The DOI matches its Crossref record; 24 of the 24 references it cites were found in a registry or an index.
The importance of mixed selectivity in complex cognitive tasks
Open accessAbstract
Single-neuron activity in the prefrontal cortex (PFC) is tuned to mixtures of multiple task-related aspects. Such mixed selectivity is highly heterogeneous, seemingly disordered and therefore difficult to interpret. We analysed the neural activity recorded in monkeys during an object sequence memory task to identify a role of mixed selectivity in subserving the cognitive functions ascribed to the PFC. We show that mixed selectivity neurons encode distributed information about all task-relevant aspects. Each aspect can be decoded from the population of neurons even when single-cell selectivity to that aspect is eliminated. Moreover, mixed selectivity offers a significant computational advantage over specialized responses in terms of the repertoire of input-output functions implementable by readout neurons. This advantage originates from the highly diverse nonlinear selectivity to mixtures of task-relevant variables, a signature of high-dimensional neural representations. Crucially, this dimensionality is predictive of animal behaviour as it collapses in error trials. Our findings recommend a shift of focus for future studies from neurons that have easily interpretable response tuning to the widely observed, but rarely analysed, mixed selectivity neurons.
Overview
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Integrity signals
Registry
Cites
Statistics
Verification
Claims the paper makes
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
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?
The source backs part of the claim, not all of it — or backs it for a different population, condition or comparison.
In the citing paper
“Additional efficiency is achieved because conceptually similar representations reuse neural populations during simulation (e.g. Rigotti et al., 2013).”
From The theory of constructed emotion: an active inference account of interoception and categorization (2016) · cites this paper as Rigotti et al., 2013
Experimental — accuracy not yet measured
Self-check
Percentages, sums and reported differences re-computed from the paper’s own numbers.
The self-check needs the paper’s full text.
Citations
Cites
Cortes, C., & Vapnik, V. (1995) · Machine Learning · doi:10.1007/bf00994018 · Cited by 59,421
Maass, W., Natschläger, T., & Markram, H. (2002) · Neural Computation · doi:10.1162/089976602760407955 · Cited by 4,025
Harnessing Nonlinearity: Predicting Chaotic Systems and Saving Energy in Wireless Communication
Jaeger, H., & Haas, H. (2004) · Science · doi:10.1126/science.1091277 · Cited by 3,811
Mullin, A., & Rosenblatt, F. F. (1963) · American Mathematical Monthly · doi:10.2307/2312103 · Cited by 2,211
How does the brain solve visual object recognition?
DiCarlo, J. J., Zoccolan, D., & Rust, N. C. (2012) · Neuron · doi:10.1016/j.neuron.2012.01.010 · Cited by 1,790
Cortex: Statistics and Geometry of Neuronal Connectivity
Braitenberg, V., & Schüz, A. (1998) · doi:10.1007/978-3-662-03733-1 · Cited by 1,178 · cited 1×
“Random connectivity in small brain regions has been suggested based on anatomical reconstructions [21] and recently observed in the connections from the olfactory bulb to the olfactory cortex [22] (see also [14] for a general discussion).”
BackgroundGenerating Coherent Patterns of Activity from Chaotic Neural Networks
Sussillo, D., & Abbott, L. F. (2009) · Neuron · doi:10.1016/j.neuron.2009.07.018 · Cited by 1,092
State-dependent computations: spatiotemporal processing in cortical networks
Buonomano, D. V., & Maass, W. (2009) · Nature reviews. Neuroscience · doi:10.1038/nrn2558 · Cited by 950
An adaptive coding model of neural function in prefrontal cortex
Duncan, J. (2001) · Nature Reviews Neuroscience · doi:10.1038/35097575 · Cited by 874
Neural Activity in the Primate Prefrontal Cortex during Associative Learning
Asaad, W. F., Rainer, G., & Miller, E. K. (1998) · Neuron · doi:10.1016/s0896-6273(00)80658-3 · Cited by 593
Self-citation
Cited by
Sorted by citations
Items 901–1,000 of 1,006
The representational geometry of cognitive maps under cognitive controlPreprint
Park, S. A., Zolfaghar, M., Russin, J., Miller, D. S., O’Reilly, R. C., & Boorman, E. D. (2023) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2023.02.04.527142 · Cited by 11
Task-specific invariant representation in auditory cortex
Heller, C. R., Hamersky, G. R., & David, S. V. (2023) · eLife · doi:10.7554/elife.89936 · Cited by 9
Neurobiological Causal Models of Language Processing
Fitz, H., Peter Hagoort, A., & Petersson, K. M. (2024) · Neurobiology of Language · doi:10.1162/nol_a_00133 · Cited by 10
The cognitive critical brain: Modulation of criticality in perception-related cortical regions
Liu, X., Fei, X., & Liu, J. (2024) · NeuroImage · doi:10.1016/j.neuroimage.2024.120964 · Cited by 8
Learning reshapes the hippocampal representation hierarchy
Chiossi, H. S. C., Nardin, M., Tkačik, G., & Csicsvari, J. (2025) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.2417025122 · Cited by 10
Category-biased patches encircle core domain-general regions in the human lateral prefrontal cortex
Assem, M., Shashidhara, S., Glasser, M. F., & Duncan, J. (2025) · Neuropsychologia · doi:10.1016/j.neuropsychologia.2025.109164 · Cited by 8
Wierda, T. S., Dora, S., Pennartz, C. M. A., & Mejías, J. F. (2025) · PLoS Computational Biology · doi:10.1371/journal.pcbi.1013559 · Cited by 8
Neural Representation of Episodic Time
Kwok, S. C., Lapate, R. C., Sakon, J. J., van Wassenhove, V., Xue, G., & Zheng, J. (2025) · Journal of Neuroscience · doi:10.1523/jneurosci.1397-25.2025 · Cited by 10
Effects of contraction bias on the decision process in the macaque prefrontal cortex
Benozzo, D., Ferrucci, L., & Genovesio, A. (2022) · Cerebral Cortex · doi:10.1093/cercor/bhac253 · Cited by 9
Constraints on the design of neuromorphic circuits set by the properties of neural population codes
Panzeri, S., Janotte, E., Pequeño-Zurro, A., Bonato, J., & Bartolozzi, C. (2023) · Neuromorphic Computing and Engineering · doi:10.1088/2634-4386/acaf9c · Cited by 9
Li, Y., Zhu, X., Qi, Y., & Wang, Y. (2023) · eLife · doi:10.7554/elife.87881 · Cited by 8
Joint encoding of stimulus and decision in monkey primary visual cortex
Yang, Y., Klon-Lipok, J., & Singer, W. (2023) · Cerebral Cortex · doi:10.1093/cercor/bhad420 · Cited by 8
Chang, W.-L., & Hen, R. (2024) · Advances in neurobiology · doi:10.1007/978-3-031-62983-9_10 · Cited by 8
Prefrontal neuronal dynamics in the absence of task execution
Pu, S., Dang, W., Qi, X.-L., & Constantinidis, C. (2024) · Nature Communications · doi:10.1038/s41467-024-50717-y · Cited by 8
Dopamine builds and reveals reward-associated latent behavioral attractors
Naudé, J., Sarazin, M., Mondoloni, S., Hannesse, B., Vicq, É., Amegandjin, F., Mourot, A., Fauré, P., & Delord, B. (2024) · Nature Communications · doi:10.1038/s41467-024-53976-x · Cited by 11
A posture subspace in the primary motor cortex
Marino, P. J., Bahureksa, L., Fisac, C. F., Oby, E. R., Smoulder, A. L., Motiwala, A., Degenhart, A. D., Grigsby, E. M., Joiner, W. M., Chase, S. M., et al. (2025) · Neuron · doi:10.1016/j.neuron.2025.07.030 · Cited by 10
Practice reshapes the geometry and dynamics of task-tailored representations
Kikumoto, A., Shibata, K., Nishio, T., & Badre, D. (2025) · Cerebral Cortex · doi:10.1093/cercor/bhaf125 · Cited by 8
Conjunctive coding in an evolved spiking model of retrosplenial cortex.
Rounds, E. L., Alexander, A. S., Nitz, D. A., & Krichmar, J. L. (2018) · Behavioral Neuroscience · doi:10.1037/bne0000236 · Cited by 8
Mione, V., Tsujimoto, S., & Genovesio, A. (2019) · Neuroscience · doi:10.1016/j.neuroscience.2019.02.023 · Cited by 8
Roth, N., & Rust, N. C. (2018) · PLoS ONE · doi:10.1371/journal.pone.0200528 · Cited by 8
Spike Train Coactivity Encodes Learned Natural Stimulus Invariances in Songbird Auditory Cortex
Theilman, B. H., Perks, K. E., & Gentner, T. Q. (2020) · Journal of Neuroscience · doi:10.1523/jneurosci.0248-20.2020 · Cited by 8
Neuronal identity and cognitive control dynamics in the PFC
Nakajima, M. (2021) · Seminars in Cell and Developmental Biology · doi:10.1016/j.semcdb.2021.08.014 · Cited by 8
Optimal Quadratic Binding for Relational Reasoning in Vector Symbolic Neural Architectures
Hiratani, N., & Sompolinsky, H. (2022) · Neural Computation · doi:10.1162/neco_a_01558 · Cited by 8
Canonical template tracking: Measuring the activation state of specific neural representations
Palenciano, A. F., Senoussi, M., Formica, S., & González‐García, C. (2023) · Frontiers in Neuroimaging · doi:10.3389/fnimg.2022.974927 · Cited by 8
The Role of Prefrontal Mixed Selectivity in Cognitive Control
Cardenas, A. R., & Viswanathan, P. (2016) · Journal of Neuroscience · doi:10.1523/jneurosci.1816-16.2016 · Cited by 8
What can neuronal populations tell us about cognition?
Arandia-Romero, I., Nogueira, R., Mochol, G., & Moreno‐Bote, R. (2017) · Current Opinion in Neurobiology · doi:10.1016/j.conb.2017.07.008 · Cited by 8
Heterogeneous value coding in orbitofrontal populations.
Enel, P., Perkins, A. Q., & Rich, E. L. (2021) · Behavioral Neuroscience · doi:10.1037/bne0000457 · Cited by 8
Common ERP responses to narrative incoherence in sentence and picture pair comprehension
Jouen, A.-L., Cazin, N., Hidot, S., Madden-Lombardi, C., Ventre‐Dominey, J., & Dominey, P. F. (2021) · Brain and Cognition · doi:10.1016/j.bandc.2021.105775 · Cited by 8
Cooper, C. P., Shafer, A. T., Armstrong, N. M., Rossi, S. L., Young, J., Herold, C., Gu, H., Yang, Y., Stein, E. A., Resnick, S. M., et al. (2021) · Cerebral Cortex · doi:10.1093/cercor/bhab257 · Cited by 8
Learning enhances behaviorally relevant representations in apical dendrites
Benezra, S. E., Patel, K., Campos, C. P., Hillman, E. M. C., & Bruno, R. M. (2024) · eLife · doi:10.7554/elife.98349.3 · Cited by 9
Pitti, A., Quoy, M., Lavandier, C., Boucenna, S., Swaileh, W., & Weidmann, C. (2022) · IEEE Transactions on Cognitive and Developmental Systems · doi:10.1109/tcds.2022.3168046 · Cited by 10
Alavash, M., Tune, S., & Obleser, J. (2021) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2021.02.22.432315 · Cited by 8
Aligned and oblique dynamics in recurrent neural networksPreprint
Schuessler, F., Mastrogiuseppe, F., Ostojic, S., & Barak, O. (2024) · eLife · doi:10.7554/elife.93060 · Cited by 11
Self-citationSeparable dorsal raphe dopamine projections mimic the facets of a loneliness-like statePreprint
Lee, C. R., Matthews, G. A., Lemieux, M., Wasserlein, E. M., Borio, M., Miranda, R. L., Keyes, L. R., Schneider, G. P., Jia, C., Tran, A., et al. (2025) · eLife · doi:10.7554/elife.105955 · Cited by 9
Wennberg, J. W., & Serences, J. T. (2024) · Attention Perception & Psychophysics · doi:10.3758/s13414-024-02933-3 · Cited by 7
Secondary motor cortex tracks decision value during the learning of a non-instructed task
Augusto, E., Kouskoff, V., Chenouard, N., Giraudet, M., Peltier, L., de Miranda, A., Louis, A., Alonso, L., & Gambino, F. (2025) · Cell Reports · doi:10.1016/j.celrep.2024.115152 · Cited by 7
Orthogonal neural representations support perceptual judgments of natural stimuli
Srinath, R., Ni, A. M., Marucci, C., Cohen, M. R., & Brainard, D. H. (2025) · Scientific Reports · doi:10.1038/s41598-025-88910-8 · Cited by 7
Mouille, A., Gaillard, C., Ästrand, E., Wardak, C., Hamed, S. B., & Hamed, S. B. (2025) · PLoS Biology · doi:10.1371/journal.pbio.3003353 · Cited by 7
Gesture encoding in human left precentral gyrus neuronal ensembles
Vargas-Irwin, C. E., Hosman, T., Gusman, J. T., Pun, T. K., Simeral, J. D., Singer-Clark, T., Kapitonava, A., Nicolas, C., Shah, N. P., Avansino, D. T., et al. (2025) · Communications Biology · doi:10.1038/s42003-025-08557-z · Cited by 7
Why is cognitive effort experienced as costly?
Otto, A. R., Westbrook, A., & Jean Daunizeau, A. (2025) · Trends in Cognitive Sciences · doi:10.1016/j.tics.2025.10.012 · Cited by 10
Oesch, L. T., Thomas, M. C., Sandberg, D., Couto, J., & Churchland, A. K. (2026) · Nature Communications · doi:10.1038/s41467-026-70639-1 · Cited by 11
Shared neural geometries for bilingual semantic representations in human hippocampal neurons
Yan, X., Chavez, A. G., Franch, M. C., Katlowitz, K. A., Gautam, I., Kim, B., Krishna, A., Shrivastava, A., Arsdel, K. V., Belanger, J. L., et al. (2026) · Cell · doi:10.1016/j.cell.2026.05.020 · Cited by 8
Nonresponsive Neurons Improve Population Coding of Object Location
Haggard, M., & Chacron, M. J. (2024) · Journal of Neuroscience · doi:10.1523/jneurosci.1068-24.2024 · Cited by 7
Huang, G.-B., Westover, M. B., Tan, E., Wang, H., Cui, D., Ma, W., Wang, T., He, Q., Wei, H., Wang, N., et al. (2024) · Neurocomputing · doi:10.1016/j.neucom.2024.129053 · Cited by 9
Contextual neural dynamics during time perception in the primate ventral premotor cortex
Díaz, H., Bayones, L., Álvarez, M., Andrade-Ortega, B., Valero, S., Zainos, A., Romo, R., & Rossi-Pool, R. (2025) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.2420356122 · Cited by 7
The cortical critical power law balances energy and information in an optimal fashion
Tatsukawa, T., & Teramae, J.-N. (2025) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.2418218122 · Cited by 8
Jahans-Price, T., Gorochowski, T. E., Wilson, M. A., Jones, M. W., & Bogacz, R. (2014) · Frontiers in Behavioral Neuroscience · doi:10.3389/fnbeh.2014.00062 · Cited by 7
Learning Recruits Neurons Representing Previously Established Associations in the Corvid Endbrain
Veit, L., Pidpruzhnykova, G., & Nieder, A. (2017) · Journal of Cognitive Neuroscience · doi:10.1162/jocn_a_01152 · Cited by 7
Ramezanpour, H., Görner, M., & Thier, P. (2021) · Journal of Neurophysiology · doi:10.1152/jn.00194.2021 · Cited by 7
Herry, C., & Jercog, D. (2022) · Current Opinion in Neurobiology · doi:10.1016/j.conb.2022.102600 · Cited by 8
Pattern Motion Direction Is Encoded in the Population Activity of Macaque Area MT
Quaia, C., Kang, I., & Cumming, B. G. (2022) · Journal of Neuroscience · doi:10.1523/jneurosci.0011-22.2022 · Cited by 7
Baumann, A. W., Schäfer, T. A. J., & Ruge, H. (2023) · NeuroImage · doi:10.1016/j.neuroimage.2023.120262 · Cited by 7
Reconfiguration of Behavioral Signals in the Anterior Cingulate Cortex Based on Emotional State
Lindsay, A. J., Gallello, I., Caracheo, B. F., & Seamans, J. K. (2024) · Journal of Neuroscience · doi:10.1523/jneurosci.1670-23.2024 · Cited by 10
A case for human systems neuroscience
Gardner, J. L. (2014) · Neuroscience · doi:10.1016/j.neuroscience.2014.06.052 · Cited by 7
Crucial Role of the Prefrontal Cortex in Conscious Perception
Lew, S., & Lau, H. C. (2017) · Elsevier eBooks · doi:10.1016/b978-0-12-803676-1.00006-4 · Cited by 7
The Emerging Role of Neurodiagnostic Informatics in Integrated Neurological and Mental Health Care
Bosl, W. J. (2018) · The Neurodiagnostic Journal · doi:10.1080/21646821.2018.1508983 · Cited by 7
Information seeking mechanism of neural populations in the lateral prefrontal cortex
Nakamura, K., & Komatsu, M. (2018) · Brain Research · doi:10.1016/j.brainres.2018.11.029 · Cited by 7
Specific excitatory connectivity for feature integration in mouse primary visual cortex
Muir, D. R., Molina-Luna, P., Roth, M., Helmchen, F., & Kampa, B. M. (2017) · PLoS Computational Biology · doi:10.1371/journal.pcbi.1005888 · Cited by 7
Computational models of motivated frontal function
O’Reilly, R. C., Russin, J., & Herd, S. A. (2019) · Handbook of clinical neurology · doi:10.1016/b978-0-12-804281-6.00017-3 · Cited by 7
Nonlinear computations in spiking neural networks through multiplicative synapses
Nardin, M., Phillips, J. W., Podlaski, W. F., & Keemink, S. W. (2021) · Peer Community Journal · doi:10.24072/pcjournal.69 · Cited by 8
Evolution of neural activity in circuits bridging sensory and abstract knowledge
Mastrogiuseppe, F., Hiratani, N., & Latham, P. E. (2023) · eLife · doi:10.7554/elife.79908 · Cited by 7
A Dynamic Bayesian Model for Characterizing Cross-Neuronal Interactions During Decision-Making
Zhou, B., Moorman, D. E., Behseta, S., Ombao, H., & Shahbaba, B. (2015) · Journal of the American Statistical Association · doi:10.1080/01621459.2015.1116988 · Cited by 8
Two frequency bands contain the most stimulus-related information in visual cortexPreprint
Lewis, C., Bosman, C. A., Brunet, N. M., Lima, B., Roberts, M. J., Womelsdorf, T., Weerd, P. D., Neuenschwander, S., Singer, W., & Fries, P. (2016) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/049718 · Cited by 7
Garrett, D. D., Epp, S. M., Perry, A., & Lindenberger, U. (2018) · Max Planck Digital Library · Cited by 7
A journey in ESN and LSTM visualisations on a language taskPreprint
Variengien, A., & Hinaut, X. (2020) · arXiv (Cornell University) · doi:10.48550/arxiv.2012.01748 · Cited by 13
Abstract representations emerge naturally in neural networks trained to perform multiple tasksPreprint
Johnston, W. J., & Fusi, S. (2021) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2021.10.20.465187 · Cited by 7
Self-citationThe Prefrontal Cortex and Human MemoryPreprint
Diamond, N. B., & Levine, B. (2018) · PsyArXiv (OSF Preprints) · doi:10.31234/osf.io/u9hgx · Cited by 8
Low-dimensional neural manifolds for the control of constrained and unconstrained movementsPreprint
Altan, E., Ma, X., Miller, L. E., Perreault, E. J., & Solla, S. A. (2023) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2023.05.25.542264 · Cited by 7
Anatomically distributed neural representations of instincts in the hypothalamusPreprint
Stagkourakis, S., Spigolon, G., Marks, M., Feyder, M. T., Kim, J. H., Perona, P., Pachitariu, M., & Anderson, D. J. (2023) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2023.11.21.568163 · Cited by 7
Somashekar, B. P., & Bhalla, U. S. (2024) · eLife · doi:10.7554/elife.100664 · Cited by 7
Park, J., Holmes, C. D., & Snyder, L. H. (2025) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2025.02.25.640211 · Cited by 9
Hippocampal-cortical interactions in the consolidation of social memory
Park, G., Kim, M. S., Lee, Y., Shin, S., Kim, S. J., Kim, S. J., Lee, Y., & Lee, Y. (2025) · Nature Communications · doi:10.1038/s41467-025-64264-7 · Cited by 7
Konoike, N., Iwaoki, H., & Nakamura, K. (2020) · Frontiers in Behavioral Neuroscience · doi:10.3389/fnbeh.2020.00156 · Cited by 6
Functional connectivity in people at clinical and familial high risk for schizophrenia
Zhang, J., Yang, Y., Liu, T., Shi, Z., Pei, G., Wang, L., Wu, J., Funahashi, S., Suo, D., Wang, C., et al. (2023) · Psychiatry Research · doi:10.1016/j.psychres.2023.115464 · Cited by 6
Bayones, L., Zainos, A., Álvarez, M., Romo, R., Franci, A., & Rossi-Pool, R. (2024) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.2316765121 · Cited by 8
Dynamic coding and sequential integration of multiple reward attributes by primate amygdala neurons
Fabian Grabenhorst, B., & Báez-Mendoza, R. (2025) · Nature Communications · doi:10.1038/s41467-025-58270-y · Cited by 6
Roth, N., & Rust, N. C. (2018) · Journal of Neurophysiology · doi:10.1152/jn.00503.2018 · Cited by 6
Self-Attention Meta-Learner for Continual Learning
Sokar, G., Mocanu, D. C., & Pechenizkiy, M. (2021) · Adaptive Agents and Multi-Agents Systems · doi:10.65109/scpy1898 · Cited by 6
Mouse frontal cortex nonlinearly encodes stimuli, choices, and outcomes
Wool, L. E., Lak, A., Carandini, M., & Harris, K. D. (2023) · Wellcome Open Research · doi:10.12688/wellcomeopenres.19693.1 · Cited by 8
Event-specific and persistent representations for contextual states in orbitofrontal neurons
Ma, F., Zhang, L., & Zhou, J. (2024) · Current Biology · doi:10.1016/j.cub.2024.01.060 · Cited by 6
Lee, N., Guo, L. L., Nestor, A., & Niemeier, M. (2024) · Journal of Neuroscience · doi:10.1523/jneurosci.2100-23.2024 · Cited by 6
Cowley, B. R., Kaufman, M. T., Churchland, M. M., Ryu, S. I., Shenoy, K. V., & Yu, B. M. (2012) · Annual International Conference of the IEEE Engineering in Medicine and Biology Society (EMBC) · doi:10.1109/embc.2012.6346993 · Cited by 6
Kuroki, S., & Isomura, T. (2018) · Frontiers in Computational Neuroscience · doi:10.3389/fncom.2018.00083 · Cited by 6
Friedman, R. (2020) · AIMS neuroscience · doi:10.3934/neuroscience.2020023 · Cited by 6
A nonlinear hidden layer enables actor–critic agents to learn multiple paired association navigation
Ganeshkumar, M., Tan, C., Libedinsky, C., Yen, S., & Tan, A. Y. Y. (2021) · Cerebral Cortex · doi:10.1093/cercor/bhab456 · Cited by 8
Feature-based attention processes in primate prefrontal cortex do not rely on feature similarity
Stalter, M., Westendorff, S., & Nieder, A. (2021) · Cell Reports · doi:10.1016/j.celrep.2021.109470 · Cited by 6
Low-Dimensional Dynamics of Brain Activity Associated with Manual Acupuncture in Healthy Subjects
Guo, X., & Wang, J. (2021) · Sensors · doi:10.3390/s21227432 · Cited by 6
Nee, D. E., & D'Esposito, M. (2015) · Elsevier eBooks · doi:10.1016/b978-0-12-397025-1.00050-6 · Cited by 6
Digital computing through randomness and order in neural networks
Pitti, A., Weidmann, C., & Quoy, M. (2022) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.2115335119 · Cited by 8
Appetitive and Aversive Systems in the Amygdala
Bernardi, S., & Salzman, D. (2016) · Elsevier eBooks · doi:10.1016/b978-0-12-805308-9.00003-8 · Cited by 6
Estimating the dimensionality of neural responses with fMRI Repetition SuppressionPreprint
Rigotti, M., & Fusi, S. (2016) · arXiv (Cornell University) · doi:10.48550/arxiv.1605.03952 · Cited by 6
Self-citationControl of Functional Connectivity in Cerebral Cortex by Basal Ganglia Mediated SynchronizationPreprint
Pouzzner, D. (2017) · arXiv (Cornell University) · doi:10.48550/arxiv.1708.00779 · Cited by 6
Inhibitory control of frontal metastability sets the temporal signature of cognitionPreprint
Fontanier, V., Sarazin, M., Stoll, F. M., Delord, B., & Procyk, E. (2020) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2020.08.20.259192 · Cited by 6
Effects of noise and metabolic cost on cortical task representationsPreprint
Stroud, J. P., Wójcik, M. J., Jensen, K. T., Kusunoki, M., Kadohisa, M., Buckley, M. J., Duncan, J., Stokes, M. G., & Lengyel, M. (2024) · eLife · doi:10.7554/elife.94961 · Cited by 7
Future movement plans interact in sequential arm movementsPreprint
Kashefi, M., Reschechtko, S., Ariani, G., Shahbazi, M., Tan, A., Diedrichsen, J., & Pruszynski, J. A. (2024) · eLife · doi:10.7554/elife.94485.2 · Cited by 6
Hue tuning curves in V4 change with visual contextPreprint
Benjamin, A. S., Ramkumar, P., Fernandes, H. L., Smith, M., & Kording, K. P. (2019) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/780478 · Cited by 6
Hierarchical sensory processing in zebrafish thalamocortical-like circuits
Trinh, A.-T., Ostenrath, A. M., del Castillo-Berges, I., Cachin, F., Koç, M., Kraus, S., Serneels, B., Kawakami, K., & Yaksi, E. (2026) · Science · doi:10.1126/science.aec2171 · Cited by 5
Hwang, S.-H., Lee, J.-W., Kim, S.-P., & Kim, H. F. (2025) · Nature Communications · doi:10.1038/s41467-025-63822-3 · Cited by 5
Causal Spike Timing-Dependent Plasticity Prevents Assembly Fusion in Recurrent Networks
Yang, X., & Doiron, B. (2025) · PRX Life · doi:10.1103/9nv2-y63v · Cited by 6
Osako, Y., Heller, G. R., Ährlund‐Richter, S., Buschman, T. J., & Sur, M. (2026) · Nature Neuroscience · doi:10.1038/s41593-026-02410-0 · Cited by 6
Metadata
- Authors
- Rigotti, M., Barak, O., Warden, M. R., Wang, X.-J., Daw, N. D., Miller, E. K., & Fusi, S.
- Affiliations
- Columbia University Irving Medical Center (US)
- Massachusetts Institute of Technology (US)
- Yale University (US)
- New York University (US)
- Corresponding author
- Fusi, Stefano
- ORCID
- Venue
- Nature
- Published
- 2013-05
- Volume
- 497
- Issue
- 7451
- Pages
- 585-590
- ISSN
- 0028-0836 (ISSN-L)
- 1476-4687
- PMC
- PMC4412347
- OpenAlex
- W2033708181
- Cited by
- 1,639
- References
- 24
- Citations by year
- 2026: 146 · 2025: 171 · 2024: 220 · 2023: 149 · 2022: 139 · 2021: 143 · 2020: 110 · 2019: 104 · 2018: 106 · 2017: 102 · 2016: 101 · 2015: 66 · 2014: 65 · 2013: 14
- FWCI
- 44.98
- Type
- journal article
- Language
- en
- Open access
- green
- www.ncbi.nlm.nih.gov
- Licence
- www.springer.com/tdm (tdm)
- Locations
- Nature (publishedVersion)
- PubMed (publishedVersion)
- PubMed Central (acceptedVersion)
- RePEc: Research Papers in Economics (submittedVersion)
- DSpace@MIT (Massachusetts Institute of Technology) (submittedVersion, cc-by-nc)
- PMC
- Funders
- Schweizerischer Nationalfonds zur Förderung der Wissenschaftlichen Forschung (133357)
- National Institute of Mental Health (R01MH091174, R37MH087027, 5-R37-MH087027-04)
- Topics
- Life Sciences › Neuroscience › Cognitive Neuroscience › Neural dynamics and brain function
- Life Sciences › Neuroscience › Cognitive Neuroscience › Memory and Neural Mechanisms
- Life Sciences › Neuroscience › Cognitive Neuroscience › Neural and Behavioral Psychology Studies
- Keywords
- mixed selectivity, prefrontal cortex, single-unit activity, population coding, error trials
- MeSH terms
- Animals, Haplorhini, Behavior, Animal, Cognition, Memory, Models, Neurological, Neurons, Prefrontal Cortex, Single-Cell Analysis
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