The DOI matches its Crossref record; 40 of the 40 references it cites were found in a registry or an index.
Internally Generated Cell Assembly Sequences in the Rat Hippocampus
Open accessAbstract
A long-standing conjecture in neuroscience is that aspects of cognition depend on the brain's ability to self-generate sequential neuronal activity. We found that reliably and continually changing cell assemblies in the rat hippocampus appeared not only during spatial navigation but also in the absence of changing environmental or body-derived inputs. During the delay period of a memory task, each moment in time was characterized by the activity of a particular assembly of neurons. Identical initial conditions triggered a similar assembly sequence, whereas different conditions gave rise to different sequences, thereby predicting behavioral choices, including errors. Such sequences were not formed in control (nonmemory) tasks. We hypothesize that neuronal representations, evolved for encoding distance in spatial navigation, also support episodic recall and the planning of action sequences.
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?
In the citing paper
“In fact, the sequential activation of place cells is thought to reflect specific episodic-like memories, occurring across similar time scales to the actual experience, all while the rat is concurrently engaged in other activities (and thus is not confusing imagined representations with current reality) [127].”
From Is episodic-like memory like episodic memory? (2024) · cites this paper as [127]
In the citing paper
“evidence suggests that place cell activity in rats can also encode information about the ‘what’ (e.g. odours and their status, i.e. match/non-match [124–126]) and ‘when’ (i.e. elapsed time [127,128]) of events.”
From Is episodic-like memory like episodic memory? (2024) · cites this paper as [127]
In the citing paper
“recent remodelling of sharp-wave-ripple events suggests that this neuronal replay often occurs at ‘real-world’ speeds that reflect actual experience [185], as observed in other studies [127].”
From Is episodic-like memory like episodic memory? (2024) · cites this paper as [127]
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
(1978) · UA Campus Repository (The University of Arizona) · Cited by 8,010
The hippocampus as a spatial map. Preliminary evidence from unit activity in the freely-moving rat
O'Keefe, J., & Dostrovsky, J. (1971) · Brain Research · doi:10.1016/0006-8993(71)90358-1 · Cited by 6,151
(1983) · Medical Entomology and Zoology · Cited by 6,051
Memory and the hippocampus: A synthesis from findings with rats, monkeys, and humans.
Squire, L. R. (1992) · Psychological Review · doi:10.1037/0033-295x.99.2.195 · Cited by 5,376
The Organization of Behavior; A Neuropsychological Theory.
Attneave, F., B., M., & Hebb, D. O. (1950) · The American Journal of Psychology · doi:10.2307/1418888 · Cited by 5,146
Reactivation of hippocampal ensemble memories during sleep
Wilson, M. A., & McNaughton, B. L. (1994) · Science · doi:10.1126/science.8036517 · Cited by 3,118
Phase relationship between hippocampal place units and the EEG theta rhythm
O'Keefe, J. M., & Recce, M. L. (1993) · Hippocampus · doi:10.1002/hipo.450030307 · Cited by 2,643
Path integration and the neural basis of the 'cognitive map'
McNaughton, B. L., Battaglia, F. P., Jensen, O., Moser, E. I., & Moser, M.-B. (2006) · Nature Reviews Neuroscience · doi:10.1038/nrn1932 · Cited by 2,024
Two-stage model of memory trace formation: A role for “noisy” brain states
Buzsáki, G. (1989) · Neuroscience · doi:10.1016/0306-4522(89)90423-5 · Cited by 1,709
Self-citationAbbott, L. F., & Regehr, W. G. (2004) · Nature · doi:10.1038/nature03010 · Cited by 1,684
Research works printed but not linked: 1
- B. L. McNaughton, F. P. Battaglia, O. Jensen, E. I. Moser, M. B. Moser, Nat. Rev. Neurosci.7, 663 (2006).
Cited by
Sorted by citations
Hippocampal sharp wave-ripple: A cognitive biomarker for episodic memory and planning
Buzsáki, G. (2015) · Hippocampus · doi:10.1002/hipo.22488 · Cited by 1,759
Memory, navigation and theta rhythm in the hippocampal-entorhinal system
Buzsáki, G., & Moser, E. I. (2013) · Nature Neuroscience · doi:10.1038/nn.3304 · Cited by 1,847
Functional organization of the hippocampal longitudinal axis
Strange, B. A., Witter, M. P., Lein, E. S., & Moser, E. I. (2014) · Nature reviews. Neuroscience · doi:10.1038/nrn3785 · Cited by 1,738
Lisman, J. E., & Jensen, O. (2013) · Neuron · doi:10.1016/j.neuron.2013.03.007 · Cited by 1,609
Neural syntax: cell assemblies, synapsembles, and readers
Buzsáki, G. (2010) · Neuron · doi:10.1016/j.neuron.2010.09.023 · Cited by 1,289
Hippocampal ‘time cells’ bridge the gap in memory for discontiguous events
MacDonald, C. J., Lepage, K. Q., Eden, U. T., & Eichenbaum, H. (2011) · Neuron · doi:10.1016/j.neuron.2011.07.012 · Cited by 1,193
Creating a False Memory in the Hippocampus
Ramirez, S., Liu, X., Lin, P.-A., Suh, J., Pignatelli, M., Redondo, R. L., Ryan, T. J., & Tonegawa, S. (2013) · Science · doi:10.1126/science.1239073 · Cited by 968
Basso, J. C., & Suzuki, W. A. (2016) · Brain Plasticity · doi:10.3233/bpl-160040 · Cited by 911
Disruption of ripple‐associated hippocampal activity during rest impairs spatial learning in the rat
Ego‐Stengel, V., & Wilson, M. A. (2010) · Hippocampus · doi:10.1002/hipo.20707 · Cited by 842
Viewpoints: how the hippocampus contributes to memory, navigation and cognition
Lisman, J., Buzsáki, G., Eichenbaum, H., Nadel, L., Ranganath, C., & Redish, A. D. (2017) · Nature Neuroscience · doi:10.1038/nn.4661 · Cited by 851
Self-citationAwake replay of remote experiences in the hippocampus
Karlsson, M. P., & Frank, L. M. (2009) · Nature Neuroscience · doi:10.1038/nn.2344 · Cited by 769
Time cells in the hippocampus: a new dimension for mapping memories
Eichenbaum, H. (2014) · Nature Reviews Neuroscience · doi:10.1038/nrn3827 · Cited by 843
Evidence for grid cells in a human memory network
Doeller, C. F., Barry, C., & Burgess, N. (2010) · Nature · doi:10.1038/nature08704 · Cited by 828
Mapping of a non-spatial dimension by the hippocampal-entorhinal circuit
Aronov, D., Nevers, R., & Tank, D. W. (2017) · Nature · doi:10.1038/nature21692 · Cited by 773
Mizuseki, K., Sirota, A., Pastalkova, E., & Buzsáki, G. (2009) · Neuron · doi:10.1016/j.neuron.2009.08.037 · Cited by 718
Self-citationPreplay of future place cell sequences by hippocampal cellular assemblies
Dragoi, G., & Tonegawa, S. (2011) · Nature · doi:10.1038/nature09633 · Cited by 716
Evidence for the Default Network's Role in Spontaneous Cognition
Andrews-Hanna, J. R., Reidler, J. S., Huang, C., & Buckner, R. L. (2010) · Journal of Neurophysiology · doi:10.1152/jn.00830.2009 · Cited by 685
Ephaptic coupling of cortical neurons
Anastassiou, C. A., Perin, R., Markram, H., & Koch, C. (2011) · Nature Neuroscience · doi:10.1038/nn.2727 · Cited by 628
Navigating cognition: Spatial codes for human thinking
Bellmund, J. L. S., Gärdenfors, P., Moser, E. I., & Doeller, C. F. (2018) · Science · doi:10.1126/science.aat6766 · Cited by 643
Spatial representation in the hippocampal formation: a history
Moser, E. I., Moser, M.-B., & McNaughton, B. L. (2017) · Nature Neuroscience · doi:10.1038/nn.4653 · Cited by 560
Internally generated reactivation of single neurons in human hippocampus during free recall
Gelbard-Sagiv, H., Mukamel, R., Harel, M., Malach, R., & Fried, I. (2008) · Science · doi:10.1126/science.1164685 · Cited by 533
Space and Time: The Hippocampus as a Sequence Generator
Buzsáki, G., & Tingley, D. (2018) · Trends in Cognitive Sciences · doi:10.1016/j.tics.2018.07.006 · Cited by 461
A 4 Hz oscillation adaptively synchronizes prefrontal, VTA, and hippocampal activities
Fujisawa, S., & Buzsáki, G. (2011) · Neuron · doi:10.1016/j.neuron.2011.08.018 · Cited by 501
“Because such goal-predicting, ‘‘prospective,’’ or ‘‘episode’’ neurons have been suggested to be a part of the working-memory network (Wood et al., 2000; Frank et al., 2000; Fujisawa et al., 2008; Pastalkova et al., 2008), we examined their relationship with LFP oscillations and compared them with nonpredicting but act…”
InfluentialSelf-citationLong-duration hippocampal sharp wave ripples improve memory
Fernández-Ruiz, A., Oliva, A., Fermino de Oliveira, E., Rocha-Almeida, F., Tingley, D., & Buzsáki, G. (2019) · Science · doi:10.1126/science.aax0758 · Cited by 490
Self-citationIntegrating time from experience in the lateral entorhinal cortex
Tsao, A., Sugar, J., Lu, L., Wang, C., Knierim, J. J., Moser, M.-B., & Moser, E. I. (2018) · Nature · doi:10.1038/s41586-018-0459-6 · Cited by 490
Concept cells: the building blocks of declarative memory functions
Quiroga, R. Q. (2012) · Nature reviews. Neuroscience · doi:10.1038/nrn3251 · Cited by 472
Encoding of fear learning and memory in distributed neuronal circuits
Herry, C., & Johansen, J. P. (2014) · Nature Neuroscience · doi:10.1038/nn.3869 · Cited by 474
Theta Phase Segregation of Input-Specific Gamma Patterns in Entorhinal-Hippocampal Networks
Schomburg, E. W., Fernández-Ruiz, A., Mizuseki, K., Berényi, A., Anastassiou, C. A., Koch, C., & Buzsáki, G. (2014) · Neuron · doi:10.1016/j.neuron.2014.08.051 · Cited by 465
The role of the hippocampus in navigation is memory
Eichenbaum, H. (2017) · Journal of Neurophysiology · doi:10.1152/jn.00005.2017 · Cited by 430
The Role of the Hippocampus in Prediction and Imagination
Buckner, R. L. (2010) · Annual Review of Psychology · doi:10.1146/annurev.psych.60.110707.163508 · Cited by 419
Hippocampal theta sequences reflect current goals
Wikenheiser, A. M., & Redish, A. D. (2015) · Nature Neuroscience · doi:10.1038/nn.3909 · Cited by 367
Ranganath, C. (2010) · Hippocampus · doi:10.1002/hipo.20852 · Cited by 375
Robust Conjunctive Item–Place Coding by Hippocampal Neurons Parallels Learning What Happens Where
Komorowski, R. W., Manns, J. R., & Eichenbaum, H. (2009) · The Journal of Neuroscience · doi:10.1523/jneurosci.1378-09.2009 · Cited by 372
Memory without Feedback in a Neural Network
Goldman, M. S. (2009) · Neuron · doi:10.1016/j.neuron.2008.12.012 · Cited by 342
Towards a functional organization of episodic memory in the medial temporal lobe
Eichenbaum, H., Sauvage, M., Fortin, N., Komorowski, R., & Lipton, P. (2012) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2011.07.006 · Cited by 354
Neuronal code for extended time in the hippocampus
Mankin, E. A., Sparks, F. T., Slayyeh, B., Sutherland, R. J., Leutgeb, S., & Leutgeb, J. K. (2012) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1214107109 · Cited by 371
Inhibition-induced theta resonance in cortical circuits
Stark, E., Eichler, R., Roux, L., Fujisawa, S., Rotstein, H. G., & Buzsáki, G. (2013) · Neuron · doi:10.1016/j.neuron.2013.09.033 · Cited by 326
Oscillatory multiplexing of population codes for selective communication in the mammalian brain
Akam, T., & Kullmann, D. M. (2014) · Nature Reviews Neuroscience · doi:10.1038/nrn3668 · Cited by 327
Recurrent network models of sequence generation and memory
Rajan, K., Harvey, C. D., & Tank, D. W. (2016) · Neuron · doi:10.1016/j.neuron.2016.02.009 · Cited by 351
Fragmentation of grid cell maps in a multicompartment environment
Derdikman, D., Whitlock, J. R., Tsao, A., Fyhn, M., Hafting, T., Moser, M.-B., & Moser, E. I. (2009) · Nature Neuroscience · doi:10.1038/nn.2396 · Cited by 330
The evolution of episodic memory
Allen, T. A., & Fortin, N. J. (2013) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1301199110 · Cited by 350
Distinct hippocampal time cell sequences represent odor memories in immobilized rats
MacDonald, C. J., Carrow, S., Place, R., & Eichenbaum, H. (2013) · The Journal of Neuroscience · doi:10.1523/jneurosci.1537-13.2013 · Cited by 312
Hippocampal CA2 activity patterns change over time to a larger extent than between spatial contexts
Mankin, E. A., Diehl, G. W., Sparks, F. T., Leutgeb, S., & Leutgeb, J. K. (2015) · Neuron · doi:10.1016/j.neuron.2014.12.001 · Cited by 279
Structuring knowledge with cognitive maps and cognitive graphs
Peer, M., Brunec, I. K., Newcombe, N. S., & Epstein, R. A. (2021) · Trends in Cognitive Sciences · doi:10.1016/j.tics.2020.10.004 · Cited by 283
Sublayer-Specific Coding Dynamics during Spatial Navigation and Learning in Hippocampal Area CA1
Danielson, N. B., Zaremba, J. D., Kaifosh, P., Bowler, J., Ladow, M., & Losonczy, A. (2016) · Neuron · doi:10.1016/j.neuron.2016.06.020 · Cited by 288
Targeted Activation of Hippocampal Place Cells Drives Memory-Guided Spatial Behavior
Robinson, N. T. M., Descamps, L. A. L., Russell, L. E., Buchholz, M. O., Bicknell, B. A., Antonov, G. K., Lau, J. Y. N., Nutbrown, R., Schmidt-Hieber, C., & Häusser, M. (2020) · Cell · doi:10.1016/j.cell.2020.09.061 · Cited by 281
Integrating what and when across the primate medial temporal lobe
Naya, Y., & Suzuki, W. A. (2011) · Science · doi:10.1126/science.1206773 · Cited by 257
Functional, But Not Anatomical, Separation of “What” and “When” in Prefrontal Cortex
Machens, C. K., Romo, R., & Brody, C. D. (2010) · The Journal of Neuroscience · doi:10.1523/jneurosci.3276-09.2010 · Cited by 260
Memory: organization and control.
Eichenbaum, H. (2017) · Annual Review of Psychology · doi:10.1146/annurev-psych-010416-044131 · Cited by 257
The role of REM sleep theta activity in emotional memory
Hutchison, I. C., & Rathore, S. (2015) · Frontiers in Psychology · doi:10.3389/fpsyg.2015.01439 · Cited by 245
Internally generated sequences in learning and executing goal-directed behavior
Pezzulo, G., van der Meer, M. A. A., Lansink, C. S., & Pennartz, C. M. A. (2014) · Trends in Cognitive Sciences · doi:10.1016/j.tics.2014.06.011 · Cited by 217
Pattern separation, completion, and categorisation in the hippocampus and neocortex
Rolls, E. T. (2016) · Neurobiology of Learning and Memory · doi:10.1016/j.nlm.2015.07.008 · Cited by 234
Prediction and memory: A predictive coding account
Barron, H. C., Auksztulewicz, R., & Friston, K. (2020) · Progress in Neurobiology · doi:10.1016/j.pneurobio.2020.101821 · Cited by 220
Causal Influence of Visual Cues on Hippocampal Directional Selectivity
Acharya, L., Aghajan, Z. M., Vuong, C., Moore, J. J., & Mehta, M. R. (2016) · Cell · doi:10.1016/j.cell.2015.12.015 · Cited by 196
Influence of local objects on hippocampal representations: Landmark vectors and memory
Deshmukh, S. S., & Knierim, J. J. (2013) · Hippocampus · doi:10.1002/hipo.22101 · Cited by 217
Planning and navigation as active inference
Kaplan, R., & Friston, K. J. (2018) · Biological Cybernetics · doi:10.1007/s00422-018-0753-2 · Cited by 203
Dimsdale-Zucker, H. R., Ritchey, M., Ekstrom, A. D., Yonelinas, A. P., & Ranganath, C. (2018) · Nature Communications · doi:10.1038/s41467-017-02752-1 · Cited by 205
Mechanisms for widespread hippocampal involvement in cognition.
Shohamy, D., & Turk-Browne, N. B. (2013) · Journal of Experimental Psychology: General · doi:10.1037/a0034461 · Cited by 187
Coordinated grid and place cell replay during rest
Ólafsdóttir, H. F., Carpenter, F., & Barry, C. (2016) · Nature Neuroscience · doi:10.1038/nn.4291 · Cited by 175
Place cells are more strongly tied to landmarks in deep than in superficial CA1
Geiller, T., Fattahi, M., Choi, J.-S., & Royer, S. (2017) · Nature Communications · doi:10.1038/ncomms14531 · Cited by 163
Buzsáki, G., & Llinás, R. (2017) · Science · doi:10.1126/science.aan8869 · Cited by 175
Self-citationMemory trace replay: The shaping of memory consolidation by neuromodulation
Atherton, L. A., Dupret, D., & Mellor, J. R. (2015) · Trends in Neurosciences · doi:10.1016/j.tins.2015.07.004 · Cited by 180
Time cells in hippocampal area CA3
Salz, D. M., Tiganj, Z., Khasnabish, S., Kohley, A., Sheehan, D., Howard, M. W., & Eichenbaum, H. (2016) · Journal of Neuroscience · doi:10.1523/jneurosci.0087-16.2016 · Cited by 183
Attention-like modulation of hippocampus place cell discharge
Fenton, A. A., Lytton, W. W., Barry, J. M., Lenck-Santini, P.-P., Zinyuk, L. E., Kubík, Š., Bureš, J., Poucet, B., Muller, R. U., & Olypher, A. V. (2010) · The Journal of Neuroscience · doi:10.1523/jneurosci.5576-09.2010 · Cited by 170
Sleep and sensorimotor integration during early vocal learning in a songbird
Shank, S. S., & Margoliash, D. (2009) · Nature · doi:10.1038/nature07615 · Cited by 178
Hippocampus and retrosplenial cortex combine path integration signals for successful navigation
Sherrill, K. R., Erdem, U. M., Ross, R. S., Brown, T. I., Hasselmo, M. E., & Stern, C. E. (2013) · The Journal of Neuroscience · doi:10.1523/jneurosci.1825-13.2013 · Cited by 167
Spatial goal coding in the hippocampal formation
Nyberg, N., Duvelle, É., Barry, C., & Spiers, H. J. (2022) · Neuron · doi:10.1016/j.neuron.2021.12.012 · Cited by 141
Chao, O. Y., de Souza Silva, M. A., Yang, Y.-M., & Huston, J. P. (2020) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2020.04.007 · Cited by 158
A distributed representation of internal time
Howard, M. W., Shankar, K. H., Aue, W. R., & Criss, A. H. (2015) · Psychological Review · doi:10.1037/a0037840 · Cited by 133
Hippocampal neurons represent events as transferable units of experience
Sun, C., Yang, W., Martin, J., & Tonegawa, S. (2020) · Nature Neuroscience · doi:10.1038/s41593-020-0614-x · Cited by 135
Knierim, J. J., & Hamilton, D. A. (2011) · Physiological Reviews · doi:10.1152/physrev.00021.2010 · Cited by 148
Wandering tales: evolutionary origins of mental time travel and language
Corballis, M. C. (2013) · Frontiers in Psychology · doi:10.3389/fpsyg.2013.00485 · Cited by 141
The hippocampus: a special place for time
Ranganath, C., & Hsieh, L.-T. (2016) · Annals of the New York Academy of Sciences · doi:10.1111/nyas.13043 · Cited by 120
Deep temporal models and active inference
Friston, K. J., Rosch, R., Parr, T., Price, C., & Bowman, H. (2018) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2018.04.004 · Cited by 119
Emergence of preconfigured and plastic time-compressed sequences in early postnatal development
Farooq, U., & Dragoi, G. (2019) · Science · doi:10.1126/science.aav0502 · Cited by 131
The why, what, where, when and how of goal-directed choice: neuronal and computational principles
Verschure, P. F. M. J., Pennartz, C. M. A., & Pezzulo, G. (2014) · Philosophical Transactions of the Royal Society B Biological Sciences · doi:10.1098/rstb.2013.0483 · Cited by 131
Hippocampal reactivation extends for several hours following novel experience
Giri, B., Miyawaki, H., Mizuseki, K., Cheng, S., & Diba, K. (2019) · The Journal of Neuroscience · doi:10.1523/jneurosci.1950-18.2018 · Cited by 99
Hippocampal Place Fields Maintain a Coherent and Flexible Map across Long Timescales
Kinsky, N. R., Sullivan, D. W., Mau, W., Hasselmo, M. E., & Eichenbaum, H. B. (2018) · Current Biology · doi:10.1016/j.cub.2018.09.037 · Cited by 105
Is hippocampal remapping the physiological basis for context
Kubie, J. L., Levy, E. R. J., & Fenton, A. A. (2020) · Hippocampus · doi:10.1002/hipo.23160 · Cited by 94
Do hippocampal pyramidal cells respond to nonspatial stimuli?
O’Keefe, J., & Krupic, J. (2021) · Physiological Reviews · doi:10.1152/physrev.00014.2020 · Cited by 93
Episodic Memory in Nonhuman Animals
Templer, V. L., & Hampton, R. R. (2013) · Current Biology · doi:10.1016/j.cub.2013.07.016 · Cited by 94
Savelli, F., & Knierim, J. J. (2019) · Journal of Experimental Biology · doi:10.1242/jeb.188912 · Cited by 93
Neurophysiology of Remembering
Buzsáki, G., McKenzie, S., & Davachi, L. (2022) · Annual Review of Psychology · doi:10.1146/annurev-psych-021721-110002 · Cited by 84
Self-citationReagh, Z. M., & Ranganath, C. (2018) · Neuroscience Letters · doi:10.1016/j.neulet.2018.04.050 · Cited by 83
Running improves pattern separation during novel object recognition
Bolz, L., Heigele, S., & Bischofberger, J. (2015) · Brain Plasticity · doi:10.3233/bpl-150010 · Cited by 80
Age-specific effects of voluntary exercise on memory and the older brain
Siette, J., Westbrook, R. F., Cotman, C., Sidhu, K., Zhu, W., Sachdev, P., & Valenzuela, M. J. (2013) · Biological Psychiatry · doi:10.1016/j.biopsych.2012.05.034 · Cited by 78
All My Circuits: Using Multiple Electrodes to Understand Functioning Neural Networks
Miller, E. K., & Wilson, M. A. (2008) · Neuron · doi:10.1016/j.neuron.2008.10.033 · Cited by 76
Stellate cells in the medial entorhinal cortex are required for spatial learning
Tennant, S. A., Fischer, L., Garden, D. L. F., Gerlei, K. Z., Martinez-Gonzalez, C., McClure, C., Wood, E. R., & Nolan, M. F. (2018) · Cell Reports · doi:10.1016/j.celrep.2018.01.005 · Cited by 71
Does metarepresentation make human mental time travel unique?
Redshaw, J. (2014) · WIREs Cognitive Science · doi:10.1002/wcs.1308 · Cited by 68
Linking hippocampal multiplexed tuning, Hebbian plasticity and navigation
Moore, J. J., Cushman, J. D., Acharya, L., Popeney, B., & Mehta, M. R. (2021) · Nature · doi:10.1038/s41586-021-03989-z · Cited by 69
Distinct neural mechanisms for remembering when an event occurred
Jenkins, L. J., & Ranganath, C. (2016) · Hippocampus · doi:10.1002/hipo.22571 · Cited by 65
Contributions of primate prefrontal cortex and medial temporal lobe to temporal-order memory
Naya, Y., Chen, H., Yang, C., & Suzuki, W. A. (2017) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1712711114 · Cited by 62
Komlósi, G., Molnár, G., Rózsa, M., Oláh, S., Barzó, P., & Tamás, G. (2012) · The Journal of Neuroscience · doi:10.1523/jneurosci.2618-12.2012 · Cited by 57
Radwan, B., Dvorak, D., & Fenton, A. A. (2016) · Neurobiology of Disease · doi:10.1016/j.nbd.2016.01.003 · Cited by 63
Consciousness, Representation, Action: The Importance of Being Goal-Directed
Pennartz, C. M. A. (2018) · Trends in Cognitive Sciences · doi:10.1016/j.tics.2017.10.006 · Cited by 49
Intrinsic timescales and predictive allostatic interoception in brain health and disease
Ibanez, A., & Northoff, G. (2024) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2023.105510 · Cited by 36
Neural and neuronal discoordination in schizophrenia: from ensembles through networks to symptoms
Krajcovic, B., Fajnerova, I., Horacek, J., Kelemen, E., Kubik, S., Svoboda, J., & Stuchlik, A. (2019) · Acta Physiologica · doi:10.1111/apha.13282 · Cited by 29
Is episodic-like memory like episodic memory?
Davies, J. R., & Clayton, N. S. (2024) · Philosophical Transactions of the Royal Society B: Biological Sciences · doi:10.1098/rstb.2023.0397 · Cited by 27
Radulovic, J., Lee, R., & Ortony, A. (2018) · Frontiers in Behavioral Neuroscience · doi:10.3389/fnbeh.2018.00259 · Cited by 26
“A compressed representation of spatial distance in the rodent hippocampus’’
Sheehan, D. J., Charczynski, S., Fordyce, B. A., Hasselmo, M. E., & Howard, M. W. (2021) · doi:10.1101/2021.02.15.431306 · Cited by 13
Metadata
- Authors
- Pastalkova, E., Itskov, V., Amarasingham, A., & Buzsáki, G.
- Affiliations
- Rutgers, The State University of New Jersey (US)
- Center for Molecular and Behavioral Neuroscience, Rutgers, The State University of New Jersey, 197 University Avenue, Newark, NJ 07102, USA.
- Corresponding author
- Itskov, Vladimir
- Venue
- Science
- Published
- 2008-09-05
- Volume
- 321
- Issue
- 5894
- Pages
- 1322-1327
- ISSN
- 0036-8075 (ISSN-L)
- 1095-9203
- PMC
- PMC2570043
- OpenAlex
- W2172122397
- Cited by
- 1,301
- References
- 40
- Citations by year
- 2026: 63 · 2025: 100 · 2024: 101 · 2023: 84 · 2022: 81 · 2021: 85 · 2020: 83 · 2019: 97 · 2018: 82 · 2017: 94 · 2016: 65 · 2015: 67 · 2014: 69 · 2013: 63 · 2012: 38
- FWCI
- 21.70
- Type
- journal article
- Language
- en
- Open access
- green
- www.ncbi.nlm.nih.gov
- Locations
- Science (publishedVersion)
- PubMed (publishedVersion)
- Europe PMC (PubMed Central) (acceptedVersion)
- PubMed Central (acceptedVersion)
- Funders
- National Institute of Mental Health (R01MH054671, MH54671)
- National Institute of Neurological Disorders and Stroke (R01NS034994, NS-34994)
- Topics
- Life Sciences › Neuroscience › Cognitive Neuroscience › Memory and Neural Mechanisms
- Life Sciences › Neuroscience › Cognitive Neuroscience › Neural dynamics and brain function
- Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Neuroscience and Neuropharmacology Research
- Keywords
- cell assemblies, hippocampus, spontaneous neuronal activity, spatial navigation, episodic memory, action planning, behavior prediction
- MeSH terms
- Action Potentials, Animals, Behavior, Animal, Choice Behavior, Cues, Hippocampus, Interneurons, Male, Memory, Models, Neurological, Motor Activity, Mental Recall, Pyramidal Cells, Maze Learning, Rats, Long-Evans, Rats
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
