Subcircuits of Deep and Superficial CA1 Place Cells Support Efficient Spatial Coding across Heterogeneous Environments
Open accessPublished version of a preprint
Abstract
The hippocampus is thought to guide navigation by forming a cognitive map of space. Different environments differ in geometry and the availability of cues that can be used for navigation. Although several spatial coding mechanisms are known to coexist in the hippocampus, how they are influenced by various environmental features is not well understood. To address this issue, we examined the spatial coding characteristics of hippocampal neurons in mice and rats navigating in different environments. We found that CA1 place cells located in the superficial sublayer were more active in cue-poor environments and preferentially used a firing rate code driven by intra-hippocampal inputs. In contrast, place cells located in the deep sublayer were more active in cue-rich environments and used a phase code driven by entorhinal inputs. Switching between these two spatial coding modes was supported by the interaction between excitatory gamma inputs and local inhibition.
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Integrity signals
Registry
Cites
Statistics
Claims the paper makes
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
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?
Spatial tuning across the hippocampus is not entirely independent but may form correlated assemblies.
“This may support recent work in rodents suggesting that spatial tuning across the hippocampus is not entirely independent but may form correlated assemblies30,31,40,45.”
From A population code for spatial representation in the zebrafish telencephalon (2024) · cites this paper as [45]
Self-check
Percentages, sums and reported differences re-computed from the paper’s own numbers.
The self-check needs the paper’s full text.
Cites
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
The hippocampus as a cognitive map
Passingham, R. E. (1979) · Neuroscience · doi:10.1016/0306-4522(79)90015-0 · Cited by 5,128 · see citing works
<b>CircStat</b> : A <i>MATLAB</i> Toolbox for Circular Statistics
Berens, P. (2009) · Journal of Statistical Software · doi:10.18637/jss.v031.i10 · Cited by 3,099 · see citing works
Phase 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 2,561 · 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
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 · see citing works
de Nó, R. L. (1934) · Cited by 1,974 · see citing works
Place units in the hippocampus of the freely moving rat
O'Keefe, J. (1976) · Experimental Neurology · doi:10.1016/0014-4886(76)90055-8 · Cited by 1,836 · see citing works
Advances in Neural Information Processing Systems 19 (NIPS 2006)
Simonotto, E., Whalley, H. C., Lawrie, S. M., Murray, L. M., McGonigle, D. J., & Storkey, A. (2006) · Cited by 1,651 · see citing works
The effects of changes in the environment on the spatial firing of hippocampal complex-spike cells
Muller, R., & Kubie, J. (1987) · The Journal of Neuroscience · doi:10.1523/jneurosci.07-07-01951.1987 · Cited by 1,581 · see citing works
Frequency of gamma oscillations routes flow of information in the hippocampus
Colgin, L. L., Denninger, T., Fyhn, M., Hafting, T., Bonnevie, T., Jensen, O. B., Moser, M., & Moser, E. I. (2009) · Nature · doi:10.1038/nature08573 · Cited by 1,425 · see citing works
Ylinen, A., Bragin, A., Nadasdy, Z., Jando, G., Szabo, I., Sik, A., & Buzsaki, G. (1995) · The Journal of Neuroscience · doi:10.1523/jneurosci.15-01-00030.1995 · Cited by 1,092 · see citing works
Self-citationNeural ensembles in CA3 transiently encode paths forward of the animal at a decision point
Johnson, A., & Redish, A. D. (2007) · The Journal of Neuroscience · doi:10.1523/jneurosci.3761-07.2007 · Cited by 1,003 · see citing works
Mechanisms of Gamma Oscillations in the Hippocampus of the Behaving Rat
Csicsvari, J., Jamieson, B. G., Wise, K. D., & Buzsáki, G. (2003) · Neuron · doi:10.1016/s0896-6273(02)01169-8 · Cited by 990 · see citing works
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 · see citing works
Barthó, P., Hirase, H., Monconduit, L., Zugaro, M. B., Harris, K. D., & Buzsáki, G. (2004) · Journal of Neurophysiology · doi:10.1152/jn.01170.2003 · Cited by 888 · see citing works
Self-citationDistinct Ensemble Codes in Hippocampal Areas CA3 and CA1
Leutgeb, S., Leutgeb, J. K., Treves, A., Moser, M., & Moser, E. I. (2004) · Science · doi:10.1126/science.1100265 · Cited by 774 · see citing works
Spike sorting for large, dense electrode arrays
Rossant, C., Kadir, S., Goodman, D. F. M., Schulman, J., Hunter, M. L. D., Saleem, A. B., Grosmark, A., Belluscio, M., Denfield, G. H., Ecker, A. S., et al. (2016) · Nature Neuroscience · doi:10.1038/nn.4268 · Cited by 760 · see citing works
Self-citationFinite scale of spatial representation in the hippocampus
Kjelstrup, K. B., Solstad, T., Brun, V. H., Hafting, T., Leutgeb, S., Witter, M. P., Moser, E. I., & Moser, M.-B. (2008) · Science · doi:10.1126/science.1157086 · Cited by 760 · see citing works
Reductive Cross‐Coupling Reactions between Two Electrophiles
Knappke, C. E. I., Grupe, S., Gärtner, D., Corpet, M., Gosmini, C., & von Wangelin, A. J. (2014) · Chemistry - A European Journal · doi:10.1002/chem.201402302 · Cited by 759 · see citing works
Temporal Encoding of Place Sequences by Hippocampal Cell Assemblies
Dragoi, G., & Buzsáki, G. (2006) · Neuron · doi:10.1016/j.neuron.2006.02.023 · Cited by 727 · see citing works
Self-citationMajor Dissociation Between Medial and Lateral Entorhinal Input to Dorsal Hippocampus
Hargreaves, E. L., Rao, G., Lee, I., & Knierim, J. J. (2005) · Science · doi:10.1126/science.1110449 · Cited by 685 · see citing works
Quantitative measures of cluster quality for use in extracellular recordings
Schmitzer-Torbert, N. C., Jackson, J. C., Henze, D. A., Harris, K., & Redish, A. D. (2005) · Neuroscience · doi:10.1016/j.neuroscience.2004.09.066 · Cited by 642 · see citing works
Role of experience and oscillations in transforming a rate code into a temporal code
Mehta, M. R., Lee, A. K., & Wilson, M. A. (2002) · Nature · doi:10.1038/nature00807 · Cited by 630 · see citing works
Independent rate and temporal coding in hippocampal pyramidal cells
Huxter, J. R., Burgess, N., & O'Keefe, J. M. (2003) · Nature · doi:10.1038/nature02058 · Cited by 594 · see citing works
O'Keefe, J. M., & Burgess, N. (2005) · Hippocampus · doi:10.1002/hipo.20115 · Cited by 547 · see citing works
Conjunctive input processing drives feature selectivity in hippocampal CA1 neurons
Bittner, K. C., Grienberger, C., Vaidya, S. P., Milstein, A. D., Macklin, J. J., Suh, J., Tonegawa, S., & Magee, J. C. (2015) · Nature Neuroscience · doi:10.1038/nn.4062 · Cited by 540 · see citing works
An Information-Theoretic Approach to Deciphering the Hippocampal Code
Skaggs, W. E., McNaughton, B. L., & Gothard, K. M. (1992) · Cited by 536 · see citing works
Hazan, L., Zugaro, M. B., & Buzsáki, G. (2006) · Journal of Neuroscience Methods · doi:10.1016/j.jneumeth.2006.01.017 · Cited by 492 · see citing works
Self-citationLong-duration hippocampal sharp wave ripples improve memory
Fernández-Ruiz, A., Oliva, A., Fermino de Oliveira, E., Rocha-Almeida, F., Tingley, D., & Buzsáki, G. (2019) · Science · doi:10.1126/science.aax0758 · Cited by 490 · see citing works
Self-citationGothard, K., Skaggs, W. E., Moore, K. L., & McNaughton, B. L. (1996) · Journal of Neuroscience · doi:10.1523/jneurosci.16-02-00823.1996 · Cited by 488 · see citing works
Theta Phase Segregation of Input-Specific Gamma Patterns in Entorhinal-Hippocampal Networks
Schomburg, E. W., Fernández-Ruiz, A., Mizuseki, K., Berényi, A., Anastassiou, C. A., Koch, C., & Buzsáki, G. (2014) · Neuron · doi:10.1016/j.neuron.2014.08.051 · Cited by 465 · see citing works
Self-citationHippocampal CA1 pyramidal cells form functionally distinct sublayers
Mizuseki, K., Diba, K., Pastalkova, E., & Buzsáki, G. (2011) · Nature Neuroscience · doi:10.1038/nn.2894 · Cited by 453 · see citing works
Self-citationComparison of population coherence of place cells in hippocampal subfields CA1 and CA3
Lee, I., Yoganarasimha, D., Rao, G., & Knierim, J. J. (2004) · Nature · doi:10.1038/nature02739 · Cited by 440 · see citing works
Spike train dynamics predicts theta-related phase precession in hippocampal pyramidal cells
Harris, K. D., Henze, D. A., Hirase, H., Leinekugel, X., Dragoi, G., Czurkó, A., & Buzsáki, G. (2002) · Nature · doi:10.1038/nature00808 · Cited by 398 · see citing works
Self-citationMultisensory Control of Hippocampal Spatiotemporal Selectivity
Ravassard, P., Kees, A. L., Willers, B., Ho, D. G., Aharoni, D. B., Cushman, J. D., Aghajan, Z. M., & Mehta, M. R. (2013) · Science · doi:10.1126/science.1232655 · Cited by 388 · see citing works
Foster, D. J., & Wilson, M. A. (2007) · Hippocampus · doi:10.1002/hipo.20345 · Cited by 381 · see citing works
Parvalbumin-Positive Basket Cells Differentiate among Hippocampal Pyramidal Cells
Lee, S.-H., Marchionni, I., Bezaire, M., Varga, C., Danielson, N., Lovett-Barron, M., Losonczy, A., & Soltesz, I. (2014) · Neuron · doi:10.1016/j.neuron.2014.03.034 · Cited by 358 · see citing works
Progressive Transformation of Hippocampal Neuronal Representations in “Morphed” Environments
Leutgeb, J. K., Leutgeb, S., Treves, A., Meyer, R. M., Barnes, C. A., McNaughton, B. L., Moser, M., & Moser, E. I. (2005) · Neuron · doi:10.1016/j.neuron.2005.09.007 · Cited by 357 · see citing works
Segmentation of spatial experience by hippocampal theta sequences
Gupta, A. S., van der Meer, M. A. A., Touretzky, D. S., & Redish, A. D. (2012) · Nature Neuroscience · doi:10.1038/nn.3138 · Cited by 352 · see citing works
Distinct contribution of adult-born hippocampal granule cells to context encoding
Danielson, N. B., Kaifosh, P., Zaremba, J. D., Lovett-Barron, M., Tsai, J., Denny, C. A., Balough, E. M., Goldberg, A. R., Drew, L. J., Hen, R., et al. (2016) · Neuron · doi:10.1016/j.neuron.2016.02.019 · Cited by 352 · see citing works
Entorhinal-CA3 Dual-Input Control of Spike Timing in the Hippocampus by Theta-Gamma Coupling
Fernández‐Ruiz, A., Oliva, A., Nagy, G. A., Maurer, A. P., Berényi, A., & Buzsáki, G. (2017) · Neuron · doi:10.1016/j.neuron.2017.02.017 · Cited by 344 · see citing works
Self-citationGrid cells require excitatory drive from the hippocampus
Bonnevie, T., Dunn, B. A., Fyhn, M., Hafting, T., Derdikman, D., Kubie, J. L., Roudi, Y., Moser, E. I., & Moser, M. (2013) · Nature Neuroscience · doi:10.1038/nn.3311 · Cited by 341 · see citing works
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 341 · see citing works
Self-citationSpatial Gene-Expression Gradients Underlie Prominent Heterogeneity of CA1 Pyramidal Neurons
Cembrowski, M. S., Bachman, J. L., Wang, L., Sugino, K., Shields, B. C., & Spruston, N. (2016) · Neuron · doi:10.1016/j.neuron.2015.12.013 · Cited by 328 · see citing works
Jensen, O. B., & Lisman, J. E. (2000) · Journal of Neurophysiology · doi:10.1152/jn.2000.83.5.2602 · Cited by 312 · see citing works
Knierim, J. J., Kudrimoti, H. S., & McNaughton, B. L. (1998) · Journal of Neurophysiology · doi:10.1152/jn.1998.80.1.425 · Cited by 297 · see citing works
High-Dimensional Cluster Analysis with the Masked EM Algorithm
Kadir, S., Goodman, D. F. M., & Harris, K. D. (2014) · Neural Computation · doi:10.1162/neco_a_00661 · Cited by 295 · see citing works
Pyramidal Cell-Interneuron Circuit Architecture and Dynamics in Hippocampal Networks
English, D. F., McKenzie, S., Evans, T., Kim, K., Yoon, E., & Buzsáki, G. (2017) · Neuron · doi:10.1016/j.neuron.2017.09.033 · Cited by 285 · see citing works
Self-citationHippocampal CA3 Output Is Crucial for Ripple-Associated Reactivation and Consolidation of Memory
Nakashiba, T., Buhl, D. L., McHugh, T. J., & Tonegawa, S. (2009) · Neuron · doi:10.1016/j.neuron.2009.05.013 · Cited by 281 · see citing works
Spatial Representation along the Proximodistal Axis of CA1
Henriksen, E. J., Colgin, L. L., Barnes, C. A., Witter, M. P., Moser, M., & Moser, E. I. (2010) · Neuron · doi:10.1016/j.neuron.2010.08.042 · Cited by 260 · see citing works
Determinants of different deep and superficial CA1 pyramidal cell dynamics during sharp-wave ripples
Valero, M., Cid, E., Averkin, R. G., Aguilar, J., Sánchez-Aguilera, A., Viney, T. J., Gómez-Domínguez, D., Bellistri, E., & de la Prida, L. M. (2015) · Nature Neuroscience · doi:10.1038/nn.4074 · Cited by 259 · see citing works
Slow and Fast Gamma Rhythms Coordinate Different Spatial Coding Modes in Hippocampal Place Cells
Bieri, K. W., Bobbitt, K. N., & Colgin, L. L. (2014) · Neuron · doi:10.1016/j.neuron.2014.03.013 · Cited by 221 · see citing works
Role of Hippocampal CA2 Region in Triggering Sharp-Wave Ripples
Oliva, A., Fernández‐Ruiz, A., Buzsáki, G., & Berényi, A. (2016) · Neuron · doi:10.1016/j.neuron.2016.08.008 · Cited by 217 · see citing works
Self-citationInfluence 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
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 216 · see citing works
Self-citationTheta phase–specific codes for two-dimensional position, trajectory and heading in the hippocampus
Huxter, J. R., Senior, T. J., Allen, K. L., & Csicsvari, J. (2008) · Nature Neuroscience · doi:10.1038/nn.2106 · Cited by 206 · see citing works
Knierim, J. J. (2002) · Journal of Neuroscience · doi:10.1523/jneurosci.22-14-06254.2002 · Cited by 193 · see citing works
Cannabinoid Control of Learning and Memory through HCN Channels
Maroso, M., Szabo, G. G., Kim, H. K., Alexander, A., Bui, A. D., Lee, S.-H., Lutz, B., & Soltész, I. (2016) · Neuron · doi:10.1016/j.neuron.2016.01.023 · Cited by 186 · see citing works
Lopes‐dos‐Santos, V., van de Ven, G. M., Morley, A., Trouche, S. G., Campo-Urriza, N., & Dupret, D. (2018) · Neuron · doi:10.1016/j.neuron.2018.09.031 · Cited by 178 · see citing works
Battaglia, F. P., Sutherland, G. R., & McNaughton, B. L. (2004) · Journal of Neuroscience · doi:10.1523/jneurosci.4896-03.2004 · Cited by 176 · see citing works
Meyers, E. M. (2013) · Frontiers in Neuroinformatics · doi:10.3389/fninf.2013.00008 · Cited by 170 · see citing works
The medial entorhinal cortex is necessary for temporal organization of hippocampal neuronal activity
Schlesiger, M. I., Cannova, C. C., Boublil, B. L., Hales, J. B., Mankin, E. A., Brandon, M. P., Leutgeb, J. K., Leibold, C., & Leutgeb, S. (2015) · Nature Neuroscience · doi:10.1038/nn.4056 · Cited by 165 · see citing works
Grienberger, C., Milstein, A. D., Bittner, K. C., Romani, S., & Magee, J. C. (2017) · Nature Neuroscience · doi:10.1038/nn.4486 · Cited by 165 · see citing works
Place cells are more strongly tied to landmarks in deep than in superficial CA1
Geiller, T., Fattahi, M., Choi, J.-S., & Royer, S. (2017) · Nature Communications · doi:10.1038/ncomms14531 · Cited by 163 · see citing works
Self-citationDynamic Reconfiguration of Hippocampal Interneuron Circuits during Spatial Learning
Dupret, D., O’Neill, J., & Csicsvari, J. (2013) · Neuron · doi:10.1016/j.neuron.2013.01.033 · Cited by 158 · see citing works
Hippocampal pyramidal cells: the reemergence of cortical lamination
Slomianka, L., Amrein, I., Knuesel, I., Sørensen, J. C. H., & Wolfer, D. P. (2011) · Brain Structure and Function · doi:10.1007/s00429-011-0322-0 · Cited by 152 · see citing works
Preexisting hippocampal network dynamics constrain optogenetically induced place fields
McKenzie, S., Huszár, R., English, D. F., Kim, K., Christensen, F., Yoon, E., & Buzsáki, G. (2021) · Neuron · doi:10.1016/j.neuron.2021.01.011 · Cited by 150 · see citing works
Self-citationQuantifying circular–linear associations: Hippocampal phase precession
Kempter, R., Leibold, C., Buzsáki, G., Diba, K., & Schmidt, R. (2012) · Journal of Neuroscience Methods · doi:10.1016/j.jneumeth.2012.03.007 · Cited by 144 · see citing works
Self-citationMasurkar, A. V., Srinivas, K. V., Brann, D. H., Warren, R., Lowes, D. C., & Siegelbaum, S. A. (2017) · Cell Reports · doi:10.1016/j.celrep.2016.12.012 · Cited by 137 · see citing works
The influence of objects on place field expression and size in distal hippocampal CA1
Burke, S. N., Maurer, A. P., Nematollahi, S., Uprety, A. R., Wallace, J. L., & Barnes, C. A. (2011) · Hippocampus · doi:10.1002/hipo.20929 · Cited by 130 · see citing works
Transformation of a Spatial Map across the Hippocampal-Lateral Septal Circuit
Tingley, D., & Buzsáki, G. (2018) · Neuron · doi:10.1016/j.neuron.2018.04.028 · Cited by 120 · see citing works
Self-citationRecalibration of path integration in hippocampal place cells
Jayakumar, R. P., Madhav, M. S., Savelli, F., Blair, H. T., Cowan, N. J., & Knierim, J. J. (2019) · Nature · doi:10.1038/s41586-019-0939-3 · Cited by 113 · see citing works
Spatial coding and physiological properties of hippocampal neurons in the Cornu Ammonis subregions
Oliva, A., Fernández‐Ruiz, A., Buzsáki, G., & Berényi, A. (2016) · Hippocampus · doi:10.1002/hipo.22659 · Cited by 113 · see citing works
Self-citationHippocampal Place Cells Couple to Three Different Gamma Oscillations during Place Field Traversal
Lasztóczi, B., & Klausberger, T. (2016) · Neuron · doi:10.1016/j.neuron.2016.05.036 · Cited by 105 · see citing works
Functional diversity along the transverse axis of hippocampal area CA1
Igarashi, K. M., Ito, H., Moser, E. I., & Moser, M. (2014) · FEBS Letters · doi:10.1016/j.febslet.2014.06.004 · Cited by 104 · see citing works
Quantifying Circular-Linear Associations: Hippocampal Phase Precession
Robert, S. (2010) · Frontiers in Computational Neuroscience · doi:10.3389/conf.fncom.2010.51.00009 · Cited by 97 · see citing works
Acute silencing of hippocampal CA3 reveals a dominant role in place field responses
Davoudi, H., & Foster, D. J. (2019) · Nature Neuroscience · doi:10.1038/s41593-018-0321-z · Cited by 89 · see citing works
Reversed theta sequences of hippocampal cell assemblies during backward travel
Cei, A., Girardeau, G., Drieu, C., Kanbi, K. E., & Zugaro, M. (2014) · Nature Neuroscience · doi:10.1038/nn.3698 · Cited by 85 · see citing works
Fernández‐Ruiz, A., Makarov, V. A., Benito, N., & Herreras, Ó. (2012) · Journal of Neuroscience · doi:10.1523/jneurosci.4499-11.2012 · Cited by 81 · see citing works
Navas-Olivé, A., Valero, M., Jurado-Parras, T., de Salas-Quiroga, A., Averkin, R. G., Gambino, G., Cid, E., & de la Prida, L. M. (2020) · Nature Communications · doi:10.1038/s41467-020-15840-6 · Cited by 81 · see citing works
Greater running speeds result in altered hippocampal phase sequence dynamics
Maurer, A. P., Burke, S. N., Lipa, P., Skaggs, W. E., & Barnes, C. A. (2011) · Hippocampus · doi:10.1002/hipo.20936 · Cited by 77 · see citing works
Dynamic control of hippocampal spatial coding resolution by local visual cues
Bourboulou, R., Marti, G., Michon, F.-X., Feghaly, E. E., Nouguier, M., Robbe, D., Koenig, J., & Epsztein, J. (2019) · eLife · doi:10.7554/elife.44487 · Cited by 76 · see citing works
Origin of Gamma Frequency Power during Hippocampal Sharp-Wave Ripples
Oliva, A., Fernández-Ruiz, A., de Oliveira, E. F., & Buzsáki, G. (2018) · Cell Reports · doi:10.1016/j.celrep.2018.10.066 · Cited by 75 · see citing works
Self-citationLópez‐Madrona, V. J., Pérez-Montoyo, E., Álvarez-Salvado, E., Moratal, D., Herreras, Ó., Pereda, E., Mirasso, C. R., & Canals, S. (2020) · eLife · doi:10.7554/elife.57313 · Cited by 72 · see citing works
Quantifying location-specific information in the discharge of rat hippocampal place cells
Olypher, A. V., Lánský, P., Muller, R. U., & Fenton, A. A. (2003) · Journal of Neuroscience Methods · doi:10.1016/s0165-0270(03)00123-7 · Cited by 71 · see citing works
Fattahi, M., Sharif, F., Geiller, T. C., & Royer, S. (2018) · Journal of Neuroscience · doi:10.1523/jneurosci.3211-17.2018 · Cited by 69 · see citing works
Self-citationCytoarchitectonic and Dynamic Origins of Giant Positive Local Field Potentials in the Dentate Gyrus
Fernández‐Ruiz, A., Muñoz, S., Sancho, M., Makarova, J., Makarov, V. A., & Herreras, Ó. (2013) · Journal of Neuroscience · doi:10.1523/jneurosci.0338-13.2013 · Cited by 60 · see citing works
Fernández‐Ruiz, A., & Herreras, Ó. (2013) · Frontiers in Computational Neuroscience · doi:10.3389/fncom.2013.00005 · Cited by 48 · see citing works
Micro-drive and headgear for chronic implant and recovery of optoelectronic probes
Chung, J., Sharif, F., Jung, D., Kim, S., & Royer, S. (2017) · Scientific Reports · doi:10.1038/s41598-017-03340-5 · Cited by 34 · see citing works
Self-citationZhou, Y., Sheremet, A., Qin, Y. F., Kennedy, J. P., DiCola, N. M., Burke, S. N., & Maurer, A. P. (2019) · eNeuro · doi:10.1523/eneuro.0142-19.2019 · Cited by 34 · see citing works
Graves, A. R., Moore, S. J., Spruston, N., Tryba, A. K., & Kaczorowski, C. C. (2016) · Journal of Neurophysiology · doi:10.1152/jn.00186.2016 · Cited by 29 · see citing works
Sariev, A., Chung, J., Jung, D., Sharif, F., Lee, J. Y., Kim, S., & Royer, S. (2017) · Journal of Visualized Experiments · doi:10.3791/56438 · Cited by 8 · see citing works
Self-citation
Flagged first, then by citations
1 of the 96 references couldn’t be matched to a known paper.
Research works printed but not linked: 2
- Fernandez-Ruiz A, Muñoz S, Sancho M, Makarov VA, Herreras O. (2013a) Cytoarchitectonic and dynamic origins of giant positive LFPs in the Dentate Gyrus. J Neurosci 33: 15518– 15532. 24068819 PMC6618450
- Save E, Nerad L, and Poucet B (2000). Contribution of multiple sensory information to place field stability in hippocampal place cells. Hippocampus 10, 64– 76. 10706218
Cited by
Sorted by citations
Gamma rhythm communication between entorhinal cortex and dentate gyrus neuronal assemblies
Fernández‐Ruiz, A., Oliva, A., Soula, M., Rocha-Almeida, F., Nagy, G. A., Martín-Vázquez, G., & Buzsáki, G. (2021) · Science · doi:10.1126/science.abf3119 · Cited by 228 · see citing works
Self-citationThe kainic acid models of temporal lobe epilepsy
Rusina, E., Bernard, C., & Williamson, A. (2021) · eneuro · doi:10.1523/eneuro.0337-20.2021 · Cited by 225 · see citing works
Over and above frequency: Gamma oscillations as units of neural circuit operations
Fernández‐Ruiz, A., Sirota, A., Lopes‐dos‐Santos, V., & Dupret, D. (2023) · Neuron · doi:10.1016/j.neuron.2023.02.026 · Cited by 167 · see citing works
Associative and predictive hippocampal codes support memory-guided behaviors
Liu, C., Todorova, R., Tang, W., Oliva, A., & Fernández‐Ruiz, A. (2023) · Science · doi:10.1126/science.adi8237 · Cited by 143 · see citing works
Prefrontal deep projection neurons enable cognitive flexibility via persistent feedback monitoring
Spellman, T., Svei, M., Kaminsky, J. C., Manzano-Nieves, G., & Liston, C. M. (2021) · Cell · doi:10.1016/j.cell.2021.03.047 · Cited by 115 · see citing works
How development sculpts hippocampal circuits and function
Cossart, R., & Khazipov, R. (2021) · Physiological Reviews · doi:10.1152/physrev.00044.2020 · Cited by 119 · see citing works
Preconfigured dynamics in the hippocampus are guided by embryonic birthdate and rate of neurogenesis
Huszár, R., Zhang, Y., Blockus, H., & Buzsáki, G. (2022) · Nature Neuroscience · doi:10.1038/s41593-022-01138-x · Cited by 104 · see citing works
Self-citationHippocampo-cortical circuits for selective memory encoding, routing, and replay
Harvey, R. E., Robinson, H. L., Liu, C., Oliva, A., & Fernandez-Ruiz, A. (2023) · Neuron · doi:10.1016/j.neuron.2023.04.015 · Cited by 101 · see citing works
The representation of context in mouse hippocampus is preserved despite neural drift
Keinath, A. T., Mosser, C., & Brandon, M. P. (2022) · Nature Communications · doi:10.1038/s41467-022-30198-7 · Cited by 92 · see citing works
MUSE-VAE: Multi-Scale VAE for Environment-Aware Long Term Trajectory Prediction
Lee, M., Sohn, S. S., Moon, S., Yoon, S., Kapadia, M., & Pavlović, V. (2022) · IEEE Computer Society Conference on Computer Vision and Pattern Recognition/Proceedings - IEEE Computer Society Conference on Computer Vision and Pattern Recognition/Proceedings · doi:10.1109/cvpr52688.2022.00226 · Cited by 87 · see citing works
Extrinsic control and intrinsic computation in the hippocampal CA1 circuit
Zutshi, I., Valero, M., Fernández‐Ruiz, A., & Buzsáki, G. (2021) · Neuron · doi:10.1016/j.neuron.2021.11.015 · Cited by 83 · see citing works
Self-citationHectoSTAR μLED Optoelectrodes for Large‐Scale, High‐Precision In Vivo Opto‐Electrophysiology
Vöröslakos, M., Kim, K., Slager, N., Ko, E., Oh, S., Parizi, S. S., Hendrix, B., Seymour, J. P., Wise, K. D., Buzsáki, G., et al. (2022) · Advanced Science · doi:10.1002/advs.202105414 · Cited by 58 · see citing works
Self-citationProbing subthreshold dynamics of hippocampal neurons by pulsed optogenetics
Valero, M., Zutshi, I., Yoon, E., & Buzsáki, G. (2022) · Science · doi:10.1126/science.abm1891 · Cited by 65 · see citing works
Self-citationCA1 pyramidal cell diversity is rooted in the time of neurogenesis
Cavalieri, D., Angelova, A., Islah, A., Lopez, C., Bocchio, M., Bollmann, Y., Baude, A., & Cossart, R. (2021) · eLife · doi:10.7554/elife.69270 · Cited by 54 · see citing works
Anxiety-related activity of ventral hippocampal interneurons
Forro, T., Volitaki, E., Malagon‐Vina, H., Klausberger, T., Nevian, T., & Ciocchi, S. (2022) · Progress in Neurobiology · doi:10.1016/j.pneurobio.2022.102368 · Cited by 46 · see citing works
van den Berg, M., Toen, D. V., Verhoye, M., & Keliris, G. A. (2023) · Frontiers in Aging Neuroscience · doi:10.3389/fnagi.2023.1081058 · Cited by 41 · see citing works
Divergent recruitment of developmentally defined neuronal ensembles supports memory dynamics
Kveim, V. A., Salm, L., Ulmer, T., Lahr, M., Kandler, S., Imhof, F., & Donato, F. (2024) · Science · doi:10.1126/science.adk0997 · Cited by 37 · see citing works
Dendritic axon origin enables information gating by perisomatic inhibition in pyramidal neurons
Hodapp, A., Kaiser, M. E., Thome, C., Ding, L., Rozov, A. V., Klumpp, M., Stevens, N. A., Stingl, M., Sackmann, T., Lehmann, N., et al. (2022) · Science · doi:10.1126/science.abj1861 · Cited by 39 · see citing works
A population code for spatial representation in the zebrafish telencephalon
Yang, C., Mammen, L., Kim, B., Li, M., Robson, D. N., & Li, J. M. (2024) · Nature · doi:10.1038/s41586-024-07867-2 · Cited by 38 · see citing works
Engram mechanisms of memory linking and identity
Choucry, A., Nomoto, M., & Inokuchi, K. (2024) · Nature reviews. Neuroscience · doi:10.1038/s41583-024-00814-0 · Cited by 40 · see citing works
Safron, A., Çatal, O., & Verbelen, T. (2022) · Frontiers in Systems Neuroscience · doi:10.3389/fnsys.2022.787659 · Cited by 33 · see citing works
What does engram encode?: Heterogeneous memory engrams for different aspects of experience
Nambu, M. F., Lin, Y.-J., Reuschenbach, J., & Tanaka, K. Z. (2022) · Current Opinion in Neurobiology · doi:10.1016/j.conb.2022.102568 · Cited by 33 · see citing works
Yaşar, T. B., Gombkötő, P., Vyssotski, A. L., Vavladeli, A., Lewis, C. M., Wu, B., Meienberg, L., Lundegardh, V., Helmchen, F., von der Behrens, W., et al. (2024) · Nature Communications · doi:10.1038/s41467-024-49226-9 · Cited by 31 · see citing works
Cooperative actions of interneuron families support the hippocampal spatial code
Valero, M., Abad-Perez, P., Gallardo, A., Picco, M., García-Hernandez, R., Brotons‐Mas, J. R., Martínez-Félix, A., Machold, R. P., Rudy, B., & Buzsáki, G. (2025) · Science · doi:10.1126/science.adv5638 · Cited by 28 · see citing works
Self-citationHeterogeneity of network and coding states in mouse CA1 place cells
Guardamagna, M., Stella, F., & Battaglia, F. P. (2023) · Cell Reports · doi:10.1016/j.celrep.2023.112022 · Cited by 28 · see citing works
Shin, J. D., & Jadhav, S. P. (2024) · Current Biology · doi:10.1016/j.cub.2024.05.018 · Cited by 29 · see citing works
Esparza, J., Quintanilla, J. P., Cid, E., Medeiros, A. C., Gallego, J. Á., & de la Prida, L. M. (2025) · Neuron · doi:10.1016/j.neuron.2025.01.022 · Cited by 26 · see citing works
Organizing the coactivity structure of the hippocampus from robust to flexible memory
Gava, G. P., Lefèvre, L., Broadbelt, T., McHugh, S. B., Lopes‐dos‐Santos, V., Brizee, D., Hartwich, K., Sjoberg, H. T., Perestenko, P. V., Toth, R., et al. (2024) · Science · doi:10.1126/science.adk9611 · Cited by 28 · see citing works
The two tales of hippocampal sharp-wave ripple content: The rigid and the plastic
Hall, A. F., & Wang, D. V. (2023) · Progress in Neurobiology · doi:10.1016/j.pneurobio.2022.102396 · Cited by 23 · see citing works
CA2 orchestrates hippocampal network dynamics
Oliva, A., Fernández‐Ruiz, A., & Karaba, L. A. (2022) · Hippocampus · doi:10.1002/hipo.23495 · Cited by 24 · see citing works
Berndt, M., Trusel, M., Roberts, T. F., Pfeiffer, B. E., & Volk, L. J. (2023) · Neuron · doi:10.1016/j.neuron.2023.08.014 · Cited by 25 · see citing works
Representation of sex-specific social memory in ventral CA1 neurons
Watarai, A., Tao, K., & Okuyama, T. (2025) · Science · doi:10.1126/science.adp3814 · Cited by 22 · see citing works
Time, space, memory and brain–body rhythms
Buzsáki, G. (2025) · Nature reviews. Neuroscience · doi:10.1038/s41583-025-00987-2 · Cited by 28 · see citing works
Self-citationJuxtacellular opto-tagging of hippocampal CA1 neurons in freely moving mice
Ding, L., Balsamo, G., Chen, H., Blanco-Hernández, E., Zouridis, I. S., Naumann, R. K., Preston‐Ferrer, P., & Burgalossi, A. (2022) · eLife · doi:10.7554/elife.71720 · Cited by 20 · see citing works
Efficient information coding and degeneracy in the nervous system
Seenivasan, P., & Narayanan, R. (2022) · Current Opinion in Neurobiology · doi:10.1016/j.conb.2022.102620 · Cited by 19 · see citing works
Deshmukh, S. S. (2021) · Journal of Neuroscience · doi:10.1523/jneurosci.2938-20.2021 · Cited by 16 · see citing works
Goal-directed hippocampal theta sweeps during memory-guided navigation
Tang, W., Mei, X., Harvey, R. E., Carbajal-Leon, E., Netzer, T., Chang, H., Oliva, A., & Fernández‐Ruiz, A. (2026) · Nature Neuroscience · doi:10.1038/s41593-026-02364-3 · Cited by 29 · see citing works
Aversive stimulus-tuned responses in the CA1 of the dorsal hippocampus
Barth, A. M., Jelitai, M., Vasarhelyi-Nagy, M. F., & Varga, V. (2023) · Nature Communications · doi:10.1038/s41467-023-42611-w · Cited by 17 · see citing works
Disruption of the autism gene and chromatin regulator KDM5A alters hippocampal cell identity
Hayek, L. E., DeVries, D., Gogate, A., Aiken, A., Kaur, K. J., & Chahrour, M. H. (2023) · Science Advances · doi:10.1126/sciadv.adi0074 · Cited by 19 · see citing works
Hippocampal ripple diversity organizes neuronal reactivation dynamics in the offline brain
Castelli, M., Lopes‐dos‐Santos, V., Gava, G. P., Lambiotte, R., & Dupret, D. (2025) · Neuron · doi:10.1016/j.neuron.2025.09.012 · Cited by 20 · see citing works
Shinohara, Y., & Kohara, K. (2023) · Hippocampus · doi:10.1002/hipo.23519 · Cited by 18 · see citing works
Functional networks of inhibitory neurons orchestrate synchrony in the hippocampus
Bocchio, M., Vorobyev, A., Sadeh, S., Brustlein, S., Dard, R. F., Reichinnek, S., Emiliani, V., Baude, A., Claudia Clopath, A., & Cossart, R. (2024) · PLoS Biology · doi:10.1371/journal.pbio.3002837 · Cited by 16 · see citing works
Shin, J., Lee, H., Jin, S., & Lee, I. (2022) · Cell Reports · doi:10.1016/j.celrep.2022.111823 · Cited by 15 · see citing works
Abbaspoor, S., & Hoffman, K. L. (2024) · Cell Reports · doi:10.1016/j.celrep.2024.114519 · Cited by 15 · see citing works
Action-driven remapping of hippocampal neuronal populations in jumping rats
Green, L., Tingley, D., Rinzel, J., & Buzsáki, G. (2022) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.2122141119 · Cited by 20 · see citing works
Self-citationSpatio-temporal organization of network activity patterns in the hippocampus
Lopes‐dos‐Santos, V., Brizee, D., & Dupret, D. (2025) · Cell Reports · doi:10.1016/j.celrep.2025.115808 · Cited by 14 · see citing works
Noncanonical circuits, states, and computations of the hippocampus
Farrell, J. S., & Soltész, I. (2025) · Science · doi:10.1126/science.adv4420 · Cited by 13 · see citing works
Subicular neurons represent multiple variables of a hippocampal-dependent task by using theta rhythm
Lee, S., Seol, J.-M., & Lee, I. (2022) · PLoS Biology · doi:10.1371/journal.pbio.3001546 · Cited by 13 · see citing works
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
From cell types to population dynamics: Making hippocampal manifolds physiologically interpretable
Esparza, J., Sebastian, E. R., & de la Prida, L. M. (2023) · Current Opinion in Neurobiology · doi:10.1016/j.conb.2023.102800 · Cited by 12 · see citing works
Laminar organization of pyramidal neuron cell types defines distinct CA1 hippocampal subregions
Pachicano, M., Mehta, S., Hurtado, A. H., Ard, T. D., Stanis, J., Breningstall, B. M., & Bienkowski, M. S. (2025) · Nature Communications · doi:10.1038/s41467-025-66613-y · Cited by 13 · see citing works
High Fidelity Theta Phase Rolling of CA1 Neurons
Sloin, H. E., Levi, A., Someck, S., Spivak, L., & Stark, E. (2022) · Journal of Neuroscience · doi:10.1523/jneurosci.2151-21.2022 · Cited by 10 · see citing works
Tentacle Microelectrode Arrays Uncover Soft Boundary Neurons in Hippocampal CA1
Lv, S., Mo, F., Xu, Z., Wang, Y., Yang, G., Han, M., Jing, L., Xu, W., Duan, Y., Liu, Y., et al. (2024) · Advanced Science · doi:10.1002/advs.202401670 · Cited by 8 · see citing works
A hippocampal population code for rapid generalizationPreprint
Tang, W., Chang, H., Liu, C., Perez-Hernandez, S., Zheng, W. Y., Park, J., Oliva, A., & Fernández‐Ruiz, A. (2025) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2025.03.15.643456 · Cited by 9 · see citing works
Subspace communication in the hippocampal–retrosplenial axis
Gonzalez, J., Vöröslakos, M., Aykan, D., Soto, N., Nitzan, N., Swanson, R., Karadas, M., Chen, Z. S., & Buzsáki, G. (2026) · Nature · doi:10.1038/s41586-026-10481-z · Cited by 7 · see citing works
Self-citationRusso, E., Becker, N., Domanski, A. P. F., Howe, T., Freud, K., Durstewitz, D., & Jones, M. W. (2024) · Nature Communications · doi:10.1038/s41467-024-52988-x · Cited by 7 · see citing works
Early and late place cells during postnatal development of the hippocampus
Wang, C., Yang, H., Chen, S., Wang, C., & Chen, X. (2024) · Nature Communications · doi:10.1038/s41467-024-54320-z · Cited by 7 · see citing works
Time or distance encoding by hippocampal neurons via heterogeneous ramping rates
Heldman, R., Pang, D., Zhao, X., Mensh, B. D., & Wang, Y. (2025) · Nature Communications · doi:10.1038/s41467-025-67038-3 · Cited by 6 · see citing works
Neural population activity for memory: Properties, computations, and codes
Dupret, D., Fusi, S., & Panzeri, S. (2025) · Neuron · doi:10.1016/j.neuron.2025.11.007 · Cited by 5 · see citing works
Hanson, M. A., Bibi, N., Safa, A., Nagarajan, D., Marshall, A. H., Johantges, A. C., & Wester, J. C. (2025) · Journal of Neuroscience · doi:10.1523/jneurosci.0737-24.2024 · Cited by 5 · see citing works
Seenivasan, P., Basak, R., & Narayanan, R. (2024) · The Journal of Physiology · doi:10.1113/jp284629 · Cited by 5 · see citing works
Large-scale 3D EM connectomics dataset of mouse hippocampal area CA1Preprint
Corteze, M., Grasso, E., Vezir, M., & Schmidt, H. (2025) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2025.04.04.647285 · Cited by 5 · see citing works
An independent coding scheme for idiothetic distance in the hippocampus
Nordlund, M., Levernier, N., Trippa, M., Bourboulou, R., Marti, G., Monasson, R., Rouault, H., Epsztein, J., & Koenig, J. (2025) · Current Biology · doi:10.1016/j.cub.2025.07.050 · Cited by 6 · see citing works
Johantges, A. C., Hanson, M. A., Marshall, A. H., Safa, A., Payne, E. K., Hariths, N. R., Bibi, N., & Wester, J. C. (2025) · Journal of Neuroscience · doi:10.1523/jneurosci.1102-25.2025 · Cited by 4 · see citing works
Cortical and subcortical activities during food rewards versus social interaction in rats
Rocha-Almeida, F., Conde-Moro, A. R., Fernández‐Ruiz, A., Delgado-Garcia, J. M., & Gruart, A. (2025) · Scientific Reports · doi:10.1038/s41598-025-87880-1 · Cited by 3 · see citing works
CA3 Circuit Model Compressing Sequential Information in Theta Oscillation and Replay
Kuroki, S., & Mizuseki, K. (2024) · Neural Computation · doi:10.1162/neco_a_01641 · Cited by 3 · see citing works
Shin, J. D., & Jadhav, S. P. (2023) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2023.12.12.571373 · Cited by 3 · see citing works
Opto-juxtacellular interrogation of neural circuits in freely moving mice
Ding, L., Balsamo, G., Diamantaki, M., Preston‐Ferrer, P., & Burgalossi, A. (2023) · Nature Protocols · doi:10.1038/s41596-023-00842-7 · Cited by 2 · see citing works
Dynamic gamma modulation of hippocampal place cells predominates development of theta sequencesPreprint
Wang, N., Wang, Y., Guo, M., Wang, L., Wang, X., Zhu, N., Yang, J., Wang, L., Zheng, C., & Ming, D. (2024) · eLife · doi:10.7554/elife.97334 · Cited by 2 · see citing works
Leprince, E., Filippi, C., Mantez, M., Dard, R. F., Dichio, V., Majnik, J., Cretella, M., Bocchio, M., Picardo, M. A., Monasson, R., et al. (2026) · Current Biology · doi:10.1016/j.cub.2026.04.053 · Cited by 1 · see citing works
Excitatory synapses onto axonic spines jump-start action potentials and route information flow
Yang, H., Wang, K., Chen, Y., Wei, K., Li, L., Tai, Y., Wang, S., Kong, Y., Wang, X., Zhang, W., et al. (2026) · Nature Neuroscience · doi:10.1038/s41593-026-02282-4 · Cited by 1 · see citing works
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 · see citing works
Tian, Y., Qing, H., & Quan, Z. (2026) · Journal of Alzheimer s Disease · doi:10.1177/13872877261473933 · Cited by 1 · see citing works
Sublayer‐ and pathway‐specific control of CA1 input processing by VIP interneurons
Iloun, P., Grenier, J., Veillette, F., & Topolnik, L. (2026) · The Journal of Physiology · doi:10.1113/jp291223 · Cited by 1 · see citing works
A cortical–hippocampal communication undergoes rebalancing after new learning
Hall, A. F., & Wang, D. V. (2026) · eLife · doi:10.7554/elife.107370.3 · Cited by 1 · see citing works
Keinath, A. T., Mosser, C., & Brandon, M. P. (2021) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2021.01.12.426395 · Cited by 1 · see citing works
Berndt, M., Trusel, M., Roberts, T. F., Volk, L. J., & Pfeiffer, B. E. (2022) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2022.10.27.514077 · Cited by 1 · see citing works
Time or distance encoding by hippocampal neurons with heterogenous ramping ratesPreprint
Heldman, R., Pang, D., Zhao, X., Mensh, B. D., & Wang, Y. (2023) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2023.03.12.532295 · Cited by 1 · see citing works
Dynamic Gamma Modulation of Hippocampal Place Cells Predominates Development of Theta SequencesPreprint
Wang, N., Wang, Y., Guo, M., Wang, L., Wang, X., Zhu, N., Yang, J., Wang, L., Zheng, C., & Ming, D. (2025) · eLife · doi:10.7554/elife.97334.2 · Cited by 1 · see citing works
Mapping environmental richness
Lewis, S. (2020) · Nature reviews. Neuroscience · doi:10.1038/s41583-020-00424-6
Functional networks of inhibitory neurons orchestrate synchrony in the hippocampusPreprint
Cossart, R., Bocchio, M., Vorobyev, A., Sadeh, S., Brustlein, S., Reichinnek, S., Emiliani, V., Claudia Clopath, A., & Dard, R. F. (2023) · Research Square · doi:10.21203/rs.3.rs-3304483/v1
Dynamic gamma modulation of hippocampal place cells predominates development of theta sequences
Wang, N., Wang, Y., Guo, M., Wang, L., Wang, X., Zhu, N., Yang, J., Wang, L., Zheng, C., & Ming, D. (2025) · eLife · doi:10.7554/elife.97334.4
Disentangling the Hippocampal Projectome
Varga, V. (2024) · Neuroscience Bulletin · doi:10.1007/s12264-024-01255-6
Cell type-specific impact of aging and Alzheimer disease on hippocampal CA1 perforant path inputPreprint
Santoro, B., Srinivas, K. V., Reyes, I., Tian, C., & Masurkar, A. V. (2024) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2024.08.27.609952
Representation of spatial information in the CA1 field
Mysin, I. E., Vasilev, A. O., Dubrovin, S. V., & Skorokhod, S. N. (2024) · Журнал высшей нервной деятельности им И П Павлова · doi:10.31857/s0044467724050019
Dynamic Gamma Modulation of Hippocampal Place Cells Predominates Development of Theta SequencesPreprint
Wang, N., Wang, Y., Guo, M., Wang, L., Wang, X., Zhu, N., Yang, J., Wang, L., Zheng, C., & Ming, D. (2025) · eLife · doi:10.7554/elife.97334.3
Representation of Spatial Information in Field CA1
Mysin, I. E., Vasilev, A. O., Dubrovin, S. V., & Skorokhod, S. N. (2025) · Neuroscience and Behavioral Physiology · doi:10.1007/s11055-025-01783-2
Brain sources composing irregular field potentials have unique temporal signatures
Muñoz-Arnaiz, R., Makarova, J., Makarov, V. A., & Herreras, Ó. (2025) · Cerebral Cortex · doi:10.1093/cercor/bhaf135
A cortical–hippocampal communication undergoes rebalancing after new learningPreprint
Hall, A. F., & Wang, D. V. (2025) · eLife · doi:10.7554/elife.107370
A cortical–hippocampal communication undergoes rebalancing after new learningPreprint
Hall, A. F., & Wang, D. V. (2025) · eLife · doi:10.7554/elife.107370.1
Maliković, J., Schönbächler, K., Destro, A. L. F., Wolfer, D. P., & Amrein, I. (2025) · Frontiers in Neuroanatomy · doi:10.3389/fnana.2025.1641787
Functional Divergence of Axon-Carrying Dendrite (AcD) and NonAcD Cells in Learning and StabilityPreprint
Hashemi, S., Shafiee, S., & Tetzlaff, C. (2025) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2025.09.15.676360
Shin, J. D., Satchell, M., Miller, P. C., & Jadhav, S. P. (2025) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2025.09.15.676366
Deriving connectivity from spiking activity in detailed models of large-scale cortical microcircuits
Moghbel, F., Hassan, M. T., Guet-McCreight, A., Yao, H. K., & Hay, E. (2025) · iScience · doi:10.1016/j.isci.2025.114313
Calbindin-containing CA1 pyramidal cells support cognitive flexibility in spatial task in micePreprint
Voigt, A., Metodieva, V. D., Alevi, D., Tukker, J. J., Stumpf, A., Parthier, D., & Schmitz, D. (2025) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.64898/2025.11.30.691413
Simultaneous path-integration recalibration in head direction and place cells
Jayakumar, R. P., Sueoka, Y., Ferreyros, M., Li, B. Y., Madhav, M. S., Chen, X., Knierim, J. J., & Cowan, N. J. (2026) · Current Biology · doi:10.1016/j.cub.2026.02.031 · Cited by 2 · see citing works
On the developmental origin of CA1 pyramidal neuron diversity in the adult mouse hippocampus
Cavalieri, D. (2021) · theses.fr (ABES) · doi:10.70675/af05b2d4zc031z48d7z9ebaz859f489a8450
Transformation of spatial representations along the mouse hippocampal circuits
Gandit, B. (2021) · theses.fr (ABES) · doi:10.70675/d646f826z0868z4becz840ez41f31240167b
Nordlund, M. (2022) · theses.fr (ABES) · doi:10.70675/85f2c44az19d3z405bza14azf37b15517fc4
All-optical interrogation of the role of interneurons in CA1 cell assemblies
Vorobyev, A. (2023) · theses.fr (ABES) · doi:10.70675/eb10a4e1za595z4f16z9e3bz115344f3d87a
- Authors
- Sharif, F., Tayebi, B., Buzsáki, G., Royer, S., & Fernandez-Ruiz, A.
- Affiliations
- Boston Children's Hospital (US)
- NYU Langone Health (US)
- Korea Institute of Science and Technology (KR)
- Corresponding author
- Royer, Sébastien
- Venue
- Neuron
- Publisher
- Elsevier BV
- Published
- 2021-01
- Volume
- 109
- Issue
- 2
- Pages
- 363-376.e6
- ISSN
- 0896-6273 (ISSN-L)
- PMC
- PMC7856084
- OpenAlex
- W3105442427
- Cited by
- 111
- References
- 96
- Citations by year
- 2026: 19 · 2025: 28 · 2024: 17 · 2023: 16 · 2022: 20 · 2021: 10 · 2020: 1
- FWCI
- 6.32
- Type
- journal article
- Language
- en
- Open access
- bronze
- doi.org
- Licence
- Locations
- Neuron (publishedVersion)
- bioRxiv (Cold Spring Harbor Laboratory) (acceptedVersion, cc-by-nc-nd)
- PubMed (publishedVersion)
- PubMed Central (acceptedVersion)
- Funders
- Brain and Behavior Research Foundation
- National Institutes of Health
- Topics
- Life Sciences › Neuroscience › Cognitive Neuroscience › Memory and Neural Mechanisms
- Physical Sciences › Engineering › Automotive Engineering › Spatial Cognition and Navigation
- Life Sciences › Neuroscience › Cognitive Neuroscience › Neural dynamics and brain function
- Keywords
- spatial coding, hippocampus, phase codes, gamma oscillations, local inhibition, cognitive maps, navigation
- MeSH terms
- Place Cells, Animals, Electrodes, Implanted, Environment Design, Male, Mice, Inbred C57BL, Nerve Net, Space Perception, Maze Learning, Rats, Long-Evans, Mice, Rats, CA1 Region, Hippocampal
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