Hippocampal sharp waves: Their origin and significance

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

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

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

Gamma (40-100 Hz) oscillation in the hippocampus of the behaving rat

Bragin, A., Jando, G., Nadasdy, Z., Hetke, J., Wise, K., & Buzsaki, G. (1995) · The Journal of Neuroscience · doi:10.1523/jneurosci.15-01-00047.1995 · Cited by 1,527 · see citing works

Control of sleep and wakefulness

Brown, R. E., Basheer, R., McKenna, J. T., Strecker, R. E., & McCarley, R. W. (2012) · Physiological Reviews · doi:10.1152/physrev.00032.2011 · Cited by 1,477 · see citing works

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 · see citing works

The Darwinian concept of stress: benefits of allostasis and costs of allostatic load and the trade-offs in health and disease

Korte, S. M., Koolhaas, J. M., Wingfield, J. C., & McEwen, B. S. (2005) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2004.08.009 · Cited by 1,097 · see citing works

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 · see citing works

Awake hippocampal sharp-wave ripples support spatial memory

Jadhav, S. P., Kemere, C., German, P. W., & Frank, L. M. (2012) · Science · doi:10.1126/science.1217230 · Cited by 924 · see citing works

Hippocampal GABAergic Inhibitory Interneurons

Pelkey, K. A., Chittajallu, R., Craig, M. T., Tricoire, L., Wester, J. C., & McBain, C. J. (2017) · Physiological Reviews · doi:10.1152/physrev.00007.2017 · Cited by 889 · see citing works

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 · 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

The reorganization and reactivation of hippocampal maps predict spatial memory performance

Dupret, D., O'Neill, J., Pleydell-Bouverie, B., & Csicsvari, J. (2010) · Nature Neuroscience · doi:10.1038/nn.2599 · Cited by 769 · see citing works

Awake replay of remote experiences in the hippocampus

Karlsson, M. P., & Frank, L. M. (2009) · Nature Neuroscience · doi:10.1038/nn.2344 · Cited by 769 · see citing works

Replay of rule-learning related neural patterns in the prefrontal cortex during sleep

Peyrache, A., Khamassi, M., Benchenane, K., Wiener, S. I., & Battaglia, F. P. (2009) · Nature Neuroscience · doi:10.1038/nn.2337 · Cited by 767 · see citing works

Neuromodulation: acetylcholine and memory consolidation

Hasselmo, M. E. (1999) · Trends in Cognitive Sciences · doi:10.1016/s1364-6613(99)01365-0 · Cited by 809 · 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

Interpreting Neuronal Population Activity by Reconstruction: Unified Framework With Application to Hippocampal Place Cells

Zhang, K., Ginzburg, I., McNaughton, B. L., & Sejnowski, T. J. (1998) · Journal of Neurophysiology · doi:10.1152/jn.1998.79.2.1017 · Cited by 741 · see citing works

Cortical membrane potential signature of optimal states for sensory signal detection

McGinley, M. J., David, S. V., & McCormick, D. A. (2015) · Neuron · doi:10.1016/j.neuron.2015.05.038 · Cited by 728 · see citing works

Origin of Slow Cortical Oscillations in Deafferented Cortical Slabs

Timofeev, I. (2000) · Cerebral Cortex · doi:10.1093/cercor/10.12.1185 · Cited by 710 · see citing works

Influences of hippocampal place cell firing in the awake state on the activity of these cells during subsequent sleep episodes

Pavlides, C., & Winson, J. (1989) · The Journal of Neuroscience · doi:10.1523/jneurosci.09-08-02907.1989 · Cited by 684 · 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

Effects of adverse experiences for brain structure and function

McEwen, B. S. (2000) · Biological Psychiatry · doi:10.1016/s0006-3223(00)00964-1 · Cited by 639 · see citing works

High acetylcholine levels set circuit dynamics for attention and encoding and low acetylcholine levels set dynamics for consolidation

Hasselmo, M. E., & McGaughy, J. (2004) · Progress in Brain Research · doi:10.1016/s0079-6123(03)45015-2 · Cited by 525 · see citing works

Why do we sleep?11Published on the World Wide Web on 7 November 2000.

Sejnowski, T. J., & Destexhe, A. (2000) · Brain Research · doi:10.1016/s0006-8993(00)03007-9 · Cited by 489 · see citing works

The hippocampal sharp wave-ripple in memory retrieval for immediate use and consolidation

Joo, H. R., & Frank, L. M. (2018) · Nature Reviews Neuroscience · doi:10.1038/s41583-018-0077-1 · Cited by 430 · see citing works

Mechanisms of late-onset cognitive decline after early-life stress

Brunson, K. L., Kramár, E., Lin, B., Chen, Y., Colgin, L. L., Yanagihara, T. K., Lynch, G., & Baram, T. Z. (2005) · The Journal of Neuroscience · doi:10.1523/jneurosci.2281-05.2005 · Cited by 479 · see citing works

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 · see citing works

Hippocampus leads ventral striatum in replay of place-reward information

Lansink, C. S., Goltstein, P. M., Lankelma, J. V., McNaughton, B. L., & Pennartz, C. M. A. (2009) · PLoS Biology · doi:10.1371/journal.pbio.1000173 · Cited by 400 · see citing works

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 · see citing works

The Role of Hippocampal Replay in Memory and Planning

Ólafsdóttir, H. F., Bush, D., & Barry, C. (2018) · Current Biology · doi:10.1016/j.cub.2017.10.073 · Cited by 413 · see citing works

Ripples in the medial temporal lobe are relevant for human memory consolidation

Axmacher, N., Elger, C. E., & Fell, J. (2008) · Brain · doi:10.1093/brain/awn103 · Cited by 372 · see citing works

Stress and hippocampal plasticity: implications for the pathophysiology of affective disorders

McEwen, B. S., & Magarinos, A. M. (2001) · Human Psychopharmacology: Clinical and Experimental · doi:10.1002/hup.266 · Cited by 349 · 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

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 · see citing works

Oscillations and hippocampal-prefrontal synchrony

Colgin, L. L. (2011) · Current Opinion in Neurobiology · doi:10.1016/j.conb.2011.04.006 · Cited by 299 · see citing works

Model of the Origin of Rhythmic Population Oscillations in the Hippocampal Slice

Traub, R. D., Miles, R., & Wong, R. K. S. (1989) · Science · doi:10.1126/science.2646715 · Cited by 315 · see citing works

Hippocampal Place Cells Acquire Location-Specific Responses to the Conditioned Stimulus during Auditory Fear Conditioning

Moita, M. A. P., Rosis, S., Zhou, Y., LeDoux, J. E., & Blair, H. T. (2003) · Neuron · doi:10.1016/s0896-6273(03)00033-3 · Cited by 295 · see citing works

The ventral striatum in off-line processing: ensemble reactivation during sleep and modulation by hippocampal ripples

Pennartz, C. M. A., Lee, E., Verheul, J., Lipa, P., Barnes, C. A., & McNaughton, B. L. (2004) · The Journal of Neuroscience · doi:10.1523/jneurosci.0575-04.2004 · Cited by 282 · 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

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

Interaction between neocortical and hippocampal networks via slow oscillations

Sirota, A., & Buzsáki, G. (2005) · Thalamus and Related Systems · doi:10.1017/s1472928807000258 · Cited by 270 · see citing works

Place-Selective Firing of CA1 Pyramidal Cells during Sharp Wave/Ripple Network Patterns in Exploratory Behavior

O'Neill, J., Senior, T., & Csicsvari, J. (2006) · Neuron · doi:10.1016/j.neuron.2005.10.037 · Cited by 281 · see citing works

Hippocampal sharp-wave ripples linked to visual episodic recollection in humans

Norman, Y., Yeagle, E. M., Khuvis, S., Harel, M., Mehta, A. D., & Malach, R. (2019) · Science · doi:10.1126/science.aax1030 · Cited by 270 · see citing works

Innervation of different peptide-containing neurons in the hippocampus by gabaergic septal afferents

Gulyás, A. I., Görcs, T. J., & Freund, T. F. (1990) · Neuroscience · doi:10.1016/0306-4522(90)90189-b · Cited by 234 · see citing works

Internally generated sequences in learning and executing goal-directed behavior

Pezzulo, G., van der Meer, M. A. A., Lansink, C. S., & Pennartz, C. M. A. (2014) · Trends in Cognitive Sciences · doi:10.1016/j.tics.2014.06.011 · Cited by 217 · see citing works

Precision and Variability in Postsynaptic Target Selection of Inhibitory Cells in the Hippocampal CA3 Region

Gulyás, A. I., Mlles, R., Hájos, N., & Freund, T. F. (1993) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.1993.tb00240.x · Cited by 226 · see citing works

Synaptic Input of Horizontal Interneurons in Stratum Oriens of the Hippocampal CA1 Subfield: Structural Basis of Feed‐back Activation

Blasco‐Ibáñez, J. M., & Freund, T. F. (1995) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.1995.tb00638.x · Cited by 212 · see citing works

LTP consolidation: Substrates, explanatory power, and functional significance

Lynch, G., Rex, C. S., & Gall, C. M. (2007) · Neuropharmacology · doi:10.1016/j.neuropharm.2006.07.027 · Cited by 214 · see citing works

Disinhibition of CA1 pyramidal cells by low-dose ketamine and other antagonists with rapid antidepressant efficacy

Widman, A. J., & McMahon, L. L. (2018) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1718883115 · Cited by 204 · see citing works

Slow Oscillations in the Mouse Hippocampus Entrained by Nasal Respiration

Yanovsky, Y., Ciatipis, M., Draguhn, A., Tort, A. B. L., & Brankačk, J. (2014) · The Journal of Neuroscience · doi:10.1523/jneurosci.5287-13.2014 · Cited by 175 · 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

Apolipoprotein E4 Causes Age-Dependent Disruption of Slow Gamma Oscillations during Hippocampal Sharp-Wave Ripples

Gillespie, A. K., Jones, E. A., Lin, Y.-H., Karlsson, M. P., Kay, K., Yoon, S. Y., Tong, L. M., Nova, P., Carr, J. S., Frank, L. M., et al. (2016) · Neuron · doi:10.1016/j.neuron.2016.04.009 · Cited by 187 · see citing works

Preferential Reactivation of Motivationally Relevant Information in the Ventral Striatum

Lansink, C. S., Goltstein, P. M., Lankelma, J. V., Joosten, R. N. J. M. A., McNaughton, B. L., & Pennartz, C. M. A. (2008) · Journal of Neuroscience · doi:10.1523/jneurosci.1054-08.2008 · Cited by 168 · see citing works

A double dissociation within the hippocampus of dopamine D1/D5 receptor and β-adrenergic receptor contributions to the persistence of long-term potentiation

Swanson-Park, J. L., Coussens, C. M., Mason-Parker, S. E., Raymond, C. R., Hargreaves, E. L., Dragunow, M., Cohen, A. S., & Abraham, W. C. (1999) · Neuroscience · doi:10.1016/s0306-4522(99)00010-x · Cited by 175 · see citing works

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

Ramadan, W., Eschenko, O., & Sara, S. J. (2009) · PLoS ONE · doi:10.1371/journal.pone.0006697 · Cited by 173 · see citing works

Hippocampal sharp-wave ripples in waking and sleeping states

Roumis, D. K., & Frank, L. M. (2015) · Current Opinion in Neurobiology · doi:10.1016/j.conb.2015.05.001 · Cited by 155 · see citing works

Attentive scanning behavior drives one-trial potentiation of hippocampal place fields

Monaco, J. D., Rao, G., Roth, E. D., & Knierim, J. J. (2014) · Nature Neuroscience · doi:10.1038/nn.3687 · Cited by 163 · see citing works

Functional fission of parvalbumin interneuron classes during fast network events

Varga, C., Oijala, M., Lish, J., Szabo, G. G., Bezaire, M., Marchionni, I., Golshani, P., & Soltesz, I. (2014) · eLife · doi:10.7554/elife.04006 · Cited by 130 · see citing works

Coherent phasic excitation during hippocampal ripples

Maier, N., Tejero-Cantero, Á., Dorrn, A. L., Winterer, J., Beed, P. S., Morris, G., Kempter, R., Poulet, J. F. A., Leibold, C., & Schmitz, D. (2011) · Neuron · doi:10.1016/j.neuron.2011.08.016 · Cited by 126 · see citing works

Memory, sleep, and dreaming: experiencing consolidation

Wamsley, E. J., & Stickgold, R. (2011) · Sleep Medicine Clinics · doi:10.1016/j.jsmc.2010.12.008 · Cited by 115 · see citing works

Grid cell co-activity patterns during sleep reflect spatial overlap of grid fields during active behaviors

Trettel, S. G., Trimper, J. B., Hwaun, E., Fiete, I. R., & Colgin, L. L. (2019) · Nature Neuroscience · doi:10.1038/s41593-019-0359-6 · Cited by 108 · see citing works

Inhibitory control of GABAergic interneurons in the hippocampus

Freund, T. F., & Gulyás, A. I. (1997) · Canadian Journal of Physiology and Pharmacology · doi:10.1139/y97-033 · Cited by 110 · see citing works

Intrinsic bursting of immature CA3 pyramidal neurons and consequent giant depolarizing potentials are driven by a persistent Na⁺ current and terminated by a slow Ca²⁺‐activated K⁺ current

Sipilä, S. T., Huttu, K., Voipio, J., & Kaila, K. (2006) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.2006.04757.x · Cited by 84 · see citing works

Control of CA3 Output by Feedforward Inhibition Despite Developmental Changes in the Excitation–Inhibition Balance

Torborg, C. L., Nakashiba, T., Tonegawa, S., & McBain, C. J. (2010) · The Journal of Neuroscience · doi:10.1523/jneurosci.3099-10.2010 · Cited by 76 · see citing works

Enhanced cortical and hippocampal neuronal excitability in mice deficient in the extracellular matrix glycoprotein tenascin-R

Gurevicius, K., Gureviciene, I., Valjakka, A., Schachner, M., & Tanila, H. (2004) · Molecular and Cellular Neuroscience · doi:10.1016/j.mcn.2003.12.001 · Cited by 58 · see citing works

Brain State Dependence of Hippocampal Subthreshold Activity in Awake Mice

Hulse, B. K., Lubenov, E. V., & Siapas, A. G. (2017) · Cell Reports · doi:10.1016/j.celrep.2016.11.084 · Cited by 40 · see citing works

A bird-brain view of episodic memory

Rattenborg, N. C., & Martinez-Gonzalez, D. (2011) · Behavioural Brain Research · doi:10.1016/j.bbr.2011.03.030 · Cited by 45 · see citing works

Different phases of afterdischarge during rapid kindling procedure in mice

Musto, A. E., Samii, M. S., & Hayes, J. F. (2009) · Epilepsy Research · doi:10.1016/j.eplepsyres.2009.02.020 · Cited by 35 · see citing works

Untitled work

McEwen (2004) · doi:10.1016/s1054-3589(04)50016-9 · Cited by 22 · see citing works