On the public citation graph
Learning cognitive maps as structured graphs for vicarious evaluation
0 signed · 73 inferred · view as graph
Inferred edges come from two machine sources: sweeps of open repository metadata (mostly SSRN and Zenodo), and a bulk OpenAlex citation snapshot. Every row below is labelled with the one it came from. Neither is a complete citation index — absence here is not evidence of absence.
Is this your work? Sign in with ORCID and put your name on the
claims that are yours.
Reference health. See whether every reference in this work resolves to a
known work and none has been retracted — and get a dated CiteStamped
badge you can embed.
What this work says
Outgoing claims: the papers this work cites, builds on, or argues with.
inferredcites →https://doi.org/10.1002/hipo.22523openalex-snapshot
Statistical learning of temporal community structure in the hippocampus
inferredcites →https://doi.org/10.1002/hipo.22750openalex-snapshot
Space, time, and episodic memory: The hippocampus is all over the cognitive map
inferredcites →https://doi.org/10.1007/7854_2016_462openalex-snapshot
Neural Activity Patterns Underlying Spatial Coding in the Hippocampus
inferredcites →https://doi.org/10.1007/978-3-319-10377-8_1openalex-snapshot
Community Detection and Visualization of Networks with the Map Equation Framework
inferredcites →https://doi.org/10.1016/j.asoc.2019.106010openalex-snapshot
Community detection in networks using bio-inspired optimization: Latest developments, new results and perspectives with a selection of recent meta-heuristics
inferredcites →https://doi.org/10.1016/j.cell.2020.10.024openalex-snapshot
The Tolman-Eichenbaum Machine: Unifying Space and Relational Memory through Generalization in the Hippocampal Formation
inferredcites →https://doi.org/10.1016/j.cobeha.2017.08.007openalex-snapshot
Memory integration constructs maps of space, time, and concepts
inferredcites →https://doi.org/10.1016/j.jtbi.2019.110089openalex-snapshot
On Markov blankets and hierarchical self-organisation
inferredcites →https://doi.org/10.1016/j.neuron.2005.09.007openalex-snapshot
Progressive Transformation of Hippocampal Neuronal Representations in “Morphed” Environments
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.2018.10.002openalex-snapshot
What Is a Cognitive Map? Organizing Knowledge for Flexible Behavior
inferredcites →https://doi.org/10.1016/j.pneurobio.2019.101717openalex-snapshot
Structure learning and the posterior parietal cortex
inferredcites →https://doi.org/10.1016/j.tics.2018.07.006openalex-snapshot
Space and Time: The Hippocampus as a Sequence Generator
inferredcites →https://doi.org/10.1016/j.tins.2008.06.008openalex-snapshot
Understanding memory through hippocampal remapping
inferredcites →https://doi.org/10.1016/s0896-6273(00)00018-0openalex-snapshot
Trajectory Encoding in the Hippocampus and Entorhinal Cortex
inferredcites →https://doi.org/10.1016/s0896-6273(00)00071-4openalex-snapshot
Hippocampal Neurons Encode Information about Different Types of Memory Episodes Occurring in the Same Location
inferredcites →https://doi.org/10.1016/s0896-6273(00)80773-4openalex-snapshot
The Hippocampus, Memory, and Place Cells
inferredcites →https://doi.org/10.1016/s0896-6273(03)00752-9openalex-snapshot
Prospective and Retrospective Memory Coding in the Hippocampus
inferredcites →https://doi.org/10.1017/cbo9780511809071openalex-snapshot
Introduction to Information Retrieval
inferredcites →https://doi.org/10.1037/a0033621openalex-snapshot
The hippocampus, time, and memory across scales.
inferredcites →https://doi.org/10.1037/h0055304openalex-snapshot
There is more than one kind of learning.
inferredcites →https://doi.org/10.1037/h0057054openalex-snapshot
Prediction of vicarious trial and error by means of the schematic sowbug.
inferredcites →https://doi.org/10.1038/416090aopenalex-snapshot
Long-term plasticity in hippocampal place-cell representation of environmental geometry
inferredcites →https://doi.org/10.1038/nature03687openalex-snapshot
Invariant visual representation by single neurons in the human brain
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/nn.3567openalex-snapshot
Integration of visual motion and locomotion in mouse visual cortex
inferredcites →https://doi.org/10.1038/nn.4656openalex-snapshot
The cognitive map in humans: spatial navigation and beyond
inferredcites →https://doi.org/10.1038/s41467-019-13760-8openalex-snapshot
A non-spatial account of place and grid cells based on clustering models of concept learning
inferredcites →https://doi.org/10.1038/s41562-017-0180-8openalex-snapshot
The successor representation in human reinforcement learning
inferredcites →https://doi.org/10.1038/s41593-019-0470-8openalex-snapshot
Learning task-state representations
inferredcites →https://doi.org/10.1073/pnas.0706851105openalex-snapshot
Maps of random walks on complex networks reveal community structure
inferredcites →https://doi.org/10.1073/pnas.1409770111openalex-snapshot
Scalable detection of statistically significant communities and hierarchies, using message passing for modularity
inferredcites →https://doi.org/10.1073/pnas.1421056111openalex-snapshot
Place cells in the hippocampus: Eleven maps for eleven rooms
inferredcites →https://doi.org/10.1093/comjnl/30.6.541openalex-snapshot
Data Compression Using Dynamic Markov Modelling
inferredcites →https://doi.org/10.1098/rstb.2008.0322openalex-snapshot
Sequence memory for prediction, inference and behaviour
inferredcites →https://doi.org/10.1101/449470openalex-snapshot
Predicting the Future with Multi-scale Successor Representations
inferredcites →https://doi.org/10.1101/565689openalex-snapshot
CA1 pyramidal cells organize an episode by segmented and ordered events
inferredcites →https://doi.org/10.1101/lm.041780.116openalex-snapshot
Active Inference, epistemic value, and vicarious trial and error
inferredcites →https://doi.org/10.1109/proc.1976.10159openalex-snapshot
Continuous speech recognition by statistical methods
inferredcites →https://doi.org/10.1111/nyas.13043openalex-snapshot
The hippocampus: a special place for time
inferredcites →https://doi.org/10.1126/sciadv.1600028openalex-snapshot
Representing higher-order dependencies in networks
inferredcites →https://doi.org/10.1126/science.1108905openalex-snapshot
Attractor Dynamics in the Hippocampal Representation of the Local Environment
inferredcites →https://doi.org/10.1126/science.271.5257.1870openalex-snapshot
Replay of Neuronal Firing Sequences in Rat Hippocampus During Sleep Following Spatial Experience
inferredcites →https://doi.org/10.1126/science.8351520openalex-snapshot
Dynamics of the Hippocampal Ensemble Code for Space
inferredcites →https://doi.org/10.1126/science.aag2612openalex-snapshot
A generative vision model that trains with high data efficiency and breaks text-based CAPTCHAs
inferredcites →https://doi.org/10.1126/science.aav5404openalex-snapshot
Schema cells in the macaque hippocampus
inferredcites →https://doi.org/10.1146/annurev.neuro.31.061307.090723openalex-snapshot
Place Cells, Grid Cells, and the Brain's Spatial Representation System
inferredcites →https://doi.org/10.1162/08997660460733976openalex-snapshot
Bayesian Computation in Recurrent Neural Circuits
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/10.1162/neco.1996.8.1.85openalex-snapshot
A Model of Spatial Map Formation in the Hippocampus of the Rat
inferredcites →https://doi.org/10.1162/netn_a_00018openalex-snapshot
The graphical brain: Belief propagation and active inference
inferredcites →https://doi.org/10.1214/aos/1176346060openalex-snapshot
On the Convergence Properties of the EM Algorithm
inferredcites →https://doi.org/10.1371/journal.pcbi.1000532openalex-snapshot
Towards a Mathematical Theory of Cortical Micro-circuits
inferredcites →https://doi.org/10.1371/journal.pcbi.1003037openalex-snapshot
Bayesian Computation Emerges in Generic Cortical Microcircuits through Spike-Timing-Dependent Plasticity
inferredcites →https://doi.org/10.1523/jneurosci.0151-18.2018openalex-snapshot
The Successor Representation: Its Computational Logic and Neural Substrates
inferredcites →https://doi.org/10.1523/jneurosci.09-07-02382.1989openalex-snapshot
Place cells and silent cells in the hippocampus of freely-behaving rats
inferredcites →https://doi.org/10.1523/jneurosci.1578-18.2018openalex-snapshot
Insensitivity of place cells to the value of spatial goals in a two-choice flexible navigation task
inferredcites →https://doi.org/10.1523/jneurosci.22-13-05760.2002openalex-snapshot
The Hippocampus and Disambiguation of Overlapping Sequences
inferredcites →https://doi.org/10.1523/jneurosci.3413-10.2011openalex-snapshot
Hippocampal Neurons Encode Different Episodes in an Overlapping Sequence of Odors Task
inferredcites →https://doi.org/10.32470/ccn.2019.1407-0openalex-snapshot
Memorize-Generalize: An online algorithm for learning higher-order sequential structure with cloned Hidden Markov Models
inferredcites →https://doi.org/10.3389/fnbeh.2017.00253openalex-snapshot
Hippocampal Remapping and Its Entorhinal Origin
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.15986openalex-snapshot
Place cells on a maze encode routes rather than destinations
inferredcites →https://doi.org/10.7554/elife.51140openalex-snapshot
Hippocampal remapping as hidden state inference
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
inferred← citeshttps://doi.org/10.1007/978-3-031-47958-8_14openalex-snapshot
Relative Representations for Cognitive Graphs
inferred← citeshttps://doi.org/10.1016/j.cobeha.2021.02.019openalex-snapshot
Reinforcement-guided learning in frontal neocortex: emerging computational concepts
inferred← citeshttps://doi.org/10.1016/j.pneurobio.2022.102329openalex-snapshot
The hippocampal formation as a hierarchical generative model supporting generative replay and continual learning
inferred← citeshttps://doi.org/10.1101/2020.09.09.290601openalex-snapshot
A detailed mathematical theory of thalamic and cortical microcircuits based on inference in a generative vision model
inferred← citeshttps://doi.org/10.1101/2020.12.31.424926openalex-snapshot
Learning attention-controllable border-ownership for objectness inference and binding
Editorial review for independent work. ICSAC — the Institute for Complexity
Science and Advanced Computing — runs a structured editorial panel for researchers
publishing outside journals, and publishes on CiteStamp rails. Submission is free
and goes through ORCID: icsacinstitute.org/submit.