Attention stabilizes the shared gain of V4 populations
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Responses of sensory neurons represent stimulus information, but are also influenced by internal state. For example, when monkeys direct their attention to a visual stimulus, the response gain of specific subsets of neurons in visual cortex changes. Here, we develop a functional model of population activity to investigate the structure of this effect. We fit the model to the spiking activity of bilateral neural populations in area V4, recorded while the animal performed a stimulus discrimination task under spatial attention. The model reveals four separate time-varying shared modulatory signals, the dominant two of which each target task-relevant neurons in one hemisphere. In attention-directed conditions, the associated shared modulatory signal decreases in variance. This finding provides an interpretable and parsimonious explanation for previous observations that attention reduces variability and noise correlations of sensory neurons. Finally, the recovered modulatory signals reflect previous reward, and are predictive of subsequent choice behavior.
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Experiments and computational models demonstrate that attention amplifies and stabilizes target cell responses, reducing their variance across trials.
“Experiments and computational models further demonstrate that attention amplifies and stabilizes target cell responses, reducing their variance across trials50,51.”
From Mechanisms underlying gain modulation in the cortex (2020) · cites this paper as [51]
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Modulation of Oscillatory Neuronal Synchronization by Selective Visual Attention
Fries, P., Reynolds, J. H., Rorie, A. E., & Desimone, R. (2001) · Science · doi:10.1126/science.1055465 · Cited by 2,786 · see citing works
Selective Attention Gates Visual Processing in the Extrastriate Cortex
Moran, J., & Desimone, R. (1985) · Science · doi:10.1126/science.4023713 · Cited by 2,433 · see citing works
The psychometric function: I. Fitting, sampling, and goodness of fit
Wichmann, F. A., & Hill, N. J. (2001) · Perception & Psychophysics · doi:10.3758/bf03194544 · Cited by 2,359 · see citing works
Shadlen, M. N., & Newsome, W. T. (1998) · The Journal of Neuroscience · doi:10.1523/jneurosci.18-10-03870.1998 · Cited by 2,178 · see citing works
Selective Attention Gates Visual Processing in the Extrastriate Cortex
Moran, J., & Desimone, R. (2003) · The MIT Press eBooks · doi:10.7551/mitpress/2834.003.0024 · Cited by 2,164 · see citing works
Mesulam, M. ‐., Mufson, E. J., Levey, A. I., & Wainer, B. H. (1983) · Journal of Comparative Neurology · doi:10.1002/cne.902140206 · Cited by 1,962 · see citing works
Context-dependent computation by recurrent dynamics in prefrontal cortex
Mante, V., Sussillo, D., Shenoy, K. V., & Newsome, W. T. (2013) · Nature · doi:10.1038/nature12742 · Cited by 1,807 · see citing works
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
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 · see citing works
Spatio-temporal correlations and visual signalling in a complete neuronal population
Pillow, J. W., Shlens, J., Paninski, L., Sher, A., Litke, A. M., Chichilnisky, E. J., & Simoncelli, E. P. (2008) · Nature · doi:10.1038/nature07140 · Cited by 1,315 · see citing works
Self-citationCorrelated neuronal discharge rate and its implications for psychophysical performance
Zohary, E., Shadlen, M. N., & Newsome, W. T. (1994) · Nature · doi:10.1038/370140a0 · Cited by 1,237 · see citing works
Dimensionality reduction for large-scale neural recordings
Cunningham, J. P., & Yu, B. M. (2014) · Nature Neuroscience · doi:10.1038/nn.3776 · Cited by 1,219 · see citing works
Attention improves performance primarily by reducing interneuronal correlations
Cohen, M. R., & Maunsell, J. H. R. (2009) · Nature Neuroscience · doi:10.1038/nn.2439 · Cited by 1,126 · see citing works
Self-citationStimulus onset quenches neural variability: A widespread cortical phenomenon
Churchland, M. M., Yu, B. M., Cunningham, J. P., Sugrue, L. P., Cohen, M. R., Corrado, G. S., Newsome, W. T., Clark, A. M., Hosseini, P., Scott, B. B., et al. (2010) · Nature Neuroscience · doi:10.1038/nn.2501 · Cited by 1,084 · see citing works
Self-citationTruccolo, W., Eden, U. T., Fellows, M. R., Donoghue, J. P., & Brown, E. N. (2004) · Journal of Neurophysiology · doi:10.1152/jn.00697.2004 · Cited by 1,063 · see citing works
Attentional modulation of visual motion processing in cortical areas MT and MST
Treue, S., & Maunsell, J. H. R. (1996) · Nature · doi:10.1038/382539a0 · Cited by 1,025 · see citing works
Harris, K. D., & Thiele, A. (2011) · Nature reviews. Neuroscience · doi:10.1038/nrn3084 · Cited by 871 · see citing works
The Effect of Correlated Variability on the Accuracy of a Population Code
Abbott, L. F., & Dayan, P. (1999) · Neural Computation · doi:10.1162/089976699300016827 · Cited by 833 · see citing works
Cortical activity in the null space: permitting preparation without movement
Kaufman, M. T., Churchland, M. M., Ryu, S. I., & Shenoy, K. V. (2014) · Nature Neuroscience · doi:10.1038/nn.3643 · Cited by 831 · see citing works
Shadlen, M., Britten, K., Newsome, W., & Movshon, J. (1996) · The Journal of Neuroscience · doi:10.1523/jneurosci.16-04-01486.1996 · Cited by 824 · see citing works
Serial dependence in visual perception
Fischer, J., & Whitney, D. C. (2014) · Nature Neuroscience · doi:10.1038/nn.3689 · Cited by 807 · see citing works
Internal brain state regulates membrane potential synchrony in barrel cortex of behaving mice
Poulet, J. F. A., & Petersen, C. C. H. (2008) · Nature · doi:10.1038/nature07150 · Cited by 796 · see citing works
Cortical membrane potential signature of optimal states for sensory signal detection
McGinley, M. J., David, S. V., & McCormick, D. A. (2015) · Neuron · doi:10.1016/j.neuron.2015.05.038 · Cited by 728 · see citing works
Pupil fluctuations track fast switching of cortical states during quiet wakefulness
Reimer, J., Froudarakis, E., Cadwell, C. R., Yatsenko, D., Denfield, G. H., & Tolias, A. S. (2014) · Neuron · doi:10.1016/j.neuron.2014.09.033 · Cited by 717 · cited 2× · see citing works
“…the estimated modulator signals against other neural or physiological signals (e.g. neurotransmitter concentrations, or pupil dilation (McGinley et al., 2015; Reimer et al., 2014), and by comparing the weights with detailed anatomical and functional properties of the neurons in the population.”
BackgroundDynamic Coding for Cognitive Control in Prefrontal Cortex
Stokes, M. G., Kusunoki, M., Sigala, N., Nili, H., Gaffan, D., & Duncan, J. (2013) · Neuron · doi:10.1016/j.neuron.2013.01.039 · Cited by 711 · see citing works
Spatial attention decorrelates intrinsic activity fluctuations in macaque area V4
Mitchell, J. F., Sundberg, K. A., & Reynolds, J. H. (2009) · Neuron · doi:10.1016/j.neuron.2009.09.013 · Cited by 710 · see citing works
Correlation between neural spike trains increases with firing rate
de la Rocha, J., Doiron, B., Shea-Brown, E., Josić, K., & Reyes, A. (2007) · Nature · doi:10.1038/nature06028 · Cited by 644 · see citing works
Decorrelated neuronal firing in cortical microcircuits
Ecker, A. S., Berens, P., Keliris, G. A., Bethge, M., Logothetis, N. K., & Tolias, A. S. (2010) · Science · doi:10.1126/science.1179867 · Cited by 640 · see citing works
Probabilistic reasoning by neurons
Yang, T., & Shadlen, M. N. (2007) · Nature · doi:10.1038/nature05852 · Cited by 581 · see citing works
Information-limiting correlations
Moreno‐Bote, R., Beck, J. M., Kanitscheider, I., Pitkow, X., Latham, P. E., & Pouget, A. (2014) · Nature Neuroscience · doi:10.1038/nn.3807 · Cited by 541 · see citing works
Slow dynamics and high variability in balanced cortical networks with clustered connections
Litwin-Kumar, A., & Doiron, B. (2012) · Nature Neuroscience · doi:10.1038/nn.3220 · Cited by 530 · see citing works
Partitioning neuronal variability
Goris, R. L. T., Movshon, J. A., & Simoncelli, E. P. (2014) · Nature Neuroscience · doi:10.1038/nn.3711 · Cited by 528 · see citing works
Self-citationNeuronal Synchronization along the Dorsal Visual Pathway Reflects the Focus of Spatial Attention
Siegel, M., Donner, T. H., Oostenveld, R., Fries, P., & Engel, A. K. (2008) · Neuron · doi:10.1016/j.neuron.2008.09.010 · Cited by 487 · see citing works
DYNAMIC RESPONSE-BY-RESPONSE MODELS OF MATCHING BEHAVIOR IN RHESUS MONKEYS
Lau, B., & Glimcher, P. W. (2005) · Journal of the Experimental Analysis of Behavior · doi:10.1901/jeab.2005.110-04 · Cited by 485 · see citing works
Mazor, O., & Laurent, G. (2005) · Neuron · doi:10.1016/j.neuron.2005.09.032 · Cited by 484 · 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
Acetylcholine contributes through muscarinic receptors to attentional modulation in V1
Herrero, J. L., Roberts, M. J., Delicato, L. S., Gieselmann, M. A., Dayan, P., & Thiele, A. (2008) · Nature · doi:10.1038/nature07141 · Cited by 459 · see citing works
Diverse coupling of neurons to populations in sensory cortex
Okun, M., Steinmetz, N. A., Cossell, L., Iacaruso, M. F., Ko, H., Barthó, P., Moore, T., Hofer, S. B., Mrsic‐Flogel, T. D., Carandini, M., et al. (2015) · Nature · doi:10.1038/nature14273 · Cited by 428 · see citing works
On simplicity and complexity in the brave new world of large-scale neuroscience
Gao, P., & Ganguli, S. (2015) · Current Opinion in Neurobiology · doi:10.1016/j.conb.2015.04.003 · Cited by 406 · see citing works
Attentional Modulation Strength in Cortical Area MT Depends on Stimulus Contrast
Martínez-Trujillo, J., & Treue, S. (2002) · Neuron · doi:10.1016/s0896-6273(02)00778-x · Cited by 402 · see citing works
A Generalization of Principal Components Analysis to the Exponential Family
Collins, M., Dasgupta, S., & Schapire, R. E. (2001) · Cited by 383 · see citing works
Treue, S., & Maunsell, J. H. R. (1999) · Journal of Neuroscience · doi:10.1523/jneurosci.19-17-07591.1999 · Cited by 366 · see citing works
Decision-related activity in sensory neurons reflects more than a neuron’s causal effect
Nienborg, H., & Cumming, B. G. (2009) · Nature · doi:10.1038/nature07821 · Cited by 360 · see citing works
Effects of Spatial Attention on Contrast Response Functions in Macaque Area V4
Williford, T., & Maunsell, J. H. R. (2006) · Journal of Neurophysiology · doi:10.1152/jn.01207.2005 · Cited by 353 · see citing works
Gain Modulation by Nicotine in Macaque V1
Disney, A. A., Aoki, C., & Hawken, M. J. (2007) · Neuron · doi:10.1016/j.neuron.2007.09.034 · Cited by 331 · see citing works
Correlations Without Synchrony
Brody, C. D. (1999) · Neural Computation · doi:10.1162/089976699300016133 · Cited by 329 · see citing works
State Dependence of Noise Correlations in Macaque Primary Visual Cortex
Ecker, A. S., Berens, P., Cotton, R. J., Subramaniyan, M., Denfield, G. H., Cadwell, C. R., Smirnakis, S. M., Bethge, M., & Tolias, A. S. (2014) · Neuron · doi:10.1016/j.neuron.2014.02.006 · Cited by 323 · see citing works
Population coding in neuronal systems with correlated noise
Sompolinsky, H., Yoon, H., Kang, K., & Shamir, M. (2001) · Physical review. E, Statistical physics, plasmas, fluids, and related interdisciplinary topics · doi:10.1103/physreve.64.051904 · Cited by 319 · 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 307 · see citing works
The Detection of Visual Contrast in the Behaving Mouse
Busse, L., Ayaz, A., Dhruv, N. T., Katzner, S., Saleem, A. B., Schölvinck, M. L., Zaharia, A. D., & Carandini, M. (2011) · Journal of Neuroscience · doi:10.1523/jneurosci.6689-10.2011 · Cited by 286 · see citing works
Effects of Attention on the Reliability of Individual Neurons in Monkey Visual Cortex
McAdams, C. J., & Maunsell, J. H. R. (1999) · Neuron · doi:10.1016/s0896-6273(01)80034-9 · Cited by 286 · see citing works
A Normalization Model of Attentional Modulation of Single Unit Responses
Lee, J., & Maunsell, J. H. R. (2009) · PLoS ONE · doi:10.1371/journal.pone.0004651 · Cited by 257 · see citing works
The Nature of Shared Cortical Variability
Lin, I.-C., Okun, M., Carandini, M., & Harris, K. D. (2015) · Neuron · doi:10.1016/j.neuron.2015.06.035 · Cited by 223 · see citing works
A new look at state-space models for neural data
Paninski, L., Ahmadian, Y., Ferreira, D. G., Koyama, S., Rad, K. R., Vidne, M., Vogelstein, J. T., & Wu, W. (2009) · Journal of Computational Neuroscience · doi:10.1007/s10827-009-0179-x · Cited by 221 · see citing works
Perceptual Learning Reduces Interneuronal Correlations in Macaque Visual Cortex
Gu, Y., Liu, S., Fetsch, C. R., Yang, Y., Fok, S., Sunkara, A., DeAngelis, G. C., & Angelaki, D. E. (2011) · Neuron · doi:10.1016/j.neuron.2011.06.015 · Cited by 218 · see citing works
Perceptual Decision-Making as Probabilistic Inference by Neural Sampling
Haefner, R. M., Berkes, P., & Fiser, J. (2016) · Neuron · doi:10.1016/j.neuron.2016.03.020 · Cited by 207 · see citing works
Cortical state determines global variability and correlations in visual cortex
Schölvinck, M. L., Saleem, A. B., Benucci, A., Harris, K. D., & Carandini, M. (2015) · The Journal of Neuroscience · doi:10.1523/jneurosci.4994-13.2015 · Cited by 198 · see citing works
Encoding and Decoding of Overlapping Odor Sequences
Broome, B. M., Jayaraman, V., & Laurent, G. (2006) · Neuron · doi:10.1016/j.neuron.2006.07.018 · Cited by 192 · see citing works
Attention can either increase or decrease spike count correlations in visual cortex
Ruff, D. A., & Cohen, M. R. (2014) · Nature Neuroscience · doi:10.1038/nn.3835 · Cited by 188 · see citing works
Self-citationEmpirical models of spiking in neural populations
Macke, J. H., Buesing, L., Cunningham, J. P., Yu, B. M., Shenoy, K. V., & Sahani, M. (2011) · Max Planck Digital Library · Cited by 172 · see citing works
A Neuronal Population Measure of Attention Predicts Behavioral Performance on Individual Trials
Cohen, M. R., & Maunsell, J. H. R. (2010) · Journal of Neuroscience · doi:10.1523/jneurosci.2171-10.2010 · Cited by 171 · see citing works
Self-citationConsistency of auditory detection judgments.
Green, D. M. (1964) · Psychological Review · doi:10.1037/h0044520 · Cited by 152 · see citing works
Herrero, J. L., Gieselmann, M. A., Sanayei, M., & Thiele, A. (2013) · Neuron · doi:10.1016/j.neuron.2013.03.029 · Cited by 151 · see citing works
Associative Learning Enhances Population Coding by Inverting Interneuronal Correlation Patterns
Jeanne, J. M., Sharpee, T. O., & Gentner, T. Q. (2013) · Neuron · doi:10.1016/j.neuron.2013.02.023 · Cited by 122 · see citing works
Common-input models for multiple neural spike-train data
Kulkarni, J. E., & Paninski, L. (2007) · Network Computation in Neural Systems · doi:10.1080/09548980701625173 · Cited by 114 · see citing works
Modeling the impact of common noise inputs on the network activity of retinal ganglion cells
Vidne, M., Ahmadian, Y., Shlens, J., Pillow, J. W., Kulkarni, J. E., Litke, A. M., Chichilnisky, E. J., Simoncelli, E. P., & Paninski, L. (2011) · Journal of Computational Neuroscience · doi:10.1007/s10827-011-0376-2 · Cited by 110 · see citing works
Self-citationRepresentational Accuracy of Stochastic Neural Populations
Wilke, S. D., & Eurich, C. W. (2002) · Neural Computation · doi:10.1162/089976602753284482 · Cited by 107 · see citing works
Improved Estimation and Interpretation of Correlations in Neural Circuits
Yatsenko, D., Josić́, K., Ecker, A. S., Froudarakis, E., Cotton, R. J., & Tolias, A. S. (2015) · PLoS Computational Biology · doi:10.1371/journal.pcbi.1004083 · Cited by 97 · see citing works
Receptive Field Inference with Localized Priors
Park, M., & Pillow, J. (2011) · PLoS Comput. Biol. · doi:10.1371/journal.pcbi.1002219 · Cited by 90 · see citing works
Task Engagement Selectively Modulates Neural Correlations in Primary Auditory Cortex
Downer, J. D., Niwa, M., & Sutter, M. L. (2015) · Journal of Neuroscience · doi:10.1523/jneurosci.4094-14.2015 · Cited by 65 · see citing works
Global Cognitive Factors Modulate Correlated Response Variability between V4 Neurons
Ruff, D. A., & Cohen, M. R. (2014) · Journal of Neuroscience · doi:10.1523/jneurosci.2750-14.2014 · Cited by 49 · see citing works
Self-citationAnalysis of response sequences in the setting of a psychophysical experiment.
Senders, V. L., & Sowards, A. (1952) · PubMed · Cited by 47 · see citing works
Analysis of Response Sequences in the Setting of a Psychophysical Experiment
Senders, V. L., & Sowards, A. (1952) · The American Journal of Psychology · doi:10.2307/1418758 · Cited by 42 · see citing works
Low-dimensional models of neural population activity in sensory cortical circuits
Archer, E., Köster, U., Pillow, J. W., & Macke, J. H. (2014) · Max Planck Digital Library · Cited by 39 · see citing works
Robust learning of low-dimensional dynamics from large neural ensembles
Pfau, D., Pnevmatikakis, E. A., & Paninski, L. (2013) · Cited by 39 · see citing works
Sensory Adaptation and Short Term Plasticity as Bayesian Correction for a Changing Brain
Stevenson, I. H., Cronin, B., Sur, M., & Kording, K. P. (2010) · PLoS ONE · doi:10.1371/journal.pone.0012436 · Cited by 16 · see citing works
Bayesian inference for low rank spatiotemporal neural receptive fields
Park, M., & Pillow, J. W. (2013) · Cited by 14 · see citing works
Point-Process Principal Components Analysis via Geometric Optimization
Solo, V., & Pasha, S. A. (2012) · Neural Computation · doi:10.1162/neco_a_00382 · Cited by 7 · see citing works
Perceptual decision-making as probabilistic inference by neural samplingPreprint
Haefner, R. M., Berkes, P., & Fiser, J. (2014) · arXiv (Cornell University) · Cited by 6 · see citing works
A model of sensory neural responses in the presence of unknown modulatory inputsPreprint
Rabinowitz, N. C., Goris, R. L. T., Ballé, J., & Simoncelli, E. P. (2015) · arXiv (Cornell University) · doi:10.48550/arxiv.1507.01497 · Cited by 4 · see citing works
Self-citationThe correlation structure induced by fluctuations in attention
Ecker, A. S., Berens, P., Tolias, A. S., & Bethge, M. (2012) · Max Planck Digital Library · Cited by 3 · see citing works
Flagged first, then by citations
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Sorted by citations
Cortical Areas Interact through a Communication Subspace
Semedo, J. D., Zandvakili, A., Machens, C. K., Yu, B. M., & Kohn, A. (2019) · Neuron · doi:10.1016/j.neuron.2019.01.026 · Cited by 383 · see citing works
Correlations and Neuronal Population Information
Kohn, A., Coen-Cagli, R., Kanitscheider, I., & Pouget, A. (2016) · Annual Review of Neuroscience · doi:10.1146/annurev-neuro-070815-013851 · Cited by 360 · see citing works
Thiele, A., & Bellgrove, M. A. (2018) · Neuron · doi:10.1016/j.neuron.2018.01.008 · Cited by 350 · see citing works
Distinct timescales of population coding across cortex
Runyan, C. A., Piasini, E., Panzeri, S., & Harvey, C. D. (2017) · Nature · doi:10.1038/nature23020 · Cited by 333 · see citing works
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 · see citing works
Williams, A. H., Kim, T. H., Wang, F. L., Vyas, S., Ryu, S. I., Shenoy, K. V., Schnitzer, M. J., Kolda, T. G., & Ganguli, S. (2018) · Neuron · doi:10.1016/j.neuron.2018.05.015 · Cited by 306 · see citing works
Behavior needs neural variability
Waschke, L., Kloosterman, N. A., Obleser, J., & Garrett, D. D. (2021) · Neuron · doi:10.1016/j.neuron.2021.01.023 · Cited by 301 · see citing works
The role of population structure in computations through neural dynamics
Dubreuil, A., Valente, A., Beiran, M., Mastrogiuseppe, F., & Ostojic, S. (2022) · Nature Neuroscience · doi:10.1038/s41593-022-01088-4 · Cited by 237 · see citing works
Perceptual Decision-Making as Probabilistic Inference by Neural Sampling
Haefner, R. M., Berkes, P., & Fiser, J. (2016) · Neuron · doi:10.1016/j.neuron.2016.03.020 · Cited by 207 · see citing works
Selective modulation of cortical state during spatial attention
Engel, T. A., Steinmetz, N. A., Gieselmann, M. A., Thiele, A., Moore, T., & Boahen, K. A. (2016) · Science · doi:10.1126/science.aag1420 · Cited by 207 · see citing works
Learning and attention reveal a general relationship between population activity and behavior
Ni, A. M., Ruff, D. A., Alberts, J. J., Symmonds, J., & Cohen, M. R. (2018) · Science · doi:10.1126/science.aao0284 · Cited by 188 · see citing works
Self-citationOrigin of information-limiting noise correlations
Kanitscheider, I., Coen-Cagli, R., & Pouget, A. (2015) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1508738112 · Cited by 160 · see citing works
Circuit Models of Low-Dimensional Shared Variability in Cortical Networks
Huang, C., Ruff, D. A., Pyle, R., Rosenbaum, R., Cohen, M. R., & Doiron, B. (2018) · Neuron · doi:10.1016/j.neuron.2018.11.034 · Cited by 144 · see citing works
Self-citationMonoaminergic Neuromodulation of Sensory Processing
Jacob, S. N., & Nienborg, H. (2018) · Frontiers in Neural Circuits · doi:10.3389/fncir.2018.00051 · Cited by 143 · see citing works
Slow Drift of Neural Activity as a Signature of Impulsivity in Macaque Visual and Prefrontal Cortex
Cowley, B. R., Snyder, A. C., Acar, K., Williamson, R. C., Yu, B. M., & Smith, M. A. (2020) · Neuron · doi:10.1016/j.neuron.2020.07.021 · Cited by 127 · see citing works
Normalization and the Cholinergic Microcircuit: A Unified Basis for Attention
Schmitz, T. W., & Duncan, J. (2018) · Trends in Cognitive Sciences · doi:10.1016/j.tics.2018.02.011 · Cited by 116 · see citing works
Analyzing biological and artificial neural networks: challenges with opportunities for synergy?
Barrett, D. G. T., Morcos, A. S., & Macke, J. H. (2019) · Current Opinion in Neurobiology · doi:10.1016/j.conb.2019.01.007 · Cited by 111 · see citing works
Scaling Properties of Dimensionality Reduction for Neural Populations and Network Models
Williamson, R. C., Cowley, B. R., Litwin-Kumar, A., Doiron, B., Kohn, A., Smith, M. A., & Yu, B. M. (2016) · PLoS Computational Biology · doi:10.1371/journal.pcbi.1005141 · Cited by 100 · see citing works
Capturing the Dynamical Repertoire of Single Neurons with Generalized Linear Models
Weber, A. I., & Pillow, J. W. (2017) · Neural Computation · doi:10.1162/neco_a_01021 · Cited by 97 · see citing works
On the Structure of Neuronal Population Activity under Fluctuations in Attentional State
Ecker, A. S., Denfield, G. H., Bethge, M., & Tolias, A. S. (2016) · The Journal of Neuroscience · doi:10.1523/jneurosci.2044-15.2016 · Cited by 88 · see citing works
Feedforward and feedback sources of choice probability in neural population responses
Cumming, B. G., & Nienborg, H. (2016) · Current Opinion in Neurobiology · doi:10.1016/j.conb.2016.01.009 · Cited by 82 · see citing works
Neuronal variability reflects probabilistic inference tuned to natural image statistics
Festa, D., Aschner, A., Davila, A., Kohn, A., & Coen-Cagli, R. (2021) · Nature Communications · doi:10.1038/s41467-021-23838-x · Cited by 78 · see citing works
Analysis of Neuronal Spike Trains, Deconstructed
Aljadeff, J., Lansdell, B., Fairhall, A. L., & Kleinfeld, D. (2016) · Neuron · doi:10.1016/j.neuron.2016.05.039 · Cited by 83 · see citing works
Stimulus complexity shapes response correlations in primary visual cortex
Bányai, M., Lazăr, A., Klein, L., Klon-Lipok, J., Stippinger, M., Singer, W., & Orbán, G. (2019) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1816766116 · Cited by 79 · see citing works
Learning is shaped by abrupt changes in neural engagement
Hennig, J. A., Oby, E. R., Golub, M. D., Bahureksa, L., Sadtler, P. T., Quick, K. M., Ryu, S. I., Tyler‐Kabara, E. C., Batista, A. P., Chase, S. M., et al. (2021) · Nature Neuroscience · doi:10.1038/s41593-021-00822-8 · Cited by 80 · see citing works
Beaman, C. B., Eagleman, S. L., & Dragoi, V. (2017) · Nature Communications · doi:10.1038/s41467-017-01030-4 · Cited by 74 · see citing works
Attentional modulation of neuronal variability in circuit models of cortex
Kanashiro, T., Ocker, G. K., Cohen, M. R., & Doiron, B. (2017) · eLife · doi:10.7554/elife.23978 · Cited by 81 · see citing works
Self-citationComputation noise in human learning and decision-making: origin, impact, function
Findling, C., & Wyart, V. (2021) · Current Opinion in Behavioral Sciences · doi:10.1016/j.cobeha.2021.02.018 · Cited by 75 · see citing works
Williamson, R. C., Doiron, B., Smith, M. A., & Yu, B. M. (2019) · Current Opinion in Neurobiology · doi:10.1016/j.conb.2018.12.009 · Cited by 64 · see citing works
Attentional fluctuations induce shared variability in macaque primary visual cortex
Denfield, G. H., Ecker, A. S., Shinn, T., Bethge, M., & Tolias, A. S. (2018) · Nature Communications · doi:10.1038/s41467-018-05123-6 · Cited by 66 · see citing works
To look or not to look: dissociating presaccadic and covert spatial attention
Li, H.-H., Hanning, N. M., & Carrasco, M. (2021) · Trends in Neurosciences · doi:10.1016/j.tins.2021.05.002 · Cited by 63 · see citing works
Cognition as a Window into Neuronal Population Space
Ruff, D. A., Ni, A. M., & Cohen, M. R. (2018) · Annual Review of Neuroscience · doi:10.1146/annurev-neuro-080317-061936 · Cited by 63 · see citing works
Self-citationNeurochemistry of Visual Attention
Lockhofen, D. E. L., & Mulert, C. (2021) · Frontiers in Neuroscience · doi:10.3389/fnins.2021.643597 · Cited by 62 · see citing works
Top-down coordination of local cortical state during selective attention
van Kempen, J., Gieselmann, M. A., Boyd, M., Steinmetz, N. A., Moore, T., Engel, T. A., & Thiele, A. (2021) · Neuron · doi:10.1016/j.neuron.2020.12.013 · Cited by 61 · see citing works
The impact of bilateral ongoing activity on evoked responses in mouse cortex
Shimaoka, D., Steinmetz, N. A., Harris, K. D., & Carandini, M. (2019) · eLife · doi:10.7554/elife.43533 · Cited by 54 · see citing works
Serotonin Decreases the Gain of Visual Responses in Awake Macaque V1
Seillier, L., Lorenz, C., Kawaguchi, K., Ott, T., Nieder, A., Pourriahi, P., & Nienborg, H. (2017) · The Journal of Neuroscience · doi:10.1523/jneurosci.1339-17.2017 · Cited by 57 · see citing works
Neural Variability Is Quenched by Attention
Arazi, A., Yeshurun, Y., & Dinstein, I. (2019) · Journal of Neuroscience · doi:10.1523/jneurosci.0355-19.2019 · Cited by 55 · see citing works
Heeger, D. J., & Mackey, W. E. (2019) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1911633116 · Cited by 54 · see citing works
Dissociation of Choice Formation and Choice-Correlated Activity in Macaque Visual Cortex
Goris, R. L. T., Ziemba, C. M., Stine, G. M., Simoncelli, E. P., & Movshon, J. A. (2017) · Journal of Neuroscience · doi:10.1523/jneurosci.3331-16.2017 · Cited by 53 · see citing works
Self-citationNew perspectives on dimensionality and variability from large-scale cortical dynamics
Engel, T. A., & Steinmetz, N. A. (2019) · Current Opinion in Neurobiology · doi:10.1016/j.conb.2019.09.003 · Cited by 53 · see citing works
Linear-nonlinear-time-warp-poisson models of neural activity
Lawlor, P. N., Perich, M. G., Miller, L. E., & Kording, K. P. (2018) · Journal of Computational Neuroscience · doi:10.1007/s10827-018-0696-6 · Cited by 51 · see citing works
The expression of established cognitive brain states stabilizes with working memory development
Montez, D. F., Calabro, F. J., & Luna, B. (2017) · eLife · doi:10.7554/elife.25606 · Cited by 52 · see citing works
Representation of visual uncertainty through neural gain variability
Hénaff, O. J., Boundy-Singer, Z. M., Meding, K., Ziemba, C. M., & Goris, R. L. T. (2020) · Nature Communications · doi:10.1038/s41467-020-15533-0 · Cited by 54 · see citing works
Self-citationDethroning the Fano Factor: A Flexible, Model-Based Approach to Partitioning Neural Variability
Charles, A. S., Park, M., Weller, J. P., Horwitz, G. D., & Pillow, J. W. (2018) · Neural Computation · doi:10.1162/neco_a_01062 · Cited by 52 · see citing works
Thiele, A., Brandt, C., Dasilva, M., Gotthardt, S., Chicharro, D., Panzeri, S., & Distler, C. (2016) · Journal of Neuroscience · doi:10.1523/jneurosci.0872-16.2016 · Cited by 49 · see citing works
Inferring Cortical Variability from Local Field Potentials
Cui, Y., Liu, L. D., McFarland, J. M., Pack, C. C., & Butts, D. A. (2016) · Journal of Neuroscience · doi:10.1523/jneurosci.2502-15.2016 · Cited by 46 · see citing works
Primary visual cortex straightens natural video trajectories
Hénaff, O. J., Bai, Y., Charlton, J. A., Nauhaus, I., Simoncelli, E. P., & Goris, R. L. T. (2021) · Nature Communications · doi:10.1038/s41467-021-25939-z · Cited by 39 · see citing works
Self-citationParallel Engagement of Regions Associated with Encoding and Later Retrieval Forms Durable Memories
Wagner, I. C., van Buuren, M., Bovy, L., & Fernández, G. (2016) · Journal of Neuroscience · doi:10.1523/jneurosci.0830-16.2016 · Cited by 44 · see citing works
Sanayei, M., Chen, X., Chicharro, D., Distler, C., Panzeri, S., & Thiele, A. (2018) · Nature Communications · doi:10.1038/s41467-018-06698-w · Cited by 46 · see citing works
Turner, M. H., Krieger, A., Pang, M. M., & Clandinin, T. R. (2022) · eLife · doi:10.7554/elife.82587 · Cited by 42 · see citing works
Can Serial Dependencies in Choices and Neural Activity Explain Choice Probabilities?
Lueckmann, J.-M., Macke, J. H., & Nienborg, H. (2018) · Journal of Neuroscience · doi:10.1523/jneurosci.2225-17.2018 · Cited by 37 · see citing works
Cell class-specific modulation of attentional signals by acetylcholine in macaque frontal eye field
Dasilva, M., Brandt, C., Gotthardt, S., Gieselmann, M. A., Distler, C., & Thiele, A. (2019) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1905413116 · Cited by 38 · see citing works
Whiteway, M. R., & Butts, D. A. (2016) · Journal of Neurophysiology · doi:10.1152/jn.00698.2016 · Cited by 37 · see citing works
Maximum entropy models as a tool for building precise neural controls
Savin, C., & Tkačik, G. (2017) · Current Opinion in Neurobiology · doi:10.1016/j.conb.2017.08.001 · Cited by 34 · see citing works
Bridging neuronal correlations and dimensionality reduction
Umakantha, A., Morina, R., Cowley, B. R., Snyder, A. C., Smith, M. A., & Yu, B. M. (2021) · Neuron · doi:10.1016/j.neuron.2021.06.028 · Cited by 39 · see citing works
The quest for interpretable models of neural population activity
Whiteway, M. R., & Butts, D. A. (2019) · Current Opinion in Neurobiology · doi:10.1016/j.conb.2019.07.004 · Cited by 35 · see citing works
Task-induced neural covariability as a signature of approximate Bayesian learning and inference
Lange, R. D., & Haefner, R. M. (2022) · PLoS Computational Biology · doi:10.1371/journal.pcbi.1009557 · Cited by 45 · see citing works
Shi, Y.-L., Steinmetz, N. A., Moore, T., Boahen, K. A., & Engel, T. A. (2022) · Nature Communications · doi:10.1038/s41467-021-27724-4 · Cited by 31 · see citing works
Park, I. M., & Pillow, J. W. (2026) · PLoS Computational Biology · doi:10.1101/178418 · Cited by 31 · see citing works
Murphy, A. J., Shaw, L. H., Hasse, J. M., Goris, R. L. T., & Briggs, F. (2020) · Journal of Computational Neuroscience · doi:10.1007/s10827-020-00754-5 · Cited by 32 · see citing works
Self-citationIncorporating behavioral and sensory context into spectro-temporal models of auditory encoding
David, S. V. (2017) · Hearing Research · doi:10.1016/j.heares.2017.12.021 · Cited by 32 · see citing works
Relating Divisive Normalization to Neuronal Response Variability
Coen-Cagli, R., & Solomon, S. S. (2019) · Journal of Neuroscience · doi:10.1523/jneurosci.0126-19.2019 · Cited by 30 · see citing works
Chen, G., & Gong, P. (2022) · Science Advances · doi:10.1126/sciadv.abl4995 · Cited by 28 · see citing works
Representations in human primary visual cortex drift over time
Roth, Z. N., & Merriam, E. P. (2023) · Nature Communications · doi:10.1038/s41467-023-40144-w · Cited by 29 · see citing works
Running modulates primate and rodent visual cortex differently
Liska, J. P., Rowley, D. P., Nguyen, T. T. K., Muthmann, J.-O., Butts, D. A., Yates, J. L., & Huk, A. C. (2024) · eLife · doi:10.7554/elife.87736.3 · Cited by 27 · see citing works
Characterizing and interpreting the influence of internal variables on sensory activity
Lange, R. D., & Haefner, R. M. (2017) · Current Opinion in Neurobiology · doi:10.1016/j.conb.2017.07.006 · Cited by 22 · see citing works
Brain noise estimation from MEG response to flickering visual stimulation
Pisarchik, A. N., Chholak, P., & Hramov, A. E. (2019) · Chaos Solitons & Fractals X · doi:10.1016/j.csfx.2019.100005 · Cited by 25 · see citing works
A flexible readout mechanism of human sensory representations
Birman, D., & Gardner, J. L. (2019) · Nature Communications · doi:10.1038/s41467-019-11448-7 · Cited by 27 · see citing works
Noise Correlations for Faster and More Robust Learning
Nassar, M. R., Scott, D., & Bhandari, A. (2021) · Journal of Neuroscience · doi:10.1523/jneurosci.3045-20.2021 · Cited by 23 · see citing works
Higher-dimensional neural representations predict better episodic memory
Sheng, J., Zhang, L., Liu, C., Liu, J., Feng, J., Zhou, Y., Hu, H., & Xue, G. (2022) · Science Advances · doi:10.1126/sciadv.abm3829 · Cited by 23 · see citing works
Transitions in dynamical regime and neural mode during perceptual decisions
Luo, T. Z., Kim, T. D., Gupta, D., Bondy, A., Kopec, C. D., Elliott, V. A., DePasquale, B., & Brody, C. D. (2025) · Nature · doi:10.1038/s41586-025-09528-4 · Cited by 46 · see citing works
Choice (-history) correlations in sensory cortex: cause or consequence?
Macke, J. H., & Nienborg, H. (2019) · Current Opinion in Neurobiology · doi:10.1016/j.conb.2019.09.005 · Cited by 21 · see citing works
Statistical neuroscience in the single trial limit
Williams, A. H., & Linderman, S. W. (2021) · Current Opinion in Neurobiology · doi:10.1016/j.conb.2021.10.008 · Cited by 22 · see citing works
Low rank mechanisms underlying flexible visual representations
Ruff, D. A., Xue, C., Kramer, L. E., Baqai, F., & Cohen, M. R. (2020) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.2005797117 · Cited by 19 · see citing works
Self-citationResponse sub-additivity and variability quenching in visual cortex
Goris, R. L. T., Coen-Cagli, R., Miller, K. D., Priebe, N. J., & Lengyel, M. (2024) · Nature reviews. Neuroscience · doi:10.1038/s41583-024-00795-0 · Cited by 26 · see citing works
Self-citationWorking memory improves developmentally as neural processes stabilize
Montez, D. F., Calabro, F. J., & Luna, B. (2019) · PLoS ONE · doi:10.1371/journal.pone.0213010 · Cited by 19 · see citing works
Data-Driven Approaches to Understanding Visual Neuron Activity
Butts, D. A. (2019) · Annual Review of Vision Science · doi:10.1146/annurev-vision-091718-014731 · Cited by 19 · see citing works
State-Dependent Regulation of Cortical Processing Speed via Gain Modulation
Wyrick, D. G., & Mazzucato, L. (2021) · Journal of Neuroscience · doi:10.1523/jneurosci.1895-20.2021 · Cited by 20 · see citing works
Internally generated population activity in cortical networks hinders information transmission
Huang, C., Pouget, A., & Doiron, B. (2022) · Science Advances · doi:10.1126/sciadv.abg5244 · Cited by 20 · see citing works
A general decoding strategy explains the relationship between behavior and correlated variability
Ni, A. M., Huang, C., Doiron, B., & Cohen, M. R. (2022) · eLife · doi:10.7554/elife.67258 · Cited by 18 · see citing works
Self-citationClery, S., Cumming, B. G., & Nienborg, H. (2016) · Journal of Neuroscience · doi:10.1523/jneurosci.2445-16.2016 · Cited by 19 · see citing works
Quiroga‐Martinez, D. R., Hansen, N. C., Højlund, A., Pearce, M. T., Brattico, E., Holmes, E., Friston, K. J., & Vuust, P. (2021) · Human Brain Mapping · doi:10.1002/hbm.25638 · Cited by 18 · see citing works
Efficient coding theory of dynamic attentional modulation
Młynarski, W. F., & Tkačik, G. (2022) · PLoS Biology · doi:10.1371/journal.pbio.3001889 · Cited by 19 · see citing works
Slow gain fluctuations limit benefits of temporal integration in visual cortex
Goris, R. L. T., Ziemba, C. M., Movshon, J. A., & Simoncelli, E. P. (2018) · Journal of Vision · doi:10.1167/18.8.8 · Cited by 24 · see citing works
Self-citationVisual information is broadcast among cortical areas in discrete channelsPreprint
Yu, Y., Stirman, J. N., Dorsett, C. R., & Smith, S. L. (2018) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/469114 · Cited by 21 · see citing works
Multi-region coordination of evidence accumulation and decision commitment in the brainPreprint
Bondy, A., Charlton, J. A., Luo, T. Z., Kopec, C. D., Stagnaro, W. M., Venditto, S. J. C., Shi, K., Xie, E. Y., Beau, M., Lynch, L. A., et al. (2024) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2024.08.21.609044 · Cited by 22 · see citing works
Compact deep neural network models of the visual cortex
Cowley, B. R., Stan, P. L., Pillow, J. W., & Smith, M. A. (2026) · Nature · doi:10.1038/s41586-026-10150-1 · Cited by 21 · see citing works
Comparing Surrogates to Evaluate Precisely Timed Higher-Order Spike Correlations
Stella, A., Bouss, P., Palm, G., & Grün, S. (2022) · eNeuro · doi:10.1523/eneuro.0505-21.2022 · Cited by 16 · see citing works
Targeted V1 comodulation supports task-adaptive sensory decisions
Haimerl, C., Ruff, D. A., Cohen, M. R., Savin, C., & Simoncelli, E. P. (2023) · Nature Communications · doi:10.1038/s41467-023-43432-7 · Cited by 16 · see citing works
Self-citationPanzeri, S., Safaai, H., Feo, V. D., & Vato, A. (2016) · Frontiers in Neuroscience · doi:10.3389/fnins.2016.00165 · Cited by 14 · see citing works
Endogenous attention improves perception in amblyopic macaques
Pham, A., Carrasco, M., & Kiorpes, L. (2018) · Journal of Vision · doi:10.1167/18.3.11 · Cited by 15 · see citing works
Circuit models of low dimensional shared variability in cortical networksPreprint
Huang, C., Ruff, D. A., Pyle, R., Rosenbaum, R., Cohen, M. R., & Doiron, B. (2017) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/217976 · Cited by 15 · see citing works
Self-citationHow spatial attention alters visual cortical representation during target anticipationPreprint
Tünçok, E., Carrasco, M., & Winawer, J. A. (2024) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2024.03.02.583127 · Cited by 15 · see citing works
Cheng, Y.-A., Sanayei, M., Chen, X., Jia, K., Li, S., Fang, F., Watanabe, T., Thiele, A., & Zhang, R. (2025) · Nature Human Behaviour · doi:10.1038/s41562-025-02149-x · Cited by 20 · see citing works
Cholinergic Control of Information Coding
van Kempen, J., Panzeri, S., & Thiele, A. (2017) · Trends in Neurosciences · doi:10.1016/j.tins.2017.06.006 · Cited by 14 · see citing works
Understanding Sensory Information Processing Through Simultaneous Multi-area Population Recordings
Zavitz, E., & Price, N. S. C. (2019) · Frontiers in Neural Circuits · doi:10.3389/fncir.2018.00115 · Cited by 14 · see citing works
Statistical mechanics of low-rank tensor decomposition*
Kadmon, J., & Ganguli, S. (2019) · Journal of Statistical Mechanics Theory and Experiment · doi:10.1088/1742-5468/ab3216 · Cited by 14 · see citing works
Weak evidence for neural correlates of task-switching in macaque V1
Lange, R. D., Gómez-Laberge, C., Berezovskii, V. K., Pletenev, A., Sherdil, A., Hartmann, T. S., Haefner, R. M., & Born, R. T. (2023) · Journal of Neurophysiology · doi:10.1152/jn.00085.2022 · Cited by 14 · see citing works
Yin, C., Melin, M. D., Rojas-Bowe, G., Sun, X. R., Couto, J., Gluf, S., Kostiuk, A., Musall, S., & Churchland, A. K. (2025) · Neuron · doi:10.1016/j.neuron.2025.06.001 · Cited by 16 · see citing works
The eyes reflect an internal cognitive state hidden in the population activity of cortical neurons
Johnston, R., Snyder, A. C., Khanna, S. B., Issar, D., & Smith, M. A. (2021) · Cerebral Cortex · doi:10.1093/cercor/bhab418 · Cited by 13 · see citing works
- Authors
- Rabinowitz, N. C., Goris, R. L., Cohen, M., & Simoncelli, E. P.
- Affiliations
- Howard Hughes Medical Institute (US)
- University of Pittsburgh (US)
- Corresponding author
- Rabinowitz, Neil C
- Simoncelli, Eero P
- Venue
- eLife
- Publisher
- eLife Sciences Publications, Ltd
- Published
- 2015-11-02
- Volume
- 4
- Pages
- e08998-e08998
- ISSN
- 2050-084X (ISSN-L)
- PMC
- PMC4758958
- OpenAlex
- W1961971483
- Cited by
- 194
- References
- 81
- Citations by year
- 2026: 16 · 2025: 7 · 2024: 15 · 2023: 15 · 2022: 14 · 2021: 24 · 2020: 15 · 2019: 24 · 2018: 22 · 2017: 23 · 2016: 18 · 2015: 1
- FWCI
- 12.84
- Type
- journal article
- Language
- en
- Open access
- gold
- doi.org
- Licence
- Locations
- eLife (publishedVersion, cc-by)
- PubMed Central (publishedVersion, cc-by)
- PubMed (publishedVersion)
- DOAJ (DOAJ: Directory of Open Access Journals) (submittedVersion, cc-by-sa)
- Funders
- Howard Hughes Medical Institute
- National Institutes of Health (4R00EY020844-03, R01 EY022930)
- Klingenstein Third Generation Foundation
- Simons Foundation
- Alfred P. Sloan Foundation (Research Fellowship)
- Topics
- Life Sciences › Neuroscience › Cognitive Neuroscience › Visual perception and processing mechanisms
- Life Sciences › Neuroscience › Cognitive Neuroscience › Neural dynamics and brain function
- Physical Sciences › Computer Science › Computer Vision and Pattern Recognition › Visual Attention and Saliency Detection
- Keywords
- visual attention, area V4, population coding, noise correlation, internal state, spiking activity, functional model, reward prediction, choice behavior, hemispheric lateralization
- MeSH terms
- Action Potentials, Animals, Haplorhini, Attention, Models, Neurological, Perception, Sensory Receptor Cells
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