On the public citation graph

A Double Error Dynamic Asymptote Model of Associative Learning

https://doi.org/10.1101/210674
0 signed · 150 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.
Claim with ORCID
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 See whether every reference in this work resolves to a known work and none has been retracted — and get a dated CiteStamped badge you can embed.
See reference health

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/10.1002/0471214426openalex-snapshot
Stevens' Handbook of Experimental Psychology
inferredcites →https://doi.org/10.1002/0471214426.pas0301openalex-snapshot
Associative Structures in Pavlovian and Instrumental Conditioning
inferredcites →https://doi.org/10.1007/978-3-540-69134-1_34openalex-snapshot
Learning to Generalize through Predictive Representations: A Computational Model of Mediated Conditioning
inferredcites →https://doi.org/10.1007/s12021-012-9172-zopenalex-snapshot
A Complete Serial Compound Temporal Difference Simulator for Compound stimuli, Configural cues and Context representation
inferredcites →https://doi.org/10.1016/0023-9690(70)90101-3openalex-snapshot
Reduction in the effectiveness of reinforcement after prior excitatory conditioning
inferredcites →https://doi.org/10.1016/0023-9690(71)90002-6openalex-snapshot
Variation in the effectiveness of reinforcement and nonreinforcement following prior inhibitory conditioning
inferredcites →https://doi.org/10.1016/0023-9690(75)90012-0openalex-snapshot
Pavlovian compound conditioning in the rabbit
inferredcites →https://doi.org/10.1016/0023-9690(82)90004-2openalex-snapshot
Representation-mediated extinction of conditioned flavor aversions
inferredcites →https://doi.org/10.1016/0023-9690(85)90023-2openalex-snapshot
Recovery of an overshadowed association achieved by extinction of the overshadowing stimulus
inferredcites →https://doi.org/10.1016/0023-9690(86)90004-4openalex-snapshot
Contextual control of negative transfer produced by prior CS-US pairings
inferredcites →https://doi.org/10.1016/0023-9690(95)90005-5openalex-snapshot
Perceptual learning in flavor aversion conditioning: Roles of stimulus comparison and latent inhibition of common stimulus elements
inferredcites →https://doi.org/10.1016/j.beproc.2009.12.007openalex-snapshot
Perceptual learning in an appetitive Pavlovian procedure: Analysis of the effectiveness of the common element
inferredcites →https://doi.org/10.1016/j.beproc.2015.09.001openalex-snapshot
Retrospective revaluation: The phenomenon and its theoretical implications
inferredcites →https://doi.org/10.1016/j.cmpb.2012.02.004openalex-snapshot
A Java simulator of Rescorla and Wagner's prediction error model and configural cue extensions
inferredcites →https://doi.org/10.1016/j.cmpb.2013.01.016openalex-snapshot
An extension of the Rescorla and Wagner Simulator for context conditioning
inferredcites →https://doi.org/10.1016/j.conb.2004.03.017openalex-snapshot
Neural coding of basic reward terms of animal learning theory, game theory, microeconomics and behavioural ecology
inferredcites →https://doi.org/10.1016/j.jmp.2008.12.005openalex-snapshot
Reinforcement learning in the brain
inferredcites →https://doi.org/10.1016/j.jmp.2014.11.003openalex-snapshot
On elemental and configural models of associative learning
inferredcites →https://doi.org/10.1016/j.jtbi.2010.06.017openalex-snapshot
The evolution of associative learning: A factor in the Cambrian explosion
inferredcites →https://doi.org/10.1016/j.neuron.2012.05.010openalex-snapshot
Hippocampal and Ventral Medial Prefrontal Activation during Retrieval-Mediated Learning Supports Novel Inference
inferredcites →https://doi.org/10.1016/j.nlm.2013.08.002openalex-snapshot
Orbitofrontal cortex inactivation impairs between- but not within-session Pavlovian extinction: An associative analysis
inferredcites →https://doi.org/10.1016/j.nlm.2016.02.014openalex-snapshot
Mini-review: Prediction errors, attention and associative learning
inferredcites →https://doi.org/10.1016/j.tics.2006.05.004openalex-snapshot
Bayesian theories of conditioning in a changing world
inferredcites →https://doi.org/10.1016/j.tics.2017.06.001openalex-snapshot
Associative Learning Should Go Deep
inferredcites →https://doi.org/10.1016/s0028-3908(98)00033-1openalex-snapshot
Goal-directed instrumental action: contingency and incentive learning and their cortical substrates
inferredcites →https://doi.org/10.1016/s0079-7421(08)60038-9openalex-snapshot
The Comparator Hypothesis: A Response Rule for The Expression of Associations
inferredcites →https://doi.org/10.1016/s0166-4328(99)00185-0openalex-snapshot
A componential view of configural cues in generalization and discrimination in Pavlovian conditioning
inferredcites →https://doi.org/10.1016/s0301-0082(02)00011-4openalex-snapshot
Dopamine and the regulation of cognition and attention
inferredcites →https://doi.org/10.1016/s0301-0511(02)00004-2openalex-snapshot
Configural learning in human Pavlovian conditioning: acquisition of a biconditional discrimination
inferredcites →https://doi.org/10.1016/s0304-3940(00)01429-4openalex-snapshot
Suppression of transient 40-Hz auditory response by haloperidol suggests modulation of human selective attention by dopamine D2 receptors
inferredcites →https://doi.org/10.1016/s0376-6357(03)00016-0openalex-snapshot
Stimulus representation in SOP: I
inferredcites →https://doi.org/10.1016/s0896-6273(01)00276-8openalex-snapshot
Ca2+ Signaling via the Neuronal Calcium Sensor-1 Regulates Associative Learning and Memory in C. elegans
inferredcites →https://doi.org/10.1016/s0896-6273(03)00873-0openalex-snapshot
Spike Train Timing-Dependent Associative Modification of Hippocampal CA3 Recurrent Synapses by Mossy Fibers
inferredcites →https://doi.org/10.1016/s1007-0214(11)70021-9openalex-snapshot
Neural correlates of human associative learning
inferredcites →https://doi.org/10.1017/cbo9780511623288openalex-snapshot
The Psychology of Associative Learning
inferredcites →https://doi.org/10.1017/cbo9780511730184.003openalex-snapshot
Latent inhibition and extinction: their signature phenomena and the role of prediction error
inferredcites →https://doi.org/10.1017/cbo9780511730184.007openalex-snapshot
Associative and nonassociative processes in latent inhibition: an elaboration of the Pearce–Hall model
inferredcites →https://doi.org/10.1017/cbo9780511921322openalex-snapshot
Formal Approaches in Categorization
inferredcites →https://doi.org/10.1017/cbo9780511921322.006openalex-snapshot
Models of attentional learning
inferredcites →https://doi.org/10.1017/s0140525x00024870openalex-snapshot
Classical conditioning beyond the reflex: An uneasy rebirth
inferredcites →https://doi.org/10.1017/s0140525x01000061openalex-snapshot
Generalization, similarity, and Bayesian inference
inferredcites →https://doi.org/10.1027/1618-3169/a000030openalex-snapshot
Reduced Summation with Common Features in Causal Judgments
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.94.1.61openalex-snapshot
A model for stimulus generalization in Pavlovian conditioning.
inferredcites →https://doi.org/10.1037//0097-7403.1.1.3openalex-snapshot
Steady state data and a quantitative model of operant generalization and discrimination.
inferredcites →https://doi.org/10.1037//0097-7403.11.3.356openalex-snapshot
Analysis of the unique cue in configural discriminations.
inferredcites →https://doi.org/10.1037//0097-7403.15.3.232openalex-snapshot
Contextual effects in conditioning, latent inhibition, and habituation: Associative and retrieval functions of contextual cues.
inferredcites →https://doi.org/10.1037//0097-7403.17.4.519openalex-snapshot
Failure of excitatory conditioning to extinguish the influence of a conditioned inhibitor.
inferredcites →https://doi.org/10.1037//0097-7403.18.3.265openalex-snapshot
A configural analysis for feature-negative discrimination learning.
inferredcites →https://doi.org/10.1037//0097-7403.19.2.180openalex-snapshot
The influence of an irrelevant stimulus on two discriminations.
inferredcites →https://doi.org/10.1037//0097-7403.2.4.313openalex-snapshot
Surprise and the attenuation of blocking.
inferredcites →https://doi.org/10.1037//0097-7403.22.2.183openalex-snapshot
Learned irrelevance: No more than the sum of CS and US preexposure effects?
inferredcites →https://doi.org/10.1037//0097-7403.22.4.395openalex-snapshot
Backward sensory preconditioning.
inferredcites →https://doi.org/10.1037//0097-7403.26.2.157openalex-snapshot
Contextual control over conditioned responding in a latent inhibition paradigm.
inferredcites →https://doi.org/10.1037//0097-7403.5.1.31openalex-snapshot
Latent inhibition of a CS during CS-US pairings.
inferredcites →https://doi.org/10.1037//0097-7403.9.1.1openalex-snapshot
Representation-mediated overshadowing and potentiation of conditioned aversions.
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.113.3.584openalex-snapshot
Elemental representations of stimuli in associative learning.
inferredcites →https://doi.org/10.1037/0033-295x.84.3.279openalex-snapshot
Scalar expectancy theory and Weber's law in animal timing.
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/10.1037/0033-295x.88.2.135openalex-snapshot
Toward a modern theory of adaptive networks: Expectation and prediction.
inferredcites →https://doi.org/10.1037/0097-7403.10.4.476openalex-snapshot
Unblocking in Pavlovian appetitive conditioning.
inferredcites →https://doi.org/10.1037/0097-7403.29.1.39openalex-snapshot
Perceptual learning in flavor aversion: Evidence for learned changes in stimulus effectiveness.
inferredcites →https://doi.org/10.1037/0097-7403.32.4.481openalex-snapshot
Stimulus salience and retrospective revaluation.
inferredcites →https://doi.org/10.1037/0097-7403.34.2.303openalex-snapshot
Comparing elemental and configural associative theories in human causal learning: A case for attention.
inferredcites →https://doi.org/10.1037/14496-000openalex-snapshot
Stochastic models for learning.
inferredcites →https://doi.org/10.1037/a0016773openalex-snapshot
Backward blocking in first-order conditioning.
inferredcites →https://doi.org/10.1037/a0017808openalex-snapshot
Context, learning, and extinction.
inferredcites →https://doi.org/10.1037/a0021460openalex-snapshot
The hide-and-seek of retrospective revaluation: Recovery from blocking is context dependent in human causal learning.
inferredcites →https://doi.org/10.1037/a0023714openalex-snapshot
Additional exposures to a compound of two preexposed stimuli deepen latent inhibition.
inferredcites →https://doi.org/10.1037/a0037018openalex-snapshot
Explaining compound generalization in associative and causal learning through rational principles of dimensional generalization.
inferredcites →https://doi.org/10.1037/a0038694openalex-snapshot
Solution of the comparator theory of associative learning.
inferredcites →https://doi.org/10.1037/h0022576openalex-snapshot
Latent inhibition: Effects of frequency of nonreinforced pre-exposure of the CS.
inferredcites →https://doi.org/10.1037/h0030694openalex-snapshot
Summation and retardation tests of latent inhibition.
inferredcites →https://doi.org/10.1037/h0032553openalex-snapshot
"Configural" conditioning in discrete-trial bar pressing.
inferredcites →https://doi.org/10.1037/h0056975openalex-snapshot
The nature of discrimination learning in animals.
inferredcites →https://doi.org/10.1037/h0058559openalex-snapshot
Toward a statistical theory of learning.
inferredcites →https://doi.org/10.1037/h0058944openalex-snapshot
Sensory pre-conditioning.
inferredcites →https://doi.org/10.1037/h0062885openalex-snapshot
The differential response in animals to stimuli varying within a single dimension.
inferredcites →https://doi.org/10.1037/h0076778openalex-snapshot
A theory of attention: Variations in the associability of stimuli with reinforcement.
inferredcites →https://doi.org/10.1037/xge0000200openalex-snapshot
The elusive nature of the blocking effect: 15 failures to replicate.
inferredcites →https://doi.org/10.1073/pnas.0404965101openalex-snapshot
The learning curve: Implications of a quantitative analysis
inferredcites →https://doi.org/10.1080/00221309.1939.10544300openalex-snapshot
Studies in Configural Conditioning: I. Historical and Preliminary Experimentation
inferredcites →https://doi.org/10.1080/02724980143000578openalex-snapshot
Outcome and Cue Properties Modulate Blocking
inferredcites →https://doi.org/10.1080/02724990042000029openalex-snapshot
Re-examination of the role of within-compound associations in the retrospective revaluation of causal judgements
inferredcites →https://doi.org/10.1080/02724990143000072openalex-snapshot
Retrospective revaluation in humans: Learning or memory?
inferredcites →https://doi.org/10.1080/02724990143000171openalex-snapshot
Summation: Further Assessment of a Configural Theory
inferredcites →https://doi.org/10.1080/02724990143000225openalex-snapshot
Analysis of the Perceptual Learning Effect in Flavour Aversion Learning: Evidence for Stimulus Differentiation
inferredcites →https://doi.org/10.1080/02724990244000133openalex-snapshot
Context-Sensitive Elemental Theory
inferredcites →https://doi.org/10.1080/02724990244000197openalex-snapshot
Learned Irrelevance and Retrospective Correlation Learning
inferredcites →https://doi.org/10.1080/02724990344000051openalex-snapshot
Superconditioning from a reduced reinforcer
inferredcites →https://doi.org/10.1080/02724990344000141openalex-snapshot
The Role of Associative History in Models of Associative Learning: A Selective Review and a Hybrid Model
inferredcites →https://doi.org/10.1080/027249999393013openalex-snapshot
Retrospective Revaluation or Mediated Conditioning? The Effect of Different Reinforcers
inferredcites →https://doi.org/10.1080/17470210802008805openalex-snapshot
Mediated Conditioning versus Retrospective Revaluation in Humans: The Influence of Physical and Functional Similarity of Cues
inferredcites →https://doi.org/10.1080/713932614openalex-snapshot
Within Compound Associations Mediate the Retrospective Revaluation of Causality Judgements
inferredcites →https://doi.org/10.1080/713932687openalex-snapshot
Backward Sensory Preconditioning when Reinforcement is Delayed
inferredcites →https://doi.org/10.1093/acprof:oso/9780198521822.001.0001openalex-snapshot
Perceptual and Associative Learning
inferredcites →https://doi.org/10.1093/acprof:oso/9780199735969.001.0001openalex-snapshot
Associative Learning and Conditioning Theory
inferredcites →https://doi.org/10.1093/brain/awm173openalex-snapshot
Disrupted prediction-error signal in psychosis: evidence for an associative account of delusions
inferredcites →https://doi.org/10.1101/100800openalex-snapshot
Associative Learning from Replayed Experience
inferredcites →https://doi.org/10.1101/lm.78804openalex-snapshot
Context and Behavioral Processes in Extinction: Table 1.
inferredcites →https://doi.org/10.1111/j.1460-9568.2011.07986.xopenalex-snapshot
Surprise! Neural correlates of Pearce–Hall and Rescorla–Wagner coexist within the brain
inferredcites →https://doi.org/10.1126/science.1151564openalex-snapshot
Rule Learning by Rats
inferredcites →https://doi.org/10.1126/science.275.5306.1593openalex-snapshot
A Neural Substrate of Prediction and Reward
inferredcites →https://doi.org/10.1146/annurev.psych.093008.100519openalex-snapshot
Learning: From Association to Cognition
inferredcites →https://doi.org/10.1146/annurev.psych.52.1.111openalex-snapshot
Theories of Associative Learning in Animals
inferredcites →https://doi.org/10.1146/annurev.psych.56.091103.070229openalex-snapshot
Behavioral Theories and the Neurophysiology of Reward
inferredcites →https://doi.org/10.1186/1744-9081-6-24openalex-snapshot
Dopamine signals for reward value and risk: basic and recent data
inferredcites →https://doi.org/10.1371/journal.pcbi.1004567openalex-snapshot
A Unifying Probabilistic View of Associative Learning
inferredcites →https://doi.org/10.1371/journal.pcbi.1005796openalex-snapshot
A Rescorla-Wagner drift-diffusion model of conditioning and timing
inferredcites →https://doi.org/10.1371/journal.pone.0102469openalex-snapshot
SSCC TD: A Serial and Simultaneous Configural-Cue Compound Stimuli Representation for Temporal Difference Learning
inferredcites →https://doi.org/10.1523/jneurosci.16-05-01936.1996openalex-snapshot
A framework for mesencephalic dopamine systems based on predictive Hebbian learning
inferredcites →https://doi.org/10.1523/jneurosci.5498-10.2012openalex-snapshot
Neural Prediction Errors Reveal a Risk-Sensitive Reinforcement-Learning Process in the Human Brain
inferredcites →https://doi.org/10.2307/1422027openalex-snapshot
Constraints on Learning: Limitations and Predispositions
inferredcites →https://doi.org/10.2307/1422092openalex-snapshot
Inhibition and Learning
inferredcites →https://doi.org/10.2307/2019960openalex-snapshot
Principles of Behavior. An Introduction to Behavior Theory
inferredcites →https://doi.org/10.3389/fpsyg.2013.00982openalex-snapshot
Revisiting the learning curve (once again)
inferredcites →https://doi.org/10.3758/bf03199432openalex-snapshot
Recovery from blocking achieved by extinguishing the blocking CS
inferredcites →https://doi.org/10.3758/bf03199919openalex-snapshot
Interval between preexposure and test determines the magnitude of latent inhibition: Implications for an interference account
inferredcites →https://doi.org/10.3758/bf03200258openalex-snapshot
An elemental model of associative learning: I. Latent inhibition and perceptual learning
inferredcites →https://doi.org/10.3758/bf03205056openalex-snapshot
Temporal primacy overrides prior training in serial compound conditioning of the rabbit’s nictitating membrane response
inferredcites →https://doi.org/10.3758/bf03209158openalex-snapshot
Encoding of the unconditioned stimulus in Pavlovian conditioning
inferredcites →https://doi.org/10.3758/bf03209459openalex-snapshot
Context change and retention interval can have additive, rather than interactive, effects after taste aversion extinction
inferredcites →https://doi.org/10.3758/bf03209681openalex-snapshot
The Kamin blocking effect with variable-duration CSs
inferredcites →https://doi.org/10.3758/bf03212309openalex-snapshot
Contextual effects in latent inhibition with an appetitive conditioning procedure
inferredcites →https://doi.org/10.3758/bf03328970openalex-snapshot
Negative patterning in classical conditioning: Summation of response tendencies to isolable and configurai components
inferredcites →https://doi.org/10.3758/brm.40.2.435openalex-snapshot
Rapid-REM: A MATLAB simulator of the replaced-elements model
inferredcites →https://doi.org/10.3758/lb.36.2.92openalex-snapshot
CS--US temporal relations in blocking
inferredcites →https://doi.org/10.3758/lb.36.3.210openalex-snapshot
Bayesian approaches to associative learning: From passive to active learning
inferredcites →https://doi.org/10.3758/lb.36.3.253openalex-snapshot
Evolution of an elemental theory of Pavlovian conditioning
inferredcites →https://doi.org/10.3758/lb.37.1.60openalex-snapshot
Spacing extinction trials alleviates renewal and spontaneous recovery
inferredcites →https://doi.org/10.3758/lb.38.1.1openalex-snapshot
An attention-modulated associative network
inferredcites →https://doi.org/10.3758/s13415-014-0277-8openalex-snapshot
Model-based and model-free Pavlovian reward learning: Revaluation, revision, and revelation
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/s13420-012-0081-7openalex-snapshot
Special issue on computational models of classical conditioning guest editors’ introduction
inferredcites →https://doi.org/10.3758/s13420-012-0083-5openalex-snapshot
Solving Pavlov's puzzle: Attentional, associative, and flexible configural mechanisms in classical conditioning
inferredcites →https://doi.org/10.3758/s13420-012-0084-4openalex-snapshot
Modeling attention in associative learning: Two processes or one?
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/10.4324/9780203803509openalex-snapshot
Clinical Applications of Learning Theory
inferredcites →https://doi.org/10.4324/9781315798820openalex-snapshot
Information Processing in Animals
inferredcites →https://doi.org/10.4324/9781315798820-6openalex-snapshot
SOP: A Model of Automatic Memory Processing in Animal Behavior
inferredcites →https://doi.org/10.4324/9781410600691openalex-snapshot
Handbook of Contemporary Learning Theories
inferredcites →https://doi.org/10.4324/9781410600691-8openalex-snapshot
A Componential Theory of Pavlovian Conditioning
inferredcites →https://doi.org/10.5220/0000145200002858openalex-snapshot
Proceedings of the 13th International Conference on Agents and Artificial Intelligence
inferredcites →https://doi.org/10.5220/0004903105440547openalex-snapshot
Computational Models of Classical Conditioning - A Qualitative Evaluation and Comparison
inferredcites →https://doi.org/10.7326/0003-4819-31-6-1133_1openalex-snapshot
Conditioned Reflexes and Neuron Organization.
inferredcites →https://doi.org/10.7551/mitpress/3119.003.0053openalex-snapshot
Computational Models of Classical Conditioning: A Comparative Study
inferredcites →https://doi.org/10.7551/mitpress/6831.003.0004openalex-snapshot
Predictive Timing under Temporal Uncertainty: The Time Derivative Model of the Conditioned Response
inferredcites →https://doi.org/10.82444/warw.33635548openalex-snapshot
A computational model of hippocampal function in trace conditioning
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.