On the public citation graph
Influence of stimulus complexity on the specificity of visual perceptual learning
0 signed · 96 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known work and none has been retracted — and get a dated CiteStamped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/10.1002/14651858.cd008388.pub2openalex-snapshot
Interventions for visual field defects in patients with stroke
inferredcites →https://doi.org/10.1007/bf02259114openalex-snapshot
The response of neurons in areas V1 and MT of the alert rhesus monkey to moving random dot patterns
inferredcites →https://doi.org/10.1016/0006-8993(71)90494-xopenalex-snapshot
Response properties and receptive fields of cells in an anatomically defined region of the superior temporal sulcus in the monkey
inferredcites →https://doi.org/10.1016/0893-6080(88)90014-7openalex-snapshot
Neocognitron: A hierarchical neural network capable of visual pattern recognition
inferredcites →https://doi.org/10.1016/j.conb.2005.03.010openalex-snapshot
Perceptual learning: specificity versus generalization
inferredcites →https://doi.org/10.1016/j.cub.2008.10.030openalex-snapshot
Complete Transfer of Perceptual Learning across Retinal Locations Enabled by Double Training
inferredcites →https://doi.org/10.1016/j.cub.2014.08.058openalex-snapshot
Training Transfers the Limits on Perception from Parietal to Ventral Cortex
inferredcites →https://doi.org/10.1016/j.neuron.2008.08.023openalex-snapshot
Fine Discrimination Training Alters the Causal Contribution of Macaque Area MT to Depth Perception
inferredcites →https://doi.org/10.1016/j.neuron.2017.06.024openalex-snapshot
The Contribution of Area MT to Visual Motion Perception Depends on Training
inferredcites →https://doi.org/10.1016/j.tics.2005.05.010openalex-snapshot
A unified model for perceptual learning
inferredcites →https://doi.org/10.1016/s0028-3932(97)00111-5openalex-snapshot
Cortical plasticity in perceptual learning demonstrated by transcranial magnetic stimulation
inferredcites →https://doi.org/10.1016/s0028-3932(97)00113-9openalex-snapshot
Cortical plasticity in perceptual learning demonstrated by transcranial magnetic stimulation
inferredcites →https://doi.org/10.1016/s0042-6989(01)00072-4openalex-snapshot
Temporal integration of optic flow, measured by contrast and coherence thresholds
inferredcites →https://doi.org/10.1016/s0042-6989(96)00308-2openalex-snapshot
Specificity of learning curvature, orientation, and vernier discriminations
inferredcites →https://doi.org/10.1017/s0952523800010269openalex-snapshot
Responses of neurons in macaque MT to stochastic motion signals
inferredcites →https://doi.org/10.1037/0033-295x.112.4.715openalex-snapshot
The Dynamics of Perceptual Learning: An Incremental Reweighting Model.
inferredcites →https://doi.org/10.1038/379725a0openalex-snapshot
A systematic map of direction preference in primary visual cortex
inferredcites →https://doi.org/10.1038/387401a0openalex-snapshot
Task difficulty and the specificity of perceptual learning
inferredcites →https://doi.org/10.1038/nature01800openalex-snapshot
Perceptual consequences of centre–surround antagonism in visual motion processing
inferredcites →https://doi.org/10.1038/nn.2304openalex-snapshot
Reinforcement learning can account for associative and perceptual learning on a visual-decision task
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/nn915openalex-snapshot
Greater plasticity in lower-level than higher-level visual motion processing in a passive perceptual learning task
inferredcites →https://doi.org/10.1038/s41598-018-37892-xopenalex-snapshot
Disentangling locus of perceptual learning in the visual hierarchy of motion processing
inferredcites →https://doi.org/10.1073/pnas.1115685109openalex-snapshot
Hierarchical processing of complex motion along the primate dorsal visual pathway
inferredcites →https://doi.org/10.1073/pnas.1312552110openalex-snapshot
An integrated reweighting theory of perceptual learning
inferredcites →https://doi.org/10.1073/pnas.1403112111openalex-snapshot
Performance-optimized hierarchical models predict neural responses in higher visual cortex
inferredcites →https://doi.org/10.1073/pnas.1524160113openalex-snapshot
Perceptual learning modifies the functional specializations of visual cortical areas
inferredcites →https://doi.org/10.1073/pnas.95.23.13988openalex-snapshot
Perceptual learning reflects external noise filtering and internal noise reduction through channel reweighting
inferredcites →https://doi.org/10.1093/brain/awaa128openalex-snapshot
Functional preservation and enhanced capacity for visual restoration in subacute occipital stroke
inferredcites →https://doi.org/10.1093/cercor/1.1.1openalex-snapshot
Distributed Hierarchical Processing in the Primate Cerebral Cortex
inferredcites →https://doi.org/10.1093/cercor/1.1.1-aopenalex-snapshot
Preface: Cerebral Cortex Has Come of Age
inferredcites →https://doi.org/10.1097/00001756-199708180-00030openalex-snapshot
Size and shape of receptive fields in the medial superior temporal area (MST) of the macaque
inferredcites →https://doi.org/10.1098/rstb.1977.0050openalex-snapshot
Plasticity of ocular dominance columns in monkey striate cortex
inferredcites →https://doi.org/10.1101/407007openalex-snapshot
Brain-Score: Which Artificial Neural Network for Object Recognition is most Brain-Like?
inferredcites →https://doi.org/10.1109/cvpr.2016.90openalex-snapshot
Deep Residual Learning for Image Recognition
inferredcites →https://doi.org/10.1109/cvpr.2017.243openalex-snapshot
Densely Connected Convolutional Networks
inferredcites →https://doi.org/10.1109/tpami.2013.50openalex-snapshot
Representation Learning: A Review and New Perspectives
inferredcites →https://doi.org/10.1145/3065386openalex-snapshot
ImageNet classification with deep convolutional neural networks
inferredcites →https://doi.org/10.1146/annurev-psych-010814-015214openalex-snapshot
Perceptual Learning: Toward a Comprehensive Theory
inferredcites →https://doi.org/10.1146/annurev-vision-102016-061249openalex-snapshot
Visual Perceptual Learning and Models
inferredcites →https://doi.org/10.1152/jn.00338.2012openalex-snapshot
Responses of MST neurons to plaid stimuli
inferredcites →https://doi.org/10.1152/jn.00629.2004openalex-snapshot
Contrast Dependence of Suppressive Influences in Cortical Area MT of Alert Macaque
inferredcites →https://doi.org/10.1152/jn.1981.46.3.621openalex-snapshot
Visual topography of striate projection zone (MT) in posterior superior temporal sulcus of the macaque.
inferredcites →https://doi.org/10.1152/jn.1984.52.6.1106openalex-snapshot
Direction and orientation selectivity of neurons in visual area MT of the macaque
inferredcites →https://doi.org/10.1152/jn.1989.62.3.642openalex-snapshot
Underlying mechanisms of the response specificity of expansion/contraction and rotation cells in the dorsal part of the medial superior temporal area of the macaque monkey
inferredcites →https://doi.org/10.1152/jn.1991.65.6.1329openalex-snapshot
Sensitivity of MST neurons to optic flow stimuli. I. A continuum of response selectivity to large-field stimuli
inferredcites →https://doi.org/10.1152/jn.1994.71.5.1597openalex-snapshot
Responses of macaque STS neurons to optic flow components: a comparison of areas MT and MST
inferredcites →https://doi.org/10.1152/jn.1998.80.4.1816openalex-snapshot
MST Neurons Respond to Optic Flow and Translational Movement
inferredcites →https://doi.org/10.1162/neco_a_01211openalex-snapshot
Approximating the Architecture of Visual Cortex in a Convolutional Network
inferredcites →https://doi.org/10.1167/12.1.4openalex-snapshot
Adaptation to sensory-motor reflex perturbations is blind to the source of errors
inferredcites →https://doi.org/10.1167/12.11.4openalex-snapshot
Transfer of perceptual learning between different visual tasks
inferredcites →https://doi.org/10.1167/15.1.17openalex-snapshot
The effect of motion on crowding: Zooming text
inferredcites →https://doi.org/10.1167/15.1.5openalex-snapshot
Moderate acute alcohol intoxication has minimal effect on surround suppression measured with a motion direction discrimination task
inferredcites →https://doi.org/10.1167/15.10.17openalex-snapshot
Confidence-based integrated reweighting model of task-difficulty explains location-based specificity in perceptual learning
inferredcites →https://doi.org/10.1167/15.10.5openalex-snapshot
Differences in perceptual learning transfer as a function of training task
inferredcites →https://doi.org/10.1167/2.10.5openalex-snapshot
Comparison of fMRI responses during discrimination under certainty and uncertainty conditions
inferredcites →https://doi.org/10.1167/2.2.5openalex-snapshot
Comparing perceptual learning across tasks: A review
inferredcites →https://doi.org/10.1167/9.3.1openalex-snapshot
Task precision at transfer determines specificity of perceptual learning
inferredcites →https://doi.org/10.1167/9.4.22openalex-snapshot
Adaptive precision pooling of model neuron activities predicts the efficiency of human visual learning
inferredcites →https://doi.org/10.1167/9.8.22openalex-snapshot
A Litmus Test for Retino- vs. Non-retinotopic Processing
inferredcites →https://doi.org/10.1371/journal.pbio.0040092openalex-snapshot
Tuning Curves, Neuronal Variability, and Sensory Coding
inferredcites →https://doi.org/10.1523/jneurosci.0203-13.2013openalex-snapshot
Diverse Suppressive Influences in Area MT and Selectivity to Complex Motion Features
inferredcites →https://doi.org/10.1523/jneurosci.07-05-01414.1987openalex-snapshot
Surface organization of orientation and direction selectivity in cat area 18
inferredcites →https://doi.org/10.1523/jneurosci.0704-10.2010openalex-snapshot
Rule-Based Learning Explains Visual Perceptual Learning and Its Specificity and Transfer
inferredcites →https://doi.org/10.1523/jneurosci.1076-14.2014openalex-snapshot
Beyond Blindsight: Properties of Visual Relearning in Cortically Blind Fields
inferredcites →https://doi.org/10.1523/jneurosci.14-01-00054.1994openalex-snapshot
Tuning of MST neurons to spiral motions
inferredcites →https://doi.org/10.1523/jneurosci.1620-17.2018openalex-snapshot
Deep Neural Networks for Modeling Visual Perceptual Learning
inferredcites →https://doi.org/10.1523/jneurosci.1661-05.2005openalex-snapshot
A Logarithmic, Scale-Invariant Representation of Speed in Macaque Middle Temporal Area Accounts for Speed Discrimination Performance
inferredcites →https://doi.org/10.1523/jneurosci.2209-18.2018openalex-snapshot
Can Deep Learning Model Perceptual Learning?
inferredcites →https://doi.org/10.1523/jneurosci.23-08-03515.2003openalex-snapshot
Contribution of Middle Temporal Area to Coarse Depth Discrimination: Comparison of Neuronal and Psychophysical Sensitivity
inferredcites →https://doi.org/10.1523/jneurosci.4121-10.2011openalex-snapshot
Improved Motion Perception and Impaired Spatial Suppression following Disruption of Cortical Area MT/V5
inferredcites →https://doi.org/10.1523/jneurosci.4882-08.2009openalex-snapshot
Perceptual Relearning of Complex Visual Motion after V1 Damage in Humans
inferredcites →https://doi.org/10.3758/bf03194543openalex-snapshot
Adaptive procedures in psychophysical research
inferredcites →https://doi.org/10.7554/elife.16167openalex-snapshot
A neural basis for the spatial suppression of visual motion perception
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
inferred← citeshttps://doi.org/10.1016/j.cub.2025.08.027openalex-snapshot
Inactivation of primate cortex reveals inductive biases in visual learning
inferred← citeshttps://doi.org/10.1016/j.visres.2022.108174openalex-snapshot
Tilt aftereffect spreads across the visual field
inferred← citeshttps://doi.org/10.1101/2022.07.25.501371openalex-snapshot
Cognitive aging and categorical representations in visual working memory
inferred← citeshttps://doi.org/10.1126/sciadv.adk7214openalex-snapshot
Decision-related activity and movement selection in primate visual cortex
inferred← citeshttps://doi.org/10.1167/jov.21.3.10openalex-snapshot
Visual perceptual learning generalizes to untrained effectors
inferred← citeshttps://doi.org/10.1167/jov.24.1.10openalex-snapshot
Asymmetric stimulus representations bias visual perceptual learning
inferred← citeshttps://doi.org/10.1167/jov.24.5.2openalex-snapshot
Feature variability determines specificity and transfer in multiorientation feature detection learning
inferred← citeshttps://doi.org/10.1177/09567976251415352openalex-snapshot
Detection of Idiosyncratic Gaze-Fingerprint Signatures in Humans
inferred← citeshttps://doi.org/10.1371/journal.pcbi.1014553openalex-snapshot
The curriculum effect in visual learning: The role of readout dimensionality
inferred← citeshttps://doi.org/10.1523/eneuro.0383-20.2020openalex-snapshot
Neural Selectivity for Visual Motion in Macaque Area V3A
inferred← citeshttps://doi.org/10.22541/au.167113388.87378584/v1openalex-snapshot
Rapid recovery from cortical visual impairment in a pediatric patient following vision training: A case study
inferred← citeshttps://doi.org/10.3233/rnn-211223openalex-snapshot
Training with optic flow stimuli promotes recovery in cortical blindness
inferred← citeshttps://doi.org/10.3233/rnn-221294openalex-snapshot
Cortical visual impairment at birth can be improved rapidly by vision training in adulthood: A case study
inferred← citeshttps://doi.org/10.3389/fnhum.2026.1882538openalex-snapshot
Semantic content of visual stimuli has a greater impact on associative equivalence learning than stimulus modality
inferred← citeshttps://doi.org/10.5772/intechopen.1009575openalex-snapshot
Perceptual-Cognitive Training Paradigms for Understanding Cognition and Cortical Visual Impairments
inferred← citeshttps://doi.org/10.64898/2026.01.30.702749openalex-snapshot
Shared gaze reflects shared aesthetic experiences
inferred← citeshttps://doi.org/10.7454/in.v7i2.351openalex-snapshot
Assessing Relations Among Visual Variables in Hotel Lobbies Using Deep Learning
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.