scholarly article | Q13442814 |
P2093 | author name string | Lorenceau J | |
Alais D | |||
P2860 | cites work | Neural representation of visual objects: encoding and top-down activation | Q30588914 |
Contour integration by the human visual system: evidence for a local "association field". | Q34361427 | ||
Reciprocal interactions between occlusion and motion computations | Q36087125 | ||
Horizontal integration and cortical dynamics | Q36331762 | ||
A closed curve is much more than an incomplete one: effect of closure in figure-ground segmentation | Q36473738 | ||
Convergence of magno- and parvocellular pathways in layer 4B of macaque primary visual cortex. | Q36795905 | ||
A theory of visual interpolation in object perception | Q37765271 | ||
Visual sensitivity and parallel retinocortical channels | Q38144704 | ||
Concurrent processing streams in monkey visual cortex | Q38203057 | ||
Psychophysical evidence for separate channels for the perception of form, color, movement, and depth | Q39680135 | ||
The analysis of visual motion: from computational theory to neuronal mechanisms | Q39763366 | ||
Aperture viewing: a review and a synthesis. | Q40349503 | ||
How parallel are the primate visual pathways? | Q40890841 | ||
Cortical dynamics of three-dimensional figure-ground perception of two-dimensional pictures | Q41551605 | ||
The influence of terminators on motion integration across space | Q43894425 | ||
Surface completion complements boundary interpolation in the visual integration of partly occluded objects | Q44048922 | ||
Neural responses to polar, hyperbolic, and Cartesian gratings in area V4 of the macaque monkey | Q46165283 | ||
Grouping of image fragments in primary visual cortex | Q48104634 | ||
Magnocellular and parvocellular contributions to the responses of neurons in macaque striate cortex. | Q48144229 | ||
Separate processing dynamics for texture elements, boundaries and surfaces in primary visual cortex of the macaque monkey | Q48150263 | ||
Neuronal selectivities to complex object features in the ventral visual pathway of the macaque cerebral cortex | Q48159037 | ||
Shape selectivity in primate lateral intraparietal cortex | Q48374523 | ||
Cortical feedback improves discrimination between figure and background by V1, V2 and V3 neurons | Q48401871 | ||
Spatial and temporal contrast sensitivities of neurones in lateral geniculate nucleus of macaque | Q48593856 | ||
Functional analysis of V3A and related areas in human visual cortex | Q48630076 | ||
Integration of what and where in the primate prefrontal cortex | Q48708944 | ||
The analysis of complex motion patterns by form/cue invariant MSTd neurons | Q48957332 | ||
Response properties of single cells in monkey striate cortex during reversible inactivation of individual lateral geniculate laminae | Q51864974 | ||
Early completion of occluded objects. | Q52182691 | ||
A computational theory for the perception of coherent visual motion | Q52564987 | ||
Responses to contour features in macaque area V4. | Q52916826 | ||
Cooperative and competitive spatial interactions in motion integration | Q57700509 | ||
Phenomenal coherence of moving visual patterns | Q59070281 | ||
Form and motion coherence activate independent, but not dorsal/ventral segregated, networks in the human brain | Q59629681 | ||
Occlusion and the solution to the aperture problem for motion | Q69412851 | ||
Increased motion linking across edges with decreased luminance contrast, edge width and duration | Q71453354 | ||
Improvement in visual sensitivity by changes in local context: Parallel studies in human observers and in V1 of alert monkeys | Q71783369 | ||
Response of monkey MST neurons to optic flow stimuli with shifted centers of motion | Q71924046 | ||
The architecture of perceptual spatial interactions | Q72262789 | ||
Learning to find a shape | Q73505078 | ||
Velocity decomposition and surface decomposition--reciprocal interactions between motion and form processing | Q73986550 | ||
Evidence for boundary-specific grouping | Q74217194 | ||
Local and global factors affecting the coherent motion of gratings presented in multiple apertures | Q77330955 | ||
P433 | issue | 7 | |
P407 | language of work or name | English | Q1860 |
P304 | page(s) | 745-751 | |
P577 | publication date | 2001-07-01 | |
P1433 | published in | Nature Neuroscience | Q1535359 |
P1476 | title | Form constraints in motion binding | |
P478 | volume | 4 |
Q27336011 | Beta, but not gamma, band oscillations index visual form-motion integration |
Q38572682 | Binocular rivalry: competition and inhibition in visual perception |
Q39143981 | Catching the voltage gradient-asymmetric boost of cortical spread generates motion signals across visual cortex: a brief review with special thanks to Amiram Grinvald. |
Q44593442 | Classification images reveal spatiotemporal contour interpolation |
Q83953849 | Conditional spatial-frequency selective pooling of one-dimensional motion signals into global two-dimensional motion |
Q52121962 | Context and the motion aftereffect: occlusion cues in the test pattern alter perceived direction. |
Q50174722 | Contour interpolation: A case study in Modularity of Mind. |
Q48361929 | Distinct functional organizations for processing different motion signals in V1, V2, and V4 of macaque |
Q36606366 | Efficiency of extracting stereo-driven object motions |
Q27304490 | From Flashes to Edges to Objects: Recovery of Local Edge Fragments Initiates Spatiotemporal Boundary Formation. |
Q51632931 | Global shape coding for motion-defined radial-frequency contours. |
Q51601165 | How do object reference frames and motion vector decomposition emerge in laminar cortical circuits? |
Q90448546 | Illusory Oscillation of the Central Rotation Axis |
Q36544347 | Is interpolation cognitively encapsulated? Measuring the effects of belief on Kanizsa shape discrimination and illusory contour formation |
Q48027968 | Local and Global Gestalt Laws: A Neurally Based Spectral Approach |
Q84421022 | Modelling the dynamics of motion integration with a new luminance-gated diffusion mechanism |
Q37842844 | Motion psychophysics: 1985-2010. |
Q37323766 | Neural substrates of perceptual integration during bistable object perception |
Q46387405 | Object motion computation for the initiation of smooth pursuit eye movements in humans |
Q46072058 | Ongoing eye movements constrain visual perception |
Q44577745 | Pattern cues disambiguate perceived direction in simple moving stimuli |
Q46051355 | S-cone signals invisible to the motion system can improve motion extraction via grouping by color. |
Q40073728 | Shape distortions and Gestalt grouping in anorthoscopic perception |
Q26795622 | Suppressive mechanisms in visual motion processing: From perception to intelligence |
Q36564553 | Temporal Asymmetry in Dark-Bright Processing Initiates Propagating Activity across Primary Visual Cortex. |
Q42497043 | The aperture problem in contoured stimuli. |
Q51121447 | The global slowdown effect: why does perceptual grouping reduce perceived speed? |
Q52091329 | The influence of motion-defined form on the perception of spatially-defined form. |
Q84373680 | The influence of orientation jitter and motion on contour saliency and object identification |
Q27302194 | The role of temporally coarse form processing during binocular rivalry |
Q51638849 | The use of facial motion and facial form during the processing of identity. |
Q42064813 | The utility of shape attributes in deciphering movements of non-rigid objects |
Q88741103 | Towards a unified perspective of object shape and motion processing in human dorsal cortex |
Q45039666 | Using the kinetic Zollner illusion to quantify the interaction between form and motion information in depth. |
Q41771081 | Voluntary attention modulates motion-induced mislocalization |
Q30669783 | What constitutes an efficient reference frame for vision? |
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