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From Distributed Resources to Limited Slots in Multiple-Item Working Memory: A Spiking Network Model with Normalization
Open accessAbstract
Recent behavioral studies have given rise to two contrasting models for limited working memory capacity: a “discrete-slot” model in which memory items are stored in a limited number of slots, and a “shared-resource” model in which the neural representation of items is distributed across a limited pool of resources. To elucidate the underlying neural processes, we investigated a continuous network model for working memory of an analog feature. Our model network fundamentally operates with a shared resource mechanism, and stimuli in cue arrays are encoded by a distributed neural population. On the other hand, the network dynamics and performance are also consistent with the discrete-slot model, because multiple objects are maintained by distinct localized population persistent activity patterns (bump attractors). We identified two phenomena of recurrent circuit dynamics that give rise to limited working memory capacity. As the working memory load increases, a localized persistent activity bump may either fade out (so the memory of the corresponding item is lost) or merge with another nearby bump (hence the resolution of mnemonic representation for the merged items becomes blurred). We identified specific dependences of these two phenomena on the strength and tuning of recurrent synaptic excitation, as well as network normalization: the overall population activity is invariant to set size and delay duration; therefore, a constant neural resource is shared by and dynamically allocated to the memorized items. We demonstrate that the model reproduces salient observations predicted by both discrete-slot and shared-resource models, and propose testable predictions of the merging phenomenon.
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“Computational models suggest that the maintenance of multiple items within a WM circuit depends on the strength of lateral inhibition (Edin et al. 2009) and on the ability to keep activity patterns separated from each other (Wei et al. 2012).”
From Linking microcircuit dysfunction to cognitive impairment: Effects of disinhibition associated with schizophrenia in a cortical working memory model (2014) · cites this paper as Wei et al. 2012
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1 retracted
Precision in Visual Working Memory Reaches a Stable Plateau When Individual Item Limits Are Exceeded
Anderson, D. E., Vogel, E. K., & Awh, E. (2011) · Journal of Neuroscience · doi:10.1523/jneurosci.4125-10.2011 · Cited by 151
RetractedThe magical number seven, plus or minus two: Some limits on our capacity for processing information.
Miller, G. A. (1956) · Psychological Review · doi:10.1037/h0043158 · Cited by 17,812
The magical number seven, plus or minus two: Some limits on our capacity for processing information.
Miller, G. A. (1994) · Psychological Review · doi:10.1037/0033-295x.101.2.343 · Cited by 17,559
Baddeley, A. (1992) · Science · doi:10.1126/science.1736359 · Cited by 5,258
The capacity of visual working memory for features and conjunctions
Luck, S. J., & Vogel, E. K. (1997) · Nature · doi:10.1038/36846 · Cited by 4,250
Mnemonic coding of visual space in the monkey's dorsolateral prefrontal cortex
Funahashi, S., Bruce, C. J., & Goldman-Rakic, P. S. (1989) · Journal of Neurophysiology · doi:10.1152/jn.1989.61.2.331 · Cited by 2,685
Cellular basis of working memory
Goldman-Rakic, P. S. (1995) · Neuron · doi:10.1016/0896-6273(95)90304-6 · Cited by 2,663
Statistical Analysis of Circular Data.
LANGE, N. D., & Fisher, N. I. (1995) · Journal of the American Statistical Association · doi:10.2307/2291098 · Cited by 2,155
Statistical Analysis of Circular Data
Fisher, N. I. (1993) · Cambridge University Press eBooks · doi:10.1017/cbo9780511564345 · Cited by 1,826
Discrete fixed-resolution representations in visual working memory
Zhang, W., & Luck, S. J. (2008) · Nature · doi:10.1038/nature06860 · Cited by 1,624
Research works printed but not linked: 1
- 10.1037/0096-1523.27.1.92 · DOI
Cited by
Sorted by citations
Changing concepts of working memory
Ma, W. J., Husain, M., & Bays, P. M. (2014) · Nature Neuroscience · doi:10.1038/nn.3655 · Cited by 1,208
Visual working memory capacity: from psychophysics and neurobiology to individual differences
Luck, S. J., & Vogel, E. K. (2013) · Trends in Cognitive Sciences · doi:10.1016/j.tics.2013.06.006 · Cited by 1,167
Wang, X., & Krystal, J. H. (2014) · Neuron · doi:10.1016/j.neuron.2014.10.018 · Cited by 326
Self-citationWorking models of working memory
Barak, O., & Tsodyks, M. V. (2013) · Current Opinion in Neurobiology · doi:10.1016/j.conb.2013.10.008 · Cited by 297
Murray, J. D., Anticevic, A., Gancsos, M., Ichinose, M., Corlett, P. R., Krystal, J. H., & Wang, X.-J. (2014) · Cerebral Cortex · doi:10.1093/cercor/bhs370 · Cited by 255
Self-citationNeural Architecture for Feature Binding in Visual Working Memory
Schneegans, S., & Bays, P. M. (2017) · Journal of Neuroscience · doi:10.1523/jneurosci.3493-16.2017 · Cited by 249
Serial dependence is absent at the time of perception but increases in visual working memory
Bliss, D. P., Sun, J. J., & D’Esposito, M. (2017) · Scientific Reports · doi:10.1038/s41598-017-15199-7 · Cited by 233
Rapid Forgetting Prevented by Retrospective Attention Cues
Pertzov, Y., Bays, P., Joseph, S., & Husain, M. (2012) · Journal of Experimental Psychology: Human Perception and Performance · doi:10.1037/a0030947 · Cited by 237
Spikes not slots: noise in neural populations limits working memory
Bays, P. M. (2015) · Trends in Cognitive Sciences · doi:10.1016/j.tics.2015.06.004 · Cited by 190
Oscillatory multiplexing of neural population codes for interval timing and working memory
Gu, B.-M., van Rijn, H., & Meck, W. H. (2014) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2014.10.008 · Cited by 164
Neural mechanisms of attending to items in working memory
Manohar, S., Zokaei, N., Fallon, S. J., Vogels, T. P., & Husain, M. (2019) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2019.03.017 · Cited by 156
Interactions between visual working memory representations
Bae, G., & Luck, S. J. (2017) · Attention Perception & Psychophysics · doi:10.3758/s13414-017-1404-8 · Cited by 132
Chunking as a rational strategy for lossy data compression in visual working memory.
Nassar, M. R., Helmers, J. C., & Frank, M. J. (2018) · Psychological Review · doi:10.1037/rev0000101 · Cited by 123
Yoon, J. H., Grandelis, A., & Maddock, R. J. (2016) · Journal of Neuroscience · doi:10.1523/jneurosci.1970-16.2016 · Cited by 130
The binding pool: A model of shared neural resources for distinct items in visual working memory
Swan, G. S., & Wyble, B. (2014) · Attention Perception & Psychophysics · doi:10.3758/s13414-014-0633-3 · Cited by 119
Synaptic Correlates of Working Memory Capacity
Mi, Y., Katkov, M., & Tsodyks, M. V. (2016) · Neuron · doi:10.1016/j.neuron.2016.12.004 · Cited by 116
The effects of delay duration on visual working memory for orientation
Shin, H., Zou, Q., & Ma, W. J. (2017) · Journal of Vision · doi:10.1167/17.14.10 · Cited by 102
Exploring brain-behavior relationships in the N-back task
Lamichhane, B., Westbrook, A., Cole, M. W., & Braver, T. S. (2020) · NeuroImage · doi:10.1016/j.neuroimage.2020.116683 · Cited by 117
No Evidence for an Item Limit in Change Detection
Keshvari, S., van den Berg, R., & Ma, W. J. (2013) · PLoS Computational Biology · doi:10.1371/journal.pcbi.1002927 · Cited by 100
50 years of mnemonic persistent activity: quo vadis?
Wang, X. (2021) · Trends in Neurosciences · doi:10.1016/j.tins.2021.09.001 · Cited by 106
Self-citationAn integrative account of constraints on cross-situational learning
Yurovsky, D., & Frank, M. C. (2015) · Cognition · doi:10.1016/j.cognition.2015.07.013 · Cited by 97
Jadi, M. P., Behabadi, B. F., Poleg-Polsky, A., Schiller, J., & Mel, B. W. (2014) · Proceedings of the IEEE · doi:10.1109/jproc.2014.2312671 · Cited by 96
Seeholzer, A., Deger, M., & Wulfram Gerstner, B. (2019) · PLoS Computational Biology · doi:10.1371/journal.pcbi.1006928 · Cited by 93
Causal Evidence for a Privileged Working Memory State in Early Visual Cortex
Zokaei, N., Manohar, S., Masud Husain, B., & Feredoes, E. A. (2013) · Journal of Neuroscience · doi:10.1523/jneurosci.2899-13.2014 · Cited by 91
Flexible frequency control of cortical oscillations enables computations required for working memory
Dipoppa, M., & Gutkin, B. S. (2013) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1303270110 · Cited by 96
Drift in Neural Population Activity Causes Working Memory to Deteriorate Over Time
Schneegans, S., & Bays, P. M. (2018) · Journal of Neuroscience · doi:10.1523/jneurosci.3440-17.2018 · Cited by 86
A resource-rational theory of set size effects in human visual working memory
van den Berg, R., & Ma, W. J. (2018) · eLife · doi:10.7554/elife.34963 · Cited by 90
Stochastic sampling provides a unifying account of visual working memory limits
Schneegans, S., Taylor, R. T., & Bays, P. M. (2020) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.2004306117 · Cited by 82
The limited capacity model of motivated mediated message processing: looking to the future
Fisher, J. T., Huskey, R., Keene, J. R., & Weber, R. (2018) · Annals of the International Communication Association · doi:10.1080/23808985.2018.1534551 · Cited by 95
Representation and computation in visual working memory
Bays, P. M., Schneegans, S., Ma, W. J., & Brady, T. F. (2024) · Nature Human Behaviour · doi:10.1038/s41562-024-01871-2 · Cited by 116
Neural circuit basis of visuo-spatial working memory precision: a computational and behavioral study
Almeida, R., Barbosa, J., & Compte, A. (2015) · Journal of Neurophysiology · doi:10.1152/jn.00362.2015 · Cited by 72
Rademaker, R. L., Park, Y. E., Sack, A. T., & Tong, F. (2018) · Journal of Experimental Psychology Human Perception & Performance · doi:10.1037/xhp0000491 · Cited by 67
An adaptive perspective on visual working memory distortions.
Chunharas, C., Rademaker, R. L., Brady, T. F., & Serences, J. T. (2022) · Journal of Experimental Psychology General · doi:10.1037/xge0001191 · Cited by 71
Jones, K. T., Peterson, D. J., Blacker, K. J., & Berryhill, M. E. (2017) · Brain Research · doi:10.1016/j.brainres.2017.05.005 · Cited by 68
Flexibility of representational states in working memory
Zokaei, N., Ning, S., Manohar, S., Feredoes, E. A., & Masud Husain, B. (2014) · Frontiers in Human Neuroscience · doi:10.3389/fnhum.2014.00853 · Cited by 65
Optimizing Working Memory with Heterogeneity of Recurrent Cortical Excitation
Kilpatrick, Z. P., Ermentrout, B., & Doiron, B. (2013) · Journal of Neuroscience · doi:10.1523/jneurosci.1641-13.2013 · Cited by 63
Serotonin Regulates Performance Nonmonotonically in a Spatial Working Memory Network
Cano-Colino, M., Almeida, R., Gómez-Cabrero, D., Artigas, F., & Compte, A. (2013) · Cerebral Cortex · doi:10.1093/cercor/bht096 · Cited by 58
Heeger, D. J., & Mackey, W. E. (2019) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1911633116 · Cited by 56
Holding Multiple Items in Short Term Memory: A Neural Mechanism
Rolls, E. T., Dempere‐Marco, L., & Deco, G. (2013) · PLoS ONE · doi:10.1371/journal.pone.0061078 · Cited by 54
Restoration of fMRI Decodability Does Not Imply Latent Working Memory States
Schneegans, S., & Bays, P. M. (2017) · Journal of Cognitive Neuroscience · doi:10.1162/jocn_a_01180 · Cited by 55
Bae, G. (2021) · NeuroImage · doi:10.1016/j.neuroimage.2021.118366 · Cited by 54
Efficient Coding in Visual Working Memory Accounts for Stimulus-Specific Variations in Recall
Taylor, R. T., & Bays, P. M. (2018) · Journal of Neuroscience · doi:10.1523/jneurosci.1018-18.2018 · Cited by 53
Synaptic mechanisms of interference in working memory
Kilpatrick, Z. P. (2018) · Scientific Reports · doi:10.1038/s41598-018-25958-9 · Cited by 52
Working Memory Load Modulates Neuronal Coupling
Pinotsis, D. A., Buschman, T. J., & Miller, E. K. (2018) · Cerebral Cortex · doi:10.1093/cercor/bhy065 · Cited by 56
Selecting and tracking multiple objects
Scimeca, J. M., & Franconeri, S. (2014) · Wiley Interdisciplinary Reviews Cognitive Science · doi:10.1002/wcs.1328 · Cited by 50
Mechanisms of Winner-Take-All and Group Selection in Neuronal Spiking Networks
Chen, Y. (2017) · Frontiers in Computational Neuroscience · doi:10.3389/fncom.2017.00020 · Cited by 48
Klink, P. C., Jeurissen, D., Theeuwes, J., Denys, D. A. J. P., & Roelfsema, P. R. (2017) · Scientific Reports · doi:10.1038/s41598-017-08608-4 · Cited by 50
A Probabilistic Palimpsest Model of Visual Short-term Memory
Matthey, L., Bays, P. M., & Dayan, P. (2015) · PLoS Computational Biology · doi:10.1371/journal.pcbi.1004003 · Cited by 51
Balanced Cortical Microcircuitry for Spatial Working Memory Based on Corrective Feedback Control
Lim, S., & Goldman, M. S. (2014) · Journal of Neuroscience · doi:10.1523/jneurosci.4602-13.2014 · Cited by 44
A neural model of retrospective attention in visual working memory
Bays, P. M., & Taylor, R. T. (2017) · Cognitive Psychology · doi:10.1016/j.cogpsych.2017.12.001 · Cited by 44
Brain works principle followed by neural information processing: a review of novel brain theory
Wang, R., Wang, Y., Xu, X., Li, Y., & Pan, X. (2023) · Artificial Intelligence Review · doi:10.1007/s10462-023-10520-5 · Cited by 43
Object tracking: Absence of long-range spatial interference supports resource theories
Holcombe, A. O., Chen, W.-Y., & Howe, P. D. L. (2014) · Journal of Vision · doi:10.1167/14.6.1 · Cited by 41
Visual working memory items drift apart due to active, not passive, maintenance.
Scotti, P. S., Hong, Y., Leber, A. B., & Golomb, J. D. (2021) · Journal of Experimental Psychology General · doi:10.1037/xge0000890 · Cited by 40
Fallon, S. J., Mattiesing, R. M., Muhammed, K., Manohar, S., & Masud Husain, B. (2017) · Cerebral Cortex · doi:10.1093/cercor/bhx242 · Cited by 39
Pereira, J., & Wang, X. (2014) · Cerebral Cortex · doi:10.1093/cercor/bhu202 · Cited by 36
Self-citationMultiple and Dissociable Effects of Sensory History on Working-Memory Performance
Hajonides, J. E., van Ede, F., Stokes, M. G., Nobre, A. C., & Myers, N. E. (2023) · Journal of Neuroscience · doi:10.1523/jneurosci.1200-22.2023 · Cited by 41
Simple measurement models for complex working-memory tasks.
Oberauer, K., & Lewandowsky, S. (2019) · Psychological Review · doi:10.1037/rev0000159 · Cited by 40
Beyond slots and resources: Grounding cognitive concepts in neural dynamics
Johnson, J. S., Simmering, V. R., & Buss, A. T. (2013) · Attention Perception & Psychophysics · doi:10.3758/s13414-013-0596-9 · Cited by 40
Neural antagonistic mechanism between default-mode and task-positive networks
Cheng, X., Yuan, Y., Wang, Y., & Wang, R. (2020) · Neurocomputing · doi:10.1016/j.neucom.2020.07.079 · Cited by 39
Serotonergic modulation of spatial working memory: predictions from a computational network model
Cano-Colino, M., Almeida, R., & Compte, A. (2013) · Frontiers in Integrative Neuroscience · doi:10.3389/fnint.2013.00071 · Cited by 34
Independent working memory resources for egocentric and allocentric spatial information
Aagten‐Murphy, D., & Bays, P. M. (2019) · PLoS Computational Biology · doi:10.1371/journal.pcbi.1006563 · Cited by 33
Representation and computation in working memoryPreprint
Bays, P. M., Schneegans, S., Ma, W. J., & Brady, T. F. (2022) · doi:10.31234/osf.io/kubr9 · Cited by 31
Koyluoglu, O. O., Pertzov, Y., Manohar, S., Husain, M., & Fiete, I. (2017) · eLife · doi:10.7554/elife.22225 · Cited by 28
Bliss, D. P., & D’Esposito, M. (2017) · PLoS ONE · doi:10.1371/journal.pone.0188927 · Cited by 27
Biophysical mechanism of the interaction between default mode network and working memory network
Yuan, Y., Pan, X., & Wang, R. (2021) · Cognitive Neurodynamics · doi:10.1007/s11571-021-09674-1 · Cited by 26
Controlling Working Memory Operations by Selective Gating: The Roles of Oscillations and Synchrony
Dipoppa, M., Marcin Szwed, A., & Gutkin, B. S. (2016) · Advances in Cognitive Psychology · doi:10.5709/acp-0199-x · Cited by 26
Towards biologically constrained attractor models of schizophrenia
Stein, H., Barbosa, J., & Compte, A. (2021) · Current Opinion in Neurobiology · doi:10.1016/j.conb.2021.10.013 · Cited by 27
Matsushima, A., & Tanaka, M. (2014) · Journal of Neuroscience · doi:10.1523/jneurosci.0295-14.2014 · Cited by 24
An interference model for visual working memory: Applications to the change detection task
Lin, H.-Y., & Oberauer, K. (2022) · Cognitive Psychology · doi:10.1016/j.cogpsych.2022.101463 · Cited by 25
Reward influences the allocation but not the availability of resources in visual working memory.
Brissenden, J. A., Adkins, T. J., Hsu, Y. T., & Lee, T. G. (2023) · Journal of Experimental Psychology General · doi:10.1037/xge0001370 · Cited by 25
Simmering, V. R., Miller, H. E., & Bohache, K. (2015) · Attention Perception & Psychophysics · doi:10.3758/s13414-015-0832-6 · Cited by 24
Competitive interactions in visual working memory drive access to awareness
van Moorselaar, D., Gayet, S., Paffen, C. L. E., Theeuwes, J., der Stigchel, S. V., & Olivers, C. N. L. (2017) · Cortex · doi:10.1016/j.cortex.2017.03.026 · Cited by 22
Setting and changing feature priorities in visual short-term memory
Kalogeropoulou, Z., Jagadeesh, A. V., Ohl, S., & Rolfs, M. (2016) · Psychonomic Bulletin & Review · doi:10.3758/s13423-016-1094-6 · Cited by 21
Scene memory and spatial inhibition in visual search
Grieben, R., Tekülve, J., Zibner, S. K. U., Lins, J., Schneegans, S., & Schöner, G. (2020) · Attention Perception & Psychophysics · doi:10.3758/s13414-019-01898-y · Cited by 25
Trade-off between Capacity and Precision in Visuospatial Working Memory
Roggeman, C., Klingberg, T., Feenstra, H. E. M., Compte, A., & Almeida, R. (2013) · Journal of Cognitive Neuroscience · doi:10.1162/jocn_a_00485 · Cited by 19
Avery, M. C., Dutt, N. D., & Krichmar, J. L. (2013) · Frontiers in Computational Neuroscience · doi:10.3389/fncom.2013.00133 · Cited by 22
Cortical Circuit Models in Psychiatry
Murray, J. D., & Wang, X. (2017) · Elsevier eBooks · doi:10.1016/b978-0-12-809825-7.00001-8 · Cited by 19
Self-citationWilsenach, C., & Makaure, P. (2018) · South African Journal of Childhood Education · doi:10.4102/sajce.v8i1.546 · Cited by 17
Ibañez, S., Luebke, J. I., Chang, W., Draguljić, D., & Weaver, C. M. (2020) · Frontiers in Computational Neuroscience · doi:10.3389/fncom.2019.00089 · Cited by 13
Visual working memory organization is subject to top-down control
van Lamsweerde, A. E., Beck, M. R., & Johnson, J. S. (2015) · Psychonomic Bulletin & Review · doi:10.3758/s13423-015-0976-3 · Cited by 16
Accessibility limits recall from visual working memory.
Rajsic, J., Swan, G. S., Wilson, D. E., & Pratt, J. (2017) · Journal of Experimental Psychology Learning Memory and Cognition · doi:10.1037/xlm0000387 · Cited by 16
An interference model for visual and verbal working memory.
Oberauer, K., & Lin, H.-Y. (2023) · Journal of Experimental Psychology Learning Memory and Cognition · doi:10.1037/xlm0001303 · Cited by 23
Spatiotemporal encoding of search strategies by prefrontal neurons
Chiang, F.-K., & Wallis, J. D. (2018) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1805044115 · Cited by 13
Buss, A. T., Magnotta, V. A., Penny, W. D., Schöner, G., Huppert, T. J., & Spencer, J. P. (2021) · Psychological Review · doi:10.1037/rev0000264 · Cited by 12
Active Working Memory and Simple Cognitive Operations
Kreither, J., Papaioannou, O., & Luck, S. J. (2021) · Journal of Cognitive Neuroscience · doi:10.1162/jocn_a_01791 · Cited by 12
Strategy-dependent effects of working-memory limitations on human perceptual decision-making
Schapiro, K. A., Josić́, K., Kilpatrick, Z. P., & Gold, J. I. (2022) · eLife · doi:10.7554/elife.73610 · Cited by 13
Testing a dynamic-field account of interactions between spatial attention and spatial working memory
Johnson, J. S., & Spencer, J. P. (2016) · Attention Perception & Psychophysics · doi:10.3758/s13414-015-1058-3 · Cited by 12
Synaptic efficacy shapes resource limitations in working memory
Krishnan, N. P., Poll, D. B., & Kilpatrick, Z. P. (2018) · Journal of Computational Neuroscience · doi:10.1007/s10827-018-0679-7 · Cited by 13
A dynamic neural field model of continuous input integration
Wojtak, W., Coombes, S., Avitabile, D., Bicho, E. G., & Erlhagen, W. (2021) · Biological Cybernetics · doi:10.1007/s00422-021-00893-7 · Cited by 11
Joyce, M. K. P., Ivanov, T. G., Krienen, F. M., Mitchell, J. F., Ma, S., Inoue, W., Nandy, A. S., Datta, D., Duque, A., Arellano, J. I., et al. (2025) · Communications Biology · doi:10.1038/s42003-025-08297-0 · Cited by 13
Dynamics of Multiple-Choice Decision Making
You, H., & Wang, D. (2013) · Neural Computation · doi:10.1162/neco_a_00473 · Cited by 11
Self-citationAdaptive memory distortion in visual working memoryPreprint
Chunharas, C., Rademaker, R. L., Brady, T. F., & Serences, J. T. (2019) · doi:10.31234/osf.io/e3m5a · Cited by 13
An interference model for visual and verbal working memoryPreprint
Oberauer, K., & Lin, H.-Y. (2023) · doi:10.31234/osf.io/eyknx · Cited by 11
On memories, neural ensembles and mental flexibility
Pinotsis, D. A., Brincat, S. L., & Miller, E. K. (2017) · NeuroImage · doi:10.1016/j.neuroimage.2017.05.068 · Cited by 10
Multiple bumps can enhance robustness to noise in continuous attractor networks
Wang, R., & Kang, L. (2022) · PLoS Computational Biology · doi:10.1371/journal.pcbi.1010547 · Cited by 10
Johnson, J. S., van Lamsweerde, A. E., Dineva, E., & Spencer, J. P. (2022) · Scientific Reports · doi:10.1038/s41598-022-22328-4 · Cited by 10
Bhat, A. A., Spencer, J. P., & Samuelson, L. K. (2020) · doi:10.31219/osf.io/kxycs · Cited by 10
Nisar, K. S., Farman, M. T., Batool, M., & Xu, C. (2024) · Cogent Engineering · doi:10.1080/23311916.2023.2301161 · Cited by 9
Zhang, Q., Li, S., Wang, X., & Che, X. (2015) · Quarterly Journal of Experimental Psychology · doi:10.1080/17470218.2015.1100206 · Cited by 9
Self-citationSlot-like capacity and resource-like coding in a neural model of multiple-item working memory
Standage, D., & Paré, M. (2018) · Journal of Neurophysiology · doi:10.1152/jn.00778.2017 · Cited by 10
Metadata
- Authors
- Wei, Z., Wang, X.-J., & Wang, D.-H.
- Affiliations
- Howard Hughes Medical Institute (US)
- Yale University (US)
- Beijing Normal University (CN)
- Venue
- The Journal of Neuroscience
- Publisher
- Society for Neuroscience
- Published
- 2012-08-15
- Volume
- 32
- Issue
- 33
- Pages
- 11228-11240
- ISSN
- 0270-6474 (ISSN-L)
- 1529-2401
- PMC
- PMC3433498
- OpenAlex
- W1980372308
- Cited by
- 163
- References
- 65
- Citations by year
- 2026: 5 · 2025: 9 · 2024: 12 · 2023: 15 · 2022: 8 · 2021: 13 · 2020: 8 · 2019: 9 · 2018: 14 · 2017: 22 · 2016: 9 · 2015: 11 · 2014: 11 · 2013: 15 · 2012: 2
- FWCI
- 6.38
- Type
- journal article
- Language
- en
- Open access
- hybrid
- doi.org
- Licence
- Locations
- Journal of Neuroscience (publishedVersion, cc-by-nc-sa)
- Europe PMC (PubMed Central) (publishedVersion)
- PubMed Central (publishedVersion)
- PubMed (publishedVersion)
- Funders
- Howard Hughes Medical Institute
- Kavli Foundation
- National Natural Science Foundation of China (60974075, 91132702)
- Beijing Normal University
- National Institutes of Health
- Fundamental Research Funds for the Central Universities
- National Institute of Mental Health (MH 062349, R01MH062349)
- Topics
- Life Sciences › Neuroscience › Cognitive Neuroscience › Neural dynamics and brain function
- Life Sciences › Neuroscience › Cognitive Neuroscience › Memory and Neural Mechanisms
- Physical Sciences › Engineering › Electrical and Electronic Engineering › Advanced Memory and Neural Computing
- Keywords
- working memory, spiking neural networks, normalization, persistent activity, recurrent excitation, memory load, population coding
- MeSH terms
- Action Potentials, Attention, Computer Simulation, Cues, Humans, Memory, Short-Term, Models, Neurological, Neural Pathways, Neurons, Photic Stimulation, Psychophysics, Time Factors, Signal Detection, Psychological, 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 ›
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