Brain rhythms and neural syntax: implications for efficient coding of cognitive content and neuropsychiatric disease.
Open accessAbstract
The perpetual activity of the cerebral cortex is largely supported by the variety of oscillations the brain generates, spanning a number of frequencies and anatomical locations, as well as behavioral correlates. First, we review findings from animal studies showing that most forms of brain rhythms are inhibition-based, producing rhythmic volleys of inhibitory inputs to principal cell populations, thereby providing alternating temporal windows of relatively reduced and enhanced excitability in neuronal networks. These inhibition-based mechanisms offer natural temporal frames to group or "chunk" neuronal activity into cell assemblies and sequences of assemblies, with more complex multi-oscillation interactions creating syntactical rules for the effective exchange of information among cortical networks. We then review recent studies in human psychiatric patients demonstrating a variety alterations in neural oscillations across all major psychiatric diseases, and suggest possible future research directions and treatment approaches based on the fundamental properties of brain rhythms.
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SOHM dynamics may help explain why oscillations tend to occur at faster rates in organisms with smaller brains, because smaller systems are likely to arrive at synchronous equilibria more quickly.
“SOHM dynamics may help to explain many kinds of rhythmic phenomena, such as the fact that oscillations tend to occur at faster rates in organisms with smaller brains (Buzsáki and Watson, 2012); all else being equal, smaller systems are likely to arrive at synchronous equilibria more quickly, with larger systems requiring relatively more time for synchronizing their micro-dynamics.”
From An Integrated World Modeling Theory (IWMT) of Consciousness (2020) · cites this paper as Buzsáki and Watson, 2012
In “Preservation of brain rhythms in the mammalian order” (page not supplied), the paper says hippocampal theta oscillations are perhaps the only known rhythm whose frequency scales inversely with brain size. It also says brain-rhythm frequencies vary little across mammals, so the cited source supports the theta example, not the broader claim that oscillations generally tend to be faster in smaller-brained organisms. The sentence presents the synchronous-equilibria explanation as the citing authors’ own reasoning, not as a claim from this source. (LLM, conf=0.87)
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Cites
Complex brain networks: graph theoretical analysis of structural and functional systems
Bullmore, E., & Sporns, O. (2009) · Nature Reviews Neuroscience · doi:10.1038/nrn2575 · Cited by 11,820 · see citing works
Self-organized criticality: An explanation of the 1/ f noise
Bak, P., Tang, C., & Wiesenfeld, K. A. (1987) · Physical Review Letters · doi:10.1103/physrevlett.59.381 · Cited by 7,644 · see citing works
Neuronal Oscillations in Cortical Networks
Buzsáki, G., & Draguhn, A. (2004) · Science · doi:10.1126/science.1099745 · Cited by 6,576 · see citing works
Self-citationBuzsáki, G. (2006) · doi:10.1093/acprof:oso/9780195301069.001.0001 · Cited by 4,873 · see citing works
Self-citationThe 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
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
Microstructure of a spatial map in the entorhinal cortex
Hafting, T., Fyhn, M., Molden, S., Moser, M.-B., & Moser, E. I. (2005) · Nature · doi:10.1038/nature03721 · Cited by 4,068 · 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-citationReactivation 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
Mechanisms of Gamma Oscillations
Buzsáki, G., & Wang, X.-J. (2012) · Annual Review of Neuroscience · doi:10.1146/annurev-neuro-062111-150444 · Cited by 2,796 · see citing works
Self-citationModulation of Oscillatory Neuronal Synchronization by Selective Visual Attention
Fries, P., Reynolds, J. H., Rorie, A. E., & Desimone, R. (2001) · Science · doi:10.1126/science.1055465 · Cited by 2,786 · 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
Experimental and theoretical approaches to conscious processing
Dehaene, S., & Changeux, J.-P. (2011) · Neuron · doi:10.1016/j.neuron.2011.03.018 · Cited by 2,573 · 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
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
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
Cortical inhibitory neurons and schizophrenia
Lewis, D. A., Hashimoto, T., & Volk, D. W. (2005) · Nature Reviews Neuroscience · doi:10.1038/nrn1648 · Cited by 2,297 · see citing works
Shadlen, M. N., & Newsome, W. T. (1998) · The Journal of Neuroscience · doi:10.1523/jneurosci.18-10-03870.1998 · Cited by 2,178 · see citing works
A default mode of brain function: a brief history of an evolving idea
Raichle, M. E., & Snyder, A. Z. (2007) · NeuroImage · doi:10.1016/j.neuroimage.2007.02.041 · Cited by 2,173 · see citing works
Abnormal neural oscillations and synchrony in schizophrenia
Uhlhaas, P. J., & Singer, W. (2010) · Nature Reviews Neuroscience · doi:10.1038/nrn2774 · Cited by 2,120 · see citing works
The functional role of cross-frequency coupling
Canolty, R. T., & Knight, R. T. (2010) · Trends in Cognitive Sciences · doi:10.1016/j.tics.2010.09.001 · Cited by 2,101 · 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
Animal models of neuropsychiatric disorders
Nestler, E. J., & Hyman, S. E. (2010) · Nature Neuroscience · doi:10.1038/nn.2647 · Cited by 2,023 · 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
Hippocampal electrical activity and voluntary movement in the rat
Vanderwolf, C. H. (1969) · Electroencephalography and Clinical Neurophysiology · doi:10.1016/0013-4694(69)90092-3 · Cited by 1,928 · see citing works
Huber, R., Felice Ghilardi, M., Massimini, M., & Tononi, G. (2004) · Nature · doi:10.1038/nature02663 · Cited by 1,854 · see citing works
Boosting slow oscillations during sleep potentiates memory
Marshall, L., Helgadóttir, H., Mölle, M., & Born, J. (2006) · Nature · doi:10.1038/nature05278 · Cited by 1,792 · 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
Self-citationCoordinated 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
The role of phase synchronization in memory processes
Fell, J., & Axmacher, N. (2011) · Nature Reviews Neuroscience · doi:10.1038/nrn2979 · Cited by 1,620 · see citing works
Tononi, G. (1998) · Science · doi:10.1126/science.282.5395.1846 · Cited by 1,561 · see citing works
von Stein, A., & Sarnthein, J. (2000) · International Journal of Psychophysiology · doi:10.1016/s0167-8760(00)00172-0 · Cited by 1,553 · see citing works
Low-frequency neuronal oscillations as instruments of sensory selection
Schroeder, C. E., & Lakatos, P. (2009) · Trends in Neurosciences · doi:10.1016/j.tins.2008.09.012 · Cited by 1,528 · 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
Self-citationStorage 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
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-citationLlinás, R. R., Ribary, U., Jeanmonod, D., Kronberg, E., & Mitra, P. P. (1999) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.96.26.15222 · Cited by 1,395 · 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
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
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
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
Neural syntax: cell assemblies, synapsembles, and readers
Buzsáki, G. (2010) · Neuron · doi:10.1016/j.neuron.2010.09.023 · Cited by 1,289 · see citing works
Self-citationResponsive cortical stimulation for the treatment of medically intractable partial epilepsy
Morrell, M. J. (2011) · Neurology · doi:10.1212/wnl.0b013e3182302056 · Cited by 1,282 · see citing works
Lakatos, P., Shah, A. S., Knuth, K. H., Ulbert, I., Karmos, G., & Schroeder, C. E. (2005) · Journal of Neurophysiology · doi:10.1152/jn.00263.2005 · Cited by 1,241 · see citing works
Correlated neuronal discharge rate and its implications for psychophysical performance
Zohary, E., Shadlen, M. N., & Newsome, W. T. (1994) · Nature · doi:10.1038/370140a0 · Cited by 1,237 · 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-citationGeometric 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
Attention improves performance primarily by reducing interneuronal correlations
Cohen, M. R., & Maunsell, J. H. R. (2009) · Nature Neuroscience · doi:10.1038/nn.2439 · Cited by 1,126 · see citing works
The Asynchronous State in Cortical Circuits
Renart, A., de la Rocha, J., Bartho, P., Hollender, L., Parga, N., Reyes, A., & Harris, K. D. (2010) · Science · doi:10.1126/science.1179850 · Cited by 1,106 · 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
Patil, S. T., Zhang, L., Martenyi, F., Lowe, S. L., Jackson, K. A., Andreev, B. V., Avedisova, A. S., Bardenstein, L. M., Gurovich, I. Y., Morozova, M. A., et al. (2007) · Nature Medicine · doi:10.1038/nm1632 · Cited by 1,040 · 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
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
Gain Modulation from Background Synaptic Input
Chance, F. S., Abbott, L. F., & Reyes, A. D. (2002) · Neuron · doi:10.1016/s0896-6273(02)00820-6 · Cited by 1,012 · see citing works
Cross-frequency coupling between neuronal oscillations
Jensen, O., & Colgin, L. L. (2007) · Trends in Cognitive Sciences · doi:10.1016/j.tics.2007.05.003 · Cited by 991 · 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
Inhibition-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
Cross-frequency coupling supports multi-item working memory in the human hippocampus
Axmacher, N., Henseler, M. M., Jensen, O. B., Weinreich, I., Elger, C. E., & Fell, J. (2010) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0911531107 · Cited by 938 · 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-citationTheta-gamma coupling increases during the learning of item-context associations
Tort, A. B. L., Komorowski, R. W., Manns, J. R., Kopell, N. J., & Eichenbaum, H. (2009) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0911331106 · Cited by 919 · see citing works
Organization of intrahippocampal projections originating from CA3 pyramidal cells in the rat
Ishizuka, N., Weber, J., & Amaral, D. G. (1990) · The Journal of Comparative Neurology · doi:10.1002/cne.902950407 · Cited by 899 · see citing works
Hasselmo, M. E., Bodelón, C., & Wyble, B. P. (2002) · Neural Computation · doi:10.1162/089976602317318965 · Cited by 875 · 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. L., 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
The Effect of Correlated Variability on the Accuracy of a Population Code
Abbott, L. F., & Dayan, P. (1999) · Neural Computation · doi:10.1162/089976699300016827 · Cited by 833 · see citing works
Closed-Loop Deep Brain Stimulation Is Superior in Ameliorating Parkinsonism
Rosin, B., Slovik, M., Mitelman, R., Rivlin-Etzion, M., Haber, S. N., Israel, Z., Vaadia, E., & Bergman, H. (2011) · Neuron · doi:10.1016/j.neuron.2011.08.023 · Cited by 793 · see citing works
Cross-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-citationKudrimoti, 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
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-citationTemporal 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-citationSteriade, M., Contreras, D., Dossi, R. C., & Núñez, Á. (1993) · Journal of Neuroscience · doi:10.1523/jneurosci.13-08-03284.1993 · Cited by 723 · 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-citationSpatial attention decorrelates intrinsic activity fluctuations in macaque area V4
Mitchell, J. F., Sundberg, K. A., & Reynolds, J. H. (2009) · Neuron · doi:10.1016/j.neuron.2009.09.013 · Cited by 710 · see citing works
Brain Oscillatory Substrates of Visual Short-Term Memory Capacity
Sauseng, P., Klimesch, W., Heise, K.-F., Gruber, W. R., Holz, E. M., Karim, A. A., Glennon, M., Gerloff, C. P., Birbaumer, N., & Hummel, F. C. (2009) · Current Biology · doi:10.1016/j.cub.2009.08.062 · Cited by 707 · 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
Very Slow Activity Fluctuations in Monkey Visual Cortex: Implications for Functional Brain Imaging
Leopold, D. A. (2003) · Cerebral Cortex · doi:10.1093/cercor/13.4.422 · Cited by 675 · see citing works
Phase Synchrony among Neuronal Oscillations in the Human Cortex
Palva, J. M., Palva, S., & Kaila, K. (2005) · Journal of Neuroscience · doi:10.1523/jneurosci.4250-04.2005 · Cited by 663 · see citing works
Gamma frequency-range abnormalities to auditory stimulation in schizophrenia
Kwon, J. S., O'Donnell, B. F., Wallenstein, G. V., Greene, R. W., Hirayasu, Y., Nestor, P. G., Hasselmo, M. E., Potts, G. F., Shenton, M. E., & McCarley, R. W. (1999) · Archives of General Psychiatry · doi:10.1001/archpsyc.56.11.1001 · Cited by 654 · 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
Decorrelated neuronal firing in cortical microcircuits
Ecker, A. S., Berens, P., Keliris, G. A., Bethge, M., Logothetis, N. K., & Tolias, A. S. (2010) · Science · doi:10.1126/science.1179867 · Cited by 640 · see citing works
Dynamics of Active Sensing and perceptual selection
Schroeder, C. E., Wilson, D. A., Radman, T., Scharfman, H. E., & Lakatos, P. (2010) · Current Opinion in Neurobiology · doi:10.1016/j.conb.2010.02.010 · Cited by 635 · see citing works
Early motor activity drives spindle bursts in the developing somatosensory cortex
Khazipov, R., Sirota, A., Leinekugel, X., Holmes, G. L., Ben‐Ari, Y., & Buzsáki, G. (2004) · Nature · doi:10.1038/nature03132 · Cited by 634 · see citing works
Self-citationAbnormal neural synchrony in schizophrenia
Spencer, K. M., Nestor, P. G., Niznikiewicz, M. A., Salisbury, D. F., Shenton, M. E., & McCarley, R. W. (2003) · The Journal of Neuroscience · doi:10.1523/jneurosci.23-19-07407.2003 · Cited by 624 · 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
Independent 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 601 · see citing works
Human EEG gamma oscillations in neuropsychiatric disorders
Herrmann, C. S., & Demıralp, T. (2005) · Clinical Neurophysiology · doi:10.1016/j.clinph.2005.07.007 · Cited by 600 · 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-citationFast-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
Hippocampal electrical activity during the development of conditioned reflexes
Grastyán, E., Lissák, K., Madarász, I., & Donhoffer, H. (1959) · Electroencephalography and Clinical Neurophysiology · doi:10.1016/0013-4694(59)90040-9 · Cited by 585 · 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-citationHippocampal theta oscillations are travelling waves
Lubenov, E. V., & Siapas, A. G. (2009) · Nature · doi:10.1038/nature08010 · Cited by 543 · 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
Impact of Network Activities on Neuronal Properties in Corticothalamic Systems
Steriade, M. (2001) · Journal of Neurophysiology · doi:10.1152/jn.2001.86.1.1 · Cited by 530 · see citing works
A 4 Hz oscillation adaptively synchronizes prefrontal, VTA, and hippocampal activities
Fujisawa, S., & Buzsáki, G. (2011) · Neuron · doi:10.1016/j.neuron.2011.08.018 · Cited by 501 · see citing works
Self-citationIsomura, 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-citationHippocampal 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-citationKahana, M. J., Seelig, D., & Madsen, J. R. (2001) · Current Opinion in Neurobiology · doi:10.1016/s0959-4388(01)00278-1 · Cited by 485 · see citing works
Closed-Loop Control of Epilepsy by Transcranial Electrical Stimulation
Berényi, A., Belluscio, M., Mao, D., & Buzsáki, G. (2012) · Science · doi:10.1126/science.1223154 · Cited by 478 · see citing works
Self-citationHegerl, U., & Juckel, G. (1993) · Biological Psychiatry · doi:10.1016/0006-3223(93)90137-3 · Cited by 472 · see citing works
Hippocampal sequence-encoding driven by a cortical multi-item working memory buffer
Jensen, O. B., & Lisman, J. E. (2004) · Trends in Neurosciences · doi:10.1016/j.tins.2004.12.001 · Cited by 467 · see citing works
Lisman, J. (2005) · Hippocampus · doi:10.1002/hipo.20121 · Cited by 435 · see citing works
A Neural Coding Scheme Formed by the Combined Function of Gamma and Theta Oscillations
Lisman, J. E., & Buzsáki, G. (2008) · Schizophrenia Bulletin · doi:10.1093/schbul/sbn060 · Cited by 433 · see citing works
Self-citationCoordinated 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
Soltész, I., & Deschênes, M. (1993) · Journal of Neurophysiology · doi:10.1152/jn.1993.70.1.97 · Cited by 410 · see citing works
Mormann, F., Fell, J., Axmacher, N., Weber, B., Lehnertz, K., Elger, C. E., & Fernández, G. (2005) · Hippocampus · doi:10.1002/hipo.20117 · Cited by 403 · see citing works
Voytek, B. (2010) · Frontiers in Human Neuroscience · doi:10.3389/fnhum.2010.00191 · Cited by 401 · see citing works
The Science of Neural Interface Systems
Hatsopoulos, N., & Donoghue, J. (2009) · Annual Review of Neuroscience · doi:10.1146/annurev.neuro.051508.135241 · Cited by 385 · see citing works
Jensen, O., & Lisman, J. E. (1996) · Learning & Memory · doi:10.1101/lm.3.2-3.279 · Cited by 383 · see citing works
Frequency analysis of olfactory system EEG in cat, rabbit, and rat
Bressler, S. L., & Freeman, W. J. (1980) · Electroencephalography and Clinical Neurophysiology · doi:10.1016/0013-4694(80)90319-3 · Cited by 382 · see citing works
Active sensation: Insights from the rodent vibrissa sensorimotor system
Kleinfeld, D., Ahissar, E., & Diamond, M. E. (2006) · Current Opinion in Neurobiology · doi:10.1016/j.conb.2006.06.009 · Cited by 374 · see citing works
EEG mu rhythm and imitation impairments in individuals with autism spectrum disorder
Bernier, R., Dawson, G., Webb, S. J., & Murias, M. (2007) · Brain and Cognition · doi:10.1016/j.bandc.2007.03.004 · Cited by 367 · see citing works
Correlated Bursts of Activity in the Neonatal Hippocampus in Vivo
Leinekugel, X., Khazipov, R., Cannon, R., Hirase, H., Ben-Ari, Y., & Buzsáki, G. (2002) · Science · doi:10.1126/science.1071111 · Cited by 362 · see citing works
Self-citationKandel, A., & Buzsáki, G. (1997) · Journal of Neuroscience · doi:10.1523/jneurosci.17-17-06783.1997 · Cited by 357 · see citing works
Self-citationAdaptive coding of visual information in neural populations
Gutnisky, D. A., & Dragoi, V. (2008) · Nature · doi:10.1038/nature06563 · Cited by 337 · see citing works
The Sniff as a Unit of Olfactory Processing
Kepecs, Á., Uchida, N., & Mainen, Z. F. (2005) · Chemical Senses · doi:10.1093/chemse/bjj016 · Cited by 326 · see citing works
Spatial spectral analysis of human electrocorticograms including the alpha and gamma bands
Freeman, W., Rogers, L. J., Holmes, M., & Silbergeld, D. L. (2000) · Journal of Neuroscience Methods · doi:10.1016/s0165-0270(99)00160-0 · Cited by 323 · see citing works
Disordered visual processing and oscillatory brain activity in autism and Williams syndrome
Grice, S. J., Spratling, M. W., Karmiloff-Smith, A., Halit, H., Csibra, G., de Haan, M., & Johnson, M. H. (2001) · Neuroreport · doi:10.1097/00001756-200108280-00021 · Cited by 322 · see citing works
Population coding in neuronal systems with correlated noise
Sompolinsky, H., Yoon, H., Kang, K., & Shamir, M. (2001) · Physical review. E, Statistical physics, plasmas, fluids, and related interdisciplinary topics · doi:10.1103/physreve.64.051904 · Cited by 319 · see citing works
Sleep-Dependent θ Oscillations in the Human Hippocampus and Neocortex
Cantero, J. L., Atienza, M., Stickgold, R., Kahana, M. J., Madsen, J. R., & Kocsis, B. (2003) · The Journal of Neuroscience · doi:10.1523/jneurosci.23-34-10897.2003 · Cited by 312 · see citing works
Hippocampal sharp wave bursts coincide with neocortical “up-state” transitions
Battaglia, F. P., Sutherland, G. R., & McNaughton, B. L. (2004) · Learning & Memory · doi:10.1101/lm.73504 · Cited by 310 · see citing works
Maurer, A. P., VanRhoads, S. R., Sutherland, G. R., Lipa, P., & McNaughton, B. L. (2005) · Hippocampus · doi:10.1002/hipo.20114 · Cited by 308 · see citing works
Clinical Utility of EEG in Attention-Deficit/Hyperactivity Disorder: A Research Update
Loo, S. K., & Makeig, S. (2012) · Neurotherapeutics · doi:10.1007/s13311-012-0131-z · Cited by 306 · see citing works
Thalamic dysfunction in schizophrenia suggested by whole-night deficits in slow and fast spindles
Ferrarelli, F., Peterson, M. J., Sarasso, S., Riedner, B. A., Murphy, M. J., Benca, R. M., Bria, P., Kalin, N. H., & Tononi, G. (2010) · American Journal of Psychiatry · doi:10.1176/appi.ajp.2010.09121731 · Cited by 301 · see citing works
T HE B IOLOGY OF E PILEPSY G ENES
Noebels, J. L. (2003) · Annual Review of Neuroscience · doi:10.1146/annurev.neuro.26.010302.081210 · Cited by 296 · see citing works
Test-retest reliability of spectral parameters of the EEG
Gasser, T., Bächer, P., & Steinberg, H.-W. (1985) · Electroencephalography and Clinical Neurophysiology · doi:10.1016/0013-4694(85)90005-7 · Cited by 290 · see citing works
Excess of High Frequency Electroencephalogram Oscillations in Boys with Autism
Orekhova, E. V., Stroganova, T. A., Nygren, G., Tsetlin, M. M., Posikera, I. N., Gillberg, C., & Elam, M. (2007) · Biological Psychiatry · doi:10.1016/j.biopsych.2006.12.029 · Cited by 286 · see citing works
Genetic variation in EEG activity during sleep in inbred mice
Franken, P., Malafosse, A., & Tafti, M. (1998) · American Journal of Physiology-Regulatory, Integrative and Comparative Physiology · doi:10.1152/ajpregu.1998.275.4.r1127 · Cited by 285 · see citing works
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
Hippocampal place cell assemblies are speed-controlled oscillators
Geisler, C. E., Robbe, D., Zugaro, M. B., Sirota, A., & Buzsáki, G. (2007) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0610121104 · Cited by 273 · see citing works
Self-citationA review of brain oscillations in cognitive disorders and the role of neurotransmitters
Başar, E., & Güntekin, B. (2008) · Brain Research · doi:10.1016/j.brainres.2008.06.103 · Cited by 270 · 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
Self-citationThe electroencephalographic fingerprint of sleep is genetically determined: A twin study
Gennaro, L. D., Marzano, C., Fratello, F., Moroni, F., Pellicciari, M. C., Ferlazzo, F., Costa, S., Couyoumdjian, A., Curcio, G., Sforza, E. A., et al. (2008) · Annals of Neurology · doi:10.1002/ana.21434 · Cited by 268 · see citing works
Guevara, M. R., & Glass, L. (1982) · Journal of Mathematical Biology · doi:10.1007/bf02154750 · Cited by 261 · see citing works
Alterations of cortical GABA neurons and network oscillations in schizophrenia
Gonzalez-Burgos, G., Hashimoto, T., & Lewis, D. A. (2010) · Current Psychiatry Reports · doi:10.1007/s11920-010-0124-8 · Cited by 260 · see citing works
Inhibition recruitment in prefrontal cortex during sleep spindles and gating of hippocampal inputs
Peyrache, A., Battaglia, F. P., & Destexhe, A. (2011) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1103612108 · Cited by 254 · see citing works
Left auditory cortex gamma synchronization and auditory hallucination symptoms in schizophrenia
Spencer, K. M., Niznikiewicz, M. A., Nestor, P. G., Shenton, M. E., & McCarley, R. W. (2009) · BMC Neuroscience · doi:10.1186/1471-2202-10-85 · Cited by 253 · see citing works
Spontaneous Changes of Neocortical Code for Associative Memory During Consolidation
Takehara‐Nishiuchi, K., & McNaughton, B. L. (2008) · Science · doi:10.1126/science.1161299 · Cited by 248 · see citing works
The Thalamic Reticular Nucleus and Schizophrenia
Ferrarelli, F., & Tononi, G. (2010) · Schizophrenia Bulletin · doi:10.1093/schbul/sbq142 · Cited by 244 · see citing works
The sequence of events that underlie quantal transmission at central glutamatergic synapses
Lisman, J. E., Raghavachari, S., & Tsien, R. W. (2007) · Nature reviews. Neuroscience · doi:10.1038/nrn2191 · Cited by 244 · see citing works
How can drug discovery for psychiatric disorders be improved?
Agid, Y., Buzsáki, G., Diamond, D. M., Frackowiak, R., Giedd, J., Girault, J.-A., Grace, A., Lambert, J. J., Manji, H., Mayberg, H., et al. (2007) · Nature Reviews Drug Discovery · doi:10.1038/nrd2217 · Cited by 240 · see citing works
Self-citationDeCoteau, W. E., Thorn, C. A., Gibson, D. J., Courtemanche, R., Mitra, P. P., Kubota, Y., & Graybiel, A. M. (2007) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0700818104 · Cited by 239 · see citing works
MECHANISM OF THALAMOCORTICAL AUGMENTATION AND REPETITION
Morison, R. S., & Dempsey, E. W. (1943) · American Journal of Physiology-Legacy Content · doi:10.1152/ajplegacy.1943.138.2.297 · Cited by 237 · see citing works
Heritability of human brain functioning as assessed by electroencephalography.
van Beijsterveldt, C. E., Molenaar, P. C. M., de Geus, E. J. C., & Boomsma, D. I. (1996) · PubMed Central · Cited by 219 · see citing works
Cohen, M. X., Elger, C. E., & Fell, J. (2008) · Journal of Cognitive Neuroscience · doi:10.1162/jocn.2008.21020 · Cited by 218 · see citing works
Quilichini, P., Sirota, A., & Buzsáki, G. (2010) · Journal of Neuroscience · doi:10.1523/jneurosci.1327-10.2010 · Cited by 217 · see citing works
Self-citationAre Smarter Brains Running Faster? Heritability of Alpha Peak Frequency, IQ, and Their Interrelation
Danielle Posthuma, B., Neale, M. C., Boomsma, D. I., & de Geus, E. J. C. (2001) · Behavior Genetics · doi:10.1023/a:1013345411774 · Cited by 215 · see citing works
Trait-like individual differences in the human sleep electroencephalogram
Buckelmüller, J., Landolt, H.-P., Stassen, H. H., & Achermann, P. (2006) · Neuroscience · doi:10.1016/j.neuroscience.2005.11.005 · Cited by 214 · see citing works
Gamma amplitudes are coupled to theta phase in human EEG during visual perception
Demıralp, T., Bayraktaroğlu, Z., Lenz, D., Junge, S., Busch, N. A., Maeß, B., Ergen, M., & Herrmann, C. S. (2006) · International Journal of Psychophysiology · doi:10.1016/j.ijpsycho.2006.07.005 · Cited by 214 · see citing works
Neural Dynamics of Saccadic Suppression
Bremmer, F., Kubischik, M., Hoffmann, K., & Krekelberg, B. (2009) · Journal of Neuroscience · doi:10.1523/jneurosci.2908-09.2009 · Cited by 213 · see citing works
Fenton, A. A., Kao, H.-Y., Neymotin, S. A., Olypher, A. V., Vayntrub, Y., Lytton, W. W., & Ludvig, N. (2008) · Journal of Neuroscience · doi:10.1523/jneurosci.2862-08.2008 · Cited by 208 · see citing works
The gamma band response may account for poor P50 suppression in schizophrenia
Clementz, B. A., Blumenfeld, L. D., & Cobb, S. R. (1997) · Neuroreport · doi:10.1097/00001756-199712220-00010 · Cited by 197 · see citing works
Wang, X. (2002) · Journal of Neurophysiology · doi:10.1152/jn.00135.2001 · Cited by 197 · see citing works
Evidence for reactive magnetic 10-Hz rhythm in the human auditory cortex
Lehtelä, L., Salmelin, R. H., & Hari, R. (1997) · Neuroscience Letters · doi:10.1016/s0304-3940(97)13361-4 · Cited by 185 · see citing works
Genetics of the human electroencephalogram (EEG) and event-related brain potentials (ERPs): a review
van Beijsterveldt, C. E. M., & Boomsma, D. I. (1994) · Human Genetics · doi:10.1007/bf00201587 · Cited by 182 · see citing works
ACTION POTENTIALS OF THE BRAIN
Davis, H. (1936) · Archives of Neurology And Psychiatry · doi:10.1001/archneurpsyc.1936.02260120061004 · Cited by 173 · see citing works
Robbe, D., & Buzsáki, G. (2009) · Journal of Neuroscience · doi:10.1523/jneurosci.2407-09.2009 · Cited by 171 · see citing works
Self-citationPreferential 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
Imaging of Thalamocortical Dysrhythmia in Neuropsychiatry
Schulman, J. J., Cancro, R., Lowe, S., Lu, F., Walton, K. D., & Llinás, R. R. (2011) · Frontiers in Human Neuroscience · doi:10.3389/fnhum.2011.00069 · Cited by 167 · see citing works
Masquelier, T., Hugues, E., Deco, G., & Thorpe, S. J. (2009) · Journal of Neuroscience · doi:10.1523/jneurosci.2207-09.2009 · Cited by 159 · see citing works
A model of episodic memory: Mental time travel along encoded trajectories using grid cells
Hasselmo, M. E. (2009) · Neurobiology of Learning and Memory · doi:10.1016/j.nlm.2009.07.005 · Cited by 157 · see citing works
Neuronal Shot Noise and Brownian 1/f2 Behavior in the Local Field Potential
Milstein, J. N., Mormann, F., Fried, I., & Christof Koch, A. (2009) · PLoS ONE · doi:10.1371/journal.pone.0004338 · Cited by 156 · see citing works
Behavioral correlates of human hippocampal delta and theta oscillations during navigation
Watrous, A. J., Fried, I., & Ekstrom, A. D. (2011) · Journal of Neurophysiology · doi:10.1152/jn.00921.2010 · Cited by 154 · see citing works
Smit, C. M., Wright, M. J., Hansell, N. K., Geffen, G. M., & Martin, N. G. (2005) · International Journal of Psychophysiology · doi:10.1016/j.ijpsycho.2005.10.004 · Cited by 147 · see citing works
Diba, K., & Buzsáki, G. (2008) · Journal of Neuroscience · doi:10.1523/jneurosci.3824-08.2008 · Cited by 145 · see citing works
Self-citationWittner, L., Henze, D. A., Záborszky, L., & Buzsáki, G. (2007) · Brain Structure and Function · doi:10.1007/s00429-007-0148-y · Cited by 142 · see citing works
Self-citationGeisler, C. E., Diba, K., Pastalkova, E., Mizuseki, K., Royer, S., & Buzsáki, G. (2010) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0912478107 · Cited by 142 · see citing works
Self-citationKetamine Disrupts Theta Modulation of Gamma in a Computer Model of Hippocampus
Neymotin, S. A., Lazarewicz, M. T., Sherif, M., Contreras, D., Finkel, L. H., & Lytton, W. W. (2011) · The Journal of Neuroscience · doi:10.1523/jneurosci.0501-11.2011 · Cited by 139 · see citing works
Human hippocampal formation EEG desynchronizes during attentiveness and movement
Halgren, E., Babb, T. L., & Crandall, P. H. (1978) · Electroencephalography and Clinical Neurophysiology · doi:10.1016/0013-4694(78)90212-2 · Cited by 138 · see citing works
Genetic contributions to long-range temporal correlations in ongoing oscillations
Linkenkaer-Hansen, K., Smit, D. J. A., Barkil, A., van Beijsterveldt, T. E. M., Brussaard, A. B., Boomsma, D. I., van Ooyen, A., & de Geus, E. J. C. (2007) · The Journal of Neuroscience · doi:10.1523/jneurosci.3083-07.2007 · Cited by 138 · see citing works
Electric activity in the neocortex of freely moving young and aged rats
Buzsáki, G., Bickford, R. G., Armstrong, D. M., Ponomareff, G., Chen, K. S., Ruiz, R., Thal, L. J., & Gage, F. H. (1988) · Neuroscience · doi:10.1016/0306-4522(88)90095-4 · Cited by 135 · see citing works
Self-citationNeuro-archaeology: pre-symptomatic architecture and signature of neurological disorders
Ben‐Ari, Y. (2008) · Trends in Neurosciences · doi:10.1016/j.tins.2008.09.002 · Cited by 135 · see citing works
Landsness, E. C., Goldstein, M. R., Peterson, M. J., Tononi, G., & Benca, R. M. (2011) · Journal of Psychiatric Research · doi:10.1016/j.jpsychires.2011.02.003 · Cited by 134 · see citing works
Maurer, A. P., Cowen, S. L., Burke, S. N., Barnes, C. A., & McNaughton, B. L. (2006) · Journal of Neuroscience · doi:10.1523/jneurosci.2882-06.2006 · Cited by 129 · see citing works
Electroencephalography-Derived Biomarkers of Antidepressant Response
Iosifescu, D. V. (2011) · Harvard Review of Psychiatry · doi:10.3109/10673229.2011.586549 · Cited by 129 · see citing works
Yordanova, J., Banaschewski, T., Kolev, V., Woerner, W., & Rothenberger, A. (2001) · Clinical Neurophysiology · doi:10.1016/s1388-2457(01)00524-7 · Cited by 126 · see citing works
Popa, D., Popescu, A. T., & Paré, D. (2009) · Journal of Neuroscience · doi:10.1523/jneurosci.4867-08.2009 · Cited by 125 · see citing works
The spectral properties of hippocampal EEG related to behaviour in man
Arnolds, D. E. A. T., Lopes, F. H. D. S., Aitink, J. W., Kamp, A., & Boeijinga, P. H. (1980) · Electroencephalography and Clinical Neurophysiology · doi:10.1016/0013-4694(80)90160-1 · Cited by 121 · see citing works
EEG, autonomic and subjective correlates of the risk for alcoholism.
Bauer, L. O., & HESSELBROCK, V. M. (1993) · Journal of Studies on Alcohol · doi:10.15288/jsa.1993.54.577 · Cited by 119 · see citing works
The use of animal models for stroke research: a review.
Casals, J. B., Pieri, N. C. G., Feitosa, M. L. T., Ercolin, A. C. M., Roballo, K. C. S., Barreto, R. S. N., Bressan, F. F., Martins, D. D. S., Miglino, M. A., & Ambrósio, C. E. (2011) · PubMed Central · Cited by 119 · see citing works
van Pelt, S., Boomsma, D. I., & Fries, P. (2012) · Journal of Neuroscience · doi:10.1523/jneurosci.5592-11.2012 · Cited by 118 · see citing works
Broadway, J. M., Holtzheimer, P. E., Hilimire, M. R., Parks, N. A., DeVylder, J., Mayberg, H. S., & Corballis, P. M. (2012) · Neuropsychopharmacology · doi:10.1038/npp.2012.23 · Cited by 116 · see citing works
Deep Brain Stimulation for Intractable Psychiatric Disorders
Goodman, W. K., & Alterman, R. L. (2010) · Annual Review of Medicine · doi:10.1146/annurev-med-052209-100401 · Cited by 115 · see citing works
Neural synchronization deficits to auditory stimulation in bipolar disorder
O’Donnell, B. F., Hetrick, W. P., Vohs, J. L., Krishnan, G. P., Carroll, C. A., & Shekhar, A. (2004) · Neuroreport · doi:10.1097/01.wnr.0000127348.64681.b2 · Cited by 110 · see citing works
Mechanisms of Phase-Locking and Frequency Control in Pairs of Coupled Neural Oscillators
Kopell, N., & Ermentrout, B. (2002) · Handbook of dynamical systems · doi:10.1016/s1874-575x(02)80022-4 · Cited by 107 · see citing works
Genetic determination of EEG frequency spectra
Lykken, D. T., Tellegen, A., & Thorkelson, K. (1974) · Biological Psychology · doi:10.1016/0301-0511(74)90001-5 · Cited by 101 · see citing works
Synchronization in noisy systems and cardiorespiratory interaction
Rosenblum, M., Kurths, J., PIKOVSKY, A. S., Schafer, C., Tass, P. A., & Abel, H. (1998) · IEEE Engineering in Medicine and Biology Magazine · doi:10.1109/51.731320 · Cited by 95 · see citing works
Deep Brain Stimulation for Treatment-Resistant Depression
Holtzheimer, P. E., & Mayberg, H. S. (2010) · American Journal of Psychiatry · doi:10.1176/appi.ajp.2010.10010141 · Cited by 93 · see citing works
Rass, O., Forsyth, J. K., Krishnan, G. P., Hetrick, W. P., Klaunig, M. J., Breier, A. F., O’Donnell, B. F., & Brenner, C. A. (2012) · Schizophrenia Research · doi:10.1016/j.schres.2012.01.003 · Cited by 92 · see citing works
Hearing voices: A role of interhemispheric auditory connectivity?
Mulert, C., Kirsch, V., Whitford, T. J., Alvarado, J., Pelavin, P. E., McCarley, R. W., Kubicki, M. R., Salisbury, D. F., & Shenton, M. E. (2011) · The World Journal of Biological Psychiatry · doi:10.3109/15622975.2011.570789 · Cited by 89 · see citing works
The structure of consciousness
Buzsáki, G. (2007) · Nature · doi:10.1038/446267a · Cited by 88 · see citing works
Self-citation
Flagged first, then by citations
Research works printed but not linked: 22
- [3]Sherrington CS. Man On His Nature.New York, NY; Cambridge, UK: The Macmillan Company; The University Press. 1941
- [11]Nunez PL. Srinivasan R. Electric Fields of the Brain: the Neurophysics of EEG. 2nd ed. New York, NY: Oxford University Press. 2005
- [39]Jerison HJ. Evolution of the Brain and Intelligence. London, UK: Academic Press. 1973
- [46]Hebb DO. The Organization of Behavior: a Neuropsychological Theory New York, NY: Wiley 1949
- [55]Johnston D. Wu SM-S. Foundations of Cellular Neurophysiology Cambridge, MA: MIT Press, Bradford Books 1994
- [68]Ahissar E. Arieli A. Figuring space by time. Neuron. 2001 32 185 201 11683990
- [81]Huerta PT. Lisman JE. Synaptic plasticity during the cholinergic thetafrequency oscillation in vitro. Hippocampus. 1996 6 58 61 8878743
- [85]Lachaux J-P. Axmacher N. Mormann F. Halgren E. Crone NE. High-frequency neural activity and human cognition: Past, present and possible future of intracranial EEG research. Prog Neurobiol In press 2012 PMC3980670 22750156
- [118]O'Keefe J. Nadel L. The Hippocampus as a Cognitive Map New York, NY: Clarendon Press 1978
- [134]Royer S. Zemelman BV. Losonczy A. et al. Control of timing, rate and bursts of hippocampal place cells by dendritic and somatic inhibition. Wat. Neurosci. 2012 15 769 775 PMC4919905 22446878
- [151]O'Neill J. Senior TJ. Allen K. Huxter JR. Csicsvari J. Reactivation of experience-dependent cell assembly patterns in the hippocampus. Wat. Neurosci. 2008 11 209 215 18193040
- [154]Girardeau G. Benchenane K. Wiener SI. Buzsaki G. Zugaro MB. Selective suppression of hippocampal ripples impairs spatial memory. Wat. Neurosci. 2009 12 1222 1223 19749750
- [156]Buzsaki G. Silva FL. High frequency oscillations in the intact brain. Prog Neurobiol In press 2012 PMC4895831 22449727
- [175]Kamondi A. Acsady L. Wang XJ. Buzsaki G. Theta oscillations in somata and dendrites of hippocampal pyramidal cells in vivo: activity-dependent phase-precession of action potentials. Hippocampus. 1998 8 244 261 9662139
- [177]Szatmáry B. Izhikevich EM. Spike-timing theory of working memory. PLoS Comput Biol In press PMC2924241 20808877
- [178]Nestler E. Hyman S. Malenka R. Molecular Neuropharmacology: A Foundation for Clinical Neuroscience, Second Edition New York, NY: McGrawHill Professional 2008
- [184]Vogel F. The genetic basis of the normal human electroencephalogram (EEG). Human Genetics. 1970 10 91 114 5528299
- [189]Matousek M. Petersen I. Automatic evaluation of EEG background activity by means of age-dependent EEG quotients. Electroencephalogr Clin Neurophysiol. 1 973 3 5 603 612 4128155
- [201]Marescaux C. Vergnes M. Depaulis A. Genetic absence epilepsy in rats from Strasbourg-a review. J Neural Trans Suppl. 1992 35 37 69 1512594
- [203]oebels JL. The biology of epilepsy genes. Ann Rev Neurosci. 2003 26 599 625 14527270
- [225]Sadock BJ. Sadock VA. Kaplan & Sadock Comprehensive Textbook of Psychiatry Philadelphia, PA: Lippincott Williams & Wilkins 2000 48 84
- [229]rivedi MH. Rush AJ. Wisniewski SR. et al. Evaluation of outcomes with citalopram for depression using measurement-based care in STAR*D: implications for clinical practice. Am J. Psychiatry. 2006 163 28 40 16390886
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- Authors
- Buzsáki, G., & Watson, B. O.
- Affiliations
- New York University (US)
- Weill Cornell Medicine (US)
- Corresponding author
- Buzsáki, György
- Venue
- Dialogues in Clinical Neuroscience
- Publisher
- Informa UK Limited
- Published
- 2012-12-31
- Volume
- 14
- Issue
- 4
- Pages
- 345-367
- ISSN
- 1294-8322 (ISSN-L)
- 1958-5969
- PMC
- PMC3553572
- OpenAlex
- W4214953342
- Cited by
- 579
- References
- 233
- Citations by year
- 2026: 37 · 2025: 47 · 2024: 40 · 2023: 36 · 2022: 64 · 2021: 61 · 2020: 50 · 2019: 48 · 2018: 41 · 2017: 33 · 2016: 47 · 2015: 34 · 2014: 24 · 2013: 9
- FWCI
- 10.98
- Type
- journal article
- Language
- en
- Open access
- diamond
- doi.org
- Licence
- Locations
- Dialogues in Clinical Neuroscience (publishedVersion, cc-by-nc-nd)
- Europe PMC (PubMed Central) (publishedVersion, cc-by-nc-nd)
- PubMed Central (publishedVersion, cc-by-nc-nd)
- PubMed (publishedVersion)
- PubMed
- Funders
- National Institute of Mental Health (R01MH054671)
- Topics
- Life Sciences › Neuroscience › Cognitive Neuroscience › Neural dynamics and brain function
- Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Neuroscience and Neuropharmacology Research
- Health Sciences › Medicine › Neurology › Neurological disorders and treatments
- Keywords
- neural oscillations, efficient coding, neuronal excitability, cell assemblies, cortical networks, mental illness, neuropsychiatric disorders, neuromodulation
- MeSH terms
- Animals, Mental Disorders, Brain, Cognition, Cortical Synchronization, Humans, Periodicity
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 ›
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