Hippocampal Sharp Wave/Ripples during Sleep for Consolidation of Associative Memory

Predictive reward signal of dopamine neurons

Schultz, W. (1998) · Journal of Neurophysiology · doi:10.1152/jn.1998.80.1.1 · Cited by 4,564 · 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

Place units in the hippocampus of the freely moving rat

O'Keefe, J. (1976) · Experimental Neurology · doi:10.1016/0014-4886(76)90055-8 · Cited by 1,836 · see citing works

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 · see citing works

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 · see citing works

Cellular bases of hippocampal EEG in the behaving rat

Buzsáki, G., Leung Lai-Wo, S., & Vanderwolf, C. H. (1983) · Brain Research Reviews · doi:10.1016/0165-0173(83)90037-1 · Cited by 1,397 · see citing works

Memory of sequential experience in the hippocampus during slow wave sleep

Lee, A. K., & Wilson, M. A. (2002) · Neuron · doi:10.1016/s0896-6273(02)01096-6 · Cited by 1,296 · see citing works

Forward and reverse hippocampal place-cell sequences during ripples

Diba, K., & Buzsáki, G. (2007) · Nature Neuroscience · doi:10.1038/nn1961 · Cited by 1,205 · 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

Temporally structured replay of awake hippocampal ensemble activity during rapid eye movement sleep

Louie, K., & Wilson, M. A. (2001) · Neuron · doi:10.1016/s0896-6273(01)00186-6 · Cited by 1,148 · see citing works

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 · see citing works

The Hippocampo-Neocortical Dialogue

Buzsáki, G. (1996) · Cerebral Cortex · doi:10.1093/cercor/6.2.81 · Cited by 938 · see citing works

Hippocampal sharp waves: Their origin and significance

Buzsáki, G. (1986) · Brain Research · doi:10.1016/0006-8993(86)91483-6 · Cited by 925 · see citing works

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 · 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

Reactivation of hippocampal cell assemblies: effects of behavioral state, experience, and EEG dynamics

Kudrimoti, H. S., Barnes, C. A., & McNaughton, B. L. (1999) · The Journal of Neuroscience · doi:10.1523/jneurosci.19-10-04090.1999 · Cited by 753 · 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

Ensemble Patterns of Hippocampal CA3-CA1 Neurons during Sharp Wave–Associated Population Events

Csicsvari, J. L., Hirase, H., Mamiya, A., & Buzsáki, G. (2000) · Neuron · doi:10.1016/s0896-6273(00)00135-5 · Cited by 503 · see citing works

Reconsolidation of memory after its reactivation

Przybyslawski, J., & Sara, S. J. (1997) · Behavioural Brain Research · doi:10.1016/s0166-4328(96)00153-2 · Cited by 493 · see citing works

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 · see citing works

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 · see citing works

Selective activation of deep layer (V-VI) retrohippocampal cortical neurons during hippocampal sharp waves in the behaving rat

Chrobak, J. J., & Buzsáki, G. (1994) · Journal of Neuroscience · doi:10.1523/jneurosci.14-10-06160.1994 · Cited by 360 · see citing works

tFast Network Oscillations in the Hippocampal CA1 Region of the Behaving Rat

Csicsvari, T., Hirase, H., Czurkó, A., Mamiya, A., & Buzsáki, G. (1999) · Journal of Neuroscience · doi:10.1523/jneurosci.19-16-j0001.1999 · Cited by 353 · see citing works

Learning‐dependent changes in sleep spindles and Stage 2 sleep

FOGEL, S. M., & SMITH, C. T. (2006) · Journal of Sleep Research · doi:10.1111/j.1365-2869.2006.00522.x · Cited by 344 · see citing works

Hippocampal Sharp Wave-Ripples Linked to Slow Oscillations in Rat Slow-Wave Sleep

Mölle, M., Yeshenko, O., Marshall, L., Sara, S. J., & Born, J. (2006) · Journal of Neurophysiology · doi:10.1152/jn.00014.2006 · Cited by 337 · see citing works

Reactivation of experience-dependent cell assembly patterns in the hippocampus

O'Neill, J., Senior, T. J., Allen, K., Huxter, J. R., & Csicsvari, J. (2008) · Nature Neuroscience · doi:10.1038/nn2037 · Cited by 318 · see citing works

Memory reprocessing in corticocortical and hippocampocortical neuronal ensembles

Qin, Y., McNaughton, B. L., Skaggs, W. E., & Barnes, C. A. (1997) · Philosophical Transactions of the Royal Society B Biological Sciences · doi:10.1098/rstb.1997.0139 · Cited by 308 · see citing works

Control of firing mode of corticotectal and corticopontine layer V burst-generating neurons by norepinephrine, acetylcholine, and 1S,3R- ACPD

Wang, Z., & McCormick, D. (1993) · The Journal of Neuroscience · doi:10.1523/jneurosci.13-05-02199.1993 · Cited by 307 · see citing works

Spatial Firing Properties of Hippocampal CA1 Populations in an Environment Containing Two Visually Identical Regions

Skaggs, W. E., & McNaughton, B. L. (1998) · The Journal of Neuroscience · doi:10.1523/jneurosci.18-20-08455.1998 · Cited by 287 · see citing works

New Experiences Enhance Coordinated Neural Activity in the Hippocampus

Cheng, S., & Frank, L. M. (2008) · Neuron · doi:10.1016/j.neuron.2007.11.035 · Cited by 286 · see citing works

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 · see citing works

Elevated Sleep Spindle Density after Learning or after Retrieval in Rats

Eschenko, O., Mölle, M., Jan Born, A., & Sara, S. J. (2006) · Journal of Neuroscience · doi:10.1523/jneurosci.3175-06.2006 · Cited by 257 · see citing works

Hippocampal Slow Oscillation: A Novel EEG State and Its Coordination with Ongoing Neocortical Activity

Wolansky, T., Clement, E., Peters, S. R., Palczak, M. A., & Dickson, C. T. (2006) · Journal of Neuroscience · doi:10.1523/jneurosci.5594-05.2006 · Cited by 226 · see citing works

Sleep after spatial learning promotes covert reorganization of brain activity

Orban, P., Rauchs, G., Balteau, E., Degueldre, C., Luxen, A., Maquet, P., & Peigneux, P. (2006) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0510198103 · Cited by 167 · see citing works

Locus coeruleus activation modulates firing rate and temporal organization of odour‐induced single‐cell responses in rat piriform cortex

Bouret, S., & Sara, S. J. (2002) · European Journal of Neuroscience · doi:10.1046/j.1460-9568.2002.02413.x · Cited by 148 · see citing works

Hebbian modification of a hippocampal population pattern in the rat

King, C., Henze, D. A., Leinekugel, X., & Buzsáki, G. (1999) · The Journal of Physiology · doi:10.1111/j.1469-7793.1999.00159.x · Cited by 122 · see citing works

Learning-Dependent, Transient Increase of Activity in Noradrenergic Neurons of Locus Coeruleus during Slow Wave Sleep in the Rat: Brain Stem–Cortex Interplay for Memory Consolidation?

Eschenko, O., & Sara, S. J. (2008) · Cerebral Cortex · doi:10.1093/cercor/bhn020 · Cited by 115 · see citing works

EEG Power Densities (0.5–20 Hz) in Different Sleep–Wake Stages in Rats

Bjorvatn, B., Fagerland, S., & Ursin, R. (1998) · Physiology & Behavior · doi:10.1016/s0031-9384(97)00460-5 · Cited by 59 · see citing works

Single-cell activity and synchronous bursting in the rat hippocampus during waking behavior and sleep

Suzuki, S. S., & Smith, G. K. (1985) · Experimental Neurology · doi:10.1016/0014-4886(85)90266-3 · Cited by 54 · see citing works

Rhythmic Constraints on Hippocampal Processing: State and Phase-Related Fluctuations of Synaptic Excitability During Theta and the Slow Oscillation

Schall, K. P., Kerber, J., & Dickson, C. T. (2007) · Journal of Neurophysiology · doi:10.1152/jn.00915.2007 · Cited by 42 · see citing works

Memory processing during human sleep as assessed by functional neuroimaging.

Maquet, P., Peigneux, P., Laureys, S., Boly, M., Dang‐Vu, T. T., Desseilles, M., & Cleeremans, A. (2003) · PubMed · Cited by 34 · see citing works

Memory and forgetting: long-term and gradual changes in memory storage.

Squire, L. R. (1994) · PubMed · Cited by 27 · see citing works

Off-line processing of memory traces during human sleep: Contribution of functional neuroimaging

Maquet, P., Peigneux, P., Laureys, S., Desseilles, M., Boly, M., & Dang‐Vu, T. T. (2003) · Sleep and Biological Rhythms · doi:10.1046/j.1446-9235.2003.00009.x · Cited by 2 · see citing works

About Sleep's Role in Memory

Rasch, B., & Born, J. (2013) · Physiological Reviews · doi:10.1152/physrev.00032.2012 · Cited by 2,783 · see citing works

Hippocampal sharp wave-ripple: A cognitive biomarker for episodic memory and planning

Buzsáki, G. (2015) · Hippocampus · doi:10.1002/hipo.22488 · Cited by 1,759 · see citing works

Rhythms of the hippocampal network

Colgin, L. L. (2016) · Nature reviews. Neuroscience · doi:10.1038/nrn.2016.21 · Cited by 654 · see citing works

Hippocampal-cortical interaction during periods of subcortical silence

Logothetis, N. K., Eschenko, O., Murayama, Y., Augath, M., Steudel, T., Evrard, H. C., Besserve, M., & Oeltermann, A. (2012) · Nature · doi:10.1038/nature11618 · Cited by 420 · see citing works

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 · see citing works

Upgrading the sleeping brain with targeted memory reactivation

Oudiette, D., & Paller, K. A. (2013) · Trends in Cognitive Sciences · doi:10.1016/j.tics.2013.01.006 · Cited by 350 · see citing works

Relationships between Hippocampal Sharp Waves, Ripples, and Fast Gamma Oscillation: Influence of Dentate and Entorhinal Cortical Activity

Sullivan, D. W., Csicsvari, J. L., Mizuseki, K., Montgomery, S. M., Diba, K., & Buzsáki, G. (2011) · Journal of Neuroscience · doi:10.1523/jneurosci.0294-11.2011 · Cited by 292 · see citing works

Light sleep versus slow wave sleep in memory consolidation: a question of global versus local processes?

Genzel, 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

Dreaming of a learning task is associated with enhanced sleep-dependent memory consolidation

Wamsley, E. J., Tucker, M., Payne, J. D., Benavides, J. A., & Stickgold, R. (2010) · Current Biology · doi:10.1016/j.cub.2010.03.027 · Cited by 255 · see citing works

Noradrenergic neurons of the locus coeruleus are phase locked to cortical up-down states during sleep

Eschenko, O., Magri, C., Panzeri, S., & Sara, S. J. (2012) · Cerebral Cortex · doi:10.1093/cercor/bhr121 · Cited by 194 · see citing works

Awake Reactivation of Prior Experiences Consolidates Memories and Biases Cognition

Tambini, A., & Davachi, L. (2019) · Trends in Cognitive Sciences · doi:10.1016/j.tics.2019.07.008 · Cited by 180 · see citing works

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 · see citing works

Local Generation and Propagation of Ripples along the Septotemporal Axis of the Hippocampus

Patel, J., Schomburg, E. W., Berényi, A., Fujisawa, S., & Buzsáki, G. (2013) · Journal of Neuroscience · doi:10.1523/jneurosci.2036-13.2013 · Cited by 167 · see citing works

Acetylcholine bidirectionally regulates learning and memory

Huang, Q., Liao, C., Ge, F., Ao, J., & Liu, T. (2022) · Journal of Neurorestoratology · doi:10.1016/j.jnrt.2022.100002 · Cited by 165 · see citing works

Cell-based transplantation strategies to promote plasticity following spinal cord injury

Ruff, C. A., Wilcox, J. T., & Fehlings, M. G. (2011) · Experimental Neurology · doi:10.1016/j.expneurol.2011.02.010 · Cited by 149 · see citing works

Inhibitory engrams in perception and memory

Barron, H. C., Vogels, T. P., Behrens, T. E., & Ramaswami, M. (2017) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1701812114 · Cited by 147 · see citing works

Sleep deprivation during a specific 3-hour time window post-training impairs hippocampal synaptic plasticity and memory

Prince, T.-M., Wimmer, M., Choi, J., Havekes, R., Aton, S., & Abel, T. (2014) · Neurobiology of Learning and Memory · doi:10.1016/j.nlm.2013.11.021 · Cited by 142 · see citing works

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 141 · see citing works

Reactivation, Replay, and Preplay: How It Might All Fit Together

Buhry, L., Azizi, A. H., & Cheng, S. (2011) · Neural Plasticity · doi:10.1155/2011/203462 · Cited by 134 · see citing works

Hippocampal memory consolidation during sleep: a comparison of mammals and birds

Rattenborg, N. C., Martı́nez-González, D., Roth, T. C., & Витальевич, П. В. (2010) · Biological reviews/Biological reviews of the Cambridge Philosophical Society · doi:10.1111/j.1469-185x.2010.00165.x · Cited by 121 · see citing works

Decreased Rhythmic GABAergic Septal Activity and Memory-Associated θ Oscillations after Hippocampal Amyloid-β Pathology in the Rat

Villette, V., Poindessous‐Jazat, F., Simon, A., Léna, C., Roullot, E., Bellessort, B., Epelbaum, J., Dutar, P., & Stéphan, A. (2010) · Journal of Neuroscience · doi:10.1523/jneurosci.6284-09.2010 · Cited by 116 · see citing works

Hippocampal Sharp-Wave Ripples Influence Selective Activation of the Default Mode Network

Kaplan, R., Adhikari, M. H., Hindriks, R., Mantini, D., Murayama, Y., Logothetis, N. K., & Deco, G. (2016) · Current Biology · doi:10.1016/j.cub.2016.01.017 · Cited by 111 · see citing works

Hippocampal output area CA1 broadcasts a generalized novelty signal during an object-place recognition task

Larkin, M. C., Lykken, C., Tye, L. D., Wickelgren, J. G., & Frank, L. M. (2014) · Hippocampus · doi:10.1002/hipo.22268 · Cited by 110 · see citing works

Selection of experience for memory by hippocampal sharp wave ripples

Yang, W., Sun, C., Huszár, R., Hainmueller, T., Kiselev, K., & Buzsáki, G. (2024) · Science · doi:10.1126/science.adk8261 · Cited by 116 · see citing works

Ripple-triggered stimulation of the locus coeruleus during post-learning sleep disrupts ripple/spindle coupling and impairs memory consolidationPreprint

Novitskaya, Y., Sara, S., Logothetis, N., & Eschenko, O. (2016) · Learning & memory (Cold Spring Harbor, N.Y.) · doi:10.1101/lm.040923.115 · Cited by 86 · see citing works

Post-learning hippocampal replay selectively reinforces spatial memory for highly rewarded locations

Michon, F., Sun, J.-J., Kim, C. Y., Ciliberti, D., & Kloosterman, F. (2019) · Current Biology · doi:10.1016/j.cub.2019.03.048 · Cited by 86 · see citing works

Sleep to Remember

Sara, S. J. (2017) · Journal of Neuroscience · doi:10.1523/jneurosci.0297-16.2017 · Cited by 100 · see citing works

What is episodic memory if it is a natural kind?

Cheng, S., & Werning, M. (2014) · Synthese · doi:10.1007/s11229-014-0628-6 · Cited by 96 · see citing works

How rhythms of the sleeping brain tune memory and synaptic plasticity

Puentes-Mestril, C., Roach, J. P., Niethard, N., Żochowski, M., & Aton, S. J. (2019) · SLEEP · doi:10.1093/sleep/zsz095 · Cited by 90 · see citing works

Learning-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

The role of replay and theta sequences in mediating hippocampal‐prefrontal interactions for memory and cognition

Zielinski, M. C., Tang, W., & Jadhav, S. P. (2017) · Hippocampus · doi:10.1002/hipo.22821 · Cited by 95 · see citing works

Sleep enhances memory consolidation in the hippocampus-dependent object-place recognition task in rats

Binder, S., Baier, P. C., Mölle, M., Inostroza, M., Jan Born, A., & Marshall, L. (2011) · Neurobiology of Learning and Memory · doi:10.1016/j.nlm.2011.12.004 · Cited by 87 · see citing works

Current findings of fMRI in panic disorder: contributions for the fear neurocircuitry and CBT effects

de Carvalho, M. R., Dias, G. P., Cosci, F., Neto, V. L. D. M., Bevilaqua, M. C. D. N., Gardino, P. F., & Nardi, A. E. (2010) · Expert Review of Neurotherapeutics · doi:10.1586/ern.09.161 · Cited by 86 · see citing works

Schema-conformant memories are preferentially consolidated during REM sleep

Durrant, S. J., Cairney, S. A., McDermott, C., & Lewis, P. A. (2015) · Neurobiology of Learning and Memory · doi:10.1016/j.nlm.2015.02.011 · Cited by 75 · see citing works

Hippocampal coupling with cortical and subcortical structures in the context of memory consolidation

Skelin, I., Kilianski, S., & McNaughton, B. L. (2018) · Neurobiology of Learning and Memory · doi:10.1016/j.nlm.2018.04.004 · Cited by 83 · see citing works

Amygdala activation and its functional connectivity during perception of emotional faces in social phobia and panic disorder

Demenescu, L. R., Kortekaas, R., Cremers, H. R., Renken, R. J., van Tol, M. J., van der Wee, N. J. A., Veltman, D. J., den Boer, J. A., Roelofs, K., & Aleman, A. (2013) · Journal of Psychiatric Research · doi:10.1016/j.jpsychires.2013.03.020 · Cited by 79 · see citing works

Rest boosts the long-term retention of spatial associative and temporal order information

Craig, M., Dewar, M., Sala, S. D., & Wolbers, T. (2015) · Hippocampus · doi:10.1002/hipo.22424 · Cited by 78 · see citing works

Nocturnal Mnemonics: Sleep and Hippocampal Memory Processing

Saletin, J., & Walker, M. P. (2012) · Frontiers in Neurology · doi:10.3389/fneur.2012.00059 · Cited by 76 · see citing works

Electrophysiological signatures of memory reactivation in humans

Schreiner, T., & Staudigl, T. (2020) · Philosophical Transactions of the Royal Society B Biological Sciences · doi:10.1098/rstb.2019.0293 · Cited by 75 · see citing works

Reactivation, Retrieval, Replay and Reconsolidation in and Out of Sleep: Connecting the Dots

Sara, S. J. (2010) · Frontiers in Behavioral Neuroscience · doi:10.3389/fnbeh.2010.00185 · Cited by 77 · see citing works

Sleep and olfactory cortical plasticity

Barnes, D. C., & Wilson, D. A. (2014) · Frontiers in Behavioral Neuroscience · doi:10.3389/fnbeh.2014.00134 · Cited by 63 · see citing works

Drug Treatment of Epilepsy Neuropsychiatric Comorbidities in Children

Holmes, G. L. (2020) · Pediatric Drugs · doi:10.1007/s40272-020-00428-w · Cited by 62 · see citing works

Caveats on psychological models of sleep and memory: A compass in an overgrown scenario

Conte, F., & Ficca, G. (2012) · Sleep Medicine Reviews · doi:10.1016/j.smrv.2012.04.001 · Cited by 60 · see citing works

Soluble amyloid beta oligomers block the learning-induced increase in hippocampal sharp wave-ripple rate and impair spatial memory formation

Nicole, O., Hadžibegović, S., Gajda, J., Bontempi, B., Bem, T., & Meyrand, P. (2016) · Scientific Reports · doi:10.1038/srep22728 · Cited by 61 · see citing works

Sharp-wave ripples as a signature of hippocampal-prefrontal reactivation for memory during sleep and waking states

Tang, W., & Jadhav, S. P. (2018) · Neurobiology of Learning and Memory · doi:10.1016/j.nlm.2018.01.002 · Cited by 62 · see citing works

Brief targeted memory reactivation during the awake state enhances memory stability and benefits the weakest memories

Tambini, A., Berners-Lee, A., & Davachi, L. (2017) · Scientific Reports · doi:10.1038/s41598-017-15608-x · Cited by 55 · see citing works

Monosynaptic Hippocampal-Prefrontal Projections Contribute to Spatial Memory Consolidation in Mice

Binder, S., Mölle, M., Lippert, M., Bruder, R., Aksamaz, S., Ohl, F. W., Wiegert, J. S., & Marshall, L. (2019) · Journal of Neuroscience · doi:10.1523/jneurosci.2158-18.2019 · Cited by 55 · see citing works

Sleep-Dependent Consolidation of Auditory Discrimination Learning in Adult Starlings

Brawn, T. P., Nusbaum, H. C., & Margoliash, D. (2010) · The Journal of Neuroscience · doi:10.1523/jneurosci.4237-09.2010 · Cited by 55 · see citing works

Hippocampal information processing across sleep/wake cycles.

Mizuseki, K., & Miyawaki, H. (2017) · Neurosciences research · doi:10.1016/j.neures.2017.04.018 · Cited by 52 · see citing works

Altered hippocampal information coding and network synchrony in APP-PS1 mice

Cayzac, S., Mons, N. E., Ginguay, A., Allinquant, B., Jeantet, Y., & Cho, Y. H. (2015) · Neurobiology of Aging · doi:10.1016/j.neurobiolaging.2015.08.023 · Cited by 51 · see citing works

Brain Rhythms During Sleep and Memory Consolidation: Neurobiological Insights

Marshall, L., Cross, N. E., Binder, S., & Dang‐Vu, T. T. (2019) · Physiology · doi:10.1152/physiol.00004.2019 · Cited by 47 · see citing works

Slow oscillations promote long-range effective communication: The key for memory consolidation in a broken-down network

Niknazar, H., Malerba, P., & Mednick, S. C. (2022) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.2122515119 · Cited by 45 · see citing works

Real-time tracking of neuronal network structure using data assimilation

Hamilton, F., Berry, T., Peixoto, N., & SAUER, T. D. (2013) · Physical Review E · doi:10.1103/physreve.88.052715 · Cited by 50 · see citing works

Recruitment of oriens-lacunosum-moleculare interneurons during hippocampal ripples

Pangalos, M., Donoso, J. R., Winterer, J., Zivkovic, A. R., Kempter, R., Maier, N., & Schmitz, D. (2013) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1215496110 · Cited by 49 · see citing works

The Role of Sleep in Human Declarative Memory Consolidation

Alger, S. E., Chambers, A. M., Cunningham, T. J., & Payne, J. D. (2014) · Current topics in behavioral neurosciences · doi:10.1007/7854_2014_341 · Cited by 49 · see citing works

The Common Effects of Sleep Deprivation on Human Long-Term Memory and Cognitive Control Processes

Kim, T., Kim, S., Kang, J., Kwon, M., & Lee, S. (2022) · Frontiers in Neuroscience · doi:10.3389/fnins.2022.883848 · Cited by 54 · see citing works

Spontaneous Entry into an “Offline” State during Wakefulness: A Mechanism of Memory Consolidation?

Wamsley, E. J., & Summer, T. (2020) · Journal of Cognitive Neuroscience · doi:10.1162/jocn_a_01587 · Cited by 40 · see citing works

Rest-related consolidation protects the fine detail of new memories

Craig, M., & Dewar, M. (2018) · Scientific Reports · doi:10.1038/s41598-018-25313-y · Cited by 43 · see citing works

Remembering to Forget: A Dual Role for Sleep Oscillations in Memory Consolidation and Forgetting

Langille, J. J. (2019) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2019.00071 · Cited by 44 · see citing works

Neural Activity Patterns Underlying Spatial Coding in the Hippocampus

Sosa, M., Gillespie, A. K., & Frank, L. M. (2016) · Current topics in behavioral neurosciences · doi:10.1007/7854_2016_462 · Cited by 39 · see citing works

Memory corticalization triggered by REM sleep: mechanisms of cellular and systems consolidation

Almeida-Filho, D. G., Queiroz, C. M., & Ribeiro, S. (2018) · Cellular and Molecular Life Sciences · doi:10.1007/s00018-018-2886-9 · Cited by 38 · see citing works

The Cognitive Role of the Globus Pallidus interna; Insights from Disease States

Gillies, M. J., Hyam, J. A., Weiss, A. R., Antoniades, C. A., Bogacz, R., FitzGerald, J. J., Aziz, T. Z., Whittington, M. A., & Green, A. L. (2017) · Experimental Brain Research · doi:10.1007/s00221-017-4905-8 · Cited by 37 · see citing works

Bidirectional relationships between sleep and amyloid-beta in the hippocampus

Dufort‐Gervais, J., Mongrain, V., & Brouillette, J. (2018) · Neurobiology of Learning and Memory · doi:10.1016/j.nlm.2018.06.009 · Cited by 36 · see citing works

Rest on it: Awake quiescence facilitates insight

Craig, M., Ottaway, G., & Dewar, M. (2018) · Cortex · doi:10.1016/j.cortex.2018.09.009 · Cited by 37 · see citing works

Synthetic peptide vaccines

Moysa, A. A., & Kolesanova, E. F. (2011) · Biomeditsinskaya Khimiya · doi:10.18097/pbmc20115701014 · Cited by 36 · see citing works

Time as the fourth dimension in the hippocampus

Banquet, J. P., Gaussier, P., Cuperlier, N., Hok, V., Save, É., Poucet, B., Quoy, M., & Wiener, S. I. (2020) · Progress in Neurobiology · doi:10.1016/j.pneurobio.2020.101920 · Cited by 33 · see citing works

Alterations of in vivo CA1 network activity in Dp(16)1Yey Down syndrome model mice

Raveau, M., Polygalov, D., Boehringer, R., Amano, K., Yamakawa, K., & McHugh, T. J. (2018) · eLife · doi:10.7554/elife.31543 · Cited by 32 · see citing works

Sniffing shapes the dynamics of olfactory bulb gamma oscillations in awake behaving rats

Pahi, M. R., & Aylwin, M. L. (2011) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.2011.07800.x · Cited by 31 · see citing works

Different effects of zolpidem and diazepam on hippocampal sharp wave—ripple activity in vitro

Koniaris, E., Drimala, P., Sotiriou, E., & Papatheodoropoulos, C. (2011) · Neuroscience · doi:10.1016/j.neuroscience.2010.11.027 · Cited by 31 · see citing works

CA2 inhibition reduces the precision of hippocampal assembly reactivation

He, H., Boehringer, R., Huang, A. J. Y., Overton, E. T. N., Polygalov, D., Okanoya, K., & McHugh, T. J. (2021) · Neuron · doi:10.1016/j.neuron.2021.08.034 · Cited by 30 · see citing works

Does sleep protect memories against interference? A failure to replicate

Bailes, C. A., Caldwell, M., Wamsley, E. J., & Tucker, M. A. (2020) · PLoS ONE · doi:10.1371/journal.pone.0220419 · Cited by 29 · see citing works

α5GABAA receptors regulate hippocampal sharp wave-ripple activity in vitro.

Papatheodoropoulos, C., & Koniaris, E. (2011) · Neuropharmacology · doi:10.1016/j.neuropharm.2010.11.022 · Cited by 30 · see citing works

Dorsal-ventral distinction of chronic stress-induced electrophysiological alterations in the rat medial prefrontal cortex

Lee, Y. A., Poirier, P., Otani, S., & Goto, Y. (2011) · Neuroscience · doi:10.1016/j.neuroscience.2011.03.039 · Cited by 30 · see citing works

Dentate Gyrus Sharp Waves, a Local Field Potential Correlate of Learning in the Dentate Gyrus of Mice

Meier, K., Merseburg, A., Isbrandt, D., Marguet, S. L., & Morellini, F. (2020) · Journal of Neuroscience · doi:10.1523/jneurosci.2275-19.2020 · Cited by 26 · see citing works

Neurophysiological Basis of Sleep’s Function on Memory and Cognition

Spencer, R. M. C. (2013) · ISRN Physiology · doi:10.1155/2013/619319 · Cited by 28 · see citing works

Ups and downs in the hippocampus: the influence of oscillatory sleep states on "neuroplasticity" at different time scales.

Dickson, C. (2010) · Behavioural Brain Research · doi:10.1016/j.bbr.2010.04.002 · Cited by 28 · see citing works

Socializing by Day May Affect Performance by Night: Vulnerability to Sleep Deprivation is Differentially Mediated by Social Exposure in Extraverts vs Introverts

Rupp, T. L., Killgore, W. D. S., & Balkin, T. J. (2010) · SLEEP · doi:10.1093/sleep/33.11.1475 · Cited by 27 · see citing works

The volumes of subcortical regions in depressed and healthy individuals are strikingly similar: a reinterpretation of the results by Schmaal et al.

Fried, E. I., & Kievit, R. (2015) · Molecular Psychiatry · doi:10.1038/mp.2015.199 · Cited by 26 · see citing works

Superficial Layer-Specific Histaminergic Modulation of Medial Entorhinal Cortex Required for Spatial Learning

He, C., Luo, F., Chen, X., Chen, F., Li, C., Ren, S., Qiao, Q., Zhang, J., de Lecea, L., Gao, D., et al. (2015) · Cerebral Cortex · doi:10.1093/cercor/bhu322 · Cited by 27 · see citing works

Neural Markers of Event Boundaries

Bilkey, D. K., & Jensen, C. S. (2019) · Topics in Cognitive Science · doi:10.1111/tops.12470 · Cited by 26 · see citing works

Deficit in hippocampal ripples does not preclude spatial memory formation in APP/PS1 mice

Jura, B., Macrez, N., Meyrand, P., & Bem, T. (2019) · Scientific Reports · doi:10.1038/s41598-019-56582-w · Cited by 26 · see citing works

A neuroscientific model of near-death experiences

Martial, C., Fritz, P., Gosseries, O., Bonhomme, V. L., Kondziella, D., Nelson, K. R., & Lejeune, N. (2025) · Nature Reviews Neurology · doi:10.1038/s41582-025-01072-z · Cited by 30 · see citing works

Effects of μ‐opioid receptor modulation on the hippocampal network activity of sharp wave and ripples

Giannopoulos, P., & Papatheodoropoulos, C. (2012) · British Journal of Pharmacology · doi:10.1111/j.1476-5381.2012.02240.x · Cited by 22 · see citing works

Hippocampal Contributions to Declarative Memory Consolidation During Sleep

Antony, J. W., & Paller, K. A. (2017) · Springer eBooks · doi:10.1007/978-3-319-50406-3_9 · Cited by 23 · see citing works

Pathological changes of brain oscillations following ischemic stroke

Satō, Y., Schmitt, O., Ip, Z., Rabiller, G., Omodaka, S., Tominaga, T., Yazdan-Shahmorad, A., & Liu, J. (2022) · Journal of Cerebral Blood Flow & Metabolism · doi:10.1177/0271678x221105677 · Cited by 22 · see citing works

Noradrenergic gating of long-lasting synaptic potentiation in the hippocampus: from neurobiology to translational biomedicine

Nguyen, P., & Gelinas, J. N. (2018) · Journal of Neurogenetics · doi:10.1080/01677063.2018.1497630 · Cited by 22 · see citing works

Patterned activation of hippocampal network (approximately 10 Hz) during in vitro sharp wave-ripples.

Papatheodoropoulos, C. (2010) · Neuroscience · doi:10.1016/j.neuroscience.2010.03.058 · Cited by 22 · see citing works

Stimulating forebrain communications: Slow sinusoidal electric fields over frontal cortices dynamically modulate hippocampal activity and cortico-hippocampal interplay during slow-wave states

Greenberg, A., Whitten, T. A., & Dickson, C. T. (2016) · NeuroImage · doi:10.1016/j.neuroimage.2016.02.070 · Cited by 20 · see citing works

Sleep facilitates spatial memory but not navigation using the Minecraft Memory and Navigation task

Simon, K. C. N. S., Clemenson, G. D., Zhang, J., Sattari, N. S., Shuster, A. E., Clayton, B., Alzueta, E., Dulai, T., de Zambotti, M., Stark, C. E. L., et al. (2022) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.2202394119 · Cited by 20 · see citing works

A Bird’s Eye View of Sleep-Dependent Memory Consolidation

Brawn, T. P., & Margoliash, D. (2014) · Current topics in behavioral neurosciences · doi:10.1007/7854_2014_349 · Cited by 20 · see citing works

Sleep changes following intensive cognitive activity

Cerasuolo, M., Conte, F., Giganti, F., & Ficca, G. (2019) · Sleep Medicine · doi:10.1016/j.sleep.2019.08.016 · Cited by 18 · see citing works

Acute Effects of Two Different Species of Amyloid-β on Oscillatory Activity and Synaptic Plasticity in the Commissural CA3-CA1 Circuit of the Hippocampus

Gauthier-Umaña, C., Muñoz-Cabrera, J., Valderrama, M. A., Múnera, A., & Nava-Mesa, M. O. (2020) · Neural Plasticity · doi:10.1155/2020/8869526 · Cited by 19 · see citing works

The Function of Oscillations in the Hippocampal Formation

Lever, C., Kaplan, R., & Burgess, N. (2014) · Springer eBooks · doi:10.1007/978-3-7091-1292-2_12 · Cited by 18 · see citing works

Mechanisms of neural organization and rhythmogenesis during hippocampal and cortical ripples

McKenzie, S., Nitzan, N., & English, D. F. (2020) · Philosophical Transactions of the Royal Society B Biological Sciences · doi:10.1098/rstb.2019.0237 · Cited by 14 · see citing works

Spontaneous and electrically modulated spatiotemporal dynamics of the neocortical slow oscillation and associated local fast activity

Greenberg, A., & Dickson, C. T. (2013) · NeuroImage · doi:10.1016/j.neuroimage.2013.07.034 · Cited by 17 · see citing works

The Monetary Incentive Delay (MID) Task Induces Changes in Sensory Processing: ERP Evidence

Krugliakova, E., Gorin, A., Fedele, T., Юрьевич, Ш. Ю., Moiseeva, V., Klucharev, V. A., & Шестакова, А. Н. (2019) · Frontiers in Human Neuroscience · doi:10.3389/fnhum.2019.00382 · Cited by 16 · see citing works

Characterizing Hippocampal Oscillatory Signatures Underlying Seizures in Temporal Lobe Epilepsy

Mokhothu, T. M., & Tanaka, K. Z. (2021) · Frontiers in Behavioral Neuroscience · doi:10.3389/fnbeh.2021.785328 · Cited by 17 · see citing works

Sleep sharp wave ripple and its functions in memory and synaptic plasticity

Zhou, Z., & Norimoto, H. (2023) · Neuroscience Research · doi:10.1016/j.neures.2023.01.011 · Cited by 16 · see citing works

Sleep Deprivation Impairs Learning-Induced Increase in Hippocampal Sharp Wave Ripples and Associated Spike Dynamics during Recovery Sleep

Li, R., Yan, J., Chen, H., Zhang, W., Yubo, H., Zhang, J., Hu, Z., Xiong, Y., Yao, Z., & Hu, B. (2021) · Cerebral Cortex · doi:10.1093/cercor/bhab247 · Cited by 16 · see citing works

Adaptive and pathological inhibition of neuroplasticity associated with circadian rhythms and sleep.

Heller, H. C., Ruby, N. F., Rolls, A., Makam, M., & Colas, D. (2014) · Behavioral Neuroscience · doi:10.1037/a0036689 · Cited by 15 · see citing works

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 · see citing works

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 · 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

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

Cortical-hippocampal dynamics during sharp-wave ripples evolve across learning

Hall, A. F., Wang, D. V., & España, R. A. (2025) · doi:10.17918/00011221