Neural syntax: cell assemblies, synapsembles, and readers
Open accessAbstract
A widely discussed hypothesis in neuroscience is that transiently active ensembles of neurons, known as "cell assemblies," underlie numerous operations of the brain, from encoding memories to reasoning. However, the mechanisms responsible for the formation and disbanding of cell assemblies and temporal evolution of cell assembly sequences are not well understood. I introduce and review three interconnected topics, which could facilitate progress in defining cell assemblies, identifying their neuronal organization, and revealing causal relationships between assembly organization and behavior. First, I hypothesize that cell assemblies are best understood in light of their output product, as detected by "reader-actuator" mechanisms. Second, I suggest that the hierarchical organization of cell assemblies may be regarded as a neural syntax. Third, constituents of the neural syntax are linked together by dynamically changing constellations of synaptic weights ("synapsembles"). The existing support for this tripartite framework is reviewed and strategies for experimental testing of its predictions are discussed.
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Integrity signals
Registry
Cites
Statistics
Claims the paper makes
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
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?
These systems are highly structured temporally, e.g., containing nested gamma and theta oscillation structures that are phase locked to sequences of place-cell responses, interfering oscillators frequency-shifted by the animal's motion velocity, tuned cellular resonances, and other neural phenomena that lie far outside a conventional artificial neural network description.
“These systems are highly structured temporally, e.g., containing nested gamma and theta oscillation structures that are phased locked to sequences of place-cell responses, interfering oscillators frequency-shifted by the animal's motion velocity (Zilli and Hasselmo, 2010), tuned cellular resonances (Giocomo et al., 2007; Buzsáki, 2010), and other neural phenomena that lie far outside a convention”
From Toward an integration of deep learning and neuroscience (2016) · cites this paper as Buzsáki, 2010
Self-check
Percentages, sums and reported differences re-computed from the paper’s own numbers.
The self-check needs the paper’s full text.
Cites
James, W. (1891) · Henry Holt and Company eBooks · doi:10.1037/11059-000 · Cited by 25,799 · see citing works
The magical number seven, plus or minus two: Some limits on our capacity for processing information.
Miller, G. A. (1994) · Psychological Review · doi:10.1037/0033-295x.101.2.343 · Cited by 17,469 · see citing works
Receptive fields, binocular interaction and functional architecture in the cat’s visual cortex
Hubel, D. H., & Wiesel, T. N. (1962) · The Journal of Physiology · doi:10.1113/jphysiol.1962.sp006837 · Cited by 13,680 · see citing works
A default mode of brain function
Raichle, M. E., MacLeod, A. M., Snyder, A. Z., Powers, W. J., Gusnard, D. A., & Shulman, G. L. (2001) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.98.2.676 · Cited by 12,190 · see citing works
Hebb, D. O. (2005) · doi:10.4324/9781410612403 · Cited by 9,825 · see citing works
(1978) · UA Campus Repository (The University of Arizona) · Cited by 8,010 · see citing works
indicated, N. A. (1950) · Journal of Consulting Psychology · doi:10.1037/h0049612 · Cited by 6,984 · see citing works
The co-ordination and regulation of movements
Bernshteĭn, N. A. (1967) · Brain Research · doi:10.1016/0006-8993(69)90278-9 · Cited by 6,389 · see citing works
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 · see citing works
The hippocampus as a cognitive map
Passingham, R. E. (1979) · Neuroscience · doi:10.1016/0306-4522(79)90015-0 · Cited by 5,128 · see citing works
Short-Term Synaptic Plasticity
Zucker, R. S., & Regehr, W. G. (2002) · Annual Review of Physiology · doi:10.1146/annurev.physiol.64.092501.114547 · Cited by 5,068 · see citing works
Buzsáki, G. (2006) · doi:10.1093/acprof:oso/9780195301069.001.0001 · Cited by 4,873 · see citing works
Self-citationMillisecond-timescale, genetically targeted optical control of neural activity
Boyden, E. S., Zhang, F., Bamberg, E., Nagel, G., & Deisseroth, K. A. (2005) · Nature Neuroscience · doi:10.1038/nn1525 · Cited by 4,831 · see citing works
The brainweb: phase synchronization and large-scale integration
Varela, F., Lachaux, J.-P., Rodriguez, E., & Martinerie, J. (2001) · Nature Reviews Neuroscience · doi:10.1038/35067550 · Cited by 4,761 · see citing works
Knowledge of Language: Its Nature, Origin, and Use.
Hornstein, N., & Chomsky, N. A. D. T. (1988) · The Philosophical Review · doi:10.2307/2185417 · Cited by 4,648 · see citing works
A mechanism for cognitive dynamics: neuronal communication through neuronal coherence.
Fries, P. (2005) · Trends in Cognitive Sciences · doi:10.1016/j.tics.2005.08.011 · Cited by 4,284 · see citing works
Maass, W., Natschläger, T., & Markram, H. (2002) · Neural Computation · doi:10.1162/089976602760407955 · Cited by 4,025 · see citing works
Regulation of Synaptic Efficacy by Coincidence of Postsynaptic APs and EPSPs
Markram, H., Lübke, J., Frotscher, M., & Sakmann, B. (1997) · Science · doi:10.1126/science.275.5297.213 · Cited by 3,832 · see citing works
Dynamic predictions: Oscillations and synchrony in top–down processing
Engel, A. K., Fries, P., & Singer, W. (2001) · Nature Reviews Neuroscience · doi:10.1038/35094565 · Cited by 3,454 · see citing works
Interneurons of the hippocampus
Freund, T. F., & Buzsáki, G. (1998) · Hippocampus · doi:10.1002/(sici)1098-1063(1996)6:4 · Cited by 3,423 · see citing works
Self-citationTheta oscillations in the hippocampus
Buzsáki, G. (2002) · Neuron · doi:10.1016/s0896-6273(02)00586-x · Cited by 3,332 · see citing works
Self-citationNeuronal ensemble control of prosthetic devices by a human with tetraplegia
Hochberg, L. R., Serruya, M. D., Friehs, G. M., Mukand, J. A., Saleh, M., Caplan, A. H., Branner, A., Chen, D., Penn, R. D., & Donoghue, J. P. (2006) · Nature · doi:10.1038/nature04970 · Cited by 3,295 · see citing works
Neuronal Population Coding of Movement Direction
Georgopoulos, A. P., Schwartz, A. B., & Kettner, R. E. (1986) · Science · doi:10.1126/science.3749885 · Cited by 3,187 · 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
PHARMACOLOGY AND FUNCTIONS OF METABOTROPIC GLUTAMATE RECEPTORS
Conn, P. J., & Pin, J. (1997) · The Annual Review of Pharmacology and Toxicology · doi:10.1146/annurev.pharmtox.37.1.205 · Cited by 3,083 · see citing works
Dynamic patterns: The self-organization of brain and behavior
(1997) · Computers & Mathematics with Applications · doi:10.1016/s0898-1221(97)90151-6 · Cited by 2,857 · see citing works
Spikes: Exploring the Neural Code
Rieke, F. M., Warland, D., van Steveninck, R. R. D. R., & Bialek, W. (1996) · Medical Entomology and Zoology · Cited by 2,844 · see citing works
The problem of serial order in behavior
Lashley, K. S. (1951) · MPG.PuRe (Max Planck Society) · Cited by 2,734 · see citing works
Rowan, W., & Tinbergen, N. (1952) · Bird-Banding · doi:10.2307/4510368 · Cited by 2,715 · see citing works
Cellular basis of working memory
Goldman-Rakic, P. S. (1995) · Neuron · doi:10.1016/0896-6273(95)90304-6 · Cited by 2,663 · see citing works
High Gamma Power Is Phase-Locked to Theta Oscillations in Human Neocortex
Canolty, R. T., Edwards, E., Dalal, S. S., Soltani, M., Nagarajan, S. S., Kirsch, H. E., Berger, M. S., Barbaro, N. M., & Knight, R. T. (2006) · Science · doi:10.1126/science.1128115 · Cited by 2,650 · see citing works
Parvalbumin neurons and gamma rhythms enhance cortical circuit performance
Sohal, V. S., Zhang, F., Yizhar, O., & Deisseroth, K. (2009) · Nature · doi:10.1038/nature07991 · Cited by 2,606 · see citing works
Driving fast-spiking cells induces gamma rhythm and controls sensory responses
Cardin, J. A., Carlén, M., Meletis, K., Knoblich, U., Zhang, F., Deisseroth, K., Tsai, L.-H., & Moore, C. I. (2009) · Nature · doi:10.1038/nature08002 · Cited by 2,603 · see citing works
Neuronal Synchrony: A Versatile Code for the Definition of Relations?
Singer, W. (1999) · Neuron · doi:10.1016/s0896-6273(00)80821-1 · Cited by 2,581 · see citing works
Phase relationship between hippocampal place units and the EEG theta rhythm
O'Keefe, J. M., & Recce, M. L. (1993) · Hippocampus · doi:10.1002/hipo.450030307 · Cited by 2,561 · see citing works
Heteromeric NMDA receptors: molecular and functional distinction of subtypes
Monyer, H., Sprengel, R., Schoepfer, R., Herb, A., Higuchi, M., Lomeli, H., Burnashev, N., Sakmann, B., & Seeburg, P. H. (1992) · Science · doi:10.1126/science.256.5060.1217 · Cited by 2,541 · see citing works
(1987) · Medical Entomology and Zoology · Cited by 2,512 · see citing works
Stimulus-specific neuronal oscillations in orientation columns of cat visual cortex
Gray, C. M., & Singer, W. (1989) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.86.5.1698 · Cited by 2,463 · see citing works
The Prefrontal Cortex: Anatomy, Physiology, and Neuropsychology of the Frontal Lobe
Fuster, J. M. (1980) · Cited by 2,367 · see citing works
Dynamics of the Hippocampal Ensemble Code for Space
Wilson, M. A., & McNaughton, B. L. (1993) · Science · doi:10.1126/science.8351520 · Cited by 2,350 · see citing works
Computing with Neural Circuits: A Model
Hopfield, J. J., & Tank, D. W. (1986) · Science · doi:10.1126/science.3755256 · Cited by 2,107 · see citing works
Synaptic mechanisms of synchronized gamma oscillations in inhibitory interneuron networks
Bartos, M., Vida, I., & Jonas, P. (2007) · Nature Reviews Neuroscience · doi:10.1038/nrn2044 · Cited by 2,070 · see citing works
Neuronal Diversity and Temporal Dynamics: The Unity of Hippocampal Circuit Operations
Klausberger, T., & Somogyi, P. (2008) · Science · doi:10.1126/science.1149381 · Cited by 2,050 · see citing works
Cover, T. M. (1965) · IEEE Transactions on Electronic Computers · doi:10.1109/pgec.1965.264137 · Cited by 2,044 · see citing works
Invariant visual representation by single neurons in the human brain
Quiroga, R. Q., Reddy, L., Kreiman, G., Koch, C., & Fried, I. (2005) · Nature · doi:10.1038/nature03687 · Cited by 1,988 · see citing works
Place Cells, Grid Cells, and the Brain's Spatial Representation System
Moser, E. I., Kropff, E., & Moser, M.-B. (2008) · Annual Review of Neuroscience · doi:10.1146/annurev.neuro.31.061307.090723 · Cited by 1,934 · see citing works
Noë, A. (2005) · Medical Entomology and Zoology · Cited by 1,875 · see citing works
Large-scale recording of neuronal ensembles
Buzsáki, G. (2004) · Nature Neuroscience · doi:10.1038/nn1233 · Cited by 1,875 · see citing works
Self-citationHuber, R., Felice Ghilardi, M., Massimini, M., & Tononi, G. (2004) · Nature · doi:10.1038/nature02663 · Cited by 1,854 · see citing works
Brain mechanisms linking language and action
Pulvermüller, F. (2005) · Nature Reviews Neuroscience · doi:10.1038/nrn1706 · Cited by 1,828 · see citing works
Learning to control a brain–machine interface for reaching and grasping by primates
Carmena, J. M., Lebedev, M. A., Crist, R. E., O'Doherty, J. E., Santucci, D. M., Dimitrov, D. F., Patil, P. G., Henriquez, C. S., & Nicolelis, M. A. L. (2003) · PLoS Biology · doi:10.1371/journal.pbio.0000042 · Cited by 1,761 · see citing works
Churchland, P. S., & Sejnowski, T. J. (1992) · doi:10.7551/mitpress/2010.001.0001 · Cited by 1,757 · 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
Single Units and Sensation: A Neuron Doctrine for Perceptual Psychology?
Barlow, H. B. (1972) · Perception · doi:10.1068/p010371 · Cited by 1,714 · 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
Self-citationSynaptic depression and cortical gain control
Abbott, L. F., Varela, J. A., Sen, K., & Nelson, S. B. (1997) · Science · doi:10.1126/science.275.5297.221 · Cited by 1,690 · see citing works
Abbott, L. F., & Regehr, W. G. (2004) · Nature · doi:10.1038/nature03010 · Cited by 1,684 · see citing works
Coordinated memory replay in the visual cortex and hippocampus during sleep
Ji, D., & Wilson, M. A. (2007) · Nature Neuroscience · doi:10.1038/nn1825 · Cited by 1,669 · see citing works
Central control of song in the canary, Serinus canarius
Nottebohm, F., Stokes, T. M., & Leonard, C. M. (1976) · The Journal of Comparative Neurology · doi:10.1002/cne.901650405 · Cited by 1,645 · see citing works
Tononi, G., Sporns, O., & Edelman, G. M. (1994) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.91.11.5033 · Cited by 1,626 · see citing works
Pattern Separation in the Dentate Gyrus and CA3 of the Hippocampus
Leutgeb, J. K., Leutgeb, S., Moser, M.-B., & Moser, E. I. (2007) · Science · doi:10.1126/science.1135801 · Cited by 1,601 · cited 2× · see citing works
“…exemplified by the strong divergence of the entorhinal cortex-dentate granule cell connectivity and the sparse responses of granule cells (Jung and McNaughton, 1993; Leutgeb et al., 2007).19 On a larger scale, the entire neocortex can (A) The reader sends an output command to optimize the sensor.”
Role of Endogenous Cannabinoids in Synaptic Signaling
Freund, T. F., Katona, I., & Piomelli, D. (2003) · Physiological Reviews · doi:10.1152/physrev.00004.2003 · Cited by 1,567 · 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
Self-citationDirect Cortical Control of 3D Neuroprosthetic Devices
Taylor, D. M., Tillery, S. I. H., & Schwartz, A. B. (2002) · Science · doi:10.1126/science.1070291 · Cited by 1,542 · 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
Synchronization of neuronal activity in hippocampus by individual GABAergic interneurons
Cobb, S. R., Buhl, E. H., Halasy, K., Paulsen, O., & Somogyi, P. (1995) · Nature · doi:10.1038/378075a0 · Cited by 1,498 · see citing works
Chomsky, N. (1975) · University of Minnesota Digital Conservancy (University of Minnesota) · Cited by 1,498 · see citing works
Real-time prediction of hand trajectory by ensembles of cortical neurons in primates
Wessberg, J., Stambaugh, C. R., Kralik, J. D., Beck, P. D., Laubach, M., Chapin, J. K., Kim, J., Biggs, S. J., Srinivasan, M. A., & Nicolelis, M. A. L. (2000) · Nature · doi:10.1038/35042582 · Cited by 1,491 · see citing works
Synaptic Modification by Correlated Activity: Hebb's Postulate Revisited
Bi, G., & Poo, M. (2001) · Annual Review of Neuroscience · doi:10.1146/annurev.neuro.24.1.139 · Cited by 1,476 · see citing works
Storage of 7 +/- 2 short-term memories in oscillatory subcycles
Lisman, J. E., & Idiart, M. A. P. (1995) · Science · doi:10.1126/science.7878473 · Cited by 1,471 · see citing works
Frequency of gamma oscillations routes flow of information in the hippocampus
Colgin, L. L., Denninger, T., Fyhn, M., Hafting, T., Bonnevie, T., Jensen, O. B., Moser, M., & Moser, E. I. (2009) · Nature · doi:10.1038/nature08573 · Cited by 1,425 · see citing works
Instant neural control of a movement signal
Serruya, M. D., Hatsopoulos, N. G., Paninski, L., Fellows, M. R., & Donoghue, J. P. (2002) · Nature · doi:10.1038/416141a · Cited by 1,415 · 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
Self-citationFeature Discovery by Competitive Learning*
Rumelhart, D. E., & Zipser, D. (1985) · Cognitive Science · doi:10.1207/s15516709cog0901_5 · Cited by 1,379 · see citing works
Modulation of Neuronal Interactions Through Neuronal Synchronization
Womelsdorf, T., Schoffelen, J.-M., Oostenveld, R., Singer, W., Desimone, R., Engel, A. K., & Fries, P. (2007) · Science · doi:10.1126/science.1139597 · Cited by 1,367 · see citing works
Balanced inhibition underlies tuning and sharpens spike timing in auditory cortex
Wehr, M., & Zador, A. M. (2003) · Nature · doi:10.1038/nature02116 · Cited by 1,363 · see citing works
A Synaptically Controlled, Associative Signal for Hebbian Plasticity in Hippocampal Neurons
Magee, J. C., & Johnston, D. (1997) · Science · doi:10.1126/science.275.5297.209 · Cited by 1,303 · see citing works
Internally Generated Cell Assembly Sequences in the Rat Hippocampus
Pastalkova, E., Itskov, V., Amarasingham, A., & Buzsáki, G. (2008) · Science · doi:10.1126/science.1159775 · Cited by 1,301 · see citing works
Grouping of brain rhythms in corticothalamic systems
Steriade, M. (2006) · Neuroscience · doi:10.1016/j.neuroscience.2005.10.029 · Cited by 1,296 · 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
Synaptic theory of working memory
Mongillo, G., Barak, O., & Tsodyks, M. (2008) · Science · doi:10.1126/science.1150769 · Cited by 1,253 · see citing works
High-frequency network oscillation in the hippocampus
Buzsáki, G., Horváth, Z., Urioste, R., Hetke, J. F., & Wise, K. D. (1992) · Science · doi:10.1126/science.1589772 · Cited by 1,223 · see citing works
Self-citationRepresentation of Geometric Borders in the Entorhinal Cortex
Solstad, T., Boccara, C. N., Kropff, E., Moser, M.-B., & Moser, E. I. (2008) · Science · doi:10.1126/science.1166466 · Cited by 1,213 · 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
Self-citationReplay 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
Real-time control of a robot arm using simultaneously recorded neurons in the motor cortex
Chapin, J. K., Moxon, K. A., Markowitz, R. S., & Nicolelis, M. A. L. (1999) · Nature Neuroscience · doi:10.1038/10223 · Cited by 1,168 · see citing works
Geometric determinants of the place fields of hippocampal neurons
O'Keefe, J., & Burgess, N. (1996) · Nature · doi:10.1038/381425a0 · Cited by 1,166 · see citing works
Identification and classification of hubs in brain networks
Sporns, O., Honey, C. J., & Kötter, R. (2007) · PLoS ONE · doi:10.1371/journal.pone.0001049 · Cited by 1,165 · see citing works
Differential signaling via the same axon of neocortical pyramidal neurons
Markram, H., Wang, Y., & Tsodyks, M. (1998) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.95.9.5323 · Cited by 1,102 · see citing works
Enforcement of Temporal Fidelity in Pyramidal Cells by Somatic Feed-Forward Inhibition
Pouille, F., & Scanziani, M. (2001) · Science · doi:10.1126/science.1060342 · Cited by 1,097 · see citing works
The Correlation Theory of Brain Function
von der Malsburg, C. (1994) · Physics of neural networks · doi:10.1007/978-1-4612-4320-5_2 · Cited by 1,086 · see citing works
The high-conductance state of neocortical neurons in vivo
Alain Destexhe, A., Rudolph, M., & Paré, D. (2003) · Nature reviews. Neuroscience · doi:10.1038/nrn1198 · Cited by 1,077 · see citing works
McNaughton, B. L., Barnes, C. A., & O'Keefe, J. (1983) · Experimental Brain Research · doi:10.1007/bf00237147 · Cited by 1,071 · 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
Fries, P., Nikolić, D., & Singer, W. (2007) · Trends in Neurosciences · doi:10.1016/j.tins.2007.05.005 · Cited by 1,044 · see citing works
Theta rhythms coordinate hippocampal-prefrontal interactions in a spatial memory task
Jones, M. W., & Wilson, M. A. (2005) · PLoS Biology · doi:10.1371/journal.pbio.0030402 · Cited by 1,036 · see citing works
Organizing principles for a diversity of GABAergic interneurons and synapses in the neocortex
Gupta, A., Wang, Y., & Markram, H. (2000) · Science · doi:10.1126/science.287.5451.273 · Cited by 1,036 · see citing works
Entrainment of Neocortical Neurons and Gamma Oscillations by the Hippocampal Theta Rhythm
Sirota, A., Montgomery, S., Fujisawa, S., Isomura, Y., Zugaro, M., & Buzsáki, G. (2008) · Neuron · doi:10.1016/j.neuron.2008.09.014 · Cited by 1,015 · see citing works
Self-citationPrefrontal phase locking to hippocampal theta oscillations
Siapas, A. G., Lubenov, E. V., & Wilson, M. A. (2005) · Neuron · doi:10.1016/j.neuron.2005.02.028 · Cited by 1,014 · see citing works
Wagner, U., Gais, S., Haider, H., Verleger, R., & Born, J. (2004) · Nature · doi:10.1038/nature02223 · Cited by 1,012 · see citing works
Wood, E. R., Dudchenko, P. A., Robitsek, R. J., & Eichenbaum, H. (2000) · Neuron · doi:10.1016/s0896-6273(00)00071-4 · Cited by 992 · see citing works
Mechanisms of Gamma Oscillations in the Hippocampus of the Behaving Rat
Csicsvari, J., Jamieson, B. G., Wise, K. D., & Buzsáki, G. (2003) · Neuron · doi:10.1016/s0896-6273(02)01169-8 · Cited by 990 · see citing works
Self-citationPath integration and cognitive mapping in a continuous attractor neural network model
Samsonovich, A., & McNaughton, B. L. (1997) · The Journal of Neuroscience · doi:10.1523/jneurosci.17-15-05900.1997 · Cited by 989 · see citing works
An ultra-sparse code underliesthe generation of neural sequences in a songbird
Hahnloser, R. H. R., Kozhevnikov, A. A., & Fee, M. S. (2002) · Nature · doi:10.1038/nature00974 · Cited by 976 · see citing works
Oscillatory coupling of hippocampal pyramidal cells and interneurons in the behaving rat
Csicsvari, J., Hirase, H., Czurkó, A., Mamiya, A., & Buzsáki, G. (1999) · The Journal of Neuroscience · doi:10.1523/jneurosci.19-01-00274.1999 · Cited by 966 · see citing works
Self-citationInhibition-based rhythms: experimental and mathematical observations on network dynamics
Whittington, M. A., Traub, R. D., Kopell, N., Ermentrout, B., & Buhl, E. (2000) · International Journal of Psychophysiology · doi:10.1016/s0167-8760(00)00173-2 · Cited by 953 · see citing works
Megı́as, M., Emri, Z., Freund, T. F., & Gulyás, A. I. (2001) · Neuroscience · doi:10.1016/s0306-4522(00)00496-6 · Cited by 950 · see citing works
Replay and Time Compression of Recurring Spike Sequences in the Hippocampus
Nádasdy, Z., Hirase, H., Czurkó, A., Csicsvari, J., & Buzsáki, G. (1999) · The Journal of Neuroscience · doi:10.1523/jneurosci.19-21-09497.1999 · Cited by 932 · see citing works
Self-citationCommunication 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 · see citing works
Self-citationA network that learns to recognize three-dimensional objects
Poggio, T., & Edelman, S. (1990) · Nature · doi:10.1038/343263a0 · Cited by 930 · see citing works
State-dependent computations: spatiotemporal processing in cortical networks
Buonomano, D. V., & Maass, W. (2009) · Nature reviews. Neuroscience · doi:10.1038/nrn2558 · Cited by 919 · see citing works
Foundations of Cellular Neurophysiology
Johnston, D., & Wu, S. M.-S. (1994) · Medical Entomology and Zoology · Cited by 918 · see citing works
Endogenous electric fields may guide neocortical network activity
Fröhlich, F., & McCormick, D. A. (2010) · Neuron · doi:10.1016/j.neuron.2010.06.005 · Cited by 913 · see citing works
Deciphering The Hippocampal Polyglot: the Hippocampus as a Path Integration System
McNaughton, B. L., Barnes, C. A., Gerrard, J. L., Gothard, K. M., Jung, M. W., Knierim, J. J., Kudrimoti, H. S., Qin, Y., Skaggs, W. E., Suster, M. S., et al. (1996) · Journal of Experimental Biology · doi:10.1242/jeb.199.1.173 · Cited by 900 · see citing works
Benchenane, K., Peyrache, A., Khamassi, M., Tierney, P. L., Gioanni, Y., Battaglia, F. P., & Wiener, S. I. (2010) · Neuron · doi:10.1016/j.neuron.2010.05.013 · Cited by 872 · see citing works
Organization of cell assemblies in the hippocampus
Harris, K. D., Csicsvari, J., Hirase, H., Dragoi, G., & Buzsáki, G. (2003) · Nature · doi:10.1038/nature01834 · Cited by 869 · see citing works
Self-citationTort, A. B. L., Kramer, M., Thorn, C. A., Gibson, D. J., Kubota, Y., Graybiel, A. M., & Kopell, N. (2008) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0810524105 · Cited by 842 · 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
A treatise concerning the principles of human knowledge, 1734
Berkeley, G. (1971) · Cited by 841 · see citing works
Synfire Chains and Cortical Songs: Temporal Modules of Cortical Activity
Ikegaya, Y., Aaron, G., Cossart, R., Aronov, D., Lampl, I., Ferster, D., & Yuste, R. (2004) · Science · doi:10.1126/science.1093173 · Cited by 838 · see citing works
Dynamical principles in neuroscience
Rabinovich, M. I., Varona, P., Selverston, A. I., & Abarbanel, H. D. I. (2006) · Reviews of Modern Physics · doi:10.1103/revmodphys.78.1213 · Cited by 819 · see citing works
Comparison of spatial firing characteristics of units in dorsal and ventral hippocampus of the rat
Jung, M. W., Wiener, S. I., & McNaughton, B. L. (1994) · Journal of Neuroscience · doi:10.1523/jneurosci.14-12-07347.1994 · Cited by 818 · see citing works
Next-Generation Optical Technologies for Illuminating Genetically Targeted Brain Circuits
Deisseroth, K. A., Feng, G., Majewska, A. K., Miesenböck, G., Ting, A. Y., & Schnitzer, M. J. (2006) · Journal of Neuroscience · doi:10.1523/jneurosci.3863-06.2006 · Cited by 812 · see citing works
Hippocampal replay of extended experience
Davidson, T. J., Kloosterman, F., & Wilson, M. A. (2009) · Neuron · doi:10.1016/j.neuron.2009.07.027 · Cited by 806 · cited 1× · see citing works
“…assembly replay during rest and sleep occurs in snippets and is faster, often compressed by at least a factor of ten compared to the behavioral timescale of neuronal activation (Davidson et al., 2009; Diba andBuzsáki, 2007; Euston et al., 2007; Foster and Wilson, 2006; Nádasdy et al., 1999).”
The tempotron: a neuron that learns spike timing–based decisions
Gütig, R., & Sompolinsky, H. (2006) · Nature Neuroscience · doi:10.1038/nn1643 · Cited by 805 · see citing works
Oscillations and Sparsening of Odor Representations in the Mushroom Body
Pérez-Orive, J., Mazor, O., Turner, G. C., Cassenaer, S., Wilson, R. I., & Laurent, G. (2002) · Science · doi:10.1126/science.1070502 · Cited by 792 · see citing works
Spatial selectivity of unit activity in the hippocampal granular layer
Jung, M. W., & McNaughton, B. L. (1993) · Hippocampus · doi:10.1002/hipo.450030209 · Cited by 789 · see citing works
Finite scale of spatial representation in the hippocampus
Kjelstrup, K. B., Solstad, T., Brun, V. H., Hafting, T., Leutgeb, S., Witter, M. P., Moser, E. I., & Moser, M.-B. (2008) · Science · doi:10.1126/science.1157086 · Cited by 760 · see citing works
Genetic Dissection of Neural Circuits
Luo, L., Callaway, E. M., & Svoboda, K. (2008) · Neuron · doi:10.1016/j.neuron.2008.01.002 · Cited by 754 · see citing works
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
Boundary Vector Cells in the Subiculum of the Hippocampal Formation
Lever, C., Burton, S., Jeewajee, A., O'Keefe, J., & Burgess, N. (2009) · The Journal of Neuroscience · doi:10.1523/jneurosci.1319-09.2009 · Cited by 753 · see citing works
The hippocampal CA3 network: An in vivo intracellular labeling study
Li, X. ‐., Somogyi, P., Ylinen, A., & Buzsáki, G. (1994) · The Journal of Comparative Neurology · doi:10.1002/cne.903390204 · Cited by 751 · see citing works
Self-citationInformation processing with population codes
Pouget, A., Dayan, P., & Zemel, R. S. (2000) · Nature reviews. Neuroscience · doi:10.1038/35039062 · Cited by 744 · see citing works
Olfactory network dynamics and the coding of multidimensional signals
Laurent, G. (2002) · Nature reviews. Neuroscience · doi:10.1038/nrn964 · Cited by 733 · see citing works
Trajectory Encoding in the Hippocampus and Entorhinal Cortex
Frank, L. M., Brown, E. N., & Wilson, M. A. (2000) · Neuron · doi:10.1016/s0896-6273(00)00018-0 · Cited by 731 · see citing works
Temporal Encoding of Place Sequences by Hippocampal Cell Assemblies
Dragoi, G., & Buzsáki, G. (2006) · Neuron · doi:10.1016/j.neuron.2006.02.023 · Cited by 727 · see citing works
Self-citationConnecting cortex to machines: recent advances in brain interfaces
Donoghue, J. P. (2002) · Nature Neuroscience · doi:10.1038/nn947 · Cited by 720 · see citing works
Mizuseki, K., Sirota, A., Pastalkova, E., & Buzsáki, G. (2009) · Neuron · doi:10.1016/j.neuron.2009.08.037 · Cited by 718 · see citing works
Self-citationMetabotropic glutamate receptors: Synaptic transmission, modulation, and plasticity
Nakanishi, S. (1994) · Neuron · doi:10.1016/0896-6273(94)90043-4 · Cited by 716 · see citing works
Target-cell-specific facilitation and depression in neocortical circuits
Reyes, A., Lujan, R., Rozov, A., Burnashev, N., Somogyi, P., & Sakmann, B. (1998) · Nature Neuroscience · doi:10.1038/1092 · Cited by 716 · cited 1× · see citing works
“…in the cortex is characterized by a large range of variation of synaptic weights (Gloveli et al., 1997; Holmgren et al., 2003; Markram et al., 1998; Reyes et al., 1998; Wang et al., 2006), which can change dynamically by both presynaptic and postsynaptic mechanisms (Chung et al., 2002; Deisz and…”
GABAergic Hub Neurons Orchestrate Synchrony in Developing Hippocampal Networks
Bonifazi, P., Goldin, M., Picardo, M. A., Jorquera, I., Cattani, A., Bianconi, G., Represa, A., Ben-Ari, Y., & Cossart, R. (2009) · Science · doi:10.1126/science.1175509 · Cited by 695 · see citing works
An oscillatory interference model of grid cell firing
Burgess, N., Barry, C., & O'Keefe, J. M. (2007) · Hippocampus · doi:10.1002/hipo.20327 · Cited by 688 · see citing works
Nonsynaptic modulation of neuronal activity in the brain: electric currents and extracellular ions
Jefferys, J. G. R. (1995) · Physiological Reviews · doi:10.1152/physrev.1995.75.4.689 · Cited by 686 · see citing works
Behavior-dependent short-term assembly dynamics in the medial prefrontal cortex
Fujisawa, S., Amarasingham, A., Harrison, M. T., & Buzsáki, G. (2008) · Nature Neuroscience · doi:10.1038/nn.2134 · Cited by 679 · see citing works
Self-citationVisual input evokes transient and strong shunting inhibition in visual cortical neurons
Graham, L. J., Monier, C., & Frégnac, Y. (1998) · Nature · doi:10.1038/30735 · Cited by 669 · see citing works
Solving the Distal Reward Problem through Linkage of STDP and Dopamine Signaling
Izhikevich, E. M. (2007) · Cerebral Cortex · doi:10.1093/cercor/bhl152 · Cited by 664 · see citing works
Hasenstaub, A. R., Shu, Y., Haider, B., Kraushaar, U., Duque, A., & McCormick, D. A. (2005) · Neuron · doi:10.1016/j.neuron.2005.06.016 · Cited by 654 · see citing works
Cerebral Mechanisms in Behavior: The Hixon Symposium
(1952) · JAMA · doi:10.1001/jama.1952.02930120090037 · Cited by 652 · see citing works
Friedemann Pulvermüller, A. (2003) · Cambridge University Press eBooks · doi:10.1017/cbo9780511615528 · Cited by 645 · see citing works
Integrative Properties of Radial Oblique Dendrites in Hippocampal CA1 Pyramidal Neurons
Losonczy, A., & Magee, J. C. (2006) · Neuron · doi:10.1016/j.neuron.2006.03.016 · Cited by 641 · see citing works
Llinás, R. R., & Paré, D. (1991) · Neuroscience · doi:10.1016/0306-4522(91)90075-y · Cited by 641 · see citing works
Interneuron Diversity series: Rhythm and mood in perisomatic inhibition
Freund, T. F. (2003) · Trends in Neurosciences · doi:10.1016/s0166-2236(03)00227-3 · Cited by 641 · see citing works
Operant Conditioning of Cortical Unit Activity
Fetz, E. E. (1969) · Science · doi:10.1126/science.163.3870.955 · Cited by 631 · see citing works
Circuit-breakers: optical technologies for probing neural signals and systems
Zhang, F., Aravanis, A. M., Adamantidis, A., de Lecea, L., & Deisseroth, K. A. (2007) · Nature reviews. Neuroscience · doi:10.1038/nrn2192 · Cited by 623 · see citing works
The hippocampus and memory for orderly stimulus relations
Dusek, J. A., & Eichenbaum, H. (1997) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.94.13.7109 · Cited by 610 · see citing works
Relating Hippocampal Circuitry to Function
Lisman, J. E. (1999) · Neuron · doi:10.1016/s0896-6273(00)81085-5 · Cited by 607 · see citing works
Reliability and State Dependence of Pyramidal Cell–Interneuron Synapses in the Hippocampus
Csicsvari, J., Hirase, H., Czurko, A., & Buzsáki, G. (1998) · Neuron · doi:10.1016/s0896-6273(00)80525-5 · Cited by 606 · see citing works
Self-citationIndependent rate and temporal coding in hippocampal pyramidal cells
Huxter, J. R., Burgess, N., & O'Keefe, J. M. (2003) · Nature · doi:10.1038/nature02058 · Cited by 594 · see citing works
Gamma Oscillations in the Entorhinal Cortex of the Freely Behaving Rat
Chrobak, J. J., & Buzsáki, G. (1998) · Journal of Neuroscience · doi:10.1523/jneurosci.18-01-00388.1998 · Cited by 590 · see citing works
Self-citationInstantaneous Modulation of Gamma Oscillation Frequency by Balancing Excitation with Inhibition
Atallah, B. V., & Scanziani, M. (2009) · Neuron · doi:10.1016/j.neuron.2009.04.027 · Cited by 588 · see citing works
Fast-Forward Playback of Recent Memory Sequences in Prefrontal Cortex During Sleep
Euston, D. R., Tatsuno, M., & McNaughton, B. L. (2007) · Science · doi:10.1126/science.1148979 · Cited by 586 · see citing works
Laminar Structure of Spontaneous and Sensory-Evoked Population Activity in Auditory Cortex
Sakata, S., & Harris, K. D. (2009) · Neuron · doi:10.1016/j.neuron.2009.09.020 · Cited by 580 · see citing works
Memory consolidation during sleep: a neurophysiological perspective
Buzsáki, G. (1998) · Journal of Sleep Research · doi:10.1046/j.1365-2869.7.s1.3.x · Cited by 578 · see citing works
Self-citationPyramidal cell communication within local networks in layer 2/3 of rat neocortex.
Holmgren, C., Harkany, T., Svennenfors, B., & Zilberter, Y. (2003) · The Journal of Physiology · doi:10.1113/jphysiol.2003.044784 · Cited by 573 · see citing works
Prospective and Retrospective Memory Coding in the Hippocampus
Ferbinteanu, J., & Shapiro, M. L. (2003) · Neuron · doi:10.1016/s0896-6273(03)00752-9 · Cited by 560 · see citing works
Synapses as associative memory elements in the hippocampal formation
Levy, W. B., & Steward, O. (1979) · Brain Research · doi:10.1016/0006-8993(79)91003-5 · Cited by 557 · see citing works
Calcium-dependent current generating the afterhyperpolarization of hippocampal neurons
Lancaster, B., & Adams, P. R. (1986) · Journal of Neurophysiology · doi:10.1152/jn.1986.55.6.1268 · Cited by 547 · cited 1× · see citing works
“Time integration of cell assemblies at the subsecond to seconds timescale can be performed by metabotropic glutamate receptors (Nakanishi, 1994), GABAB receptors (Deisz and Prince, 1989), and slow afterhyperpolarization-associated conductances (Lancaster and Adams, 1986).”
Hippocampal theta oscillations are travelling waves
Lubenov, E. V., & Siapas, A. G. (2009) · Nature · doi:10.1038/nature08010 · Cited by 543 · see citing works
Sparse optical microstimulation in barrel cortex drives learned behaviour in freely moving mice
Huber, D., Petreanu, L., Ghitani, N., Ranade, S., Hromádka, T., Mainen, Z., & Svoboda, K. (2008) · Nature · doi:10.1038/nature06445 · Cited by 539 · see citing works
Internally generated reactivation of single neurons in human hippocampus during free recall
Gelbard-Sagiv, H., Mukamel, R., Harel, M., Malach, R., & Fried, I. (2008) · Science · doi:10.1126/science.1164685 · Cited by 533 · see citing works
Mind time: the temporal factor in consciousness
(2004) · Choice Reviews Online · doi:10.5860/choice.42-0932 · Cited by 533 · see citing works
Experience-dependent rescaling of entorhinal grids
Barry, C., Hayman, R. M. A., Burgess, N., & Jeffery, K. J. (2007) · Nature Neuroscience · doi:10.1038/nn1905 · Cited by 532 · see citing works
Temporal association in asymmetric neural networks.
Sompolinsky, H., & Kanter, I. (1986) · Physical Review Letters · doi:10.1103/physrevlett.57.2861 · Cited by 531 · see citing works
Chung, S., Li, X., & Nelson, S. B. (2002) · Neuron · doi:10.1016/s0896-6273(02)00659-1 · Cited by 530 · cited 2× · see citing works
“The chaining of such assemblies by some internal mechanisms (Hebb’s ‘‘phase sequences’’), in turn, would provide the basis by which complex cognitive processes, such as memory recall, thinking, planning, and decision making, could flow independently of direct control from the environment or the body (Churchland and Se…”
Oscillatory Entrainment of Striatal Neurons in Freely Moving Rats
Berke, J. D., Okatan, M., Skurski, J., & Eichenbaum, H. (2004) · Neuron · doi:10.1016/j.neuron.2004.08.035 · Cited by 507 · 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
Self-citationHeterogeneity in the pyramidal network of the medial prefrontal cortex
Wang, Y., Markram, H., Goodman, P. H., Berger, T. K., Ma, J., & Goldman-Rakic, P. S. (2006) · Nature Neuroscience · doi:10.1038/nn1670 · Cited by 503 · see citing works
Isomura, Y., Sirota, A., Özen, S., Montgomery, S., Mizuseki, K., Henze, D. A., & Buzsáki, G. (2006) · Neuron · doi:10.1016/j.neuron.2006.10.023 · Cited by 500 · see citing works
Self-citationMillisecond-Timescale Optical Control of Neural Dynamics in the Nonhuman Primate Brain
Han, X., Qian, X., Bernstein, J. G., Zhou, H., Franzesi, G. T., Stern, P., Bronson, R. T., Graybiel, A. M., Desimone, R., & Boyden, E. S. (2009) · Neuron · doi:10.1016/j.neuron.2009.03.011 · Cited by 497 · see citing works
Using temperature to analyse temporal dynamics in the songbird motor pathway
Long, M. A., & Fee, M. S. (2008) · Nature · doi:10.1038/nature07448 · Cited by 494 · see citing works
The structure and precision of retinal spike trains
Berry, M. J., Warland, D. K., & Meister, M. (1997) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.94.10.5411 · Cited by 490 · see citing works
Modalities, Modes, and Models in Functional Neuroimaging
Friston, K. J. (2009) · Science · doi:10.1126/science.1174521 · Cited by 489 · see citing works
Hippocampal network patterns of activity in the mouse
Buzsáki, G., Buhl, D. L., Harris, K. D., Csicsvari, J., Czéh, B., & Morozov, A. (2003) · Neuroscience · doi:10.1016/s0306-4522(02)00669-3 · Cited by 486 · see citing works
Self-citationMazor, O., & Laurent, G. (2005) · Neuron · doi:10.1016/j.neuron.2005.09.032 · Cited by 484 · see citing works
Writing Memories with Light-Addressable Reinforcement Circuitry
Claridge-Chang, A., Roorda, R. D., Vrontou, E., Sjulson, L., Li, H., Hirsh, J., & Miesenböck, G. (2009) · Cell · doi:10.1016/j.cell.2009.08.034 · Cited by 484 · see citing works
Principles of neural ensemble physiology underlying the operation of brain–machine interfaces
Nicolelis, M. A. L., & Lebedev, M. (2009) · Nature reviews. Neuroscience · doi:10.1038/nrn2653 · Cited by 477 · see citing works
Restoration of neural output from a paralyzed patient by a direct brain connection
Kennedy, P. R., & Bakay, R. A. E. (1998) · Neuroreport · doi:10.1097/00001756-199806010-00007 · Cited by 475 · see citing works
I of the Vortex: From Neurons to Self
Llinás, R. R. (2000) · Cited by 470 · see citing works
Transient Dynamics for Neural Processing
Rabinovich, M., Huerta, R., & Laurent, G. (2008) · Science · doi:10.1126/science.1155564 · Cited by 458 · see citing works
Edge of chaos and prediction of computational performance for neural circuit models
Legenstein, R. A., & Maass, W. (2007) · Neural Networks · doi:10.1016/j.neunet.2007.04.017 · Cited by 455 · see citing works
Odor Encoding as an Active, Dynamical Process: Experiments, Computation, and Theory
Laurent, G., Stopfer, M., Friedrich, R. W., Rabinovich, M. I., Volkovskii, A., & Abarbanel, H. D. I. (2001) · Annual Review of Neuroscience · doi:10.1146/annurev.neuro.24.1.263 · Cited by 450 · see citing works
Neural signatures of cell assembly organization
Harris, K. D. (2005) · Nature reviews. Neuroscience · doi:10.1038/nrn1669 · Cited by 443 · see citing works
Gamma oscillations dynamically couple hippocampal CA3 and CA1 regions during memory task performance
Montgomery, S. M., & Buzsáki, G. (2007) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0701826104 · Cited by 431 · see citing works
Self-citationWhisker movements evoked by stimulation of single pyramidal cells in rat motor cortex
Brecht, M., Schneider, M., Sakmann, B. J., & Margrie, T. W. (2004) · Nature · doi:10.1038/nature02266 · Cited by 429 · see citing works
Membrane potential dynamics of GABAergic neurons in the barrel cortex of behaving mice
Gentet, L. J., Avermann, M., Matyas, F., Staiger, J. F., & Petersen, C. C. H. (2010) · Neuron · doi:10.1016/j.neuron.2010.01.006 · Cited by 429 · cited 2× · see citing works
“In the neocortex, inhibition can have either a positive or inverse correlation with excitatory thalamic input (Ferster, 1986; Gentet et al., 2010; Wehr and Zador, 2003;).”
Optimizing Sound Features for Cortical Neurons
deCharms, R. C., Blake, D. T., & Merzenich, M. M. (1998) · Science · doi:10.1126/science.280.5368.1439 · Cited by 426 · see citing works
Corticonics: Neural Circuits of the Cerebral Cortex
Braitenberg, V. (1992) · Trends in Neurosciences · doi:10.1016/0166-2236(92)90361-b · Cited by 425 · see citing works
Coordinated Reactivation of Distributed Memory Traces in Primate Neocortex
Hoffman, K. L., & McNaughton, B. L. (2002) · Science · doi:10.1126/science.1073538 · Cited by 420 · see citing works
Submillisecond AMPA receptor-mediated signaling at a principal neuron-interneuron synapse
Geiger, J. R. P., Lübke, J., Roth, A., Frotscher, M., & Jonas, P. (1997) · Neuron · doi:10.1016/s0896-6273(00)80339-6 · Cited by 407 · see citing works
Rao, S. G., Williams, G. V., & Goldman-Rakic, P. S. (2000) · The Journal of Neuroscience · doi:10.1523/jneurosci.20-01-00485.2000 · Cited by 407 · see citing works
Flagged first, then by citations
Research works printed but not linked: 2
- Pikovsky M Rosenblum Kurths J Synchronization: a unified approach to nonlinear science 2001 Cambridge Cambridge University Press
- Rumelhart DE McLelland JL the PDP Research Group Parallel Distributed Processing: Explorations in the Microstructure of cognition - Vol. 1 Foundations 1986 Cambridge, MA MIT Press
Cited by
Sorted by citations
The origin of extracellular fields and currents — EEG, ECoG, LFP and spikes
Buzsáki, G., Anastassiou, C. A., & Koch, C. (2012) · Nature Reviews Neuroscience · doi:10.1038/nrn3241 · Cited by 4,225 · see citing works
Self-citationFrontal theta as a mechanism for cognitive control
Cavanagh, J. F., & Frank, M. J. (2014) · Trends in Cognitive Sciences · doi:10.1016/j.tics.2014.04.012 · Cited by 2,726 · see citing works
Canonical Microcircuits for Predictive Coding
Bastos, A. M., Usrey, W. M., Adams, R. A., Mangun, G. R., Fries, P., & Friston, K. J. (2012) · Neuron · doi:10.1016/j.neuron.2012.10.038 · Cited by 2,421 · see citing works
“This view has re-emerged in recent years, with the development of the requisite recording and analytic techniques for evaluating this proposal (Buzsáki, 2010; Canolty et al., 2010; Singer et al., 1997; Lopes-dos-Santos et al., 2011).”
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
Self-citationMemory, navigation and theta rhythm in the hippocampal-entorhinal system
Buzsáki, G., & Moser, E. I. (2013) · Nature Neuroscience · doi:10.1038/nn.3304 · Cited by 1,847 · see citing works
Self-citationIntegrated information theory: from consciousness to its physical substrate
Tononi, G., Boly, M., Massimini, M., & Koch, C. (2016) · Nature Reviews Neuroscience · doi:10.1038/nrn.2016.44 · Cited by 1,727 · see citing works
Functional organization of the hippocampal longitudinal axis
Strange, B. A., Witter, M. P., Lein, E. S., & Moser, E. I. (2014) · Nature reviews. Neuroscience · doi:10.1038/nrn3785 · Cited by 1,738 · see citing works
Lisman, J. E., & Jensen, O. (2013) · Neuron · doi:10.1016/j.neuron.2013.03.007 · Cited by 1,609 · see citing works
Millan, M. J., Agid, Y., Brüne, M., Bullmore, E. T., Carter, C. S., Clayton, N. S., Connor, R., Davis, S., Deakin, B., DeRubeis, R. J., et al. (2012) · Nature Reviews Drug Discovery · doi:10.1038/nrd3628 · Cited by 1,292 · see citing works
Cortical tracking of hierarchical linguistic structures in connected speech
Ding, N., Melloni, L., Zhang, H., Tian, X., & Poeppel, D. (2016) · Nature Neuroscience · doi:10.1038/nn.4186 · Cited by 1,059 · see citing works
‘Activity-silent’ working memory in prefrontal cortex: a dynamic coding framework
Stokes, M. G. (2015) · Trends in Cognitive Sciences · doi:10.1016/j.tics.2015.05.004 · Cited by 850 · see citing works
Viewpoints: how the hippocampus contributes to memory, navigation and cognition
Lisman, J., Buzsáki, G., Eichenbaum, H., Nadel, L., Ranganath, C., & Redish, A. D. (2017) · Nature Neuroscience · doi:10.1038/nn.4661 · Cited by 851 · see citing works
Self-citationCross-Frequency Phase–Phase Coupling between Theta and Gamma Oscillations in the Hippocampus
Belluscio, M. A., Mizuseki, K., Schmidt, R., Kempter, R., & Buzsáki, G. (2012) · The Journal of Neuroscience · doi:10.1523/jneurosci.4122-11.2012 · Cited by 784 · see citing works
Self-citationBuzsáki, G., & Watson, B. O. (2012) · Dialogues in Clinical Neuroscience · doi:10.31887/dcns.2012.14.4/gbuzsaki · Cited by 579 · see citing works
Self-citationA New Unifying Account of the Roles of Neuronal Entrainment
Lakatos, P., Gross, J., & Thut, G. (2019) · Current Biology · doi:10.1016/j.cub.2019.07.075 · Cited by 508 · see citing works
van de Ven, G. M., Trouche, S., McNamara, C. G., Allen, K., & Dupret, D. (2016) · Neuron · doi:10.1016/j.neuron.2016.10.020 · Cited by 320 · see citing works
Structural and synaptic plasticity in stress-related disorders
Christoffel, D. J., Golden, S. A., & Russo, S. J. (2011) · Reviews in the Neurosciences · doi:10.1515/rns.2011.044 · Cited by 334 · see citing works
CA1 pyramidal cell diversity enabling parallel information processing in the hippocampus
Soltesz, I., & Losonczy, A. (2018) · Nature Neuroscience · doi:10.1038/s41593-018-0118-0 · Cited by 333 · see citing works
State-dependent architecture of thalamic reticular subnetworks
Halassa, M. M., Chen, Z., Wimmer, R. D., Brunetti, P. M., Zhao, S., Zikopoulos, B., Wang, F., Brown, E. N., & Wilson, M. A. (2014) · Cell · doi:10.1016/j.cell.2014.06.025 · Cited by 309 · see citing works
Identification of a Functional Connectome for Long-Term Fear Memory in Mice
Wheeler, A. L., Teixeira, C. M., Wang, A. H., Xiong, X., Kovacevic, N., Lerch, J. P., McIntosh, A. R., Parkinson, J., & Frankland, P. W. (2013) · PLoS Computational Biology · doi:10.1371/journal.pcbi.1002853 · Cited by 315 · see citing works
Visual stimuli recruit intrinsically generated cortical ensembles
Miller, J.-E. K., Ayzenshtat, I., Carrillo-Reid, L., & Yuste, R. (2014) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1406077111 · Cited by 288 · see citing works
Tasks for inhibitory interneurons in intact brain circuits
Roux, L., & Buzsáki, G. (2015) · Neuropharmacology · doi:10.1016/j.neuropharm.2014.09.011 · Cited by 218 · see citing works
Self-citationSelective entrainment of gamma subbands by different slow network oscillations
Zhong, W., Ciatipis, M., Wolfenstetter, T., Jessberger, J., Müller, C., Ponsel, S., Yanovsky, Y., Brankačk, J., Tort, A. B. L., & Draguhn, A. (2017) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1617249114 · Cited by 155 · see citing works
Ephaptic coupling to endogenous electric field activity: Why bother?
Anastassiou, C. A., & Koch, C. (2015) · Current Opinion in Neurobiology · doi:10.1016/j.conb.2014.09.002 · Cited by 171 · see citing works
Portraits of communication in neuronal networks
Hahn, G., Ponce-Alvarez, A., Deco, G., Aertsen, A., & Kumar, A. (2019) · Nature reviews. Neuroscience · doi:10.1038/s41583-018-0094-0 · Cited by 171 · see citing works
Pfarr, S., Meinhardt, M. W., Klee, M. L., Hansson, A. C., Vengeliene, V., Schonig, K., Bartsch, D., Hope, B. T., Spanagel, R., & Sommer, W. H. (2015) · Journal of Neuroscience · doi:10.1523/jneurosci.0684-15.2015 · Cited by 143 · see citing works
Bazan, N. G. (2018) · Molecular Aspects of Medicine · doi:10.1016/j.mam.2018.09.003 · Cited by 148 · see citing works
Cognit activation: a mechanism enabling temporal integration in working memory
Fuster, J. M., & Bressler, S. L. (2012) · Trends in Cognitive Sciences · doi:10.1016/j.tics.2012.03.005 · Cited by 139 · see citing works
Neural versus alternative integrative systems: molecular insights into origins of neurotransmitters
Moroz, L. L., Romanova, D. Y., & Kohn, A. B. (2021) · Philosophical Transactions of the Royal Society B · doi:10.1098/rstb.2019.0762 · Cited by 130 · see citing works
Basu, J., Srinivas, K. V., Cheung, S. K., Taniguchi, H., Huang, Z. J., & Siegelbaum, S. A. (2013) · Neuron · doi:10.1016/j.neuron.2013.07.001 · Cited by 122 · see citing works
Early Cognitive Experience Prevents Adult Deficits in a Neurodevelopmental Schizophrenia Model
Lee, H., Dvorak, D., Kao, H.-Y., Duffy, Á. M., Scharfman, H. E., & Fenton, A. A. (2012) · Neuron · doi:10.1016/j.neuron.2012.06.016 · Cited by 122 · see citing works
Toward an integration of deep learning and neuroscience
Marblestone, A. H., Wayne, G., & Kording, K. P. (2016) · Frontiers in Computational Neuroscience · doi:10.3389/fncom.2016.00094 · Cited by 119 · see citing works
Is hippocampal remapping the physiological basis for context
Kubie, J. L., Levy, E. R. J., & Fenton, A. A. (2020) · Hippocampus · doi:10.1002/hipo.23160 · Cited by 94 · see citing works
Cognitive and Physiologic Impacts of the Infraslow Oscillation
Watson, B. O. (2018) · Frontiers in Systems Neuroscience · doi:10.3389/fnsys.2018.00044 · Cited by 74 · see citing works
Multiple Origins of Neurons From Secretory Cells
Moroz, L. L. (2021) · Frontiers in Cell and Developmental Biology · doi:10.3389/fcell.2021.669087 · Cited by 67 · see citing works
Radwan, B., Dvorak, D., & Fenton, A. A. (2016) · Neurobiology of Disease · doi:10.1016/j.nbd.2016.01.003 · Cited by 63 · see citing works
Syringe-injectable electronics with a plug-and-play input/output interface.
Schuhmann, T. G., Yao, J., Hong, G., Fu, T.-M., & Lieber, C. M. (2017) · Nano Letters · doi:10.1021/acs.nanolett.7b03081 · Cited by 63 · see citing works
Chronic stress disrupts neural coherence between cortico-limbic structures
Oliveira, J. F., Dias, N. S., Correia, M., Gama-Pereira, F., Sardinha, V. M., Lima, A., Oliveira, A. F., Jacinto, L. R., Ferreira, D. S., Silva, A. M., et al. (2013) · Frontiers in Neural Circuits · doi:10.3389/fncir.2013.00010 · Cited by 55 · see citing works
Xu, X., An, L., Mi, X., & Zhang, T. (2013) · PLoS ONE · doi:10.1371/journal.pone.0077796 · Cited by 49 · see citing works
Pulvermüller, F. (2014) · Trends in Cognitive Sciences · doi:10.1016/j.tics.2014.01.001 · Cited by 46 · see citing works
Neural and phenotypic representation under the free-energy principle
Ramstead, M. J. D., Hesp, C., Tschantz, A., Smith, R., Constant, A., & Friston, K. (2021) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2020.11.024 · Cited by 43 · see citing works
Beker, S., Foxe, J. J., & Molholm, S. (2021) · Journal of Neurophysiology · doi:10.1152/jn.00329.2021 · Cited by 35 · see citing works
Neural ensembles: role of intrinsic excitability and its plasticity
Hansel, C., & Yuste, R. (2024) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2024.1440588 · Cited by 33 · see citing works
The generative grammar of the brain: a critique of internally generated representations
Dragoi, G. (2024) · Nature Reviews Neuroscience · doi:10.1038/s41583-023-00763-0 · Cited by 28 · see citing works
Dynamical Emergence Theory (DET): A Computational Account of Phenomenal Consciousness
Moyal, R., Fekete, T., & Edelman, S. (2020) · Minds and Machines · doi:10.1007/s11023-020-09516-9 · Cited by 26 · see citing works
Neural and neuronal discoordination in schizophrenia: from ensembles through networks to symptoms
Krajcovic, B., Fajnerova, I., Horacek, J., Kelemen, E., Kubik, S., Svoboda, J., & Stuchlik, A. (2019) · Acta Physiologica · doi:10.1111/apha.13282 · Cited by 29 · see citing works
Differential Impact of Acute and Chronic Stress on CA1 Spatial Coding and Gamma Oscillations
Tomar, A., Polygalov, D., & McHugh, T. J. (2021) · Frontiers in Behavioral Neuroscience · doi:10.3389/fnbeh.2021.710725 · Cited by 21 · see citing works
- Authors
- Buzsáki, G.
- Affiliations
- Rutgers, The State University of New Jersey (US)
- Corresponding author
- Buzsáki, György
- ORCID
- Buzsáki, György
- Venue
- Neuron
- Publisher
- Elsevier BV
- Published
- 2010-11
- Volume
- 68
- Issue
- 3
- Pages
- 362-385
- ISSN
- 0896-6273 (ISSN-L)
- PMC
- PMC3005627
- OpenAlex
- W1996874802
- Cited by
- 1,289
- References
- 351
- Citations by year
- 2026: 78 · 2025: 88 · 2024: 93 · 2023: 73 · 2022: 90 · 2021: 108 · 2020: 83 · 2019: 92 · 2018: 93 · 2017: 82 · 2016: 93 · 2015: 90 · 2014: 77 · 2013: 71 · 2012: 46
- FWCI
- 3.37
- Type
- journal article
- Language
- en
- Open access
- bronze
- doi.org
- Licence
- www.elsevier.com/tdm/userlicense/1.0/ (tdm)
- www.elsevier.com/legal/tdmrep-license (tdm)
- www.elsevier.com/open-access/userlicense/1.0/ (vor, 989 d)
- doi.org/10.15223/policy-017 (stm-asf)
- doi.org/10.15223/policy-037 (stm-asf)
- doi.org/10.15223/policy-012 (stm-asf)
- doi.org/10.15223/policy-029 (stm-asf)
- doi.org/10.15223/policy-004 (stm-asf)
- Locations
- Neuron (publishedVersion)
- PubMed (publishedVersion)
- Europe PMC (PubMed Central) (acceptedVersion)
- PubMed Central (acceptedVersion)
- Funders
- National Science Foundation (SBE 0542013)
- National Institutes of Health (MH54671, NS034994)
- Topics
- Life Sciences › Neuroscience › Cognitive Neuroscience › Neural dynamics and brain function
- Life Sciences › Neuroscience › Cognitive Neuroscience › Memory and Neural Mechanisms
- Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Neuroscience and Neuropharmacology Research
- Keywords
- cell assemblies, synaptic weights, memory encoding, neural basis of behavior
- MeSH terms
- Animals, Brain, Electrophysiology, Humans, Models, Neurological, Neural Pathways, Neurons, Synapses
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
