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What is a cognitive map? Organising knowledge for flexible behaviour
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1 of the 135 references listed on this page is in the Retraction Watch database as retracted (export 2026-11-04): 10.7554/elife.12248 (notice 2018-04-12).
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What this work says
Outgoing claims: the papers this work cites, builds on, or argues with.
inferredcites →https://doi.org/10.1002/hipo.20504openalex-snapshot
Progressive increase in grid scale from dorsal to ventral medial entorhinal cortex
inferredcites →https://doi.org/10.1002/hipo.22101openalex-snapshot
Influence of local objects on hippocampal representations: Landmark vectors and memory
inferredcites →https://doi.org/10.1002/hipo.450010207openalex-snapshot
Experience‐dependent modifications of hippocampal place cell firing
inferredcites →https://doi.org/10.1006/jcss.1995.1013openalex-snapshot
On the Computational Power of Neural Nets
inferredcites →https://doi.org/10.1007/11871842_29openalex-snapshot
Bandit Based Monte-Carlo Planning
inferredcites →https://doi.org/10.1007/3-540-44668-0_13openalex-snapshot
Learning to Learn Using Gradient Descent
inferredcites →https://doi.org/10.1016/0031-9384(87)90205-8openalex-snapshot
Effects of selective lesions of Fimbria-Fornix on learning set in the rat
inferredcites →https://doi.org/10.1016/j.beproc.2011.12.001openalex-snapshot
Transitive inference in pigeons: Measuring the associative values of Stimuli B and D
inferredcites →https://doi.org/10.1016/j.beproc.2016.12.012openalex-snapshot
The representation of space in the brain
inferredcites →https://doi.org/10.1016/j.cub.2014.07.078openalex-snapshot
Higher-Order Conditioning Is Impaired by Hippocampal Lesions
inferredcites →https://doi.org/10.1016/j.neuron.2010.02.027openalex-snapshot
Separable Learning Systems in the Macaque Brain and the Role of Orbitofrontal Cortex in Contingent Learning
inferredcites →https://doi.org/10.1016/j.neuron.2011.02.027openalex-snapshot
Model-Based Influences on Humans' Choices and Striatal Prediction Errors
inferredcites →https://doi.org/10.1016/j.neuron.2011.05.014openalex-snapshot
Frontal Cortex and Reward-Guided Learning and Decision-Making
inferredcites →https://doi.org/10.1016/j.neuron.2013.11.005openalex-snapshot
Orbitofrontal Cortex as a Cognitive Map of Task Space
inferredcites →https://doi.org/10.1016/j.neuron.2014.08.031openalex-snapshot
The Neural Network Underlying Incentive-Based Learning: Implications for Interpreting Circuit Disruptions in Psychiatric Disorders
inferredcites →https://doi.org/10.1016/j.neuron.2014.10.049openalex-snapshot
The Orbitofrontal Oracle: Cortical Mechanisms for the Prediction and Evaluation of Specific Behavioral Outcomes
inferredcites →https://doi.org/10.1016/j.neuron.2015.06.011openalex-snapshot
A Map for Social Navigation in the Human Brain
inferredcites →https://doi.org/10.1016/j.neuron.2015.07.006openalex-snapshot
Using Grid Cells for Navigation
inferredcites →https://doi.org/10.1016/j.neuron.2015.09.051openalex-snapshot
Hippocampal Remapping after Partial Inactivation of the Medial Entorhinal Cortex
inferredcites →https://doi.org/10.1016/j.neuron.2016.01.039openalex-snapshot
Grid Cell Responses in 1D Environments Assessed as Slices through a 2D Lattice
inferredcites →https://doi.org/10.1016/j.neuron.2016.02.014openalex-snapshot
Two Anatomically and Computationally Distinct Learning Signals Predict Changes to Stimulus-Outcome Associations in Hippocampus
inferredcites →https://doi.org/10.1016/j.neuron.2016.02.018openalex-snapshot
Reward-Guided Learning with and without Causal Attribution
inferredcites →https://doi.org/10.1016/j.neuron.2016.02.031openalex-snapshot
Unmasking Latent Inhibitory Connections in Human Cortex to Reveal Dormant Cortical Memories
inferredcites →https://doi.org/10.1016/j.neuron.2016.08.019openalex-snapshot
Human Orbitofrontal Cortex Represents a Cognitive Map of State Space
inferredcites →https://doi.org/10.1016/j.neuron.2017.03.025openalex-snapshot
A Multiplexed, Heterogeneous, and Adaptive Code for Navigation in Medial Entorhinal Cortex
inferredcites →https://doi.org/10.1016/j.neuron.2017.08.003openalex-snapshot
Suppression of Ventral Hippocampal Output Impairs Integrated Orbitofrontal Encoding of Task Structure
inferredcites →https://doi.org/10.1016/j.neuron.2018.06.008openalex-snapshot
A Dedicated Population for Reward Coding in the Hippocampus
inferredcites →https://doi.org/10.1016/j.tics.2006.11.004openalex-snapshot
Self-projection and the brain
inferredcites →https://doi.org/10.1017/s0140525x16001837openalex-snapshot
Building machines that learn and think like people
inferredcites →https://doi.org/10.1037//0097-7403.17.3.334openalex-snapshot
Transitive inference formation in pigeons.
inferredcites →https://doi.org/10.1037//0097-7403.22.1.105openalex-snapshot
Concurrent conditional discrimination tests of transitive inference by macaque monkeys: List linking.
inferredcites →https://doi.org/10.1037/0033-295x.102.3.419openalex-snapshot
Why there are complementary learning systems in the hippocampus and neocortex: Insights from the successes and failures of connectionist models of learning and memory.
inferredcites →https://doi.org/10.1037/a0030306openalex-snapshot
Cognitive mechanisms for transitive inference performance in rhesus monkeys: Measuring the influence of associative strength and inferred order.
inferredcites →https://doi.org/10.1037/com0000065openalex-snapshot
Transitive inference in humans (Homo sapiens) and rhesus macaques (Macaca mulatta) after massed training of the last two list items.
inferredcites →https://doi.org/10.1037/h0053944openalex-snapshot
Studies in spatial learning. I. Orientation and the short-cut.
inferredcites →https://doi.org/10.1038/17605openalex-snapshot
The global record of memory in hippocampal neuronal activity
inferredcites →https://doi.org/10.1038/22268openalex-snapshot
Neural correlates of decision variables in parietal cortex
inferredcites →https://doi.org/10.1038/30918openalex-snapshot
Collective dynamics of ‘small-world’ networks
inferredcites →https://doi.org/10.1038/381607a0openalex-snapshot
Emergence of simple-cell receptive field properties by learning a sparse code for natural images
inferredcites →https://doi.org/10.1038/nature03687openalex-snapshot
Invariant visual representation by single neurons in the human brain
inferredcites →https://doi.org/10.1038/nature03721openalex-snapshot
Microstructure of a spatial map in the entorhinal cortex
inferredcites →https://doi.org/10.1038/nature04676openalex-snapshot
Neurons in the orbitofrontal cortex encode economic value
inferredcites →https://doi.org/10.1038/nature04766openalex-snapshot
Cortical substrates for exploratory decisions in humans
inferredcites →https://doi.org/10.1038/nature05601openalex-snapshot
Hippocampal remapping and grid realignment in entorhinal cortex
inferredcites →https://doi.org/10.1038/nature08704openalex-snapshot
Evidence for grid cells in a human memory network
inferredcites →https://doi.org/10.1038/nature10754openalex-snapshot
Neuron-type-specific signals for reward and punishment in the ventral tegmental area
inferredcites →https://doi.org/10.1038/nature12742openalex-snapshot
Context-dependent computation by recurrent dynamics in prefrontal cortex
inferredcites →https://doi.org/10.1038/nature14236openalex-snapshot
Human-level control through deep reinforcement learning
inferredcites →https://doi.org/10.1038/nature16961openalex-snapshot
Mastering the game of Go with deep neural networks and tree search
inferredcites →https://doi.org/10.1038/nature21682openalex-snapshot
Neural ensemble dynamics underlying a long-term associative memory
inferredcites →https://doi.org/10.1038/nature21692openalex-snapshot
Mapping of a non-spatial dimension by the hippocampal–entorhinal circuit
inferredcites →https://doi.org/10.1038/ncomms12554openalex-snapshot
A dynamic code for economic object valuation in prefrontal cortex neurons
inferredcites →https://doi.org/10.1038/nn.2957openalex-snapshot
Expectancy-related changes in firing of dopamine neurons depend on orbitofrontal cortex
inferredcites →https://doi.org/10.1038/nn.3331openalex-snapshot
Neural representations of events arise from temporal community structure
inferredcites →https://doi.org/10.1038/nn.3466openalex-snapshot
Direct recordings of grid-like neuronal activity in human spatial navigation
inferredcites →https://doi.org/10.1038/nn.3981openalex-snapshot
Model-based choices involve prospective neural activity
inferredcites →https://doi.org/10.1038/nn.4042openalex-snapshot
A neural network that finds a naturalistic solution for the production of muscle activity
inferredcites →https://doi.org/10.1038/nn.4244openalex-snapshot
Using goal-driven deep learning models to understand sensory cortex
inferredcites →https://doi.org/10.1038/nn.4300openalex-snapshot
Neuronal remapping and circuit persistence in economic decisions
inferredcites →https://doi.org/10.1038/nn.4613openalex-snapshot
Dorsal hippocampus contributes to model-based planning
inferredcites →https://doi.org/10.1038/nn1560openalex-snapshot
Uncertainty-based competition between prefrontal and dorsolateral striatal systems for behavioral control
inferredcites →https://doi.org/10.1038/nn1954openalex-snapshot
Learning the value of information in an uncertain world
inferredcites →https://doi.org/10.1038/nrn.2016.56openalex-snapshot
Over the river, through the woods: cognitive maps in the hippocampus and orbitofrontal cortex
inferredcites →https://doi.org/10.1038/nrn3785openalex-snapshot
Functional organization of the hippocampal longitudinal axis
inferredcites →https://doi.org/10.1038/s41562-017-0180-8openalex-snapshot
The successor representation in human reinforcement learning
inferredcites →https://doi.org/10.1038/s41586-018-0102-6openalex-snapshot
Vector-based navigation using grid-like representations in artificial agents
inferredcites →https://doi.org/10.1038/s41586-019-1077-7openalex-snapshot
Object-vector coding in the medial entorhinal cortex
inferredcites →https://doi.org/10.1038/s41593-017-0049-1openalex-snapshot
Human entorhinal cortex represents visual space using a boundary-anchored grid
inferredcites →https://doi.org/10.1038/s41593-017-0050-8openalex-snapshot
Hexadirectional coding of visual space in human entorhinal cortex
inferredcites →https://doi.org/10.1038/s41593-017-0062-4openalex-snapshot
Grid cells map the visual world
inferredcites →https://doi.org/10.1038/s41593-018-0147-8openalex-snapshot
Prefrontal cortex as a meta-reinforcement learning system
inferredcites →https://doi.org/10.1073/pnas.0610561104openalex-snapshot
Patients with hippocampal amnesia cannot imagine new experiences
inferredcites →https://doi.org/10.1073/pnas.0802631105openalex-snapshot
The discovery of structural form
inferredcites →https://doi.org/10.1073/pnas.1209918109openalex-snapshot
Grid cell firing patterns signal environmental novelty by expansion
inferredcites →https://doi.org/10.1073/pnas.1414219112openalex-snapshot
Interplay of approximate planning strategies
inferredcites →https://doi.org/10.1073/pnas.1609094113openalex-snapshot
Adaptive integration of habits into depth-limited planning defines a habitual-goal–directed spectrum
inferredcites →https://doi.org/10.1073/pnas.1611835114openalex-snapshot
Overcoming catastrophic forgetting in neural networks
inferredcites →https://doi.org/10.1073/pnas.94.13.7109openalex-snapshot
The hippocampus and memory for orderly stimulus relations
inferredcites →https://doi.org/10.1093/cercor/bhk039openalex-snapshot
Frontal-Temporal Disconnection Abolishes Object Discrimination Learning Set in Macaque Monkeys
inferredcites →https://doi.org/10.1101/196758openalex-snapshot
Offline Replay Supports Planning: fMRI Evidence from Reward Revaluation
inferredcites →https://doi.org/10.1101/245720openalex-snapshot
Value Representations in the Rodent Orbitofrontal Cortex Drive Learning, not Choice
inferredcites →https://doi.org/10.1101/421461openalex-snapshot
Intuitive planning: global navigation through cognitive maps based on grid-like codes
inferredcites →https://doi.org/10.1109/tnn.1998.712192openalex-snapshot
Reinforcement Learning: An Introduction
inferredcites →https://doi.org/10.1109/tnn.2004.842673openalex-snapshot
Reinforcement Learning: An Introduction
inferredcites →https://doi.org/10.1126/science.1094285openalex-snapshot
Dissociable Roles of Ventral and Dorsal Striatum in Instrumental Conditioning
inferredcites →https://doi.org/10.1126/science.1114037openalex-snapshot
Independent Codes for Spatial and Episodic Memory in Hippocampal Neuronal Ensembles
inferredcites →https://doi.org/10.1126/science.1166466openalex-snapshot
Representation of Geometric Borders in the Entorhinal Cortex
inferredcites →https://doi.org/10.1126/science.1222403openalex-snapshot
Neural Representations of Location Composed of Spatially Periodic Bands
inferredcites →https://doi.org/10.1126/science.1227489openalex-snapshot
Orbitofrontal Cortex Supports Behavior and Learning Using Inferred But Not Cached Values
inferredcites →https://doi.org/10.1126/science.1255514openalex-snapshot
A critical time window for dopamine actions on the structural plasticity of dendritic spines
inferredcites →https://doi.org/10.1126/science.1500816openalex-snapshot
Connecting multiple spatial scales to decode the population activity of grid cells
inferredcites →https://doi.org/10.1126/science.275.5306.1593openalex-snapshot
A Neural Substrate of Prediction and Reward
inferredcites →https://doi.org/10.1126/science.aab3050openalex-snapshot
Human-level concept learning through probabilistic program induction
inferredcites →https://doi.org/10.1126/science.aaf0941openalex-snapshot
Organizing conceptual knowledge in humans with a gridlike code
inferredcites →https://doi.org/10.1126/science.aak9589openalex-snapshot
Vectorial representation of spatial goals in the hippocampus of bats
inferredcites →https://doi.org/10.1126/science.aao3474openalex-snapshot
Social place-cells in the bat hippocampus
inferredcites →https://doi.org/10.1126/science.aao3898openalex-snapshot
Spatial representations of self and other in the hippocampus
inferredcites →https://doi.org/10.1146/annurev.neuro.29.051605.113038openalex-snapshot
The Neural Basis of Decision Making
inferredcites →https://doi.org/10.1162/jocn_a_00203openalex-snapshot
The Human Ventromedial Prefrontal Cortex Is Critical for Transitive Inference
inferredcites →https://doi.org/10.1162/neco.1993.5.4.613openalex-snapshot
Improving Generalization for Temporal Difference Learning: The Successor Representation
inferredcites →https://doi.org/10.1177/1073858411435128openalex-snapshot
Information Processing in Decision-Making Systems
inferredcites →https://doi.org/10.1371/journal.pcbi.1000291openalex-snapshot
Accurate Path Integration in Continuous Attractor Network Models of Grid Cells
inferredcites →https://doi.org/10.1371/journal.pcbi.1002235openalex-snapshot
Grid Cells, Place Cells, and Geodesic Generalization for Spatial Reinforcement Learning
inferredcites →https://doi.org/10.1371/journal.pcbi.1004523openalex-snapshot
Implicit Value Updating Explains Transitive Inference Performance: The Betasort Model
inferredcites →https://doi.org/10.1371/journal.pcbi.1004584openalex-snapshot
Computing the Local Field Potential (LFP) from Integrate-and-Fire Network Models
inferredcites →https://doi.org/10.1523/jneurosci.0091-11.2011openalex-snapshot
Dissociable Effects of Subtotal Lesions within the Macaque Orbital Prefrontal Cortex on Reward-Guided Behavior
inferredcites →https://doi.org/10.1523/jneurosci.10-02-00420.1990openalex-snapshot
Head-direction cells recorded from the postsubiculum in freely moving rats. I. Description and quantitative analysis
inferredcites →https://doi.org/10.1523/jneurosci.1319-09.2009openalex-snapshot
Boundary Vector Cells in the Subiculum of the Hippocampal Formation
inferredcites →https://doi.org/10.1523/jneurosci.1378-09.2009openalex-snapshot
Robust Conjunctive Item–Place Coding by Hippocampal Neurons Parallels Learning What Happens Where
inferredcites →https://doi.org/10.1523/jneurosci.1532-04.2004openalex-snapshot
Entorhinal Cortex Lesions Disrupt the Relational Organization of Memory in Monkeys
inferredcites →https://doi.org/10.1523/jneurosci.16-23-07478.1996openalex-snapshot
D1/D5 Dopamine Receptor Activation Increases the Magnitude of Early Long-Term Potentiation at CA1 Hippocampal Synapses
inferredcites →https://doi.org/10.1523/jneurosci.2631-10.2010openalex-snapshot
Differential Contributions of the Primate Ventrolateral Prefrontal and Orbitofrontal Cortex to Serial Reversal Learning
inferredcites →https://doi.org/10.1523/jneurosci.3761-07.2007openalex-snapshot
Neural Ensembles in CA3 Transiently Encode Paths Forward of the Animal at a Decision Point
inferredcites →https://doi.org/10.2307/1416950openalex-snapshot
An Experimental Study of Apparent Behavior
inferredcites →https://doi.org/10.2307/1419876openalex-snapshot
The Staircase-Method in Psychophysics
inferredcites →https://doi.org/10.2307/3331482openalex-snapshot
The Senses Considered as Perceptual Systems
inferredcites →https://doi.org/10.48550/arxiv.1606.04474openalex-snapshot
Learning to learn by gradient descent by gradient descent
inferredcites →https://doi.org/10.48550/arxiv.1606.05336openalex-snapshot
On the Expressive Power of Deep Neural Networks
inferredcites →https://doi.org/10.48550/arxiv.1703.03400openalex-snapshot
Model-Agnostic Meta-Learning for Fast Adaptation of Deep Networks
inferredcites →https://doi.org/10.48550/arxiv.1703.04200openalex-snapshot
Continual Learning Through Synaptic Intelligence
inferredcites →https://doi.org/10.48550/arxiv.1803.07770openalex-snapshot
Emergence of grid-like representations by training recurrent neural networks to perform spatial localization
inferredcites →https://doi.org/10.48550/arxiv.1805.09042openalex-snapshot
Generalisation of structural knowledge in the hippocampal-entorhinal system
inferredcites →https://doi.org/10.48550/arxiv.1806.01830openalex-snapshot
Relational Deep Reinforcement Learning
inferredcites →https://doi.org/10.7554/elife.06063openalex-snapshot
Hippocampal place cells construct reward related sequences through unexplored space
inferredcites →https://doi.org/10.7554/elife.06633openalex-snapshot
Ventromedial hypothalamic neurons control a defensive emotion state
inferredcites →https://doi.org/10.7554/elife.09685openalex-snapshot
Retroactive modulation of spike timing-dependent plasticity by dopamine
inferredcites →https://doi.org/10.7554/elife.10094openalex-snapshot
Extracting grid cell characteristics from place cell inputs using non-negative principal component analysis
inferredcites →https://doi.org/10.7554/elife.12248openalex-snapshot
RETRACTED: A mathematical model explains saturating axon guidance responses to molecular gradients
inferredcites →https://doi.org/10.7554/elife.17086openalex-snapshot
A map of abstract relational knowledge in the human hippocampal–entorhinal cortex
inferredcites →https://doi.org/10.7554/elife.20010openalex-snapshot
Genetic evidence that Nkx2.2 acts primarily downstream of Neurog3 in pancreatic endocrine lineage development
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
inferred← citeshttps://doi.org/10.1016/j.neuropsychologia.2020.107477openalex-snapshot
The radiation of autonoetic consciousness in cognitive neuroscience: A functional neuroanatomy perspective
inferred← citeshttps://doi.org/10.1038/s41467-019-13472-zopenalex-snapshot
Human confidence judgments reflect reliability-based hierarchical integration of contextual information
inferred← citeshttps://doi.org/10.1073/pnas.1809298115openalex-snapshot
Dopaminergic basis for signaling belief updates, but not surprise, and the link to paranoia
inferred← citeshttps://doi.org/10.1101/2021.07.21.453253openalex-snapshot
Transfer of learned cognitive flexibility to novel stimuli and task sets
inferred← citeshttps://doi.org/10.1101/2025.03.24.645064openalex-snapshot
Recasting adaptation as strategy inference
inferred← citeshttps://doi.org/10.1101/433862openalex-snapshot
Neurons remap to represent memories in the human entorhinal cortex
inferred← citeshttps://doi.org/10.3233/faia210207openalex-snapshot
Social Media User Profiling Based on Genre Extraction
inferred← citeshttps://doi.org/10.70675/e5b36e93za976z4c91zbe75z1fa58bfb6985openalex-snapshot
Spatial resolution of the cognitive map : investigation on the influence of proximal visual cues on spatial coding resolution in area CA1 of the dorsal hippocampus using virtual reality
inferred← citeshttps://doi.org/10.7554/elife.56477openalex-snapshot
Private–public mappings in human prefrontal cortex
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