Reduction of Theta Rhythm Dissociates Grid Cell Spatial Periodicity from Directional Tuning

Phase relationship between hippocampal place units and the EEG theta rhythm

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Head-direction cells recorded from the postsubiculum in freely moving rats. I. Description and quantitative analysis

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Conjunctive Representation of Position, Direction, and Velocity in Entorhinal Cortex

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Spatial representation in the entorhinal cortex

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Representation of Geometric Borders in the Entorhinal Cortex

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Loss of Hippocampal Theta Rhythm Results in Spatial Memory Deficit in the Rat

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Boundary Vector Cells in the Subiculum of the Hippocampal Formation

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An oscillatory interference model of grid cell firing

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Development of the Spatial Representation System in the Rat

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Development of the Hippocampal Cognitive Map in Preweanling Rats

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Voltage dependence of subthreshold resonance frequency in layer ii of medial entorhinal cortex

Shay, C. F., Boardman, I., James, N. M., & Hasselmo, M. E. (2012) · Hippocampus · doi:10.1002/hipo.22008 · Cited by 26

Heterogeneity in hippocampal place coding

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The activity of thalamic nucleus reuniens is critical for memory retrieval, but not essential for the early phase of “off-line” consolidationPreprint

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Examination of rhythmicity of extracellularly recorded neurons in the entorhinal cortex

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The Art of Grid Fields: Geometry of Neuronal Time

SHILNIKOV, A. L., & Maurer, A. P. (2016) · Frontiers in Neural Circuits · doi:10.3389/fncir.2016.00012 · Cited by 24

From grid cells to place cells with realistic field sizes

Neher, T., Azizi, A. H., & Cheng, S. (2017) · PLoS ONE · doi:10.1371/journal.pone.0181618 · Cited by 27

The Role of the Medial Septum—Associated Networks in Controlling Locomotion and Motivation to Move

Mocellin, P., & Mikulovic, S. (2021) · Frontiers in Neural Circuits · doi:10.3389/fncir.2021.699798 · Cited by 30

In vivo cholinergic modulation of the cellular properties of medial entorhinal cortex neurons

Tsuno, Y., Schultheiss, N. W., & Hasselmo, M. E. (2013) · The Journal of Physiology · doi:10.1113/jphysiol.2012.250431 · Cited by 27

Grid cell disruption in a mouse model of early Alzheimer’s disease reflects reduced integration of self-motion cues

Ying, J., Reboreda, A., Yoshida, M., & Brandon, M. P. (2023) · Current Biology · doi:10.1016/j.cub.2023.04.065 · Cited by 26

Expression and Functional Roles of Kv7/KCNQ/M-Channels in Rat Medial Entorhinal Cortex Layer II Stellate Cells

Nigro, M. J., Mateos‐Aparicio, P., & Storm, J. F. (2014) · Journal of Neuroscience · doi:10.1523/jneurosci.4153-13.2014 · Cited by 23

Head Direction Cells: From Generation to Integration

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Spatial synchronization codes from coupled rate-phase neurons

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Head direction maps remain stable despite grid map fragmentation

Whitlock, J. R., & Derdikman, D. (2012) · Frontiers in Neural Circuits · doi:10.3389/fncir.2012.00009 · Cited by 24

A systems model of alternating theta sweeps via firing rate adaptation

Ji, Z., Chu, T., Wu, S., & Burgess, N. (2025) · Current Biology · doi:10.1016/j.cub.2024.08.059 · Cited by 26

Two septal-entorhinal GABAergic projections differentially control coding properties of spatially tuned neurons in the medial entorhinal cortex

Schlesiger, M. I., Ruff, T., MacLaren, D. A. A., Barriuso-Ortega, I., Saidov, K. M., Yen, T.-Y., & Monyer, H. (2021) · Cell Reports · doi:10.1016/j.celrep.2021.108801 · Cited by 24

Optogenetic pacing of medial septum parvalbumin-positive cells disrupts temporal but not spatial firing in grid cells

Lepperød, M. E., Christensen, A. C., Lensjø, K. K., Buccino, A. P., Yu, J. Y., Fyhn, M., & Hafting, T. (2021) · Science Advances · doi:10.1126/sciadv.abd5684 · Cited by 24

Septo-hippocampal dynamics and the encoding of space and time

Robinson, J. C., Wilmot, J. H., & Hasselmo, M. E. (2023) · Trends in Neurosciences · doi:10.1016/j.tins.2023.06.004 · Cited by 33

Modelling effects on grid cells of sensory input during self‐motion

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Potential roles of cholinergic modulation in the neural coding of location and movement speed

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Efficacy of nonselective optogenetic control of the medial septum over hippocampal oscillations: the influence of speed and implications for cognitive enhancement

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Systemic administration of two different anxiolytic drugs decreases local field potential theta frequency in the medial entorhinal cortex without affecting grid cell firing fields

Monaghan, C. K., Chapman, G. W., & Hasselmo, M. E. (2017) · Neuroscience · doi:10.1016/j.neuroscience.2017.08.056 · Cited by 21

Entorhinal Stellate Cells Show Preferred Spike Phase-Locking to Theta Inputs That Is Enhanced by Correlations in Synaptic Activity

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Reduced grid-like theta modulation in schizophrenia

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Merging information in the entorhinal cortex: what can we learn from robotics experiments and modeling?

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To be a Grid Cell: Shuffling procedures for determining “Gridness”Preprint

Barry, C., & Burgess, N. (2017) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/230250 · Cited by 19

Spatial memory requires hypocretins to elevate medial entorhinal gamma oscillations

Liao, Y., Wen, R., Fu, S., Cheng, X., Ren, S., Lu, M., Qian, L., Luo, F., Wang, Y., Xiao, Q., et al. (2023) · Neuron · doi:10.1016/j.neuron.2023.10.012 · Cited by 19

The Function of Oscillations in the Hippocampal Formation

Lever, C., Kaplan, R., & Burgess, N. (2014) · Springer eBooks · doi:10.1007/978-3-7091-1292-2_12 · Cited by 20

Harnessing the power of theta: natural manipulations of cognitive performance during hippocampal theta-contingent eyeblink conditioning

Hoffmann, L. C., Cicchese, J. J., & Berry, S. D. (2015) · Frontiers in Systems Neuroscience · doi:10.3389/fnsys.2015.00050 · Cited by 20

From A to Z: a potential role for grid cells in spatial navigation

Barry, C., & Bush, D. (2012) · Neural Systems & Circuits · doi:10.1186/2042-1001-2-6 · Cited by 18

Identifying Core Regions for Path Integration on Medial Entorhinal Cortex of Hippocampal Formation

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The transformation from grid cells to place cells is robust to noise in the grid pattern

Azizi, A. H., Schieferstein, N., & Cheng, S. (2014) · Hippocampus · doi:10.1002/hipo.22306 · Cited by 17

Modular microcircuit organization of the presubicular head-direction map

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Optogenetic silencing of medial septal GABAergic neurons disrupts grid cell spatial and temporal coding in the medial entorhinal cortex

Robinson, J. C., Ying, J., Hasselmo, M. E., & Brandon, M. P. (2024) · Cell Reports · doi:10.1016/j.celrep.2024.114590 · Cited by 21

Infusion of GAT1-saporin into the medial septum/vertical limb of the diagonal band disrupts self-movement cue processing and spares mnemonic function

Köppen, J. R., Winter, S. S., Stuebing, S. L., Cheatwood, J. L., & Wallace, D. G. (2012) · Brain Structure and Function · doi:10.1007/s00429-012-0449-7 · Cited by 15

Medial Entorhinal Grid Cells and Head Direction Cells Rotate with a T-Maze More Often During Less Recently Experienced Rotations

Gupta, K., Beer, N. J., Keller, L. A., & Hasselmo, M. E. (2013) · Cerebral Cortex · doi:10.1093/cercor/bht020 · Cited by 17

Medial entorhinal cortex commissural input regulates the activity of spatially and object-tuned cells contributing to episodic memory

Caputi, A., Liu, X., Fuchs, E. C., Liu, Y., & Monyer, H. (2022) · Neuron · doi:10.1016/j.neuron.2022.08.013 · Cited by 17

A septal-ventral tegmental area circuit drives exploratory behavior

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Hippocampal Discoveries: Spatial View Cells, Connectivity, and Computations for Memory and Navigation, in Primates Including Humans

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Models of spatial and temporal dimensions of memory

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Parallel and convergent processing in grid cell, head‐direction cell, boundary cell, and place cell networks

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Reduced spiking in entorhinal cortex during the delay period of a cued spatial response taskPreprint

Gupta, K., Keller, L. A., & Hasselmo, M. E. (2012) · Learning & Memory · doi:10.1101/lm.025866.112 · Cited by 14

Optogenetic reduction of theta oscillations reveals that a single reliable time cell sequence is not required for working memoryPreprint

Yong, H. C., Chang, H., & Brandon, M. P. (2022) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2022.06.25.497592 · Cited by 16

Spatial Maps in the Entorhinal Cortex and Adjacent Structures

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Membrane potential‐dependent integration of synaptic inputs in entorhinal stellate neurons

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Modality-specific Subpopulations of Place Fields Coexist in the Hippocampus

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Sharp Tuning of Head Direction and Angular Head Velocity Cells in the Somatosensory Cortex

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Temporal dynamics of cholinergic activity in the septo-hippocampal system

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Comparison of Properties of Medial Entorhinal Cortex Layer II Neurons in Two Anatomical Dimensions with and without Cholinergic Activation

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How to build a grid cell

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Linking minimal and detailed models of CA1 microcircuits reveals how theta rhythms emerge and their frequencies controlled

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Development of the SPEAR Model: Separate Phases of Encoding and Retrieval Are Necessary for Storing Multiple Overlapping Associative Memories

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A unified hierarchical oscillatory network model of head direction cells, spatially periodic cells, and place cells

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Retrosplenial inputs drive visual representations in the medial entorhinal cortex

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How Does the Brain Solve the Computational Problems of Spatial Navigation?

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Histamine Enhances Theta-Coupled Spiking and Gamma Oscillations in the Medial Entorhinal Cortex Consistent With Successful Spatial Recognition

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Excitatory-inhibitory recurrent dynamics produce robust visual grids and stable attractors

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A Brain-Inspired Goal-Oriented Robot Navigation System

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Hippocampal Signatures of Episodic Memory: Evidence from Single-Unit Recording Studies

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Grid codes underlie multiple cognitive maps in the human brain

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Optogenetic Stimulation of CA1 Pyramidal Neurons at Theta Enhances Recognition Memory in Brain Injured Animals

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How reduction of theta rhythm by medial septum inactivation may covary with disruption of entorhinal grid cell responses due to reduced cholinergic transmission

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Path integration impairments reveal early cognitive changes in subjective cognitive decline

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Models of Path Integration in the Hippocampal Complex

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Learning Spatiotemporal Properties of Hippocampal Place Cells

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Rebound spiking properties of mouse medial entorhinal cortex neurons in vivo

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Hippocampal place cell and inhibitory neuron activity in disrupted-in-schizophrenia-1 mutant mice: implications for working memory deficits

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Computational Models of Grid Cell Firing

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Nucleus incertus projections to rat medial septum and entorhinal cortex: rare collateralization and septal-gating of temporal lobe theta rhythm activity

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Acetylcholine contributes to the integration of self-movement cues in head direction cells.

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Speed modulation of hippocampal theta frequency and amplitude predicts water maze learning

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Modeling of grid cell activity demonstrates in vivo entorhinal ‘look-ahead’ properties

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Inducing theta oscillations in the entorhinal hippocampal network in vitro

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Phase Precession Relative to Turning Angle in Theta‐Modulated Head Direction Cells

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Remapping to Discriminate Contexts with Hippocampal Population Codes

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If I had a million neurons

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Visual boundary cues suffice to anchor place and grid cells in virtual reality

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Critical Points and Traveling Wave in Locomotion: Experimental Evidence and Some Theoretical Considerations

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Intrinsic theta oscillation in the attractor network of grid cells

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Beyond correlation: optimal transport metrics for characterizing representational stability and remapping in neurons encoding spatial memory

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Variational log‐ Gaussian point‐process methods for grid cells

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Hippocampal Remapping Is Constrained by Sparseness rather than Capacity

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Retrosplenial Segregation Reflects the Navigation Load During Ambulatory Movement

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PEDOT-Citrate/SIKVAV modified bioaffinity microelectrode arrays for detecting theta rhythm cells in the retrosplenial cortex of rats under sensory conflict

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Phase precession of grid cells in a network model without external pacemaker

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The Role of Hierarchical Dynamical Functions in Coding for Episodic Memory and Cognition

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Time Makes Space: Emergence of Place Fields in Networks Encoding Temporally Continuous Sensory ExperiencesPreprint

Wang, Z., DiTullio, R. W., Rooke, S., & Balasubramanian, V. (2024) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2024.08.11.607484 · Cited by 10

Spatial coding dysfunction and network instability in the aging medial entorhinal cortex

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Spatial Representation: Maps in a Temporal Void

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Organization of a Latent Space structure in VAE/GAN trained by navigation data

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Dynamical self-organization and efficient representation of space by grid cells

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Contribution of muscarinic M1 receptors to the cholinergic suppression of synaptic responses in layer II of the entorhinal cortex

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Spatio-temporal mechanisms of consolidation, recall and reconsolidation in reward-related memory trace

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