Cited by 872Memory and Neural MechanismsNeural dynamics and brain functionSpatial Cognition and Navigation

The DOI matches its Crossref record; 206 of the 209 references it cites were found in a registry or an index.

Theta rhythm of navigation: Link between path integration and landmark navigation, episodic and semantic memory

Buzsáki, György·2005·Hippocampus

DOI 10.1002/hipo.20113

Open this paper in CoChat — free account

Abstract

Five key topics have been reverberating in hippocampal‐entorhinal cortex (EC) research over the past five decades: episodic and semantic memory, path integration (“dead reckoning”) and landmark (“map”) navigation, and theta oscillation. We suggest that the systematic relations between single cell discharge and the activity of neuronal ensembles reflected in local field theta oscillations provide a useful insight into the relationship among these terms. In rats trained to run in direction‐guided (1‐dimensional) tasks, hippocampal cell assemblies discharge sequentially, with different assemblies active on opposite runs, i.e., place cells are unidirectional. Such tasks do not require map representation and are formally identical with learning sequentially occurring items in an episode. Hebbian plasticity, acting within the temporal window of the theta cycle, converts the travel distances into synaptic strengths between the sequentially activated and unidirectionally connected assemblies. In contrast, place representations by hippocampal neurons in 2‐dimensional environments are typically omnidirectional, characteristic of a map. Generation of a map requires exploration, essentially a dead reckoning behavior. We suggest that omnidirectional navigation through the same places (junctions) during exploration gives rise to omnidirectional place cells and, consequently, maps free of temporal context. Analogously, multiple crossings of common junction(s) of episodes convert the common junction(s) into context‐free or semantic memory. Theta oscillation can hence be conceived as the navigation rhythm through both physical and mnemonic space, facilitating the formation of maps and episodic/semantic memories. © 2005 Wiley‐Liss, Inc.

Integrity signals

Registry

Crossref · 10.1002/hipo.20113

Cites

206 of 206 references verified0 citation errors · 0 not checkable

Statistics

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

Claims the paper makes

This paper’s full text isn’t openly available, so its claims and self-check weren’t run. The registry and citation checks still apply.

Claims other papers make about this one

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

Untitled work
(1978) · UA Campus Repository (The University of Arizona) · Cited by 8,010
LOSS OF RECENT MEMORY AFTER BILATERAL HIPPOCAMPAL LESIONS
Scoville, W. B., & Milner, B. (1957) · Journal of Neurology, Neurosurgery & Psychiatry · doi:10.1136/jnnp.20.1.11 · Cited by 7,322
Neuronal Oscillations in Cortical Networks
Buzsáki, G., & Draguhn, A. (2004) · Science · doi:10.1126/science.1099745 · Cited by 6,576
The hippocampus as a spatial map. Preliminary evidence from unit activity in the freely-moving rat
O'Keefe, J., & Dostrovsky, J. (1971) · Brain Research · doi:10.1016/0006-8993(71)90358-1 · Cited by 6,151
Memory and the hippocampus: A synthesis from findings with rats, monkeys, and humans.
Squire, L. R. (1992) · Psychological Review · doi:10.1037/0033-295x.99.2.195 · Cited by 5,376
Why there are complementary learning systems in the hippocampus and neocortex: insights from the successes and failures of connectionist models of learning and memory
McClelland, J. L., McNaughton, B. L., & O'Reilly, R. C. (1995) · Psychological Review · doi:10.1037/0033-295x.102.3.419 · Cited by 5,256
Episodic memory: from mind to brain
Tulving, E. (2002) · Annual Review of Psychology · doi:10.1146/annurev.psych.53.100901.135114 · Cited by 4,950
Untitled work
(1987) · Medical Entomology and Zoology · Cited by 4,269
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
Episodic and semantic memory
(2007) · Cognitive Psychology · doi:10.4135/9781446212967.n15 · Cited by 3,749
Theta oscillations in the hippocampus
Buzsáki, G. (2002) · Neuron · doi:10.1016/s0896-6273(02)00586-x · Cited by 3,332
Self-citation
Reactivation of hippocampal ensemble memories during sleep
Wilson, M. A., & McNaughton, B. L. (1994) · Science · doi:10.1126/science.8036517 · Cited by 3,118
Simple memory: a theory for archicortex
Marr, D. (1971) · Philosophical Transactions of the Royal Society of London. B, Biological Sciences · doi:10.1098/rstb.1971.0078 · Cited by 2,771
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 2,643
The human hippocampus and spatial and episodic memory
Burgess, N., Maguire, E. A., & O'Keefe, J. (2002) · Neuron · doi:10.1016/s0896-6273(02)00830-9 · Cited by 2,401
The Hippocampus as a Cognitive Map
Ranck, J. B. (1979) · American Journal of Psychiatry · doi:10.1176/ajp.136.10.1353 · Cited by 2,373
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
Perception and the conditioned reflex
Granger, G. W. (1964) · Behaviour Research and Therapy · doi:10.1016/0005-7967(64)90061-0 · Cited by 2,209
The organization of recent and remote memories
Frankland, P. W., & Bontempi, B. (2005) · Nature Reviews Neuroscience · doi:10.1038/nrn1607 · Cited by 2,138
Perception and the Conditioned Reflex
Hay, J. C., & Sokolov, Y. N. (1966) · The American Journal of Psychology · doi:10.2307/1420734 · Cited by 2,123
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
Memory consolidation, retrograde amnesia and the hippocampal complex
Nadel, L., & Moscovitch, M. (1997) · Current Opinion in Neurobiology · doi:10.1016/s0959-4388(97)80010-4 · Cited by 1,924
A cortical–hippocampal system for declarative memory
Eichenbaum, H. (2000) · Nature reviews. Neuroscience · doi:10.1038/35036213 · Cited by 1,817
Differential Effects of Early Hippocampal Pathology on Episodic and Semantic Memory
Vargha-Khadem, F., Gadian, D. G., Watkins, K. E., Connelly, A., Van Paesschen, W., & Mishkin, M. (1997) · Science · doi:10.1126/science.277.5324.376 · Cited by 1,746
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
Self-citation
The effects of changes in the environment on the spatial firing of hippocampal complex-spike cells
Muller, R., & Kubie, J. (1987) · The Journal of Neuroscience · doi:10.1523/jneurosci.07-07-01951.1987 · Cited by 1,581
Memory, amnesia, and the hippocampal system
(1994) · Choice Reviews Online · doi:10.5860/choice.31-5148 · Cited by 1,533
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
Organization of Memory
Battig, W. F., Tulving, E., & Donaldson, W. (1973) · The American Journal of Psychology · doi:10.2307/1421962 · Cited by 1,428
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
Self-citation
HIPPOCAMPAL ELECTRICAL ACTIVITY IN AROUSAL
Green, J. D., & Arduini, A. (1954) · Journal of Neurophysiology · doi:10.1152/jn.1954.17.6.533 · Cited by 1,396
Brain-state- and cell-type-specific firing of hippocampal interneurons in vivo
Klausberger, T., Magill, P. J., Márton, L. F., Roberts, J. D. B., Cobden, P. M., Buzsáki, G., & Somogyi, P. (2003) · Nature · doi:10.1038/nature01374 · Cited by 1,345
Self-citation
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 1,340
Spatial representation in the entorhinal cortex
Fyhn, M., Molden, S., Witter, M. P., Moser, E. I., & Moser, M.-B. (2004) · Science · doi:10.1126/science.1099901 · Cited by 1,339
Cognitive Neuroscience and the Study of Memory
Milner, B. A., Squire, L. R., & Kandel, E. R. (1998) · Neuron · doi:10.1016/s0896-6273(00)80987-3 · Cited by 1,335
Hippocampal synaptic enhancement and information storage within a distributed memory system
McNaughton, B. L., & Morris, R. G. M. (1987) · Trends in Neurosciences · doi:10.1016/0166-2236(87)90011-7 · Cited by 1,304
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
Selected Writings of John Hughlings Jackson
SCOTT, J. (1959) · American Journal of Psychiatry · doi:10.1176/ajp.116.5.479-a · Cited by 1,291
Computational analysis of the role of the hippocampus in memory
Treves, A., & Rolls, E. T. (1994) · Hippocampus · doi:10.1002/hipo.450040319 · Cited by 1,272
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
Self-citation
The role of sleep in learning and memory
Maquet, P. (2001) · Science · doi:10.1126/science.1062856 · Cited by 1,177
Replay of neuronal firing sequences in rat hippocampus during sleep following spatial experience
Skaggs, W. E., & McNaughton, B. L. (1996) · Science · doi:10.1126/science.271.5257.1870 · Cited by 1,173
Geometric determinants of the place fields of hippocampal neurons
O'Keefe, J., & Burgess, N. (1996) · Nature · doi:10.1038/381425a0 · Cited by 1,166
The Structure and Organization of Memory
Squire, L. R., Knowlton, B. J., & Musen, G. (1993) · Annual Review of Psychology · doi:10.1146/annurev.ps.44.020193.002321 · Cited by 1,159
Radical embodiment: neural dynamics and consciousness
Thompson, E., & Varela, F. J. (2001) · Trends in Cognitive Sciences · doi:10.1016/s1364-6613(00)01750-2 · Cited by 1,144
Sharp wave-associated high-frequency oscillation (200 Hz) in the intact hippocampus: network and intracellular mechanisms
Ylinen, A., Bragin, A., Nadasdy, Z., Jando, G., Szabo, I., Sik, A., & Buzsaki, G. (1995) · The Journal of Neuroscience · doi:10.1523/jneurosci.15-01-00030.1995 · Cited by 1,092
Self-citation
The contributions of position, direction, and velocity to single unit activity in the hippocampus of freely-moving rats
McNaughton, B. L., Barnes, C. A., & O'Keefe, J. (1983) · Experimental Brain Research · doi:10.1007/bf00237147 · Cited by 1,071
The Hippocampus, Memory, and Place Cells
Eichenbaum, H., Dudchenko, P., Wood, E., Shapiro, M., & Tanila, H. (1999) · Neuron · doi:10.1016/s0896-6273(00)80773-4 · Cited by 1,064
Memory consolidation and the medial temporal lobe: a simple network model.
Alvarez, P., & Squire, L. R. (1994) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.91.15.7041 · Cited by 1,054
The physiology and pharmacology of hippocampal formation theta rhythms
Bland, B. H. (1986) · Progress in Neurobiology · doi:10.1016/0301-0082(86)90019-5 · Cited by 1,039
Hippocampal place units in the freely moving rat: Why they fire where they fire
O'Keefe, J. M., & Conway, D. H. (1978) · Experimental Brain Research · doi:10.1007/bf00239813 · Cited by 1,028
Sleep inspires insight
Wagner, U., Gais, S., Haider, H., Verleger, R., & Born, J. (2004) · Nature · doi:10.1038/nature02223 · Cited by 1,012
Path 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
Sparse Distributed Memory
Kanerva, P. (1988) · Medical Entomology and Zoology · Cited by 976
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
Self-citation
A model for recognition memory: REM—retrieving effectively from memory
Shiffrin, R. M., & Steyvers, M. (1997) · Psychonomic Bulletin & Review · doi:10.3758/bf03209391 · Cited by 956
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 · cited 2×
“…are compressed into the 150 ms sharp wave event than in several seconds of theta (Wilson and McNaughton, 1994; Skaggs and McNaughton, 1996; Kudrimoti et al., 1999; Nádasdy et al., 1999; Lee and Wilson, 2002), creating opportunities for crossing episodes at the timescale of synaptic plasticity.”
BackgroundSelf-citation
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 914
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 901
Self-citation
Iso-orientation domains in cat visual cortex are arranged in pinwheel-like patterns
Bonhoeffer, T., & Grinvald, A. (1991) · Nature · doi:10.1038/353429a0 · Cited by 873
The cognitive neuroscience of sleep: neuronal systems, consciousness and learning
Hobson, J. A., & Pace-Schott, E. F. (2002) · Nature Reviews Neuroscience · doi:10.1038/nrn915 · Cited by 835
Neurophysiology of the states of sleep.
Jouvet, M. (1967) · Physiological Reviews · doi:10.1152/physrev.1967.47.2.117 · Cited by 814
Two types of hippocampal rhythmical slow activity in both the rabbit and the rat: Relations to behavior and effects of atropine, diethyl ether, urethane, and pentobarbital
Kramis, R., Vanderwolf, C. H., & Bland, B. H. (1975) · Experimental Neurology · doi:10.1016/0014-4886(75)90195-8 · Cited by 791
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
Distinct Ensemble Codes in Hippocampal Areas CA3 and CA1
Leutgeb, S., Leutgeb, J. K., Treves, A., Moser, M., & Moser, E. I. (2004) · Science · doi:10.1126/science.1100265 · Cited by 774
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 760
Reactivation of hippocampal cell assemblies: effects of behavioral state, experience, and EEG dynamics
Kudrimoti, H. S., Barnes, C. A., & McNaughton, B. L. (1999) · The Journal of Neuroscience · doi:10.1523/jneurosci.19-10-04090.1999 · Cited by 753
Conservation of hippocampal memory function in rats and humans
Bunsey, M. D., & Eichenbaum, H. (1996) · Nature · doi:10.1038/379255a0 · Cited by 752
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
Self-citation
Homing by path integration in a mammal
Mittelstaedt, M.-L., & Mittelstaedt, H. (1980) · Die Naturwissenschaften · doi:10.1007/bf00450672 · Cited by 728
What's new with the amnesic patient H.M.?
Corkin, S. (2002) · Nature Reviews Neuroscience · doi:10.1038/nrn726 · Cited by 726
The global record of memory in hippocampal neuronal activity
Wood, E. R., Dudchenko, P. A., & Eichenbaum, H. (1999) · Nature · doi:10.1038/17605 · Cited by 707
Interactions between location and task affect the spatial and directional firing of hippocampal neurons
Markus, E. J., Qin, Y., Leonard, B. W., Skaggs, W. E., McNaughton, B. L., & Barnes, C. A. (1995) · Journal of Neuroscience · doi:10.1523/jneurosci.15-11-07079.1995 · Cited by 698
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
Self-citation
Role of experience and oscillations in transforming a rate code into a temporal code
Mehta, M. R., Lee, A. K., & Wilson, M. A. (2002) · Nature · doi:10.1038/nature00807 · Cited by 630
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 610
Relating Hippocampal Circuitry to Function
Lisman, J. E. (1999) · Neuron · doi:10.1016/s0896-6273(00)81085-5 · Cited by 607
Associative retrieval processes in free recall
Kahana, M. J. (1996) · Memory & Cognition · doi:10.3758/bf03197276 · Cited by 605
High-Frequency Oscillations in the Output Networks of the Hippocampal–Entorhinal Axis of the Freely Behaving Rat
Chrobak, J. J., & Buzsáki, G. (1996) · The Journal of Neuroscience · doi:10.1523/jneurosci.16-09-03056.1996 · Cited by 587
Self-citation
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
Hippocampus as comparator: Role of the two input and two output systems of the hippocampus in selection and registration of information
Vinogradova, O. S. (2001) · Hippocampus · doi:10.1002/hipo.1073 · Cited by 550
The hippocampus as an associator of discontiguous events
Wallenstein, G. V., Hasselmo, M. E., & Eichenbaum, H. (1998) · Trends in Neurosciences · doi:10.1016/s0166-2236(97)01220-4 · Cited by 545
Experience-dependent, asymmetric expansion of hippocampal place fields
Mehta, M. R., Barnes, C. A., & McNaughton, B. L. (1997) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.94.16.8918 · Cited by 536
Ensemble Patterns of Hippocampal CA3-CA1 Neurons during Sharp Wave–Associated Population Events
Csicsvari, J., Hirase, H., Mamiya, A., & Buzsáki, G. (2000) · Neuron · doi:10.1016/s0896-6273(00)00135-5 · Cited by 523
Self-citation
Hippocampal mediation of stimulus representation: A computational theory
Gluck, M. A., & Myers, C. E. (1993) · Hippocampus · doi:10.1002/hipo.450030410 · Cited by 502
Theta returns
Kahana, M. J., Seelig, D., & Madsen, J. R. (2001) · Current Opinion in Neurobiology · doi:10.1016/s0959-4388(01)00278-1 · Cited by 485
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
The hippocampus and behavioral maturation
Altman, J., Brunner, R. L., & Bayer, S. A. (1973) · Behavioral Biology · doi:10.1016/s0091-6773(73)80144-0 · Cited by 460
Cerebral Activity and Behavior: Control by Central Cholinergic and Serotonergic Systems
Vanderwolf, C. H. (1988) · International review of neurobiology · doi:10.1016/s0074-7742(08)60050-1 · Cited by 455
The positional firing properties of medial entorhinal neurons: description and comparison with hippocampal place cells
Quirk, G., Muller, R., Kubie, J., & Ranck, J. B. (1992) · Journal of Neuroscience · doi:10.1523/jneurosci.12-05-01945.1992 · Cited by 428
Storage, recall, and novelty detection of sequences by the hippocampus: Elaborating on the SOCRATIC model to account for normal and aberrant effects of dopamine
Lisman, J. E., & Otmakhova, N. A. (2001) · Hippocampus · doi:10.1002/hipo.1071 · Cited by 414
Low acetylcholine during slow-wave sleep is critical for declarative memory consolidation
Gais, S., & Born, J. (2004) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0305404101 · Cited by 412
Hippocampal Plasticity across Multiple Days of Exposure to Novel Environments
Frank, L. M., Stanley, G. B., & Brown, E. N. (2004) · The Journal of Neuroscience · doi:10.1523/jneurosci.1958-04.2004 · Cited by 410
Spike train dynamics predicts theta-related phase precession in hippocampal pyramidal cells
Harris, K. D., Henze, D. A., Hirase, H., Leinekugel, X., Dragoi, G., Czurkó, A., & Buzsáki, G. (2002) · Nature · doi:10.1038/nature00808 · Cited by 398
Self-citation
Multiple memory systems and consciousness.
Tulving, E. (1987) · PubMed · Cited by 396
Contextual variability and serial position effects in free recall.
Howard, M. W., & Kahana, M. J. (1999) · Journal of Experimental Psychology Learning Memory and Cognition · doi:10.1037//0278-7393.25.4.923 · Cited by 393
The hippocampus as a cognitive graph.
Muller, R. U., Stead, M., & Pach, J. (1996) · The Journal of general physiology · doi:10.1085/jgp.107.6.663 · Cited by 391
Object and Place Memory in the Macaque Entorhinal Cortex
SUZUKI, W. A., Miller, E. K., & Desimone, R. (1997) · Journal of Neurophysiology · doi:10.1152/jn.1997.78.2.1062 · Cited by 388
Memory for places learned long ago is intact after hippocampal damage
Teng, E., & Squire, L. R. (1999) · Nature · doi:10.1038/23276 · Cited by 372
Selective activation of deep layer (V-VI) retrohippocampal cortical neurons during hippocampal sharp waves in the behaving rat
Chrobak, J. J., & Buzsáki, G. (1994) · Journal of Neuroscience · doi:10.1523/jneurosci.14-10-06160.1994 · Cited by 360
Self-citation
Semantic Memory and the Human Hippocampus
Manns, J. R., Hopkins, R. O., & Squire, L. R. (2003) · Neuron · doi:10.1016/s0896-6273(03)00146-6 · Cited by 354
A Quarter of a Century of Place Cells
Muller, R. U. (1996) · Neuron · doi:10.1016/s0896-6273(00)80214-7 · Cited by 350
Electrical activity of the archicortex
Karmos, G. (1986) · Electroencephalography and Clinical Neurophysiology · doi:10.1016/0013-4694(86)90135-5 · Cited by 343
Cortico-Hippocampal Interplay and the Representation of Contexts in the Brain
Miller, R. J. (1991) · Studies of brain function · doi:10.1007/978-3-662-21732-0 · Cited by 339
Patterns of hippocampal theta rhythm in the freely moving rat
Winson, J. (1974) · Electroencephalography and Clinical Neurophysiology · doi:10.1016/0013-4694(74)90171-0 · Cited by 332
Unilateral temporal lobectomy patients show lateralized topographical and episodic memory deficits in a virtual town
Spiers, H. J. (2001) · Brain · doi:10.1093/brain/124.12.2476 · Cited by 329
Sustained activation of hippocampal pyramidal cells by ‘space clamping’ in a running wheel
Czurkó, A., Hirase, H., Csicsvari, J., & Buzsáki, G. (1999) · European Journal of Neuroscience · doi:10.1046/j.1460-9568.1999.00446.x · Cited by 327
Self-citation
On the directional firing properties of hippocampal place cells
Muller, R., Bostock, E., Taube, J., & Kubie, J. (1994) · The Journal of Neuroscience · doi:10.1523/jneurosci.14-12-07235.1994 · Cited by 322
Place cells, navigational accuracy, and the human hippocampus
O'Keefe, J. M., Burgess, N., Donnett, J. G., Jeffery, K. J., & Maguire, E. A. (1998) · Philosophical Transactions of the Royal Society B Biological Sciences · doi:10.1098/rstb.1998.0287 · Cited by 314
Contextual variability and serial position effects in free recall.
Howard, M. W., & Kahana, M. J. (1999) · Journal of Experimental Psychology Learning Memory and Cognition · doi:10.1037/0278-7393.25.4.923 · Cited by 313
Distribution of spatial and nonspatial information in dorsal hippocampus
Hampson, R. E., Simeral, J. D., & Deadwyler, S. A. (1999) · Nature · doi:10.1038/45154 · Cited by 306
The temporal context model in spatial navigation and relational learning: toward a common explanation of medial temporal lobe function across domains
Howard, M. W., Fotedar, M. S., Datey, A. V., & Hasselmo, M. E. (2005) · Psychological Review · doi:10.1037/0033-295x.112.1.75 · Cited by 283 · cited 2×
“2; Kahana, 1996; Howard and Kahana, 1999; Howard et al., 2005).”
Background
Synchrony between limbic system theta activity and rhythmical behavior in rats.
Komisaruk, B. R. (1970) · Journal of Comparative and Physiological Psychology · doi:10.1037/h0028709 · Cited by 282
Neural encoding of individual words and faces by the human hippocampus and amygdala
Heit, G., Smith, M. E., & Halgren, E. (1988) · Nature · doi:10.1038/333773a0 · Cited by 281
Hippocampal Slow Waves
ADEY, W. R. (1960) · Archives of Neurology · doi:10.1001/archneur.1960.00450010074007 · Cited by 278
Sodium amobarbital, the hippocampal theta rhythm, and the partial reinforcement extinction effect.
Gray, J. A. (1970) · Psychological Review · doi:10.1037/h0029804 · Cited by 266
Considerations arising from a complementary learning systems perspective on hippocampus and neocortex
McClelland, J. L., & Goddard, N. (1996) · Hippocampus · doi:10.1002/(sici)1098-1063(1996)6:6 · Cited by 264
A Double Dissociation between Hippocampal Subfields
Lee, I., Rao, G., & Knierim, J. J. (2004) · Neuron · doi:10.1016/j.neuron.2004.05.010 · Cited by 246
NMDA Receptor Antagonism Blocks Experience-Dependent Expansion of Hippocampal “Place Fields”
Ekstrom, A. D., Meltzer, J., McNaughton, B. L., & Barnes, C. A. (2001) · Neuron · doi:10.1016/s0896-6273(01)00401-9 · Cited by 246
Hippocampal theta rhythm and the firing of neurons in walking and urethane anesthetized rats
Fox, S. E., Wolfson, S., & Ranck, J. B. (1986) · Experimental Brain Research · doi:10.1007/bf00236028 · Cited by 244
Relationship between hippocampal theta activity and running speed in the rat.
McFarland, W. L., Teitelbaum, H., & Hedges, E. K. (1975) · Journal of Comparative and Physiological Psychology · doi:10.1037/h0076177 · Cited by 237
Interspecies differences in the occurrence of theta
Winson, J. (1972) · Behavioral Biology · doi:10.1016/s0091-6773(72)80210-4 · Cited by 231
Place Representation within Hippocampal Networks Is Modified by Long-Term Potentiation
Dragoi, G., Harris, K. D., & Buzsáki, G. (2003) · Neuron · doi:10.1016/s0896-6273(03)00465-3 · Cited by 219
Self-citation
Hippocampus as a memory map: Synaptic plasticity and memory encoding by hippocampal neurons
Shapiro, M. L., & Eichenbaum, H. (1999) · Hippocampus · doi:10.1002/(sici)1098-1063(1999)9:4 · Cited by 209
Eine Methodik der Ableitung Iokalisierter Potentialschwankungen aus subcorticalen Hirngebieten
Jung, R., & Kornmüller, A. E. (1938) · European Archives of Psychiatry and Clinical Neuroscience · doi:10.1007/bf02157817 · Cited by 204
Stopping behavior: constraints on exploration in rats (Rattus norvegicus)
Golani, I., Benjamini, Y., & Eilam, D. (1993) · Behavioural Brain Research · doi:10.1016/s0166-4328(05)80263-3 · Cited by 192
Local Sensory Cues and Place Cell Directionality: Additional Evidence of Prospective Coding in the Hippocampus
Battaglia, F. P., Sutherland, G. R., & McNaughton, B. L. (2004) · Journal of Neuroscience · doi:10.1523/jneurosci.4896-03.2004 · Cited by 183
Dentate gyrus-selective colchicine lesion and disruption of performance in spatial tasks: Difficulties in ?place strategy? because of a lack of flexibility in the use of environmental cues?
Xavier, G. F., Oliveira-Filho, F. J. B., & Santos, A. M. G. (1999) · Hippocampus · doi:10.1002/(sici)1098-1063(1999)9:6 · Cited by 182
Hippocampectomized rats are capable of homing by path integration.
Alyan, S. H., & McNaughton, B. L. (1999) · Behavioral Neuroscience · doi:10.1037//0735-7044.113.1.19 · Cited by 180
Head direction cells: properties and functional significance
Muller, R. U., Ranck, J. B., & Taube, J. S. (1996) · Current Opinion in Neurobiology · doi:10.1016/s0959-4388(96)80073-0 · Cited by 171
The relation of hippocampal theta activity to arousal, attentive behaviour and somato-motor movements in unrestrained cats
Kemp, I. R., & Kaada, B. R. (1975) · Brain Research · doi:10.1016/0006-8993(75)90110-9 · Cited by 169
Hippocampal EEG and behavior: effects of variation in body temperature and relation of EEG to vibrissae movement, swimming and shivering
Whishaw, I. Q., & Vanderwolf, C. H. (1971) · Physiology & Behavior · doi:10.1016/0031-9384(71)90172-7 · Cited by 168
The hippocampal electrical correlates of the homeostatic regulation of motivation
Grastyán, E., Karmos, G., Vereczkey, L., & Kellényi, L. (1966) · Electroencephalography and Clinical Neurophysiology · doi:10.1016/0013-4694(66)90057-5 · Cited by 162
Preserved spatial memory after hippocampal lesions: effects of extensive experience in a complex environment
Winocur, G., Moscovitch, M., Fogel, S., Rosenbaum, R. S., & Sekeres, M. (2005) · Nature Neuroscience · doi:10.1038/nn1401 · Cited by 161
Consolidation of Long-Term Memory: Evidence and Alternatives.
Meeter, M., & Murre, J. M. J. (2004) · Psychological Bulletin · doi:10.1037/0033-2909.130.6.843 · Cited by 148
Slam on the brakes: A critique of Altman, Brunner, and Bayer's response-inhibition model of hippocampal function
Nadel, L., O'Keefe, J. M., & Black, A. H. (1975) · Behavioral Biology · doi:10.1016/s0091-6773(75)90148-0 · Cited by 145
Reaction to rhythmic stimuli with attempt to synchronize.
Dunlap, K. (1910) · Psychological Review · doi:10.1037/h0074736 · Cited by 139
The hippocampus, time and working memory
Rawlins, J. N. P., & Tsaltas, E. (1983) · Behavioural Brain Research · doi:10.1016/0166-4328(83)90033-5 · Cited by 132
Computer simulation of hippocampal place cells
Sharp, P. E. (1991) · Psychobiology · doi:10.3758/bf03327179 · Cited by 131
A simple neural network model of the hippocampus suggesting its pathfinding role in episodic memory retrievalPreprint
Samsonovich, A. V., & Ascoli, G. A. (2005) · Learning & Memory · doi:10.1101/lm.85205 · Cited by 127
Intracellular records of carbachol-induced theta rhythm in hippocampal slices
Bland, B. H., Colom, L. V., Konopacki, J., & Roth, S. H. (1988) · Brain Research · doi:10.1016/0006-8993(88)91141-9 · Cited by 126
Spike phase precession persists after transient intrahippocampal perturbation
Zugaro, M., Monconduit, L., & Buzsáki, G. (2004) · Nature Neuroscience · doi:10.1038/nn1369 · Cited by 125
Self-citation
Origins of Timing Errors in Human Sensorimotor Coordination
Chen, Y., Ding, M., & Kelso, J. A. S. (2001) · Journal of Motor Behavior · doi:10.1080/00222890109601897 · Cited by 121
Two‐Phase Computational Model Training Long‐Term Memories in the Entorhinal‐Hippocampal Region
Lörincz, A., & Buzsáki, G. (2000) · Annals of the New York Academy of Sciences · doi:10.1111/j.1749-6632.2000.tb06721.x · Cited by 119
Self-citation
Temporal relationships between hippocampal slow waves and exploratory sniffing in hamsters
Macrides, F. (1975) · Behavioral Biology · doi:10.1016/s0091-6773(75)90419-8 · Cited by 116
Hippocampal States and Functional Relations with Corticosubcortical Systems in Attention and Learning
ADEY, W. R. (1967) · Progress in brain research · doi:10.1016/s0079-6123(08)63102-7 · Cited by 106
Effects of septal driving of the hippocampal theta rhythm on resistance to extinction
Gray, J. A. (1972) · Physiology & Behavior · doi:10.1016/0031-9384(72)90333-2 · Cited by 104
Failure to acquire new semantic knowledge in patients with large medial temporal lobe lesions
Bayley, P. J., & Squire, L. R. (2004) · Hippocampus · doi:10.1002/hipo.20057 · Cited by 102
Electrophysiological correlates of copulatory behavior in the male rat: Evidence for a sexual inhibitory process.
Kurtz, R. G., & Adler, N. T. (1973) · Journal of Comparative and Physiological Psychology · doi:10.1037/h0035265 · Cited by 100
Avoidance training of hippocampal theta waves in flaxedilized dogs and its relation to skeletal movement.
Black, A. H., Young, G. A., & Batenchuk, C. (1970) · Journal of Comparative and Physiological Psychology · doi:10.1037/h0028393 · Cited by 98
Hippocampal evoked potentials and EEG changes during classical conditioning in the rat
Buzsáki, G., Grastyán, E., Tveritskaia, I. N., & Czopf, J. (1979) · Electroencephalography and Clinical Neurophysiology · doi:10.1016/0013-4694(79)90033-6 · Cited by 90
Self-citation
Modeling goal-directed spatial navigation in the rat based on physiological data from the hippocampal formation
Koene, R. A., Anatoli Gorchetchnikov, A., Cannon, R. C., & Hasselmo, M. E. (2003) · Neural Networks · doi:10.1016/s0893-6080(03)00106-0 · Cited by 89
Hippocampal Theta: a Sensory-inhibition Theory of Function
Sainsbury, R. S. (1998) · Neuroscience & Biobehavioral Reviews · doi:10.1016/s0149-7634(97)00011-0 · Cited by 87
Hippocampal Slow Wave Activity as a Correlate of Basic Behavioral Mechanisms in the Rat
PICKENHAIN, L., & Klingberg, F. (1967) · Progress in brain research · doi:10.1016/s0079-6123(08)63101-5 · Cited by 83
Hippocampal place fields: Relationship between degree of field overlap and cross-correlations within ensembles of hippocampal neurons
Hampson, R. E., Byrd, D. R., Konstantopoulos, J. K., Bunn, T., & Deadwyler, S. A. (1996) · Hippocampus · doi:10.1002/(sici)1098-1063(1996)6:3 · Cited by 82
Frequency and phase of hippocampal theta activity in the spontaneously behaving cat
Brown, B. B. (1968) · Electroencephalography and Clinical Neurophysiology · doi:10.1016/0013-4694(68)90066-7 · Cited by 82
Changes in excitability of the theta activity generating substrate by ACTH 4–10 in the rat
Urban, I. J. A., & de Wied, D. (1976) · Experimental Brain Research · doi:10.1007/bf00235019 · Cited by 80
Electrical activity of the entorhinal cortex during conditioned behavior
Holmes, J., & ADEY, W. R. (1960) · American Journal of Physiology-Legacy Content · doi:10.1152/ajplegacy.1960.199.5.741 · Cited by 80
Hippocampal activity during natural behavior in the guinea pig
Sainsbury, R. S. (1970) · Physiology & Behavior · doi:10.1016/0031-9384(70)90104-6 · Cited by 78
Hippocampal theta activity and the attention component of discrimination learning
Bennett, T. L., Hébert, P. N., & Moss, D. E. (1973) · Behavioral Biology · doi:10.1016/s0091-6773(73)80017-3 · Cited by 77
The primate hippocampus: ontogeny, early insult and memory
Bachevalier, J., & Vargha‐Khadem, F. (2005) · Current Opinion in Neurobiology · doi:10.1016/j.conb.2005.03.015 · Cited by 76
Hippocampal theta activity and response inhibition
Bennett, T. L., & Gottfried, J. (1970) · Electroencephalography and Clinical Neurophysiology · doi:10.1016/0013-4694(70)90123-9 · Cited by 75
Relationships of hippocampal theta cycles with bar pressing during self-stimulation
Buño, W., & Velluti, J. C. (1977) · Physiology & Behavior · doi:10.1016/0031-9384(77)90035-x · Cited by 74
Hippocampal EEG and behaviour in dog. I. Hippocampal EEG correlates of gross motor behaviour
Arnolds, D. E. A. T., Lopes, F. H. D. S., Aitink, J. W., & Kamp, A. (1979) · Electroencephalography and Clinical Neurophysiology · doi:10.1016/0013-4694(79)90009-9 · Cited by 72
Classic conditioning in aged rabbits: Delay, trace, and long-delay conditioning.
Solomon, P. R., & Groccia-Ellison, M. (1996) · Behavioral Neuroscience · doi:10.1037//0735-7044.110.3.427 · Cited by 70
Classic conditioning in aged rabbits: Delay, trace, and long-delay conditioning.
Solomon, P. R., & Groccia-Ellison, M. (1996) · Behavioral Neuroscience · doi:10.1037/0735-7044.110.3.427 · Cited by 68
Time and the Brain
(2000) · CRC Press eBooks · doi:10.1201/9781482284102 · Cited by 65
Phase of the theta wave in relation to different limb movements in awake rats
Semba, K., & Komisaruk, B. R. (1978) · Electroencephalography and Clinical Neurophysiology · doi:10.1016/0013-4694(78)90105-0 · Cited by 63
Effects of electric stimulation of brain stem reticular formation on hippocampal theta rhythm and muscle activity in unanesthetized, cervical- and midbrain-transected rats
Klemm, W. R. (1972) · Brain Research · doi:10.1016/0006-8993(72)90506-9 · Cited by 62
Idiothetic input into object-place configuration as the contribution to memory of the monkey and human hippocampus: a review
Gaffan, D. (1998) · Experimental Brain Research · doi:10.1007/s002210050562 · Cited by 60
The effects of centrally blocking hippocampal theta activity on learning and retention
Bennett, T. L. (1973) · Behavioral Biology · doi:10.1016/s0091-6773(73)80049-5 · Cited by 59
V1 Neurons Signal Acquisition of an Internal Representation of Stimulus Location
Sharma, J., Dragoi, V., Tenenbaum, J. B., Miller, E. K., & Sur, M. (2003) · Science · doi:10.1126/science.1081721 · Cited by 58
Instrumental conditioning of hippocampal theta and subsequent response persistence.
Glazer, H. I. (1974) · Journal of Comparative and Physiological Psychology · doi:10.1037/h0035954 · Cited by 53
Hippocampal theta frequency shifts and operant behaviour
Silva, F. H. L. D., & Kamp, A. (1969) · Electroencephalography and Clinical Neurophysiology · doi:10.1016/0013-4694(69)90204-1 · Cited by 53
Hippocampal slow wave activity during appetitive and aversive conditioning in the cat
Buzsáki, G., Haubenreiser, J., Grastyán, E., Czopf, J., & Kellényi, L. (1981) · Electroencephalography and Clinical Neurophysiology · doi:10.1016/0013-4694(81)90141-3 · Cited by 50
Self-citation
Triple-loop model of path control by head direction and place cells
Mittelstaedt, H. (2000) · Biological Cybernetics · doi:10.1007/s004220000169 · Cited by 46
Autonomic-somatic interaction and hippocampal theta activity.
Powell, D. A., & Joseph, J. A. (1974) · Journal of Comparative and Physiological Psychology · doi:10.1037/h0037209 · Cited by 45
Chapter 1 Neuromodulation and the hippocampus: memory function and dysfunction in a network simulation
Hasselmo, M. E. (1999) · Progress in brain research · doi:10.1016/s0079-6123(08)63064-2 · Cited by 44
Computational theories on the function of theta oscillations
Lengyel, M., Huhn, Z., & Érdi, P. (2005) · Biological Cybernetics · doi:10.1007/s00422-005-0567-x · Cited by 42
A frequency shift in the hippocampal theta activity: an electrical correlate of central action of ACTH analogues in the dog?
Urban, I. J. A., Lopes, F. H. D. S., van Leeuwen, W. S., & de Wied, D. (1974) · Brain Research · doi:10.1016/0006-8993(74)90015-8 · Cited by 39
Classical conditioning of hippocampal theta patterns in the rat.
Teitelbaum, H., McFarland, W. L., & Mattsson, J. L. (1977) · Journal of Comparative and Physiological Psychology · doi:10.1037/h0077344 · Cited by 35
Analysis of temporal relations among units and slow waves in rabbit hippocampus
Berry, S. D., Rinaldi, P. C., Thompson, R. F., & Verzeano, M. (1978) · Brain Research Bulletin · doi:10.1016/0361-9230(78)90080-1 · Cited by 32
Two types of diencephalically driven RSA (theta) as a means of studying memory formation in mice
Destrade, C. (1982) · Brain Research · doi:10.1016/0006-8993(82)90892-7 · Cited by 31
Hippocampal and cortical activity during sexual behavior in the female rat.
Kurtz, R. G. (1975) · Journal of Comparative and Physiological Psychology · doi:10.1037/h0076650 · Cited by 29
Information compression in biological systems
Haken, H. (1987) · Biological Cybernetics · doi:10.1007/bf00333063 · Cited by 27
A study of a possible "dreaming" mechanism in the cat.
Grastyán, E., & Karmos, G. (1961) · PubMed · Cited by 26
Behavioral and hippocampal electrical changes during operant learning in cats and effects of stimulating two hypothalamic-hippocampal systems
Coleman, J. R., & Lindsley, D. B. (1977) · Electroencephalography and Clinical Neurophysiology · doi:10.1016/0013-4694(77)90168-7 · Cited by 23
Hippocampal rhythmic slow activity (RSA) during animal hypnosis in the rabbit
Fontani, G., Grazzi, F., Lombardi, G., & Carli, G. (1982) · Behavioural Brain Research · doi:10.1016/0166-4328(82)90078-x · Cited by 20
Dentate granule cell discharge during conditioning
West, M. O., Christian, E. P., Robinson, J. H., & Deadwyler, S. A. (1981) · Experimental Brain Research · doi:10.1007/bf00236566 · Cited by 20
Instrumental response persistence following induction of hippocampal theta frequency during fixed-ratio responding in rats.
Glazer, H. I. (1974) · Journal of Comparative and Physiological Psychology · doi:10.1037/h0037646 · Cited by 19
A test of the reverberatory activity hypothesis for hippocampal ‘place’ cells
Moser, E. I., Moser, M., Lipa, P., Newton, M., Houston, F. P., Barnes, C. A., & McNaughton, B. L. (2004) · Neuroscience · doi:10.1016/j.neuroscience.2004.09.044 · Cited by 17
[Comparator function of the hippocampus].
Vinogradova, O. S., & Dudaeva, K. I. (1972) · PubMed · Cited by 16
Correlation of hippocampal theta rhythm with changes in cutaneous temperature
Jm, H., Ma, S., & Karem, R. D. (1974) · American Journal of Physiology-Legacy Content · doi:10.1152/ajplegacy.1974.227.3.635 · Cited by 15
Hippocampal theta in nervous pointer dogs
Lucas, E., Powell, E. W., & Murphree, O. D. (1974) · Physiology & Behavior · doi:10.1016/0031-9384(74)90210-8 · Cited by 14
Electrical activity of the cat hippocampus during the species-typical gape response: Evidence against the voluntary movement hypothesis
Bennett, T. L., & French, J. (1977) · Behavioral Biology · doi:10.1016/s0091-6773(77)90266-8 · Cited by 8
Hippocampal Theta and Disinhibition: A Counterreply
Douglas, R. J. (1969) · Psychological Reports · doi:10.2466/pr0.1969.24.2.583 · Cited by 7
Columbus's Method of Determining Longitude: An Analytical View
Pickering, K. (1996) · Journal of Navigation · doi:10.1017/s037346330001314x · Cited by 7
Species-typical IRMs in CA1-3 hippocampi and habituation memory in area dentata
McLardy, T. (1981) · Medical Hypotheses · doi:10.1016/0306-9877(81)90142-0 · Cited by 4
Power spectral density of hippocampal theta activity during rhombencephalic sleep, after physostigmine administration and during orienting reaction.
Radil-Weiss, T. (1974) · PubMed · Cited by 4
A peculiar dreamlike stage of sleep in the cat.
Lissák, K., Karmos, G., & Grastyán, E. (1962) · PubMed · Cited by 4

Research works printed but not linked: 7

10.1037/0735-7044.113.1.19 · DOI
Huizinga J, 1955, Homo ludens
10.1002/(SICI)1098-1063(1996)6:6<579::AID-HIPO3>3.0.CO;2-C · DOI
Ranck JB, 1985, Electrical activity of the archicortex, 217
10.1002/(SICI)1098-1063(1996)6:6<601::AID-HIPO5>3.0.CO;2-J · DOI
10.1002/(SICI)1098-1063(1996)6:3<247::AID-HIPO4>3.0.CO;2-K · DOI
10.1002/(SICI)1098-1063(1996)6:3<271::AID-HIPO5>3.0.CO;2-Q · DOI

Sorted by citations

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
Self-citation
Memory, 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
Self-citation
Entrainment of Neuronal Oscillations as a Mechanism of Attentional Selection
Lakatos, P., Karmos, G., Mehta, A. D., Ulbert, I., & Schroeder, C. E. (2008) · Science · doi:10.1126/science.1154735 · Cited by 1,719
Motivation, emotion, and their inhibitory control mirrored in brain oscillations
Knyazev, G. G. (2006) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2006.10.004 · Cited by 1,034
The effects of acute exercise on mood, cognition, neurophysiology, and neurochemical pathways: a review.
Basso, J. C., & Suzuki, W. A. (2016) · Brain Plasticity · doi:10.3233/bpl-160040 · Cited by 911

See all 872

Authors: Buzsáki, G.
Affiliations: Rutgers, The State University of New Jersey (US)
Corresponding author: Buzsáki, György
ORCID: Buzsáki, György
Venue: Hippocampus
Publisher: Wiley
Published: 2005-01
Volume: 15
Issue: 7
Pages: 827-840
ISSN: 1050-9631 (ISSN-L)
1098-1063
DOI: 10.1002/hipo.20113
OpenAlex: W2084694708
Cited by: 872
References: 209
Citations by year: 2026: 23 · 2025: 44 · 2024: 67 · 2023: 38 · 2022: 47 · 2021: 36 · 2020: 39 · 2019: 58 · 2018: 47 · 2017: 50 · 2016: 38 · 2015: 44 · 2014: 46 · 2013: 49 · 2012: 39
FWCI: 2.31
Type: journal article
Language: en
Open access: closed
Licence: onlinelibrary.wiley.com/termsAndConditions#vor (vor, 249 d)
Locations: Hippocampus (publishedVersion)
PubMed (publishedVersion)
Funders: National Institute of Mental Health (R01MH054671, MH54671)
National Institute of Neurological Disorders and Stroke (NS 43157, R01NS043157, R01NS034994, NS-34994)
Topics: Life Sciences › Neuroscience › Cognitive Neuroscience › Memory and Neural Mechanisms
Life Sciences › Neuroscience › Cognitive Neuroscience › Neural dynamics and brain function
Social Sciences › Psychology › Experimental and Cognitive Psychology › Spatial Cognition and Navigation
Keywords: theta oscillations, path integration, dead reckoning, landmark navigation, map representation, place cells, episodic memory, semantic memory, entorhinal cortex, Hebbian plasticity, neuronal ensembles, exploration
MeSH terms: Animals, Biological Clocks, Hippocampus, Humans, Memory, Neural Pathways, Synaptic Transmission, Neuronal Plasticity, Orientation, Space Perception, Theta Rhythm

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

Theta rhythm of navigation: Link between path integration and landmark navigation, episodic and semantic memory

Abstract

Overview

Integrity signals

Verification

Claims the paper makes

Claims other papers make about this one

Citations

Cites

Cited by

Related

Metadata

Record

About these checks