Cited by 133Memory and Neural MechanismsMemory Processes and InfluencesSleep and Wakefulness Research

The DOI matches its Crossref record; 184 of the 184 references it cites were found in a registry or an index.

Memory consolidation as an adaptive process

Open access

Cowan, Emily T., Schapiro, Anna C., Dunsmoor, Joseph E., Murty, Vishnu P.·2021·Psychonomic Bulletin & Review

DOI 10.3758/s13423-021-01978-x

Open this paper in CoChat — free account Open PDF

Abstract

We rely on our long-term memories to guide future behaviors, making it adaptive to prioritize the retention of goal-relevant, salient information in memory. In this review, we discuss findings from rodent and human research to demonstrate that active processes during post-encoding consolidation support the selective stabilization of recent experience into adaptive, long-term memories. Building upon literatures focused on dynamics at the cellular level, we highlight that consolidation also transforms memories at the systems level to support future goal-relevant behavior, resulting in more generalized memory traces in the brain and behavior. We synthesize previous literatures spanning animal research, human cognitive neuroscience, and cognitive psychology to propose an integrative framework for adaptive consolidation by which goal-relevant memoranda are "tagged" for subsequent consolidation, resulting in selective transformations to the structure of memories that support flexible, goal-relevant behaviors.

Integrity signals

Registry

Crossref · 10.3758/s13423-021-01978-x

Cites

184 of 184 references verified0 citation errors · 0 not checkable

Statistics

Recomputing p-values needs the paper’s full text.

Claims the paper makes

We couldn’t retrieve this paper’s full text, so its claims and self-check weren’t run. The registry and citation checks still apply.

Claims other papers make about this one

Each is checked against this paper’s own text: does it say what the citing paper says it does?

Why there are complementary learning systems in the hippocampus and neocortex: insights from the successes and failures of connectionist models of learning and memory
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
Depth of Processing and the Retention of Words in Episodic Memory
Craik, F. I. M., & Tulving, E. (1975) · Journal of Experimental Psychology: General · doi:10.1037/0096-3445.104.3.268 · Cited by 4,121
Reactivation of hippocampal ensemble memories during sleep
Wilson, M. A., & McNaughton, B. L. (1994) · Science · doi:10.1126/science.8036517 · Cited by 3,118
About Sleep's Role in Memory
Rasch, B., & Born, J. (2013) · Physiological Reviews · doi:10.1152/physrev.00032.2012 · Cited by 2,783
Remembering the past to imagine the future: the prospective brain
Schacter, D. L., Addis, D. R., & Buckner, R. L. (2007) · Nature Reviews Neuroscience · doi:10.1038/nrn2213 · Cited by 2,394
The organization of recent and remote memories
Frankland, P. W., & Bontempi, B. (2005) · Nature Reviews Neuroscience · doi:10.1038/nrn1607 · Cited by 2,138
The hippocampal-VTA loop: controlling the entry of information into long-term memory
Lisman, J. E., & Grace, A. A. (2005) · Neuron · doi:10.1016/j.neuron.2005.05.002 · Cited by 1,983
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
The cognitive neuroscience of constructive memory: remembering the past and imagining the future
Schacter, D. L., & Addis, D. R. (2007) · Philosophical Transactions of the Royal Society B: Biological Sciences · doi:10.1098/rstb.2007.2087 · Cited by 1,836
Cognitive neuroscience of emotional memory
LaBar, K. S., & Cabeza, R. (2006) · Nature Reviews Neuroscience · doi:10.1038/nrn1825 · Cited by 1,834
Synaptic tagging and long-term potentiation
Frey, U., & Morris, R. G. M. (1997) · Nature · doi:10.1038/385533a0 · Cited by 1,736
Reverse replay of behavioural sequences in hippocampal place cells during the awake state
Foster, D. J., & Wilson, M. A. (2006) · Nature · doi:10.1038/nature04587 · Cited by 1,727
Two-stage model of memory trace formation: A role for “noisy” brain states
Buzsáki, G. (1989) · Neuroscience · doi:10.1016/0306-4522(89)90423-5 · Cited by 1,709
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
Mechanisms of emotional arousal and lasting declarative memory.
Cahill, L., & McGaugh, J. L. (1998) · Trends in Neurosciences · doi:10.1016/s0166-2236(97)01214-9 · Cited by 1,575
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
Grouping of brain rhythms in corticothalamic systems
Steriade, M. (2006) · Neuroscience · doi:10.1016/j.neuroscience.2005.10.029 · Cited by 1,296
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
Hippocampal 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
Forward and reverse hippocampal place-cell sequences during ripples
Diba, K., & Buzsáki, G. (2007) · Nature Neuroscience · doi:10.1038/nn1961 · Cited by 1,205
Replay of neuronal firing sequences in rat hippocampus during sleep following spatial experience
Skaggs, W. E., & McNaughton, B. L. (1996) · Science · doi:10.1126/science.271.5257.1870 · Cited by 1,173
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
Sleep-Dependent Learning and Memory Consolidation
Walker, M. P., & Stickgold, R. (2004) · Neuron · doi:10.1016/j.neuron.2004.08.031 · Cited by 1,113
Episodic memory and beyond: the hippocampus and neocortex in transformation
Moscovitch, M., Cabeza, R., Winocur, G., & Nadel, L. (2016) · Annual Review of Psychology · doi:10.1146/annurev-psych-113011-143733 · Cited by 1,062
What Is a Cognitive Map? Organizing Knowledge for Flexible Behavior
Behrens, T. E. J., Muller, T. H., Whittington, J. C. R., Mark, S., Baram, A. B., Stachenfeld, K. L., & Kurth-Nelson, Z. (2018) · Neuron · doi:10.1016/j.neuron.2018.10.002 · Cited by 1,055
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
Coordinated interactions between hippocampal Ripples and Cortical Spindles during Slow-Wave Sleep
Siapas, A. G., & Wilson, M. A. (1998) · Neuron · doi:10.1016/s0896-6273(00)80629-7 · Cited by 1,052
Arousal-Biased Competition in Perception and Memory
Mather, M., & Sutherland, M. R. (2011) · Perspectives on Psychological Science · doi:10.1177/1745691611400234 · Cited by 1,013
Sleep inspires insight
Wagner, U., Gais, S., Haider, H., Verleger, R., & Born, J. (2004) · Nature · doi:10.1038/nature02223 · Cited by 1,012
The hippocampus as a predictive map
Stachenfeld, K. L., Botvinick, M. M., & Gershman, S. J. (2017) · Nature Neuroscience · doi:10.1038/nn.4650 · Cited by 1,000
Reward-motivated learning: mesolimbic activation precedes memory formation
Adcock, R. A., Thangavel, A., Whitfield-Gabrieli, S., Knutson, B., & Gabrieli, J. D. E. (2006) · Neuron · doi:10.1016/j.neuron.2006.03.036 · Cited by 977
Hippocampal replay in the awake state: a potential substrate for memory consolidation and retrieval
Carr, M. F., Jadhav, S. P., & Frank, L. M. (2011) · Nature Neuroscience · doi:10.1038/nn.2732 · Cited by 958
Communication between neocortex and hippocampus during sleep in rodents
Sirota, A., Csicsvari, J., Buhl, D., & Buzsáki, G. (2003) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0437938100 · Cited by 930
Orbitofrontal Cortex as a Cognitive Map of Task Space
Wilson, R. C., Takahashi, Y. K., Schoenbaum, G., & Niv, Y. (2014) · Neuron · doi:10.1016/j.neuron.2013.11.005 · Cited by 885
Learning-dependent increases in sleep spindle density
Gais, S., Mölle, M., Helms, K., & Born, J. (2002) · The Journal of Neuroscience · doi:10.1523/jneurosci.22-15-06830.2002 · Cited by 859
Hierarchical nesting of slow oscillations, spindles and ripples in the human hippocampus during sleep
Staresina, B. P., Bergmann, T. O., Bonnefond, M., van der Meij, R., Jensen, O., Deuker, L., Elger, C. E., Axmacher, N., & Fell, J. (2015) · Nature Neuroscience · doi:10.1038/nn.4119 · Cited by 831
Making memories last: the synaptic tagging and capture hypothesis
Redondo, R. L., & Morris, R. G. M. (2011) · Nature Reviews Neuroscience · doi:10.1038/nrn2963 · Cited by 792
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
Sleep-dependent memory triage: evolving generalization through selective processing
Stickgold, R., & Walker, M. P. (2013) · Nature Neuroscience · doi:10.1038/nn.3303 · Cited by 755
The Consolidation and Transformation of Memory
Dudai, Y., Karni, A., & Born, J. (2015) · Neuron · doi:10.1016/j.neuron.2015.09.004 · Cited by 741
Dopamine and adaptive memory
Shohamy, D., & Adcock, R. A. (2010) · Trends in Cognitive Sciences · doi:10.1016/j.tics.2010.08.002 · Cited by 736
Hippocampal replay is not a simple function of experience
Gupta, A. S., van der Meer, M. A. A., Touretzky, D. S., & Redish, A. D. (2010) · Neuron · doi:10.1016/j.neuron.2010.01.034 · Cited by 733
Are affective events richly recollected or simply familiar? The experience and process of recognizing feelings past.
Ochsner, K. N. (2000) · Journal of Experimental Psychology: General · doi:10.1037/0096-3445.129.2.242 · Cited by 704
Reward-related FMRI activation of dopaminergic midbrain is associated with enhanced hippocampus-dependent long-term memory formation
Wittmann, B. C., Schott, B. H., Guderian, S., Frey, J. U., Heinze, H.-J., & Düzel, E. (2005) · Neuron · doi:10.1016/j.neuron.2005.01.010 · Cited by 698
Hippocampo-cortical coupling mediates memory consolidation during sleep
Maingret, N., Girardeau, G., Todorova, R., Goutierre, M., & Zugaro, M. (2016) · Nature Neuroscience · doi:10.1038/nn.4304 · Cited by 667
The Tolman-Eichenbaum machine: unifying space and relational memory through generalization in the hippocampal formation
Whittington, J. C. R., Muller, T. H., Mark, S., Chen, G., Barry, C., Burgess, N., & Behrens, T. E. J. (2020) · Cell · doi:10.1016/j.cell.2020.10.024 · Cited by 660
Neuronal Plasticity in Thalamocortical Networks during Sleep and Waking Oscillations
Steriade, M., & Timofeev, I. (2003) · Neuron · doi:10.1016/s0896-6273(03)00065-5 · Cited by 659
Synaptic tagging: implications for late maintenance of hippocampal long-term potentiation
Frey, U., & Morris, R. G. M. (1998) · Trends in Neurosciences · doi:10.1016/s0166-2236(97)01189-2 · Cited by 615
REM sleep, prefrontal theta, and the consolidation of human emotional memory
Nishida, M., Pearsall, J., Buckner, R. L., & Walker, M. P. (2009) · Cerebral Cortex · doi:10.1093/cercor/bhn155 · Cited by 603
Human orbitofrontal cortex represents a cognitive map of state space
Schuck, N. W., Cai, M. B., Wilson, R. C., & Niv, Y. (2016) · Neuron · doi:10.1016/j.neuron.2016.08.019 · Cited by 602
Remembering one year later: role of the amygdala and the medial temporal lobe memory system in retrieving emotional memories
Dolcos, F., LaBar, K. S., & Cabeza, R. (2005) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0409848102 · Cited by 601
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
Dopamine-dependent facilitation of LTP induction in hippocampal CA1 by exposure to spatial novelty
Li, S., Cullen, W. K., Anwyl, R., & Rowan, M. J. (2003) · Nature Neuroscience · doi:10.1038/nn1049 · Cited by 568
Sleep Spindles and Their Significance for Declarative Memory Consolidation
Schabus, M., Gruber, G., Parapatics, S., Sauter, C., Klösch, G., Anderer, P., Klimesch, W., Saletu, B., & Zeitlhofer, J. (2004) · Sleep · doi:10.1093/sleep/27.7.1479 · Cited by 560
Memory Transformation and Systems Consolidation
Winocur, G., & Moscovitch, M. (2011) · Journal of the International Neuropsychological Society · doi:10.1017/s1355617711000683 · Cited by 557
Declarative memory consolidation in humans: A prospective functional magnetic resonance imaging study
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
D1/D5 receptor agonists induce a protein synthesis-dependent late potentiation in the CA1 region of the hippocampus.
Huang, Y.-Y., & Kandel, E. R. (1995) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.92.7.2446 · Cited by 544
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
Human replay spontaneously reorganizes experience
Liu, Y., Dolan, R. J., Kurth-Nelson, Z., & Behrens, T. E. J. (2019) · Cell · doi:10.1016/j.cell.2019.06.012 · Cited by 497
Paired-associate learning as a function of arousal and interpolated interval.
Kleinsmith, L. J., & Kaplan, S. (1963) · Journal of Experimental Psychology · doi:10.1037/h0040288 · Cited by 495
Hemodynamic cerebral correlates of sleep spindles during human non-rapid eye movement sleep
Schabus, M., Dang-Vu, T. T., Albouy, G., Balteau, E., Boly, M., Carrier, J., Darsaud, A., Degueldre, C., Desseilles, M., Gais, S., et al. (2007) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0703084104 · Cited by 488
Dopaminergic neurons promote hippocampal reactivation and spatial memory persistence
McNamara, C. G., Tejero-Cantero, Á., Trouche, S., Campo-Urriza, N., & Dupret, D. (2014) · Nature Neuroscience · doi:10.1038/nn.3843 · Cited by 486
Dopamine controls persistence of long-term memory storage
Rossato, J. I., Bevilaqua, L. R. M., Izquierdo, I., Medina, J. H., & Cammarota, M. (2009) · Science · doi:10.1126/science.1172545 · Cited by 486
Sleep spindle activity is associated with the integration of new memories and existing knowledge
Tamminen, J., Payne, J. D., Stickgold, R., Wamsley, E. J., & Gaskell, M. G. (2010) · The Journal of Neuroscience · doi:10.1523/jneurosci.3028-10.2010 · Cited by 478
Persistent schema-dependent hippocampal-neocortical connectivity during memory encoding and postencoding rest in humans
van Kesteren, M. T. R., Fernández, G., Norris, D. G., & Hermans, E. J. (2010) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0914892107 · Cited by 449
Memory modulation.
Roozendaal, B., & McGaugh, J. L. (2011) · Behavioral Neuroscience · doi:10.1037/a0026187 · Cited by 445
Memory integration: neural mechanisms and implications for behavior
Schlichting, M. L., & Preston, A. R. (2014) · Current Opinion in Behavioral Sciences · doi:10.1016/j.cobeha.2014.07.005 · Cited by 442
Sleep preferentially enhances memory for emotional components of scenes
Payne, J. D., Stickgold, R., Swanberg, K., & Kensinger, E. A. (2008) · Psychological Science · doi:10.1111/j.1467-9280.2008.02157.x · Cited by 440
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
Decay happens: the role of active forgetting in memory
Hardt, O., Nader, K., & Nadel, L. (2013) · Trends in Cognitive Sciences · doi:10.1016/j.tics.2013.01.001 · Cited by 416
Human relational memory requires time and sleep
Ellenbogen, J. M., Hu, P. T., Payne, J. D., Titone, D., & Walker, M. P. (2007) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0700094104 · Cited by 415
Pattern-Specific Associative Long-Term Potentiation Induced by a Sleep Spindle-Related Spike Train
Rosanova, M., & Ulrich, D. (2005) · The Journal of Neuroscience · doi:10.1523/jneurosci.2149-05.2005 · Cited by 413
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
Sleep transforms the cerebral trace of declarative memories
Gais, S., Albouy, G., Boly, M., Dang-Vu, T. T., Darsaud, A., Desseilles, M., Rauchs, G., Schabus, M., Sterpenich, V., Vandewalle, G., et al. (2007) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0705454104 · Cited by 412
Overnight verbal memory retention correlates with the number of sleep spindles
Clemens, Z., Fabó, D., & Halász, P. (2005) · Neuroscience · doi:10.1016/j.neuroscience.2005.01.011 · Cited by 405
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
Temporal coupling of parahippocampal ripples, sleep spindles and slow oscillations in humans
Clemens, Z., Molle, M., Eross, L., Barsi, P., Halasz, P., & Born, J. (2007) · Brain · doi:10.1093/brain/awm146 · Cited by 398
Sleep selectively enhances memory expected to be of future relevance
Wilhelm, I., Diekelmann, S., Molzow, I., Ayoub, A., Mölle, M., & Born, J. (2011) · The Journal of Neuroscience · doi:10.1523/jneurosci.3575-10.2011 · Cited by 397
Rewarded Outcomes Enhance Reactivation of Experience in the Hippocampus
Singer, A. C., & Frank, L. M. (2009) · Neuron · doi:10.1016/j.neuron.2009.11.016 · Cited by 385
How arousal modulates memory: disentangling the effects of attention and retention
Sharot, T., & Phelps, E. A. (2004) · Cognitive, Affective, & Behavioral Neuroscience · doi:10.3758/cabn.4.3.294 · Cited by 375
Induction of long-term memory by exposure to novelty requires protein synthesis: evidence for a behavioral tagging
Moncada, D., & Viola, H. (2007) · The Journal of Neuroscience · doi:10.1523/jneurosci.1083-07.2007 · Cited by 370
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
Over the river, through the woods: cognitive maps in the hippocampus and orbitofrontal cortex
Wikenheiser, A. M., & Schoenbaum, G. M. (2016) · Nature reviews. Neuroscience · doi:10.1038/nrn.2016.56 · Cited by 368
Sleep facilitates consolidation of emotional declarative memory
Hu, P., Stylos-Allan, M., & Walker, M. P. (2006) · Psychological Science · doi:10.1111/j.1467-9280.2006.01799.x · Cited by 355
The slow forgetting of emotional episodic memories: an emotional binding account
Yonelinas, A. P., & Ritchey, M. (2015) · Trends in Cognitive Sciences · doi:10.1016/j.tics.2015.02.009 · Cited by 341
The Persistence and Transience of Memory
Richards, B. A., & Frankland, P. W. (2017) · Neuron · doi:10.1016/j.neuron.2017.04.037 · Cited by 338
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
Self-citation
Hippocampal ripples and memory consolidation
Girardeau, G., & Zugaro, M. (2011) · Current Opinion in Neurobiology · doi:10.1016/j.conb.2011.02.005 · Cited by 330
Hippocampal place cells construct reward related sequences through unexplored space
Ólafsdóttir, H. F., Barry, C., Saleem, A. B., Hassabis, D., & Spiers, H. J. (2015) · eLife · doi:10.7554/elife.06063 · Cited by 319
Behavioral tagging is a general mechanism of long-term memory formation
Ballarini, F., Moncada, D., Martinez, M. C., Alen, N., & Viola, H. (2009) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0907078106 · Cited by 301
Differential roles for medial prefrontal and medial temporal cortices in schema-dependent encoding: From congruent to incongruent
van Kesteren, M. T. R., Beul, S. F., Takashima, A., Henson, R. N., Ruiter, D. J., & Fernández, G. (2013) · Neuropsychologia · doi:10.1016/j.neuropsychologia.2013.05.027 · Cited by 298
Reverse replay of hippocampal place cells is uniquely modulated by changing reward
Ambrose, R. E., Pfeiffer, B. E., & Foster, D. J. (2016) · Neuron · doi:10.1016/j.neuron.2016.07.047 · Cited by 292
Hippocampal SWR Activity Predicts Correct Decisions during the Initial Learning of an Alternation Task
Singer, A. C., Carr, M. F., Karlsson, M. P., & Frank, L. M. (2013) · Neuron · doi:10.1016/j.neuron.2013.01.027 · Cited by 289
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
Memory consolidation is linked to spindle-mediated information processing during sleep
Cairney, S. A., Guttesen, A. Á. V., El Marj, N., & Staresina, B. P. (2018) · Current Biology · doi:10.1016/j.cub.2018.01.087 · Cited by 289
Human hippocampal replay during rest prioritizes weakly learned information and predicts memory performance
Schapiro, A. C., McDevitt, E. A., Rogers, T. T., Mednick, S. C., & Norman, K. A. (2018) · Nature Communications · doi:10.1038/s41467-018-06213-1 · Cited by 282
Self-citation
Sustained increase in hippocampal sharp-wave ripple activity during slow-wave sleep after learning
Eschenko, O., Ramadan, W., Mölle, M., Born, J., & Sara, S. J. (2008) · Learning & Memory · doi:10.1101/lm.726008 · Cited by 277
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
Consolidating memories
McGaugh, J. L. (2015) · Annual Review of Psychology · doi:10.1146/annurev-psych-010814-014954 · Cited by 271
Slow oscillations orchestrating fast oscillations and memory consolidation
Mölle, M., & Born, J. (2011) · Progress in Brain Research · doi:10.1016/b978-0-444-53839-0.00007-7 · Cited by 270
Dopamine and Memory: Modulation of the Persistence of Memory for Novel Hippocampal NMDA Receptor-Dependent Paired Associates
Bethus, I., Tse, D., & Morris, R. G. M. (2010) · The Journal of Neuroscience · doi:10.1523/jneurosci.2721-09.2010 · Cited by 270
Sleep spindles in midday naps enhance learning in preschool children
Kurdziel, L., Duclos, K., & Spencer, R. M. C. (2013) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1306418110 · Cited by 266
Details, gist and schema: hippocampal–neocortical interactions underlying recent and remote episodic and spatial memory
Robin, J., & Moscovitch, M. (2017) · Current Opinion in Behavioral Sciences · doi:10.1016/j.cobeha.2017.07.016 · Cited by 266
Sleep-related hippocampo-cortical interplay during emotional memory recollection
Sterpenich, V., Albouy, G., Boly, M., Vandewalle, G., Darsaud, A., Balteau, E., Dang-Vu, T. T., Desseilles, M., D'Argembeau, A., Gais, S., et al. (2007) · PLoS Biology · doi:10.1371/journal.pbio.0050282 · Cited by 265
Enhanced Emotional Memory: Cognitive and Neural Mechanisms
Talmi, D. (2013) · Current Directions in Psychological Science · doi:10.1177/0963721413498893 · Cited by 257
Differential time-dependent effects of emotion on recollective experience and memory for contextual information.
Sharot, T., & Yonelinas, A. (2008) · Cognition · doi:10.1016/j.cognition.2007.03.002 · Cited by 246
Consolidation Promotes the Emergence of Representational Overlap in the Hippocampus and Medial Prefrontal Cortex
Tompary, A., & Davachi, L. (2017) · Neuron · doi:10.1016/j.neuron.2017.09.005 · Cited by 235
Encoding Difficulty Promotes Postlearning Changes in Sleep Spindle Activity during Napping
Schmidt, C., Peigneux, P., Muto, V., Schenkel, M., Knoblauch, V., Münch, M. Y., de Quervain, D. J. ‐., Wirz‐Justice, A., & Cajochen, C. (2006) · Journal of Neuroscience · doi:10.1523/jneurosci.2464-06.2006 · Cited by 230
Sleep spindle-related reactivation of category-specific cortical regions after learning face-scene associations
Bergmann, T. O., Mölle, M., Diedrichs, J., Born, J., & Siebner, H. R. (2012) · NeuroImage · doi:10.1016/j.neuroimage.2011.10.036 · Cited by 228
Basolateral amygdala lesions block glucocorticoid-induced modulation of memory for spatial learning.
Roozendaal, B., Portillo-Marquez, G., & McGaugh, J. L. (1996) · Behavioral Neuroscience · doi:10.1037//0735-7044.110.5.1074 · Cited by 221
The Role of Memory Reactivation during Wakefulness and Sleep in Determining Which Memories Endure
Oudiette, D., Antony, J. W., Creery, J. D., & Paller, K. A. (2013) · Journal of Neuroscience · doi:10.1523/jneurosci.5497-12.2013 · Cited by 220
Sleep Spindles and Hippocampal Functional Connectivity in Human NREM Sleep
Andrade, K. C., Spoormaker, V. I., Dresler, M., Wehrle, R., Holsboer, F., Sämann, P., & Czisch, M. (2011) · Journal of Neuroscience · doi:10.1523/jneurosci.5660-10.2011 · Cited by 218
Sleep promotes the neural reorganization of remote emotional memory
Sterpenich, V., Albouy, G., Darsaud, A., Schmidt, C., Vandewalle, G., Dang Vu, T. T., Desseilles, M., Phillips, C., Degueldre, C., Balteau, E., et al. (2009) · The Journal of Neuroscience · doi:10.1523/jneurosci.0561-09.2009 · Cited by 217
Post-learning hippocampal dynamics promote preferential retention of rewarding events
Gruber, M. J., Ritchey, M., Wang, S.-F., Doss, M. K., & Ranganath, C. (2016) · Neuron · doi:10.1016/j.neuron.2016.01.017 · Cited by 212
Sleep spindle refractoriness segregates periods of memory reactivation
Antony, J. W., Piloto, L., Wang, M., Pacheco, P., Norman, K. A., & Paller, K. A. (2018) · Current Biology · doi:10.1016/j.cub.2018.04.020 · Cited by 208
Role of Amygdala Connectivity in the Persistence of Emotional Memories Over Time: An Event-Related fMRI Investigation
Ritchey, M., Dolcos, F., & Cabeza, R. E. L. (2008) · Cerebral Cortex · doi:10.1093/cercor/bhm262 · Cited by 204
Anticipated reward enhances offline learning during sleep.
Fischer, S., & Born, J. (2009) · Journal of Experimental Psychology: Learning, Memory, and Cognition · doi:10.1037/a0017256 · Cited by 186
The content of hippocampal “replay”
Pfeiffer, B. E. (2017) · Hippocampus · doi:10.1002/hipo.22824 · Cited by 184
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 184
Memory trace replay: The shaping of memory consolidation by neuromodulation
Atherton, L. A., Dupret, D., & Mellor, J. R. (2015) · Trends in Neurosciences · doi:10.1016/j.tins.2015.07.004 · Cited by 180
Twenty-four hours retention of visuospatial memory correlates with the number of parietal sleep spindles
Clemens, Z., Fabó, D., & Halász, P. (2006) · Neuroscience Letters · doi:10.1016/j.neulet.2006.04.035 · Cited by 179
Ventromedial Prefrontal and Anterior Cingulate Cortex Adopt Choice and Default Reference Frames during Sequential Multi-Alternative Choice
Boorman, E. D., Rushworth, M. F. S., & Behrens, T. E. J. (2013) · Journal of Neuroscience · doi:10.1523/jneurosci.3022-12.2013 · Cited by 178
Sleep leads to changes in the emotional memory trace: evidence from FMRI
Payne, J. D., & Kensinger, E. A. (2011) · Journal of Cognitive Neuroscience · doi:10.1162/jocn.2010.21526 · Cited by 169
The reorganisation of memory during sleep
Landmann, N., Kühn, M., Piosczyk, H., Feige, B., Baglioni, C., Spiegelhalder, K., Frase, L., Riemann, D. W., Sterr, A., & Nissen, C. (2014) · Sleep Medicine Reviews · doi:10.1016/j.smrv.2014.03.005 · Cited by 167
Involvement of spindles in memory consolidation is slow wave sleep-specific
Cox, R., Hofman, W. F., & Talamini, L. M. (2012) · Learning & Memory · doi:10.1101/lm.026252.112 · Cited by 163
Consolidation power of extrinsic rewards: Reward cues enhance long-term memory for irrelevant past events.
Murayama, K., & Kitagami, S. (2013) · Journal of Experimental Psychology General · doi:10.1037/a0031992 · Cited by 163
Role of conceptual knowledge in learning and retention of conditioned fear
Dunsmoor, J. E., Martin, A. D., & LaBar, K. S. (2011) · Biological Psychology · doi:10.1016/j.biopsycho.2011.11.002 · Cited by 160
Self-citation
What Are Memories For? The Hippocampus Bridges Past Experience with Future Decisions
Biderman, N., Bakkour, A., & Shohamy, D. (2020) · Trends in Cognitive Sciences · doi:10.1016/j.tics.2020.04.004 · Cited by 160
Hippocampal Contributions to Model-Based Planning and Spatial Memory
Vikbladh, O. M., Meager, M. R., King, J. A., Blackmon, K., Devinsky, O., Shohamy, D., Burgess, N., & Daw, N. D. (2019) · Neuron · doi:10.1016/j.neuron.2019.02.014 · Cited by 159
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
Self-citation
The role of sleep spindles and slow-wave activity in integrating new information in semantic memory
Tamminen, J., Lambon Ralph, M. A., & Lewis, P. A. (2013) · The Journal of Neuroscience · doi:10.1523/jneurosci.5093-12.2013 · Cited by 152
Locus Coeruleus Activity Strengthens Prioritized Memories Under Arousal
Clewett, D. V., Huang, R., Velasco, R., Lee, T.-H., & Mather, M. (2018) · The Journal of Neuroscience · doi:10.1523/jneurosci.2097-17.2017 · Cited by 152
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
Sleep Spindle Density Predicts the Effect of Prior Knowledge on Memory Consolidation
Hennies, N., Ralph, M. A. L., Kempkes, M., Cousins, J. N., & Lewis, P. A. (2016) · Journal of Neuroscience · doi:10.1523/jneurosci.3162-15.2016 · Cited by 149
Evolving schema representations in orbitofrontal ensembles during learning
Zhou, J., Jia, C., Montesinos-Cartagena, M., Gardner, M., Zong, W., & Schoenbaum, G. M. (2020) · Nature · doi:10.1038/s41586-020-03061-2 · Cited by 148
Sleep Spindles and Memory Reprocessing
Antony, J. W., Schönauer, M., Staresina, B. P., & Cairney, S. A. (2019) · Trends in Neurosciences · doi:10.1016/j.tins.2018.09.012 · Cited by 146
Selectivity in Postencoding Connectivity with High-Level Visual Cortex Is Associated with Reward-Motivated Memory
Murty, V. P., Tompary, A., Adcock, R. A., & Davachi, L. (2016) · Journal of Neuroscience · doi:10.1523/jneurosci.4032-15.2016 · Cited by 141
Self-citation
Decoding material-specific memory reprocessing during sleep in humans
Schönauer, M., Alizadeh, S., Jamalabadi, H., Abraham, A., Pawlizki, A., & Gais, S. (2017) · Nature Communications · doi:10.1038/ncomms15404 · Cited by 139
Sleep-Dependent Facilitation of Episodic Memory Details
van der Helm, E., Gujar, N., Nishida, M., & Walker, M. P. (2011) · PLoS ONE · doi:10.1371/journal.pone.0027421 · Cited by 138
Money enhances memory consolidation – But only for boring material
Murayama, K., & Kuhbandner, C. (2011) · Cognition · doi:10.1016/j.cognition.2011.01.001 · Cited by 130
Echoes of Emotions Past: How Neuromodulators Determine What We Recollect
Clewett, D., & Murty, V. P. (2019) · eNeuro · doi:10.1523/eneuro.0108-18.2019 · Cited by 127
Self-citation
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
Overnight Consolidation Aids the Transfer of Statistical Knowledge from the Medial Temporal Lobe to the Striatum
Durrant, S. J., Cairney, S. A., & Lewis, P. A. (2013) · Cerebral Cortex · doi:10.1093/cercor/bhs244 · Cited by 124
Two Anatomically and Computationally Distinct Learning Signals Predict Changes to Stimulus-Outcome Associations in Hippocampus
Boorman, E. D., Rajendran, V. G., O’Reilly, J. X., & Behrens, T. E. J. (2016) · Neuron · doi:10.1016/j.neuron.2016.02.014 · Cited by 116
Retroactive and graded prioritization of memory by reward
Braun, E. K., Wimmer, G. E., & Shohamy, D. (2018) · Nature Communications · doi:10.1038/s41467-018-07280-0 · Cited by 112
Sleep Supports Selective Retention of Associative Memories Based on Relevance for Future Utilization
van Dongen, E. V., Thielen, J.-W., Takashima, A., Barth, M., & Fernández, G. (2012) · PLoS ONE · doi:10.1371/journal.pone.0043426 · Cited by 110 · cited 1×
“…have shown specific benefits of sleep for the retention of task goals (Diekelmann et al., 2013; Scullin & McDaniel, 2010) and content determined to be relevant for future use ( van Dongen et al., 2012; van Rijn et al., 2017; Wilhelm et al., 2011; cf.: Reverberi et al., 2020; Wamsley et al., 2016).”
Background
Ventromedial Prefrontal Cortex Is Necessary for Normal Associative Inference and Memory Integration
Spalding, K. N., Schlichting, M. L., Zeithamová, D., Preston, A. R., Tranel, D., Duff, M. C., & Warren, D. E. (2018) · Journal of Neuroscience · doi:10.1523/jneurosci.2501-17.2018 · Cited by 109
Remembering to Execute a Goal: Sleep on It!
Scullin, M. K., & McDaniel, M. A. (2010) · Psychological Science · doi:10.1177/0956797610373373 · Cited by 106
Deliberating trade-offs with the future
Bulley, A., & Schacter, D. L. (2020) · Nature Human Behaviour · doi:10.1038/s41562-020-0834-9 · Cited by 105
Sleep facilitates learning a new linguistic rule
Batterink, L. J., Oudiette, D., Reber, P. J., & Paller, K. A. (2014) · Neuropsychologia · doi:10.1016/j.neuropsychologia.2014.10.024 · Cited by 101
Consolidation of Associative and Item Memory Is Related to Post-Encoding Functional Connectivity between the Ventral Tegmental Area and Different Medial Temporal Lobe Subregions during an Unrelated Task
Tompary, A., Duncan, K. D., & Davachi, L. (2015) · Journal of Neuroscience · doi:10.1523/jneurosci.4816-14.2015 · Cited by 98
Awake reactivation of emotional memory traces through hippocampal–neocortical interactions
de Voogd, L. D., Fernández, G., & Hermans, E. J. (2016) · NeuroImage · doi:10.1016/j.neuroimage.2016.04.026 · Cited by 97
Transferring structural knowledge across cognitive maps in humans and models
Mark, S., Moran, R., Parr, T., Kennerley, S. W., & Behrens, T. E. J. (2020) · Nature Communications · doi:10.1038/s41467-020-18254-6 · Cited by 97
Sleep spindles promote the restructuring of memory representations in ventromedial prefrontal cortex through enhanced hippocampal-cortical functional connectivity
Cowan, E., Liu, A., Henin, S., Kothare, S., Devinsky, O., & Davachi, L. (2020) · The Journal of Neuroscience · doi:10.1523/jneurosci.1946-19.2020 · Cited by 97
Self-citation
Short‐ and medium‐term plasticity associated with augmenting responses in cortical slabs and spindles in intact cortex of cats in vivo
Timofeev, I., Grenier, F., Bazhenov, M., Houweling, A. R., Sejnowski, T. J., & Steriade, M. (2002) · The Journal of Physiology · doi:10.1113/jphysiol.2001.013479 · Cited by 93
Sleep Benefits Memory for Semantic Category Structure While Preserving Exemplar-Specific Information
Schapiro, A. C., McDevitt, E. A., Chen, L., Norman, K. A., Mednick, S. C., & Rogers, T. T. (2017) · Scientific Reports · doi:10.1038/s41598-017-12884-5 · Cited by 91
Self-citation
A mechanism for learning with sleep spindles
Peyrache, A., & Seibt, J. (2020) · Philosophical Transactions of the Royal Society B: Biological Sciences · doi:10.1098/rstb.2019.0230 · Cited by 89
Threat of Punishment Motivates Memory Encoding via Amygdala, Not Midbrain, Interactions with the Medial Temporal Lobe
Murty, V. P., LaBar, K. S., & Adcock, R. A. (2012) · Journal of Neuroscience · doi:10.1523/jneurosci.0094-12.2012 · Cited by 88
Self-citation
Memory trace stabilization leads to large-scale changes in the retrieval network: A functional MRI study on associative memoryPreprint
Takashima, A., Nieuwenhuis, I. L. C., Rijpkema, M., Petersson, K. M., Jensen, O. B., & Fernández, G. (2007) · Learning & Memory · doi:10.1101/lm.605607 · Cited by 81
Episodic memory and Pavlovian conditioning: ships passing in the night
Dunsmoor, J. E., & Kroes, M. C. W. (2018) · Current Opinion in Behavioral Sciences · doi:10.1016/j.cobeha.2018.09.019 · Cited by 77
Self-citation
Individual differences in working memory capacity predict sleep-dependent memory consolidation.
Fenn, K. M., & Hambrick, D. Z. (2012) · Journal of Experimental Psychology: General · doi:10.1037/a0025268 · Cited by 75
Relational Memory: A Daytime Nap Facilitates the Abstraction of General Concepts
Lau, H., Alger, S. E., & Fishbein, W. (2011) · PLoS ONE · doi:10.1371/journal.pone.0027139 · Cited by 75
Age-related Changes in the Sleep-dependent Reorganization of Declarative Memories
Baran, B., Mantua, J., & Spencer, R. M. C. (2016) · Journal of Cognitive Neuroscience · doi:10.1162/jocn_a_00938 · Cited by 72
Perirhinal-Hippocampal Connectivity during Reactivation Is a Marker for Object-Based Memory Consolidation
Vilberg, K. L., & Davachi, L. (2013) · Neuron · doi:10.1016/j.neuron.2013.07.013 · Cited by 71
Complementary Task Structure Representations in Hippocampus and Orbitofrontal Cortex during an Odor Sequence Task
Zhou, J., Montesinos-Cartagena, M., Wikenheiser, A. M., Gardner, M., Niv, Y., & Schoenbaum, G. M. (2019) · Current Biology · doi:10.1016/j.cub.2019.08.040 · Cited by 64
The effects of non-contingent extrinsic and intrinsic rewards on memory consolidation
Nielson, K. A., & Bryant, T. A. (2005) · Neurobiology of Learning and Memory · doi:10.1016/j.nlm.2005.03.004 · Cited by 63
Event-Related Nociceptive Arousal Enhances Memory Consolidation for Neutral Scenes
Schwarze, U., Bingel, U., & Sommer, T. (2012) · The Journal of Neuroscience · doi:10.1523/jneurosci.4497-11.2012 · Cited by 63
Sleep Promotes the Extraction of Grammatical Rules
Nieuwenhuis, I. L. C., Folia, V., Forkstam, C., Jensen, O. B., & Petersson, K. M. (2013) · PLoS ONE · doi:10.1371/journal.pone.0065046 · Cited by 62
A nap to recap or how reward regulates hippocampal-prefrontal memory networks during daytime sleep in humans
Iglói, K., Gaggioni, G., Virginie Sterpenich, A., & Schwartz, S. (2015) · eLife · doi:10.7554/elife.07903 · Cited by 59
Generalizing memories over time: Sleep and reinforcement facilitate transitive inference
Werchan, D. M., & Gómez, R. L. (2012) · Neurobiology of Learning and Memory · doi:10.1016/j.nlm.2012.12.006 · Cited by 57
Reward Learning over Weeks Versus Minutes Increases the Neural Representation of Value in the Human Brain
Wimmer, G. E., Li, J. K., Gorgolewski, K. J., & Poldrack, R. A. (2018) · Journal of Neuroscience · doi:10.1523/jneurosci.0075-18.2018 · Cited by 57
Sleep Improves Prospective Remembering by Facilitating Spontaneous-Associative Retrieval Processes
Diekelmann, S., Wilhelm, I., Wagner, U., & Jan Born, A. (2013) · PLoS ONE · doi:10.1371/journal.pone.0077621 · Cited by 54
Prior knowledge promotes hippocampal separation but cortical assimilation in the left inferior frontal gyrus
Bein, O., Reggev, N., & Maril, A. (2020) · Nature Communications · doi:10.1038/s41467-020-18364-1 · Cited by 52
Dopamine D2-like Receptor Activation Wipes Out Preferential Consolidation of High over Low Reward Memories during Human Sleep
Feld, G. B., Besedovsky, L., Kaida, K., Münte, T. F., & Jan Born, A. (2014) · Journal of Cognitive Neuroscience · doi:10.1162/jocn_a_00629 · Cited by 51
Semantic influences on episodic memory distortions.
Tompary, A., & Thompson‐Schill, S. L. (2021) · Journal of Experimental Psychology General · doi:10.1037/xge0001017 · Cited by 51
The effects of prior knowledge on the encoding of episodic contextual details
Dewitt, M. R., Knight, J. B., Hicks, J. L., & Ball, B. H. (2012) · Psychonomic Bulletin & Review · doi:10.3758/s13423-011-0196-4 · Cited by 51
Emotional learning retroactively enhances item memory but distorts source attributionPreprint
Hennings, A. C., Lewis‐Peacock, J. A., & Dunsmoor, J. E. (2021) · Learning & Memory · doi:10.1101/lm.053371.120 · Cited by 46
Self-citation
Pain anticipation recruits the mesolimbic system and differentially modulates subsequent recognition memory
Bauch, E. M., Rausch, V. H., & Bunzeck, N. (2014) · Human Brain Mapping · doi:10.1002/hbm.22497 · Cited by 36
Neural correlates of sleep, stress, and selective memory consolidation
Kim, S. Y., & Payne, J. D. (2020) · Current Opinion in Behavioral Sciences · doi:10.1016/j.cobeha.2019.12.009 · Cited by 33
Test Expectation Enhances Memory Consolidation across Both Sleep and Wake.
Wamsley, E. J., Hamilton, K., Graveline, Y., Manceor, S., & Parr, E. (2016) · PLoS ONE · doi:10.1371/journal.pone.0165141 · Cited by 29
Human hippocampal replay during rest prioritizes weakly-learned information and predicts memory performancePreprint
Schapiro, A. C., McDevitt, E. A., Rogers, T. T., Mednick, S. C., & Norman, K. A. (2017) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/173021 · Cited by 26
Self-citation
Functional connectivity in category‐selective brain networks after encoding predicts subsequent memory
Collins, J. A., & Dickerson, B. C. (2018) · Hippocampus · doi:10.1002/hipo.23003 · Cited by 24
No evidence for an effect of explicit relevance instruction on consolidation of associative memories
Reverberi, S., Kohn, N., & Fernández, G. (2020) · Neuropsychologia · doi:10.1016/j.neuropsychologia.2020.107491 · Cited by 20
Sleep‐dependent memory consolidation is related to perceived value of learned material
van Rijn, E., Lucignoli, C., Izura, C., & Blagrove, M. (2017) · Journal of Sleep Research · doi:10.1111/jsr.12457 · Cited by 18

Sorted by citations

Is it harmful or helpful? Examining the causes and consequences of generative AI usage among university students
Abbas, M., Jam, F. A., & Khan, T. I. (2024) · International Journal of Educational Technology in Higher Education · doi:10.1186/s41239-024-00444-7 · Cited by 531
“Active learning, which involves active cognitive engagement with the content, is crucial for memory consolidation and retention (Cowan et al., 2021).”
Background
Neurobiology and systems biology of stress resilience
Kalisch, R., Russo, S. J., & Müller, M. B. (2024) · Physiological Reviews · doi:10.1152/physrev.00042.2023 · Cited by 149
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
Laboratory models of post-traumatic stress disorder: The elusive bridge to translation
Dunsmoor, J. E., Cisler, J. M., Fonzo, G. A., Creech, S. K., & Nemeroff, C. B. (2022) · Neuron · doi:10.1016/j.neuron.2022.03.001 · Cited by 101
Self-citation
A model of autonomous interactions between hippocampus and neocortex driving sleep-dependent memory consolidation
Singh, D., Norman, K. A., & Schapiro, A. C. (2022) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.2123432119 · Cited by 81
Self-citation

See all 133

Authors: Cowan, E. T., Schapiro, A. C., Dunsmoor, J. E., & Murty, V. P.
Affiliations: Temple University (US)
University of Pennsylvania (US)
The University of Texas at Austin (US)
Corresponding author: Murty, Vishnu P.
ORCID: Cowan, Emily T.
Schapiro, Anna C.
Dunsmoor, Joseph E.
Murty, Vishnu P.
Venue: Psychonomic Bulletin & Review
Publisher: Springer Science and Business Media LLC
Published: 2021-07-29
Volume: 28
Issue: 6
Pages: 1796-1810
ISSN: 1069-9384 (ISSN-L)
1531-5320
DOI: 10.3758/s13423-021-01978-x
OpenAlex: W3184949359
Cited by: 133
References: 184
Citations by year: 2026: 20 · 2025: 30 · 2024: 42 · 2023: 20 · 2022: 17 · 2021: 4
FWCI: 3.07
Type: journal article
Language: en
Open access: bronze
doi.org
Licence: www.springernature.com/gp/researchers/text-and-data-mining (tdm)
www.springernature.com/gp/researchers/text-and-data-mining (vor)
Locations: Psychonomic Bulletin & Review (publishedVersion)
PubMed (publishedVersion)
Funders: National Institute on Drug Abuse (R21DA043568)
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, adaptive memory, memory stabilization, memory tagging, memory generalization, behavioral flexibility, long-term memory, rodent models
MeSH terms: Memory Consolidation, Cognitive Psychology, Animals, Brain, Motivation, Memory, Long-Term

About these checks

Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.

Statistics and arithmetic are recomputed, not judged.

Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.

What counts as a claim ›How we measure confidence ›How we check this ›

Are you an author, or do you see a problem with this page? Request a review

Memory consolidation as an adaptive process

Abstract

Overview

Integrity signals

Verification

Claims the paper makes

Claims other papers make about this one

Citations

Cites

Cited by

Related

Metadata

Record

About these checks