threshold function of voltage and voltage responses include significant noise. We show that the resulting average spike rate is well described by an expansive power law of the average voltage (averaged over multiple trials), provided that average voltage remains less than about 1.5 SDs of the noise above threshold. Finally, we use this model to show that the noise levels recorded by Anderson et al. are consistent with the degree to which the orientation tuning of spiking responses is more sharply tuned relative to the orientation tuning of voltage responses. Thus neuronal noise can robustly generate power-law input-output functions of the form frequently postulated for simple cells.
Integrity signals
Registry
Cites
Statistics
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?
Synaptically driven fluctuations in Vm smooth the transformation from Vm depolarization to spike output, creating a power-law relationship between the mean Vm and the mean firing rate.
“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 [63]
Vm fluctuations may contribute to contrast-invariant tuning in neurons of the visual cortex of cats and rodents.
“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 [63]
Cites
Dynamics of ongoing activity: explanation of the large variability in evoked cortical responses
Arieli, A., Sterkin, A., Grinvald, A., & Aertsen, A. (1996) · Science · doi:10.1126/science.273.5283.1868 · Cited by 1,660 · see citing works
Striate cortex of monkey and cat: contrast response function.
Albrecht, D. G., & Hamilton, D. B. (1982) · Journal of Neurophysiology · doi:10.1152/jn.1982.48.1.217 · Cited by 956 · 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
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 · see citing works
Linking Spontaneous Activity of Single Cortical Neurons and the Underlying Functional Architecture
Tsodyks, M. V., Kenet, T., Grinvald, A., & Arieli, A. (1999) · Science · doi:10.1126/science.286.5446.1943 · Cited by 702 · 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
Self-citationCoding of image contrast in central visual pathways of the macaque monkey
Sclar, G., Maunsell, J. H. R., & Lennie, P. (1990) · Vision Research · doi:10.1016/0042-6989(90)90123-3 · Cited by 663 · see citing works
Paré, D., Shink, É., Gaudreau, H., Alain Destexhe, A., & Lang, E. J. (1998) · Journal of Neurophysiology · doi:10.1152/jn.1998.79.3.1450 · Cited by 453 · see citing works
Motion selectivity and the contrast-response function of simple cells in the visual cortex
Albrecht, D. G., & Geisler, W. S. (1991) · Visual Neuroscience · doi:10.1017/s0952523800010336 · Cited by 433 · 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
Self-citationThe Contribution of Noise to Contrast Invariance of Orientation Tuning in Cat Visual Cortex
Anderson, J. S., Lampl, I., Gillespie, D. C., & Ferster, D. (2000) · Science · doi:10.1126/science.290.5498.1968 · Cited by 422 · 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
Orientation selectivity in the cat's striate cortex is invariant with stimulus contrast
Sclar, G., & Freeman, R. D. (1982) · Experimental Brain Research · doi:10.1007/bf00238641 · Cited by 339 · see citing works
Skottun, B. C., Bradley, A., Sclar, G., Ohzawa, I., & Freeman, R. D. (1987) · Journal of Neurophysiology · doi:10.1152/jn.1987.57.3.773 · Cited by 298 · cited 2× · see citing works
“…basis for the observation that orientation tuning of visual cortical neurons is contrast invariant, i.e., changing stimulus contrast simply scales the magnitude of a neuron’s response, without changing the shape of its orientation tuning curve (Sclar and Freeman 1982; Skottun et al. 1987).”
BackgroundSynaptic Background Activity Enhances the Responsiveness of Neocortical Pyramidal Neurons
Hô, N., & Destexhe, A. (2000) · Journal of Neurophysiology · doi:10.1152/jn.2000.84.3.1488 · Cited by 281 · see citing works
Computational models of cortical visual processing.
Heeger, D. J., Simoncelli, E. P., & Movshon, J. A. (1996) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.93.2.623 · Cited by 280 · see citing works
Half-squaring in responses of cat striate cells
Heeger, D. J. (1992) · Visual Neuroscience · doi:10.1017/s095252380001124x · Cited by 262 · see citing works
McLaughlin, D. W., Shapley, R. M., Shelley, M., & Wielaard, D. J. (2000) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.110135097 · Cited by 259 · see citing works
Modeling simple-cell direction selectivity with normalized, half-squared, linear operators
Heeger, D. J. (1993) · Journal of Neurophysiology · doi:10.1152/jn.1993.70.5.1885 · Cited by 240 · see citing works
Neural Mechanisms for Processing Binocular Information I. Simple Cells
Anzai, A., Ohzawa, I., & Freeman, R. D. (1999) · Journal of Neurophysiology · doi:10.1152/jn.1999.82.2.891 · Cited by 212 · see citing works
Jagadeesh, B., Wheat, H. S., & Ferster, D. (1993) · Science · doi:10.1126/science.8266083 · Cited by 204 · see citing works
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 · see citing works
Self-citationAlbrecht, D. G. (1995) · Visual Neuroscience · doi:10.1017/s0952523800006817 · Cited by 158 · see citing works
A single spike suffices: the simplest form of stochastic resonance in model neurons
Stemmler, M. (1996) · Network Computation in Neural Systems · doi:10.1088/0954-898x_7_4_005 · Cited by 134 · see citing works
Direction Selectivity of Synaptic Potentials in Simple Cells of the Cat Visual Cortex
Jagadeesh, B., Wheat, H. S., Kontsevich, L. L., Tyler, C. W., & Ferster, D. (1997) · Journal of Neurophysiology · doi:10.1152/jn.1997.78.5.2772 · Cited by 123 · see citing works
Linear and nonlinear contributions to orientation tuning of simple cells in the cat's striate cortex
Gardner, J. L., Anzai, A., Ohzawa, I., & Freeman, R. D. (1999) · Visual Neuroscience · doi:10.1017/s0952523899166112 · Cited by 115 · 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
Linearity and Gain Control in V1 Simple Cells
Carandini, M., Heeger, D. J., & Movshon, J. A. (1999) · Cerebral cortex · doi:10.1007/978-1-4615-4903-1_7 · Cited by 94 · see citing works
Rectification in the goldfish retina: Analysis by sinusoidal and auxiliary stimulation
Spekreijse, H. (1969) · Vision Research · doi:10.1016/0042-6989(69)90062-5 · Cited by 91 · see citing works
Lampl, I., Anderson, J. S., Gillespie, D. C., & Ferster, D. (2001) · Neuron · doi:10.1016/s0896-6273(01)00278-1 · Cited by 82 · see citing works
Comparison of the selectivity of postsynaptic potentials and spike responses in cat visual cortex
Volgushev, M., Pernberg, J., & Eysel, U. T. (2000) · European Journal of Neuroscience · doi:10.1046/j.1460-9568.2000.00909.x · Cited by 57 · see citing works
Laminar differences in the spatiotemporal structure of simple cell receptive fields in cat area 17
MURTHY, A., Humphrey, A. L., SAUL, A. B., & Feidler, J. C. (1998) · Visual Neuroscience · doi:10.1017/s0952523898152045 · Cited by 32 · see citing works
Emerson, R. C., Korenberg, M. J., & Citron, M. C. (1989) · Springer eBooks · doi:10.1007/978-1-4613-9789-2_5 · Cited by 30 · see citing works
Linking Linear Threshold Units with Quadratic Models of Motion Perception
Suarez, H. H., & Koch, C. (1989) · Neural Computation · doi:10.1162/neco.1989.1.3.318 · Cited by 17 · see citing works
Flagged first, then by citations
Cited by
Sorted by citations
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 · see citing works
Power-Law Scaling in the Brain Surface Electric Potential
Miller, K. J., Sorensen, L. B., Ojemann, J. G., & den Nijs, M. (2009) · PLoS Computational Biology · doi:10.1371/journal.pcbi.1000609 · Cited by 742 · see citing works
Self-citationShunting 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 · see citing works
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 483 · see citing works
Silver, R. A. (2010) · Nature Reviews Neuroscience · doi:10.1038/nrn2864 · Cited by 481 · see citing works
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 · see citing works
Self-citationRapid Neocortical Dynamics: Cellular and Network Mechanisms
Haider, B., & McCormick, D. A. (2009) · Neuron · doi:10.1016/j.neuron.2009.04.008 · Cited by 441 · see citing works
Parallel processing by cortical inhibition enables context-dependent behavior
Kuchibhotla, K. V., Gill, J. V., Lindsay, G. W., Papadoyannis, E. S., Field, R. E., Sten, T. H., Miller, K. D., & Froemke, R. C. (2016) · Nature Neuroscience · doi:10.1038/nn.4436 · Cited by 350 · see citing works
Self-citationInhibition, 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 · see citing works
Rubin, D. B., Hooser, S. D. V., & Miller, K. D. (2015) · Neuron · doi:10.1016/j.neuron.2014.12.026 · Cited by 334 · see citing works
Self-citationMechanisms 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 · see citing works
The Slow Oscillation in Cortical and Thalamic Networks: Mechanisms and Functions
Neske, G. T. (2016) · Frontiers in Neural Circuits · doi:10.3389/fncir.2015.00088 · Cited by 283 · see citing works
Maximum Likelihood Estimation of a Stochastic Integrate-and-Fire Neural Encoding Model
Paninski, L., Pillow, J. W., & Simoncelli, E. P. (2004) · Neural Computation · doi:10.1162/0899766042321797 · Cited by 270 · see citing works
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 · see citing works
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 · see citing works
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 · see citing works
On 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 246 · see citing works
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 · see citing works
Adverse Listening Conditions and Memory Load Drive a Common Alpha Oscillatory Network
Obleser, J., Wöstmann, M., Hellbernd, N., Wilsch, A., & Maess, B. (2012) · The Journal of Neuroscience · doi:10.1523/jneurosci.4908-11.2012 · Cited by 224 · see citing works
“Importantly, the alpha-change pattern also showed a significant interaction, best characterized as an “expansive” (i.e., nonlinear) response function (Miller and Troyer, 2002; Duong and Freeman, 2008; Fig.”
BackgroundA 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 · see citing works
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 · see citing works
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 · see citing works
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 · see citing works
Sensory stimulation shifts visual cortex from synchronous to asynchronous states
Tan, A. Y. Y., Chen, Y., Scholl, B., Seidemann, E., & Priebe, N. J. (2014) · Nature · doi:10.1038/nature13159 · Cited by 206 · see citing works
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 · see citing works
Zagha, E., & McCormick, D. A. (2014) · Current Opinion in Neurobiology · doi:10.1016/j.conb.2014.09.010 · Cited by 184 · see citing works
Mechanisms underlying cross-orientation suppression in cat visual cortex
Priebe, N. J., & Ferster, D. (2006) · Nature Neuroscience · doi:10.1038/nn1660 · Cited by 184 · see citing works
Liu, B.-H., Li, Y.-T., Ma, W.-P., Pan, C.-J., Zhang, L. I., & Tao, H. W. (2011) · Neuron · doi:10.1016/j.neuron.2011.06.017 · Cited by 173 · see citing works
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 163 · see citing works
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 · see citing works
Hennequin, G., Ahmadian, Y., Rubin, D. B., Lengyel, M., & Miller, K. D. (2018) · Neuron · doi:10.1016/j.neuron.2018.04.017 · Cited by 167 · see citing works
Self-citationInhibitory 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 157 · see citing works
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 · see citing works
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 · see citing works
Self-citationAnalysis 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 · see citing works
Self-citationNeuronal Spike Timing Adaptation Described with a Fractional Leaky Integrate-and-Fire Model
Teka, W. W., Marinov, T. M., & Santamarı́a, F. (2014) · PLoS Computational Biology · doi:10.1371/journal.pcbi.1003526 · Cited by 140 · see citing works
What is the dynamical regime of cerebral cortex?
Ahmadian, Y., & Miller, K. D. (2021) · Neuron · doi:10.1016/j.neuron.2021.07.031 · Cited by 140 · see citing works
Self-citationCanonical computations of cerebral cortex
Miller, K. D. (2016) · Current Opinion in Neurobiology · doi:10.1016/j.conb.2016.01.008 · Cited by 130 · see citing works
Self-citationMechanisms 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 125 · see citing works
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 112 · see citing works
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 113 · see citing works
Attentional modulation of firing rate and synchrony in a model cortical network
Buia, C., & Tiesinga, P. H. E. (2006) · Journal of Computational Neuroscience · doi:10.1007/s10827-006-6358-0 · Cited by 112 · see citing works
Nowak, L. G., Sanchez-Vives, M. V., & McCormick, D. A. (2007) · Cerebral Cortex · doi:10.1093/cercor/bhm137 · Cited by 96 · see citing works
Cardin, J. A., Palmer, L. A., & Contreras, D. (2008) · Neuron · doi:10.1016/j.neuron.2008.05.002 · Cited by 90 · see citing works
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 · see citing works
Rasmussen, R. N., Nicholas, E., Petersen, N., Dietz, A. G., Xu, Q., Sun, Q., & Nedergaard, M. (2019) · Cell Reports · doi:10.1016/j.celrep.2019.06.082 · Cited by 85 · see citing works
Frazor, R. A., Albrecht, D. G., Geisler, W. S., & Crane, A. M. (2004) · Journal of Neurophysiology · doi:10.1152/jn.00858.2003 · Cited by 85 · see citing works
Multiplication and stimulus invariance in a looming-sensitive neuron
Gabbiani, F., Krapp, H. G., Hatsopoulos, N. G., Mo, C., Christof Koch, A., & Laurent, G. (2004) · Journal of Physiology-Paris · doi:10.1016/j.jphysparis.2004.03.001 · Cited by 83 · see citing works
A human-specific modifier of cortical connectivity and circuit function
Schmidt, E. R. E., Zhao, H. T., Park, J. M., Dipoppa, M., Monsalve-Mercado, M. M., Dahan, J. B., Rodgers, C. C., Lejeune, A., Hillman, E. M. C., Miller, K. D., et al. (2021) · Nature · doi:10.1038/s41586-021-04039-4 · Cited by 82 · see citing works
Self-citationRoxin, A. (2011) · Frontiers in Computational Neuroscience · doi:10.3389/fncom.2011.00008 · Cited by 78 · see citing works
Visual Clutter Causes High-Magnitude Errors
Baldassi, S., Megna, N., & Burr, D. (2006) · PLoS Biology · doi:10.1371/journal.pbio.0040056 · Cited by 88 · see citing works
Ohshiro, T., Angelaki, D. E., & DeAngelis, G. C. (2017) · Neuron · doi:10.1016/j.neuron.2017.06.043 · Cited by 77 · see citing works
Petersen, P. C., & Berg, R. W. (2016) · eLife · doi:10.7554/elife.18805 · Cited by 76 · see citing works
Understanding Layer 4 of the Cortical Circuit: A Model Based on Cat V1
Miller, K. D. (2002) · Cerebral Cortex · doi:10.1093/cercor/13.1.73 · Cited by 75 · see citing works
Self-citationFernandez, F. R., & White, J. A. (2008) · Journal of Neuroscience · doi:10.1523/jneurosci.5658-07.2008 · Cited by 73 · see citing works
Dynamics of Normalization Underlying Masking in Human Visual Cortex
Tsai, J. J., Wade, A. R., & Norcia, A. M. (2012) · Journal of Neuroscience · doi:10.1523/jneurosci.4485-11.2012 · Cited by 71 · see citing works
del Molino, L. C. G., Yang, G. R., Mejías, J. F., & Wang, X. (2017) · eLife · doi:10.7554/elife.29742 · Cited by 70 · see citing works
A recurrent circuit implements normalization, simulating the dynamics of V1 activity
Heeger, D. J., & Zemlianova, K. O. (2020) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.2005417117 · Cited by 69 · see citing works
Linking structure and activity in nonlinear spiking networks
Ocker, G. K., Josić́, K., Shea‐Brown, E., & Buice, M. A. (2017) · PLoS Computational Biology · doi:10.1371/journal.pcbi.1005583 · Cited by 61 · see citing works
A spherical model for orientation and spatial–frequency tuning in a cortical hypercolumn
Bressloff, P. C., & Cowan, J. D. (2002) · Philosophical Transactions of the Royal Society B Biological Sciences · doi:10.1098/rstb.2002.1109 · Cited by 65 · see citing works
Vanni, S., Hokkanen, H., Werner, F., & Angelucci, A. (2019) · Cerebral Cortex · doi:10.1093/cercor/bhz322 · Cited by 62 · see citing works
Visual Orientation and Directional Selectivity through Thalamic Synchrony
Stanley, G. B., Jin, J., Wang, Y., Desbordes, G., Wang, Q., Black, M. J., & Alonso, J. (2012) · Journal of Neuroscience · doi:10.1523/jneurosci.4968-11.2012 · Cited by 66 · see citing works
Xiong, X. R., Liang, F., Li, H., Mesik, L., Zhang, K. K., Polley, D. B., Tao, H. W., Xiao, Z., & Zhang, L. I. (2013) · Neuron · doi:10.1016/j.neuron.2013.06.012 · Cited by 63 · see citing works
Fractional-order leaky integrate-and-fire model with long-term memory and power law dynamics
Teka, W. W., Upadhyay, R. K., & Mondal, A. (2017) · Neural Networks · doi:10.1016/j.neunet.2017.05.007 · Cited by 62 · see citing works
The Operating Point of the Cortex: Neurons as Large Deviation Detectors
Ringach, D. L., & Malone, B. J. (2007) · Journal of Neuroscience · doi:10.1523/jneurosci.1048-07.2007 · Cited by 55 · see citing works
Mathematical Equivalence of Two Common Forms of Firing Rate Models of Neural Networks
Miller, K. D., & Fumarola, F. (2011) · Neural Computation · doi:10.1162/neco_a_00221 · Cited by 55 · see citing works
Self-citationCalcium imaging with genetically encoded indicators in behaving primates
Seidemann, E., Chen, Y., Bai, Y., Chen, S. C., Mehta, P., Kajs, B. L., Geisler, W. S., & Zemelman, B. V. (2016) · eLife · doi:10.7554/elife.16178 · Cited by 54 · see citing works
LGN Input to Simple Cells and Contrast-Invariant Orientation Tuning: An Analysis
Troyer, T. W., Krukowski, A. E., & Miller, K. D. (2002) · Journal of Neurophysiology · doi:10.1152/jn.2002.87.6.2741 · Cited by 53 · see citing works
Self-citationXing, D., Ringach, D. L., Hawken, M. J., & Shapley, R. M. (2011) · Journal of Neuroscience · doi:10.1523/jneurosci.2245-11.2011 · Cited by 48 · see citing works
Fernandez, F. R., Broicher, T., Truong, A., & White, J. A. (2011) · Journal of Neuroscience · doi:10.1523/jneurosci.5076-10.2011 · Cited by 44 · see citing works
Emergence of Adaptive Computation by Single Neurons in the Developing Cortex
Mease, R. A., Famulare, M., Gjorgjieva, J., Moody, W. J., & Fairhall, A. L. (2013) · Journal of Neuroscience · doi:10.1523/jneurosci.3263-12.2013 · Cited by 45 · see citing works
How effective delays shape oscillatory dynamics in neuronal networks
Roxin, A., & Montbrió, E. (2010) · Physica D Nonlinear Phenomena · doi:10.1016/j.physd.2010.09.009 · Cited by 44 · see citing works
Strabismus Disrupts Binocular Synaptic Integration in Primary Visual Cortex
Scholl, B., Tan, A. Y. Y., & Priebe, N. J. (2013) · Journal of Neuroscience · doi:10.1523/jneurosci.1831-13.2013 · Cited by 44 · see citing works
Adaptive Integration in the Visual Cortex by Depressing Recurrent Cortical Circuits
van Rossum, M. C. W., van der Meer, M. A. A., Xiao, D., & Oram, M. W. (2008) · Neural Computation · doi:10.1162/neco.2008.06-07-546 · Cited by 44 · see citing works
Geis, H.-R. A. P., & Borst, J. G. G. (2009) · Journal of Neurophysiology · doi:10.1152/jn.90966.2008 · Cited by 43 · see citing works
Orientation selectivity in visual cortex by fluctuation-controlled criticality
Tao, L., Cai, D., McLaughlin, D. W., Shelley, M., & Shapley, R. M. (2006) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0605415103 · Cited by 41 · see citing works
Persi, E., Hansel, D., Nowak, L. G., Barone, P., & van Vreeswijk, C. (2011) · PLoS Computational Biology · doi:10.1371/journal.pcbi.1001078 · Cited by 41 · see citing works
Computational Diversity in Complex Cells of Cat Primary Visual Cortex
Finn, I. M., & Ferster, D. (2007) · Journal of Neuroscience · doi:10.1523/jneurosci.2119-07.2007 · Cited by 37 · see citing works
Cross-Correlation in the Auditory Coincidence Detectors of Owls
Fischer, B. J., Christianson, G. B., & Peña, J. L. (2008) · Journal of Neuroscience · doi:10.1523/jneurosci.1969-08.2008 · Cited by 35 · see citing works
May, K. A., & Georgeson, M. A. (2007) · Vision Research · doi:10.1016/j.visres.2007.02.012 · Cited by 34 · see citing works
Gold, J. I., Law, C.-T., Connolly, P. M., & Bennur, S. (2009) · Journal of Neurophysiology · doi:10.1152/jn.00744.2009 · Cited by 31 · see citing works
How to Modify a Neural Network Gradually Without Changing Its Input-Output Functionality
DiMattina, C., & Zhang, K. (2009) · Neural Computation · doi:10.1162/neco.2009.05-08-781 · Cited by 31 · see citing works
Marken, R. S. (2013) · Attention Perception & Psychophysics · doi:10.3758/s13414-013-0552-8 · Cited by 31 · see citing works
Learning shapes cortical dynamics to enhance integration of relevant sensory input
Chadwick, A., Khan, A. G., Poort, J., Blot, A., Hofer, S. B., Mrsic‐Flogel, T. D., & Sahani, M. (2022) · Neuron · doi:10.1016/j.neuron.2022.10.001 · Cited by 38 · see citing works
Spectrotemporal Processing in Spectral Tuning Modules of Cat Primary Auditory Cortex
Atencio, C. A., & Schreiner, C. E. (2012) · PLoS ONE · doi:10.1371/journal.pone.0031537 · Cited by 31 · see citing works
Divisive Gain Modulation of Motoneurons by Inhibition Optimizes Muscular Control
Vestergaard, M., & Berg, R. W. (2015) · Journal of Neuroscience · doi:10.1523/jneurosci.3899-14.2015 · Cited by 30 · see citing works
A neurophysiologically plausible population code model for human contrast discrimination
Goris, R. L. T., Wichmann, F. A., & Henning, G. B. (2009) · Journal of Vision · doi:10.1167/9.7.15 · Cited by 30 · see citing works
Synaptic Mechanisms for Bandwidth Tuning in Awake Mouse Primary Auditory Cortex
Li, H., Liang, F., Zhong, W., Yan, L., Mesik, L., Xiao, Z., Tao, H. W., & Zhang, L. I. (2018) · Cerebral Cortex · doi:10.1093/cercor/bhy165 · Cited by 30 · see citing works
Contrast invariance of functional maps in cat primary visual cortex
Carandini, M., & Sengpiel, F. (2004) · Journal of Vision · doi:10.1167/4.3.1 · Cited by 31 · see citing works
Stabilized supralinear network can give rise to bistable, oscillatory, and persistent activity
Kraynyukova, N., & Tchumatchenko, T. (2018) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1700080115 · Cited by 29 · see citing works
Optimal Stimulus Coding by Neural Populations Using Rate Codes
Johnson, D. H., & Ray, W. (2004) · Journal of Computational Neuroscience · doi:10.1023/b:jcns.0000014106.09948.83 · Cited by 29 · see citing works
Arthurs, O. J., Stephenson, C., Rice, K. M., Lupson, V. C., Spiegelhalter, D. J., Boniface, S. J., & Bullmore, E. T. (2003) · NeuroImage · doi:10.1016/j.neuroimage.2003.09.067 · Cited by 29 · see citing works
Physiological Noise: Definition, Estimation, and Characterization in Complex Biomedical Signals
Scarciglia, A., Catrambone, V., Bonanno, C., & Valenza, G. (2023) · IEEE Transactions on Biomedical Engineering · doi:10.1109/tbme.2023.3291538 · Cited by 28 · see citing works
Contrast Adaptation Contributes to Contrast-Invariance of Orientation Tuning of Primate V1 Cells
Nowak, L. G., & Barone, P. (2009) · PLoS ONE · doi:10.1371/journal.pone.0004781 · Cited by 27 · see citing works
Mondal, A., & Upadhyay, R. K. (2017) · Nonlinear Dynamics · doi:10.1007/s11071-017-3944-9 · Cited by 26 · see citing works
Optimum signal in a simple neuronal model with signal-dependent noise
Greenwood, P. E., & Lánský, P. (2005) · Biological Cybernetics · doi:10.1007/s00422-005-0545-3 · Cited by 26 · see citing works
Multiplexing working memory and time in the trajectories of neural networks
Zhou, S., Seay, M. J., Taxidis, J., Golshani, P., & Buonomano, D. V. (2023) · Nature Human Behaviour · doi:10.1038/s41562-023-01592-y · Cited by 25 · see citing works
Cortical synaptic architecture supports flexible sensory computations
Scholl, B., & Fitzpatrick, D. (2020) · Current Opinion in Neurobiology · doi:10.1016/j.conb.2020.01.013 · Cited by 22 · see citing works
Population codes enable learning from few examples by shaping inductive bias
Bordelon, B., & Pehlevan, C. (2022) · eLife · doi:10.7554/elife.78606 · Cited by 23 · see citing works
Cellular-resolution optogenetics reveals attenuation-by-suppression in visual cortical neurons
LaFosse, P. K., Zhou, Z., O’Rawe, J. F., Friedman, N. G., Scott, V. M., Deng, Y., & Histed, M. H. (2024) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.2318837121 · Cited by 24 · see citing works
- Authors
- Miller, K. D., & Troyer, T. W.
- Affiliations
- University of California, San Francisco (US)
- University of Maryland, College Park (US)
- Venue
- Journal of Neurophysiology
- Publisher
- American Physiological Society
- Published
- 2002-02-01
- Volume
- 87
- Issue
- 2
- Pages
- 653-659
- ISSN
- 0022-3077 (ISSN-L)
- 1522-1598
- OpenAlex
- W1961056875
- Cited by
- 207
- References
- 35
- Citations by year
- 2026: 6 · 2025: 10 · 2024: 4 · 2023: 8 · 2022: 10 · 2021: 13 · 2020: 10 · 2019: 3 · 2018: 7 · 2017: 12 · 2016: 13 · 2015: 8 · 2014: 6 · 2013: 9 · 2012: 12
- FWCI
- 4.51
- Type
- journal article
- Language
- en
- Open access
- closed
- Locations
- Journal of Neurophysiology (publishedVersion)
- PubMed (publishedVersion)
- Funders
- National Eye Institute (R01EY011001, EY11001)
- Topics
- Life Sciences › Neuroscience › Cognitive Neuroscience › Visual perception and processing mechanisms
- Life Sciences › Neuroscience › Cognitive Neuroscience › Neural dynamics and brain function
- Physical Sciences › Physics and Astronomy › Statistical and Nonlinear Physics › stochastic dynamics and bifurcation
- Keywords
- neural noise, power nonlinearity, input-output function, linear threshold functions, simple cells, primary visual cortex, orientation tuning, contrast invariance, voltage noise, spike frequency
- MeSH terms
- Action Potentials, Animals, Computer Simulation, Models, Neurological, Neurons, Visual Cortex, Nonlinear Dynamics
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