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Dorsal hippocampus contributes to model-based planning

https://doi.org/10.1101/096594
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Outgoing claims: the papers this work cites, builds on, or argues with.

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Hippocampectomy disrupts auditory trace fear conditioning and contextual fear conditioning in the rat
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Do hippocampal pyramidal cells signal non-spatial as well as spatial information?
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A model of hippocampally dependent navigation, using the temporal difference learning rule
inferredcites →https://doi.org/10.1002/hipo.20127openalex-snapshot
Inactivation of the dorsal hippocampus does not affect learning during exploration of a novel environment
inferredcites →https://doi.org/10.1006/nlme.1996.0007openalex-snapshot
Inactivation of Hippocampus or Caudate Nucleus with Lidocaine Differentially Affects Expression of Place and Response Learning
inferredcites →https://doi.org/10.1016/0006-8993(71)90358-1openalex-snapshot
The hippocampus as a spatial map. Preliminary evidence from unit activity in the freely-moving rat
inferredcites →https://doi.org/10.1016/0006-8993(78)90930-7openalex-snapshot
Hippocampal connections and spatial discrimination
inferredcites →https://doi.org/10.1016/0028-3932(79)90042-3openalex-snapshot
Spatial memory and hippocampal function
inferredcites →https://doi.org/10.1016/0031-9384(81)90209-2openalex-snapshot
Latent learning in hippocampal-lesioned rats
inferredcites →https://doi.org/10.1016/0031-9384(82)90258-xopenalex-snapshot
Further evidence for latent learning in hippocampal-lesioned rats
inferredcites →https://doi.org/10.1016/0304-3940(91)90784-qopenalex-snapshot
Autoradiographic estimation of the extent of reversible inactivation produced by microinjection of lidocaine and muscimol in the rat
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Hybrid Monte Carlo
inferredcites →https://doi.org/10.1016/j.conb.2008.01.003openalex-snapshot
Integrating hippocampus and striatum in decision-making
inferredcites →https://doi.org/10.1016/j.conb.2011.12.005openalex-snapshot
Sequence learning and the role of the hippocampus in rodent navigation
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.2011.02.027openalex-snapshot
Model-Based Influences on Humans' Choices and Striatal Prediction Errors
inferredcites →https://doi.org/10.1016/j.neuron.2012.03.042openalex-snapshot
Dopamine Enhances Model-Based over Model-Free Choice Behavior
inferredcites →https://doi.org/10.1016/j.neuron.2013.08.009openalex-snapshot
Disruption of Dorsolateral Prefrontal Cortex Decreases Model-Based in Favor of Model-free Control in Humans
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.neuron.2013.11.005openalex-snapshot
Orbitofrontal Cortex as a Cognitive Map of Task Space
inferredcites →https://doi.org/10.1016/j.neuron.2013.11.028openalex-snapshot
Neural Computations Underlying Arbitration between Model-Based and Model-free Learning
inferredcites →https://doi.org/10.1016/j.neuron.2014.07.032openalex-snapshot
Can We Reconcile the Declarative Memory and Spatial Navigation Views on Hippocampal Function?
inferredcites →https://doi.org/10.1016/j.neuron.2014.12.009openalex-snapshot
The 2014 Nobel Prize in Physiology or Medicine: A Spatial Model for Cognitive Neuroscience
inferredcites →https://doi.org/10.1016/j.tics.2014.06.011openalex-snapshot
Internally generated sequences in learning and executing goal-directed behavior
inferredcites →https://doi.org/10.1016/s0893-6080(03)00106-0openalex-snapshot
Modeling goal-directed spatial navigation in the rat based on physiological data from the hippocampal formation
inferredcites →https://doi.org/10.1016/s0896-6273(00)80773-4openalex-snapshot
The Hippocampus, Memory, and Place Cells
inferredcites →https://doi.org/10.1017/s0140525x00062713openalex-snapshot
Hippocampus, space, and memory
inferredcites →https://doi.org/10.1037//0735-7044.100.5.729openalex-snapshot
Hippocampus and trace conditioning of the rabbit's classically conditioned nictitating membrane response.
inferredcites →https://doi.org/10.1037//0735-7044.115.6.1357openalex-snapshot
Excitotoxic lesions of the hippocampus leave sensory preconditioning intact: Implications for models of hippocampal functioning.
inferredcites →https://doi.org/10.1037/a0013990openalex-snapshot
Hippocampal involvement in the acquisition of relational associations, but not in the expression of a transitive inference task in mice.
inferredcites →https://doi.org/10.1037/h0058944openalex-snapshot
Sensory pre-conditioning.
inferredcites →https://doi.org/10.1037/h0061626openalex-snapshot
Cognitive maps in rats and men.
inferredcites →https://doi.org/10.1038/297681a0openalex-snapshot
Place navigation impaired in rats with hippocampal lesions
inferredcites →https://doi.org/10.1038/379255a0openalex-snapshot
Conservation of hippocampal memory function in rats and humans
inferredcites →https://doi.org/10.1038/nature12112openalex-snapshot
Hippocampal place-cell sequences depict future paths to remembered goals
inferredcites →https://doi.org/10.1038/ncomms3264openalex-snapshot
Orbitofrontal and striatal circuits dynamically encode the shift between goal-directed and habitual actions
inferredcites →https://doi.org/10.1038/nn.3068openalex-snapshot
Mapping value based planning and extensively trained choice in the human brain
inferredcites →https://doi.org/10.1038/nn.3648openalex-snapshot
A solution to dependency: using multilevel analysis to accommodate nested data
inferredcites →https://doi.org/10.1038/nn.3909openalex-snapshot
Hippocampal theta sequences reflect current goals
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/nn1961openalex-snapshot
Forward and reverse hippocampal place-cell sequences during ripples
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/nrn2753openalex-snapshot
A new perspective on the role of the orbitofrontal cortex in adaptive behaviour
inferredcites →https://doi.org/10.1073/pnas.94.13.7109openalex-snapshot
The hippocampus and memory for orderly stimulus relations
inferredcites →https://doi.org/10.1073/pnas.96.14.8200openalex-snapshot
Immediate thalamic sensory plasticity depends on corticothalamic feedback
inferredcites →https://doi.org/10.1080/14640748108400816openalex-snapshot
Instrumental Responding following Reinforcer Devaluation
inferredcites →https://doi.org/10.1093/acprof:oso/9780199600434.003.0001openalex-snapshot
Trial-by-trial data analysis using computational models
inferredcites →https://doi.org/10.1098/rstb.2012.0510openalex-snapshot
Space in the brain: how the hippocampal formation supports spatial cognition
inferredcites →https://doi.org/10.1101/096339openalex-snapshot
Identifying Model-Based and Model-Free Patterns in Behavior on Multi-Step Tasks
inferredcites →https://doi.org/10.1111/j.1460-9568.2007.05525.xopenalex-snapshot
The effects of selective amygdala, orbital frontal cortex or hippocampal formation lesions on reward assessment in nonhuman primates
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/10.1146/annurev-neuro-061010-113648openalex-snapshot
Neurobiology of Economic Choice: A Good-Based Model
inferredcites →https://doi.org/10.1146/annurev.psych.60.110707.163508openalex-snapshot
The Role of the Hippocampus in Prediction and Imagination
inferredcites →https://doi.org/10.1177/0956797612463080openalex-snapshot
The Curse of Planning
inferredcites →https://doi.org/10.1201/9780429258411openalex-snapshot
Bayesian Data Analysis
inferredcites →https://doi.org/10.1371/journal.pcbi.1002055openalex-snapshot
Speed/Accuracy Trade-Off between the Habitual and the Goal-Directed Processes
inferredcites →https://doi.org/10.1371/journal.pcbi.1004463openalex-snapshot
Model-Based Reasoning in Humans Becomes Automatic with Training
inferredcites →https://doi.org/10.1371/journal.pcbi.1004648openalex-snapshot
Simple Plans or Sophisticated Habits? State, Transition and Learning Interactions in the Two-Step Task
inferredcites →https://doi.org/10.1371/journal.pcbi.1005090openalex-snapshot
When Does Model-Based Control Pay Off?
inferredcites →https://doi.org/10.1523/jneurosci.19-15-06610.1999openalex-snapshot
Orbitofrontal Cortex and Representation of Incentive Value in Associative Learning
inferredcites →https://doi.org/10.1523/jneurosci.1921-04.2004openalex-snapshot
Bilateral Orbital Prefrontal Cortex Lesions in Rhesus Monkeys Disrupt Choices Guided by Both Reward Value and Reward Contingency
inferredcites →https://doi.org/10.1523/jneurosci.20-11-04233.2000openalex-snapshot
The Role of the Hippocampus in Instrumental Conditioning
inferredcites →https://doi.org/10.1523/jneurosci.22-24-10976.2002openalex-snapshot
Sensitivity to Instrumental Contingency Degradation Is Mediated by the Entorhinal Cortex and Its Efferents via the Dorsal Hippocampus
inferredcites →https://doi.org/10.1523/jneurosci.2618-15.2015openalex-snapshot
Memory and Space: Towards an Understanding of the Cognitive Map
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/10.1523/jneurosci.4202-10.2011openalex-snapshot
Memory for the Order of Events in Specific Sequences: Contributions of the Hippocampus and Medial Prefrontal Cortex
inferredcites →https://doi.org/10.1523/jneurosci.4647-10.2011openalex-snapshot
Neural Correlates of Forward Planning in a Spatial Decision Task in Humans
inferredcites →https://doi.org/10.1523/jneurosci.5443-06.2007openalex-snapshot
Orbitofrontal Cortex Mediates Outcome Encoding in Pavlovian But Not Instrumental Conditioning
inferredcites →https://doi.org/10.1523/jneurosci.5499-10.2011openalex-snapshot
Ventral Striatum and Orbitofrontal Cortex Are Both Required for Model-Based, But Not Model-Free, Reinforcement Learning
inferredcites →https://doi.org/10.18637/jss.v076.i01openalex-snapshot
Stan : A Probabilistic Programming Language
inferredcites →https://doi.org/10.1901/jeab.1980.34-297openalex-snapshot
THE EFFECT OF CONTINGENCY UPON THE APPETITIVE CONDITIONING OF FREE‐OPERANT BEHAVIOR
inferredcites →https://doi.org/10.1901/jeab.2005.110-04openalex-snapshot
DYNAMIC RESPONSE-BY-RESPONSE MODELS OF MATCHING BEHAVIOR IN RHESUS MONKEYS
inferredcites →https://doi.org/10.3389/neuro.07.006.2007openalex-snapshot
Endocannabinoid signaling is critical for habit formation
inferredcites →https://doi.org/10.3758/bf03343139openalex-snapshot
Hippocampal lesions and delayed alternation in the rat

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Incoming claims: where this work appears in other papers’ reference lists and arguments.

inferred← citeshttps://doi.org/10.1016/j.neuron.2017.08.003openalex-snapshot
Suppression of Ventral Hippocampal Output Impairs Integrated Orbitofrontal Encoding of Task Structure
inferred← citeshttps://doi.org/10.1016/j.neuron.2019.02.014openalex-snapshot
Hippocampal Contributions to Model-Based Planning and Spatial Memory
inferred← citeshttps://doi.org/10.1016/j.neuron.2020.11.024openalex-snapshot
Entorhinal and ventromedial prefrontal cortices abstract and generalize the structure of reinforcement learning problems
inferred← citeshttps://doi.org/10.1017/9781009026949.009openalex-snapshot
Representational Exchange in Human Social Learning
inferred← citeshttps://doi.org/10.1101/359232openalex-snapshot
Two Sides of the Same Coin: The Hippocampus as a Common Neural Substrate for Model-Based Planning and Spatial Memory
inferred← citeshttps://doi.org/10.4216/jpssj.50.0_51openalex-snapshot
How and What Deep Learning Learns
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