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Episodic Memory and Beyond: The Hippocampus and Neocortex in Transformation
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The last decade has seen dramatic technological and conceptual changes in research on episodic memory and the brain. New technologies, and increased use of more naturalistic observations, have enabled investigators to delve deeply into the structures that mediate episodic memory, particularly the hippocampus, and to track functional and structural interactions among brain regions that support it. Conceptually, episodic memory is increasingly being viewed as subject to lifelong transformations that are reflected in the neural substrates that mediate it. In keeping with this dynamic perspective, research on episodic memory (and the hippocampus) has infiltrated domains, from perception to language and from empathy to problem solving, that were once considered outside its boundaries. Using the component process model as a framework, and focusing on the hippocampus, its subfields, and specialization along its longitudinal axis, along with its interaction with other brain regions, we consider these new developments and their implications for the organization of episodic memory and its contribution to functions in other domains.
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“In mammals, allocentric navigation is thought to involve the operation of an extended cortico-hippocampal network that conveys highly processed visual and multisensory information to the hippocampal circuits for further processing and transformation into “world-centered” relational spatial representations [74,76,79,188,189,190,191,192].”
From Spatial Cognition in Teleost Fish: Strategies and Mechanisms (2021) · cites this paper as [191]
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“These cortical nodes appear to be associated with different aspects of episodic memory: the PCC with autobiographical recall, RSC with spatial navigation, mPFC with regulation of memory encoding and recall, and the AG with elaboration of the contents of memory.”
From 20 years of the default mode network: A review and synthesis. (2023) · cites this paper as [50]
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“Studies on this topic have indicated that episodic memory may be recruited for additional tasks where particular details of past experiences are leveraged to generate, or assemble and maintain, mental content that incorporates specific elements of prior events.”
From Neural Mechanisms of Episodic Retrieval Support Divergent Creative Thinking (2019) · cites this paper as Moscovitch et al. 2016
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“Strikingly, during the past decade, episodic memory, and the neural processes that support it, have been found to be engaged during tasks beyond simple remembering that may also involve the retrieval and reconstruction of episodic details for completion, such as future thinking or simulation, decision making, and problem solving (for review, see Schacter et al. 2012;Moscovitch et al. 2016;Schacter”
From Neural Mechanisms of Episodic Retrieval Support Divergent Creative Thinking (2019) · cites this paper as Moscovitch et al. 2016
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“Recent conceptual work has suggested that engagement of the hippocampus (and core network more broadly) is exhibited during generative tasks that nominally involve the retrieval and reconstruction of episodic details for completion, such as simulation, decision making, and problem solving”
From Neural Mechanisms of Episodic Retrieval Support Divergent Creative Thinking (2019) · cites this paper as Moscovitch et al. 2016
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“the collective results reported here converge on the idea that the boundary conditions and neural expressions of a constructive episodic memory system lie beyond simple remembering”
From Neural Mechanisms of Episodic Retrieval Support Divergent Creative Thinking (2019) · cites this paper as Moscovitch et al. 2016
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“First, episodic memories depend on many brain regions for their creation and persistence.”
From Episodic Memory in AI Agents Poses Risks that Should be Studied and Mitigated (2025) · cites this paper as [70]
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“According to the hippocampal indexing theory [69], an encoding of an episode in the hippocampus serves as a kind of index that points to and binds together representations in the neocortex that form the basis of the episode, such as multimodal sensory representations along with associated emotional and conceptual information [70].”
From Episodic Memory in AI Agents Poses Risks that Should be Studied and Mitigated (2025) · cites this paper as [70]
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“Moreover, the typical delay for hippocampal consolidation processes starts at approximately one hour (for shorter delays it may rather relate to short-term memory, relying distinct mechanisms) [128–131].”
From First-person view of one’s body in immersive virtual reality: Influence on episodic memory (2019) · cites this paper as [131]
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Citations
Cites
James, W. (1891) · Personality Culture Society · doi:10.1037/11059-000 · Cited by 25,876
(1978) · UA Campus Repository (The University of Arizona) · Cited by 8,010
Self-citationREMEMBERING: A STUDY IN EXPERIMENTAL AND SOCIAL PSYCHOLOGY
Bartlett, F. C., & Burt, C. (1933) · British Journal of Educational Psychology · doi:10.1111/j.2044-8279.1933.tb02913.x · Cited by 7,475
(1983) · Medical Entomology and Zoology · Cited by 6,051
McClelland, J. L., McNaughton, B. L., & O'Reilly, R. C. (1995) · Psychological Review · doi:10.1037/0033-295x.102.3.419 · Cited by 5,256
The hippocampus as a cognitive map
Passingham, R. E. (1979) · Neuroscience · doi:10.1016/0306-4522(79)90015-0 · Cited by 5,128
Episodic memory: from mind to brain
Tulving, E. (2002) · Annual Review of Psychology · doi:10.1146/annurev.psych.53.100901.135114 · Cited by 4,950
Diekelmann, S., & Born, J. (2010) · Nature Reviews Neuroscience · doi:10.1038/nrn2762 · Cited by 3,760
Memory: A Contribution to Experimental Psychology
Ebbinghaus, H. (2013) · Annals of Neurosciences · doi:10.5214/ans.0972.7531.200408 · Cited by 2,827
The Medial Temporal Lobe and Recognition Memory
Eichenbaum, H., Yonelinas, A. P., & Ranganath, C. (2007) · Annual Review of Neuroscience · doi:10.1146/annurev.neuro.30.051606.094328 · Cited by 2,580
Spreng, R. N., Mar, R. A., & Kim, A. S. N. (2009) · Journal of Cognitive Neuroscience · doi:10.1162/jocn.2008.21029 · Cited by 2,143
The organization of recent and remote memories
Frankland, P. W., & Bontempi, B. (2005) · Nature Reviews Neuroscience · doi:10.1038/nrn1607 · Cited by 2,138
Zola-Morgan, S., Squire, L., & Amaral, D. (1986) · The Journal of Neuroscience · doi:10.1523/jneurosci.06-10-02950.1986 · Cited by 1,997
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
Self-citationMemory, 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
Aging and autobiographical memory: dissociating episodic from semantic retrieval
Levine, B., Svoboda, E., Hay, J. F., Winocur, G., & Moscovitch, M. (2002) · Psychology and Aging · doi:10.1037/0882-7974.17.4.677 · Cited by 1,521
Self-citationThe future of memory: remembering, imagining, and the brain
Schacter, D. L., Addis, D. R., Hassabis, D., Martin, V. C., Spreng, R. N., & Szpunar, K. K. (2012) · Neuron · doi:10.1016/j.neuron.2012.11.001 · Cited by 1,398
Interplay of Hippocampus and Prefrontal Cortex in Memory
Preston, A. R., & Eichenbaum, H. (2013) · Current Biology · doi:10.1016/j.cub.2013.05.041 · Cited by 1,389
Frontal theta activity in humans increases with memory load in a working memory task
Jensen, O., & Tesche, C. D. (2002) · European Journal of Neuroscience · doi:10.1046/j.1460-9568.2002.01975.x · Cited by 1,379
Two cortical systems for memory-guided behaviour
Ranganath, C., & Ritchey, M. (2012) · Nature Reviews Neuroscience · doi:10.1038/nrn3338 · Cited by 1,377
The hippocampus and memory: insights from spatial processing
Bird, C. M., & Burgess, N. (2008) · Nature Reviews Neuroscience · doi:10.1038/nrn2335 · Cited by 1,313
Memory; a contribution to experimental psychology,
Ebbinghaus, H., Bussenius, C. E., & Ruger, H. A. (n.d.) · University of Michigan Library Repository · Cited by 1,281
The 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
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
Eling, P. (1993) · Acta Psychologica · doi:10.1016/0001-6918(93)90027-o · Cited by 1,198
The Molecular and Systems Biology of Memory
Kandel, E. R., Dudai, Y., & Mayford, M. R. (2014) · Cell · doi:10.1016/j.cell.2014.03.001 · Cited by 1,134
The brain's default network and its adaptive role in internal mentation
Andrews-Hanna, J. R. (2012) · The Neuroscientist · doi:10.1177/1073858411403316 · Cited by 1,114
Long-axis specialization of the human hippocampus
Poppenk, J., Evensmoen, H. R., Moscovitch, M., & Nadel, L. (2013) · Trends in Cognitive Sciences · doi:10.1016/j.tics.2013.03.005 · Cited by 1,100
Self-citationPattern Separation in the Human Hippocampal CA3 and Dentate Gyrus
Bakker, A., Kirwan, C. B., Miller, M. I., & Stark, C. E. L. (2008) · Science · doi:10.1126/science.1152882 · Cited by 1,050
Kopelman, M. D., Wilson, B. A., & Baddeley, A. (1989) · Journal of Clinical and Experimental Neuropsychology · doi:10.1080/01688638908400928 · Cited by 983
Prefrontal and medial temporal lobe interactions in long-term memory
Simons, J. S., & Spiers, H. J. (2003) · Nature Reviews Neuroscience · doi:10.1038/nrn1178 · Cited by 961
Cross-frequency coupling supports multi-item working memory in the human hippocampus
Axmacher, N., Henseler, M. M., Jensen, O. B., Weinreich, I., Elger, C. E., & Fell, J. (2010) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0911531107 · Cited by 929
Memory Deficit Produced by Bilateral Lesions in the Hippocampal Zone
Penfield, W. G. (1958) · Archives of Neurology And Psychiatry · doi:10.1001/archneurpsyc.1958.02340050003001 · Cited by 913
How 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
Time cells in the hippocampus: a new dimension for mapping memories
Eichenbaum, H. (2014) · Nature Reviews Neuroscience · doi:10.1038/nrn3827 · Cited by 843
Memory and Working-with-Memory: A Component Process Model Based on Modules and Central Systems
Moscovitch, M. (1992) · Journal of Cognitive Neuroscience · doi:10.1162/jocn.1992.4.3.257 · Cited by 822
Self-citationA single standard for memory: The case for reconsolidation
Nader, K., & Hardt, O. (2009) · Nature Reviews Neuroscience · doi:10.1038/nrn2590 · Cited by 811
Brain networks underlying episodic memory retrieval
Rugg, M. D., & Vilberg, K. L. (2013) · Current Opinion in Neurobiology · doi:10.1016/j.conb.2012.11.005 · Cited by 751
Josselyn, S. A., Köhler, S., & Frankland, P. W. (2015) · Nature reviews. Neuroscience · doi:10.1038/nrn4000 · Cited by 749
The Cognitive Neuroscience of Human Memory Since H.M.
Squire, L. R., & Wixted, J. T. (2011) · Annual Review of Neuroscience · doi:10.1146/annurev-neuro-061010-113720 · Cited by 749
A model for memory systems based on processing modes rather than consciousness
Henke, K. (2010) · Nature reviews. Neuroscience · doi:10.1038/nrn2850 · Cited by 739
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
Self-citationTheta and gamma oscillations predict encoding and retrieval of declarative memory
Osipova, D., Takashima, A., Oostenveld, R., Fernández, G., Maris, E., & Jensen, O. (2006) · The Journal of Neuroscience · doi:10.1523/jneurosci.1948-06.2006 · Cited by 671
The Restless Engram: Consolidations Never End
Dudai, Y. (2012) · Annual Review of Neuroscience · doi:10.1146/annurev-neuro-062111-150500 · Cited by 644
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 596
Yassa, M. A., Lacy, J. W., Stark, S. M., Albert, M. S., Gallagher, M., & Stark, C. E. L. (2011) · Hippocampus · doi:10.1002/hipo.20808 · Cited by 595
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 581
Hippocampal-Neocortical Interactions in Memory Formation, Consolidation, and Reconsolidation
Wang, S., & Morris, R. (2009) · Annual Review of Psychology · doi:10.1146/annurev.psych.093008.100523 · Cited by 570
Functional role of gamma and theta oscillations in episodic memory
Nyhus, E., & Curran, T. (2010) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2009.12.014 · Cited by 564
Memory Transformation and Systems Consolidation
Winocur, G., & Moscovitch, M. (2011) · Journal of the International Neuropsychological Society · doi:10.1017/s1355617711000683 · Cited by 557
Self-citationIntegrating Memories in the Human Brain: Hippocampal-Midbrain Encoding of Overlapping Events
Shohamy, D., & Wagner, A. D. (2008) · Neuron · doi:10.1016/j.neuron.2008.09.023 · Cited by 553
Preference by Association: How Memory Mechanisms in the Hippocampus Bias Decisions
Wimmer, G. E., & Shohamy, D. (2012) · Science · doi:10.1126/science.1223252 · Cited by 533
Conway, M. A. (2009) · Neuropsychologia · doi:10.1016/j.neuropsychologia.2009.02.003 · Cited by 519
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 · cited 1×
“With respect to episodic memory, there is evidence that recollection can be preserved or degraded and transformed to familiarity, but the conditions that lead to one or the other outcome, and the neural mechanisms involved, have yet to be elucidated (Lewis & Durrant 2011).”
The role of the hippocampus in flexible cognition and social behavior
Rubin, R. D., Watson, P. D., Duff, M. C., & Cohen, N. J. (2014) · Frontiers in Human Neuroscience · doi:10.3389/fnhum.2014.00742 · Cited by 489
Winocur, G., Moscovitch, M., & Bontempi, B. (2010) · Neuropsychologia · doi:10.1016/j.neuropsychologia.2010.04.016 · Cited by 486
Self-citationThe construction system of the brain
Hassabis, D., & Maguire, E. A. (2009) · Philosophical Transactions of the Royal Society B: Biological Sciences · doi:10.1098/rstb.2008.0296 · Cited by 483
Concept cells: the building blocks of declarative memory functions
Quiroga, R. Q. (2012) · Nature reviews. Neuroscience · doi:10.1038/nrn3251 · Cited by 472
Hippocampal sequence-encoding driven by a cortical multi-item working memory buffer
Jensen, O. B., & Lisman, J. E. (2004) · Trends in Neurosciences · doi:10.1016/j.tins.2004.12.001 · Cited by 467
Autobiographical memory and sense of self.
Prebble, S. C., Addis, D. R., & Tippett, L. J. (2013) · Psychological Bulletin · doi:10.1037/a0030146 · Cited by 466
Engel, A. K., Kreiter, A. K., Peter König, B., & Singer, W. (1991) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.88.14.6048 · Cited by 461
Cortical Representations Are Reinstated by the Hippocampus during Memory Retrieval
Tanaka, K. Z., Pevzner, A., Hamidi, A., Nakazawa, Y., Graham, J. A., & Wiltgen, B. J. (2014) · Neuron · doi:10.1016/j.neuron.2014.09.037 · Cited by 437
A neural mechanism mediating the impact of episodic prospection on farsighted decisions
Benoit, R. G., Gilbert, S. J., & Burgess, P. W. (2011) · The Journal of Neuroscience · doi:10.1523/jneurosci.6559-10.2011 · Cited by 422
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
Memory engram storage and retrieval
Tonegawa, S., Pignatelli, M., Roy, D. S., & Ryan, T. J. (2015) · Current Opinion in Neurobiology · doi:10.1016/j.conb.2015.07.009 · Cited by 415
Working Memory for Conjunctions Relies on the Medial Temporal Lobe
Olson, I. R., Page, K., Moore, K. S., Chatterjee, A. K., & Verfaellie, M. H. (2006) · Journal of Neuroscience · doi:10.1523/jneurosci.1923-05.2006 · Cited by 412
Hyman, J. M., Wyble, B., Goyal, V., Rossi, C. A., & Hasselmo, M. E. (2003) · Journal of Neuroscience · doi:10.1523/jneurosci.23-37-11725.2003 · Cited by 404
The ghosts of brain states past: Remembering reactivates the brain regions engaged during encoding.
Danker, J. F., & Anderson, J. R. (2010) · Psychological Bulletin · doi:10.1037/a0017937 · Cited by 400
The hippocampus: a manifesto for change
Maguire, E. A., & Mullally, S. L. (2013) · Journal of Experimental Psychology: General · doi:10.1037/a0033650 · Cited by 393 · cited 4×
“…in healthy controls in fMRI studies, was similar to that obtained on recall of autobiographical episodes (BenYakov & Dudai 2011, Furman et al. 2012, Maguire & Mullally 2013) [Supplemental Figure 3 (follow the Supplemental Material link in the online version of this article or at http://…”
InfluentialEffects of Healthy Aging on Hippocampal and Rhinal Memory Functions: An Event-Related fMRI Study
Daselaar, S. M., Fleck, M. S., Dobbins, I. G., Madden, D. J., & Cabeza, R. (2005) · Cerebral Cortex · doi:10.1093/cercor/bhj112 · Cited by 392
Self-citationPersonal semantics: at the crossroads of semantic and episodic memory
Renoult, L., Davidson, P. S. R., Palombo, D. J., Moscovitch, M., & Levine, B. (2012) · Trends in Cognitive Sciences · doi:10.1016/j.tics.2012.09.003 · Cited by 391
Self-citationNeural Activity in Human Hippocampal Formation Reveals the Spatial Context of Retrieved Memories
Miller, J. F., Neufang, M., Solway, A., Brandt, A., Trippel, M., Mader, I., Hefft, S., Merkow, M. B., Polyn, S. M., Jacobs, J., et al. (2013) · Science · doi:10.1126/science.1244056 · Cited by 390
Inferences about mental states
Mitchell, J. P. (2009) · Philosophical Transactions of the Royal Society B: Biological Sciences · doi:10.1098/rstb.2008.0318 · Cited by 387
Recollective qualities modulate hippocampal activation during autobiographical memory retrieval
Addis, D. R., Moscovitch, M., Crawley, A. P., & McAndrews, M. P. (2004) · Hippocampus · doi:10.1002/hipo.10215 · Cited by 383
Self-citationEvent memory: A theory of memory for laboratory, autobiographical, and fictional events.
Rubin, D. C., & Umanath, S. (2015) · Psychological Review · doi:10.1037/a0037907 · Cited by 379
Cognitive contributions of the ventral parietal cortex: an integrative theoretical account
Cabeza, R., Ciaramelli, E., & Moscovitch, M. (2012) · Trends in Cognitive Sciences · doi:10.1016/j.tics.2012.04.008 · Cited by 373
Self-citationThe hippocampal indexing theory and episodic memory: Updating the index
Teyler, T. J., & Rudy, J. W. (2007) · Hippocampus · doi:10.1002/hipo.20350 · Cited by 373
Piolino, P., Desgranges, B., & Eustache, F. (2009) · Neuropsychologia · doi:10.1016/j.neuropsychologia.2009.01.020 · Cited by 370
Yonelinas, A. P. (2013) · Behavioural Brain Research · doi:10.1016/j.bbr.2013.05.030 · Cited by 362
The Eyes Have It: Hippocampal Activity Predicts Expression of Memory in Eye Movements
Hannula, D. E., & Ranganath, C. (2009) · Neuron · doi:10.1016/j.neuron.2009.08.025 · Cited by 352
The hippocampus supports multiple cognitive processes through relational binding and comparison
Olsen, R. K., Moses, S. N., Riggs, L., & Ryan, J. D. (2012) · Frontiers in Human Neuroscience · doi:10.3389/fnhum.2012.00146 · Cited by 348
Bartsch, T., Döhring, J., Rohr, A., Jansen, O., & Deuschl, G. (2011) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1110266108 · Cited by 345
Aggleton, J. P. (2011) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2011.09.005 · Cited by 339
Emotional learning selectively and retroactively strengthens memories for related events
Dunsmoor, J. E., Murty, V. P., Davachi, L., & Phelps, E. A. (2015) · Nature · doi:10.1038/nature14106 · Cited by 332
How the hippocampus preserves order: the role of prediction and context
Davachi, L., & DuBrow, S. (2015) · Trends in Cognitive Sciences · doi:10.1016/j.tics.2014.12.004 · Cited by 328
Penfield, W. G. (1974) · Archives of Neurology · doi:10.1001/archneur.1974.00490390027001 · Cited by 327
Specificity of priming: a cognitive neuroscience perspective
Schacter, D. L., Dobbins, I. G., & Schnyer, D. M. (2004) · Nature reviews. Neuroscience · doi:10.1038/nrn1534 · Cited by 324
Neural Similarity Between Encoding and Retrieval is Related to Memory Via Hippocampal Interactions
Ritchey, M., Wing, E. A., LaBar, K. S., & Cabeza, R. E. L. (2012) · Cerebral Cortex · doi:10.1093/cercor/bhs258 · Cited by 324
Self-citationHunsaker, M. R., & Kesner, R. P. (2012) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2012.09.014 · Cited by 311
Howard, L. R., Javadi, A. H., Yu, Y., Mill, R. D., Morrison, L. C., Knight, R., Loftus, M. M., Staskute, L., & Spiers, H. J. (2014) · Current Biology · doi:10.1016/j.cub.2014.05.001 · Cited by 298
The hippocampus and the flexible use and processing of language
Duff, M. C., & Brown‐Schmidt, S. (2012) · Frontiers in Human Neuroscience · doi:10.3389/fnhum.2012.00069 · Cited by 297
Effect of unitization on associative recognition in amnesia
Quamme, J., Yonelinas, A., & Norman, K. A. (2007) · Hippocampus · doi:10.1002/hipo.20257 · Cited by 297
Remote spatial memory in an amnesic person with extensive bilateral hippocampal lesions
Rosenbaum, R. S., Priselac, S., Köhler, S., Black, S. E., Gao, F., Nadel, L., & Moscovitch, M. (2000) · Nature Neuroscience · doi:10.1038/79867 · Cited by 293
Self-citationPerirhinal Cortex Supports Encoding and Familiarity-Based Recognition of Novel Associations
Haskins, A., Yonelinas, A. P., Quamme, J. R., & Ranganath, C. (2008) · Neuron · doi:10.1016/j.neuron.2008.07.035 · Cited by 293
Poppenk, J., & Moscovitch, M. (2011) · Neuron · doi:10.1016/j.neuron.2011.10.014 · Cited by 292
Self-citationThe Hippocampus and Imagining the Future: Where Do We Stand?
Addis, D. R., & Schacter, D. L. (2012) · Frontiers in Human Neuroscience · doi:10.3389/fnhum.2011.00173 · Cited by 285
The Frontal Cortex and Working with Memory
Moscovitch, M., & Winocur, G. (2002) · Oxford University Press eBooks · doi:10.1093/acprof:oso/9780195134971.003.0012 · Cited by 278
Self-citationShift 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
The hippocampus and visual perception
Lee, A. C. H., Yeung, L., & Barense, M. D. (2012) · Frontiers in Human Neuroscience · doi:10.3389/fnhum.2012.00091 · Cited by 268
Rozin, P., Dow, S., Moscovitch, M., & Rajaram, S. (1998) · Psychological Science · doi:10.1111/1467-9280.00073 · Cited by 265
Self-citationRobinson, E., Aveyard, P. N., Daley, A., Jolly, K. B., Lewis, A. L., Lycett, D., & Higgs, S. (2013) · American Journal of Clinical Nutrition · doi:10.3945/ajcn.112.045245 · Cited by 259
Enhanced Emotional Memory: Cognitive and Neural Mechanisms
Talmi, D. (2013) · Current Directions in Psychological Science · doi:10.1177/0963721413498893 · Cited by 257
Norman, K. A. (2010) · Hippocampus · doi:10.1002/hipo.20855 · Cited by 247
NMDA Receptor Antagonism Blocks Experience-Dependent Expansion of Hippocampal “Place Fields”
Ekstrom, A. D., Meltzer, J., McNaughton, B. L., & Barnes, C. A. (2001) · Neuron · doi:10.1016/s0896-6273(01)00401-9 · Cited by 246
Moscovitch, M. (2008) · Canadian Journal of Experimental Psychology/Revue canadienne de psychologie expérimentale · doi:10.1037/1196-1961.62.1.62 · Cited by 245
Self-citationNeural correlates of recollection and familiarity: A review of neuroimaging and patient data
Skinner, E. I., & Fernandes, M. A. (2007) · Neuropsychologia · doi:10.1016/j.neuropsychologia.2007.03.007 · Cited by 243
Creativity and Memory: Effects of an Episodic-Specificity Induction on Divergent Thinking
Madore, K. P., Addis, D. R., & Schacter, D. L. (2015) · Psychological Science · doi:10.1177/0956797615591863 · Cited by 242
Ben-Yakov, A., & Dudai, Y. (2011) · Journal of Neuroscience · doi:10.1523/jneurosci.0702-11.2011 · Cited by 238
Decoding Individual Episodic Memory Traces in the Human Hippocampus
Chadwick, M. J., Hassabis, D., Weiskopf, N., & Maguire, E. A. (2010) · Current Biology · doi:10.1016/j.cub.2010.01.053 · Cited by 235
Dissociation Between Memory Accuracy and Memory Confidence Following Bilateral Parietal Lesions
Simons, J. S., Peers, P. V., Mazuz, Y. S., Berryhill, M. E., & Olson, I. R. (2009) · Cerebral Cortex · doi:10.1093/cercor/bhp116 · Cited by 232
Rapid neocortical acquisition of long-term arbitrary associations independent of the hippocampus
Sharon, T., Moscovitch, M., & Gilboa, A. (2011) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1005238108 · Cited by 229
Self-citationBenoit, R. G., Szpunar, K. K., & Schacter, D. L. (2014) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1419274111 · Cited by 223
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
Does lateral parietal cortex support episodic memory?
Davidson, P. S. R., Anaki, D., Ciaramelli, E., Cohn, M., Kim, A. S. N., Murphy, K. J., Troyer, A. K., Moscovitch, M., & Levine, B. (2008) · Neuropsychologia · doi:10.1016/j.neuropsychologia.2008.01.011 · Cited by 216
Self-citationRecovered consciousness: A hypothesis concerning modularity and episodic memory
Moscovitch, M. (1995) · Journal of Clinical and Experimental Neuropsychology · doi:10.1080/01688639508405123 · Cited by 212
Self-citationThe role of the ventromedial prefrontal cortex in memory consolidation
Nieuwenhuis, I. L. C., & Takashima, A. (2010) · Behavioural Brain Research · doi:10.1016/j.bbr.2010.12.009 · Cited by 211
Towards a Cognitive and Neurobiological Model of Motivated Forgetting
Anderson, M. C., & Huddleston, E. (2011) · Nebraska Symposium on Motivation/The Nebraska symposium on motivation · doi:10.1007/978-1-4614-1195-6_3 · Cited by 208
Distances between real-world locations are represented in the human hippocampus
Morgan, L. K., MacEvoy, S. P., Aguirre, G. K., & Epstein, R. A. (2011) · The Journal of Neuroscience · doi:10.1523/jneurosci.4667-10.2011 · Cited by 203
McCormick, C., St‐Laurent, M., Ty, A., Valiante, T. A., & McAndrews, M. P. (2013) · Cerebral Cortex · doi:10.1093/cercor/bht324 · Cited by 192
Spatial Cognition and the Hippocampus: The Anterior–Posterior Axis
Nadel, L., Hoscheidt, S. M., & Ryan, L. (2012) · Journal of Cognitive Neuroscience · doi:10.1162/jocn_a_00313 · Cited by 191
Self-citationRosenbaum, R. S., Gilboa, A., Levine, B., Winocur, G., & Moscovitch, M. (2008) · Neuropsychologia · doi:10.1016/j.neuropsychologia.2008.11.028 · Cited by 190
Self-citationAttenuated Boundary Extension Produces a Paradoxical Memory Advantage in Amnesic Patients
Mullally, S. L., Intraub, H., & Maguire, E. A. (2012) · Current Biology · doi:10.1016/j.cub.2012.01.001 · Cited by 184
Nichols, E. A., Kao, Y.-C., Verfaellie, M. H., & Gabrieli, J. D. E. (2006) · Hippocampus · doi:10.1002/hipo.20190 · Cited by 180
Subsequent memory effect in intracranial and scalp EEG
Long, N. M., Burke, J. F., & Kahana, M. J. (2013) · NeuroImage · doi:10.1016/j.neuroimage.2013.08.052 · Cited by 179
Episodic simulation and episodic memory can increase intentions to help others
Gaesser, B., & Schacter, D. L. (2014) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1402461111 · Cited by 175
Parsing the role of sleep in memory processing
Stickgold, R. (2013) · Current Opinion in Neurobiology · doi:10.1016/j.conb.2013.04.002 · Cited by 173
Permanent present tense: the unforgettable life of the amnesic patient, H.M
(2013) · Choice Reviews Online · doi:10.5860/choice.51-1171 · Cited by 165
Pertzov, Y., Miller, T. D., Gorgoraptis, N., Caine, D., Schott, J. M., Butler, C., & Husain, M. (2013) · Brain · doi:10.1093/brain/awt129 · Cited by 165
The hippocampus, time, and memory across scales.
Howard, M. W., & Eichenbaum, H. (2013) · Journal of Experimental Psychology General · doi:10.1037/a0033621 · Cited by 163
Memory Systems, Processing Modes, and Components: Functional Neuroimaging Evidence
Cabeza, R., & Moscovitch, M. (2013) · Perspectives on Psychological Science · doi:10.1177/1745691612469033 · Cited by 163
Self-citationSheldon, S., McAndrews, M. P., & Moscovitch, M. (2011) · Neuropsychologia · doi:10.1016/j.neuropsychologia.2011.04.021 · Cited by 161
Self-citationMeasuring recollection and familiarity: Improving the remember/know procedure
Migo, E. M., Mayes, A. R., & Montaldi, D. (2012) · Consciousness and Cognition · doi:10.1016/j.concog.2012.04.014 · Cited by 157
Schema representation in patients with ventromedial PFC lesions
Ghosh, V. E., Moscovitch, M., Melo Colella, B., & Gilboa, A. (2014) · The Journal of Neuroscience · doi:10.1523/jneurosci.0740-14.2014 · Cited by 155
Self-citationHippocampal immediate poststimulus activity in the encoding of consecutive naturalistic episodes
Ben-Yakov, A., Eshel, N., & Dudai, Y. (2013) · Journal of Experimental Psychology: General · doi:10.1037/a0033558 · Cited by 153
Baldo, J. V., & Shimamura, A. P. (2002) · Cited by 151
An episodic specificity induction enhances means-end problem solving in young and older adults.
Madore, K. P., & Schacter, D. L. (2014) · Psychology and Aging · doi:10.1037/a0038209 · Cited by 150
Delay-dependent contributions of medial temporal lobe regions to episodic memory retrieval
Ritchey, M., Montchal, M. E., Yonelinas, A. P., & Ranganath, C. (2015) · eLife · doi:10.7554/elife.05025 · Cited by 148
Palombo, D. J., Keane, M. M., & Verfaellie, M. (2015) · Hippocampus · doi:10.1002/hipo.22376 · Cited by 145
In vivo quantification of hippocampal subfields using 4.7 T fast spin echo imaging
Malykhin, N. V., Lebel, R. M., Coupland, N. J., Wilman, A. H., & Carter, R. (2009) · NeuroImage · doi:10.1016/j.neuroimage.2009.09.042 · Cited by 145
Schnider, A. (2008) · Oxford University Press eBooks · doi:10.1093/med/9780199206759.001.0001 · Cited by 145
Is the hippocampus necessary for visual and verbal binding in working memory?
Baddeley, A., Allen, R. J., & Vargha‐Khadem, F. (2009) · Neuropsychologia · doi:10.1016/j.neuropsychologia.2009.12.009 · Cited by 140
Divergent thinking and constructing episodic simulations
Addis, D. R., Pan, L., Musicaro, R., & Schacter, D. L. (2016) · Memory · doi:10.1080/09658211.2014.985591 · Cited by 140
Kim, H. (2014) · Hippocampus · doi:10.1002/hipo.22387 · Cited by 133
The Neural Basis of Involuntary Episodic Memories
Hall, S. A., Rubin, D. C., Miles, A. N., Davis, S. W., Wing, E. A., Cabeza, R. E. L., & Berntsen, D. (2014) · Journal of Cognitive Neuroscience · doi:10.1162/jocn_a_00633 · Cited by 130
Self-citationHuman medial temporal lobe neurons respond preferentially to personally relevant images
Viskontas, I. V., Quiroga, R. Q., & Fried, I. (2009) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0902319106 · Cited by 127
Memory reactivation during rest supports upcoming learning of related content
Schlichting, M. L., & Preston, A. R. (2014) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1404396111 · Cited by 126
Burgess, A. P., & Ali, L. (2002) · International Journal of Psychophysiology · doi:10.1016/s0167-8760(02)00108-3 · Cited by 126
The spatial scaffold: The effects of spatial context on memory for events.
Robin, J., Wynn, J. S., & Moscovitch, M. (2015) · Journal of Experimental Psychology Learning Memory and Cognition · doi:10.1037/xlm0000167 · Cited by 125
Self-citationDetecting Changes in Scenes: The Hippocampus Is Critical for Strength-Based Perception
Aly, M., Ranganath, C., & Yonelinas, A. P. (2013) · Neuron · doi:10.1016/j.neuron.2013.04.018 · Cited by 124
Scenes, Spaces, and Memory Traces
Maguire, E. A., Intraub, H., & Mullally, S. L. (2015) · The Neuroscientist · doi:10.1177/1073858415600389 · Cited by 114
Sheldon, S., & Moscovitch, M. (2011) · Hippocampus · doi:10.1002/hipo.20985 · Cited by 108
Self-citationNeuroimaging the Serial Position Curve
Talmi, D., Grady, C. L., Goshen‐Gottstein, Y., & Moscovitch, M. (2005) · Psychological Science · doi:10.1111/j.1467-9280.2005.01601.x · Cited by 108
Self-citationShallice, T., & Cooper, R. (2011) · Cortex · doi:10.1016/j.cortex.2011.07.004 · Cited by 101
Neglected Time: Impaired Temporal Perception of Multisecond Intervals in Unilateral Neglect
Danckert, J. A., Ferber, S., Pun, C., Broderick, C., Striemer, C. L., Rock, S., & Stewart, D. J. (2007) · Journal of Cognitive Neuroscience · doi:10.1162/jocn.2007.19.10.1706 · Cited by 101
Hirshhorn, M., Grady, C. L., Rosenbaum, R. S., Winocur, G., & Moscovitch, M. (2011) · Hippocampus · doi:10.1002/hipo.20944 · Cited by 100
Self-citationMerhav, M., Karni, A., & Gilboa, A. (2015) · NeuroImage · doi:10.1016/j.neuroimage.2015.05.027 · Cited by 99
Bowles, B., Crupi, C., Pigott, S. E., Parrent, A. G., Wiebe, S., Janzen, L. A., & Köhler, S. (2010) · Neuropsychologia · doi:10.1016/j.neuropsychologia.2010.05.010 · Cited by 99
Robin, J., & Moscovitch, M. (2013) · Journal of Experimental Psychology Learning Memory and Cognition · doi:10.1037/a0034886 · Cited by 98
Self-citationNadel, L., & Peterson, M. A. (2013) · Journal of Experimental Psychology General · doi:10.1037/a0033690 · Cited by 97
Self-citationKwan, D. T., Craver, C. F., Green, L., Myerson, J., & Rosenbaum, R. S. (2013) · Journal of Experimental Psychology General · doi:10.1037/a0034001 · Cited by 97
Memory, scene construction, and the human hippocampus
Kim, S., Dede, A. J. O., Hopkins, R. O., & Squire, L. R. (2015) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1503863112 · Cited by 97
Impaired Category Fluency in Medial Temporal Lobe Amnesia: The Role of Episodic Memory
Greenberg, D. L., Keane, M. M., Ryan, L., & Verfaellie, M. H. (2009) · Journal of Neuroscience · doi:10.1523/jneurosci.1202-09.2009 · Cited by 94
Empathy in Hippocampal Amnesia
Beadle, J. N., Tranel, D., Cohen, N. J., & Duff, M. C. (2013) · Frontiers in Psychology · doi:10.3389/fpsyg.2013.00069 · Cited by 94
Continuous Theta Burst Stimulation of Angular Gyrus Reduces Subjective Recollection
Yazar, Y., Bergström, Z. M., & Simons, J. S. (2014) · PLoS ONE · doi:10.1371/journal.pone.0110414 · Cited by 93
Representations 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 91
Berryhill, M. E. (2012) · Frontiers in Integrative Neuroscience · doi:10.3389/fnint.2012.00031 · Cited by 91
Sheldon, S., & Levine, B. (2013) · NeuroImage · doi:10.1016/j.neuroimage.2013.06.082 · Cited by 90
Intracranial recordings and human memory
Johnson, E. L., & Knight, R. T. (2014) · Current Opinion in Neurobiology · doi:10.1016/j.conb.2014.07.021 · Cited by 88
The perceptual richness of complex memory episodes is compromised by medial temporal lobe damage
St‐Laurent, M., Moscovitch, M., Jadd, R., & McAndrews, M. P. (2014) · Hippocampus · doi:10.1002/hipo.22249 · Cited by 85
Self-citationComparison of explicit and incidental learning strategies in memory-impaired patients
Smith, C. N., Urgolites, Z. J., Hopkins, R. O., & Squire, L. R. (2013) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1322263111 · Cited by 83
Gerraty, R. T., Davidow, J. Y., Wimmer, G. E., Kahn, I., & Shohamy, D. (2014) · Journal of Neuroscience · doi:10.1523/jneurosci.0185-14.2014 · Cited by 80
The hippocampus extrapolates beyond the view in scenes: an fMRI study of boundary extension
Chadwick, M. J., Mullally, S. L., & Maguire, E. A. (2013) · Cortex · doi:10.1016/j.cortex.2012.11.010 · Cited by 80
CA3 size predicts the precision of memory recall
Chadwick, M. J., Bonnici, H. M., & Maguire, E. A. (2014) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1319641111 · Cited by 80
Gaesser, B., Spreng, R. N., McLelland, V. C., Addis, D. R., & Schacter, D. L. (2013) · Hippocampus · doi:10.1002/hipo.22152 · Cited by 78
Evensmoen, H. R., Ladstein, J., Hansen, T. I., Møller, J. A., Witter, M. P., Nadel, L., & Håberg, A. K. (2015) · Hippocampus · doi:10.1002/hipo.22357 · Cited by 75
Self-citationFurman, O., Mendelsohn, A., & Dudai, Y. (2012) · Learning & Memory · doi:10.1101/lm.025965.112 · Cited by 75
The Hippocampus and Context Revisited
Nadel, L. (2008) · Hippocampal Place Fields · doi:10.1093/acprof:oso/9780195323245.003.0002 · Cited by 74
Self-citationAssessing recollection and familiarity of similar lures in a behavioral pattern separation task
Kim, J., & Yassa, M. A. (2013) · Hippocampus · doi:10.1002/hipo.22087 · Cited by 73
Viard, A., Desgranges, B., Eustache, F., & Piolino, P. (2012) · Brain and Cognition · doi:10.1016/j.bandc.2012.05.004 · Cited by 71
Individualized Theory of Mind (iToM): When Memory Modulates Empathy
Ciaramelli, E., Bernardi, F., & Moscovitch, M. (2013) · Frontiers in Psychology · doi:10.3389/fpsyg.2013.00004 · Cited by 71
Self-citationMemory as Social Glue: Close Interpersonal Relationships in Amnesic Patients
Davidson, P. S. R., Drouin, H., Kwan, D. T., Moscovitch, M., & Rosenbaum, R. S. (2012) · Frontiers in Psychology · doi:10.3389/fpsyg.2012.00531 · Cited by 70
Self-citationMedial temporal lobe amnesia impairs performance on a free association task
Sheldon, S., Romero, K., & Moscovitch, M. (2013) · Hippocampus · doi:10.1002/hipo.22099 · Cited by 69
Self-citationRobin, J., Hirshhorn, M., Rosenbaum, R. S., Winocur, G., Moscovitch, M., & Grady, C. L. (2014) · Hippocampus · doi:10.1002/hipo.22352 · Cited by 68
Self-citationRemembering Preservation in Hippocampal Amnesia
Clark, I. A., & Maguire, E. A. (2015) · Annual Review of Psychology · doi:10.1146/annurev-psych-122414-033739 · Cited by 68
Levine, B., Svoboda, E., Turner, G. R., Mandic, M., & Mackey, A. R. (2008) · Neuropsychologia · doi:10.1016/j.neuropsychologia.2008.12.026 · Cited by 68
The neural correlates of recollection: Hippocampal activation declines as episodic memory fades
Viskontas, I. V., Carr, V. A., Engel, S. A., & Knowlton, B. J. (2008) · Hippocampus · doi:10.1002/hipo.20503 · Cited by 67
Periodically reactivated context memory retains its precision and dependence on the hippocampus
Alvares, L. D. O., Einarsson, E. Ö., Santana, F., Crestani, A. P., Haubrich, J., Cassini, L. F., Nader, K., & Quillfeldt, J. A. (2011) · Hippocampus · doi:10.1002/hipo.20983 · Cited by 67
Impaired perception of mnemonic oldness, but not mnemonic newness, after parietal lobe damage
Hower, K. H., Wixted, J. T., Berryhill, M. E., & Olson, I. R. (2014) · Neuropsychologia · doi:10.1016/j.neuropsychologia.2014.02.014 · Cited by 62
Neocortical catastrophic interference in healthy and amnesic adults: A paradoxical matter of time
Merhav, M., Karni, A., & Gilboa, A. (2014) · Hippocampus · doi:10.1002/hipo.22353 · Cited by 59
Episodic memory and event construction in aging and amnesia
Romero, K., & Moscovitch, M. (2012) · Journal of Memory and Language · doi:10.1016/j.jml.2012.05.002 · Cited by 58
Self-citationIntact Learning of New Relations in Amnesia as Achieved through Unitization
Ryan, J. D., Moses, S. N., Barense, M. D., & Rosenbaum, R. S. (2013) · Journal of Neuroscience · doi:10.1523/jneurosci.0169-13.2013 · Cited by 57
Ben-Yakov, A., Rubinson, M., & Dudai, Y. (2014) · Journal of Neuroscience · doi:10.1523/jneurosci.1892-14.2014 · Cited by 57
Verfaellie, M. H., Bousquet, K., & Keane, M. M. (2014) · Neuropsychologia · doi:10.1016/j.neuropsychologia.2014.06.018 · Cited by 57
Rapid consolidation of new knowledge in adulthood via fast mapping
Coutanche, M. N., & Thompson‐Schill, S. L. (2015) · Trends in Cognitive Sciences · doi:10.1016/j.tics.2015.06.001 · Cited by 51
The hippocampus, a time machine that makes errors
Barba, G. D., & Corte, V. L. (2013) · Trends in Cognitive Sciences · doi:10.1016/j.tics.2013.01.005 · Cited by 51
When recognition memory is independent of hippocampal function
Smith, C. N., Jeneson, A., Frascino, J. C., Kirwan, C. B., Hopkins, R. O., & Squire, L. R. (2014) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1409878111 · Cited by 49
Recollective performance advantages for implicit memory tasks
Sheldon, S., & Moscovitch, M. (2010) · Memory · doi:10.1080/09658211.2010.499876 · Cited by 49
Self-citationRenoult, L., Davidson, P. S. R., Schmitz, E. M., Park, L., Campbell, K., Moscovitch, M., & Levine, B. (2014) · Journal of Cognitive Neuroscience · doi:10.1162/jocn_a_00689 · Cited by 48
Self-citationRecollection versus strength as the primary determinant of hippocampal engagement at retrieval
Cohn, M., Moscovitch, M., Lahat, A., & McAndrews, M. P. (2009) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0908651106 · Cited by 42
Self-citation
Research works printed but not linked: 4
- Addis DR, 2011, Front. Hum. Neurosci., 5, 173
- Craik FIM, 1986, Human Memory and Cognitive Capabilities, 409
- James W, 1950, Principles of Psychology, 1
- Moscovitch M, 1992, The Encyclopedia of Learning and Memory: A Volume in Neuropsychology, 182
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Metadata
- Authors
- Moscovitch, M., Cabeza, R., Winocur, G., & Nadel, L.
- Affiliations
- University of Toronto (CA)
- Duke University (US)
- University of Arizona (US)
- Venue
- Annual Review of Psychology
- Publisher
- Annual Reviews
- Published
- 2016-01-04
- Volume
- 67
- Issue
- 1
- Pages
- 105-134
- ISSN
- 0066-4308 (ISSN-L)
- 1545-2085
- PMC
- PMC5060006
- OpenAlex
- W1702555102
- Cited by
- 1,062
- References
- 213
- Citations by year
- 2026: 77 · 2025: 122 · 2024: 154 · 2023: 88 · 2022: 91 · 2021: 129 · 2020: 120 · 2019: 105 · 2018: 86 · 2017: 60 · 2016: 27
- FWCI
- 9.73
- Type
- journal article
- Language
- en
- Open access
- green
- www.ncbi.nlm.nih.gov
- Locations
- Annual Review of Psychology (publishedVersion)
- PubMed (publishedVersion)
- PubMed Central (acceptedVersion)
- Funders
- Canadian Institutes of Health Research (MGP6694)
- National Institute on Aging (R01AG019731, AG 19731)
- Topics
- Life Sciences › Neuroscience › Cognitive Neuroscience › Memory and Neural Mechanisms
- Life Sciences › Neuroscience › Cognitive Neuroscience › Memory Processes and Influences
- Social Sciences › Psychology › Experimental and Cognitive Psychology › Cognitive Functions and Memory
- Keywords
- episodic memory, hippocampus, neocortex, hippocampal subfields, Component Process Model, neural substrates of memory, hippocampal-neocortical interaction, memory and perception, language and memory
- MeSH terms
- Animals, Brain Mapping, Hippocampus, Humans, Magnetic Resonance Imaging, Neocortex, Rats, Memory, Episodic
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