| scholarly article | Q13442814 |
| P356 | DOI | 10.1016/S0896-6273(02)01174-1 |
| P698 | PubMed publication ID | 12546827 |
| P50 | author | Nikos K. Logothetis | Q897072 |
| Mark Augath | Q124164636 | ||
| Christian F Altmann | Q59693751 | ||
| P2093 | author name string | Andreas S Tolias | |
| Zoe Kourtzi | |||
| P2860 | cites work | Event-related functional MRI: Past, present, and future | Q22066199 |
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| Neurophysiological investigation of the basis of the fMRI signal | Q27860853 | ||
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| The neurophysiology of figure-ground segregation in primary visual cortex | Q72575609 | ||
| RECEPTIVE FIELDS AND FUNCTIONAL ARCHITECTURE IN TWO NONSTRIATE VISUAL AREAS (18 AND 19) OF THE CAT | Q28201959 | ||
| 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 | ||
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| Computational neuroimaging of human visual cortex | Q30573119 | ||
| Estimating receptive field size from fMRI data in human striate and extrastriate visual cortex | Q30665592 | ||
| 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 | ||
| Receptive fields and functional architecture of monkey striate cortex | Q34053190 | ||
| 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 | ||
| Horizontal integration and cortical dynamics | Q36331762 | ||
| A closed curve is much more than an incomplete one: effect of closure in figure-ground segmentation | Q36473738 | ||
| Relationship between intrinsic connections and functional architecture revealed by optical imaging and in vivo targeted biocytin injections in primate striate cortex | Q36656162 | ||
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| Parametric analysis of fMRI data using linear systems methods. | Q36882945 | ||
| Psychophysical evidence for fast region-based segmentation processes in motion and color. | Q37508235 | ||
| Visual processing in monkey extrastriate cortex | Q39594248 | ||
| Stimulus specific responses from beyond the classical receptive field: neurophysiological mechanisms for local-global comparisons in visual neurons | Q39817499 | ||
| Corticocortical connections in the visual system: structure and function | Q40576726 | ||
| Adaptation to contingencies in macaque primary visual cortex | Q40840069 | ||
| Inferotemporal cortex and object vision | Q41132609 | ||
| Pattern-selective adaptation in visual cortical neurones | Q41582398 | ||
| Response modulation by texture surround in primate area V1: correlates of "popout" under anesthesia | Q41607319 | ||
| Response profiles to texture border patterns in area V1. | Q41750029 | ||
| Adult cortical dynamics | Q41751235 | ||
| Brightness perception and filling-in | Q42097916 | ||
| Neuronal responses to static texture patterns in area V1 of the alert macaque monkey | Q43960085 | ||
| Visual properties of neurons in inferotemporal cortex of the Macaque | Q44351941 | ||
| The unresponsive regions of visual cortical receptive fields | Q44685362 | ||
| Experiencing and perceiving visual surfaces | Q44985133 | ||
| Length and width tuning of neurons in the cat's primary visual cortex. | Q45937806 | ||
| Collinear stimuli regulate visual responses depending on cell's contrast threshold. | Q46004153 | ||
| Visual areas in macaque cortex measured using functional magnetic resonance imaging. | Q46362114 | ||
| Linear systems analysis of functional magnetic resonance imaging in human V1. | Q46703850 | ||
| fMRI of human visual cortex | Q48105271 | ||
| The representation of illusory and real contours in human cortical visual areas revealed by functional magnetic resonance imaging. | Q48108878 | ||
| Rapid adaptation in visual cortex to the structure of images. | Q48126247 | ||
| Cortical point-spread function and long-range lateral interactions revealed by real-time optical imaging of macaque monkey primary visual cortex. | Q48126372 | ||
| Functional imaging of the monkey brain | Q48134538 | ||
| Separate processing dynamics for texture elements, boundaries and surfaces in primary visual cortex of the macaque monkey | Q48150263 | ||
| Contrast's effect on spatial summation by macaque V1 neurons | Q48158343 | ||
| Topography of contextual modulations mediated by short-range interactions in primary visual cortex | Q48176281 | ||
| Endstopped neurons in the visual cortex as a substrate for calculating curvature | Q48198605 | ||
| Integration of surface information in primary visual cortex | Q48240047 | ||
| Processing of color, form and disparity information in visual areas VP and V2 of ventral extrastriate cortex in the macaque monkey | Q48313682 | ||
| Multiple visual areas in the caudal superior temporal sulcus of the macaque | Q48333727 | ||
| 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 | ||
| Organization of suppression in receptive fields of neurons in cat visual cortex | Q48460385 | ||
| Signals in macaque striate cortical neurons that support the perception of glass patterns. | Q48488342 | ||
| Functional-anatomic correlates of object priming in humans revealed by rapid presentation event-related fMRI. | Q48517857 | ||
| Characteristics of surround inhibition in cat area 17. | Q48605383 | ||
| A neural mechanism for working and recognition memory in inferior temporal cortex | Q48622090 | ||
| Distortions of visuotopic map match orientation singularities in primary visual cortex | Q48685141 | ||
| Object-completion effects in the human lateral occipital complex | Q48692720 | ||
| Motion processing in the macaque: revisited with functional magnetic resonance imaging. | Q48740747 | ||
| Orientation selectivity and the arrangement of horizontal connections in tree shrew striate cortex. | Q48765018 | ||
| fMR-adaptation: a tool for studying the functional properties of human cortical neurons | Q48859141 | ||
| Contextual modulation in primary visual cortex. | Q48860387 | ||
| A hierarchical axis of object processing stages in the human visual cortex | Q48933507 | ||
| The representation of brightness in primary visual cortex | Q48940355 | ||
| Neural mechanisms of visual working memory in prefrontal cortex of the macaque | Q48942845 | ||
| Cortical mechanisms specific to explicit visual object recognition | Q48959881 | ||
| Contextual modulation in primary visual cortex of macaques. | Q48974618 | ||
| Differential processing of objects under various viewing conditions in the human lateral occipital complex. | Q50108251 | ||
| Lateral inhibition between orientation detectors in the cat's visual cortex | Q51108012 | ||
| Perceptual sensitivity maps within globally defined visual shapes. | Q52057008 | ||
| Contextual influences on orientation discrimination: binding local and global cues. | Q52133876 | ||
| 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 | ||
| Isolating excitatory and inhibitory nonlinear spatial interactions involved in contrast detection. | Q52299698 | ||
| Mechanisms of contour perception in monkey visual cortex. I. Lines of pattern discontinuity. | Q52868065 | ||
| Representation of Perceived Object Shape by the Human Lateral Occipital Complex | Q59665058 | ||
| Neuronal Correlates of Pop-out in Cat Striate Cortex | Q60508450 | ||
| Collinear interactions and contour integration. | Q64977365 | ||
| Visuotopic organization and extent of V3 and V4 of the macaque | Q68416694 | ||
| Receptive field properties of neurons in area V3 of macaque monkey extrastriate cortex | Q69028798 | ||
| Mechanisms of contour perception in monkey visual cortex. II. Contours bridging gaps | Q69614452 | ||
| Columnar specificity of intrinsic horizontal and corticocortical connections in cat visual cortex | Q69653762 | ||
| Lateral interactions between spatial channels: suppression and facilitation revealed by lateral masking experiments | Q70748422 | ||
| Visual topography of V2 in the macaque | Q70946139 | ||
| 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 | ||
| P433 | issue | 2 | |
| P407 | language of work or name | English | Q1860 |
| P921 | main subject | functional magnetic resonance imaging | Q903809 |
| P304 | page(s) | 333-346 | |
| P577 | publication date | 2003-01-01 | |
| P1433 | published in | Neuron | Q3338676 |
| P1476 | title | Integration of local features into global shapes: monkey and human FMRI studies | |
| P478 | volume | 37 |
| Q30424382 | A century of Gestalt psychology in visual perception: I. Perceptual grouping and figure-ground organization |
| Q34291260 | A century of Gestalt psychology in visual perception: II. Conceptual and theoretical foundations |
| Q37475626 | A comparison of fMRI adaptation and multivariate pattern classification analysis in visual cortex |
| Q24616769 | A putative model of multisensory object representation |
| Q43085930 | Adaptation to implied tilt: extensive spatial extrapolation of orientation gradients. |
| Q36705810 | An event-related potential examination of contour integration deficits in schizophrenia |
| Q34993047 | An fMRI examination of visual integration in schizophrenia |
| Q30427273 | Animal models and measures of perceptual processing in schizophrenia. |
| Q28660557 | Are non-human primates capable of rhythmic entrainment? Evidence for the gradual audiomotor evolution hypothesis |
| Q28237325 | Attention to form or surface properties modulates different regions of human occipitotemporal cortex |
| Q48387621 | BOLD adaptation in vibrotactile stimulation: neuronal networks involved in frequency discrimination |
| Q34460604 | Bilateral theta-burst TMS to influence global gestalt perception |
| Q28757119 | Brain areas selective for both observed and executed movements |
| Q30439622 | Brain networks supporting perceptual grouping and contour selection |
| Q39117607 | Bringing the real world into the fMRI scanner: repetition effects for pictures versus real objects |
| Q36008518 | Categorization training results in shape- and category-selective human neural plasticity |
| Q79741609 | Closure facilitates contour integration |
| Q34490015 | Collinear stimuli induce local and cross-areal coherence in the visual cortex of behaving monkeys |
| Q33411768 | Common cortical loci are activated during visuospatial interpolation and orientation discrimination judgements |
| Q41846754 | Computing local edge probability in natural scenes from a population of oriented simple cells |
| Q48706298 | Contour Integration over Time: Psychophysical and fMRI Evidence |
| Q43121495 | Contour integration and aging: the effects of element spacing, orientation alignment and stimulus duration. |
| 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 |
| 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 |
| Q30500951 | Differential effect of contrast polarity reversals in closed squares and open L-junctions |
| Q48320427 | Differential human brain activation by vertical and horizontal global visual textures |
| Q40314553 | Distinct effects of contour smoothness and observer bias on visual persistence |
| Q37221877 | Distinguishing conjoint and independent neural tuning for stimulus features with fMRI adaptation |
| Q24810399 | Distributed neural plasticity for shape learning in the human visual cortex |
| Q42118362 | Do we need another neural correlate of contour integration? |
| Q44890760 | Electrophysiological correlates of lateral interactions in human visual cortex |
| Q48888043 | Emergence of perceptual Gestalts in the human visual cortex: the case of the configural-superiority effect |
| Q30939194 | Ensemble Empirical Mode Decomposition Analysis of EEG Data Collected during a Contour Integration Task |
| Q48508936 | Equivalent representation of real and illusory contours in macaque V4. |
| Q37210476 | Exploring the brains of Baduk (Go) experts: gray matter morphometry, resting-state functional connectivity, and graph theoretical analysis. |
| Q33283993 | FMRI reveals a dissociation between grasping and perceiving the size of real 3D objects |
| Q33883323 | Face inversion reduces the persistence of global form and its neural correlates |
| Q48188318 | Functional magnetic resonance imaging adaptation reveals the cortical networks for processing grasp-relevant object properties. |
| Q26852273 | Future trends in Neuroimaging: Neural processes as expressed within real-life contexts |
| Q40982153 | Gestalt Perceptual Organization of Visual Stimuli Captures Attention Automatically: Electrophysiological Evidence |
| Q35750320 | Global contour processing in amblyopia |
| Q39125271 | Haptic shape processing in visual cortex |
| Q48442758 | Heterogeneous structure in face-selective human occipito-temporal cortex |
| 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 |
| Q37154607 | Identification of everyday objects on the basis of fragmented outline versions |
| Q35944521 | Image segregation in strabismic amblyopia |
| 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. |
| Q21091087 | Investigating the mechanisms of hallucinogen-induced visions using 3,4-methylenedioxyamphetamine (MDA): a randomized controlled trial in humans |
| Q35092414 | Local and global limits on visual processing in schizophrenia |
| Q33747732 | MEG responses to the perception of global structure within glass patterns. |
| Q36930734 | Mapping the connectivity with structural equation modeling in an fMRI study of shape-from-motion task |
| Q81420102 | Multi-component correlate for lateral collinear interactions in the human visual cortex |
| Q38827597 | Multiple asynchronous stimulus- and task-dependent hierarchies (STDH) within the visual brain's parallel processing systems |
| Q30489822 | Multisensory visual-tactile object related network in humans: insights gained using a novel crossmodal adaptation approach |
| Q52146707 | Neural Discriminability of Object Features Predicts Perceptual Organization. |
| Q37190501 | Neural representations of faces and body parts in macaque and human cortex: a comparative FMRI study. |
| Q80210951 | Neural substrates differentiating global/local processing of bilateral visual inputs |
| Q34039754 | Neuronal oscillations form parietal/frontal networks during contour integration |
| Q48925694 | Neurons in macaque area V4 acquire directional tuning after adaptation to motion stimuli |
| Q37350700 | Normal susceptibility to visual illusions in abnormal development: evidence from Williams syndrome |
| Q46065712 | Object representation in inferior temporal cortex is organized hierarchically in a mosaic-like structure |
| Q33379100 | On the functional significance of the P1 and N1 effects to illusory figures in the notch mode of presentation. |
| Q35632478 | Optimization and validation of a visual integration test for schizophrenia research |
| Q37322491 | Organizational principles of human visual cortex revealed by receptor mapping. |
| Q27312200 | Orientation-cue invariant population responses to contrast-modulated and phase-reversed contour stimuli in macaque V1 and V2 |
| Q34974645 | Orientation-selective adaptation to first- and second-order patterns in human visual cortex |
| Q33972564 | Parallel processing in the brain's visual form system: an fMRI study |
| Q34471276 | Parallel processing of face and house stimuli by V1 and specialized visual areas: a magnetoencephalographic (MEG) study |
| Q37715674 | Parallelism in the brain's visual form system |
| Q48218209 | Parietal cortex mediates conscious perception of illusory gestalt. |
| Q30550039 | Pattern randomness aftereffect |
| Q30491461 | Perception measurement in clinical trials of schizophrenia: promising paradigms from CNTRICS. |
| Q49134777 | Perceptual continuity and the emergence of perceptual persistence in the ventral visual pathway |
| Q46626742 | Perceptual integration and attention in human extrastriate cortex |
| Q33941784 | Perceptual organization impairment in schizophrenia and associated brain mechanisms: review of research from 2005 to 2010. |
| Q41904542 | Perceptual representation and effectiveness of local figure-ground cues in natural contours |
| Q36652957 | Piecing it together: infants' neural responses to face and object structure |
| Q43275684 | Population response to contextual influences in the primary visual cortex. |
| Q33621851 | Posterior-Anterior Brain Maturation Reflected in Perceptual, Motor and Cognitive Performance |
| Q35920817 | Radial Frequency Analysis of Contour Shapes in the Visual Cortex |
| Q47233224 | Reading acquisition enhances an early visual process of contour integration |
| 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 |
| Q41714338 | Regular Is Longer. |
| Q28078708 | Repetition suppression: a means to index neural representations using BOLD? |
| Q90090227 | Resolving the spatial profile of figure enhancement in human V1 through population receptive field modeling |
| 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 |
| Q83231130 | Seeing grating-textured surface begins at the border |
| Q81019531 | Short-term visual deprivation alters neural processing of tactile form |
| Q57522506 | Spatially Specific fMRI Repetition Effects in Human Visual Cortex |
| Q34046637 | Speed dependence of tuning to one-dimensional features in V1. |
| Q30381464 | Subsecond timing in primates: comparison of interval production between human subjects and rhesus monkeys |
| Q38994590 | The Faces of Predictive Coding. |
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| Q48216889 | The cortical representation of objects rotating in depth. |
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