| scholarly article | Q13442814 |
| P50 | author | Martin Rolfs | Q39187707 |
| P2093 | author name string | Patrick Cavanagh | |
| Arash Afraz | |||
| Amelia R Hunt | |||
| P2860 | cites work | Control of goal-directed and stimulus-driven attention in the brain | Q27860553 |
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| Computational modelling of visual attention | Q28205343 | ||
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| The representation of visual salience in monkey parietal cortex | Q48536671 | ||
| Spatial invariance of visual receptive fields in parietal cortex neurons | Q48539975 | ||
| The updating of the representation of visual space in parietal cortex by intended eye movements | Q48550550 | ||
| The existence and role of retinotopic and spatiotopic forms of visual persistence | Q48863428 | ||
| Trans-saccadic perception | Q48865055 | ||
| Dissociable neural mechanisms supporting visual short-term memory for objects | Q48940698 | ||
| Limits of attentive tracking reveal temporal properties of attention | Q49049215 | ||
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| Spatial processing in the monkey frontal eye field. II. Memory responses. | Q52016414 | ||
| Integration of Form across Saccadic Eye Movements | Q52239070 | ||
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| Localized effects of spatial frequency adaptation | Q70431382 | ||
| Facilitatory and inhibitory after-effect of spatially localized grating adaptation | Q70692191 | ||
| Neurons in the monkey superior colliculus predict the visual result of impending saccadic eye movements | Q71923794 | ||
| Stroboscopic movement based on change of phenomenal rather than retinal location | Q79064014 | ||
| Spatiotopic transfer of visual-form adaptation across saccadic eye movements | Q81328728 | ||
| Attentional resolution | Q83168832 | ||
| Perceptual evidence for saccadic updating of color stimuli | Q83191966 | ||
| Post-saccadic location judgments reveal remapping of saccade targets to non-foveal locations | Q84565232 | ||
| Capacity limit of visual short-term memory in human posterior parietal cortex | Q28256604 | ||
| Visual and eye movement functions of the posterior parietal cortex | Q28268897 | ||
| Neuronal mechanisms of visual stability | Q28282153 | ||
| Saccade target selection and object recognition: evidence for a common attentional mechanism | Q28287057 | ||
| The role of attention in the programming of saccades | Q28296532 | ||
| Subcortical modulation of attention counters change blindness | Q28298546 | ||
| Maps of visual space in human occipital cortex are retinotopic, not spatiotopic. | Q30483049 | ||
| Prefrontal and parietal contributions to spatial working memory | Q31023172 | ||
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| Updating of the visual representation in monkey striate and extrastriate cortex during saccades | Q34021579 | ||
| A sensorimotor account of vision and visual consciousness. | Q34150234 | ||
| Feature analysis in early vision: Evidence from search asymmetries | Q34175755 | ||
| The time course of perisaccadic receptive field shifts in the lateral intraparietal area of the monkey | Q34180492 | ||
| Change blindness: past, present, and future | Q34382751 | ||
| The maintenance of spatial accuracy by the perisaccadic remapping of visual receptive fields | Q35093838 | ||
| Attentional modulation of visual processing. | Q35817099 | ||
| Visual and oculomotor selection: links, causes and implications for spatial attention. | Q36392384 | ||
| Salience, relevance, and firing: a priority map for target selection | Q36537303 | ||
| The native coordinate system of spatial attention is retinotopic | Q37012708 | ||
| Direction selectivity of neurons in the macaque lateral intraparietal area | Q37086548 | ||
| Attention and active vision | Q37216971 | ||
| Decoding reveals the contents of visual working memory in early visual areas | Q37259708 | ||
| The gender-specific face aftereffect is based in retinotopic not spatiotopic coordinates across several natural image transformations | Q37473179 | ||
| Spatially global representations in human primary visual cortex during working memory maintenance. | Q39355571 | ||
| Predictive remapping of visual features precedes saccadic eye movements | Q40200980 | ||
| Spatial processing in the monkey frontal eye field. I. Predictive visual responses | Q40881710 | ||
| The role of location indexes in spatial perception: a sketch of the FINST spatial-index model | Q41316990 | ||
| Evidence for the predictive remapping of visual attention | Q41827029 | ||
| The reference frame of the tilt aftereffect | Q43167351 | ||
| The reference frame of the motion aftereffect is retinotopic | Q43275878 | ||
| Psychophysical evidence for spatiotopic processing in area MT in a short-term memory for motion task | Q43289482 | ||
| The Activity of the Stapedius Muscle in Man During Vocalization | Q44441660 | ||
| Spatiotopic temporal integration of visual motion across saccadic eye movements. | Q44519475 | ||
| Topography of the motion aftereffect with and without eye movements. | Q46161672 | ||
| A dynamic model of how feature cues guide spatial attention | Q46166469 | ||
| The reviewing of object files: object-specific integration of information | Q46227218 | ||
| Saccade-related remapping of target representations between topographic maps: a neural network study | Q48102167 | ||
| Neural mechanisms for timing visual events are spatially selective in real-world coordinates. | Q48236248 | ||
| P433 | issue | 4 | |
| P921 | main subject | attention | Q6501338 |
| P304 | page(s) | 147-153 | |
| P577 | publication date | 2010-02-26 | |
| P1433 | published in | Trends in Cognitive Sciences | Q7838299 |
| P1476 | title | Visual stability based on remapping of attention pointers | |
| P478 | volume | 14 |
| Q48169057 | A "blanking effect" for surface features: Transsaccadic spatial-frequency discrimination is improved by postsaccadic blanking |
| Q48581156 | A neural mechanism for coordinate transformation predicts pre-saccadic remapping |
| Q36566618 | A reinvestigation of the reference frame of the tilt-adaptation aftereffect |
| Q43967132 | A retinotopic attentional trace after saccadic eye movements: evidence from event-related potentials |
| Q40831932 | A soft handoff of attention between cerebral hemispheres |
| Q50676363 | Adaptation of scanning saccades co-occurs in different coordinate systems. |
| Q39506791 | Allocation of attention across saccades |
| Q35931447 | An Attention-Sensitive Memory Trace in Macaque MT Following Saccadic Eye Movements |
| Q37037378 | An object-mediated updating account of insensitivity to transsaccadic change. |
| Q21133943 | Apparent motion from outside the visual field, retinotopic cortices may register extra-retinal positions |
| Q38631906 | Attention in Active Vision: A Perspective on Perceptual Continuity Across Saccades. |
| Q47135127 | Attention modulates perception of visual space |
| Q47341171 | Attention modulates trans-saccadic integration. |
| Q51762296 | Attention points to the future. |
| Q48595659 | Attentional load interferes with target localization across saccades. |
| Q35560112 | Attentional trade-offs maintain the tracking of moving objects across saccades |
| Q41495125 | Binocular fusion and invariant category learning due to predictive remapping during scanning of a depthful scene with eye movements |
| Q42158035 | Breaking Object Correspondence Across Saccadic Eye Movements Deteriorates Object Recognition. |
| Q30409245 | Buildup of spatial information over time and across eye-movements |
| Q35954012 | Causal Inference for Spatial Constancy across Saccades |
| Q47858872 | Chances and challenges for an active visual search perspective. |
| Q42935001 | Changing viewer perspectives reveals constraints to implicit visual statistical learning |
| Q90076529 | Characterizing and dissociating multiple time-varying modulatory computations influencing neuronal activity |
| Q47194059 | Characterizing ensemble statistics: mean size is represented across multiple frames of reference |
| Q38961409 | Circuits for presaccadic visual remapping |
| Q38663266 | Coherent alpha oscillations link current and future receptive fields during saccades |
| Q30604343 | Constructing stable spatial maps of the world |
| Q49052164 | Context dependence of receptive field remapping in superior colliculus |
| Q40011977 | Cortical Dynamics of Figure-Ground Separation in Response to 2D Pictures and 3D Scenes: How V2 Combines Border Ownership, Stereoscopic Cues, and Gestalt Grouping Rules |
| Q47273636 | Decoding trans-saccadic memory |
| Q48733859 | Differentiating between verbal and spatial encoding using eye-movement recordings |
| Q49185767 | Distractor displacements during saccades are reflected in the time-course of saccade curvature |
| Q36532623 | Division of labor in frontal eye field neurons during presaccadic remapping of visual receptive fields |
| Q36390911 | Dynamics of visual receptive fields in the macaque frontal eye field |
| Q35850695 | Electrophysiological recordings in humans reveal reduced location-specific attentional-shift activity prior to recentering saccades. |
| Q50576793 | Emotional stimuli capture spatial attention but do not modulate spatial memory. |
| Q36723850 | Eye movement sequence generation in humans: Motor or goal updating? |
| Q35162877 | Eye movements help link different views in scene-selective cortex |
| Q41729574 | Eye movements reset visual perception |
| Q90629651 | Eye movements shape visual learning |
| Q50519934 | Feature-based attention across saccades and immediate postsaccadic selection. |
| Q33650598 | Feature-binding errors after eye movements and shifts of attention |
| Q34091162 | Fine-scale plasticity of microscopic saccades |
| Q38083442 | Flexible cognitive resources: competitive content maps for attention and memory |
| Q34464855 | Forgetting what was where: the fragility of object-location binding |
| Q39451933 | Habitual versus goal-driven attention |
| Q30528055 | Higher level visual cortex represents retinotopic, not spatiotopic, object location |
| Q46440071 | Holding visual attention for 400millionyears: A model of tectum and torus longitudinalis in teleost fishes |
| Q33639534 | Integrating retinotopic features in spatiotopic coordinates |
| Q51028995 | Location and identity memory of saccade targets. |
| Q47826404 | Memory as Perception of the Past: Compressed Time inMind and Brain. |
| Q30505237 | Motion and tilt aftereffects occur largely in retinal, not in object, coordinates in the Ternus-Pikler display |
| Q51023108 | Multiple reference frames for saccadic planning in the human parietal cortex. |
| Q41239069 | Multiple visual objects are sampled sequentially |
| Q27308555 | No Evidence for Automatic Remapping of Stimulus Features or Location Found with fMRI |
| Q36127246 | Nonretinotopic exogenous attention |
| Q49506051 | Object discrepancy modulates feature prediction across eye movements. |
| Q52759541 | Object-location binding across a saccade: A retinotopic spatial congruency bias. |
| Q39178244 | Oculomotor Prediction: A Window into the Psychotic Mind |
| Q37024933 | Oculomotor Remapping of Visual Information to Foveal Retinotopic Cortex |
| Q35674594 | Onset rivalry: the initial dominance phase is independent of ongoing perceptual alternations |
| Q57481204 | Optimal Trans-saccadic integration relies on visual working memory |
| Q35138377 | Parallax-sensitive remapping of visual space in occipito-parietal alpha-band activity during whole-body motion |
| Q48595410 | Paying attention through eye movements: a computational investigation of the premotor theory of spatial attention |
| Q34115460 | Perceptual learning beyond retinotopic reference frame |
| Q49579882 | Perceptual learning while preparing saccades |
| Q36123461 | Peri-saccadic compression to two locations in a two-target choice saccade task |
| Q26768206 | Perisaccadic Updating of Visual Representations and Attentional States: Linking Behavior and Neurophysiology |
| Q34539221 | Position specificity of adaptation-related face aftereffects |
| Q60923760 | Pre-saccadic remapping relies on dynamics of spatial attention |
| Q34429773 | Pre-saccadic shifts of visual attention |
| Q39801310 | Predictive remapping of attention across eye movements |
| Q64107023 | Presaccadic attention improves or impairs performance by enhancing sensitivity to higher spatial frequencies |
| Q38844562 | Presaccadic motion integration between current and future retinotopic locations of attended objects |
| Q101049838 | Rapid spatial oculomotor updating across saccades is malleable |
| Q49231025 | Rapid updating of spatial working memory across saccades |
| Q39475899 | Remapped visual masking |
| Q42137481 | Remapping attention in multiple object tracking |
| Q47115624 | Remapping high-capacity, pre-attentive, fragile sensory memory |
| Q33861650 | Remapping of border ownership in the visual cortex. |
| Q48627746 | Remapping of the line motion illusion across eye movements |
| Q36982901 | Remapping, Spatial Stability, and Temporal Continuity: From the Pre-Saccadic to Postsaccadic Representation of Visual Space in LIP. |
| Q35749924 | Retinotopic memory is more precise than spatiotopic memory |
| Q51367474 | Retinotopy of visual masking and non-retinotopic perception during masking. |
| Q26822997 | Saccade adaptation as a model of flexible and general motor learning |
| Q55267341 | Saccade-synchronized rapid attention shifts in macaque visual cortical area MT. |
| Q52577296 | Saccades Trigger Predictive Updating of Attentional Topography in Area V4. |
| Q34786127 | Saccades and shifting receptive fields: anticipating consequences or selecting targets? |
| Q30359865 | Saccades create similar mislocalizations in visual and auditory space |
| Q36166951 | Saccadic remapping of object-selective information |
| Q33614340 | Salient distractors can induce saccade adaptation |
| Q48155213 | Selective attention within the foveola. |
| Q55425140 | Selective modulation of visual sensitivity during fixation. |
| Q37578385 | Shape selectivity and remapping in dorsal stream visual area LIP |
| Q104111186 | Sounds are remapped across saccades |
| Q50595627 | Spatial constancy of attention across eye movements is mediated by the presence of visual objects. |
| Q37767160 | Spatial maps for time and motion. |
| Q41864711 | Spatial reference frame of attention in a large outdoor environment |
| Q44072163 | Spatio-temporal templates of transient attention revealed by classification images |
| Q33795528 | Spatiotopic coding and remapping in humans |
| Q30474848 | Spatiotopic coding of BOLD signal in human visual cortex depends on spatial attention |
| Q48939481 | Spatiotopic perceptual learning mediated by retinotopic processing and attentional remapping |
| Q41237843 | Spatiotopic updating facilitates perception immediately after saccades |
| Q34303228 | Spontaneous microsaccades reflect shifts in covert attention |
| Q101121149 | Stimulus blanking reveals contrast-dependent transsaccadic feature transfer |
| Q92583142 | Target Localization after Saccades and at Fixation: Nontargets both Facilitate and Bias Responses |
| Q37346837 | Temporally flexible feedback signal to foveal cortex for peripheral object recognition |
| Q64947009 | The Limits of Predictive Remapping of Attention Across Eye Movements. |
| Q36134193 | The Role of the Oculomotor System in Updating Visual-Spatial Working Memory across Saccades |
| Q44975883 | The background is remapped across saccades |
| Q28685555 | The efference cascade, consciousness, and its self: naturalizing the first person pivot of action control |
| Q85048785 | The missing link for attention pointers: comment on Cavanagh et al |
| Q28596441 | The phase of ongoing EEG oscillations predicts the amplitude of peri-saccadic mislocalization |
| Q47242846 | The reference frame for encoding and retention of motion depends on stimulus set size |
| Q92891905 | The resonant brain: How attentive conscious seeing regulates action sequences that interact with attentive cognitive learning, recognition, and prediction |
| Q50697507 | The role of motor response in implicit encoding: evidence from intertrial priming in pop-out search. |
| Q52657974 | The spatial profile of mask-induced compression for perception and action. |
| Q50502293 | The spatiotopic representation of visual objects across time. |
| Q51093606 | The temporal evolution of coarse location coding of objects: evidence for feedback. |
| Q30459911 | Trans-saccadic priming in hemianopia: sighted-field sensitivity is boosted by a blind-field prime |
| Q36600693 | Transient spatiotopic integration across saccadic eye movements mediates visual stability |
| Q92310545 | Transsaccadic integration benefits are not limited to the saccade target |
| Q64892397 | Transsaccadic integration is dominated by early, independent noise. |
| Q38266189 | Transsaccadic processing: stability, integration, and the potential role of remapping |
| Q27334910 | Two distinct types of remapping in primate cortical area V4. |
| Q41658618 | Unmasking saccadic uncrowding. |
| Q41211354 | Use of NeuroEyeCoach™ to Improve Eye Movement Efficacy in Patients with Homonymous Visual Field Loss. |
| Q82489923 | Visual Suppression in the Superior Colliculus Around the Time of Microsaccades |
| Q37829534 | Visual attention and stability |
| Q41852737 | Visual attention is available at a task-relevant location rapidly after a saccade. |
| Q37844208 | Visual cognition |
| Q35219052 | Visual perception and saccadic eye movements |
| Q58761946 | Visual percepts modify iconic memory in humans |
| Q42585588 | Visual stability |
| Q41583650 | Visual stability-what is the problem? |
| Q88877158 | Visuospatial Working Memory as a Fundamental Component of the Eye Movement System |
| Q41771081 | Voluntary attention modulates motion-induced mislocalization |
| Q39034170 | When circles become triangular: how transsaccadic predictions shape the perception of shape |
| Q40803057 | Where's Waldo? How perceptual, cognitive, and emotional brain processes cooperate during learning to categorize and find desired objects in a cluttered scene |
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