Memory Consolidation
Open accessAbstract
Conscious memory for a new experience is initially dependent on information stored in both the hippocampus and neocortex. Systems consolidation is the process by which the hippocampus guides the reorganization of the information stored in the neocortex such that it eventually becomes independent of the hippocampus. Early evidence for systems consolidation was provided by studies of retrograde amnesia, which found that damage to the hippocampus-impaired memories formed in the recent past, but typically spared memories formed in the more remote past. Systems consolidation has been found to occur for both episodic and semantic memories and for both spatial and nonspatial memories, although empirical inconsistencies and theoretical disagreements remain about these issues. Recent work has begun to characterize the neural mechanisms that underlie the dialogue between the hippocampus and neocortex (e.g., "neural replay," which occurs during sharp wave ripple activity). New work has also identified variables, such as the amount of preexisting knowledge, that affect the rate of consolidation. The increasing use of molecular genetic tools (e.g., optogenetics) can be expected to further improve understanding of the neural mechanisms underlying consolidation.
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Humans gradually summarize common structure from past episodes and organize it into abstractions through memory consolidation.
“Humans do not treat every new situation as entirely unfamiliar; instead, they gradually summarize common structure from past episodes and organize it into abstractions through memory consolidation (McClelland et al., 1995; Squire et al., 2015; Dudai et al., 2015; Moscovitch et al., 2016; Sun et al., 2023; Bartlett, 1932).”
From Useful Memories Become Faulty When Continuously Updated by LLMs (2026) · cites this paper as Squire et al., 2015
The Conclusions (page unavailable) describe gradual reorganization of memory and its relationship to existing schemas. But Interpreting Behavioral Measures and Cognitive Factors (page unavailable) says that extracting gist from learned instances is a proposed interpretation of animal data and that an extraction mechanism may not be required. The paper therefore supports gradual consolidation and a possible route to abstraction, but not the claim that humans necessarily summarize past episodes into abstractions through that process. (LLM, conf=0.84)
Experimental — accuracy not yet measuredCognitive theories of memory describe two complementary processes: a fast episodic system that stores individual experiences, and a slow process that extracts compact schemas-abstractions over many episodes that integrate with prior knowledge to support future generalization.
“Cognitive theories of memory describe two complementary processes: a fast episodic system that stores individual experiences, and a slow process that extracts compact schemas -abstractions over many episodes that integrate with prior knowledge to support future generalization (McClelland et al., 1995; Squire et al., 2015; Dudai et al., 2015; Moscovitch et al., 2016).”
From Useful Memories Become Faulty When Continuously Updated by LLMs (2026) · cites this paper as Squire et al., 2015
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Experimental — accuracy not yet measuredHuman memory relies on complementary learning systems.
“Human memory relies on complementary learning systems (McClelland et al., 1995), where memory consolidation (Squire et al., 2015) progressively transforms rapid episodic encoding into more stable semantic structures (Cowan et al., 2021).”
From TiMem: Temporal-Hierarchical Memory Consolidation for Long-Horizon Conversational Agents (2026) · cites this paper as Squire et al., 2015
Memory consolidation progressively transforms rapid episodic encoding into more stable semantic structures.
“Human memory relies on complementary learning systems (McClelland et al., 1995), where memory consolidation (Squire et al., 2015) progressively transforms rapid episodic encoding into more stable semantic structures (Cowan et al., 2021).”
From TiMem: Temporal-Hierarchical Memory Consolidation for Long-Horizon Conversational Agents (2026) · cites this paper as Squire et al., 2015
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Cites
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 · see citing works
Self-citationMcClelland, J. L., McNaughton, B. L., & O'Reilly, R. C. (1995) · Psychological Review · doi:10.1037/0033-295x.102.3.419 · Cited by 5,256 · see citing works
The hippocampus as a cognitive map
Passingham, R. E. (1979) · Neuroscience · doi:10.1016/0306-4522(79)90015-0 · Cited by 5,128 · see citing works
Diekelmann, S., & Born, J. (2010) · Nature Reviews Neuroscience · doi:10.1038/nrn2762 · Cited by 3,760 · see citing works
Reactivation of hippocampal ensemble memories during sleep
Wilson, M. A., & McNaughton, B. L. (1994) · Science · doi:10.1126/science.8036517 · Cited by 3,118 · see citing works
Simple memory: a theory for archicortex
Marr, D. (1971) · Philosophical Transactions of the Royal Society of London. B, Biological Sciences · doi:10.1098/rstb.1971.0078 · Cited by 2,771 · see citing works
Fear memories require protein synthesis in the amygdala for reconsolidation after retrieval
Nader, K., Schafe, G. E., & Le Doux, J. E. (2000) · Nature · doi:10.1038/35021052 · Cited by 2,706 · see citing works
Modality-Specific Retrograde Amnesia of Fear
Kim, J. J., & Fanselow, M. S. (1992) · Science · doi:10.1126/science.1585183 · Cited by 2,483 · see citing works
Tononi, G., & Cirelli, C. (2014) · Neuron · doi:10.1016/j.neuron.2013.12.025 · Cited by 2,356 · see citing works
Sleep function and synaptic homeostasis
Tononi, G., & Cirelli, C. (2006) · Sleep Medicine Reviews · doi:10.1016/j.smrv.2005.05.002 · Cited by 2,151 · see citing works
The organization of recent and remote memories
Frankland, P. W., & Bontempi, B. (2005) · Nature Reviews Neuroscience · doi:10.1038/nrn1607 · Cited by 2,138 · see citing works
Hippocampus, space, and memory
Olton, D. S., Becker, J. T., & Handelmann, G. E. (1979) · Behavioral and Brain Sciences · doi:10.1017/s0140525x00062713 · Cited by 2,018 · see citing works
Place Cells, Grid Cells, and the Brain's Spatial Representation System
Moser, E. I., Kropff, E., & Moser, M.-B. (2008) · Annual Review of Neuroscience · doi:10.1146/annurev.neuro.31.061307.090723 · Cited by 1,934 · see citing works
Memory consolidation, retrograde amnesia and the hippocampal complex
Nadel, L., & Moscovitch, M. (1997) · Current Opinion in Neurobiology · doi:10.1016/s0959-4388(97)80010-4 · Cited by 1,924 · see citing works
Coordinated memory replay in the visual cortex and hippocampus during sleep
Ji, D., & Wilson, M. A. (2007) · Nature Neuroscience · doi:10.1038/nn1825 · Cited by 1,669 · see citing works
Selective suppression of hippocampal ripples impairs spatial memory
Girardeau, G., Benchenane, K., Wiener, S. I., Buzsáki, G., & Zugaro, M. B. (2009) · Nature Neuroscience · doi:10.1038/nn.2384 · Cited by 1,560 · see citing works
Retrograde amnesia and memory consolidation: a neurobiological perspective
Squire, L. R., & Alvarez, P. (1995) · Current Opinion in Neurobiology · doi:10.1016/0959-4388(95)80023-9 · Cited by 1,412 · see citing works
Self-citationThe functional neuroanatomy of autobiographical memory: a meta-analysis
Svoboda, E., McKinnon, M. C., & Levine, B. (2006) · Neuropsychologia · doi:10.1016/j.neuropsychologia.2006.05.023 · Cited by 1,274 · see citing works
Schemas and Memory Consolidation.
Tse, D., Langston, R. F., Kakeyama, M., Bethus, I., Spooner, P. A., Wood, E. R., Witter, M. P., & Morris, R. G. M. (2007) · Science · doi:10.1126/science.1135935 · Cited by 1,244 · see citing works
Self-citationHippocampal place-cell sequences depict future paths to remembered goals
Pfeiffer, B. E., & Foster, D. J. (2013) · Nature · doi:10.1038/nature12112 · Cited by 1,216 · see citing works
Odor cues during slow-wave sleep prompt declarative memory consolidation
Rasch, B., Büchel, C., Gais, S., & Born, J. (2007) · Science · doi:10.1126/science.1138581 · Cited by 1,181 · see citing works
Memory consolidation and the medial temporal lobe: a simple network model.
Alvarez, P., & Squire, L. R. (1994) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.91.15.7041 · Cited by 1,054 · see citing works
Self-citationThe Involvement of the Anterior Cingulate Cortex in Remote Contextual Fear Memory
Frankland, P., Bontempi, B., Talton, L., Kaczmarek, L., & Silva, A. J. (2004) · Science · doi:10.1126/science.1094804 · Cited by 952 · see citing works
Kopelman, M. D., Wilson, B. A., & Baddeley, A. (1989) · Journal of Clinical and Experimental Neuropsychology · doi:10.1080/01688638908400928 · Cited by 939 · see citing works
Regional Slow Waves and Spindles in Human Sleep
Nir, Y., Staba, R. J., Andrillon, T., Vyazovskiy, V. V., Cirelli, C., Fried, I., & Tononi, G. (2011) · Neuron · doi:10.1016/j.neuron.2011.02.043 · Cited by 924 · see citing works
Awake hippocampal sharp-wave ripples support spatial memory
Jadhav, S. P., Kemere, C., German, P. W., & Frank, L. M. (2012) · Science · doi:10.1126/science.1217230 · Cited by 924 · see citing works
Retrieval and reconsolidation: Toward a neurobiology of remembering
Sara, S. J. (2000) · Learning & Memory · doi:10.1101/lm.7.2.73 · Cited by 919 · see citing works
The Primate Hippocampal Formation: Evidence for a Time-Limited Role in Memory Storage
Zola-Morgan, S. M., & Squire, L. R. (1990) · Science · doi:10.1126/science.2218534 · Cited by 863 · see citing works
Self-citationHow schema and novelty augment memory formation
van Kesteren, M. T. R., Ruiter, D. J., Fernández, G., & Henson, R. N. (2012) · Trends in Neurosciences · doi:10.1016/j.tins.2012.02.001 · Cited by 860 · see citing works
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 · see citing works
Hippocampal replay of extended experience
Davidson, T. J., Kloosterman, F., & Wilson, M. A. (2009) · Neuron · doi:10.1016/j.neuron.2009.07.027 · Cited by 806 · cited 2× · see citing works
“2010), and longer memories seem to be replayed across multiple sharp wave ripples (Davidson et al. 2009).”
Awake replay of remote experiences in the hippocampus
Karlsson, M. P., & Frank, L. M. (2009) · Nature Neuroscience · doi:10.1038/nn.2344 · Cited by 769 · see citing works
The reorganization and reactivation of hippocampal maps predict spatial memory performance
Dupret, D., O'Neill, J., Pleydell-Bouverie, B., & Csicsvari, J. (2010) · Nature Neuroscience · doi:10.1038/nn.2599 · Cited by 769 · see citing works
Replay of rule-learning related neural patterns in the prefrontal cortex during sleep
Peyrache, A., Khamassi, M., Benchenane, K., Wiener, S. I., & Battaglia, F. P. (2009) · Nature Neuroscience · doi:10.1038/nn.2337 · Cited by 767 · see citing works
Are spatial memories strengthened in the human hippocampus during slow wave sleep?
Peigneux, P., Laureys, S., Fuchs, S., Collette, F., Perrin, F., Reggers, J., Phillips, C., Degueldre, C., Del Fiore, G., Aerts, J., et al. (2004) · Neuron · doi:10.1016/j.neuron.2004.10.007 · Cited by 766 · see citing works
Obliviscence during sleep and waking
Jenkins, J. G., & Dallenbach, K. M. (1924) · The American Journal of Psychology · doi:10.2307/1414040 · Cited by 741 · see citing works
Functional neuroimaging of autobiographical memory
Cabeza, R., & St Jacques, P. (2007) · Trends in Cognitive Sciences · doi:10.1016/j.tics.2007.02.005 · Cited by 736 · see citing works
Time-dependent reorganization of brain circuitry underlying long-term memory storage
Bontempi, B., Laurent-Demir, C., Destrade, C., & Jaffard, R. (1999) · Nature · doi:10.1038/23270 · Cited by 673 · see citing works
The cognitive neuroscience of remote episodic, semantic and spatial memory
Moscovitch, M., Nadel, L., Winocur, G., Gilboa, A., & Rosenbaum, R. S. (2006) · Current Opinion in Neurobiology · doi:10.1016/j.conb.2006.03.013 · Cited by 660 · see citing works
Sites of Neocortical Reorganization Critical for Remote Spatial Memory
Maviel, T., Durkin, T., Menzaghi, F., & Bontempi, B. (2004) · Science · doi:10.1126/science.1098180 · Cited by 659 · see citing works
Anagnostaras, S., Maren, S., & Fanselow, M. S. (1999) · Journal of Neuroscience · doi:10.1523/jneurosci.19-03-01106.1999 · Cited by 656 · see citing works
The Restless Engram: Consolidations Never End
Dudai, Y. (2012) · Annual Review of Neuroscience · doi:10.1146/annurev-neuro-062111-150500 · Cited by 644 · see citing works
Schema-dependent gene activation and memory encoding in neocortex
Tse, D., Takeuchi, T., Kakeyama, M., Kajii, Y., Okuno, H., Tohyama, C., Bito, H., & Morris, R. G. M. (2011) · Science · doi:10.1126/science.1205274 · Cited by 618 · see citing works
Self-citationSleep promotes branch-specific formation of dendritic spines after learning
Yang, G., Lai, C. S. W., Cichon, J., Ma, L., Li, W., & Gan, W.-B. (2014) · Science · doi:10.1126/science.1249098 · Cited by 616 · see citing works
Human cognition : learning, understanding, and remembering
Bransford, J. D. (1979) · Medical Entomology and Zoology · Cited by 604 · see citing works
Alberini, C. M. (2005) · Trends in Neurosciences · doi:10.1016/j.tins.2004.11.001 · Cited by 594 · see citing works
Fast-Forward Playback of Recent Memory Sequences in Prefrontal Cortex During Sleep
Euston, D. R., Tatsuno, M., & McNaughton, B. L. (2007) · Science · doi:10.1126/science.1148979 · Cited by 586 · see citing works
Enhanced Brain Correlations during Rest Are Related to Memory for Recent Experiences
Tambini, A., Ketz, N., & Davachi, L. (2010) · Neuron · doi:10.1016/j.neuron.2010.01.001 · Cited by 570 · see citing works
Memory Transformation and Systems Consolidation
Winocur, G., & Moscovitch, M. (2011) · Journal of the International Neuropsychological Society · doi:10.1017/s1355617711000683 · Cited by 557 · see citing works
Takashima, A., Petersson, K. M., Rutters, F., Tendolkar, I., Jensen, O., Zwarts, M. J., McNaughton, B. L., & Fernández, G. (2006) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0507774103 · Cited by 557 · see citing works
Dynamics of Retrieval Strategies for Remote Memories
Goshen, I., Brodsky, M., Prakash, R., Wallace, J. L., Gradinaru, V., Ramakrishnan, C., & Deisseroth, K. A. (2011) · Cell · doi:10.1016/j.cell.2011.09.033 · Cited by 546 · see citing works
Strengthening Individual Memories by Reactivating Them During Sleep
Rudoy, J. D., Voss, J. L., Westerberg, C. E., & Paller, K. A. (2009) · Science · doi:10.1126/science.1179013 · Cited by 532 · see citing works
What is a memory schema? A historical perspective on current neuroscience literature
Ghosh, V. E., & Gilboa, A. (2014) · Neuropsychologia · doi:10.1016/j.neuropsychologia.2013.11.010 · Cited by 529 · see citing works
Overlapping memory replay during sleep builds cognitive schemata
Lewis, P. A., & Durrant, S. J. (2011) · Trends in Cognitive Sciences · doi:10.1016/j.tics.2011.06.004 · Cited by 512 · see citing works
Sleep Spindles in Humans: Insights from Intracranial EEG and Unit Recordings
Andrillon, T., Nir, Y., Staba, R. J., Ferrarelli, F., Cirelli, C., Tononi, G., & Fried, I. (2011) · The Journal of Neuroscience · doi:10.1523/jneurosci.2604-11.2011 · Cited by 504 · see citing works
Reversible neural inactivation reveals hippocampal participation in several memory processes
Riedel, G., Micheau, J., Lam, A. G. M., Roloff, E. V. L., Martin, S. J., Bridge, H., de Hoz, L., Poeschel, B., McCulloch, J., & Morris, R. (1999) · Nature Neuroscience · doi:10.1038/13202 · Cited by 478 · see citing works
Self-citationGilboa, A. (2004) · Cerebral Cortex · doi:10.1093/cercor/bhh082 · Cited by 459 · see citing works
Yiu, A. P., Mercaldo, V., Chen, Y., Richards, B. A., Rashid, A. J., Hsiang, H., Pressey, J. C., Mahadevan, V., Tran, M. M., Kushner, S. A., et al. (2014) · Neuron · doi:10.1016/j.neuron.2014.07.017 · Cited by 442 · see citing works
The case of K.C.: contributions of a memory-impaired person to memory theory
Rosenbaum, R. S., Köhler, S., Schacter, D. L., Moscovitch, M., Westmacott, R., Black, S. E., Gao, F., & Tulving, E. (2005) · Neuropsychologia · doi:10.1016/j.neuropsychologia.2004.10.007 · Cited by 433 · see citing works
Hippocampus leads ventral striatum in replay of place-reward information
Lansink, C. S., Goltstein, P. M., Lankelma, J. V., McNaughton, B. L., & Pennartz, C. M. A. (2009) · PLoS Biology · doi:10.1371/journal.pbio.1000173 · Cited by 400 · see citing works
Differential remoteness and emotional tone modulate the neural correlates of autobiographical memory
Piefke, M. (2003) · Brain · doi:10.1093/brain/awg064 · Cited by 391 · see citing works
Early Tagging of Cortical Networks Is Required for the Formation of Enduring Associative Memory
Lesburguères, E., Gobbo, O. L., Alaux‐Cantin, S., Hambücken, A., Trifilieff, P., & Bontempi, B. (2011) · Science · doi:10.1126/science.1196164 · Cited by 390 · see citing works
Memory for places learned long ago is intact after hippocampal damage
Teng, E., & Squire, L. R. (1999) · Nature · doi:10.1038/23276 · Cited by 372 · see citing works
Self-citationDirect Reactivation of a Coherent Neocortical Memory of Context
Cowansage, K. K., Shuman, T., Dillingham, B. C., Chang, A., Golshani, P., & Mayford, M. R. (2014) · Neuron · doi:10.1016/j.neuron.2014.09.022 · Cited by 359 · see citing works
Biasing the content of hippocampal replay during sleep
Bendor, D., & Wilson, M. A. (2012) · Nature Neuroscience · doi:10.1038/nn.3203 · Cited by 359 · see citing works
Semantic Memory and the Human Hippocampus
Manns, J. R., Hopkins, R. O., & Squire, L. R. (2003) · Neuron · doi:10.1016/s0896-6273(03)00146-6 · Cited by 354 · see citing works
Self-citationAnterograde and retrograde amnesia in rats with dorsal hippocampal or dorsomedial thalamic lesions
Winocur, G. (1990) · Behavioural Brain Research · doi:10.1016/0166-4328(90)90012-4 · Cited by 352 · see citing works
Role for a cortical input to hippocampal area CA1 in the consolidation of a long-term memory
Remondes, M., & Schuman, E. M. (2004) · Nature · doi:10.1038/nature02965 · Cited by 352 · see citing works
Retrograde Amnesia: Temporal Gradient in Very Long Term Memory Following Electroconvulsive Therapy
Squire, L. R., Slater, P. C., & Chace, P. M. (1975) · Science · doi:10.1126/science.1109228 · Cited by 338 · see citing works
Self-citationExperimentelle Beiträge zur Lehre vom Gedächtnis
Ephrussi, P. (1904) · University of Michigan Library Repository · Cited by 332 · see citing works
Race, E., Keane, M. M., & Verfaellie, M. (2011) · Journal of Neuroscience · doi:10.1523/jneurosci.1145-11.2011 · Cited by 328 · see citing works
Memory for context becomes less specific with timePreprint
Wiltgen, B. J., & Silva, A. J. (2007) · Learning & Memory · doi:10.1101/lm.430907 · Cited by 319 · see citing works
Identification of a Functional Connectome for Long-Term Fear Memory in Mice
Wheeler, A. L., Teixeira, C. M., Wang, A. H., Xiong, X., Kovacevic, N., Lerch, J. P., McIntosh, A. R., Parkinson, J., & Frankland, P. W. (2013) · PLoS Computational Biology · doi:10.1371/journal.pcbi.1002853 · Cited by 315 · see citing works
Priming of semantic autobiographical knowledge: A case study of retrograde amnesia
Tulving, E., Schacter, D. L., McLachlan, D. R., & Moscovitch, M. (1988) · Brain and Cognition · doi:10.1016/0278-2626(88)90035-8 · Cited by 312 · see citing works
The neuroscience of remote memory
Squire, L. R., & Bayley, P. J. (2007) · Current Opinion in Neurobiology · doi:10.1016/j.conb.2007.02.006 · Cited by 309 · see citing works
Self-citationThe Hippocampus Plays a Selective Role in the Retrieval of Detailed Contextual Memories
Wiltgen, B. J., Zhou, M., Cai, Y., Balaji, J., Karlsson, M. G., Parivash, S. N., Li, W., & Silva, A. J. (2010) · Current Biology · doi:10.1016/j.cub.2010.06.068 · Cited by 300 · see citing works
Memory for remote events in anterograde amnesia: Recognition of public figures from newsphotographs
Marslen‐Wilson, W. D., & Teuber, H. (1975) · Neuropsychologia · doi:10.1016/0028-3932(75)90013-5 · Cited by 289 · see citing works
State-dependent spike-timing relationships between hippocampal and prefrontal circuits during sleep
Wierzynski, C. M., Lubenov, E. V., Gu, M., & Siapas, A. G. (2009) · Neuron · doi:10.1016/j.neuron.2009.01.011 · Cited by 289 · see citing works
Shift from hippocampal to neocortical centered retrieval network with consolidation
Takashima, A., Nieuwenhuis, I. L. C., Jensen, O., Talamini, L. M., Rijpkema, M., & Fernández, G. (2009) · The Journal of Neuroscience · doi:10.1523/jneurosci.0799-09.2009 · Cited by 276 · see citing works
McClelland, J. L. (2013) · Journal of Experimental Psychology General · doi:10.1037/a0033812 · Cited by 273 · see citing works
100 Years of Consolidation— Remembering Müller and PilzeckerPreprint
Lechner, H., Squire, L. R., & Byrne, J. H. (1999) · Learning & Memory · doi:10.1101/lm.6.2.77 · Cited by 272 · see citing works
Self-citationSteinvorth, S., Levine, B., & Corkin, S. (2005) · Neuropsychologia · doi:10.1016/j.neuropsychologia.2005.01.001 · Cited by 267 · see citing works
An opportunistic theory of cellular and systems consolidation
Mednick, S. C., Cai, D. J., Shuman, T., Anagnostaras, S., & Wixted, J. T. (2011) · Trends in Neurosciences · doi:10.1016/j.tins.2011.06.003 · Cited by 267 · see citing works
Self-citationGenzel, L., Kroes, M. C. W., Dresler, M., & Battaglia, F. P. (2013) · Trends in Neurosciences · doi:10.1016/j.tins.2013.10.002 · Cited by 259 · see citing works
Self-citationInhibition recruitment in prefrontal cortex during sleep spindles and gating of hippocampal inputs
Peyrache, A., Battaglia, F. P., & Destexhe, A. (2011) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1103612108 · Cited by 254 · see citing works
Spontaneous Changes of Neocortical Code for Associative Memory During Consolidation
Takehara‐Nishiuchi, K., & McNaughton, B. L. (2008) · Science · doi:10.1126/science.1161299 · Cited by 248 · see citing works
Detecting Representations of Recent and Remote Autobiographical Memories in vmPFC and Hippocampus
Bonnici, H. M., Chadwick, M. J., Lutti, A., Hassabis, D., Weiskopf, N., & Maguire, E. A. (2012) · Journal of Neuroscience · doi:10.1523/jneurosci.2475-12.2012 · Cited by 245 · see citing works
Mechanisms of sleep-dependent consolidation of cortical plasticity
Aton, S. J., Seibt, J., Dumoulin, M., Jha, S. K., Steinmetz, N., Coleman, T., Naidoo, N., & Frank, M. G. (2009) · Neuron · doi:10.1016/j.neuron.2009.01.007 · Cited by 244 · see citing works
Sleep states, memory processes and synaptic plasticity
Smith, C. T. (1996) · Behavioural Brain Research · doi:10.1016/0166-4328(95)00218-9 · Cited by 230 · see citing works
Persistence of hippocampal multivoxel patterns into postencoding rest is related to memory
Tambini, A., & Davachi, L. (2013) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1308499110 · Cited by 230 · see citing works
Stark, C. E. L., & Okado, Y. (2003) · Journal of Neuroscience · doi:10.1523/jneurosci.23-17-06748.2003 · Cited by 220 · see citing works
Awake reactivation predicts memory in humans
Staresina, B. P., Alink, A., Kriegeskorte, N., & Henson, R. N. (2013) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1311989110 · Cited by 219 · see citing works
Consolidation of human memory over decades revealed by functional magnetic resonance imaging
Haist, F., Gore, J. B., & Mao, H. Z. (2001) · Nature Neuroscience · doi:10.1038/nn739 · Cited by 214 · see citing works
Hippocampus and remote spatial memory in rats
Clark, R. E., Broadbent, N., & Squire, L. R. (2004) · Hippocampus · doi:10.1002/hipo.20056 · Cited by 209 · see citing works
Self-citationRetrograde amnesia after hippocampal damage: Recent vs. remote memories in two tasks
Sutherland, R. J., Weisend, M. P., Mumby, D. G., Astur, R. S., Hanlon, F. M., Koerner, A., Thomas, M. J., Wu, Y., Moses, S. N., Cole, C., et al. (2001) · Hippocampus · doi:10.1002/1098-1063(2001)11:1 · Cited by 190 · see citing works
Self-citationLateral Asymmetry in the Hippocampal Response to the Remoteness of Autobiographical Memories
Maguire, E. A., & Frith, C. (2003) · Journal of Neuroscience · doi:10.1523/jneurosci.23-12-05302.2003 · Cited by 181 · see citing works
Memory retrieval deficits based upon altered contextual cues: A paradox.
Riccio, D. C., Richardson, R., & Ebner, D. L. (1984) · Psychological Bulletin · doi:10.1037/0033-2909.96.1.152 · Cited by 180 · see citing works
Bayley, P. J., Hopkins, R. O., & Squire, L. R. (2003) · Neuron · doi:10.1016/s0896-6273(03)00156-9 · Cited by 178 · see citing works
Self-citationThe Neuroanatomy of Remote Memory
Bayley, P. J., Gold, J. J., Hopkins, R. O., & Squire, L. R. (2005) · Neuron · doi:10.1016/j.neuron.2005.04.034 · Cited by 178 · see citing works
Self-citationMartin, S. J., de Hoz, L., & Morris, R. (2004) · Neuropsychologia · doi:10.1016/j.neuropsychologia.2004.07.007 · Cited by 151 · see citing works
Self-citationTulving, E. (2003) · The MIT Press eBooks · doi:10.7551/mitpress/2834.003.0045 · Cited by 150 · see citing works
Patterns across multiple memories are identified over time
Richards, B. A., Xia, F., Santoro, A., Husse, J., Woodin, M. A., Josselyn, S. A., & Frankland, P. W. (2014) · Nature Neuroscience · doi:10.1038/nn.3736 · Cited by 150 · see citing works
Maguire, E. A., Henson, R. N., Mummery, C. J., & Frith, C. (2001) · Neuroreport · doi:10.1097/00001756-200103050-00004 · Cited by 146 · see citing works
Bolhuis, J. J., Stewart, C., & Forrest, E. M. (1994) · PubMed · doi:10.1080/14640749408401353 · Cited by 145 · see citing works
Smith, C. N., & Squire, L. R. (2009) · Journal of Neuroscience · doi:10.1523/jneurosci.4545-08.2009 · Cited by 140 · see citing works
Self-citationBroadbent, N., Squire, L. R., & Clark, R. E. (2006) · Learning & Memory · doi:10.1101/lm.134706 · Cited by 138 · see citing works
Self-citationSutherland, R. J., O'Brien, J., & Lehmann, H. (2008) · Hippocampus · doi:10.1002/hipo.20431 · Cited by 137 · see citing works
Temporally-specific retrograde amnesia in two cases of discrete bilateral hippocampal pathology
Kapur, N., & Brooks, D. J. (1999) · Hippocampus · doi:10.1002/(sici)1098-1063(1999)9:3 · Cited by 135 · see citing works
Lehmann, H., Lacanilao, S., & Sutherland, R. J. (2007) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.2007.05374.x · Cited by 129 · see citing works
The Fate of Old Memories after Medial Temporal Lobe Damage
Bayley, P. J., Hopkins, R. O., & Squire, L. R. (2006) · Journal of Neuroscience · doi:10.1523/jneurosci.4262-06.2006 · Cited by 126 · see citing works
Self-citationMisattribution, false recognition and the sins of memory
Schacter, D. L., & Dodson, C. S. (2001) · Philosophical Transactions of the Royal Society B Biological Sciences · doi:10.1098/rstb.2001.0938 · Cited by 126 · see citing works
Clark, R. E., Broadbent, N., & Squire, L. R. (2005) · Hippocampus · doi:10.1002/hipo.20076 · Cited by 119 · see citing works
Self-citationRetroactive Amnesia: Illustrative Cases and a Tentative Explanation
Burnham, W. H. (1903) · The American Journal of Psychology · doi:10.2307/1412310 · Cited by 117 · see citing works
The Hippocampus and Spatial Memory: Findings with a Novel Modification of the Water Maze
Clark, R. E., Broadbent, N., & Squire, L. R. (2007) · Journal of Neuroscience · doi:10.1523/jneurosci.0913-07.2007 · Cited by 110 · see citing works
Self-citationRekkas, P. V., & Constable, R. T. (2005) · Journal of Cognitive Neuroscience · doi:10.1162/089892905775008652 · Cited by 109 · see citing works
Bright, P., Buckman, J., Fradera, A., Yoshimasu, H., Colchester, A. C. F., & Kopelman, M. D. (2006) · Learning & Memory · doi:10.1101/lm.265906 · Cited by 101 · see citing works
Niki, K., & Jing, L. (2002) · Journal of Cognitive Neuroscience · doi:10.1162/089892902317362010 · Cited by 101 · see citing works
Douville, K. L., Woodard, J. L., Seidenberg, M., Miller, S. K., Leveroni, C. L., Nielson, K. A., Franczak, M. B., Antuono, P., & Rao, S. M. (2004) · Neuropsychologia · doi:10.1016/j.neuropsychologia.2004.09.005 · Cited by 100 · see citing works
Detailed recollection of remote autobiographical memory after damage to the medial temporal lobe
Kirwan, C. B., Bayley, P. J., Galván, V. V., & Squire, L. R. (2008) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0712155105 · Cited by 99 · see citing works
Self-citationThe hippocampal region is involved in successful recognition of both remote and recent famous faces
Bernard, F., Bullmore, E. T., Graham, K. S., Thompson, S., Hodges, J. R., & Fletcher, P. C. (2004) · NeuroImage · doi:10.1016/j.neuroimage.2004.03.036 · Cited by 91 · see citing works
Spooner, R. I., Thomson, A. C., Hall, J., Morris, R., & Salter, S. H. (1994) · Learning & Memory · doi:10.1101/lm.1.3.203 · Cited by 89 · see citing works
Self-citationLearning-Induced Plasticity Regulates Hippocampal Sharp Wave-Ripple Drive
Girardeau, G., Cei, A., & Zugaro, M. B. (2014) · Journal of Neuroscience · doi:10.1523/jneurosci.4288-13.2014 · Cited by 88 · see citing works
To consolidate or not to consolidate: what are the questions?
Dudai, Y., & Morris, R. (2000) · Oxford University Press eBooks · doi:10.1093/acprof:oso/9780198524823.003.0011 · Cited by 87 · see citing works
Self-citationRepresentations of recent and remote autobiographical memories in hippocampal subfields
Bonnici, H. M., Chadwick, M. J., & Maguire, E. A. (2013) · Hippocampus · doi:10.1002/hipo.22155 · Cited by 80 · see citing works
Emotional Autobiographical Memories in Amnesic Patients with Medial Temporal Lobe Damage
Buchanan, T. W., Tranel, D., & Adolphs, R. (2005) · The Journal of Neuroscience · doi:10.1523/jneurosci.4735-04.2005 · Cited by 78 · see citing works
Forgetting, Reminding, and Remembering: The Retrieval of Lost Spatial Memory
de Hoz, L., Martin, S. J., & Morris, R. (2004) · PLoS Biology · doi:10.1371/journal.pbio.0020225 · Cited by 75 · see citing works
Self-citationLiang, K., Hon, W., Tyan, Y. M., & Liao, W. L. (1994) · PubMed · Cited by 74 · see citing works
Söderlund, H., Moscovitch, M., Kumar, N., Mandic, M., & Levine, B. (2011) · Hippocampus · doi:10.1002/hipo.20927 · Cited by 68 · see citing works
Furman, O., Mendelsohn, A., & Dudai, Y. (2012) · Learning & Memory · doi:10.1101/lm.025965.112 · Cited by 65 · see citing works
The Hippocampus Remains Activated over the Long Term for the Retrieval of Truly Episodic Memories
Harand, C., Bertran, F., Joie, R. L., Landeau, B., Mézenge, F., Desgranges, B., Peigneux, P., Eustache, F., & Rauchs, G. (2012) · PLoS ONE · doi:10.1371/journal.pone.0043495 · Cited by 64 · see citing works
Viard, A., Lebreton, K., Chételat, G., Desgranges, B., Landeau, B., Young, A., de la Sayette, V., Eustache, F., & Piolino, P. (2009) · Hippocampus · doi:10.1002/hipo.20601 · Cited by 63 · see citing works
Dudai, Y., & Morris, R. (2013) · Neuron · doi:10.1016/j.neuron.2013.09.039 · Cited by 59 · see citing works
Self-citationField Potential Signature of Distinct Multicellular Activity Patterns in the Mouse Hippocampus
Reichinnek, S., Künsting, T., Draguhn, A., & Both, M. (2010) · Journal of Neuroscience · doi:10.1523/jneurosci.2535-10.2010 · Cited by 56 · see citing works
Broadbent, N., & Clark, R. E. (2013) · Neurobiology of Learning and Memory · doi:10.1016/j.nlm.2013.08.008 · Cited by 51 · see citing works
Yamashita, K.-I., Hirose, S., Kunimatsu, A., Aoki, S., Chikazoe, J., Jimura, K., Masutani, Y., Abe, O., Ohtomo, K., Miyashita, Y., et al. (2009) · The Journal of Neuroscience · doi:10.1523/jneurosci.1328-09.2009 · Cited by 51 · see citing works
Structured cognition and neural systems: From rats to language
Battaglia, F. P., Borensztajn, G., & Bod, R. (2012) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2012.04.004 · Cited by 47 · see citing works
Hippocampal lesions produce both nongraded and temporally graded retrograde amnesia in the same rat
Winocur, G., Sekeres, M. J., Binns, M. A., & Moscovitch, M. (2013) · Hippocampus · doi:10.1002/hipo.22093 · Cited by 45 · see citing works
Autobiographical Memory After Temporal Lobe Lesions
Eslinger, P. J. (1998) · Neurocase · doi:10.1080/13554799808410641 · Cited by 41 · see citing works
Sparks, F. T., Lehmann, H., Hernandez, K., & Sutherland, R. J. (2011) · PLoS ONE · doi:10.1371/journal.pone.0027426 · Cited by 38 · see citing works
Misattribution, false recognition and the sins of memory
Schacter, D. L., & Dodson, C. S. (2002) · Oxford University Press eBooks · doi:10.1093/acprof:oso/9780198508809.003.0005 · Cited by 25 · see citing works
Autobiographical memory of the recent past following frontal cortex or temporal lobe excisions
Thaiss, L., & Petrides, M. (2008) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.2008.06381.x · Cited by 24 · see citing works
Dynamics of Retrieval Strategies for Remote Memories
Goshen, I., Brodsky, M., Prakash, R., Wallace, J. L., Gradinaru, V., Ramakrishnan, C., & Deisseroth, K. A. (2011) · Cell · doi:10.1016/j.cell.2011.11.006 · Cited by 22 · see citing works
Kopelman, M. D., & Bright, P. (2012) · Neuropsychologia · doi:10.1016/j.neuropsychologia.2012.07.028 · Cited by 20 · see citing works
Broadbent, N., Squire, L. R., & Clark, R. E. (2009) · Hippocampus · doi:10.1002/hipo.20722 · Cited by 19 · see citing works
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Replication and Analysis of Ebbinghaus’ Forgetting Curve
Murre, J. M. J., & Dros, J. (2015) · PLOS ONE · doi:10.1371/journal.pone.0120644 · Cited by 777 · see citing works
The hippocampal sharp wave-ripple in memory retrieval for immediate use and consolidation
Joo, H. R., & Frank, L. M. (2018) · Nature Reviews Neuroscience · doi:10.1038/s41583-018-0077-1 · Cited by 430 · see citing works
A contextual binding theory of episodic memory: systems consolidation reconsidered
Yonelinas, A. P., Charan Ranganath, A., Ekstrom, A. D., & Wiltgen, B. J. (2019) · Nature reviews. Neuroscience · doi:10.1038/s41583-019-0150-4 · Cited by 446 · see citing works
XMem: Long-Term Video Object Segmentation with an Atkinson-Shiffrin Memory Model
Cheng, H. K., & Schwing, A. G. (2022) · Lecture Notes in Computer Science · doi:10.1007/978-3-031-19815-1_37 · Cited by 449 · see citing works
Foster, D. J. (2017) · Annual Review of Neuroscience · doi:10.1146/annurev-neuro-072116-031538 · Cited by 375 · see citing works
The Role of Hippocampal Replay in Memory and Planning
Ólafsdóttir, H. F., Bush, D., & Barry, C. (2018) · Current Biology · doi:10.1016/j.cub.2017.10.073 · Cited by 413 · see citing works
The hippocampus and related neocortical structures in memory transformation
Sekeres, M. J., Winocur, G., & Moscovitch, M. (2018) · Neuroscience Letters · doi:10.1016/j.neulet.2018.05.006 · Cited by 370 · see citing works
Physical Activity and Brain Health
Liegro, C. M. D., Schiera, G., Proia, P., & Liegro, I. D. (2019) · Genes · doi:10.3390/genes10090720 · Cited by 392 · see citing works
van de Ven, G. M., Trouche, S., McNamara, C. G., Allen, K., & Dupret, D. (2016) · Neuron · doi:10.1016/j.neuron.2016.10.020 · Cited by 320 · see citing works
From Knowing to Remembering: The Semantic–Episodic Distinction
Renoult, L., Irish, M., Moscovitch, M., & Rugg, M. D. (2019) · Trends in Cognitive Sciences · doi:10.1016/j.tics.2019.09.008 · Cited by 346 · see citing works
Representational drift in primary olfactory cortex
Schoonover, C. E., Ohashi, S. N., Axel, R., & Fink, A. J. P. (2021) · Nature · doi:10.1038/s41586-021-03628-7 · Cited by 313 · see citing works
Novelty and Dopaminergic Modulation of Memory Persistence: A Tale of Two Systems
Duszkiewicz, A. J., McNamara, C. G., Takeuchi, T., & Genzel, L. (2018) · Trends in Neurosciences · doi:10.1016/j.tins.2018.10.002 · Cited by 307 · see citing works
Self-citationAstrocyte glycogen and lactate: New insights into learning and memory mechanisms
Alberini, C. M., Cruz, E., Descalzi, G., Bessières, B., & Gao, V. (2017) · Glia · doi:10.1002/glia.23250 · Cited by 286 · see citing works
Robin, J., & Moscovitch, M. (2017) · Current Opinion in Behavioral Sciences · doi:10.1016/j.cobeha.2017.07.016 · Cited by 266 · see citing works
Computational Principles of Supervised Learning in the Cerebellum
Raymond, J. L., & Medina, J. F. (2018) · Annual Review of Neuroscience · doi:10.1146/annurev-neuro-080317-061948 · Cited by 231 · see citing works
Infantile Amnesia: A Critical Period of Learning to Learn and Remember
Alberini, C. M., & Travaglia, A. (2017) · Journal of Neuroscience · doi:10.1523/jneurosci.0324-17.2017 · Cited by 209 · see citing works
Remote Memory and the Hippocampus: A Constructive Critique
Barry, D. N., & Maguire, E. A. (2018) · Trends in Cognitive Sciences · doi:10.1016/j.tics.2018.11.005 · Cited by 196 · see citing works
BDNF effects on dendritic spine morphology and hippocampal function
von Bohlen und Halbach, O., & von Bohlen und Halbach, V. (2018) · Cell and Tissue Research · doi:10.1007/s00441-017-2782-x · Cited by 218 · see citing works
Early-Onset Alzheimer’s Disease: What Is Missing in Research?
Ayodele, T., Rogaeva, E. A., Kurup, J. T., Beecham, G. W., & Reitz, C. (2021) · Current Neurology and Neuroscience Reports · doi:10.1007/s11910-020-01090-y · Cited by 198 · see citing works
Physical exercise induces hippocampal neurogenesis and prevents cognitive decline
Ma, C., Ma, X., Wang, J., Liu, H., Chen, Y., & Yang, Y. (2016) · Behavioural Brain Research · doi:10.1016/j.bbr.2016.09.067 · Cited by 192 · see citing works
Gilboa, A., & Moscovitch, M. (2021) · Neuron · doi:10.1016/j.neuron.2021.04.025 · Cited by 174 · see citing works
Early-life adversity and neurological disease: age-old questions and novel answers
Short, A. K., & Baram, T. Z. (2019) · Nature Reviews Neurology · doi:10.1038/s41582-019-0246-5 · Cited by 180 · see citing works
Myelin: A gatekeeper of activity-dependent circuit plasticity?
Bonetto, G., Belin, D., & Káradóttir, R. T. (2021) · Science · doi:10.1126/science.aba6905 · Cited by 186 · see citing works
Neuronal Computation Underlying Inferential Reasoning in Humans and Mice
Barron, H. C., Reeve, H. M., Koolschijn, R. S., Perestenko, P. V., Shpektor, A., Nili, H., Rothaermel, R., Campo-Urriza, N., O’Reilly, J. X., Bannerman, D. M., et al. (2020) · Cell · doi:10.1016/j.cell.2020.08.035 · Cited by 179 · see citing works
MovieChat: From Dense Token to Sparse Memory for Long Video Understanding
Song, E., Chai, W., Wang, G., Zhang, Y., Zhou, H., Wu, F., Chi, H., Guo, X., Ye, T., Zhang, Y., et al. (2024) · 2024 IEEE/CVF Conference on Computer Vision and Pattern Recognition (CVPR) · doi:10.1109/cvpr52733.2024.01725 · Cited by 176 · see citing works
MovieChat: From Dense Token to Sparse Memory for Long Video Understanding
Song, E., Chai, W., Wang, G., Zhang, Y., Zhou, H., Wu, F., Chi, H., Guo, X., Ye, T., Zhang, Y., et al. (2023) · arXiv · doi:10.48550/arxiv.2307.16449 · Cited by 176 · see citing works
A Rapid Form of Offline Consolidation in Skill Learning
Bönstrup, M., Iturrate, I., Thompson, R., Cruciani, G., Censor, N., & Cohen, L. G. (2019) · Current Biology · doi:10.1016/j.cub.2019.02.049 · Cited by 167 · see citing works
Reward retroactively enhances memory consolidation for related itemsPreprint
Patil, A., Murty, V. P., Dunsmoor, J. E., Phelps, E. A., & Davachi, L. (2016) · Learning & Memory · doi:10.1101/lm.042978.116 · Cited by 152 · see citing works
Norman, Y., Raccah, O., Liu, S., Parvizi, J., & Malach, R. (2021) · Neuron · doi:10.1016/j.neuron.2021.06.020 · Cited by 140 · see citing works
Engram neurons: Encoding, consolidation, retrieval, and forgetting of memory
Guskjolen, A. J., & Cembrowski, M. S. (2023) · Molecular Psychiatry · doi:10.1038/s41380-023-02137-5 · Cited by 148 · see citing works
The hippocampus, ventromedial prefrontal cortex, and episodic and semantic memory
Rolls, E. T. (2022) · Progress in Neurobiology · doi:10.1016/j.pneurobio.2022.102334 · Cited by 144 · see citing works
Translational Control in the Brain in Health and Disease
Sossin, W. S., & Costa-Mattioli, M. (2019) · Cold Spring Harbor Perspectives in Biology · doi:10.1101/cshperspect.a032912 · Cited by 138 · see citing works
van Dongen, E. V., Kersten, I., Wagner, I. C., Morris, R., & Fernández, G. (2016) · Current Biology · doi:10.1016/j.cub.2016.04.071 · Cited by 136 · see citing works
Self-citationTao, L., Liu, Q., Zhang, F., Fu, Y., Zhu, X. D., Weng, X., Han, H., Huang, Y., Suo, Y., Chen, L., et al. (2021) · Light Science & Applications · doi:10.1038/s41377-021-00617-3 · Cited by 133 · see citing works
Surget, A., & Belzung, C. (2021) · Molecular Psychiatry · doi:10.1038/s41380-021-01136-8 · Cited by 122 · see citing works
The anterior thalamic nuclei: core components of a tripartite episodic memory system
Aggleton, J. P., & O’Mara, S. M. (2022) · Nature reviews. Neuroscience · doi:10.1038/s41583-022-00591-8 · Cited by 112 · see citing works
The neuroplastic brain: current breakthroughs and emerging frontiers
Gazerani, P. (2025) · Brain Research · doi:10.1016/j.brainres.2025.149643 · Cited by 132 · see citing works
Tadi, M., Allaman, I., Lengacher, S., Grenningloh, G., & Magistretti, P. J. (2015) · PLoS ONE · doi:10.1371/journal.pone.0141568 · Cited by 106 · see citing works
Organizing memories for generalization in complementary learning systems
Sun, W., Advani, M., Spruston, N., Saxe, A., & Fitzgerald, J. E. (2023) · Nature Neuroscience · doi:10.1038/s41593-023-01382-9 · Cited by 103 · see citing works
Rosenbaum, R. S., Kim, A. S. N., & Baker, S. (2017) · Elsevier eBooks · doi:10.1016/b978-0-12-809324-5.21037-7 · Cited by 109 · see citing works
Chen, H., Gilmore, A. W., Nelson, S. M., & McDermott, K. B. (2017) · Journal of Neuroscience · doi:10.1523/jneurosci.1534-16.2017 · Cited by 98 · see citing works
Time-dependent memory transformation along the hippocampal anterior–posterior axis
Dandolo, L., & Schwabe, L. (2018) · Nature Communications · doi:10.1038/s41467-018-03661-7 · Cited by 97 · see citing works
Understanding the physical basis of memory: Molecular mechanisms of the engram
Luis, C. O. S., & Ryan, T. J. (2022) · Journal of Biological Chemistry · doi:10.1016/j.jbc.2022.101866 · Cited by 103 · see citing works
Replay and compositional computation
Kurth-Nelson, Z. L., Behrens, T. E. J., Wayne, G., Miller, K. J., Luettgau, L., Dolan, R. J., Liu, Y., & Schwartenbeck, P. (2023) · Neuron · doi:10.1016/j.neuron.2022.12.028 · Cited by 93 · see citing works
Sekeres, M. J., Winocur, G., Moscovitch, M., Anderson, J. A. E., Pishdadian, S., Wojtowicz, J. M., St‐Laurent, M., McAndrews, M. P., & Grady, C. L. (2018) · Hippocampus · doi:10.1002/hipo.23009 · Cited by 95 · see citing works
Mechanisms of offline motor learning at a microscale of seconds in large-scale crowdsourced data
Bönstrup, M., Iturrate, I., Hebart, M. N., Censor, N., & Cohen, L. G. (2020) · npj Science of Learning · doi:10.1038/s41539-020-0066-9 · Cited by 94 · see citing works
Retrieving fear memories, as time goes by…
Monte, F. H. D., Quirk, G. J., Li, B., & Penzo, M. A. (2016) · Molecular Psychiatry · doi:10.1038/mp.2016.78 · Cited by 95 · see citing works
A generative model of memory construction and consolidation
Spens, E., & Burgess, N. (2024) · Nature Human Behaviour · doi:10.1038/s41562-023-01799-z · Cited by 101 · see citing works
First-person view of one’s body in immersive virtual reality: Influence on episodic memory
Bréchet, L., Mange, R., Herbelin, B., Theillaud, Q., Gauthier, B., Serino, A., & Blanke, O. (2019) · PLOS ONE · doi:10.1371/journal.pone.0197763 · Cited by 85 · see citing works
PROLIDASE: A Review from Discovery to its Role in Health and Disease
Eni-Aganga, I., Lanaghan, Z. M., Balasubramaniam, M., Dash, C., & Pandhare, J. (2021) · Frontiers in Molecular Biosciences · doi:10.3389/fmolb.2021.723003 · Cited by 85 · see citing works
Schemas provide a scaffold for neocortical integration of new memories over time
Audrain, S., & McAndrews, M. P. (2022) · Nature Communications · doi:10.1038/s41467-022-33517-0 · Cited by 76 · see citing works
Cognitive neuroscience perspective on memory: overview and summary
Sridhar, S., Khamaj, A., & Asthana, M. K. (2023) · Frontiers in Human Neuroscience · doi:10.3389/fnhum.2023.1217093 · Cited by 80 · see citing works
The Interplay of Hippocampus and Ventromedial Prefrontal Cortex in Memory-Based Decision Making
Weilbächer, R. A., & Gluth, S. (2016) · Brain Sciences · doi:10.3390/brainsci7010004 · Cited by 78 · see citing works
Singh, D., Norman, K. A., & Schapiro, A. C. (2022) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.2123432119 · Cited by 72 · see citing works
Neurostimulation techniques to enhance sleep and improve cognition in aging
Grimaldi, D., Papalambros, N. A., Zee, P. C., & Malkani, R. G. (2020) · Neurobiology of Disease · doi:10.1016/j.nbd.2020.104865 · Cited by 76 · see citing works
Wang, X., Kooijman, S., Gao, Y., Tzeplaeff, L., Cosquer, B., Milanova, I. V., Wolff, S. E. C., Korpel, N. L., Champy, M., Petit‐Demoulière, B., et al. (2021) · Molecular Psychiatry · doi:10.1038/s41380-021-01169-z · Cited by 74 · see citing works
Hippocampal function in rodents
Zemla, R., & Basu, J. (2017) · Current Opinion in Neurobiology · doi:10.1016/j.conb.2017.04.005 · Cited by 71 · see citing works
DNA methylation: a permissive mark in memory formation and maintenancePreprint
Oliveira, A. M. M. (2016) · Learning & Memory · doi:10.1101/lm.042739.116 · Cited by 74 · see citing works
Brain-transportable dipeptides across the blood-brain barrier in mice
Tanaka, M., Dohgu, S., Komabayashi, G., Kiyohara, H., Takata, F., Kataoka, Y., Nirasawa, T., Maebuchi, M., & Matsui, T. (2019) · Scientific Reports · doi:10.1038/s41598-019-42099-9 · Cited by 73 · see citing works
Initial memory consolidation and the synaptic tagging and capture hypothesis
Okuda, K., Højgaard, K., Privitera, L., Bayraktar, G., & Takeuchi, T. (2020) · European Journal of Neuroscience · doi:10.1111/ejn.14902 · Cited by 71 · see citing works
Do sex differences in rumination explain sex differences in depression?
Shors, T. J., Millon, E. M., Chang, H. Y. M., Olson, R. L., & Alderman, B. L. (2017) · Journal of Neuroscience Research · doi:10.1002/jnr.23976 · Cited by 70 · see citing works
Chow, T. E., & Rissman, J. (2017) · Annals of the New York Academy of Sciences · doi:10.1111/nyas.13353 · Cited by 68 · see citing works
Replay of Learned Neural Firing Sequences during Rest in Human Motor Cortex
Eichenlaub, J., Jarosiewicz, B., Saab, J., Franco, B., Kelemen, J. N., Halgren, E., Hochberg, L. R., & Cash, S. S. (2020) · Cell Reports · doi:10.1016/j.celrep.2020.107581 · Cited by 83 · see citing works
Quiroga, R. Q. (2019) · Cell · doi:10.1016/j.cell.2019.10.016 · Cited by 66 · see citing works
An historical perspective on Endel Tulving's episodic-semantic distinction
Renoult, L., & Rugg, M. D. (2020) · Neuropsychologia · doi:10.1016/j.neuropsychologia.2020.107366 · Cited by 71 · see citing works
Evidence supporting a time-limited hippocampal role in retrieving autobiographical memories
Gilmore, A. W., Quach, A., Kalinowski, S. E., González-Araya, E. I., Gotts, S. J., Schacter, D. L., & Martin, A. D. (2021) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.2023069118 · Cited by 66 · see citing works
No Pattern Separation in the Human Hippocampus
Quiroga, R. Q. (2020) · Trends in Cognitive Sciences · doi:10.1016/j.tics.2020.09.012 · Cited by 63 · see citing works
A Synaptic Framework for the Persistence of Memory Engrams
Rao‐Ruiz, P., Visser, E., Mitrić, M. M., Smit, A. B., & van den Oever, M. C. (2021) · Frontiers in Synaptic Neuroscience · doi:10.3389/fnsyn.2021.661476 · Cited by 65 · see citing works
Moscovitch, M., & Gilboa, A. (2021) · doi:10.31234/osf.io/yxbrs · Cited by 62 · see citing works
Titi Monkeys as a Novel Non-Human Primate Model for the Neurobiology of Pair Bonding .
Bales, K. L., Razo, R. A., Conklin, Q. A., Hartman, S., Mayer, H. S., Rogers, F. D., Simmons, T. C., Smith, L. K., Williams, A. V., Williams, D. R., et al. (2017) · Europe PMC (PubMed Central) · Cited by 62 · see citing works
Computer Vision Based Two-stage Waste Recognition-Retrieval Algorithm for Waste Classification
Zhang, S., Chen, Y., Yang, Z., & Gong, H. (2021) · Resources Conservation and Recycling · doi:10.1016/j.resconrec.2021.105543 · Cited by 62 · see citing works
Mechanistic flexibility of the retrosplenial cortex enables its contribution to spatial cognition
Stacho, M., & Manahan‐Vaughan, D. (2022) · Trends in Neurosciences · doi:10.1016/j.tins.2022.01.007 · Cited by 61 · see citing works
Semantic memory in developmental amnesia
Elward, R. L., & Vargha‐Khadem, F. (2018) · Neuroscience Letters · doi:10.1016/j.neulet.2018.04.040 · Cited by 59 · see citing works
The molecular memory code and synaptic plasticity: A synthesis
Gershman, S. J. (2023) · Biosystems · doi:10.1016/j.biosystems.2022.104825 · Cited by 61 · see citing works
Boccia, M., Teghil, A., & Guariglia, C. (2019) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2019.09.003 · Cited by 58 · see citing works
Contributions of post-learning REM and NREM sleep to memory retrieval
MacDonald, K. J., & Côté, K. A. (2021) · Sleep Medicine Reviews · doi:10.1016/j.smrv.2021.101453 · Cited by 59 · see citing works
Ali, M. A., Menze, E. T., Tadros, M., & Tolba, M. F. (2020) · Neuropharmacology · doi:10.1016/j.neuropharm.2020.108334 · Cited by 60 · see citing works
What can we teach Lymnaea and what can Lymnaea teach us?
Rivi, V., Benatti, C., Lukowiak, K., Colliva, C., Alboni, S., Tascedda, F., & Blom, J. M. C. (2021) · Biological reviews/Biological reviews of the Cambridge Philosophical Society · doi:10.1111/brv.12716 · Cited by 59 · see citing works
Perez, D. M. (2021) · Frontiers in Cell and Developmental Biology · doi:10.3389/fcell.2021.652152 · Cited by 57 · see citing works
Evans, H. T., Bodea, L., & Götz, J. (2020) · eLife · doi:10.7554/elife.52990 · Cited by 54 · see citing works
Cassel, J., Ferraris, M., Quilichini, P., Cholvin, T., Boch, L., Stéphan, A., & de Vasconcelos, A. P. (2021) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2021.03.023 · Cited by 54 · see citing works
Hrybouski, S., MacGillivray, M., Huang, Y., Madan, C. R., Carter, R., Seres, P., & Malykhin, N. V. (2019) · NeuroImage · doi:10.1016/j.neuroimage.2019.01.061 · Cited by 53 · see citing works
Causal Contribution of Awake Post-encoding Processes to Episodic Memory Consolidation
Tambini, A., & D’Esposito, M. (2020) · Current Biology · doi:10.1016/j.cub.2020.06.063 · Cited by 53 · see citing works
Tortella, G., Seabra, A. B., Padrão, J., & Juan, R. D.-S. (2021) · Brain Sciences · doi:10.3390/brainsci11050552 · Cited by 58 · see citing works
Smolen, P., Baxter, D. A., & Byrne, J. H. (2019) · Learning & Memory · doi:10.1101/lm.049395.119 · Cited by 53 · see citing works
A theory of hippocampal function: New developments
Rolls, E. T., & Treves, A. (2024) · Progress in Neurobiology · doi:10.1016/j.pneurobio.2024.102636 · Cited by 52 · see citing works
Network-wide abnormalities explain memory variability in hippocampal amnesia
Argyropoulos, G. P. D., Loane, C., Roca‐Fernández, A., Lage-Martinez, C., Gurau, O., Irani, S. R., & Butler, C. (2019) · eLife · doi:10.7554/elife.46156 · Cited by 50 · see citing works
Ugolini, F., Lana, D., Nardiello, P., Nosi, D., Pantano, D., Casamenti, F., & Giovannini, M. G. (2018) · Frontiers in Aging Neuroscience · doi:10.3389/fnagi.2018.00372 · Cited by 50 · see citing works
Emerging neurodevelopmental perspectives on mathematical learning
Menon, V., & Chang, H. (2021) · Developmental Review · doi:10.1016/j.dr.2021.100964 · Cited by 58 · see citing works
Memory Retrieval in Mice and MenPreprint
Ben-Yakov, A., Dudai, Y., & Mayford, M. R. (2015) · Cold Spring Harbor Perspectives in Biology · doi:10.1101/cshperspect.a021790 · Cited by 50 · see citing works
Task-dependent mixed selectivity in the subiculum
Ledergerber, D., Battistin, C., Blackstad, J. S., Gardner, R. J., Witter, M. P., Moser, M., Roudi, Y., & Moser, E. I. (2021) · Cell Reports · doi:10.1016/j.celrep.2021.109175 · Cited by 49 · see citing works
Hippocampal area CA1 and remote memory in ratsPreprint
Ocampo, A. C., Squire, L. R., & Clark, R. E. (2017) · Learning & Memory · doi:10.1101/lm.045781.117 · Cited by 49 · see citing works
Self-citationA double dissociation between savings and long-term memory in motor learning
Hadjiosif, A. M., Morehead, J. R., & Smith, M. A. (2023) · PLoS Biology · doi:10.1371/journal.pbio.3001799 · Cited by 49 · see citing works
Hypertension is associated with reduced hippocampal connectivity and impaired memory
Feng, R., Rolls, E. T., Cheng, W., & Feng, J. (2020) · EBioMedicine · doi:10.1016/j.ebiom.2020.103082 · Cited by 49 · see citing works
Understanding the dynamic and destiny of memories
Alvares, L. D. O., & Monte, F. H. D. (2021) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2021.03.009 · Cited by 47 · see citing works
Early- and Late-Onset Alzheimer’s Disease: Two Sides of the Same Coin?
Valdez-Gaxiola, C. A., Rosales-Leycegui, F., Gaxiola-Rubio, A., Moreno-Ortíz, J. M., & Figuera, L. E. (2024) · Diseases · doi:10.3390/diseases12060110 · Cited by 50 · see citing works
Sugden, A. U., Zaremba, J. D., Sugden, L. A., McGuire, K. L., Lutas, A., Ramesh, R. N., Alturkistani, O., Lensjø, K. K., Burgess, C. R., & Andermann, M. L. (2020) · Nature Neuroscience · doi:10.1038/s41593-020-0651-5 · Cited by 46 · see citing works
Naïve to expert: Considering the role of previous knowledge in memory
Alonso, A., van der Meij, J., Tse, D., & Genzel, L. (2020) · Brain and Neuroscience Advances · doi:10.1177/2398212820948686 · Cited by 46 · see citing works
Self-citationVirtual reality modulating dynamics of neuroplasticity: Innovations in neuro-motor rehabilitation
Wankhede, N. L., Koppula, S., Ballal, S., Doshi, H., Kumawat, R., Raju, S., Arora, I., Sammeta, S. S., Khalid, M., Zafar, A., et al. (2024) · Neuroscience · doi:10.1016/j.neuroscience.2024.12.040 · Cited by 47 · see citing works
Engram stability and maturation during systems consolidation
Refaeli, R., Kreisel, T., Groysman, M., Adamsky, A., & Goshen, I. (2023) · Current Biology · doi:10.1016/j.cub.2023.07.042 · Cited by 42 · see citing works
- Authors
- Squire, L. R., Genzel, L., Wixted, J. T., & Morris, R. G.
- Affiliations
- University of California San Diego (US)
- University of Edinburgh (GB)
- Venue
- Cold Spring Harbor Perspectives in Biology
- Publisher
- Cold Spring Harbor Laboratory
- Published
- 2015-08
- Volume
- 7
- Issue
- 8
- Pages
- a021766
- ISSN
- 1943-0264 (ISSN-L)
- PMC
- PMC4526749
- OpenAlex
- W4247532959
- Cited by
- 700
- References
- 148
- Citations by year
- 2026: 70 · 2025: 97 · 2024: 100 · 2023: 78 · 2022: 83 · 2021: 83 · 2020: 68 · 2019: 45 · 2018: 26 · 2017: 27 · 2016: 14 · 2015: 6 · 2014: 1
- Type
- posted content
- Language
- en
- Open access
- bronze
- doi.org
- Locations
- Cold Spring Harbor Perspectives in Biology (publishedVersion)
- Europe PMC (PubMed Central) (publishedVersion)
- PubMed Central (publishedVersion)
- PubMed (publishedVersion)
- Funders
- U.S. Department of Veterans Affairs
- U.S. Public Health Service (24600)
- National Institute of Mental Health (24600, Grant 24600)
- Topics
- Life Sciences › Neuroscience › Cognitive Neuroscience › Memory and Neural Mechanisms
- Life Sciences › Neuroscience › Cognitive Neuroscience › Memory Processes and Influences
- Life Sciences › Neuroscience › Cognitive Neuroscience › Sleep and Wakefulness Research
- Keywords
- memory consolidation, systems consolidation, hippocampus, neocortex, retrograde amnesia, episodic memory, semantic memory, spatial memory, neural replay, sharp-wave ripples, optogenetics
- MeSH terms
- Animals, Hippocampus, Humans, Memory, Neocortex
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