scholarly article | Q13442814 |
P2093 | author name string | McCollough C | |
P433 | issue | 3688 | |
P407 | language of work or name | English | Q1860 |
P304 | page(s) | 1115-1116 | |
P577 | publication date | 1965-09-01 | |
P1433 | published in | Science | Q192864 |
P1476 | title | Color Adaptation of Edge-Detectors in the Human Visual System | |
P478 | volume | 149 |
Q52271378 | "Extinction" of the McCollough effect does not transfer interocularly. |
Q74595314 | 3D after-effects are due to shape and not disparity adaptation |
Q67441299 | A Comparison of Fourier Analysis and Feature Analysis in Pattern-Specific Color Aftereffects |
Q50918881 | A color-contingent prism displacement aftereffect |
Q73005134 | A contingent aftereffect in the auditory system |
Q71961464 | A model for after-effects of seen movement |
Q67877204 | A neural network model of the McCollough effect |
Q66963144 | A re-evaluation of curvature-specific chromatic aftereffects |
Q71312890 | A reevaluation of angle-contingent color aftereffects |
Q44721823 | A synaptic model for spatial frequency adaptation |
Q33797271 | A trained perceptual bias that lasts for weeks |
Q36332795 | Absence of Sex-Contingent Gaze Direction Aftereffects Suggests a Limit to Contingencies in Face Aftereffects. |
Q69149366 | Adaptation in single units in visual cortex: the tuning of aftereffects in the temporal domain |
Q45977875 | Adaptation of gender derived from biological motion. |
Q37611731 | Adaptation to Complex Pictures: Exposure to Emotional Valence Induces Assimilative Aftereffects |
Q38472028 | Adaptation to asymmetrically distorted faces and its lack of effect on mirror images |
Q42949579 | Adaptation to combinations of form, colour, and movement. |
Q40840069 | Adaptation to contingencies in macaque primary visual cortex |
Q52307410 | Adaptation to displaced vision: evidence for prolonged after-effects. |
Q59084473 | Adaptation to invisible gratings and the site of binocular rivalry suppression |
Q37316756 | Adaptation to numerosity requires only brief exposures, and is determined by number of events, not exposure duration |
Q51952789 | Adaptation to sensory-motor temporal misalignment: instrumental or perceptual learning? |
Q34076766 | Adapting internal statistical models for interpreting visual cues to depth |
Q30488367 | Adapting to altered image statistics using processed video |
Q90100290 | Adaptive Efficient Coding of Correlated Acoustic Properties |
Q30411821 | Adaptive coding is constrained to midline locations in a spatial listening task |
Q81255606 | Adaptive modulation of color salience contingent upon global form coding and task relevance |
Q70742638 | Age-related differences in the magnitude of pattern-contingent color aftereffects |
Q52069386 | Amnesia for the mccollough effect following unilateral electroconvulsive therapy: implications for laterality |
Q41045958 | An assessment of a property analyzer model in predicting adaptation patterns of simple and complex figures |
Q56893973 | Applying visual psychophysics to user interface design |
Q46006982 | Are You Smiling, or Have I Seen You Before? Familiarity Makes Faces Look Happier. |
Q33839086 | Are cortical models really bound by the "binding problem"? |
Q35099209 | Are high-level aftereffects perceptual? |
Q52193060 | Assessing a new analysis of contingent color aftereffects. |
Q48872425 | Asynchronous processing in vision: color leads motion. |
Q50581744 | Attention-based long-lasting sensitization and suppression of colors |
Q36956328 | Blood oxygen level-dependent activation of the primary visual cortex predicts size adaptation illusion |
Q37097057 | Body Image Distortion and Exposure to Extreme Body Types: Contingent Adaptation and Cross Adaptation for Self and Other |
Q91867800 | Body Size Adaptation Alters Perception of Test Stimuli, Not Internal Body Image |
Q59088291 | Border and Colour Coding in the Retina of the Frog |
Q51970890 | Broadly tuned, view-specific coding of face shape: opposing figural aftereffects can be induced in different views. |
Q52096247 | Characteristics of the indirect McCollough effect. |
Q71489893 | Checkerboard-specific color aftereffects: a failure to find effects of perceptual organization |
Q52165835 | Cholinergic agents and the McCollough effect. |
Q41517707 | Chromatic Induction Effects in the Hermann Grid Illusion |
Q48590132 | Chromatic substitution with stabilized images: Evidence for chromatic-specific pattern processing in the human visual system |
Q50468983 | Chromatic tuning of contour-shape mechanisms revealed through the shape-frequency and shape-amplitude after-effects |
Q48375415 | Coding and binding of color and form in visual cortex |
Q48766171 | Color Adaptation of Spatial Frequency Detectors in the Human Visual System |
Q38875008 | Color Afterimages in Autistic Adults |
Q38482405 | Color aftereffect contingent on text |
Q44525860 | Color and edge sensitive channels converge on stereo-depth analyzers |
Q44690933 | Color constancy and the functional significance of McCollough effects |
Q35859334 | Color improves speed of processing but not perception in a motion illusion |
Q50475977 | Color naming, unique hues, and hue cancellation predicted from singularities in reflection properties |
Q66928202 | Color selectivity and interocular transfer of color specific tilt aftereffects |
Q70598677 | Color- and Edge-Sensitive Channels in the Human Visual System: Tuning for Orientation |
Q44087932 | Color-selective analysis of luminance-varying stimuli |
Q73812977 | Color-specific depth mechanisms revealed by a color-contingent depth aftereffect |
Q72106283 | Color: A Motion-Contingent Aftereffect |
Q53830096 | Colored aftereffects contingent on patterns generated by Lie transformation groups. |
Q54323160 | Colour Selectivity in Motion After-effect |
Q77797868 | Colour at edges and colour spreading in McCollough effects |
Q70892013 | Colour selectivity in the tilt after-effect: Comments upon Wade and Wenderoth |
Q70035159 | Colour-contingent after-effects are really wavelength-contingent |
Q48598953 | Colour-spatial vision |
Q71052307 | Comments on the use of perceptually ambiguous figures as McCollough-effect stimuli |
Q44225660 | Common mechanisms for 2D tilt and 3D slant after-effects |
Q44729357 | Comparison of normal and dichoptic colour mixing |
Q52811883 | Concept of visual sensation |
Q52257009 | Conditioning and blocking of the McCollough effect. |
Q44017443 | Context effects in visual length perception: role of ocular, retinal, and spatial location |
Q71807039 | Contextual influences on a spatial-frequency-contingent color aftereffect |
Q52255257 | Contingency and the McCollough effect. |
Q92161319 | Contingent adaptation in masking and surround suppression |
Q45971246 | Contingent aftereffects distinguish conscious and preconscious color processing. |
Q70201680 | Contingent aftereffects: lateral interactions between color and motion |
Q52197618 | Contingent color aftereffects: reassessing old conclusions. |
Q67371366 | Contour specificity of the McCollough effect |
Q41704004 | Contrast and frequency competition for orientation-contingent color aftereffects |
Q69763278 | Cortical dynamics of three-dimensional form, color, and brightness perception: II. Binocular theory |
Q38429703 | Cross-category adaptation: exposure to faces produces gender aftereffects in body perception. |
Q31103866 | Cross-category adaptation: objects produce gender adaptation in the perception of faces |
Q69777146 | Curvature Detectors in Human Vision? |
Q69563646 | Curvature as a Feature of Pattern Vision |
Q83317076 | Decline of the McCollough effect by orientation-specific post-adaptation exposure to achromatic gratings |
Q52308218 | Delayed one-trial extinction of the McCollough effect |
Q30476597 | Demonstration of cue recruitment: change in visual appearance by means of Pavlovian conditioning |
Q90285617 | Desirability, availability, credit assignment, category learning, and attention: Cognitive-emotional and working memory dynamics of orbitofrontal, ventrolateral, and dorsolateral prefrontal cortices |
Q50776922 | Dichoptically viewed colour aftereffects produced by monocular adaptation |
Q70347081 | Differences in apparent straightness of dot and line stimuli |
Q35889288 | Distinct mechanism for long-term contrast adaptation |
Q93599478 | Does testing initiate decay of McCollough effects? |
Q38658333 | Dynamics of color contrast adaptation |
Q50962646 | Dynamics of walking adaptation aftereffects induced in static images of walking actors |
Q36711460 | Early visual mechanisms do not contribute to synesthetic color experience |
Q71249459 | Effective luminance contrast as a parameter in contingent aftereffects |
Q70562517 | Effects of spatial filtering and lack of effects of visual imagery on pattern-contingent color aftereffects |
Q30471198 | Efficient coding and statistically optimal weighting of covariance among acoustic attributes in novel sounds |
Q48531959 | Electrophysiological evidence for colour channels in human pattern vision |
Q37977517 | Ergonomic aspects of the health and safety of VDT work in Japan: a review |
Q36165763 | Ergonomics of digital imaging |
Q46955133 | Evidence for a role of action in colour perception. |
Q38759965 | Explaining Delusions: Reducing Uncertainty Through Basic and Computational Neuroscience |
Q52585457 | Exploring the functional nature of synaesthetic colour: Dissociations from colour perception and imagery. |
Q37251868 | Face adaptation aftereffects reveal anterior medial temporal cortex role in high level category representation. |
Q35218418 | Face adaptation does not improve performance on search or discrimination tasks |
Q48676475 | Failure of colour and contrast polarity identification at threshold for detection of motion and global form |
Q52191467 | False categories in cognition: the Not-the-Liver fallacy. |
Q48476705 | Feature binding across different visual dimensions |
Q36382882 | Feature binding of a continuously changing object |
Q38318289 | Feature confirmation in object perception: Feature integration theory 26 years on from the Treisman Bartlett lecture |
Q48527901 | Features and Objects: The Fourteenth Bartlett Memorial Lecture |
Q69812918 | Form-specific colour after effects in scotopic illumination |
Q54028444 | Frequency specific chromatic adaptation in the human visual system. |
Q35088394 | From single cells to social perception |
Q37238815 | Functional computational model for optimal color coding |
Q52278543 | Further evidence against the classical conditioning model of McCollough effects. |
Q43669074 | Gaze direction modulates visual aftereffects in depth and color |
Q44326793 | Gaze modulation of visual aftereffects |
Q41479949 | Guided search for triple conjunctions |
Q34714294 | Habituation and sensitization to an electrical shock in the crab Chasmagnathus. Effect of background illumination |
Q57519312 | Hallucinatory aspects of normal vision |
Q36496981 | Hour-long adaptation in the awake early visual system |
Q42907873 | How the deployment of attention determines what we see. |
Q46889162 | Hue difference contours can be used in processing orientation information |
Q54079136 | Identification and adaptation of hue: parallels in the operation of mechanisms that underlie categorical perception in vision and in audition. |
Q80787839 | Illusory colors promote interocular grouping during binocular rivalry |
Q93599481 | Imagery effects on early visual processing |
Q30583529 | Images created in a model eye during simulated cataract surgery can be the basis for images perceived by patients during cataract surgery. |
Q69863672 | Individual differences in McCollough effects: a study of twins |
Q67398161 | Induction of the McCollough effect I: figural variables |
Q67444239 | Induction of the McCollough effect II: two different mechanisms |
Q46709841 | Initial activation state, stimulation intensity and timing of stimulation interact in producing behavioral effects of TMS. |
Q46591265 | Inter-ocular transfer of the tilt illusion shows that monocular orientation mechanisms are colour selective |
Q30804387 | Interactions of afterimages for orientation and color: experimental data and model simulations. |
Q37092631 | Interdependent Mechanisms for Processing Gender and Emotion: The Special Status of Angry Male Faces |
Q68033158 | Interference with McCollough effects via pre- and postinduction exposure to achromatic gratings: time course and magnitude of aftereffect decrement |
Q71089149 | Interocular transfer of orientation-contingent color aftereffects with external and internal adaptation |
Q52954069 | Investigation of temporal integration by video sampling. |
Q71337907 | Investigations of perception and imagery using CAEs: the role of experimental design and psychophysical method |
Q72154891 | Is Orientation-Specific Color Adaptation in Human Vision Due to Edge Detectors, Afterimages, or "Dipoles"? |
Q69736627 | Is spatial masking selective to wavelength? |
Q41703909 | Is the “contour specificity” of McCollough effects an example of anomalous transfer? Comments on Sharpe and Tees (1978) |
Q70705265 | Laterality differences in sensitivity to line orientation as a function of adaptation duration |
Q51951405 | Learning and the wisdom of the body. |
Q37127471 | Learning to Associate Orientation with Color in Early Visual Areas by Associative Decoded fMRI Neurofeedback |
Q48189742 | Learning to adapt: Dynamics of readaptation to geometrical distortions |
Q34273775 | Less is more: latent learning is maximized by shorter training sessions in auditory perceptual learning |
Q69779142 | Letter: McCollough colour after effect |
Q46380025 | Long-lasting sensitization to a given colour after visual search |
Q37078830 | Long-term renormalization of chromatic mechanisms following cataract surgery |
Q69654743 | Luminance Thresholds for Motion Contingent on Colour |
Q69555470 | Making ambiguous displays unambiguous: the influence of real colors and colored aftereffects on perceptual alternation |
Q52278544 | McCollough effect acquisition depends on duration of exposure to inducing stimuli, not number of stimulus presentations. |
Q70636299 | McCollough effect analogs of two-color projections |
Q48223315 | McCollough effect and eye optics |
Q39673526 | McCollough effect: A theory based on the anatomy of the lateral geniculate body |
Q77809678 | Motion after-effects and word contingency |
Q36727183 | Motion aftereffects specific to surface depth order: beyond binocular disparity |
Q67345975 | Movement aftereffects contingent on the colour or pattern of a stationary surround |
Q48294249 | Multiple orientation-contingent chromatic after-effects |
Q50518291 | Mystery of the anti-McCollough effect |
Q52244272 | Negative afterimages and the McCollough effect. |
Q30401084 | Neural Adaptation Effects in Conceptual Processing |
Q55040130 | Neuronal Mechanism for Compensation of Longitudinal Chromatic Aberration-Derived Algorithm. |
Q33839076 | Neuronal synchrony: a versatile code for the definition of relations? |
Q48723983 | Normal McCollough effect in Alzheimer's disease and global amnesia |
Q48121878 | On the Development of Speech Perception: Mechanisms and Analogies |
Q48561792 | Opponent-colour cells in different layers of foveal striate cortex |
Q48388061 | Orientation specific colour adaptation at a binocular site |
Q68474673 | Orientation-contingent color aftereffects are determined by real color, not induced color |
Q52230484 | Orientation-contingent color aftereffects mediated by subjective transparent structures. |
Q69509057 | Orientation-sensitive after-effects or dichoptically presented colour and form |
Q52241165 | Orientation-specific luminance aftereffects. |
Q52247374 | Overprediction and blocking in the McCollough aftereffect. |
Q59600756 | Parallel processing: Giving up without a fight |
Q41537123 | Past, present, and future of the recombination procedure |
Q69970022 | Pattern-contingent color aftereffects on noninduced patterns |
Q52289859 | Perceptual learning of illusory contours and colour. |
Q36355022 | Persistent states in vision break universality and time invariance. |
Q70742631 | Pigeons experience orientation-contingent chromatic aftereffects |
Q52285121 | Practice does not facilitate acquisition of McCollough effects: evidence against a learning model. |
Q48942840 | Preattentive binding of auditory and visual stimulus features |
Q50608150 | Preserved striate cortex is not sufficient to support the McCollough effect: evidence from two patients with cerebral achromatopsia. |
Q93089835 | Preview of partial stimulus information in search prioritizes features and conjunctions, not locations |
Q48498207 | Probing the visual representation of faces with adaptation: A view from the other side of the mean |
Q93588748 | Prolonged complementary chromatopsia in users of video display terminals |
Q52319303 | Proposals for the study of anomalous perceptual schemata. |
Q44461070 | Psychophysical measurement of cortical color mechanisms not sensitive to spatial frequency |
Q67818254 | Psychophysical measurement of spectral sensitivity and color vision in red-light-reared tree shrews (Tupaia belangeri) |
Q41275196 | Psychophysical ‘measurement’ of Cortical Colour Mechanisms: Reply to Meyer |
Q59201388 | Psykologins bidrag till utveckling av bildskärmar |
Q45785427 | Rapid Discrimination of McCollough Effects |
Q30475151 | Rapid efficient coding of correlated complex acoustic properties |
Q33966527 | Recent advances in electrical recording from the human brain |
Q37334632 | Receptoral and postreceptoral visual processes in recovery from chromatic adaptation |
Q59064994 | Reduction or Disappearance of Visual After Effect of Movement in the Absence of Patterned Surround |
Q33816605 | Response normalization and blur adaptation: data and multi-scale model |
Q60050104 | Response to short-term deprivation of the human adult visual cortex measured with 7T BOLD |
Q48182150 | Response variability and orientation discrimination of single cells in striate cortex of cat |
Q48343258 | Right hemispheric sensitivity for the McCollough effect |
Q54519619 | Role of Retinal Image Motion in Evoking the McCollough Effect |
Q49186528 | STEP--a System for Teaching Experimental Psychology using E-Prime |
Q37209789 | Seeing the invisible: the scope and limits of unconscious processing in binocular rivalry |
Q35540070 | Selectivity for the configural cues that identify the gender, ethnicity, and identity of faces in human cortex |
Q35677234 | Sensing limb movements in the motor cortex: how humans sense limb movement |
Q35008619 | Sensory memory of illusory depth in structure-from-motion. |
Q35810105 | Shared or separate mechanisms for self-face and other-face processing? Evidence from adaptation. |
Q50601049 | Simple and contingent aftereffects of perceived duration in vision and audition |
Q43845442 | Simultaneous color contrast from McCollough effects is spatially contingent |
Q53170345 | Simultaneous perceptual and response biases on sequential face attractiveness judgments. |
Q33597598 | Single units and visual cortical organization |
Q47393595 | Size Adaptation: A New Aftereffect |
Q59679641 | Sleep facilitates long-term face adaptation |
Q35875629 | Sleep's influence on a reflexive form of memory that does not require voluntary attention |
Q73454020 | Solutions to the binding problem: progress through controversy and convergence |
Q40874352 | Something for the future |
Q69510124 | Spatial Frequency Dependent Chromatic After-effects |
Q67441297 | Spatial Frequency—Contingent Color Aftereffects |
Q38275529 | Spatial and temporal aspects of chromatic adaptation and their functional significance for colour constancy |
Q52263619 | Spatial attention in vision. Evidence for early selection. |
Q77732722 | Spatial characteristics of the second-order visual pathway revealed by positional adaptation |
Q41211180 | Spatial contingency and the McCollough effect. |
Q70705311 | Spatial frequency content of visual imagery |
Q69641909 | Spatial frequency phase effects in human vision |
Q44008261 | Spatial frequency, orientation and color: Interocular effects of adaptation on the perceived duration of gratings |
Q68076251 | Spatial-frequency-contingent color aftereffects: adaptation with one-dimensional stimuli |
Q46829047 | Spatial-frequency-contingent color aftereffects: adaptation with two-dimensional stimulus patterns |
Q33839082 | Specialized representations in visual cortex: a role for binding? |
Q45273144 | Specific and general contour adaptation effects found using a selective adaptation paradigm |
Q41272722 | Spectral and orientation specificity of single cells in foveal striate cortex of the vervet monkey,Cercopithecus aethiops |
Q48477391 | Stabilized images: Probe analysis of pattern and color analytic mechanisms |
Q52330529 | Stereoscopic Depth Aftereffect Produced without Monocular Cues |
Q48230119 | Storage of Spatially Specific Threshold Elevation |
Q51871160 | Subjective colours and brain function |
Q85205070 | Surface boundaries do not constrain a depth aftereffect |
Q34088010 | Surface color from boundaries: a new 'watercolor' illusion |
Q86450838 | Surround-contingent motion aftereffect |
Q28144831 | Synchrony unbound: a critical evaluation of the temporal binding hypothesis |
Q41873453 | Synesthesia and the McCollough Effect |
Q57022307 | Temporal contingencies determine whether adaptation strengthens or weakens normalization |
Q38465423 | Text-contingent color aftereffects: a reexamination |
Q52119122 | Thalamocortical dynamics of the McCollough effect: boundary-surface alignment through perceptual learning. |
Q35898794 | The McCollough effect and facial emotion discrimination in patients with schizophrenia and their unaffected relatives |
Q48552695 | The McCollough effect as a measure of central cholinergic activity in man |
Q57944515 | The McCollough effect in pigeons: tests of persistence and spatial-frequency specificity |
Q57381968 | The McCollough effect reveals orientation discrimination in a case of cortical blindness |
Q42795273 | The McCollough effect with plaids and gratings: evidence for a plaid-selective visual mechanism |
Q52222584 | The McCollough effect: dissociating retinal from spatial coordinates. |
Q34390252 | The binding problem |
Q73453997 | The binding problem |
Q42581410 | The company they keep: background similarity influences transfer of aftereffects from second- to first-order stimuli |
Q52124711 | The conjunction of feature and depth information. |
Q73412668 | The effect of orientation learning on contrast sensitivity |
Q69493148 | The effects of electrical stimulation of the eye upon increment threshold for square-wave gratings |
Q50849371 | The graph-paper effect: subjective stereoscopic patterns induced by moving gratings |
Q74524544 | The influence of adaptation on perceived visual location |
Q70705315 | The influence of imagery ability on color aftereffects produced by physically present and imagined induction stimuli |
Q69522294 | The influence of wavelength on visual adaptation to spatially periodic stimuli |
Q40840416 | The knowledge used in vision and where it comes from |
Q48891500 | The perceived spatial frequency shift: evidence for frequency-selective neurones in the human brain |
Q41519589 | The photopigment bleaching hypothesis of complementary after-images: A psychophysical test |
Q36241924 | The physiology and psychophysics of the color-form relationship: a review |
Q33839059 | The psychophysical evidence for a binding problem in human vision |
Q67371374 | The quantitative measure of pattern representation in images using orientation-specific color aftereffects |
Q42011315 | The role of background statistics in face adaptation |
Q54037289 | The role of intervening patterns in the storage of the movement aftereffect. |
Q33839065 | The role of neural mechanisms of attention in solving the binding problem |
Q52303080 | The role of test pattern background hue in the McCollough effect |
Q69789242 | The roles of pattern orthogonality and color contrast in the generation of pattern-contingent color aftereffects |
Q44414059 | The slippery context effect in psychophysics: intensive, extensive, and qualitative continua |
Q51639018 | The spatial tuning of chromatic adaptation. |
Q33839069 | The temporal correlation hypothesis of visual feature integration: still alive and well |
Q37037895 | The watercolor effect: quantitative evidence for luminance-dependent mechanisms of long-range color assimilation |
Q33839091 | The what and why of binding: the modeler's perspective |
Q52199854 | The widespread influence of the Rescorla-Wagner model. |
Q56902649 | Time course of contrast adaptation to VDU-displayed text |
Q51647808 | Top-down learning of low-level vision tasks. |
Q72923403 | Transmission of edge information in the human visual system |
Q38586694 | Two new contingent aftereffects: Perceived auditory duration contingent on pitch and on temporal order |
Q52003109 | Unconscious orientation processing. |
Q51594078 | Using structural equation modeling to examine McCollough Effects (orientation-contingent color aftereffects): influence of dissociative experiences and age on illusory aftereffects. |
Q34752003 | Vision contingent auditory pitch aftereffects |
Q33533801 | Vision: modular analysis--or not? |
Q39222161 | Visual Construction of Color Is Digital |
Q93076026 | Visual Cortical Plasticity in Retinitis Pigmentosa |
Q72416360 | Visual Motion Perception: Experimental Modification |
Q36753984 | Visual adaptation: physiology, mechanisms, and functional benefits |
Q33646727 | Visual after-effects associated with the use of high-resolution visual display units |
Q50752288 | Visual aftereffect of texture density contigent on color of frame |
Q46386499 | Visual illusions and neurobiology |
Q66928189 | Visual movement aftereffect: Evidence for independent adaptation to moving target and stationary surround |
Q66938763 | What causes decay of pattern-contingent chromatic aftereffects? |
Q35949500 | You Don't See What I See: Individual Differences in the Perception of Meaning from Visual Stimuli |
Q54332251 | [Selective analysis of movement direction and velocity in the human visual system (author's transl)]. |
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