scholarly article | Q13442814 |
P50 | author | Heinrich Bülthoff | Q1596905 |
Christian F Altmann | Q59693751 | ||
Zoe Kourtzi | Q61302299 | ||
P2860 | cites work | Borders of multiple visual areas in humans revealed by functional magnetic resonance imaging | Q22337051 |
Neurophysiological investigation of the basis of the fMRI signal | Q27860853 | ||
Distributed hierarchical processing in the primate cerebral cortex | Q28266250 | ||
Mapping striate and extrastriate visual areas in human cerebral cortex | Q28279618 | ||
Feedforward, horizontal, and feedback processing in the visual cortex | Q28283667 | ||
Collinear interactions and contour integration. | Q64977365 | ||
Lateral interactions between spatial channels: suppression and facilitation revealed by lateral masking experiments | Q70748422 | ||
Improvement in visual sensitivity by changes in local context: Parallel studies in human observers and in V1 of alert monkeys | Q71783369 | ||
The architecture of perceptual spatial interactions | Q72262789 | ||
The neurophysiology of figure-ground segregation in primary visual cortex | Q72575609 | ||
Visual responses in monkey areas V1 and V2 to three-dimensional surface configurations | Q73119755 | ||
Integrating contours within and through depth | Q73348723 | ||
Shape-coding in IT cells generalizes over contrast and mirror reversal, but not figure-ground reversal | Q74441732 | ||
Integrated model of visual processing | Q77110173 | ||
Retinotopic organization in human visual cortex and the spatial precision of functional MRI | Q28306912 | ||
Visual Object Recognition | Q30047650 | ||
Integration of contours: new insights | Q33774272 | ||
Object-related activity revealed by functional magnetic resonance imaging in human occipital cortex | Q33950103 | ||
Seeing beyond the receptive field in primary visual cortex | Q34029080 | ||
The distinct modes of vision offered by feedforward and recurrent processing | Q34080505 | ||
Selective averaging of rapidly presented individual trials using fMRI. | Q34111241 | ||
Contour integration by the human visual system: evidence for a local "association field". | Q34361427 | ||
Dynamics of spatial summation in primary visual cortex of alert monkeys | Q35732891 | ||
Figure-ground activity in primary visual cortex is suppressed by anesthesia | Q35985602 | ||
Task-dependent influences of attention on the activation of human primary visual cortex | Q36312174 | ||
Horizontal integration and cortical dynamics | Q36331762 | ||
A closed curve is much more than an incomplete one: effect of closure in figure-ground segmentation | Q36473738 | ||
Functional imaging of human visual recognition | Q36848252 | ||
Parametric analysis of fMRI data using linear systems methods. | Q36882945 | ||
Stimulus specific responses from beyond the classical receptive field: neurophysiological mechanisms for local-global comparisons in visual neurons | Q39817499 | ||
Inferotemporal cortex and object vision | Q41132609 | ||
Response modulation by texture surround in primate area V1: correlates of "popout" under anesthesia | Q41607319 | ||
Task-related modulation of visual cortex | Q41740792 | ||
Response profiles to texture border patterns in area V1. | Q41750029 | ||
Adult cortical dynamics | Q41751235 | ||
Activity in primary visual cortex predicts performance in a visual detection task | Q41758676 | ||
Brightness perception and filling-in | Q42097916 | ||
Neuronal responses to static texture patterns in area V1 of the alert macaque monkey | Q43960085 | ||
Experiencing and perceiving visual surfaces | Q44985133 | ||
Linear systems analysis of functional magnetic resonance imaging in human V1. | Q46703850 | ||
A human extrastriate area functionally homologous to macaque V4. | Q46851622 | ||
Separate processing dynamics for texture elements, boundaries and surfaces in primary visual cortex of the macaque monkey | Q48150263 | ||
Integration of surface information in primary visual cortex | Q48240047 | ||
The role of the primary visual cortex in higher level vision | Q48361996 | ||
Cue-invariant activation in object-related areas of the human occipital lobe | Q48414956 | ||
Contextual modulation in primary visual cortex. | Q48860387 | ||
Cortical mechanisms specific to explicit visual object recognition | Q48959881 | ||
Contextual modulation in primary visual cortex of macaques. | Q48974618 | ||
Perceptual sensitivity maps within globally defined visual shapes. | Q52057008 | ||
Shape-selective stereo processing in human object-related visual areas. | Q52124131 | ||
The dynamics of object-selective activation correlate with recognition performance in humans. | Q52166695 | ||
Cortical regions involved in perceiving object shape. | Q52169046 | ||
Contextual influence on orientation discrimination of humans and responses of neurons in V1 of alert monkeys. | Q52171064 | ||
Contour integration across depth | Q52339952 | ||
Representation of Perceived Object Shape by the Human Lateral Occipital Complex | Q59665058 | ||
Texture Segregation in the Human Visual Cortex: A Functional MRI Study | Q60508438 | ||
P433 | issue | 4 | |
P407 | language of work or name | English | Q1860 |
P1104 | number of pages | 8 | |
P304 | page(s) | 342-349 | |
P577 | publication date | 2003-02-01 | |
P1433 | published in | Current Biology | Q1144851 |
P1476 | title | Perceptual organization of local elements into global shapes in the human visual cortex | |
P478 | volume | 13 |
Q30424382 | A century of Gestalt psychology in visual perception: I. Perceptual grouping and figure-ground organization |
Q50310650 | A new approach to the study of detail perception in Autism Spectrum Disorder (ASD): investigating visual feedforward, horizontal and feedback processing |
Q21559607 | Abnormal contextual modulation of visual contour detection in patients with schizophrenia |
Q43085930 | Adaptation to implied tilt: extensive spatial extrapolation of orientation gradients. |
Q49555618 | Alterations in the inferior longitudinal fasciculus in autism and associations with visual processing: a diffusion-weighted MRI study |
Q34993047 | An fMRI examination of visual integration in schizophrenia |
Q30427273 | Animal models and measures of perceptual processing in schizophrenia. |
Q48344765 | Asymmetric priming effects in visual processing of occlusion patterns |
Q48874875 | Attentional modulation of perceptual grouping in human visual cortex: ERP studies. |
Q48913969 | Attentional modulation of perceptual grouping in human visual cortex: functional MRI studies. |
Q33542989 | BOLD signal in both ipsilateral and contralateral retinotopic cortex modulates with perceptual fading |
Q34460604 | Bilateral theta-burst TMS to influence global gestalt perception |
Q30439622 | Brain networks supporting perceptual grouping and contour selection |
Q79741609 | Closure facilitates contour integration |
Q30010513 | Cognitive representation of "musical fractals": Processing hierarchy and recursion in the auditory domain |
Q35161160 | Collinear facilitation and contour integration in autism: evidence for atypical visual integration |
Q99724129 | Collinear facilitation and contour integration in autistic adults: Examining lateral and feedback connectivity |
Q33411768 | Common cortical loci are activated during visuospatial interpolation and orientation discrimination judgements |
Q33785887 | Connecting the dots: how local structure affects global integration in infants |
Q34031983 | Context modulates the ERP signature of contour integration |
Q41455747 | Contour Integration in Dynamic Scenes: Impaired Detection Performance in Extended Presentations. |
Q48706298 | Contour Integration over Time: Psychophysical and fMRI Evidence |
Q36607927 | Contour discontinuities subserve two types of form analysis that underlie motion processing |
Q43121495 | Contour integration and aging: the effects of element spacing, orientation alignment and stimulus duration. |
Q88163716 | Contour integration with corners |
Q50174722 | Contour interpolation: A case study in Modularity of Mind. |
Q36973262 | Contributions of low and high spatial frequency processing to impaired object recognition circuitry in schizophrenia |
Q30377892 | Cortical contributions to impaired contour integration in schizophrenia |
Q35601131 | Crowding, grouping, and object recognition: A matter of appearance |
Q52007271 | Cue combination in a combined feature contrast detection and figure identification task. |
Q34885341 | Decoding of coherent but not incoherent motion signals in early dorsal visual cortex |
Q33938867 | Defining the units of competition: influences of perceptual organization on competitive interactions in human visual cortex. |
Q52086816 | Detection of contour continuity and closure in three-month-olds. |
Q76377940 | Development of contour integration in macaque monkeys |
Q36028271 | Development of sensitivity to global form and motion in macaque monkeys (Macaca nemestrina) |
Q48761749 | Development of spatial integration depends on top-down and interhemispheric connections that can be perturbed in migraine: a DCM analysis |
Q35347152 | Director field model of the primary visual cortex for contour detection. |
Q37341051 | Disruptions in neural connectivity associated with reduced susceptibility to a depth inversion illusion in youth at ultra high risk for psychosis |
Q40314553 | Distinct effects of contour smoothness and observer bias on visual persistence |
Q34766876 | Early stages of figure-ground segregation during perception of the face-vase |
Q35658203 | Effects of Spatial Frequency Similarity and Dissimilarity on Contour Integration |
Q48888043 | Emergence of perceptual Gestalts in the human visual cortex: the case of the configural-superiority effect |
Q33883323 | Face inversion reduces the persistence of global form and its neural correlates |
Q46364047 | Feedforward and recurrent processing in scene segmentation: electroencephalography and functional magnetic resonance imaging. |
Q64056783 | Fragmented ambiguous objects: Stimuli with stable low-level features for object recognition tasks |
Q40982153 | Gestalt Perceptual Organization of Visual Stimuli Captures Attention Automatically: Electrophysiological Evidence |
Q21129133 | Global processing in amblyopia: a review |
Q27026988 | Hierarchical processing in music, language, and action: Lashley revisited |
Q37598282 | How Configural Is the Configural Superiority Effect? A Neuroimaging Investigation of Emergent Features in Visual Cortex |
Q50735343 | Impaired texture segregation but spared contour integration following damage to right posterior parietal cortex. |
Q91279892 | Integrated assessment of visual perception abnormalities in psychotic disorders and relationship with clinical characteristics |
Q98200392 | Integration of contours defined by second-order contrast-modulation of texture |
Q42979408 | Inter-element orientation and distance influence the duration of persistent contour integration |
Q48600959 | Interhemispheric integration at different spatial scales: the evidence from EEG coherence and FMRI. |
Q28731032 | Layer-specific fMRI reflects different neuronal computations at different depths in human V1 |
Q33763214 | Low level constraints on dynamic contour path integration |
Q33747732 | MEG responses to the perception of global structure within glass patterns. |
Q48247171 | Motion fading is driven by perceived, not actual angular velocity |
Q52146707 | Neural Discriminability of Object Features Predicts Perceptual Organization. |
Q80210951 | Neural substrates differentiating global/local processing of bilateral visual inputs |
Q34039754 | Neuronal oscillations form parietal/frontal networks during contour integration |
Q48487839 | Object ensemble processing in human anterior-medial ventral visual cortex. |
Q34002642 | Object grouping based on real-world regularities facilitates perception by reducing competitive interactions in visual cortex |
Q42220791 | Orientation perception in Williams Syndrome: discrimination and integration |
Q30491461 | Perception measurement in clinical trials of schizophrenia: promising paradigms from CNTRICS. |
Q41699463 | Perceptual Grouping of Closed Contours Is Disrupted by the Interpretation of the Scene Layout |
Q49134777 | Perceptual continuity and the emergence of perceptual persistence in the ventral visual pathway |
Q64099559 | Perceptual inference employs intrinsic alpha frequency to resolve perceptual ambiguity |
Q47161630 | Perceptual integration rapidly activates dorsal visual pathway to guide local processing in early visual areas. |
Q41904542 | Perceptual representation and effectiveness of local figure-ground cues in natural contours |
Q58588706 | Phase-selective masking with radial frequency contours |
Q33621851 | Posterior-Anterior Brain Maturation Reflected in Perceptual, Motor and Cognitive Performance |
Q35920817 | Radial Frequency Analysis of Contour Shapes in the Visual Cortex |
Q34192897 | Rapid shape detection signals in area V4. |
Q47572188 | Recurrent Processing of Contour Integration in the Human Visual Cortex as Revealed By fMRI-Guided TMS. |
Q33817886 | Regions of mid-level human visual cortex sensitive to the global coherence of local image patches |
Q51968013 | Representation of shapes, edges, and surfaces across multiple cues in the human visual cortex. |
Q62578839 | Response priming evidence for feedforward processing of snake contours but not of ladder contours and textures |
Q27335028 | Responses in early visual areas to contour integration are context dependent |
Q87246803 | Right-hemisphere specialization for contour grouping |
Q48822868 | Rotational and translational motion interact independently with form |
Q40959471 | Suppressive and enhancing effects in early visual cortex during illusory shape perception: A comment on. |
Q48465934 | The "mosaic stage" in amodal completion as characterized by magnetoencephalography responses |
Q46334459 | The effect of aging on contour integration |
Q83463851 | The effects of aging on contour discrimination in clutter |
Q82871696 | The effects of spatial proximity and collinearity on contour integration in adults and children |
Q52783981 | The forest or the trees: preference for global over local image processing is reversed by prior experience in honeybees. |
Q81176524 | The influences of visibility and anomalous integration processes on the perception of global spatial form versus motion in human amblyopia |
Q38441115 | The moon illusion and size-distance scaling--evidence for shared neural patterns. |
Q33543149 | The neural correlates of visuospatial perceptual and oculomotor extrapolation |
Q48535387 | The neural mechanisms underlying the Müller-Lyer illusion and its interaction with visuospatial judgments |
Q50785390 | The role of shape complexity in the detection of closed contours. |
Q45848460 | The role of temporo-parietal junction (TPJ) in global Gestalt perception |
Q30459086 | Top-down control in contour grouping |
Q34582346 | Top-down modulations in the visual form pathway revealed with dynamic causal modeling |
Q48439072 | Toward a common circle: interhemispheric contextual modulation in human early visual areas. |
Q89516482 | Ventral stream hierarchy underlying perceptual organization in adolescents with autism |
Q34044956 | Vision first? The development of primary visual cortical networks is more rapid than the development of primary motor networks in humans |
Q38954274 | Visual Perception Disturbances in Schizophrenia: A Unified Model |
Q34377355 | Visual crowding illustrates the inadequacy of local vs. global and feedforward vs. feedback distinctions in modeling visual perception |
Q36849530 | Visual integration dysfunction in schizophrenia arises by the first psychotic episode and worsens with illness duration. |
Q50433204 | Visual training improves perceptual grouping based on basic stimulus features. |
Q50342399 | Visuoperceptual processing in children with neurofibromatosis type 1: True deficit or artefact? |
Q51847204 | Visuospatial encoding deficits and compensatory strategies in schizophrenia revealed by eye movement analysis during a working memory task. |
Q43247363 | Visuospatial interpolation in typically developing children and in people with Williams Syndrome |
Q52086779 | [Cognitive function evaluation in school-age children from economically impoverished community: results of enriched education program]. |
Q30571270 | fMRI correlates of object-based attentional facilitation vs. suppression of irrelevant stimuli, dependent on global grouping and endogenous cueing |
Q48123134 | fMRI reveals that non-local processing in ventral retinotopic cortex underlies perceptual grouping by temporal synchrony |
Search more.