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The promise of low-tech intervention in a high-tech era: Remodeling pathological brain circuits using behavioral reverse engineering

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Grid codes underlie multiple cognitive maps in the human brain

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Lost in space(s): Multimodal neuroimaging of disorientation along the Alzheimer's disease continuum

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Bats

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Territorial blueprint in the hippocampal system

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Transitional gradation and the distinction between episodic and semantic memory

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Sensory cortex plasticity supports auditory social learning

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Neuronal ensemble dynamics in social memory

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Sense of self impacts spatial navigation and hexadirectional coding in human entorhinal cortexPreprint

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Advertisement vocalizations support home-range defense in the singing mouse

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Extending neural systems for navigation to hunting behavior

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What is a cognitive map? Organising knowledge for flexible behaviourPreprint

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Temporal encoding in deep reinforcement learning agents

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Evaluation of alfaxalone and midazolam with or without flumazenil reversal in Egyptian fruit bats (Rousettus aegyptiacus)

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Socio-sexual processing in cortical circuits

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Hippocampus and Hippocampal Neurons

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A unifying mechanism governing inter-brain neural relationship during social interactions

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Neuronal activity underlying vocal production in bats

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Hippocampal Revolutions

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Social Learning of a Spatial Task by Observation Alone

Doublet, T., Nosrati, M., & Kentros, C. G. (2022) · Frontiers in Behavioral Neuroscience · doi:10.3389/fnbeh.2022.902675 · Cited by 8

Mental Time Travel: A Retrospective

Redish, A. D. (2024) · Hippocampus · doi:10.1002/hipo.23661 · Cited by 8

Navigation in a Space With Moving Objects: Rats Can Avoid Specific Locations Defined With Respect to a Moving Robot

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

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Superposition mechanism as a neural basis for understanding others

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Social navigation modulates the anterior and posterior hippocampal circuits in the resting brain

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Quantifying Extrinsic Curvature in Neural Manifolds

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Imagining and Experiencing the Self on Cognitive Maps

Arzy, S., & Dafni‐Merom, A. (2020) · Cambridge University Press eBooks · doi:10.1017/9781108580298.020 · Cited by 7

Single-neuron representations of spatial targets in humansPreprint

Tsitsiklis, M., Miller, J., Qasim, S. E., Inman, C. S., Gross, R. E., Willie, J. T., Smith, E. H., Sheth, S. A., Schevon, C. A., Sperling, M. R., et al. (2019) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/523753 · Cited by 6

Hippocampal Morphological Alterations and Oxidative Stress in Autism Spectrum Disorder Model Induced by Prenatal Exposure to Valproic Acid in Male and Female Mice

Bouargane, Z., Moubarrad, F. L., Anouar, Y., Boukhzar, L., Bennis, M., & Ba-M’hamed, S. (2025) · Hippocampus · doi:10.1002/hipo.70024 · Cited by 5

Primate neuroethology: a new synthesis

Parodi, F., Kording, K. P., & Platt, M. L. (2025) · Trends in Cognitive Sciences · doi:10.1016/j.tics.2025.09.002 · Cited by 4

Linking cognitive strategy, neural mechanism, and movement statistics in group foraging behaviors

Urbaniak, R., Xie, M., & Mackevicius, E. L. (2024) · Scientific Reports · doi:10.1038/s41598-024-71931-0 · Cited by 4

Brain Rhythms Provide a Framework for Neural Syntax

Buzsáki, G. (2019) · Oxford University Press eBooks · doi:10.1093/oso/9780190905385.003.0006 · Cited by 3

Double Electrode Experiments Reveal the Processes Occurring at PEDOT-Coated Neural Electrode Arrays

Zhang, Y., Chen, Y., Contera, S., & Compton, R. G. (2024) · ACS Applied Materials & Interfaces · doi:10.1021/acsami.4c05204 · Cited by 4

Brain rhythms that help us to detect borders

Spiers, H. J. (2020) · Nature · doi:10.1038/d41586-020-03576-8 · Cited by 4

Five discoveries of Volodymyr Betz. Part one. Betz and the islands of entorhinal cortex

Medvediev, V. V., Cherkasov, V., Vaslovych, V. V., & Tsymbaliuk, V. (2023) · Ukrainian Scientific Medical Youth Journal · doi:10.32345/usmyj.1(136).2023.30-59 · Cited by 5

Social spatial cognition: social distance dynamics as an identifier of social interactions

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Author response: Neural Trajectories of Conceptually Related Events

Schafer, M., Kamilar-Britt, P., Sahani, V., Bachi, K., & Schiller, D. (2024) · eLife · doi:10.7554/elife.96895.1.sa3 · Cited by 3

Asymmetric Social Representations in the Prefrontal Cortex for Cooperative BehaviorPreprint

Cheng, Y., Chen, Y., Kwak, M., Kempner, R. P., Singha, R. G., Winslow, J., Liu, R., Khan, U., Spangler, T., Khan, A., et al. (2025) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2025.08.27.672249 · Cited by 4

Constructing Memories, Episodic and Semantic

Gentry, H. (2025) · Cognitive Science · doi:10.1111/cogs.70113 · Cited by 3

20 years of concept cells: From invariant responses to a unique coding of human memory

Quiroga, R. Q. (2026) · Neuron · doi:10.1016/j.neuron.2026.01.026 · Cited by 3

Sparse-to-dense coding transformation between hippocampal areas CA3 and CA1

Maimon, S. R., Eliav, T., Aljadeff, J., Shalev, A., Gronich, Y., Finger, N. M., Eveland, K. E., Moss, C. F., Las, L., & Ulanovsky, N. (2026) · Nature · doi:10.1038/s41586-026-10537-0 · Cited by 7

Fifty years of the brain’s sense of space

Low, I. I. C., & Giocomo, L. M. (2021) · Nature · doi:10.1038/d41586-021-03010-7 · Cited by 3

Navigating space and the developing mind

Németh, A. R., Stojić, S., & Nádasdy, Z. (2025) · Frontiers in Psychology · doi:10.3389/fpsyg.2025.1521487 · Cited by 4

Auditory object representation in the bat hippocampus

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Linking global top-down views to first-person views in the brain

Xing, J., Chrastil, E. R., Nitz, D. A., & Krichmar, J. L. (2022) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.2202024119 · Cited by 3

Auditory cortical regions show resting-state functional connectivity with the default mode-like network in echolocating bats

Washington, S. D., Shattuck, K. F., Steckel, J., Peremans, H., Jonckers, E., Hinz, R., Venneman, T., van den Berg, M., Ruijssevelt, L. V., Verellen, T., et al. (2024) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.2306029121 · Cited by 3

Impaired remapping of social relationships in older adults

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Dissecting social decision-making: A spotlight on oxytocinergic transmission

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Hippocampal coding of conspecific position

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The Problem

Buzsáki, G. (2019) · Oxford University Press eBooks · doi:10.1093/oso/9780190905385.003.0001 · Cited by 4

Neural Trajectories of Conceptually Related EventsPreprint

Schafer, M., Kamilar-Britt, P., Sahani, V., Bachi, K., & Schiller, D. (2023) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2023.12.04.569670 · Cited by 4

Home Ranges of Animals

Powell, R. A. (2025) · Oxford University Press eBooks · doi:10.1093/9780191949142.001.0001 · Cited by 2

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

A Comprehensive Review of Brain-inspired Navigation

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Asymmetric prefrontal representations for leader–follower dynamics

Cheng, Y., Chen, Y., Kwak, M., Kempner, R. P., Singha, R. G., Winslow, J., Liu, R., Khan, U., Spangler, T., Khan, A., et al. (2026) · Nature · doi:10.1038/s41586-026-10900-1 · Cited by 4

100 bats and a long, dark tunnel: one neuroscientist’s quest to unlock the secrets of 3D navigation

Abbott, A. (2018) · Nature · doi:10.1038/d41586-018-05648-2 · Cited by 2

Distance- rather than location-based temporal judgments are more accurate during episodic recall in a real-world task

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Mice integrate conspecific and contextual information in forming social episodic-like memories under spontaneous recognition task conditions

Ross, T. W., Poulter, S. L., Lever, C., & Easton, A. (2024) · Scientific Reports · doi:10.1038/s41598-024-66403-4 · Cited by 4

Neurobiology of social interactions across species

Keysers, C., & Gazzola, V. (2025) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2025.106001 · Cited by 2

Diminished Social Memory and Hippocampal Correlates of Social Interactions in Chronic Social Defeat Stress Susceptibility

Larosa, A., Zhang, T. R., Wong, A. S., Fung, C. Y. H., Long, X. L. Y. (., Singh, P., Fung, B. C. M., & Wong, T. P. (2025) · Biological Psychiatry Global Open Science · doi:10.1016/j.bpsgos.2025.100455 · Cited by 2

Internally Organized Cell Assembly Trajectories

Buzsáki, G. (2019) · Oxford University Press eBooks · doi:10.1093/oso/9780190905385.003.0007 · Cited by 1

Recording central nervous system responses of freely-swimming marine and freshwater fishes with a customizable, implantable AC differential amplifier

Gibbs, B. J., Strother, J. A., & Liao, J. C. (2023) · Journal of Neuroscience Methods · doi:10.1016/j.jneumeth.2023.109850 · Cited by 2

Perception from Action

Buzsáki, G. (2019) · Oxford University Press eBooks · doi:10.1093/oso/9780190905385.003.0003 · Cited by 1

Advancements in the study of neural mechanisms underlying mammalian grouping behaviour

Kelly, A. M. (2023) · Frontiers in Ethology · doi:10.3389/fetho.2023.1273613 · Cited by 1

Competition and cooperation of assembly sequences in recurrent neural networks

Stöber, T. M., Lehr, A. B., Nikzad, A., Ganjtabesh, M., Fyhn, M., & Kumar, A. (2025) · PLoS Computational Biology · doi:10.1371/journal.pcbi.1013403 · Cited by 1

Social remapping of spatial coding along the dorsoventral axis of the mouse prefrontal cortex

Cohen, L., Mohapatra, A. N., Netser, S., Wagner, S., & Stark, E. (2025) · Cell Reports · doi:10.1016/j.celrep.2025.116319 · Cited by 1

Foraging Optimally for a Home Range

Powell, R. A. (2025) · Oxford University Press eBooks · doi:10.1093/9780191949142.003.0008 · Cited by 1

Territories

Powell, R. A. (2025) · Oxford University Press eBooks · doi:10.1093/9780191949142.003.0002 · Cited by 1

A Framework for Sensory‐to‐Memory Weighting During Navigation

Finger, N. M., Drieskens, D. C., & Moss, C. F. (2025) · Annals of the New York Academy of Sciences · doi:10.1111/nyas.70112 · Cited by 2

An 'other' kind of place cell

Bray, N. (2018) · Nature reviews. Neuroscience · doi:10.1038/nrn.2018.12 · Cited by 1

Causation and Logic in Neuroscience

Buzsáki, G. (2019) · Oxford University Press eBooks · doi:10.1093/oso/9780190905385.003.0002 · Cited by 1

Challenges for Place and Grid Cell Models

Soldatkina, O., Schönsberg, F., & Treves, A. (2021) · Advances in experimental medicine and biology · doi:10.1007/978-3-030-89439-9_12 · Cited by 1

Space and Time in the Brain

Buzsáki, G. (2019) · Oxford University Press eBooks · doi:10.1093/oso/9780190905385.003.0010 · Cited by 1

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

Not so griddy: Internal representations of RNNs path integrating more than one agent

Redman, W. T., Acosta–Mendoza, S., Acosta–Mendoza, S., & Miolane, N. (2024) · neural information processing systems · doi:10.52202/079017-0713 · Cited by 2

The hippocampus encodes delay and value information during delay-discounting decision makingPreprint

Masuda, A., Sano, C., Zhang, Q., Goto, H., McHugh, T. J., Fujisawa, S., & Itohara, S. (2018) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/495598 · Cited by 1

The role of hippocampus during observational learningPreprint

Fuentealba, Y., & Valdés, J. L. (2019) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/832758 · Cited by 2

Hippocampal Place-like Signal in Latent SpacePreprint

Schafer, M., Kamilar-Britt, P., Sahani, V., Bachi, K., & Schiller, D. (2022) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2022.07.15.499827 · Cited by 1

Entorhinal grid-like codes and time-locked network dynamics track others navigating through spacePreprint

Wagner, I. C., Graichen, L. P., Todorova, B., Lüttig, A., Omer, D. B., Stangl, M., & Lamm, C. (2022) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2022.10.08.511403 · Cited by 1

Observational activation of anterior cingulate cortical neurons coordinates hippocampal replay in social learningPreprint

Mou, X., & Ji, D. (2024) · eLife · doi:10.7554/elife.97884 · Cited by 3

Observational activation of anterior cingulate cortical neurons coordinates hippocampal replay in social learningPreprint

Mou, X., & Ji, D. (2024) · eLife · doi:10.7554/elife.97884.1 · Cited by 1

Information transfer from spatial to social distance in rats: implications for the role of the posterior parietal cortex in spatial-social integrationPreprint

Wise, T. B., Templer, V. L., & Burwell, R. D. (2024) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2024.10.14.618305 · Cited by 1

A neuro‐behavioural model of neophobia

Dorfman, A., Subach, A., & Scharf, I. (2026) · Biological Reviews · doi:10.1002/brv.70151

‘Bat-nav’ reveals how the brain tracks other animals

Abbott, A. (2018) · Nature · doi:10.1038/d41586-018-00484-w

Gain and Abstraction

Buzsáki, G. (2019) · Oxford University Press eBooks · doi:10.1093/oso/9780190905385.003.0011

Everything Is a Relationship

Buzsáki, G. (2019) · Oxford University Press eBooks · doi:10.1093/oso/9780190905385.003.0012

Internalization of Experience

Buzsáki, G. (2019) · Oxford University Press eBooks · doi:10.1093/oso/9780190905385.003.0005

The Brain’s Best Guess

Buzsáki, G. (2019) · Oxford University Press eBooks · doi:10.1093/oso/9780190905385.003.0013

Enhancing Brain Performance by Externalizing Thought

Buzsáki, G. (2019) · Oxford University Press eBooks · doi:10.1093/oso/9780190905385.003.0009

Internally Organized Activity During Offline Brain States

Buzsáki, G. (2019) · Oxford University Press eBooks · doi:10.1093/oso/9780190905385.003.0008

Neuronal Assembly

Buzsáki, G. (2019) · Oxford University Press eBooks · doi:10.1093/oso/9780190905385.003.0004

Neuroscientists are questing to unlock the secrets of three-dimensional navigation in the brains of bats

Fu, Z., Tang, J., & Chen, Q.-C. (2019) · Chinese Science Bulletin (Chinese Version) · doi:10.1360/tb-2019-0404

The Rise of Endothermy

Striedter, G. F., & Northcutt, R. G. (2019) · Oxford University Press eBooks · doi:10.1093/oso/9780195125689.003.0006

Biological Reinforcement Learning via Predictive Spacetime EncodingPreprint

Yang, M. A., Lee, J. H., & Lee, S. W. (2020) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2020.08.21.260844

Epilogue

Buzsáki, G. (2019) · Oxford University Press eBooks · doi:10.1093/oso/9780190905385.003.0014

Understanding from the Inside

Rizzolatti, G., & Sinigaglia, C. (2023) · Oxford University Press eBooks · doi:10.1093/oso/9780198871705.003.0006

An 'other' kind of place cell

Bray, N. (2018) · Nature reviews. Neuroscience · doi:10.1038/nrn.2018.12 · Cited by 1

Multiplexed representation of others in the hippocampal CA1 subfield of female mice

Zhang, X., Cao, Q., Gao, K., Chen, C., Cheng, S., Li, A. A., Zhou, Y., Liu, R., Hao, J., Kropff, E., et al. (2024) · Nature Communications · doi:10.1038/s41467-024-47453-8 · Cited by 18

Hippocampal coding of identity, sex, hierarchy, and affiliation in a social group of wild fruit bats

Ray, S., Yona, I., Elami, N., Palgi, S., Latimer, K. W., Jacobsen, B., Witter, M. P., Las, L., & Ulanovsky, N. (2025) · Science · doi:10.1126/science.adk9385 · Cited by 35

Spatial representations of self and other in the hippocampus

Danjo, T., Toyoizumi, T., & Fujisawa, S. (2018) · Science · doi:10.1126/science.aao3898 · Cited by 264

Social Spaces: Place Cells Represent the Locations of Others

Duvelle, É., & Jeffery, K. J. (2018) · Current Biology · doi:10.1016/j.cub.2018.02.017 · Cited by 20