On the public citation graph

How learning unfolds in the brain: toward an optimization view

0 signed · 199 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 See whether every reference in this work resolves to a known work and none has been retracted — and get a dated CiteStamped badge you can embed.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/10.1007/978-0-387-77064-2_24openalex-snapshot
Time Scales, Difficulty/Skill Duality, and the Dynamics of Motor Learning
inferredcites →https://doi.org/10.1007/978-1-4614-5465-6_1openalex-snapshot
Model-Based and Model-Free Mechanisms of Human Motor Learning
inferredcites →https://doi.org/10.1007/978-3-031-01581-6openalex-snapshot
Lifelong Machine Learning
inferredcites →https://doi.org/10.1007/bf00992696openalex-snapshot
Simple statistical gradient-following algorithms for connectionist reinforcement learning
inferredcites →https://doi.org/10.1007/s00221-001-0928-1openalex-snapshot
Modulation of saccadic eye movements by predicted reward outcome
inferredcites →https://doi.org/10.1016/j.cell.2017.07.021openalex-snapshot
Dynamic Reorganization of Neuronal Activity Patterns in Parietal Cortex
inferredcites →https://doi.org/10.1016/j.conb.2015.12.005openalex-snapshot
Brain–computer interfaces for dissecting cognitive processes underlying sensorimotor control
inferredcites →https://doi.org/10.1016/j.conb.2017.06.004openalex-snapshot
Using computational theory to constrain statistical models of neural data
inferredcites →https://doi.org/10.1016/j.conb.2017.08.002openalex-snapshot
Parsing learning in networks using brain–machine interfaces
inferredcites →https://doi.org/10.1016/j.conb.2019.09.011openalex-snapshot
Harnessing behavioral diversity to understand neural computations for cognition
inferredcites →https://doi.org/10.1016/j.cub.2009.01.036openalex-snapshot
Motor Task Variation Induces Structural Learning
inferredcites →https://doi.org/10.1016/j.cub.2012.08.058openalex-snapshot
Neuronal Circuits Underlying Persistent Representations Despite Time Varying Activity
inferredcites →https://doi.org/10.1016/j.cub.2013.01.027openalex-snapshot
Volitional Control of Neural Activity Relies on the Natural Motor Repertoire
inferredcites →https://doi.org/10.1016/j.cub.2017.11.035openalex-snapshot
Brain-Computer Interface with Inhibitory Neurons Reveals Subtype-Specific Strategies
inferredcites →https://doi.org/10.1016/j.cub.2021.01.068openalex-snapshot
Prefrontal cortex represents heuristics that shape choice bias and its integration into future behavior
inferredcites →https://doi.org/10.1016/j.jmp.2008.12.005openalex-snapshot
Reinforcement learning in the brain
inferredcites →https://doi.org/10.1016/j.neuron.2007.04.030openalex-snapshot
Motor Learning with Unstable Neural Representations
inferredcites →https://doi.org/10.1016/j.neuron.2011.06.015openalex-snapshot
Perceptual Learning Reduces Interneuronal Correlations in Macaque Visual Cortex
inferredcites →https://doi.org/10.1016/j.neuron.2012.03.016openalex-snapshot
Not Noisy, Just Wrong: The Role of Suboptimal Inference in Behavioral Variability
inferredcites →https://doi.org/10.1016/j.neuron.2012.08.001openalex-snapshot
The Spike-Timing Dependence of Plasticity
inferredcites →https://doi.org/10.1016/j.neuron.2013.02.023openalex-snapshot
Associative Learning Enhances Population Coding by Inverting Interneuronal Correlation Patterns
inferredcites →https://doi.org/10.1016/j.neuron.2015.05.037openalex-snapshot
Learning Enhances Sensory and Multiple Non-sensory Representations in Primary Visual Cortex
inferredcites →https://doi.org/10.1016/j.neuron.2016.02.009openalex-snapshot
Recurrent Network Models of Sequence Generation and Memory
inferredcites →https://doi.org/10.1016/j.neuron.2017.03.002openalex-snapshot
Computing by Robust Transience: How the Fronto-Parietal Network Performs Sequential, Category-Based Decisions
inferredcites →https://doi.org/10.1016/j.neuron.2017.05.023openalex-snapshot
Motor Cortical Visuomotor Feedback Activity Is Initially Isolated from Downstream Targets in Output-Null Neural State Space Dimensions
inferredcites →https://doi.org/10.1016/j.neuron.2018.01.040openalex-snapshot
Neural Population Dynamics Underlying Motor Learning Transfer
inferredcites →https://doi.org/10.1016/j.neuron.2018.04.017openalex-snapshot
The Dynamical Regime of Sensory Cortex: Stable Dynamics around a Single Stimulus-Tuned Attractor Account for Patterns of Noise Variability
inferredcites →https://doi.org/10.1016/j.neuron.2018.09.030openalex-snapshot
A Neural Population Mechanism for Rapid Learning
inferredcites →https://doi.org/10.1016/j.neuron.2019.07.003openalex-snapshot
Convergent Temperature Representations in Artificial and Biological Neural Networks
inferredcites →https://doi.org/10.1016/j.neuron.2019.08.034openalex-snapshot
Engineering a Less Artificial Intelligence
inferredcites →https://doi.org/10.1016/j.neuron.2020.06.014openalex-snapshot
Deep Reinforcement Learning and Its Neuroscientific Implications
inferredcites →https://doi.org/10.1016/j.neuron.2020.07.021openalex-snapshot
Slow Drift of Neural Activity as a Signature of Impulsivity in Macaque Visual and Prefrontal Cortex
inferredcites →https://doi.org/10.1016/j.pneurobio.2013.02.002openalex-snapshot
From fixed points to chaos: Three models of delayed discrimination
inferredcites →https://doi.org/10.1016/j.tics.2016.05.002openalex-snapshot
Taking Aim at the Cognitive Side of Learning in Sensorimotor Adaptation Tasks
inferredcites →https://doi.org/10.1016/j.tins.2016.12.001openalex-snapshot
Neuronal Adaptation: Tired Neurons or Wired Networks?
inferredcites →https://doi.org/10.1016/j.tins.2020.11.007openalex-snapshot
A Network Perspective on Sensorimotor Learning
inferredcites →https://doi.org/10.1016/s0896-6273(01)00301-4openalex-snapshot
Neuronal Correlates of Motor Performance and Motor Learning in the Primary Motor Cortex of Monkeys Adapting to an External Force Field
inferredcites →https://doi.org/10.1016/s0959-4388(00)00153-7openalex-snapshot
Complementary roles of basal ganglia and cerebellum in learning and motor control
inferredcites →https://doi.org/10.1016/s1364-6613(99)01294-2openalex-snapshot
Catastrophic forgetting in connectionist networks
inferredcites →https://doi.org/10.1017/9781108891530.017openalex-snapshot
Deep Reinforcement Learning
inferredcites →https://doi.org/10.1017/s0140525x16001837openalex-snapshot
Building machines that learn and think like people
inferredcites →https://doi.org/10.1037/0022-3514.46.3.610openalex-snapshot
Choking under pressure: Self-consciousness and paradoxical effects of incentives on skillful performance.
inferredcites →https://doi.org/10.1038/35087601openalex-snapshot
Practising orientation identification improves orientation coding in V1 neurons
inferredcites →https://doi.org/10.1038/417351aopenalex-snapshot
What songbirds teach us about learning
inferredcites →https://doi.org/10.1038/nature06390openalex-snapshot
Performance variability enables adaptive plasticity of ‘crystallized’ adult birdsong
inferredcites →https://doi.org/10.1038/nature10845openalex-snapshot
Corticostriatal plasticity is necessary for learning intentional neuroprosthetic skills
inferredcites →https://doi.org/10.1038/nature11057openalex-snapshot
Brain-wide neuronal dynamics during motor adaptation in zebrafish
inferredcites →https://doi.org/10.1038/nature12742openalex-snapshot
Context-dependent computation by recurrent dynamics in prefrontal cortex
inferredcites →https://doi.org/10.1038/nature13235openalex-snapshot
Emergence of reproducible spatiotemporal activity during motor learning
inferredcites →https://doi.org/10.1038/nature13665openalex-snapshot
Neural constraints on learning
inferredcites →https://doi.org/10.1038/nature14236openalex-snapshot
Human-level control through deep reinforcement learning
inferredcites →https://doi.org/10.1038/nature24056openalex-snapshot
Network control principles predict neuron function in the Caenorhabditis elegans connectome
inferredcites →https://doi.org/10.1038/ncomms6319openalex-snapshot
Formation and maintenance of neuronal assemblies through synaptic plasticity
inferredcites →https://doi.org/10.1038/ncomms7454openalex-snapshot
Choice-correlated activity fluctuations underlie learning of neuronal category representation
inferredcites →https://doi.org/10.1038/nn.3805openalex-snapshot
Perceptual training continuously refines neuronal population codes in primary visual cortex
inferredcites →https://doi.org/10.1038/nn.3807openalex-snapshot
Information-limiting correlations
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.4061openalex-snapshot
Learning enhances the relative impact of top-down processing in the visual cortex
inferredcites →https://doi.org/10.1038/nn.4158openalex-snapshot
Inferring learning rules from distributions of firing rates in cortical neurons
inferredcites →https://doi.org/10.1038/nn.4242openalex-snapshot
The mechanics of state-dependent neural correlations
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.4405openalex-snapshot
Unstable neurons underlie a stable learned behavior
inferredcites →https://doi.org/10.1038/nn2070openalex-snapshot
Neural correlates of perceptual learning in a sensory-motor, but not a sensory, cortical area
inferredcites →https://doi.org/10.1038/nrn2699openalex-snapshot
Experience-dependent structural synaptic plasticity in the mammalian brain
inferredcites →https://doi.org/10.1038/s41467-018-04537-6openalex-snapshot
Concurrence of form and function in developing networks and its role in synaptic pruning
inferredcites →https://doi.org/10.1038/s41467-019-11786-6openalex-snapshot
A critique of pure learning and what artificial neural networks can learn from animal brains
inferredcites →https://doi.org/10.1038/s41467-021-25437-2openalex-snapshot
Stable representation of a naturalistic movie emerges from episodic activity with gain variability
inferredcites →https://doi.org/10.1038/s41583-020-00395-8openalex-snapshot
If deep learning is the answer, what is the question?
inferredcites →https://doi.org/10.1038/s41583-020-0277-3openalex-snapshot
Backpropagation and the brain
inferredcites →https://doi.org/10.1038/s41586-019-1787-xopenalex-snapshot
Distributed coding of choice, action and engagement across the mouse brain
inferredcites →https://doi.org/10.1038/s41586-020-03051-4openalex-snapshot
Mastering Atari, Go, chess and shogi by planning with a learned model
inferredcites →https://doi.org/10.1038/s41586-020-2130-2openalex-snapshot
Fundamental bounds on the fidelity of sensory cortical coding
inferredcites →https://doi.org/10.1038/s41586-021-03628-7openalex-snapshot
Representational drift in primary olfactory cortex
inferredcites →https://doi.org/10.1038/s41586-021-04329-xopenalex-snapshot
Cortical preparatory activity indexes learned motor memories
inferredcites →https://doi.org/10.1038/s41593-017-0028-6openalex-snapshot
Flexible timing by temporal scaling of cortical responses
inferredcites →https://doi.org/10.1038/s41593-018-0095-3openalex-snapshot
Learning by neural reassociation
inferredcites →https://doi.org/10.1038/s41593-018-0147-8openalex-snapshot
Prefrontal cortex as a meta-reinforcement learning system
inferredcites →https://doi.org/10.1038/s41593-019-0340-4openalex-snapshot
Optimality and heuristics in perceptual neuroscience
inferredcites →https://doi.org/10.1038/s41593-019-0502-4openalex-snapshot
Single-trial neural dynamics are dominated by richly varied movements
inferredcites →https://doi.org/10.1038/s41593-019-0520-2openalex-snapshot
A deep learning framework for neuroscience
inferredcites →https://doi.org/10.1038/s41593-020-0671-1openalex-snapshot
Cortical-like dynamics in recurrent circuits optimized for sampling-based probabilistic inference
inferredcites →https://doi.org/10.1038/s41593-021-00822-8openalex-snapshot
Learning is shaped by abrupt changes in neural engagement
inferredcites →https://doi.org/10.1038/s41593-021-00980-9openalex-snapshot
Large-scale neural recordings call for new insights to link brain and behavior
inferredcites →https://doi.org/10.1038/s41593-021-01007-zopenalex-snapshot
Mice alternate between discrete strategies during perceptual decision-making
inferredcites →https://doi.org/10.1038/s42256-019-0025-4openalex-snapshot
Reinforcement learning in artificial and biological systems
inferredcites →https://doi.org/10.1073/pnas.0808113105openalex-snapshot
Functional network reorganization during learning in a brain-computer interface paradigm
inferredcites →https://doi.org/10.1073/pnas.1820296116openalex-snapshot
New neural activity patterns emerge with long-term learning
inferredcites →https://doi.org/10.1098/rstb.2016.0161openalex-snapshot
Variance and invariance of neuronal long-term representations
inferredcites →https://doi.org/10.1101/2021.03.14.435278openalex-snapshot
A Synthesis of the Many Errors and Learning Processes of Visuomotor Adaptation
inferredcites →https://doi.org/10.1101/2021.06.21.449346openalex-snapshot
Heterogeneous ‘cell types’ can improve performance of deep neural networks
inferredcites →https://doi.org/10.1109/cec.2008.4631255openalex-snapshot
Natural Evolution Strategies
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/10.1123/jsep.32.1.61openalex-snapshot
Experienced Golfers’ Perspectives on Choking Under Pressure
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.277.5327.821openalex-snapshot
Neural Correlates of Motor Memory Consolidation
inferredcites →https://doi.org/10.1126/science.aao0284openalex-snapshot
Learning and attention reveal a general relationship between population activity and behavior
inferredcites →https://doi.org/10.1126/science.aao6058openalex-snapshot
Evidence for a neural law of effect
inferredcites →https://doi.org/10.1126/science.aav3932openalex-snapshot
Thirst regulates motivated behavior through modulation of brainwide neural population dynamics
inferredcites →https://doi.org/10.1126/science.aav7893openalex-snapshot
Spontaneous behaviors drive multidimensional, brainwide activity
inferredcites →https://doi.org/10.1126/science.aay2400openalex-snapshot
Superhuman AI for multiplayer poker
inferredcites →https://doi.org/10.1145/3291801.3291829openalex-snapshot
Lifelong Machine Learning
inferredcites →https://doi.org/10.1146/annurev-neuro-072116-031548openalex-snapshot
The Role of Variability in Motor Learning
inferredcites →https://doi.org/10.1146/annurev.ne.08.030185.001013openalex-snapshot
Birdsong: From Behavior to Neuron
inferredcites →https://doi.org/10.1146/annurev.neuro.051508.135516openalex-snapshot
Synaptic Mechanisms for Plasticity in Neocortex
inferredcites →https://doi.org/10.1146/annurev.neuro.27.070203.144238openalex-snapshot
CEREBELLUM-DEPENDENT LEARNING: The Role of Multiple Plasticity Mechanisms
inferredcites →https://doi.org/10.1146/annurev.neuro.28.061604.135722openalex-snapshot
Multiple Dopamine Functions at Different Time Courses
inferredcites →https://doi.org/10.1152/jn.00266.2007openalex-snapshot
Sensory Prediction Errors Drive Cerebellum-Dependent Adaptation of Reaching
inferredcites →https://doi.org/10.1152/jn.00373.2013openalex-snapshot
Rapid acquisition of novel interface control by small ensembles of arbitrarily selected primary motor cortex neurons
inferredcites →https://doi.org/10.1152/jn.00466.2018openalex-snapshot
Distinct types of neural reorganization during long-term learning
inferredcites →https://doi.org/10.1152/jn.00761.2010openalex-snapshot
Learning on Multiple Timescales in Smooth Pursuit Eye Movements
inferredcites →https://doi.org/10.1152/jn.01012.2010openalex-snapshot
Recording from the same neurons chronically in motor cortex
inferredcites →https://doi.org/10.1152/jn.01311.2006openalex-snapshot
Model of Birdsong Learning Based on Gradient Estimation by Dynamic Perturbation of Neural Conductances
inferredcites →https://doi.org/10.1162/089976605774320539openalex-snapshot
Learning Curves for Stochastic Gradient Descent in Linear Feedforward Networks
inferredcites →https://doi.org/10.1162/089976698300017214openalex-snapshot
Chaotic Balanced State in a Model of Cortical Circuits
inferredcites →https://doi.org/10.1162/isal_a_00200openalex-snapshot
Self-optimization in a Hopfield neural network based on the
inferredcites →https://doi.org/10.1162/jocn_a_00789openalex-snapshot
The Effects of Short-term and Long-term Learning on the Responses of Lateral Intraparietal Neurons to Visually Presented Objects
inferredcites →https://doi.org/10.1184/r1/6607196openalex-snapshot
Mechanisms of skill acquisition and the law of practice
inferredcites →https://doi.org/10.1201/9781351006620-6openalex-snapshot
Deep Reinforcement Learning
inferredcites →https://doi.org/10.12688/f1000research.19793.1openalex-snapshot
Recent advances in understanding the role of phasic dopamine activity
inferredcites →https://doi.org/10.13140/rg.2.2.16025.88169openalex-snapshot
Weight Agnostic Neural Networks
inferredcites →https://doi.org/10.1371/journal.pbio.0030153openalex-snapshot
Vocal Experimentation in the Juvenile Songbird Requires a Basal Ganglia Circuit
inferredcites →https://doi.org/10.1371/journal.pbio.0040179openalex-snapshot
Interacting Adaptive Processes with Different Timescales Underlie Short-Term Motor Learning
inferredcites →https://doi.org/10.1371/journal.pbio.1000130openalex-snapshot
Crystal Structure of a Yeast Aquaporin at 1.15 Å Reveals a Novel Gating Mechanism
inferredcites →https://doi.org/10.1371/journal.pbio.1000153openalex-snapshot
Emergence of a Stable Cortical Map for Neuroprosthetic Control
inferredcites →https://doi.org/10.1371/journal.pcbi.1002012openalex-snapshot
Learning from Sensory and Reward Prediction Errors during Motor Adaptation
inferredcites →https://doi.org/10.1371/journal.pcbi.1003963openalex-snapshot
Deep Neural Networks Rival the Representation of Primate IT Cortex for Core Visual Object Recognition
inferredcites →https://doi.org/10.1371/journal.pcbi.1007074openalex-snapshot
Perturbing low dimensional activity manifolds in spiking neuronal networks
inferredcites →https://doi.org/10.1371/journal.pcbi.1007514openalex-snapshot
Dimensionality, information and learning in prefrontal cortex
inferredcites →https://doi.org/10.1371/journal.pcbi.1008621openalex-snapshot
Neural manifold under plasticity in a goal driven learning behaviour
inferredcites →https://doi.org/10.1371/journal.pone.0214096openalex-snapshot
Choking under the pressure of competition: A complete statistical investigation of pressure kicks in the NFL, 2000–2017
inferredcites →https://doi.org/10.1523/jneurosci.1370-17.2019openalex-snapshot
Medial prefrontal cortex population activity is plastic irrespective of learning
inferredcites →https://doi.org/10.1523/jneurosci.1831-12.2012openalex-snapshot
Population Rate Dynamics and Multineuron Firing Patterns in Sensory Cortex
inferredcites →https://doi.org/10.1523/jneurosci.2072-19.2019openalex-snapshot
Information-Limiting Correlations in Large Neural Populations
inferredcites →https://doi.org/10.1523/jneurosci.2125-20.2021openalex-snapshot
Did We Get Sensorimotor Adaptation Wrong? Implicit Adaptation as Direct Policy Updating Rather than Forward-Model-Based Learning
inferredcites →https://doi.org/10.1523/jneurosci.2325-10.2010openalex-snapshot
Latent Inputs Improve Estimates of Neural Encoding in Motor Cortex
inferredcites →https://doi.org/10.1523/jneurosci.2656-14.2015openalex-snapshot
Persistent Residual Errors in Motor Adaptation Tasks: Reversion to Baseline and Exploratory Escape
inferredcites →https://doi.org/10.1523/jneurosci.3244-14.2015openalex-snapshot
Reward-Dependent Modulation of Movement Variability
inferredcites →https://doi.org/10.1523/jneurosci.3967-10.2010openalex-snapshot
Incorporating Feedback from Multiple Sensory Modalities Enhances Brain–Machine Interface Control
inferredcites →https://doi.org/10.1523/jneurosci.4406-10.2012openalex-snapshot
Change in Choice-Related Response Modulation in Area MT during Learning of a Depth-Discrimination Task is Consistent with Task Learning
inferredcites →https://doi.org/10.1523/jneurosci.5792-11.2012openalex-snapshot
Muscle Coordination Is Habitual Rather than Optimal
inferredcites →https://doi.org/10.3389/fnbeh.2015.00019openalex-snapshot
Choking under pressure: the neuropsychological mechanisms of incentive-induced performance decrements
inferredcites →https://doi.org/10.3389/fncom.2016.00094openalex-snapshot
Toward an Integration of Deep Learning and Neuroscience
inferredcites →https://doi.org/10.3389/fpsyg.2013.00623openalex-snapshot
Perceptual estimation obeys Occam's razor
inferredcites →https://doi.org/10.3758/s13423-020-01865-xopenalex-snapshot
Prolonged response time helps eliminate residual errors in visuomotor adaptation
inferredcites →https://doi.org/10.4324/9780203728178openalex-snapshot
Cognitive Skills and Their Acquisition
inferredcites →https://doi.org/10.48550/arxiv.1502.04156openalex-snapshot
Towards Biologically Plausible Deep Learning
inferredcites →https://doi.org/10.48550/arxiv.1703.03864openalex-snapshot
Evolution Strategies as a Scalable Alternative to Reinforcement Learning
inferredcites →https://doi.org/10.48550/arxiv.1706.01905openalex-snapshot
Parameter Space Noise for Exploration
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.1808.05377openalex-snapshot
Neural Architecture Search: A Survey
inferredcites →https://doi.org/10.48550/arxiv.2010.11765openalex-snapshot
Identifying Learning Rules From Neural Network Observables
inferredcites →https://doi.org/10.5555/2627435.2638566openalex-snapshot
Natural evolution strategies
inferredcites →https://doi.org/10.7554/elife.06346openalex-snapshot
Serotonergic neurons signal reward and punishment on multiple timescales
inferredcites →https://doi.org/10.7554/elife.18044openalex-snapshot
Dopamine neurons learn relative chosen value from probabilistic rewards
inferredcites →https://doi.org/10.7554/elife.36774openalex-snapshot
Constraints on neural redundancy
inferredcites →https://doi.org/10.7554/elife.38242openalex-snapshot
'Artiphysiology' reveals V4-like shape tuning in a deep network trained for image classification
inferredcites →https://doi.org/10.7554/elife.51121openalex-snapshot
Stable task information from an unstable neural population
inferredcites →https://doi.org/10.7554/elife.63550openalex-snapshot
The brain in motion: How ensemble fluidity drives memory-updating and flexibility
inferredcites →https://doi.org/10.7554/elife.66175openalex-snapshot
Mice in a labyrinth show rapid learning, sudden insight, and efficient exploration

What points at this work

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

inferred← citeshttps://doi.org/10.2139/ssrn.4660873openalex-extracted
inferred← citeshttps://doi.org/10.1007/978-3-031-64487-0_1openalex-snapshot
On Cyber-Social Learning: A Critique of Artificial Intelligence in Education
inferred← citeshttps://doi.org/10.1007/s44163-022-00029-1openalex-snapshot
Artificial intelligence in the long view: from mechanical intelligence to cyber-social systems
inferred← citeshttps://doi.org/10.1016/j.biosystems.2025.105515openalex-snapshot
Codes across (life)sciences
inferred← citeshttps://doi.org/10.1016/j.celrep.2025.115289openalex-snapshot
Prospective and retrospective representations of saccadic movements in primate prefrontal cortex
inferred← citeshttps://doi.org/10.1016/j.cogsys.2024.101260openalex-snapshot
Exploring biological challenges in building a thinking machine
inferred← citeshttps://doi.org/10.1016/j.conb.2021.10.015openalex-snapshot
Towards the next generation of recurrent network models for cognitive neuroscience
inferred← citeshttps://doi.org/10.1016/j.conb.2023.102759openalex-snapshot
Signatures of task learning in neural representations
inferred← citeshttps://doi.org/10.1016/j.conb.2026.103267openalex-snapshot
But what behavior?
inferred← citeshttps://doi.org/10.1016/j.cub.2024.03.003openalex-snapshot
Learning leaves a memory trace in motor cortex
inferred← citeshttps://doi.org/10.1016/j.neubiorev.2026.106927openalex-snapshot
Reframing motor skill organisation: Dynamics, mechanisms, and impact in surgical settings
inferred← citeshttps://doi.org/10.1016/j.tics.2025.06.017openalex-snapshot
Brain–computer interfaces as a causal probe for scientific inquiry
inferred← citeshttps://doi.org/10.1038/s41467-025-64976-wopenalex-snapshot
Fluctuation-learning relationship in recurrent neural networks
inferred← citeshttps://doi.org/10.1038/s41562-023-01662-1openalex-snapshot
Developmental changes in exploration resemble stochastic optimization
inferred← citeshttps://doi.org/10.1038/s41593-024-01626-2openalex-snapshot
Dimensionality reduction beyond neural subspaces with slice tensor component analysis
inferred← citeshttps://doi.org/10.1038/s41598-024-69666-zopenalex-snapshot
Vagus nerve stimulation during training fails to improve learning in healthy rats
inferred← citeshttps://doi.org/10.1080/00131857.2022.2033213openalex-snapshot
The cybernetics of learning
inferred← citeshttps://doi.org/10.1101/2021.10.29.465647openalex-snapshot
Inter-trial variations in EEG predict the individual differences in social tasks
inferred← citeshttps://doi.org/10.1101/2022.07.05.498856openalex-snapshot
Learning alters neural activity to simultaneously support memory and action
inferred← citeshttps://doi.org/10.1101/2022.12.08.519453openalex-snapshot
BCI Learning Phenomena Can Be Explained by Gradient-Based Optimization
inferred← citeshttps://doi.org/10.1101/2023.03.11.532146openalex-snapshot
Comparing Sites of Plasticity in Models of Adaptation to Manifold-Based Perturbations in Brain-Computer Interfaces
inferred← citeshttps://doi.org/10.1101/2023.08.09.552699openalex-snapshot
Cell-type-specific plasticity shapes neocortical dynamics for motor learning
inferred← citeshttps://doi.org/10.1101/2025.04.02.646788openalex-snapshot
Neural signatures of motor memories emerge in neural network models
inferred← citeshttps://doi.org/10.1101/cshperspect.a041507openalex-snapshot
Modeling Normal and Abnormal Circuit Development with Recurrent Neural Networks
inferred← citeshttps://doi.org/10.1109/icassp48485.2024.10447409openalex-snapshot
Fixed Inter-Neuron Covariability Induces Adversarial Robustness
inferred← citeshttps://doi.org/10.1109/tbme.2023.3319956openalex-snapshot
Efficient Estimation of Directed Connectivity in Nonlinear and Nonstationary Spiking Neuron Networks
inferred← citeshttps://doi.org/10.1113/jp283291openalex-snapshot
Heksor: the central nervous system substrate of an adaptive behaviour
inferred← citeshttps://doi.org/10.1152/jn.00474.2021openalex-snapshot
De novo motor learning of a bimanual control task over multiple days of practice
inferred← citeshttps://doi.org/10.1371/journal.pcbi.1012492openalex-snapshot
De novo sensorimotor learning through reuse of movement components
inferred← citeshttps://doi.org/10.1371/journal.pcbi.1014719openalex-snapshot
Manifold-constrained plasticity enables stable learning in recurrent neural circuits
inferred← citeshttps://doi.org/10.21203/rs.3.rs-2073831/v1openalex-snapshot
Investigation of Factors Affecting Motif-Based Short- and Long-Term Memory Behaviour in Biological Networks
inferred← citeshttps://doi.org/10.31202/ecjse.1523210openalex-snapshot
Investigation of Factors Affecting Motif-Based Short- and Long-Term Memory Behaviour in Brain Neuron Networks
inferred← citeshttps://doi.org/10.31234/osf.io/9f4k3openalex-snapshot
Developmental changes resemble stochastic optimization
inferred← citeshttps://doi.org/10.3389/fneur.2026.1753883openalex-snapshot
Editorial: Integrating multimodal approaches to unravel neural mechanisms of learning and cognition
inferred← citeshttps://doi.org/10.37843/rted.v18i1.630openalex-snapshot
La Fascinante Conexión entre la Neurociencia y el Aprendizaje Matemático
inferred← citeshttps://doi.org/10.70675/60817e4dzd012z4c1eza527z519c2d5bf260openalex-snapshot
The effect of age on spatial working memory and topography of dopamine neurons in the ventral tegmental area in a mouse model of healthy aging
inferred← citeshttps://doi.org/10.7554/elife.106871openalex-snapshot
Neural signatures of motor memories emerge in neural network models
inferred← citeshttps://doi.org/10.7554/elife.106871.1openalex-snapshot
Neural signatures of motor memories emerge in neural network models
inferred← citeshttps://doi.org/10.7554/elife.91839openalex-snapshot
Fundamental processes in sensorimotor learning: Reasoning, refinement, and retrieval
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.