The DOI matches its Crossref record; 32 of the 32 references it cites were found in a registry or an index.
Finite Scale of Spatial Representation in the Hippocampus
Abstract
To determine how spatial scale is represented in the pyramidal cell population of the hippocampus, we recorded neural activity at multiple longitudinal levels of this brain area while rats ran back and forth on an 18-meter-long linear track. CA3 cells had well-defined place fields at all levels. The scale of representation increased almost linearly from <1 meter at the dorsal pole to approximately 10 meters at the ventral pole. The results suggest that the place-cell map includes the entire hippocampus and that environments are represented in the hippocampus at a topographically graded but finite continuum of scales.
Overview
Integrity signals
Registry
Cites
Statistics
Verification
Claims the paper makes
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?
In the citing paper
“the anterior HF contains cells with larger place fields than the posterior HF”
From Delay-dependent contributions of medial temporal lobe regions to episodic memory retrieval (2015) · cites this paper as Kjelstrup et al., 2008
Citations
Cites
(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
Microstructure of a spatial map in the entorhinal cortex
Hafting, T., Fyhn, M., Molden, S., Moser, M.-B., & Moser, E. I. (2005) · Nature · doi:10.1038/nature03721 · Cited by 4,068
Self-citationPhase 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
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
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-citationSpatial 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
Self-citationLamellar organization of hippocampal excitatory pathways
Andersen, P. N., Bliss, T. V. P., & Skrede, K. K. (1971) · Experimental Brain Research · doi:10.1007/bf00234087 · Cited by 969
Moser, E., Moser, M. ‐., & Andersen, P. N. (1993) · Journal of Neuroscience · doi:10.1523/jneurosci.13-09-03916.1993 · Cited by 953
Self-citationFunctional organization of the extrinsic and intrinsic circuitry of the parahippocampal region
Witter, M. P., Groenewegen, H. J., Lopes, F. H. D. S., & Lohman, A. H. M. (1989) · Progress in Neurobiology · doi:10.1016/0301-0082(89)90009-9 · Cited by 918
Self-citation
Flagged first, then by citations
Research works printed but not linked: 3
- P. Andersen, T. V. P. Bliss, K. K. Skrede, Exp. Brain Res.13, 222 (1971).
- E. I. Moser E. Kropff M.-B. Moser. Annu. Rev. Neurosci. 31 in press.
- T. Solstad, V. H. Brun, K. B. Kjelstrup, M. Fyhn, M. P. Witter, E. I. Moser, M.-B. Moser. Soc. Neurosci. Abstr.33, 93.2 (2007).
Cited by
Sorted by citations
Are the Dorsal and Ventral Hippocampus Functionally Distinct Structures?
Fanselow, M. S., & Dong, H.-W. (2010) · Neuron · doi:10.1016/j.neuron.2009.11.031 · Cited by 3,358
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-citationFunctional organization of the hippocampal longitudinal axis
Strange, B. A., Witter, M. P., Lein, E. S., & Moser, E. I. (2014) · Nature reviews. Neuroscience · doi:10.1038/nrn3785 · Cited by 1,738
Self-citationThe role of medial prefrontal cortex in memory and decision making
Euston, D. R., Gruber, A. J., & McNaughton, B. L. (2012) · Neuron · doi:10.1016/j.neuron.2012.12.002 · Cited by 1,541
Neural syntax: cell assemblies, synapsembles, and readers
Buzsáki, G. (2010) · Neuron · doi:10.1016/j.neuron.2010.09.023 · Cited by 1,289
Long-axis specialization of the human hippocampus
Poppenk, J., Evensmoen, H. R., Moscovitch, M., & Nadel, L. (2013) · Trends in Cognitive Sciences · doi:10.1016/j.tics.2013.03.005 · Cited by 1,100
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
Self-citationAdult hippocampal neurogenesis and cognitive flexibility — linking memory and mood
Anacker, C., & Hen, R. (2017) · Nature Reviews Neuroscience · doi:10.1038/nrn.2017.45 · Cited by 1,014
The hippocampus as a predictive map
Stachenfeld, K. L., Botvinick, M. M., & Gershman, S. J. (2017) · Nature Neuroscience · doi:10.1038/nn.4650 · Cited by 1,000
Hippocampal replay in the awake state: a potential substrate for memory consolidation and retrieval
Carr, M. F., Jadhav, S. P., & Frank, L. M. (2011) · Nature Neuroscience · doi:10.1038/nn.2732 · Cited by 958
A pathophysiological framework of hippocampal dysfunction in ageing and disease
Small, S. A., Schobel, S., Buxton, R. B., Witter, M. P., & Barnes, C. A. (2011) · Nature reviews. Neuroscience · doi:10.1038/nrn3085 · Cited by 955
Self-citationPrefrontal–hippocampal interactions in episodic memory
Eichenbaum, H. (2017) · Nature Reviews Neuroscience · doi:10.1038/nrn.2017.74 · Cited by 870
Adhikari, A., Topiwala, M. A., & Gordon, J. A. (2010) · Neuron · doi:10.1016/j.neuron.2009.12.002 · Cited by 729
Differential Control of Learning and Anxiety along the Dorsoventral Axis of the Dentate Gyrus
Kheirbek, M. A., Drew, L. J., Burghardt, N. S., Costantini, D. O., Tannenholz, L., Ahmari, S. E., Zeng, H., Fenton, A. A., & Hen, R. (2013) · Neuron · doi:10.1016/j.neuron.2012.12.038 · Cited by 713
Hippocampal–prefrontal input supports spatial encoding in working memory
Spellman, T., Rigotti, M., Ahmari, S. E., Fusi, S., Gogos, J. A., & Gordon, J. A. (2015) · Nature · doi:10.1038/nature14445 · Cited by 693
Whittington, J. C. R., Muller, T. H., Mark, S., Chen, G., Barry, C., Burgess, N., & Behrens, T. E. J. (2020) · Cell · doi:10.1016/j.cell.2020.10.024 · Cited by 660
Navigating cognition: Spatial codes for human thinking
Bellmund, J. L. S., Gärdenfors, P., Moser, E. I., & Doeller, C. F. (2018) · Science · doi:10.1126/science.aat6766 · Cited by 643
Self-citationCortical travelling waves: mechanisms and computational principles
Muller, L., Chavane, F., Reynolds, J. H., & B, T. J. S. A. (2018) · Nature reviews. Neuroscience · doi:10.1038/nrn.2018.20 · Cited by 617
Anterior hippocampus: the anatomy of perception, imagination and episodic memory
Zeidman, P., & Maguire, E. A. (2016) · Nature Reviews Neuroscience · doi:10.1038/nrn.2015.24 · Cited by 542
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
Self-citationCortex and memory: emergence of a new paradigm
Fuster, J. M. (2009) · Journal of Cognitive Neuroscience · doi:10.1162/jocn.2009.21280 · Cited by 559
Hippocampal theta oscillations are travelling waves
Lubenov, E. V., & Siapas, A. G. (2009) · Nature · doi:10.1038/nature08010 · Cited by 523
Assessing Spatial Learning and Memory in Rodents
Vorhees, C. V., & Williams, M. T. (2014) · ILAR Journal · doi:10.1093/ilar/ilu013 · Cited by 582
Place Cells, Grid Cells, and MemoryPreprint
Moser, M., Rowland, D. C., & Moser, E. I. (2015) · Cold Spring Harbor Perspectives in Biology · doi:10.1101/cshperspect.a021808 · Cited by 596
Self-citationSpace in the brain: How the hippocampal formation supports spatial cognition
Hartley, T., Lever, C., Burgess, N., & O'Keefe, J. (2014) · Philosophical Transactions of the Royal Society B: Biological Sciences · doi:10.1098/rstb.2012.0510 · Cited by 495
A map of visual space in the primate entorhinal cortex
Killian, N. J., Jutras, M. J., & Buffalo, E. A. (2012) · Nature · doi:10.1038/nature11587 · Cited by 501
Space and Time: The Hippocampus as a Sequence Generator
Buzsáki, G., & Tingley, D. (2018) · Trends in Cognitive Sciences · doi:10.1016/j.tics.2018.07.006 · Cited by 461
Powell, R. A., & Mitchell, M. S. (2012) · Journal of Mammalogy · doi:10.1644/11-mamm-s-177.1 · Cited by 415
Theta and Alpha Oscillations Are Traveling Waves in the Human Neocortex
Zhang, H., Watrous, A. J., Patel, A., & Jacobs, J. (2018) · Neuron · doi:10.1016/j.neuron.2018.05.019 · Cited by 396
Buzsáki, G. (2019) · doi:10.1093/oso/9780190905385.001.0001 · Cited by 383
Distinct Representations and Theta Dynamics in Dorsal and Ventral Hippocampus
Royer, S., Sirota, A., Patel, J., & Buzsáki, G. (2010) · Journal of Neuroscience · doi:10.1523/jneurosci.4681-09.2010 · Cited by 356
Selective information routing by ventral hippocampal CA1 projection neurons
Ciocchi, S., Passecker, J., Malagon‐Vina, H., Mikuš, N., & Klausberger, T. (2015) · Science · doi:10.1126/science.aaa3245 · Cited by 357
Fragmentation of grid cell maps in a multicompartment environment
Derdikman, D., Whitlock, J. R., Tsao, A., Fyhn, M., Hafting, T., Moser, M.-B., & Moser, E. I. (2009) · Nature Neuroscience · doi:10.1038/nn.2396 · Cited by 330
Self-citationUsing Grid Cells for Navigation
Bush, D., Barry, C., Manson, D., & Burgess, N. (2015) · Neuron · doi:10.1016/j.neuron.2015.07.006 · Cited by 347
Memory and Space: Towards an Understanding of the Cognitive Map
Schiller, D., Eichenbaum, H., Buffalo, E. A., Davachi, L., Foster, D. J., Leutgeb, S., & Ranganath, C. (2015) · Journal of Neuroscience · doi:10.1523/jneurosci.2618-15.2015 · Cited by 340
Self-citationProgressive increase in grid scale from dorsal to ventral medial entorhinal cortex
Brun, V. H., Solstad, T., Kjelstrup, K. B., Fyhn, M., Witter, M. P., Moser, E. I., & Moser, M. (2008) · Hippocampus · doi:10.1002/hipo.20504 · Cited by 322
Self-citationHippocampal-Prefrontal Interactions in Cognition, Behavior and Psychiatric Disease
Sigurdsson, T., & Duvarci, S. (2016) · Frontiers in Systems Neuroscience · doi:10.3389/fnsys.2015.00190 · Cited by 309
Traveling Theta Waves along the Entire Septotemporal Axis of the Hippocampus
Patel, J., Fujisawa, S., Berényi, A., Royer, S., & Buzsáki, G. (2012) · Neuron · doi:10.1016/j.neuron.2012.07.015 · Cited by 302
Grid cells and theta as oscillatory interference: Theory and predictions
Burgess, N. (2008) · Hippocampus · doi:10.1002/hipo.20518 · Cited by 294
Sublayer-Specific Coding Dynamics during Spatial Navigation and Learning in Hippocampal Area CA1
Danielson, N. B., Zaremba, J. D., Kaifosh, P., Bowler, J., Ladow, M., & Losonczy, A. (2016) · Neuron · doi:10.1016/j.neuron.2016.06.020 · Cited by 288
Prediction, sequences and the hippocampus
Lisman, J. E., & Redish, A. D. (2009) · Philosophical Transactions of the Royal Society B Biological Sciences · doi:10.1098/rstb.2008.0316 · Cited by 299
The hippocampal-striatal axis in learning, prediction and goal-directed behavior
Pennartz, C. M. A., Ito, R., Verschure, P. F. M. J., Battaglia, F. P., & Robbins, T. W. (2011) · Trends in Neurosciences · doi:10.1016/j.tins.2011.08.001 · Cited by 287
Structuring knowledge with cognitive maps and cognitive graphs
Peer, M., Brunec, I. K., Newcombe, N. S., & Epstein, R. A. (2021) · Trends in Cognitive Sciences · doi:10.1016/j.tics.2020.10.004 · Cited by 283
Multiple Scales of Representation along the Hippocampal Anteroposterior Axis in Humans
Brunec, I. K., Bellana, B., Ozubko, J. D., Man, V. Y., Robin, J., Liu, Z., Grady, C. L., Rosenbaum, R. S., Winocur, G., Barense, M. D., et al. (2018) · Current Biology · doi:10.1016/j.cub.2018.05.016 · Cited by 305
Kanoski, S. E., & Grill, H. J. (2015) · Biological Psychiatry · doi:10.1016/j.biopsych.2015.09.011 · Cited by 294
Theta rhythm and the encoding and retrieval of space and time
Hasselmo, M. E., & Stern, C. E. (2013) · NeuroImage · doi:10.1016/j.neuroimage.2013.06.022 · Cited by 291
Spatial cognition in bats and rats: from sensory acquisition to multiscale maps and navigation
Geva‐Sagiv, M., Las, L., Yovel, Y., & Ulanovsky, N. (2015) · Nature reviews. Neuroscience · doi:10.1038/nrn3888 · Cited by 273
PKMζ Maintains Spatial, Instrumental, and Classically Conditioned Long-Term Memories
Serrano, P. A., Friedman, E., Kenney, J., Taubenfeld, S. M., Zimmerman, J., Hanna, J., Alberini, C. M., Kelley, A. E., Maren, S., Rudy, J. W., et al. (2008) · PLoS Biology · doi:10.1371/journal.pbio.0060318 · Cited by 267
Heterogeneity within classical cell types is the rule: lessons from hippocampal pyramidal neurons
Cembrowski, M. S., & Spruston, N. (2019) · Nature Reviews Neuroscience · doi:10.1038/s41583-019-0125-5 · Cited by 258
The Cognitive Architecture of Spatial Navigation: Hippocampal and Striatal Contributions
Chersi, F., & Burgess, N. (2015) · Neuron · doi:10.1016/j.neuron.2015.09.021 · Cited by 240
Time cells in the human hippocampus and entorhinal cortex support episodic memory
Umbach, G. S., Kantak, P. A., Jacobs, J., Kahana, M. J., Pfeiffer, B. E., Sperling, M. R., & Lega, B. C. (2020) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.2013250117 · Cited by 247
A cognitive map for object memory in the hippocampusPreprint
Manns, J. R., & Eichenbaum, H. (2009) · Learning & Memory · doi:10.1101/lm.1484509 · Cited by 249
Computational Models of Grid Cells
Giocomo, L. M., Moser, M., & Moser, E. I. (2011) · Neuron · doi:10.1016/j.neuron.2011.07.023 · Cited by 236
Self-citationHippocampal size predicts rapid learning of a cognitive map in humans
Schinazi, V. R., Nardi, D., Newcombe, N. S., Shipley, T. F., & Epstein, R. A. (2013) · Hippocampus · doi:10.1002/hipo.22111 · Cited by 231
Pereira, F., Alessio, A., Sercheli, M. S., Pedro, T., Bilevicius, E., Rondina, J. M., Ozelo, H. F., Castellano, G., Covolan, R. J. M., Damasceno, B. P., et al. (2010) · BMC Neuroscience · doi:10.1186/1471-2202-11-66 · Cited by 228
Human hippocampus represents space and time during retrieval of real-world memories
Nielson, D. M., Smith, T. A., Sreekumar, V., Dennis, S. J., & Sederberg, P. B. (2015) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1507104112 · Cited by 245
Tompary, A., & Davachi, L. (2017) · Neuron · doi:10.1016/j.neuron.2017.09.005 · Cited by 235
Activity dynamics and behavioral correlates of CA3 and CA1 hippocampal pyramidal neurons
Mizuseki, K., Royer, S., Diba, K., & Buzsáki, G. (2012) · Hippocampus · doi:10.1002/hipo.22002 · Cited by 226
Rowland, D. C., Roudi, Y., Moser, M., & Moser, E. I. (2016) · Annual Review of Neuroscience · doi:10.1146/annurev-neuro-070815-013824 · Cited by 227
Self-citationInternally generated sequences in learning and executing goal-directed behavior
Pezzulo, G., van der Meer, M. A. A., Lansink, C. S., & Pennartz, C. M. A. (2014) · Trends in Cognitive Sciences · doi:10.1016/j.tics.2014.06.011 · Cited by 217
Moser, E. I., & Moser, M. (2008) · Hippocampus · doi:10.1002/hipo.20483 · Cited by 228
Self-citationFenton, A. A., Kao, H.-Y., Neymotin, S. A., Olypher, A. V., Vayntrub, Y., Lytton, W. W., & Ludvig, N. (2008) · Journal of Neuroscience · doi:10.1523/jneurosci.2862-08.2008 · Cited by 224
Ketamine Modulates Theta and Gamma Oscillations
Lazarewicz, M. T., Ehrlichman, R. S., Maxwell, C. R., Gandal, M. J., Finkel, L. H., & Siegel, S. J. (2009) · Journal of Cognitive Neuroscience · doi:10.1162/jocn.2009.21305 · Cited by 216
Bowman, C. R., & Zeithamová, D. (2018) · Journal of Neuroscience · doi:10.1523/jneurosci.2811-17.2018 · Cited by 215
A Unified Mathematical Framework for Coding Time, Space, and Sequences in the Hippocampal Region
Howard, M. W., MacDonald, C. J., Tiganj, Z., Shankar, K. H., Du, Q., Hasselmo, M. E., & Eichenbaum, H. (2014) · Journal of Neuroscience · doi:10.1523/jneurosci.5808-12.2014 · Cited by 203
The Neuroscience of Learning: Beyond the Hebbian Synapse
Gallistel, C. R., & Matzel, L. D. (2012) · Annual Review of Psychology · doi:10.1146/annurev-psych-113011-143807 · Cited by 212
Disambiguating the similar: The dentate gyrus and pattern separation
Schmidt, B., Marrone, D. F., & Markus, E. J. (2012) · Behavioural Brain Research · doi:10.1016/j.bbr.2011.08.039 · Cited by 198
From Rapid Place Learning to Behavioral Performance: A Key Role for the Intermediate Hippocampus
Bast, T., Wilson, I. A., Witter, M. P., & Morris, R. (2009) · PLoS Biology · doi:10.1371/journal.pbio.1000089 · Cited by 204
Self-citationEpisodic memory: Neuronal codes for what, where, and when
Sugar, J., & Moser, M. (2019) · Hippocampus · doi:10.1002/hipo.23132 · Cited by 216
Self-citationSpatial Cognition and the Hippocampus: The Anterior–Posterior Axis
Nadel, L., Hoscheidt, S. M., & Ryan, L. (2012) · Journal of Cognitive Neuroscience · doi:10.1162/jocn_a_00313 · Cited by 191
Traveling Theta Waves in the Human Hippocampus
Zhang, H., & Jacobs, J. (2015) · Journal of Neuroscience · doi:10.1523/jneurosci.5102-14.2015 · Cited by 196
Ventral Hippocampal Neurons Are Shaped by Experience to Represent Behaviorally Relevant Contexts
Komorowski, R. W., Garcia, C., Wilson, A., Hattori, S., Howard, M. W., & Eichenbaum, H. (2013) · Journal of Neuroscience · doi:10.1523/jneurosci.5458-12.2013 · Cited by 188
Home ranges and the value of spatial information
Spencer, W. D. (2012) · Journal of Mammalogy · doi:10.1644/12-mamm-s-061.1 · Cited by 188
Large environments reveal the statistical structure governing hippocampal representations
Rich, P. D., Liaw, H.-P., & Lee, A. K. (2014) · Science · doi:10.1126/science.1255635 · Cited by 188
Feng, T., Silva, D., & Foster, D. J. (2015) · Journal of Neuroscience · doi:10.1523/jneurosci.2614-14.2015 · Cited by 185
Dordek, Y., Soudry, D., Meir, R., & Derdikman, D. (2016) · eLife · doi:10.7554/elife.10094 · Cited by 183
Modulating Neuronal Competition Dynamics in the Dentate Gyrus to Rejuvenate Aging Memory Circuits
McAvoy, K. M., Scobie, K. N., Berger, S. M., Russo, C., Guo, N., Decharatanachart, P., Vega-Ramirez, H., Miake-Lye, S., Whalen, M. J., Nelson, M., et al. (2016) · Neuron · doi:10.1016/j.neuron.2016.08.009 · Cited by 184
Local Generation and Propagation of Ripples along the Septotemporal Axis of the Hippocampus
Patel, J., Schomburg, E. W., Berényi, A., Fujisawa, S., & Buzsáki, G. (2013) · Journal of Neuroscience · doi:10.1523/jneurosci.2036-13.2013 · Cited by 181
Ito, R., & Lee, A. C. H. (2016) · Behavioural Brain Research · doi:10.1016/j.bbr.2016.07.039 · Cited by 188
A manifold of spatial maps in the brain
Derdikman, D., & Moser, E. I. (2010) · Trends in Cognitive Sciences · doi:10.1016/j.tics.2010.09.004 · Cited by 175
Self-citationThe physiological control of eating: signals, neurons, and networks
Watts, A. G., Kanoski, S. E., Sanchez-Watts, G., & Langhans, W. (2022) · Physiological Reviews · doi:10.1152/physrev.00028.2020 · Cited by 168
Korotkova, T. M., Ponomarenko, A. A., Monaghan, C. K., Poulter, S. L., Cacucci, F., Wills, T. J., Hasselmo, M. E., & Lever, C. (2017) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2017.09.004 · Cited by 173
Intrinsic excitability of CA1 pyramidal neurones from the rat dorsal and ventral hippocampus
Dougherty, K. A., Islam, T., & Johnston, D. (2012) · The Journal of Physiology · doi:10.1113/jphysiol.2012.242693 · Cited by 158
What do grid cells contribute to place cell firing?
Bush, D., Barry, C., & Burgess, N. (2014) · Trends in Neurosciences · doi:10.1016/j.tins.2013.12.003 · Cited by 170
Topography of Place Maps along the CA3-to-CA2 Axis of the Hippocampus
Lu, L., Igarashi, K. M., Witter, M. P., Moser, E. I., & Moser, M. (2015) · Neuron · doi:10.1016/j.neuron.2015.07.007 · Cited by 163
Self-citationTheta Modulation in the Medial and the Lateral Entorhinal Cortices
Deshmukh, S. S., Yoganarasimha, D., Voicu, H., & Knierim, J. J. (2010) · Journal of Neurophysiology · doi:10.1152/jn.01141.2009 · Cited by 158
Delay-dependent contributions of medial temporal lobe regions to episodic memory retrieval
Ritchey, M., Montchal, M. E., Yonelinas, A. P., & Ranganath, C. (2015) · eLife · doi:10.7554/elife.05025 · Cited by 148
Vorhees, C. V., & Williams, M. T. (2014) · Neurotoxicology and Teratology · doi:10.1016/j.ntt.2014.07.003 · Cited by 152
Stress‐induced dynamic routing of hippocampal connectivity: A hypothesis
Segal, M., Richter‐Levin, G., & Maggio, N. (2010) · Hippocampus · doi:10.1002/hipo.20751 · Cited by 146
Park, E., Dvořák, D., & Fenton, A. A. (2011) · PLoS ONE · doi:10.1371/journal.pone.0022349 · Cited by 150
Optimal Population Codes for Space: Grid Cells Outperform Place Cells
Mathis, A., Herz, A. V. M., & Stemmler, M. (2012) · Neural Computation · doi:10.1162/neco_a_00319 · Cited by 153
Anterior hippocampus and goal-directed spatial decision making
Viard, A., Doeller, C. F., Hartley, T., Bird, C. M., & Burgess, N. (2011) · The Journal of Neuroscience · doi:10.1523/jneurosci.4640-10.2011 · Cited by 144
Agster, K. L., & Burwell, R. D. (2013) · Behavioural Brain Research · doi:10.1016/j.bbr.2013.07.005 · Cited by 143
Topography of Head Direction Cells in Medial Entorhinal Cortex
Giocomo, L. M., Stensola, T., Bonnevie, T., Cauter, T. V., Moser, M., & Moser, E. I. (2014) · Current Biology · doi:10.1016/j.cub.2013.12.002 · Cited by 152
Self-citationGeisler, C. E., Diba, K., Pastalkova, E., Mizuseki, K., Royer, S., & Buzsáki, G. (2010) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0912478107 · Cited by 144
Alexander, A. S., & Nitz, D. A. (2017) · Current Biology · doi:10.1016/j.cub.2017.04.036 · Cited by 146
Updating hippocampal representations: CA2 joins the circuit
Jones, M. W., & McHugh, T. J. (2011) · Trends in Neurosciences · doi:10.1016/j.tins.2011.07.007 · Cited by 147
Douchamps, V., Jeewajee, A., Blundell-Birtill, P., Burgess, N., & Lever, C. (2013) · Journal of Neuroscience · doi:10.1523/jneurosci.4483-12.2013 · Cited by 150
Lee, J., Lee, E., Kim, J., Lee, Y., Jeong, Y., Choi, B. S., Kim, J., & Staab, J. P. (2018) · Human Brain Mapping · doi:10.1002/hbm.24080 · Cited by 143
Boundaries Shape Cognitive Representations of Spaces and Events
Brunec, I. K., Moscovitch, M., & Barense, M. D. (2018) · Trends in Cognitive Sciences · doi:10.1016/j.tics.2018.03.013 · Cited by 149
Metadata
- Authors
- Kjelstrup, K. B., Solstad, T., Brun, V. H., Hafting, T., Leutgeb, S., Witter, M. P., Moser, E. I., & Moser, M.-B.
- Affiliations
- Norwegian University of Science and Technology (NO)
- Corresponding author
- Moser, Edvard I.
- ORCID
- Venue
- Science
- Published
- 2008-07-04
- Volume
- 321
- Issue
- 5885
- Pages
- 140-143
- ISSN
- 0036-8075 (ISSN-L)
- 1095-9203
- OpenAlex
- W2052918792
- Cited by
- 760
- References
- 32
- Citations by year
- 2026: 36 · 2025: 64 · 2024: 52 · 2023: 52 · 2022: 35 · 2021: 53 · 2020: 48 · 2019: 45 · 2018: 41 · 2017: 48 · 2016: 34 · 2015: 50 · 2014: 37 · 2013: 35 · 2012: 37
- FWCI
- 16.05
- Type
- journal article
- Language
- en
- Open access
- closed
- Locations
- Science (publishedVersion)
- PubMed (publishedVersion)
- Pure Amsterdam UMC (publishedVersion)
- Amsterdam UMC (VU Amsterdam) - Institutional Repository (publishedVersion)
- Data Archiving and Networked Services (DANS) (submittedVersion)
- 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
- hippocampus, spatial representation, place cells, place fields, CA3, spatial scale, topographic map, pyramidal neurons, rats, dorsal-ventral gradient
- MeSH terms
- Action Potentials, Algorithms, Animals, Brain Mapping, Electrodes, Implanted, Hippocampus, Learning, Male, Space Perception, Spatial Behavior, Theta Rhythm, Linear Models, Pyramidal Cells, Rats, Long-Evans, 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