Cited by 606Memory and Neural MechanismsSpatial Cognition and NavigationNeurogenesis and neuroplasticity mechanisms

The DOI matches its Crossref record; 24 of the 24 references it cites were found in a registry or an index.

Place Cells and Place Recognition Maintained by Direct Entorhinal-Hippocampal Circuitry

Brun, Vegard H., Otnæss, Mona K., Molden, Sturla, Steffenach, Hill-Aina, Witter, Menno P., Moser, May-Britt, Moser, Edvard I.·2002·Science

DOI 10.1126/science.1071089

Open this paper in CoChat — free account

Abstract

Place cells in hippocampal area CA1 may receive positional information from the intrahippocampal associative network in area CA3 or directly from the entorhinal cortex. To determine whether direct entorhinal connections support spatial firing and spatial memory, we removed all input from areas CA3 to CA1, thus isolating the CA1 area. Pyramidal cells in the isolated CA1 area developed sharp and stable place fields. Rats with an isolated CA1 area showed normal acquisition of an associative hippocampal-dependent spatial recognition task. Spatial recall was impaired. These results suggest that the hippocampus contains two functionally separable memory circuits: The direct entorhinal-CA1 system is sufficient for recollection-based recognition memory, but recall depends on intact CA3-CA1 connectivity.

Integrity signals

Registry

Crossref · 10.1126/science.1071089

Cites

24 of 24 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
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
The three-dimensional organization of the hippocampal formation: A review of anatomical data
Amaral, D. G., & Witter, M. P. (1989) · Neuroscience · doi:10.1016/0306-4522(89)90424-7 · Cited by 2,180
Self-citation
A cortical–hippocampal system for declarative memory
Eichenbaum, H. (2000) · Nature reviews. Neuroscience · doi:10.1038/35036213 · Cited by 1,817
Recognition memory: What are the roles of the perirhinal cortex and hippocampus?
Brown, M. W., & Aggleton, J. P. (2001) · Nature reviews. Neuroscience · doi:10.1038/35049064 · Cited by 1,624
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
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
Spatial learning with a minislab in the dorsal hippocampus.
Moser, M., Moser, E. I., Forrest, E., Andersen, P. N., & Morris, R. (1995) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.92.21.9697 · Cited by 944
Self-citation
Neural Networks and Brain Function
Rolls, E. T., & Treves, A. (1997) · Oxford University Press eBooks · doi:10.1093/acprof:oso/9780198524328.001.0001 · Cited by 885

Flagged first, then by citations

Show all 24 references

Research works printed but not linked: 3

Dostrovsky J., Brain Res. 34, 171 (1971).
K. Nakazawa et al. Science in press; published online 30 May 2002 (10.1126/science.1071795). · DOI
We thank R. Biegler and R. G. M. Morris for discussion and I. M. F. Hammer K. Haugen K. Jenssen and R. Ulriksen for technical assistance. Supported by the European Commission (Framework 5; QLG3-CT-1999-00192) and the Norwegian Research Council (139786/300 133958/420). Supporting Online Material www.sciencemag.org/cgi/content/full/296/5576/2243/DC1 Materials and Methods Fig. S1 Movie S1

Sorted by citations

Items 401–500 of 599

Predictive Place-Cell Sequences for Goal-Finding Emerge from Goal Memory and the Cognitive Map: A Computational Model
Gönner, L., Vitay, J., & Hamker, F. H. (2017) · Frontiers in Computational Neuroscience · doi:10.3389/fncom.2017.00084 · Cited by 16
Spatial Navigation
Jin, W., Qin, H., Zhang, K., & Chen, X. (2020) · Advances in experimental medicine and biology · doi:10.1007/978-981-15-7086-5_7 · Cited by 15
Parallel processing of information about location in the amygdala, entorhinal cortex and hippocampus
Gaskin, S., & White, N. M. (2013) · Hippocampus · doi:10.1002/hipo.22179 · Cited by 12
Low-Resolution Place and Response Learning Capacities in Down Syndrome
Bostelmann, M., Costanzo, F., Martorana, L., Menghini, D., Vicari, S., Lavenex, P. B., & Lavenex, P. (2018) · Frontiers in Psychology · doi:10.3389/fpsyg.2018.02049 · Cited by 13
A low noise remotely controllable wireless telemetry system for single-unit recording in rats navigating in a vertical maze
Chen, H., Wu, J.-S., Hyland, B. I., Lu, X.-D., & Chen, J. J. J. (2008) · Medical & Biological Engineering & Computing · doi:10.1007/s11517-008-0355-6 · Cited by 13
Maternal exposure to TCDD during gestation advanced sensory-motor development, but induced impairments of spatial learning and memory in adult male rat offspring
Zhang, H.-J., Liu, Y.-N., Xian, P., Ma, J., Sun, Y., Chen, J., Chen, X., & Tang, N. (2018) · Chemosphere · doi:10.1016/j.chemosphere.2018.08.118 · Cited by 13
Postnatal development of the entorhinal cortex: A stereological study in macaque monkeys
Piguet, O., Chareyron, L. J., Lavenex, P. B., Amaral, D. G., & Lavenex, P. (2020) · The Journal of Comparative Neurology · doi:10.1002/cne.24897 · Cited by 12
Local activation of CA1 pyramidal cells induces theta-phase precession
Sloin, H. E., Spivak, L., Levi, A., Gattegno, R., Someck, S., & Stark, E. (2024) · Science · doi:10.1126/science.adk2456 · Cited by 12
Paradoxical Sleep as a Tool for Understanding the Hippocampal Mechanisms of Contextual Memory
Silkis, I. G. (2009) · Neuroscience and Behavioral Physiology · doi:10.1007/s11055-009-9230-7 · Cited by 12
Proximodistal Heterogeneity in Learning-promoted Pathway-specific Plasticity at Dorsal CA1 Synapses
Paw-Min-Thein-Oo, Sakimoto, Y., Kida, H., & Mitsushima, D. (2020) · Neuroscience · doi:10.1016/j.neuroscience.2020.04.040 · Cited by 12
The Hippocampal System as the Cortical Resource Manager: A Model Connecting Psychology, Anatomy and Physiology
Coward, L. A. (2009) · Advances in experimental medicine and biology · doi:10.1007/978-0-387-79100-5_18 · Cited by 13
The Ins and Outs of Hippocampal Circuits
Tonegawa, S., & McHugh, T. J. (2008) · Neuron · doi:10.1016/j.neuron.2008.01.005 · Cited by 12
Reactivating Memories for Consolidation
Jadhav, S. P., & Frank, L. M. (2009) · Neuron · doi:10.1016/j.neuron.2009.06.002 · Cited by 12
Organization of cortico-hippocampal networks in rats related to learning and memory
Witter, M. P. (2003) · International Congress Series · doi:10.1016/s0531-5131(03)01014-8 · Cited by 12
Self-citation
Sound-induced hyperpolarization of hippocampal neurons
Abe, R., Sakaguchi, T., Matsumoto, N., Matsuki, N., & Ikegaya, Y. (2014) · Neuroreport · doi:10.1097/wnr.0000000000000206 · Cited by 12
Place-cell capacity and volatility with grid-like inputs
Yim, M. Y., Sadun, L. A., Fiete, I., & Taillefumier, T. O. (2021) · eLife · doi:10.7554/elife.62702 · Cited by 13
A Critical Review of Spatial Abilities in Down and Williams Syndromes: Not All Space Is Created Equal
Lavenex, P. B., & Lavenex, P. (2021) · Frontiers in Psychiatry · doi:10.3389/fpsyt.2021.669320 · Cited by 11
Frequency-Dependent Synaptic Dynamics Differentially Tune CA1 and CA2 Pyramidal Neuron Responses to Cortical Input
Sun, Q., Buss, E. W., Jiang, Y., Santoro, B., Brann, D. H., Nicholson, D. A., & Siegelbaum, S. A. (2021) · Journal of Neuroscience · doi:10.1523/jneurosci.0451-20.2021 · Cited by 11
The Watermaze
Morris, R. (2014) · Neuromethods · doi:10.1007/978-1-4939-2159-1_3 · Cited by 11
Hippocampal place cells as a window into cognitive aging
Wilson, I. A. (2005) · Cited by 11
Gender and cytoarchitecture differences: Functional connectivity of the hippocampal sub-regions
Alahmadi, A. A. S., Alotaibi, N. O., Hakami, N. Y., Almutairi, R. S., Darwesh, A. M. F., Abdeen, R. H., Alghamdi, J., Abdulaal, O. M., Alsharif, W. M., Sultan, S. R., et al. (2023) · Heliyon · doi:10.1016/j.heliyon.2023.e20389 · Cited by 10
Direct entorhinal control of CA1 temporal coding
Guardamagna, M., Chadney, O. M. T., Stella, F., Zhang, Q., Kentros, C. G., & Battaglia, F. P. (2025) · Nature Communications · doi:10.1038/s41467-025-61453-2 · Cited by 10
Machine learning-based segmentation of the rodent hippocampal CA2 area from Nissl-stained sections
Takeuchi, Y., Yamashiro, K., Noguchi, A., Liu, J., Mitsui, S., Ikegaya, Y., & Matsumoto, N. (2023) · Frontiers in Neuroanatomy · doi:10.3389/fnana.2023.1172512 · Cited by 10
The Structure of Hippocampal CA1 Interactions Optimizes Spatial Coding across Experience
Nardin, M., Csicsvari, J., Tkačik, G., & Savin, C. (2023) · Journal of Neuroscience · doi:10.1523/jneurosci.0194-23.2023 · Cited by 11
Experience on the Barnes Spatial Maze Influences PKCγ Levels in the Hippocampus
Nithianantharajah, J., & Murphy, M. (2009) · International Journal of Neuroscience · doi:10.1080/00207450802328508 · Cited by 10
Situationally appropriate behavior: translating situations into appetitive behavior modes
Behrendt, R. (2013) · Reviews in the Neurosciences · doi:10.1515/revneuro-2013-0037 · Cited by 9
Early classification of Alzheimer's disease phenotype based on hippocampal electrophysiology in the TgF344-AD rat model
Moradi, F., van den Berg, M., Mirjebreili, S. M., Kosten, L., Verhoye, M., Amiri, M., & Keliris, G. A. (2023) · iScience · doi:10.1016/j.isci.2023.107454 · Cited by 9
Ten Traps for Non-Representational Theory in Human Geography
Torrens, P. M. (2024) · Geographies · doi:10.3390/geographies4020016 · Cited by 9
How Many Gammas? Redefining Hippocampal Theta-Gamma Dynamic During Spatial Learning
Aguilera, M., Douchamps, V., Battaglia, D. A., & Goutagny, R. (2022) · Frontiers in Behavioral Neuroscience · doi:10.3389/fnbeh.2022.811278 · Cited by 9
Computational Models of Hippocampal Functions
Rolls, E. T. (2008) · Elsevier eBooks · doi:10.1016/b978-012370509-9.00084-x · Cited by 9
Somatic Depolarization Enhances Hippocampal CA1 Dendritic Spike Propagation and Distal Input-Driven Synaptic Plasticity
Bock, T., Negrean, A., & Siegelbaum, S. A. (2022) · Journal of Neuroscience · doi:10.1523/jneurosci.0780-21.2022 · Cited by 11
Hierarchical consciousness: the Nested Observer Windows model
Riddle, J., & Schooler, J. W. (2024) · Neuroscience of Consciousness · doi:10.1093/nc/niae010 · Cited by 8
Potential role of oxytocin in the regulation of memories and treatment of memory disorders
Walia, V., Wal, P., Mishra, S., Agrawal, A., Kosey, S., & Patil, A. D. (2024) · Peptides · doi:10.1016/j.peptides.2024.171222 · Cited by 9
The mantle of the heavens: Reflections on the 2014 nobel prize for medicine or physiology
Morris, R. (2015) · Hippocampus · doi:10.1002/hipo.22455 · Cited by 8
Sources of the spatial code within the hippocampus
Brandon, M. P., & Hasselmo, M. E. (2009) · F1000 Biology Reports · doi:10.3410/b1-3 · Cited by 8
Pattern Completion and Pattern Separation Mechanisms in the Hippocampus
Rolls, E. T. (2015) · Springer eBooks · doi:10.1007/978-3-319-15759-7_4 · Cited by 9
A computational grid-to-place-cell transformation model indicates a synaptic driver of place cell impairment in early-stage Alzheimer’s Disease
Ness, N., & Schultz, S. R. (2021) · PLoS Computational Biology · doi:10.1371/journal.pcbi.1009115 · Cited by 8
Cerebral perfusion mapping during retrieval of spatial memory in rats
Holschneider, D. P., Givrad, T. K., Yang, J., Stewart, S. A., Francis, S., Wang, Z., & Maarek, J. (2019) · Behavioural Brain Research · doi:10.1016/j.bbr.2019.112116 · Cited by 9
Post-training N-methyl-d-aspartate receptor blockade offers protection from retrograde interference but does not affect consolidation of weak or strong memory traces in the water maze
Day, M., & Langston, R. F. (2005) · Neuroscience · doi:10.1016/j.neuroscience.2005.08.040 · Cited by 8
Organization of cell assemblies that code temporal sequences in a hippocampal CA3-CA1 model
Yoshida, M., & Hayashi, H. (2005) · International Joint Conference on Neural Networks (IJCNN) · doi:10.1109/ijcnn.2004.1379959 · Cited by 8
Hippocampus and Neural Representations
Moser, E. I., & Moser, M. (2009) · Elsevier eBooks · doi:10.1016/b978-008045046-9.00767-1 · Cited by 8
Self-citation
The Hippocampal Ensemble Code for Spatial Navigation and Episodic Memory
TAKAHASHI, S. Y. (2018) · Advances in neurobiology · doi:10.1007/978-3-319-94593-4_3 · Cited by 9
Subfield variations in hippocampal processing—components of a spatial navigation system
Hartley, M., Taylor, N. R., & Taylor, J. G. (2005) · Neural Networks · doi:10.1016/j.neunet.2005.06.028 · Cited by 7
Involvement of intracellular Zn2+ signaling in LTP at perforant pathway–CA1 pyramidal cell synapse
Tamano, H., Nishio, R., & Takeda, A. (2017) · Hippocampus · doi:10.1002/hipo.22730 · Cited by 7
Learning allocentric representations of space for navigation
Zhao, D., Si, B., & Xiaoli Li, A. (2020) · Neurocomputing · doi:10.1016/j.neucom.2020.10.013 · Cited by 7
Social Interactions of Dat-Het Epi-Genotypes Differing for Maternal Origins: The Development of a New Preclinical Model of Socio-Sexual Apathy
Brancato, A., Russo, S. L. M. L., Liberati, A. S., Carbone, C., Zelli, S., Giovanni Laviola, A., Cannizzaro, C., & Adriani, W. (2021) · Biomedicines · doi:10.3390/biomedicines9070778 · Cited by 7
Dissociations in perceptual discrimination following selective damage to the dentate gyrus versus CA1 subfield of the hippocampus
Mitchnick, K. A., Labardo, S., & Rosenbaum, R. S. (2024) · Cortex · doi:10.1016/j.cortex.2024.06.020 · Cited by 6
Impaired spatial coding of the hippocampus in a dentate gyrus hypoplasia mouse model
Chen, X., Cheng, N., Wang, C., & Knierim, J. J. (2025) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.2416214122 · Cited by 7
A Place and a Grid in the Sun
Kandel, E. R. (2014) · Cell · doi:10.1016/j.cell.2014.11.033 · Cited by 7
Spine Head Calcium as a Measure of Summed Postsynaptic Activity for Driving Synaptic Plasticity
Graham, B. P., Saudargienė, A., & Cobb, S. (2014) · Neural Computation · doi:10.1162/neco_a_00640 · Cited by 6
A nonlinear hidden layer enables actor–critic agents to learn multiple paired association navigation
Ganeshkumar, M., Tan, C., Libedinsky, C., Yen, S., & Tan, A. Y. Y. (2021) · Cerebral Cortex · doi:10.1093/cercor/bhab456 · Cited by 8
Effect of ramosetron, a 5-HT3 receptor antagonist on the severity of seizures and memory impairment in electrical amygdala kindled rats
Sayahi, Z., Komaki‬, A., Jam, M. S., Karimi, S. A., Raoufi, S., Mardani, P., Naderishahab, M., Sarihi, A., & Mirnajafi‐Zadeh, J. (2022) · The Journal of Physiological Sciences · doi:10.1186/s12576-022-00825-5 · Cited by 6
Associative Memory Models of Hippocampal Areas CA1 and CA3
Graham, B. P., Cutsuridis, V., & Hunter, R. (2010) · Springer eBooks · doi:10.1007/978-1-4419-0996-1_16 · Cited by 6
Regulatory role of the cell adhesion molecule nectin‐1 in GABA ergic inhibitory synaptic transmission in the CA 3 region of mouse hippocampus
Geng, X., Mandai, K., Maruo, T., Wang, S., Fujiwara, T., Mizoguchi, A., Takai, Y., & Mori, M. (2015) · Genes to Cells · doi:10.1111/gtc.12322 · Cited by 6
Beyond the bolus: transgenic tools for investigating the neurophysiology of learning and memoryPreprint
Lykken, C. M., & Kentros, C. G. (2014) · Learning & Memory · doi:10.1101/lm.036152.114 · Cited by 6
Wire together, fire apart
Krupic, J. (2017) · Science · doi:10.1126/science.aao4159 · Cited by 7
Le codage de l’espace
Rondi‐Reig, L. (2015) · médecine/sciences · doi:10.1051/medsci/20153102018 · Cited by 6
Scene-selectivity in CA1/subicular complex: Multivoxel pattern analysis at 7T
Read, M., Berry, S. C., Graham, K. S., Voets, N., Zhang, J., Aggleton, J. P., Lawrence, A. D., & Hodgetts, C. J. (2023) · Neuropsychologia · doi:10.1016/j.neuropsychologia.2023.108783 · Cited by 6
Self-sustaining non-repetitive activity in a large scale neuronal-level model of the hippocampal circuit
Scorcioni, R., Hamilton, D. J., & Ascoli, G. A. (2008) · Neural Networks · doi:10.1016/j.neunet.2008.05.006 · Cited by 5
Neural Representations Supporting Spatial Navigation and Memory
Brown, J. E., & Taube, J. S. (2007) · Springer eBooks · doi:10.1007/978-4-431-73021-7_9 · Cited by 5
Crystals of the brain
Moser, M., & Moser, E. I. (2011) · EMBO Molecular Medicine · doi:10.1002/emmm.201000118 · Cited by 5
Self-citation
Labile glutamate signaling onto CA1 pyramidal cells in the developing hippocampus depends mechanistically on input pathway
Ma, R., Xiao, M., & Gustafsson, B. (2016) · Neuroscience · doi:10.1016/j.neuroscience.2016.09.008 · Cited by 5
Memory Development During Infancy and Early Childhood across Cultures
Hayne, H., Imuta, K., & Scarf, D. (2015) · Elsevier eBooks · doi:10.1016/b978-0-08-097086-8.23062-6 · Cited by 5
Brain region-specific gain modulation of place cells by VIP neurons
Lenkey, N., Garvert, A. C., Neubrandt, M., Kriener, B., & Vervaeke, K. (2025) · Nature Communications · doi:10.1038/s41467-025-60679-4 · Cited by 5
Repeated Morphine Exposure Alters Temporoamonic-CA1 Synaptic Plasticity in Male Rat Hippocampus
Anvari, S., Javan, M., Mirnajafi‐Zadeh, J., & Fathollahi, Y. (2024) · Neuroscience · doi:10.1016/j.neuroscience.2024.03.015 · Cited by 4
Social spatial cognition: social distance dynamics as an identifier of social interactions
Dorfman, A., & Eilam, D. (2020) · Animal Cognition · doi:10.1007/s10071-020-01441-9 · Cited by 4
In the Place Space
Bilkey, D. K. (2004) · Science · doi:10.1126/science.1102895 · Cited by 4
Investigating the role of the hippocampal formation in episodic and spatial memory
Stevenson, C. H. (2011) · ERA · Cited by 4
Dynamic Updating of Cognitive Maps via Traces of Experience in the Subiculum
Wang, F., & Bičanski, A. (2026) · Hippocampus · doi:10.1002/hipo.70078 · Cited by 4
Failure to detect entorhinal grid-like signals in a passive navigation human fMRI study
Kransberg, J., Bråthen, A. C. S., FALCH, E., Øverbye, K., Garrido, P. F., Fjell, A. M., Stangl, M., Wolbers, T., Sneve, M. H., & Walhovd, K. B. (2026) · Imaging Neuroscience · doi:10.1162/imag.a.1196 · Cited by 3
Evidence for complementary learning systems within the hippocampus
Singh, D., & Schapiro, A. C. (2026) · Philosophical Transactions of the Royal Society B Biological Sciences · doi:10.1098/rstb.2025.0243 · Cited by 3
Asynchronous inputs and NMDA conductances predict excitatory responses in the cortical-CA1 pathway of the hippocampus
Longden, K. D., & Willshaw, D. J. (2007) · Network Computation in Neural Systems · doi:10.1080/09548980701587100 · Cited by 3
Rhythmic Activity in the Hippocampus and Entorhinal Cortex is Impaired in a Model of Kainate Neurotoxicity in Rats in Free Behavior
Malkov, A., Shevkova, L., Latyshkova, A. A., & Kitchigina, V. F. (2020) · Neuroscience and Behavioral Physiology · doi:10.1007/s11055-020-01041-7 · Cited by 3
Bases neurales de la mémoire et de la navigation spatiale
Tran, T.-H., Mahzoum, R. E., Fricker, D., Cohen, I., & Bonnot, A. (2023) · médecine/sciences · doi:10.1051/medsci/2023072 · Cited by 4
Neural Encoding: The Brain’s Representation of Space
O'Flanagan, R. A., & Stevens, C. F. (2005) · Current Biology · doi:10.1016/j.cub.2005.08.006 · Cited by 3
Spatial NavigatioN iN geometric mazeS: a computatioNal model of rodeNt Behavior
Pol, É., & Lausanne, F. D. (2007) · Cited by 3
Spatial Perception and Cognition, Insights From Virtual Reality Experiments
Török, Á. (2016) · Eötvös Loránd Tudományegyetem · doi:10.15476/elte.2015.213 · Cited by 3
Alcohol outcomes on anxiety, impulsivity and spatial memory: Possible Omega-3 amelioration effects
Cabrera, V., Abate, P., Balaszczuk, V., & Macchione, A. F. (2025) · Progress in Neuro-Psychopharmacology and Biological Psychiatry · doi:10.1016/j.pnpbp.2025.111281 · Cited by 2
Thalamocortical white matter connectivity and the entorhinal cortex as neural correlates of electroconvulsive therapy response in patients with schizophrenia spectrum disorder
Kim, M., Choe, E., Park, H., Lho, S. K., Moon, S., Oh, S., & Kwon, J. S. (2025) · Brain stimulation · doi:10.1016/j.brs.2025.06.007 · Cited by 2
The navigation system of the brain
Venkhatesh, P., V (2015) · Resonance · doi:10.1007/s12045-015-0198-z · Cited by 2
Neuroligin-3-Mediated Synapse Formation Strengthens Interactions between Hippocampus and Barrel Cortex in Associative Memory
Xiao, H., Xu, Y., Cui, S., & Wang, J.-H. (2024) · International Journal of Molecular Sciences · doi:10.3390/ijms25020711 · Cited by 2
The Inner Ear and Aging Brain: A Cross-Sectional Study of Vestibular Function and Morphometric Variations in the Entorhinal and Trans-Entorhinal Cortex
Vania, C. J., Padova, D., Ratnanather, J. T., & Agrawal, Y. (2025) · Journal of the Association for Research in Otolaryngology · doi:10.1007/s10162-025-00977-2 · Cited by 2
Investigating the relationship between allocentric spatial working memory and biomarker status in preclinical and prodromal Alzheimer’s disease
Lorentzen, I. M., Espenes, J., Eliassen, I. V., Hessen, E., Waterloo, K. K., Nakling, A. E., Gísladóttir, B., Jarholm, J. A., Fladby, T., & Kirsebom, B. (2023) · Applied Neuropsychology Adult · doi:10.1080/23279095.2023.2236262 · Cited by 2
Estimating neuronal firing density: A quantitative analysis of firing rate map algorithms
Grieves, R. M. (2023) · PLoS Computational Biology · doi:10.1371/journal.pcbi.1011763 · Cited by 4
Cortical Morphometric Similarity Remodeling in Traumatic Brain Injury Links Cognitive Impairments with Transcriptional Changes and Type‐Specific Cells
Pan, Y., Wang, Z., Zhang, X., Zhao, W., Zhang, H., Li, X., Jia, X., Ji, Q., Yin, B., Bai, G., et al. (2025) · Advanced Science · doi:10.1002/advs.202415262 · Cited by 2
Heterosynaptic modulation of evoked synaptic potentials in layer II of the entorhinal cortex by activation of the parasubiculum
Sparks, D. W., & Chapman, C. A. (2016) · Journal of Neurophysiology · doi:10.1152/jn.00095.2016 · Cited by 2
Changes in brain synapse–related molecules with age
Mizutani, K., & Takai, Y. (2021) · Elsevier eBooks · doi:10.1016/b978-0-12-817990-1.00017-2 · Cited by 2
Dendritic spiking accounts for rate and phase coding in a biophysical model of a hippocampal place cell
Huhn, Z., Lengyel, M., Orbán, G., & Érdi, P. (2004) · Neurocomputing · doi:10.1016/j.neucom.2004.10.026 · Cited by 2
Constraining the function of CA1 in associative memory models of the hippocampus
Longden, K. D. (2005) · ERA · Cited by 2
Neural representations of Euclidean space
Solstad, T. (2009) · BIBSYS Brage (BIBSYS (Norway)) · Cited by 2
An Oscillatory Network Model of Head Direction, Spatially Periodic Cells and Place Cells Using Locomotor InputsPreprint
Soman, K., Muralidharan, V., & Chakravarthy, V. S. (2016) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/080267 · Cited by 2
Extra-field activity shifts the place field center of mass to encode aversion experiencePreprint
Mamad, O., Agayby, B., Stumpp, L. I., Reilly, R. B., & Tsanov, M. (2017) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/218180 · Cited by 2
GABAA Receptor Subtypes: Memory Function and Neurological Disorders
Fritschy, J., Crestani, F., Rudolph, U., & Möhler, H. (2003) · Springer eBooks · doi:10.1007/978-1-4615-0039-1_14 · Cited by 2
The Map’s Design: Evolution’s Impact on Navigation and Spatial Cognition
Olynik-McLaughlin, I. S., & Marrone, D. F. (2025) · Animals · doi:10.3390/ani15243628 · Cited by 1
Entorhinal Silencing Reveals Energy Cascade Organization of Hippocampal Oscillations
Zhao, B., Qin, Y. F., Burke, S. N., & Maurer, A. P. (2025) · Hippocampus · doi:10.1002/hipo.70050 · Cited by 1
Methods for the Modulation and Analysis of NF-κB-dependent Adult Neurogenesis
Widera, D., Müller, J., Imielski, Y., Heimann, P., Kaltschmidt, C., & Kaltschmidt, B. (2014) · Journal of Visualized Experiments · doi:10.3791/50870 · Cited by 1
Software for analyzing the behavioural test “Morris Water Maze”
Zorin, A., Chernyuk, D., Власова, О. Л., Bolsunovskaya, M. V., & Борисович, Б. И. (2020) · E3S Web of Conferences · doi:10.1051/e3sconf/202020301029 · Cited by 1
Rapid Spectral Dynamics in Hippocampal Oscillons
Zobaer, M. S., Domenico, C., Perotti, L., Ji, D.-Y., & Dabaghian, Y. (2022) · Frontiers in Computational Neuroscience · doi:10.3389/fncom.2022.880742 · Cited by 1
Brain–computer interface for simultaneous dual‐region spatial coding in hippocampal and somatosensory cortex of freely behaving rats
Li, M., Xu, W., Xu, Z., Mo, F., Yang, G., Lv, S., Cao, H., Liu, J., & Cai, X. (2024) · Electronics Letters · doi:10.1049/ell2.70013 · Cited by 1
The Entorhinal Cortex
Kanter, B. R., Moser, E. I., & Witter, M. P. (2025) · Oxford University Press eBooks · doi:10.1093/med/9780190065324.003.0012 · Cited by 1
Self-citation

Authors: Brun, V. H., Otnæss, M. K., Molden, S., Steffenach, H.-A., Witter, M. P., Moser, M.-B., & Moser, E. I.
Affiliations: Norwegian University of Science and Technology (NO)
Amsterdam UMC Location Vrije Universiteit Amsterdam (NL)
Corresponding author: Moser, Edvard I.
ORCID: Brun, Vegard H.
Witter, Menno P.
Moser, May-Britt
Moser, Edvard I.
Venue: Science
Publisher: American Association for the Advancement of Science (AAAS)
Published: 2002-06-21
Volume: 296
Issue: 5576
Pages: 2243-2246
ISSN: 0036-8075 (ISSN-L)
1095-9203
DOI: 10.1126/science.1071089
OpenAlex: W2004974848
Cited by: 606
References: 24
Citations by year: 2026: 13 · 2025: 20 · 2024: 15 · 2023: 17 · 2022: 17 · 2021: 26 · 2020: 20 · 2019: 18 · 2018: 18 · 2017: 26 · 2016: 35 · 2015: 39 · 2014: 33 · 2013: 25 · 2012: 31
FWCI: 13.98
Type: journal article
Language: en
Open access: closed
Locations: Science (publishedVersion)
PubMed (publishedVersion)
Topics: Life Sciences › Neuroscience › Cognitive Neuroscience › Memory and Neural Mechanisms
Social Sciences › Psychology › Experimental and Cognitive Psychology › Spatial Cognition and Navigation
Life Sciences › Neuroscience › Developmental Neuroscience › Neurogenesis and neuroplasticity mechanisms
Keywords: place cells, entorhinal cortex, hippocampal CA1, spatial memory, recollection
MeSH terms: Action Potentials, Animals, Brain Mapping, Denervation, Electrodes, Implanted, Hippocampus, Interneurons, Memory, Nerve Net, Neural Pathways, Mental Recall, Space Perception, Pyramidal Cells, Entorhinal Cortex, Maze Learning, Rats

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

Place Cells and Place Recognition Maintained by Direct Entorhinal-Hippocampal Circuitry

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