Place units in the hippocampus of the freely moving rat

Cognitive maps in rats and men

Tolman, E. C. (1948) · Psychological Review · doi:10.1037/h0061626 · Cited by 6,641 · see citing works

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 · 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

Studies on single neurons in dorsal hippocampal formation and septum in unrestrained rats

Ranck, J. B. (1973) · Experimental Neurology · doi:10.1016/0014-4886(73)90290-2 · Cited by 1,322 · see citing works

Glass-coated platinum-plated tungsten microelectrodes

Merrill, E. G., & Ainsworth, A. (1972) · Medical & Biological Engineering & Computing · doi:10.1007/bf02476084 · Cited by 597 · see citing works

Limbic-diencephalic mechanisms of voluntary movement.

Vanderwolf, C. H. (1971) · Psychological Review · doi:10.1037/h0030672 · Cited by 491 · see citing works

Fornix lesions selectively abolish place learning in the rat

O'Keefe, J. M., Nadel, L., Keightley, S. J., & Kill, D. (1975) · Experimental Neurology · doi:10.1016/0014-4886(75)90230-7 · Cited by 337 · see citing works

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 · see citing works

Studies on single neurons in dorsal hippocampal formation and septum in unrestrained rats

Feder, R., & Ranck, J. B. (1973) · Experimental Neurology · doi:10.1016/0014-4886(73)90291-4 · Cited by 182 · see citing works

Diencephalic, Hippocampal, and Neocortical Mechanisms in Voluntary Movement

Vanderwolf, C. H., Bland, B. H., & Whishaw, I. Q. (1973) · Elsevier eBooks · doi:10.1016/b978-0-12-476950-2.50014-2 · Cited by 110 · see citing works

Place navigation impaired in rats with hippocampal lesions

Morris, R. G. M., Garrud, P., Rawlins, J. N. P., & O'Keefe, J. (1982) · Nature · doi:10.1038/297681a0 · Cited by 6,340 · see citing works

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 · 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

Memory deficits associated with senescence: A neurophysiological and behavioral study in the rat.

Barnes, C. A. (1979) · Journal of Comparative and Physiological Psychology · doi:10.1037/h0077579 · Cited by 2,088 · see citing works

Path integration and the neural basis of the 'cognitive map'

McNaughton, B. L., Battaglia, F. P., Jensen, O., Moser, E. I., & Moser, M.-B. (2006) · Nature Reviews Neuroscience · doi:10.1038/nrn1932 · Cited by 2,024 · 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 sharp wave-ripple: A cognitive biomarker for episodic memory and planning

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

Geometric determinants of the place fields of hippocampal neurons

O'Keefe, J., & Burgess, N. (1996) · Nature · doi:10.1038/381425a0 · Cited by 1,166 · see citing works

The Molecular and Systems Biology of Memory

Kandel, E. R., Dudai, Y., & Mayford, M. R. (2014) · Cell · doi:10.1016/j.cell.2014.03.001 · Cited by 1,134 · see citing works

On the role of the hippocampus in learning and memory in the rat.

Jarrard, L. E. (1993) · Behavioral and Neural Biology · doi:10.1016/0163-1047(93)90664-4 · Cited by 1,125 · see citing works

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 · see citing works

Visual Place Recognition: A Survey

Lowry, S., Sünderhauf, N., Newman, P., Leonard, J. J., Cox, D., Corke, P., & Milford, M. J. (2016) · IEEE Transactions on Robotics · doi:10.1109/tro.2015.2496823 · Cited by 1,079 · see citing works

Remembering the past and imagining the future: A neural model of spatial memory and imagery.

Byrne, P., Becker, S., & Burgess, N. (2007) · Psychological Review · doi:10.1037/0033-295x.114.2.340 · Cited by 1,011 · see citing works

The anatomy of memory: an interactive overview of the parahippocampal–hippocampal network

van Strien, N. M., Cappaert, N. L. M., & Witter, M. P. (2009) · Nature Reviews Neuroscience · doi:10.1038/nrn2614 · Cited by 1,041 · see citing works

Hippocampal Neurons Encode Information about Different Types of Memory Episodes Occurring in the Same Location

Wood, E. R., Dudchenko, P. A., Robitsek, R. J., & Eichenbaum, H. (2000) · Neuron · doi:10.1016/s0896-6273(00)00071-4 · Cited by 992 · see citing works

The hippocampus—what does it do?

Eichenbaum, H., Otto, T., & Cohen, N. J. (1992) · Behavioral and Neural Biology · doi:10.1016/0163-1047(92)90724-i · Cited by 867 · see citing works

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

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

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

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

Hippocampal synaptic plasticity, spatial memory and anxiety

Bannerman, D. M., Sprengel, R., Sanderson, D. J., McHugh, S. B., Rawlins, J. N. P., Monyer, H., & Seeburg, P. H. (2014) · Nature Reviews Neuroscience · doi:10.1038/nrn3677 · Cited by 688 · see citing works

The Restless Engram: Consolidations Never End

Dudai, Y. (2012) · Annual Review of Neuroscience · doi:10.1146/annurev-neuro-062111-150500 · Cited by 644 · see citing works

Rhythms of the hippocampal network

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

Spatial representation in the hippocampal formation: a history

Moser, E. I., Moser, M.-B., & McNaughton, B. L. (2017) · Nature Neuroscience · doi:10.1038/nn.4653 · Cited by 560 · see citing works

<i>Spatial Cognition and the Brain</i>

Burgess, N. (2008) · Annals of the New York Academy of Sciences · doi:10.1196/annals.1440.002 · Cited by 614 · see citing works

Spatial memory deficits in patients with lesions to the right hippocampus and to the right parahippocampal cortex

Bohbot, V. D., Kalina, M., Stepankova, K., Spackova, N., Petrides, M., & Nadel, L. (1998) · Neuropsychologia · doi:10.1016/s0028-3932(97)00161-9 · Cited by 516 · see citing works

What is the function of hippocampal theta rhythm?--Linking behavioral data to phasic properties of field potential and unit recording data

Hasselmo, M. E. (2005) · Hippocampus · doi:10.1002/hipo.20116 · Cited by 502 · see citing works

Dopaminergic neurons promote hippocampal reactivation and spatial memory persistence

McNamara, C. G., Tejero-Cantero, Á., Trouche, S., Campo-Urriza, N., & Dupret, D. (2014) · Nature Neuroscience · doi:10.1038/nn.3843 · Cited by 486 · see citing works

Complementary Roles of Cholecystokinin- and Parvalbumin-Expressing GABAergic Neurons in Hippocampal Network Oscillations

Klausberger, T., Marton, L. F., O'Neill, J., Huck, J. H. J., Dalezios, Y., Fuentealba, P., Suen, W. Y., Papp, E., Kaneko, T., Watanabe, M., et al. (2005) · The Journal of Neuroscience · doi:10.1523/jneurosci.3269-05.2005 · Cited by 469 · see citing works

Functional correlates of the lateral and medial entorhinal cortex: objects, path integration and local-global reference frames

Knierim, J. J., Neunuebel, J. P., & Deshmukh, S. S. (2014) · Philosophical Transactions of the Royal Society B Biological Sciences · doi:10.1098/rstb.2013.0369 · Cited by 425 · see citing works

The Boundary Vector Cell Model of Place Cell Firing and Spatial Memory

Barry, C., Lever, C., Hayman, R., Hartley, T., Burton, S., O'Keefe, J., Jeffery, K., & Burgess, Ν. (2006) · Reviews in the Neurosciences · doi:10.1515/revneuro.2006.17.1-2.71 · Cited by 401 · see citing works

The need for integrative approaches to understand and conserve migratory ungulates.

Bolger, D. T., Newmark, W. D., Morrison, T. A., & Doak, D. F. (2008) · Ecology Letters · doi:10.1111/j.1461-0248.2007.01109.x · Cited by 410 · see citing works

A Dedicated Population for Reward Coding in the Hippocampus

Gauthier, J. L., & Tank, D. W. (2018) · Neuron · doi:10.1016/j.neuron.2018.06.008 · Cited by 394 · see citing works

Memory for items and memory for relations in the procedural/declarative memory framework

Cohen, N. J., Poldrack, R. A., & Eichenbaum, H. (1997) · Memory · doi:10.1080/741941149 · Cited by 383 · see citing works

Neuronal Diversity in GABAergic Long-Range Projections from the Hippocampus

Jinno, S., Klausberger, T., Marton, L. F., Dalezios, Y., Roberts, J. D. B., Fuentealba, P., Bushong, E. A., Henze, D., Buzsáki, G., & Somogyi, P. (2007) · The Journal of Neuroscience · doi:10.1523/jneurosci.1847-07.2007 · Cited by 369 · see citing works

Neuronal code for extended time in the hippocampus

Mankin, E. A., Sparks, F. T., Slayyeh, B., Sutherland, R. J., Leutgeb, S., & Leutgeb, J. K. (2012) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1214107109 · Cited by 371 · see citing works

Object-vector coding in the medial entorhinal cortex

Høydal, Ø. A., Skytøen, E. R., Andersson, S. O., Moser, M.-B., & Moser, E. I. (2019) · Nature · doi:10.1038/s41586-019-1077-7 · Cited by 366 · see citing works

Oscillatory multiplexing of population codes for selective communication in the mammalian brain

Akam, T., & Kullmann, D. M. (2014) · Nature Reviews Neuroscience · doi:10.1038/nrn3668 · Cited by 327 · see citing works

Grid cells and cortical representation

Moser, E. I., Roudi, Y., Witter, M. P., Kentros, C., Bonhoeffer, T., & Moser, M.-B. (2014) · Nature Reviews Neuroscience · doi:10.1038/nrn3766 · Cited by 335 · see citing works

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 · see citing works

Cell Type-Specific Tuning of Hippocampal Interneuron Firing during Gamma Oscillations<i>In Vivo</i>

Tukker, J. J., Fuentealba, P., Hartwich, K., Somogyi, P., & Klausberger, T. (2007) · The Journal of Neuroscience · doi:10.1523/jneurosci.1685-07.2007 · Cited by 304 · see citing works

Navigation

Montello, D. R. (2005) · The Cambridge Handbook of Visuospatial Thinking · doi:10.1017/cbo9780511610448.008 · Cited by 305 · see citing works

Traces of experience in the lateral entorhinal cortex

Tsao, A., Moser, M.-B., & Moser, E. I. (2013) · Current Biology · doi:10.1016/j.cub.2013.01.036 · Cited by 290 · see citing works

Slow waves, sharp waves, ripples, and REM in sleeping dragons

Shein-Idelson, M., Ondracek, J. M., Liaw, H.-P., Reiter, S., & Laurent, G. (2016) · Science · doi:10.1126/science.aaf3621 · Cited by 274 · see citing works

Corticosterone effects on BDNF expression in the hippocampus. Implications for memory formation

Schaaf, M. J. M., De Kloet, E. R., & Vreugdenhil, E. (2000) · Stress · doi:10.3109/10253890009001124 · Cited by 270 · see citing works

Navigating from hippocampus to parietal cortex

Whitlock, J. R., Sutherland, R. J., Witter, M. P., Moser, M.-B., & Moser, E. I. (2008) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0804216105 · Cited by 267 · see citing works

How do (some) people make a cognitive map? Routes, places, and working memory.

Weisberg, S. M., & Newcombe, N. S. (2016) · Journal of Experimental Psychology: Learning, Memory, and Cognition · doi:10.1037/xlm0000200 · Cited by 219 · see citing works

Pattern separation, pattern completion, and new neuronal codes within a continuous CA3 map

Leutgeb, S., & Leutgeb, J. K. (2007) · Learning &amp; Memory · doi:10.1101/lm.703907 · Cited by 234 · see citing works

A neural-level model of spatial memory and imagery

Bicanski, A., & Burgess, N. (2018) · eLife · doi:10.7554/elife.33752 · Cited by 230 · see citing works

Prediction and memory: A predictive coding account

Barron, H. C., Auksztulewicz, R., & Friston, K. (2020) · Progress in Neurobiology · doi:10.1016/j.pneurobio.2020.101821 · Cited by 220 · see citing works

Building an allocentric travelling direction signal via vector computation

Lyu, C., Abbott, L. F., & Maimon, G. (2022) · Nature · doi:10.1038/s41586-021-04067-0 · Cited by 215 · see citing works

Hippocampal Function in Cognition

Sweatt, J. D. (2004) · Psychopharmacology · doi:10.1007/s00213-004-1795-9 · Cited by 217 · see citing works

Influence of local objects on hippocampal representations: Landmark vectors and memory

Deshmukh, S. S., & Knierim, J. J. (2013) · Hippocampus · doi:10.1002/hipo.22101 · Cited by 217 · see citing works

Event-related brain potential correlates of the processing of novel visual and auditory information in autism

Courchesne, E., Lincoln, A. J., Kilman, B. A., & Galambos, R. (1985) · Journal of Autism and Developmental Disorders · doi:10.1007/bf01837899 · Cited by 198 · see citing works

Neuronal vector coding in spatial cognition

Bicanski, A., & Burgess, N. (2020) · Nature Reviews Neuroscience · doi:10.1038/s41583-020-0336-9 · Cited by 172 · see citing works

Hippocampal remapping as hidden state inference

Sanders, H., Wilson, M. A., & Gershman, S. J. (2020) · eLife · doi:10.7554/elife.51140 · Cited by 163 · see citing works

Landmark stability is a prerequisite for spatial but not discrimination learning

Biegler, R., & Morris, R. G. M. (1993) · Nature · doi:10.1038/361631a0 · Cited by 181 · see citing works

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

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

Spatial firing properties of hippocampal theta cells

Kubie, J., Muller, R., & Bostock, E. (1990) · The Journal of Neuroscience · doi:10.1523/jneurosci.10-04-01110.1990 · Cited by 163 · see citing works

Spatial goal coding in the hippocampal formation

Nyberg, N., Duvelle, É., Barry, C., & Spiers, H. J. (2022) · Neuron · doi:10.1016/j.neuron.2021.12.012 · Cited by 141 · see citing works

New and Distinct Hippocampal Place Codes Are Generated in a New Environment during Septal Inactivation

Brandon, M. P., Koenig, J., Leutgeb, J. K., & Leutgeb, S. (2014) · Neuron · doi:10.1016/j.neuron.2014.04.013 · Cited by 145 · see citing works

Framing Spatial Cognition: Neural Representations of Proximal and Distal Frames of Reference and Their Roles in Navigation

Knierim, J. J., & Hamilton, D. A. (2011) · Physiological Reviews · doi:10.1152/physrev.00021.2010 · Cited by 148 · see citing works

Place Field Repetition and Purely Local Remapping in a Multicompartment Environment

Spiers, H. J., Hayman, R. M. A., Jovalekic, A., Marozzi, E., & Jeffery, K. J. (2015) · Cerebral Cortex · doi:10.1093/cercor/bht198 · Cited by 138 · see citing works

Medial Parietal Cortex Encodes Perceived Heading Direction in Humans

Baumann, O., & Mattingley, J. B. (2010) · The Journal of Neuroscience · doi:10.1523/jneurosci.3077-10.2010 · Cited by 137 · see citing works

Cocaine Place Conditioning Strengthens Location-Specific Hippocampal Coupling to the Nucleus Accumbens

Sjulson, L., Peyrache, A., Cumpelik, A., Cassataro, D., & Buzsáki, G. (2018) · Neuron · doi:10.1016/j.neuron.2018.04.015 · Cited by 123 · see citing works

Orientation selectivity and noise correlation in awake monkey area V1 are modulated by the gamma cycle

Womelsdorf, T., Lima, B., Vinck, M., Oostenveld, R., Singer, W., Neuenschwander, S., & Fries, P. (2012) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1114223109 · Cited by 119 · see citing works

Conflicts between local and global spatial frameworks dissociate neural representations of the lateral and medial entorhinal cortex

Neunuebel, J. P., Yoganarasimha, D., Rao, G., & Knierim, J. J. (2013) · The Journal of Neuroscience · doi:10.1523/jneurosci.0946-13.2013 · Cited by 126 · see citing works

Coherent phasic excitation during hippocampal ripples

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

Hippocampal Place Fields Maintain a Coherent and Flexible Map across Long Timescales

Kinsky, N. R., Sullivan, D. W., Mau, W., Hasselmo, M. E., & Eichenbaum, H. B. (2018) · Current Biology · doi:10.1016/j.cub.2018.09.037 · Cited by 105 · see citing works

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

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

Subcircuits of Deep and Superficial CA1 Place Cells Support Efficient Spatial Coding across Heterogeneous Environments

Sharif, F., Tayebi, B., Buzsáki, G., Royer, S., & Fernandez-Ruiz, A. (2021) · Neuron · doi:10.1016/j.neuron.2020.10.034 · Cited by 111 · see citing works

Do hippocampal pyramidal cells respond to nonspatial stimuli?

O’Keefe, J., & Krupic, J. (2021) · Physiological Reviews · doi:10.1152/physrev.00014.2020 · Cited by 93 · see citing works

Origin and role of path integration in the cognitive representations of the hippocampus: computational insights into open questions

Savelli, F., & Knierim, J. J. (2019) · Journal of Experimental Biology · doi:10.1242/jeb.188912 · Cited by 93 · see citing works

Intranasal Adeno-Associated Virus Mediated Gene Delivery and Expression of Human Iduronidase in the Central Nervous System: A Noninvasive and Effective Approach for Prevention of Neurologic Disease in Mucopolysaccharidosis Type I

Belur, L. R., Temme, A., Podetz-Pedersen, K. M., Riedl, M., Vulchanova, L., Robinson, N., Hanson, L. R., Kozarsky, K. F., Orchard, P. J., Frey, W. H., et al. (2017) · Human Gene Therapy · doi:10.1089/hum.2017.187 · Cited by 67 · see citing works

Neural and behavioural state switching during hippocampal dentate spikes

Farrell, J. S., Hwaun, E., Dudok, B., & Soltesz, I. (2024) · Nature · doi:10.1038/s41586-024-07192-8 · Cited by 47 · see citing works

Brain State Dependence of Hippocampal Subthreshold Activity in Awake Mice

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

Temporal Organization of GABAergic Interneurons in the Intermediate CA1 Hippocampus During Network Oscillations

Forro, T., Valenti, O., Lasztoczi, B., & Klausberger, T. (2015) · Cerebral Cortex · doi:10.1093/cercor/bht316 · Cited by 38 · see citing works

A stable hippocampal representation of a space requires its direct experience

Rowland, D. C., Yanovich, Y., & Kentros, C. G. (2011) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1105445108 · Cited by 40 · see citing works

Enhancement of Neocortical-Medial Temporal EEG Correlations during Non-REM Sleep

Axmacher, N., Helmstaedter, C., Elger, C. E., & Fell, J. (2008) · Neural Plasticity · doi:10.1155/2008/563028 · Cited by 22 · see citing works

Differential Impact of Acute and Chronic Stress on CA1 Spatial Coding and Gamma Oscillations

Tomar, A., Polygalov, D., & McHugh, T. J. (2021) · Frontiers in Behavioral Neuroscience · doi:10.3389/fnbeh.2021.710725 · Cited by 21 · see citing works

From Text to Space: Mapping Abstract Spatial Models in LLMs during a Grid-World Navigation Task

Martorell, N. (2025) · arXiv · doi:10.48550/arxiv.2502.16690

Hippocampal Place Cell Activity During Overtly Purposeful Behavior

Fenton, A. A., Bureš, J., Cimadevilla, J. M., Olypher, A. V., Wesierska, M., & Zinyuk, L. E. (2002) · Springer eBooks · doi:10.1007/978-1-4615-0887-8_4 · Cited by 4 · see citing works

Altered hippocampal place cell representation and theta rhythmicity following moderate prenatal alcohol exposurePreprint

Harvey, R. E., Berkowitz, L. E., Savage, D. D., Hamilton, D. A., & Clark, B. J. (2020) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2020.02.11.944173 · Cited by 2 · see citing works

Sensory Reception and Somatesthesia

Sturkie, P. D. (1981) · doi:10.1007/978-1-4613-8081-8_5

Spatial Firing of Hippocampal Place Cells in Blind Rats

Save, É., Cressant, A., Thinus‐Blanc, C., & Poucet, B. (1998) · Journal of Neuroscience · doi:10.1523/jneurosci.18-05-01818.1998 · Cited by 193 · see citing works

Comparison of the effect of β-amyloid peptide 25-35 on hippocampal and septal neurons in vitroi

Zhao, Y. (2004)