Hippocampal Remapping and Its Entorhinal Origin

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Abolition of Long-Term Stability of New Hippocampal Place Cell Maps by NMDA Receptor Blockade

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Altered Hippocampal Place Cell Representation and Theta Rhythmicity following Moderate Prenatal Alcohol Exposure

Harvey, R. E., Berkowitz, L. E., Savage, D. D., Hamilton, D. A., & Clark, B. J. (2020) · Current Biology · doi:10.1016/j.cub.2020.06.077 · Cited by 26 · see citing works

Neuronal signature of spatial decision-making during navigation by freely moving rats by using calcium imaging

Gobbo, F., Mitchell‐Heggs, R., Tse, D., Omrani, M. A., Spooner, P. A., Schultz, S. R., & Morris, R. (2022) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.2212152119 · Cited by 24 · see citing works

Grid cell remapping under three-dimensional object and social landmarks detected by implantable microelectrode arrays for the medial entorhinal cortex

Xu, Z., Mo, F., Yang, G., Fan, P., Wang, Y., Lu, B., Xie, J., Dai, Y., Song, Y., He, E., et al. (2022) · Microsystems & Nanoengineering · doi:10.1038/s41378-022-00436-5 · Cited by 24 · see citing works

Learning produces a hippocampal cognitive map in the form of an orthogonalized state machinePreprint

Sun, W., Winnubst, J., Natrajan, M., Lai, C., Kajikawa, K., Michaelos, M., Gattoni, R., Stringer, C., Flickinger, D., Fitzgerald, J. E., et al. (2023) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2023.08.03.551900 · Cited by 24 · see citing works

Calcium Imaging Reveals Fast Tuning Dynamics of Hippocampal Place Cells and CA1 Population Activity during Free Exploration Task in Mice

Sotskov, V. P., Pospelov, N., Plusnin, V. V., & Anokhin, K. V. (2022) · International Journal of Molecular Sciences · doi:10.3390/ijms23020638 · Cited by 18 · see citing works

Modular microcircuit organization of the presubicular head-direction map

Balsamo, G., Blanco-Hernández, E., Liang, F., Naumann, R. K., Coletta, S., Burgalossi, A., & Preston‐Ferrer, P. (2022) · Cell Reports · doi:10.1016/j.celrep.2022.110684 · Cited by 17 · see citing works

Dream to Explore: 5-HT2a as Adaptive Temperature Parameter for Sophisticated Affective Inference

Safron, A., & Sheikhbahaee, Z. (2021) · Communications in computer and information science · doi:10.1007/978-3-030-93736-2_56 · Cited by 13 · see citing works

Single-trial dynamics of hippocampal spatial representations are modulated by reward value

Michon, F., Krul, E., Sun, J., & Kloosterman, F. (2021) · Current Biology · doi:10.1016/j.cub.2021.07.058 · Cited by 14 · see citing works

Single-Neuron Detection of Place Cells Remapping in Short-Term Memory Using Motion Microelectrode Arrays

Mo, F., Xu, Z., Yang, G., Fan, P., Wang, Y., Lu, B., Liu, J., Wang, M., Jing, L., Xu, W., et al. (2022) · Biosensors and Bioelectronics · doi:10.1016/j.bios.2022.114726 · Cited by 13 · see citing works

Firing patterns of ventral hippocampal neurons predict the exploration of anxiogenic locations

Malagon‐Vina, H., Ciocchi, S., & Klausberger, T. (2023) · eLife · doi:10.7554/elife.83012 · Cited by 12 · see citing works

Integrated Three-Electrode Dual-Mode Detection Chip for Place Cell Analysis: Dopamine Facilitates the Role of Place Cells in Encoding Spatial Locations of Novel Environments and Rewards

Mo, F., Kong, F., Yang, G., Xu, Z., Liang, W. J., Liu, J., Zhang, K., Liu, Y., Lv, S., Han, M., et al. (2023) · ACS Sensors · doi:10.1021/acssensors.3c01864 · Cited by 10 · see citing works

The generalized spatial representation in the prefrontal cortex is inherited from the hippocampusPreprint

Nardin, M., Kaefer, K., & Csicsvari, J. L. (2021) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2021.09.30.462269 · Cited by 10 · see citing works

Graded remapping of hippocampal ensembles under sensory conflicts

Fetterhoff, D., Sobolev, A., & Leibold, C. (2021) · Cell Reports · doi:10.1016/j.celrep.2021.109661 · Cited by 9 · see citing works

Adult Neurogenesis, Context Encoding, and Pattern Separation: A Pathway for Treating Overgeneralization

Chang, W.-L., & Hen, R. (2024) · Advances in neurobiology · doi:10.1007/978-3-031-62983-9_10 · Cited by 8 · see citing works

Changes in spatial self-consciousness elicit grid cell–like representation in the entorhinal cortex

Moon, H.-J., Albert, L., Falco, E. D., Tasu, C., Gauthier, B., Park, H.-D., & Blanke, O. (2024) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.2315758121 · Cited by 9 · see citing works

Learning cognitive maps as structured graphs for vicarious evaluationPreprint

Rikhye, R. V., Gothoskar, N., Guntupalli, J. S., Dedieu, A., Lázaro-Gredilla, M., & George, D. (2019) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/864421 · Cited by 8 · see citing works

Multiple representations in geospatial databases, the brain’s spatial cells, and deep learning algorithms

Yuan, M. (2023) · Cartography and Geographic Information Science · doi:10.1080/15230406.2023.2264758 · Cited by 7 · see citing works

Border cells without theta rhythmicity in the medial prefrontal cortex

Long, X., Deng, B., Shen, R., Yang, L. S., Chen, L., Ran, Q., Du, X., & Zhang, S. (2024) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.2321614121 · Cited by 5 · see citing works

Neural Oscillations as Representations

Martínez, M., & Artiga, M. (2021) · The British Journal for the Philosophy of Science · doi:10.1086/714914 · Cited by 6 · see citing works

Binding in hippocampal-entorhinal circuits enables compositionality in cognitive maps

Kymn, C., Mazelet, S., Thomas, A., Kleyko, D. V., Frady, E. P., Sommer, F. T., & Olshausen, B. A. (2024) · neural information processing systems · doi:10.52202/079017-1235 · Cited by 5 · see citing works

Why the neural ingredients for a language of thought are not like spatial cells (commentary on Kazanina & Poeppel, 2023)

van Bree, S. (2024) · European Journal of Neuroscience · doi:10.1111/ejn.16329 · Cited by 4 · see citing works

Gateway identity and spatial remapping in a combined grid and place cell attractor

Baumann, T., & Mallot, H. A. (2022) · Neural Networks · doi:10.1016/j.neunet.2022.10.019 · Cited by 4 · see citing works

Global remapping emerges as the mechanism for renewal of context-dependent behavior in a reinforcement learning model

Kappel, D., & Cheng, S. (2025) · Frontiers in Computational Neuroscience · doi:10.3389/fncom.2024.1462110 · Cited by 3 · see citing works

Accounting for Bias in the Estimation ofr2between Two Sets of Noisy Neural Responses

Pospisil, D. A., & Bair, W. (2022) · Journal of Neuroscience · doi:10.1523/jneurosci.0198-22.2022 · Cited by 3 · see citing works

Bimodal Remapping of Visual GridsPreprint

Long, X., Cai, J., Deng, B., Chen, Z. S., & Zhang, S. (2021) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2021.10.30.466568 · Cited by 3 · see citing works

Representational similarity supports rapid context retrieval during fear discrimination in ventral hippocampusPreprint

Rozeske, R. R., Runtz, L., Keinath, A. T., Sossin, A., & Brandon, M. P. (2023) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2023.09.08.556889 · Cited by 3 · see citing works

Learning Conjunctive RepresentationsPreprint

Pettersen, M. B., Rogge, F. S., & Lepperød, M. E. (2024) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2024.05.30.596595 · Cited by 3 · see citing works

Adaptation of hippocampal spatial and contextual representations to task structure

Nyilas, R., Kelemen, A. B., Lükő, B., Sümegi, M., Ujfalussy, B. B., & Makara, J. K. (2025) · Science Advances · doi:10.1126/sciadv.adu4899 · Cited by 3 · see citing works

The relevance of context in memory tasks influences the magnitude of hippocampal remapping

Tarcsay, G., Masala, N., Yi, J. D., Igarashi, M. K., Redic, U. J., & Ewell, L. A. (2025) · Cell Reports · doi:10.1016/j.celrep.2025.116682 · Cited by 3 · see citing works

Behavioural interference at event boundaries reduces long-term memory performance in the virtual water maze task without affecting working memory performance

Pahlenkemper, M., Bernhard, H., Reithler, J., & Roberts, M. J. (2024) · Cognition · doi:10.1016/j.cognition.2024.105859 · Cited by 2 · see citing works

Developmental exposure to legacy environmental contaminants, medial temporal lobe volumes and spatial navigation memory in late adolescents

Bastien, K., Muckle, G., Ayotte, P., Dodge, N. C., Jacobson, J. L., Jacobson, S. W., & Saint‐Amour, D. (2025) · Environmental Research · doi:10.1016/j.envres.2025.120830 · Cited by 2 · see citing works

Object-translocation induces event coding in the rat hippocampus

Duan, Y., Hu, S.-Y., Ge, X.-F., Long, J.-L., Deng, C., Sun, Y.-M., Li, C.-J., Zhang, R., Cai, X., & Lu, L. (2025) · Communications Biology · doi:10.1038/s42003-025-08241-2 · Cited by 2 · see citing works

A Brain-Inspired Adaptive Space Representation Model Based on Grid Cells and Place Cells

Han, K., Wu, D., & Lai, L. (2020) · Computational Intelligence and Neuroscience · doi:10.1155/2020/1492429 · Cited by 2 · see citing works

Anxiety and personality

McNaughton, N., & Gray, J. A. (2024) · Oxford University Press eBooks · doi:10.1093/oso/9780198843313.003.0012 · Cited by 2 · 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

Gateway Identity and Spatial Remapping in a Combined Grid and Place Cell AttractorPreprint

Baumann, T., & Mallot, H. A. (2022) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2022.05.11.491479 · Cited by 2 · see citing works

Transient DREADD Manipulation of the Dorsal Dentate Gyrus in Rats Impairs Initial Learning of Place‐Outcome Associations

Lim, J., Souiki, A., Ahmad, P., Oomen, C. A., Veld, G. H. I. ’., Lansink, C. S., Pennartz, C. M. A., & Olcese, U. (2025) · Hippocampus · doi:10.1002/hipo.70014 · Cited by 1 · see citing works

Partial EC outputs by degraded cues are amplified in hippocampal CA3 circuits for retrieving stored patterns

Eom, K. (2023) · PLoS ONE · doi:10.1371/journal.pone.0281458 · Cited by 1 · see citing works

Fundamentals of the septo-hippocampal system

McNaughton, N., & Gray, J. A. (2024) · Oxford University Press eBooks · doi:10.1093/oso/9780198843313.003.0009 · Cited by 1 · see citing works

Memory and the septo-hippocampal system

McNaughton, N., & Gray, J. A. (2024) · Oxford University Press eBooks · doi:10.1093/oso/9780198843313.003.0008 · Cited by 1 · see citing works

Hippocampal Physiology in the Behaving Animal

Krupic, J., & O'Keefe, J. M. (2025) · Oxford University Press eBooks · doi:10.1093/med/9780190065324.003.0011 · Cited by 1 · see citing works

Growth Hormone Alters Remapping in the Hippocampal Area CA1 in a Novel Environment

Haugland, K. G., Jordbræk, S. V., Knutsen, E., Kjelstrup, K. B., & Brun, V. H. (2025) · eNeuro · doi:10.1523/eneuro.0237-24.2024 · Cited by 1 · see citing works

Attenuated heterogeneity of hippocampal neuron subsets in response to novelty induced by amyloid-β

Ren, X., Wang, Y., Li, X., Wang, X., Liu, Z., Yang, J., Wang, L., & Zheng, C. (2025) · Cognitive Neurodynamics · doi:10.1007/s11571-025-10237-x · Cited by 1 · see citing works

The Neural Ingredients for a Language of Thought are AvailablePreprint

Kazanina, N., & Poeppel, D. (2023) · doi:10.31234/osf.io/7rqkb · Cited by 1 · see citing works

Does Bodily Action Shape Spatial Representation? Evidence from Virtual Reality, Sensory Augmentation and Map LearningPreprint

Kuske, N., & Clay, V. (2023) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2023.10.15.562402 · Cited by 1 · see citing works

Transient DREADD manipulation of the dorsal Dentate Gyrus in rats impairs disambiguation of similar place-outcome associationsPreprint

Lim, J., Souiki, A., Ahmad, P., Oomen, C. A., Veld, G. H. I. ’., Lansink, C. S., Pennartz, C. M. A., & Olcese, U. (2024) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2024.02.20.581173 · Cited by 1 · see citing works

Modeling flexible behavior with remapping-based hippocampal sequence learningPreprint

Ito, Y., & Toyoizumi, T. (2025) · eLife · doi:10.7554/elife.106506 · Cited by 2 · see citing works

Dentate gyrus amplifies rate-based coding while sparing global remapping across the CA3 transverse axisPreprint

Hu, S.-Y., Duan, Y.-L., Long, J.-L., Cai, X., & Lu, L. (2025) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.64898/2025.12.04.692471 · Cited by 1 · see citing works

Cellular- and network-level regulation of place cell activity mediated by activity-dependent gene, Arc

Yuan, L. (2019) · doi:10.32657/10220/49828

Brain-Inspired Spatial Representation Based on Grid Cells with Finite-Spacing Firing Field

Han, K., Wu, D., & Lai, L. (2019) · Chinese Automation Congress · doi:10.1109/cac48633.2019.8996913

Grid Cells Lose Coherence in Realistic Environments

Luo, Y., Toso, M., Si, B., Stella, F., & Treves, A. (2021) · IntechOpen eBooks · doi:10.5772/intechopen.100310

Drift and stabilization of cortical response selectivity

Schmidt, A. (2021) · doi:10.53846/goediss-8733

Adult born hippocampal granule cells promote pattern separation by bidirectionally modulating the remapping of place and cue cellsPreprint

Tuncdemir, S. N., Grosmark, A., Chung, H., Luna, V. M., Lacefield, C., Losonczy, A., & Hen, R. (2022) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2022.12.08.519632

Homogenous HippocampusPreprint

McNaughton, N., & Bannerman, D. M. (2024) · doi:10.31219/osf.io/a458n

What do hippocampal cell fields represent?

McNaughton, N., & Gray, J. A. (2024) · Oxford University Press eBooks · doi:10.1093/oso/9780198843313.003.0007

Overview

McNaughton, N., & Gray, J. A. (2024) · Oxford University Press eBooks · doi:10.1093/oso/9780198843313.003.0001

The neurology of anxiety—planning circuits

McNaughton, N., & Gray, J. A. (2024) · Oxford University Press eBooks · doi:10.1093/oso/9780198843313.003.0011

A theory of the septo-hippocampal system (SHS)

McNaughton, N., & Gray, J. A. (2024) · Oxford University Press eBooks · doi:10.1093/oso/9780198843313.003.0010

Symptoms and syndromes of anxiety

McNaughton, N., & Gray, J. A. (2024) · Oxford University Press eBooks · doi:10.1093/oso/9780198843313.003.0013

The neurology of anxiety—survival circuits

McNaughton, N., & Gray, J. A. (2024) · Oxford University Press eBooks · doi:10.1093/oso/9780198843313.003.0006

Ethology and anxiety

McNaughton, N., & Gray, J. A. (2024) · Oxford University Press eBooks · doi:10.1093/oso/9780198843313.003.0002

The treatment of anxiety and fear disorders

McNaughton, N., & Gray, J. A. (2024) · Oxford University Press eBooks · doi:10.1093/oso/9780198843313.003.0014

Epigraph

McNaughton, N., & Gray, J. A. (2024) · Oxford University Press eBooks · doi:10.1093/oso/9780198843313.002.0011

Coda

McNaughton, N., & Gray, J. A. (2024) · Oxford University Press eBooks · doi:10.1093/oso/9780198843313.003.0015

Abbreviations

McNaughton, N., & Gray, J. A. (2024) · Oxford University Press eBooks · doi:10.1093/oso/9780198843313.002.0009

The anxiolytic drugs—our key tool

McNaughton, N., & Gray, J. A. (2024) · Oxford University Press eBooks · doi:10.1093/oso/9780198843313.003.0004

Learning theory and anxiety

McNaughton, N., & Gray, J. A. (2024) · Oxford University Press eBooks · doi:10.1093/oso/9780198843313.003.0003

List of online appendices and reviews

McNaughton, N., & Gray, J. A. (2024) · Oxford University Press eBooks · doi:10.1093/oso/9780198843313.002.0010

A conceptual theory of the goal inhibition system

McNaughton, N., & Gray, J. A. (2024) · Oxford University Press eBooks · doi:10.1093/oso/9780198843313.003.0005

Preface

McNaughton, N., & Gray, J. A. (2024) · Oxford University Press eBooks · doi:10.1093/oso/9780198843313.002.0006

Copyright Page

McNaughton, N., & Gray, J. A. (2024) · Oxford University Press eBooks · doi:10.1093/oso/9780198843313.002.0004

Dedication

McNaughton, N., & Gray, J. A. (2024) · Oxford University Press eBooks · doi:10.1093/oso/9780198843313.002.0005

References

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Object-translocation induces event coding in the hippocampusPreprint

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Modeling flexible behavior with remapping-based hippocampal sequence learning

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Redefining Driver Education and Training for Automated VehiclesPreprint

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Localized Space Coding and Phase Coding Complement Each Other to Achieve Robust and Efficient Spatial RepresentationPreprint

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The intermediate hippocampus integrates shock-observation and spatial information during observational fear memory in male rats

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Modeling flexible behavior with remapping-based hippocampal sequence learningPreprint

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A disynaptic pathway linking the cerebellum to the hippocampus

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Remapping of Place Cells in the Dorsal and Ventral Hippocampus in Response to Environmental Change

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