On the public citation graph
Associative Learning from Replayed Experience
0 signed · 110 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known work and none has been retracted — and get a dated CiteStamped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/10.1001/archneurpsyc.1930.02220110256018openalex-snapshot
Conditioned Reflexes: An Investigation of the Physiological Activity of the Cerebral Cortex.
inferredcites →https://doi.org/10.1006/jmps.2001.1388openalex-snapshot
A Distributed Representation of Temporal Context
inferredcites →https://doi.org/10.1006/lmot.1994.1008openalex-snapshot
Cue Competition in Causality Judgments: The Role of Nonpresentation of Compound Stimulus Elements
inferredcites →https://doi.org/10.1007/bf00992699openalex-snapshot
Self-improving reactive agents based on reinforcement learning, planning and teaching
inferredcites →https://doi.org/10.1007/bf00993104openalex-snapshot
Prioritized Sweeping: Reinforcement Learning with Less Data and Less Time
inferredcites →https://doi.org/10.1016/0023-9690(91)90009-wopenalex-snapshot
Trace conditioning of the rabbit's nictitating membrane response as a function of CS-US interstimulus interval and trials per session
inferredcites →https://doi.org/10.1016/0031-9384(77)90123-8openalex-snapshot
Disruption of rabbit (Oryctolagus cuniculus) nictitating membrane conditioning by posttrial electrical stimulation of hippocampus
inferredcites →https://doi.org/10.1016/b978-1-55860-141-3.50030-4openalex-snapshot
Integrated Architectures for Learning, Planning, and Reacting Based on Approximating Dynamic Programming
inferredcites →https://doi.org/10.1016/c2009-0-62209-1openalex-snapshot
The Psychology of Learning and Motivation: Advances in Research and Theory
inferredcites →https://doi.org/10.1016/j.beproc.2007.07.003openalex-snapshot
Pavlovian backward conditioned inhibition in humans: Summation and retardation tests
inferredcites →https://doi.org/10.1016/j.beth.2012.11.001openalex-snapshot
Preventing Return of Fear in an Animal Model of Anxiety: Additive Effects of Massive Extinction and Extinction in Multiple Contexts
inferredcites →https://doi.org/10.1016/j.cobeha.2015.08.010openalex-snapshot
Integrating memories to guide decisions
inferredcites →https://doi.org/10.1016/j.neunet.2005.08.009openalex-snapshot
Hippocampal replay contributes to within session learning in a temporal difference reinforcement learning model
inferredcites →https://doi.org/10.1016/j.neuron.2009.07.027openalex-snapshot
Hippocampal Replay of Extended Experience
inferredcites →https://doi.org/10.1016/j.neuron.2010.01.034openalex-snapshot
Hippocampal Replay Is Not a Simple Function of Experience
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.2013.09.007openalex-snapshot
Goals and Habits in the Brain
inferredcites →https://doi.org/10.1016/j.sleep.2007.03.011openalex-snapshot
Sleep-dependent memory consolidation and reconsolidation
inferredcites →https://doi.org/10.1016/j.tics.2016.05.004openalex-snapshot
What Learning Systems do Intelligent Agents Need? Complementary Learning Systems Theory Updated
inferredcites →https://doi.org/10.1016/s0005-7894(71)80064-3openalex-snapshot
Phobias and preparedness
inferredcites →https://doi.org/10.1016/s0079-7421(08)60422-3openalex-snapshot
Human Memory: A Proposed System and its Control Processes
inferredcites →https://doi.org/10.1023/a:1022689900470openalex-snapshot
Instance-Based Learning Algorithms
inferredcites →https://doi.org/10.1037//0033-2909.114.1.80openalex-snapshot
Context, time, and memory retrieval in the interference paradigms of Pavlovian learning.
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//0033-295x.97.2.285openalex-snapshot
Connectionist models of recognition memory: Constraints imposed by learning and forgetting functions.
inferredcites →https://doi.org/10.1037//0096-3445.125.4.370openalex-snapshot
Biological significance in forward and backward blocking: Resolution of a discrepancy between animal conditioning and human causal judgment.
inferredcites →https://doi.org/10.1037//0097-7403.10.3.360openalex-snapshot
Context specificity of conditioning, extinction, and latent inhibition.
inferredcites →https://doi.org/10.1037//0097-7403.18.2.182openalex-snapshot
Rapid reacquisition in conditioning of the rabbit's nictitating membrane response.
inferredcites →https://doi.org/10.1037//0278-7393.17.5.837openalex-snapshot
Trial order affects cue interaction in contingency judgment.
inferredcites →https://doi.org/10.1037/0033-2909.116.2.220openalex-snapshot
Dual-task interference in simple tasks: Data and theory.
inferredcites →https://doi.org/10.1037/0033-2909.117.3.363openalex-snapshot
Assessment of the Rescorla-Wagner model.
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/10.1037/0033-295x.113.3.584openalex-snapshot
Elemental representations of stimuli in associative learning.
inferredcites →https://doi.org/10.1037/0033-295x.87.6.532openalex-snapshot
A model for Pavlovian learning: Variations in the effectiveness of conditioned but not of unconditioned stimuli.
inferredcites →https://doi.org/10.1037/0097-7403.31.1.107openalex-snapshot
Retrospective Revaluation as Simple Associative Learning.
inferredcites →https://doi.org/10.1037/0097-7403.34.2.185openalex-snapshot
Is the number of trials a primary determinant of conditioned responding?
inferredcites →https://doi.org/10.1037/a0014212openalex-snapshot
Does incubation enhance problem solving? A meta-analytic review.
inferredcites →https://doi.org/10.1037/a0014815openalex-snapshot
Spontaneous recovery of excitation and inhibition.
inferredcites →https://doi.org/10.1037/a0016425openalex-snapshot
Within-subject effects of number of trials in rat conditioning procedures.
inferredcites →https://doi.org/10.1037/a0020886openalex-snapshot
A memory-based account of retrospective revaluation.
inferredcites →https://doi.org/10.1037/a0030844openalex-snapshot
Retrospective revaluation in sequential decision making: A tale of two systems.
inferredcites →https://doi.org/10.1037/h0028974openalex-snapshot
Paradoxical enhancement of learned fear.
inferredcites →https://doi.org/10.1037/h0046700openalex-snapshot
Latent inhibition: The effect of nonreinforced pre-exposure to the conditional stimulus.
inferredcites →https://doi.org/10.1037/h0048509openalex-snapshot
Statistical theory of spontaneous recovery and regression.
inferredcites →https://doi.org/10.1037/h0054388openalex-snapshot
A mathematical model for simple learning.
inferredcites →https://doi.org/10.1037/h0076778openalex-snapshot
A theory of attention: Variations in the associability of stimuli with reinforcement.
inferredcites →https://doi.org/10.1038/nature04286openalex-snapshot
Sleep-dependent memory consolidation
inferredcites →https://doi.org/10.1038/nature14236openalex-snapshot
Human-level control through deep reinforcement learning
inferredcites →https://doi.org/10.1038/nature17955openalex-snapshot
A shared neural ensemble links distinct contextual memories encoded close in time
inferredcites →https://doi.org/10.1038/nn.3203openalex-snapshot
Biasing the content of hippocampal replay during sleep
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/npp.2009.131openalex-snapshot
Human and Rodent Homologies in Action Control: Corticostriatal Determinants of Goal-Directed and Habitual Action
inferredcites →https://doi.org/10.1038/s41562-017-0180-8openalex-snapshot
The successor representation in human reinforcement learning
inferredcites →https://doi.org/10.1073/pnas.1311989110openalex-snapshot
Awake reactivation predicts memory in humans
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/10.1080/00221309.1978.9920877openalex-snapshot
Spontaneous Recovery in Rabbit Eyelid Conditioning
inferredcites →https://doi.org/10.1080/02724990344000042openalex-snapshot
Within-compound associations in retrospective revaluation and in direct learning: A challenge for comparator theory
inferredcites →https://doi.org/10.1080/713932614openalex-snapshot
Within Compound Associations Mediate the Retrospective Revaluation of Causality Judgements
inferredcites →https://doi.org/10.1098/rsos.160734openalex-snapshot
The power of associative learning and the ontogeny of optimal behaviour
inferredcites →https://doi.org/10.1098/rstb.1985.0010openalex-snapshot
Actions and habits: the development of behavioural autonomy
inferredcites →https://doi.org/10.1126/science.1148979openalex-snapshot
Fast-Forward Playback of Recent Memory Sequences in Prefrontal Cortex During Sleep
inferredcites →https://doi.org/10.1126/science.1217230openalex-snapshot
Awake Hippocampal Sharp-Wave Ripples Support Spatial Memory
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.287.5451.248openalex-snapshot
Memory--a Century of Consolidation
inferredcites →https://doi.org/10.1126/science.290.5492.812openalex-snapshot
Song Replay During Sleep and Computational Rules for Sensorimotor Vocal Learning
inferredcites →https://doi.org/10.1126/science.8036517openalex-snapshot
Reactivation of Hippocampal Ensemble Memories During Sleep
inferredcites →https://doi.org/10.1145/1390156.1390278openalex-snapshot
Sample-based learning and search with permanent and transient memories
inferredcites →https://doi.org/10.1146/annurev.psych.52.1.111openalex-snapshot
Theories of Associative Learning in Animals
inferredcites →https://doi.org/10.1162/neco.2008.11-07-654openalex-snapshot
Stimulus Representation and the Timing of Reward-Prediction Errors in Models of the Dopamine System
inferredcites →https://doi.org/10.1177/105971239300100403openalex-snapshot
Efficient Learning and Planning Within the Dyna Framework
inferredcites →https://doi.org/10.1523/jneurosci.0255-08.2008openalex-snapshot
Tripartite Mechanism of Extinction Suggested by Dopamine Neuron Activity and Temporal Difference Model
inferredcites →https://doi.org/10.1523/jneurosci.0414-13.2013openalex-snapshot
Memory Consolidation by Replay of Stimulus-Specific Neural Activity
inferredcites →https://doi.org/10.1523/jneurosci.21-02-00682.2001openalex-snapshot
Latent Acquisition of Timed Responses in Cerebellar Cortex
inferredcites →https://doi.org/10.3758/bf03192912openalex-snapshot
Extinction revisited: Similarities between extinction and reductions in US intensity in classical conditioning of the rabbit’s nictitating membrane response
inferredcites →https://doi.org/10.3758/bf03198931openalex-snapshot
Trial spacing effects in pavlovian conditioning: A role for local context
inferredcites →https://doi.org/10.3758/bf03198940openalex-snapshot
One-trial context fear conditioning as a function of the interstimulus interval
inferredcites →https://doi.org/10.3758/bf03199210openalex-snapshot
Spontaneous recovery without interference: Why remembering is adaptive
inferredcites →https://doi.org/10.3758/bf03199432openalex-snapshot
Recovery from blocking achieved by extinguishing the blocking CS
inferredcites →https://doi.org/10.3758/bf03200771openalex-snapshot
The sequential view: From rapidly fading stimulus traces to the organization of memory and the abstract concept of number
inferredcites →https://doi.org/10.3758/bf03342473openalex-snapshot
The effects of ITI interpolated stimuli and CS intensity on classical conditioning of the nictitating membrane response of the rabbit
inferredcites →https://doi.org/10.3758/s13420-012-0080-8openalex-snapshot
Exploring a latent cause theory of classical conditioning
inferredcites →https://doi.org/10.3758/s13420-012-0082-6openalex-snapshot
Evaluating the TD model of classical conditioning
inferredcites →https://doi.org/10.3819/ccbr.2010.50001openalex-snapshot
Time and Associative Learning.
inferredcites →https://doi.org/10.4018/978-1-60960-021-1.ch006openalex-snapshot
A Primer on Reinforcement Learning in the Brain
inferredcites →https://doi.org/10.48550/arxiv.1206.3285openalex-snapshot
Dyna-Style Planning with Linear Function Approximation and Prioritized Sweeping
inferredcites →https://doi.org/10.82444/warw.33635548openalex-snapshot
A computational model of hippocampal function in trace conditioning
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
inferred← citeshttps://doi.org/10.1016/b978-0-12-812098-9.00007-3openalex-snapshot
Competition and Cooperation Between Multiple Reinforcement Learning Systems
inferred← citeshttps://doi.org/10.1016/j.beproc.2018.12.009openalex-snapshot
Comparative inspiration: From puzzles with pigeons to novel discoveries with humans in risky choice
inferred← citeshttps://doi.org/10.1037/rev0000147openalex-snapshot
A double error dynamic asymptote model of associative learning.
inferred← citeshttps://doi.org/10.1038/s41593-018-0232-zopenalex-snapshot
Prioritized memory access explains planning and hippocampal replay
inferred← citeshttps://doi.org/10.1038/s41593-020-0651-5openalex-snapshot
Cortical reactivations of recent sensory experiences predict bidirectional network changes during learning
inferred← citeshttps://doi.org/10.1038/s41593-026-02206-2openalex-snapshot
Duration between rewards controls the rate of behavioral and dopaminergic learning
inferred← citeshttps://doi.org/10.1038/s41598-021-81157-zopenalex-snapshot
Context-dependent extinction learning emerging from raw sensory inputs: a reinforcement learning approach
inferred← citeshttps://doi.org/10.1080/17470218.2015.1014378openalex-snapshot
Cue Competition Effects in Human Causal Learning
inferred← citeshttps://doi.org/10.1093/oxfordhb/9780190917982.013.12openalex-snapshot
Conditioning and Associative Learning
inferred← citeshttps://doi.org/10.1101/104091openalex-snapshot
Information seeking and simulation: Roles of attention in guiding a goal-directed behavior
inferred← citeshttps://doi.org/10.1101/196758openalex-snapshot
Offline Replay Supports Planning: fMRI Evidence from Reward Revaluation
inferred← citeshttps://doi.org/10.1101/210674openalex-snapshot
A Double Error Dynamic Asymptote Model of Associative Learning
inferred← citeshttps://doi.org/10.1101/245720openalex-snapshot
Value Representations in the Rodent Orbitofrontal Cortex Drive Learning, not Choice
inferred← citeshttps://doi.org/10.1162/jocn_a_01170openalex-snapshot
Imaginative Reinforcement Learning: Computational Principles and Neural Mechanisms
inferred← citeshttps://doi.org/10.1371/journal.pcbi.1005768openalex-snapshot
Predictive representations can link model-based reinforcement learning to model-free mechanisms
inferred← citeshttps://doi.org/10.3410/f.734918397.793583295openalex-snapshot
Faculty Opinions recommendation of Habits without values.
inferred← citeshttps://doi.org/10.7554/elife.32548openalex-snapshot
Offline replay supports planning in human reinforcement learning
inferred← citeshttps://doi.org/10.7554/elife.64575openalex-snapshot
Value representations in the rodent orbitofrontal cortex drive learning, not choice
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.