The DOI matches its Crossref record.
The Psychophysics Toolbox
Abstract
The Psychophysics Toolbox is a software package that supports visual psychophysics. Its routines provide an interface between a high-level interpreted language (MATLAB on the Macintosh) and the video display hardware. A set of example programs is included with the Toolbox distribution.
Overview
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Integrity signals
Registry
Cites
Statistics
Verification
Claims the paper makes
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Self-check
Percentages, sums and reported differences re-computed from the paper’s own numbers.
The self-check needs the paper’s full text.
Citations
Cited by
Items 101–200 of 430
Runyan, C. A., Schummers, J., Van Wart, A., Kuhlman, S. J., Wilson, N. R., Huang, Z. J., & Sur, M. (2010) · Neuron · doi:10.1016/j.neuron.2010.08.006 · Cited by 244
A spike-timing mechanism for action selection
von Reyn, C. R., Breads, P., Peek, M. Y., Zheng, G. Z., Williamson, W. R., Yee, A. L., Leonardo, A., & Card, G. M. (2014) · Nature Neuroscience · doi:10.1038/nn.3741 · Cited by 254
Neurons in anterior cingulate cortex multiplex information about reward and action
Hayden, B. Y., & Platt, M. L. (2010) · The Journal of Neuroscience · doi:10.1523/jneurosci.4874-09.2010 · Cited by 236
Brewer, R., Biotti, F., Catmur, C., Press, C., Happé, F., Cook, R., & Bird, G. (2016) · Autism Research · doi:10.1002/aur.1508 · Cited by 233
A Distinct Role of the Temporal-Parietal Junction in Predicting Socially Guided Decisions
Carter, R. M., Bowling, D. L., Reeck, C., & Huettel, S. A. (2012) · Science · doi:10.1126/science.1219681 · Cited by 238
Microstimulation of visual cortex affects the speed of perceptual decisions
Ditterich, J., Mazurek, M. E., & Shadlen, M. N. (2003) · Nature Neuroscience · doi:10.1038/nn1094 · Cited by 234
Milne, E. (2011) · Frontiers in Psychology · doi:10.3389/fpsyg.2011.00051 · Cited by 217
Episodic reinstatement in the medial temporal lobe
Staresina, B. P., Henson, R. N. A., Kriegeskorte, N., & Alink, A. (2012) · The Journal of Neuroscience · doi:10.1523/jneurosci.4156-12.2012 · Cited by 228
A neural mechanism of speed-accuracy tradeoff in macaque area LIP
Hanks, T., Kiani, R., & Shadlen, M. N. (2014) · eLife · doi:10.7554/elife.02260 · Cited by 222
Separate Neural Mechanisms Underlie Choices and Strategic Preferences in Risky Decision Making
Venkatraman, V., Payne, J. W., Bettman, J. R., Luce, M. F., & Huettel, S. A. (2009) · Neuron · doi:10.1016/j.neuron.2009.04.007 · Cited by 222
Konen, C. S., & Kastner, S. (2008) · The Journal of Neuroscience · doi:10.1523/jneurosci.1930-08.2008 · Cited by 221
Genetic origins of social networks in rhesus macaques
Brent, L. J. N., Heilbronner, S. R., Horvath, J. E., Gonzalez-Martinez, J., Ruiz-Lambides, A., Robinson, A. G., Skene, J. H. P., & Platt, M. L. (2013) · Scientific Reports · doi:10.1038/srep01042 · Cited by 220
Mixed selectivity morphs population codes in prefrontal cortex
Parthasarathy, A., Herikstad, R., Bong, J. H., Medina, F. S., Libedinsky, C., & Yen, S.-C. (2017) · Nature Neuroscience · doi:10.1038/s41593-017-0003-2 · Cited by 219
Selective and invariant neural responses to spoken and written narratives
Regev, M., Honey, C. J., Simony, E., & Hasson, U. (2013) · The Journal of Neuroscience · doi:10.1523/jneurosci.1580-13.2013 · Cited by 215
Hotson, G., McMullen, D. P., Fifer, M. S., Johannes, M. S., Katyal, K. D., Para, M. P., Armiger, R., Anderson, W. S., Thakor, N. V., Wester, B. A., et al. (2016) · Journal of Neural Engineering · doi:10.1088/1741-2560/13/2/026017 · Cited by 201
Locomotion Enhances Neural Encoding of Visual Stimuli in Mouse V1
Dadarlat, M. C., & Stryker, M. P. (2017) · The Journal of Neuroscience · doi:10.1523/jneurosci.2728-16.2017 · Cited by 205
An acetylcholine-activated microcircuit drives temporal dynamics of cortical activity
Chen, N., Sugihara, H., & Sur, M. (2015) · Nature Neuroscience · doi:10.1038/nn.4002 · Cited by 210
Analysis of face gaze in autism using “bubbles”
Spezio, M. L., Adolphs, R., Hurley, R. S. E., & Piven, J. (2007) · Neuropsychologia · doi:10.1016/j.neuropsychologia.2006.04.027 · Cited by 209
Critical Period Plasticity Matches Binocular Orientation Preference in the Visual Cortex
Wang, B.-S., Sarnaik, R., & Cang, J. (2010) · Neuron · doi:10.1016/j.neuron.2010.01.002 · Cited by 209
Making the ineffable explicit: estimating the information employed for face classifications
Mangini, M. C., & Biederman, I. (2004) · Cognitive Science · doi:10.1207/s15516709cog2802_4 · Cited by 208
A neural measure of precision in visual working memory
Ester, E. F., Anderson, D. E., Serences, J. T., & Awh, E. (2013) · Journal of Cognitive Neuroscience · doi:10.1162/jocn_a_00357 · Cited by 207
Recruitment of the default mode network during a demanding act of executive control
Crittenden, B. M., Mitchell, D. J., & Duncan, J. (2015) · eLife · doi:10.7554/elife.06481 · Cited by 176
Magnetic Stimulation of Extrastriate Body Area Impairs Visual Processing of Nonfacial Body Parts
Urgesi, C., Berlucchi, G., & Aglioti, S. M. (2004) · Current Biology · doi:10.1016/j.cub.2004.11.031 · Cited by 204
Bifurcation in brain dynamics reveals a signature of conscious processing independent of report
Sergent, C., Corazzol, M., Labouret, G., Stockart, F., Wexler, M., King, J.-R., Meyniel, F., & Pressnitzer, D. (2021) · Nature Communications · doi:10.1038/s41467-021-21393-z · Cited by 200
Cueing attention after the stimulus is gone can retrospectively trigger conscious perception
Sergent, C., Wyart, V., Babo-Rebelo, M., Cohen, L., Naccache, L., & Tallon-Baudry, C. (2013) · Current Biology · doi:10.1016/j.cub.2012.11.047 · Cited by 195
Rapid Encoding of New Memories by Individual Neurons in the Human Brain
Ison, M. J., Quian Quiroga, R., & Fried, I. (2015) · Neuron · doi:10.1016/j.neuron.2015.06.016 · Cited by 184
Causal evidence for frontal cortex organization for perceptual decision making
Rahnev, D., Nee, D. E., Riddle, J., Larson, A. S., & D’Esposito, M. (2016) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1522551113 · Cited by 200
Layer-specific fMRI reflects different neuronal computations at different depths in human V1
Olman, C. A., Harel, N., Feinberg, D. A., He, S., Zhang, P., Ugurbil, K., & Yacoub, E. (2012) · PLoS ONE · doi:10.1371/journal.pone.0032536 · Cited by 194
Shape Perception Simultaneously Up- and Downregulates Neural Activity in the Primary Visual Cortex
Kok, P., & de Lange, F. P. (2014) · Current Biology · doi:10.1016/j.cub.2014.05.042 · Cited by 163
Maps of visual space in human occipital cortex are retinotopic, not spatiotopic
Gardner, J. L., Merriam, E. P., Movshon, J. A., & Heeger, D. J. (2008) · The Journal of Neuroscience · doi:10.1523/jneurosci.5476-07.2008 · Cited by 192
Cognitive and neural contributors to emotion regulation in aging
Winecoff, A., LaBar, K. S., Madden, D. J., Cabeza, R., & Huettel, S. A. (2011) · Social Cognitive and Affective Neuroscience · doi:10.1093/scan/nsq030 · Cited by 191
Reinstatement of associative memories in early visual cortex is signaled by the hippocampus
Bosch, S. E., Jehee, J. F. M., Fernández, G., & Doeller, C. F. (2014) · The Journal of Neuroscience · doi:10.1523/jneurosci.0805-14.2014 · Cited by 157
Snow, J. C., Allen, H. A., Rafal, R. D., & Humphreys, G. W. (2009) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0810086106 · Cited by 188
Oxytocin enhances inter-brain synchrony during social coordination in male adults
Mu, Y., Guo, C., & Han, S. (2016) · Social Cognitive and Affective Neuroscience · doi:10.1093/scan/nsw106 · Cited by 177
The neural dynamics of hierarchical Bayesian causal inference in multisensory perception
Rohe, T., Ehlis, A.-C., & Noppeney, U. (2019) · Nature Communications · doi:10.1038/s41467-019-09664-2 · Cited by 187
Venkatraman, V., Rosati, A. G., Taren, A. A., & Huettel, S. A. (2009) · The Journal of Neuroscience · doi:10.1523/jneurosci.2708-09.2009 · Cited by 186
Optogenetic Localization and Genetic Perturbation of Saccade-Generating Neurons in Zebrafish
Schoonheim, P. J., Arrenberg, A. B., Del Bene, F., & Baier, H. (2010) · The Journal of Neuroscience · doi:10.1523/jneurosci.5193-09.2010 · Cited by 185
Weakened center-surround interactions in visual motion processing in schizophrenia
Tadin, D., Kim, J., Doop, M. L., Gibson, C., Lappin, J. S., Blake, R., & Park, S. (2006) · The Journal of Neuroscience · doi:10.1523/jneurosci.2592-06.2006 · Cited by 182
Consolidating the Effects of Waking and Sleep on Motor-Sequence Learning
Brawn, T. P., Fenn, K. M., Nusbaum, H. C., & Margoliash, D. (2010) · The Journal of Neuroscience · doi:10.1523/jneurosci.3295-10.2010 · Cited by 181
Schreiner, T., Petzka, M., Staudigl, T., & Staresina, B. P. (2021) · Nature Communications · doi:10.1038/s41467-021-23520-2 · Cited by 161
Brain–phenotype models fail for individuals who defy sample stereotypes
Greene, A. S., Shen, X., Noble, S., Horien, C., Hahn, C. A., Arora, J., Tokoglu, F., Spann, M. N., Carrión, C. I., Barron, D. S., et al. (2022) · Nature · doi:10.1038/s41586-022-05118-w · Cited by 167
Expectations accelerate entry of visual stimuli into awareness
Pinto, Y., van Gaal, S., de Lange, F. P., Lamme, V. A. F., & Seth, A. K. (2015) · Journal of Vision · doi:10.1167/15.8.13 · Cited by 159
Motion psychophysics: 1985-2010.
Burr, D., & Thompson, P. (2011) · Vision Research · doi:10.1016/j.visres.2011.02.008 · Cited by 178
Multisensory integration of looming signals by rhesus monkeys
Maier, J. X., Neuhoff, J. G., Logothetis, N. K., & Ghazanfar, A. A. (2004) · Neuron · doi:10.1016/j.neuron.2004.06.027 · Cited by 172
Memory failure predicted by attention lapsing and media multitasking
Madore, K. P., Khazenzon, A. M., Backes, C. W., Jiang, J., Uncapher, M. R., Norcia, A. M., & Wagner, A. D. (2020) · Nature · doi:10.1038/s41586-020-2870-z · Cited by 184
Smaller Primary Visual Cortex Is Associated with Stronger, but Less Precise Mental Imagery
Bergmann, J., Genç, E., Kohler, A., Singer, W., & Pearson, J. (2016) · Cerebral Cortex · doi:10.1093/cercor/bhv186 · Cited by 177
Linde-Domingo, J., Treder, M. S., Kerrén, C., & Wimber, M. (2019) · Nature Communications · doi:10.1038/s41467-018-08080-2 · Cited by 152
Visual sensitivity underlying changes in visual consciousness
Alais, D., Cass, J., O'Shea, R. P., & Blake, R. (2010) · Current Biology · doi:10.1016/j.cub.2010.06.015 · Cited by 166
Theta phase synchronization is the glue that binds human associative memory
Clouter, A., Shapiro, K. L., & Hanslmayr, S. (2017) · Current Biology · doi:10.1016/j.cub.2017.09.001 · Cited by 170
Changing value through cued approach: an automatic mechanism of behavior change
Schonberg, T., Bakkour, A., Hover, A. M., Mumford, J. A., Nagar, L., Perez, J., & Poldrack, R. A. (2014) · Nature Neuroscience · doi:10.1038/nn.3673 · Cited by 161
The signal processing architecture underlying subjective reports of sensory awareness
Maniscalco, B., & Lau, H. (2016) · Neuroscience of Consciousness · doi:10.1093/nc/niw002 · Cited by 133
Representation of accumulating evidence for a decision in two parietal areas
de Lafuente, V., Jazayeri, M., & Shadlen, M. N. (2015) · The Journal of Neuroscience · doi:10.1523/jneurosci.2451-14.2015 · Cited by 162
“Experimental control and stimulus presentation were achieved with either REX (Hays et al., 1982) in combination with the Psychophysics toolbox (Brainard, 1997) or with EXPO (developed by Peter Lennie, currently maintained by Rod Dotson, Center for Neural Science at New York University, New York,…”
MethodFusion of visual cues is not mandatory in children
Nardini, M., Bedford, R., & Mareschal, D. (2010) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1001699107 · Cited by 161
Economic principles motivating social attention in humans
Hayden, B. Y., Parikh, P. C., Deaner, R. O., & Platt, M. L. (2007) · Proceedings of the Royal Society B: Biological Sciences · doi:10.1098/rspb.2007.0368 · Cited by 160
Neural mechanisms of social decision-making in the primate amygdala
Chang, S. W. C., Fagan, N. A., Toda, K., Utevsky, A. V., Pearson, J. M., & Platt, M. L. (2015) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1514761112 · Cited by 157
Exogenous attention and color perception: Performance and appearance of saturation and hue
Fuller, S., & Carrasco, M. (2006) · Vision Research · doi:10.1016/j.visres.2006.07.014 · Cited by 157
Relating inter-individual differences in metacognitive performance on different perceptual tasks
Song, C., Kanai, R., Fleming, S. M., Weil, R. S., Schwarzkopf, D. S., & Rees, G. (2011) · Consciousness and Cognition · doi:10.1016/j.concog.2010.12.011 · Cited by 158
Multivoxel neurofeedback selectively modulates confidence without changing perceptual performance
Cortese, A., Amano, K., Koizumi, A., Kawato, M., & Lau, H. (2016) · Nature Communications · doi:10.1038/ncomms13669 · Cited by 157
Direct injection of noise to the visual cortex decreases accuracy but increases decision confidence
Rahnev, D. A., Maniscalco, B., Luber, B., Lau, H., & Lisanby, S. H. (2012) · Journal of Neurophysiology · doi:10.1152/jn.00985.2011 · Cited by 156
Feature Integration Drives Probabilistic Behavior in the Drosophila Escape Response
von Reyn, C. R., Nern, A., Williamson, W. R., Breads, P., Wu, M., Namiki, S., & Card, G. M. (2017) · Neuron · doi:10.1016/j.neuron.2017.05.036 · Cited by 156
Neural mediators of changes of mind about perceptual decisions
Fleming, S. M., van der Putten, E. J., & Daw, N. D. (2018) · Nature Neuroscience · doi:10.1038/s41593-018-0104-6 · Cited by 155
Neural Basis for Looming Size and Velocity Encoding in the Drosophila Giant Fiber Escape Pathway
Ache, J. M., Polsky, J., Alghailani, S., Parekh, R., Breads, P., Peek, M. Y., Bock, D. D., von Reyn, C. R., & Card, G. M. (2019) · Current Biology · doi:10.1016/j.cub.2019.01.079 · Cited by 153
Comparing Bayesian and non-Bayesian accounts of human confidence reports
Adler, W. T., & Ma, W. J. (2018) · PLoS Computational Biology · doi:10.1371/journal.pcbi.1006572 · Cited by 118
Milne, E., Scope, A., Pascalis, O., Buckley, D., & Makeig, S. (2009) · Biological Psychiatry · doi:10.1016/j.biopsych.2008.07.017 · Cited by 148
Kozai, T. D. Y., Li, X., Bodily, L. M., Caparosa, E. M., Zenonos, G. A., Carlisle, D. L., Friedlander, R. M., & Cui, X. T. (2014) · Biomaterials · doi:10.1016/j.biomaterials.2014.08.006 · Cited by 136
Representation of retrieval confidence by single neurons in the human medial temporal lobe
Rutishauser, U., Ye, S., Koroma, M., Tudusciuc, O., Ross, I. B., Chung, J. M., & Mamelak, A. N. (2015) · Nature Neuroscience · doi:10.1038/nn.4041 · Cited by 147
Breakdown of the brain’s functional network modularity with awareness
Godwin, D., Barry, R. L., & Marois, R. (2015) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1414466112 · Cited by 145
Psilocybin links binocular rivalry switch rate to attention and subjective arousal levels in humans
Carter, O. L., Hasler, F., Pettigrew, J. D., Wallis, G. M., Liu, G. B., & Vollenweider, F. X. (2007) · Psychopharmacology · doi:10.1007/s00213-007-0930-9 · Cited by 146
Krishnan, K., Wang, B.-S., Lu, J., Wang, L., Maffei, A., Cang, J., & Huang, Z. J. (2015) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1506499112 · Cited by 146
Crittenden, B. M., Mitchell, D. J., & Duncan, J. (2016) · The Journal of Neuroscience · doi:10.1523/jneurosci.4590-15.2016 · Cited by 143
Visual Imagery and Perception Share Neural Representations in the Alpha Frequency Band
Xie, S., Kaiser, D., & Cichy, R. M. (2020) · Current Biology · doi:10.1016/j.cub.2020.04.074 · Cited by 139
Kay, L., Keogh, R., Andrillon, T., & Pearson, J. (2022) · eLife · doi:10.7554/elife.72484 · Cited by 142
Error Rates in Users of Automatic Face Recognition Software
White, D., Dunn, J. D., Schmid, A. C., & Kemp, R. I. (2015) · PLOS ONE · doi:10.1371/journal.pone.0139827 · Cited by 141
Distinct transfer effects of training different facets of working memory capacity.
von Bastian, C. C., & Oberauer, K. (2013) · Journal of Memory and Language · doi:10.1016/j.jml.2013.02.002 · Cited by 139
Plug-and-play control of a brain–computer interface through neural map stabilization
Silversmith, D. B., Abiri, R., Hardy, N. F., Natraj, N., Tu-Chan, A., Chang, E. F., & Ganguly, K. (2021) · Nature Biotechnology · doi:10.1038/s41587-020-0662-5 · Cited by 126
Confidence Is the Bridge between Multi-stage Decisions
van den Berg, R., Zylberberg, A., Kiani, R., Shadlen, M. N., & Wolpert, D. M. (2016) · Current Biology · doi:10.1016/j.cub.2016.10.021 · Cited by 125
Confidence controls perceptual evidence accumulation
Balsdon, T., Wyart, V., & Mamassian, P. (2020) · Nature Communications · doi:10.1038/s41467-020-15561-w · Cited by 137
A predictive coding account of bistable perception - a model-based fMRI study
Weilnhammer, V., Stuke, H., Hesselmann, G., Sterzer, P., & Schmack, K. (2017) · PLOS Computational Biology · doi:10.1371/journal.pcbi.1005536 · Cited by 120
A Demonstration of the Transition from Ready-to-Hand to Unready-to-Hand
Dotov, D. G., Nie, L., & Chemero, A. (2010) · PLoS ONE · doi:10.1371/journal.pone.0009433 · Cited by 135
Working memory and fear conditioning
Carter, R. M., Hofstötter, C., Tsuchiya, N., & Koch, C. (2003) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0334049100 · Cited by 134
Attentional bias for nondrug reward is magnified in addiction.
Anderson, B. A., Faulkner, M. L., Rilee, J. J., Yantis, S., & Marvel, C. L. (2013) · Experimental and Clinical Psychopharmacology · doi:10.1037/a0034575 · Cited by 131
The manifold structure of limb coordination in walking Drosophila
DeAngelis, B. D., Zavatone-Veth, J. A., & Clark, D. A. (2019) · eLife · doi:10.7554/elife.46409 · Cited by 104
“Visual stimuli (Figure 8) Visual stimuli were designed using Matlab and its associated Psychophysics Toolbox (Brainard, 1997; Kleiner et al., 2007; Pelli, 1997).”
MethodBehavioral, Modeling, and Electrophysiological Evidence for Supramodality in Human Metacognition
Faivre, N., Filevich, E., Solovey, G., Kühn, S., & Blanke, O. (2018) · The Journal of Neuroscience · doi:10.1523/jneurosci.0322-17.2017 · Cited by 129
Maniscalco, B., Peters, M. A. K., & Lau, H. (2016) · Attention, Perception, & Psychophysics · doi:10.3758/s13414-016-1059-x · Cited by 129
Multisensory Integration in Complete Unawareness: Evidence From Audiovisual Congruency Priming
Faivre, N., Mudrik, L., Schwartz, N., & Koch, C. (2014) · Psychological Science · doi:10.1177/0956797614547916 · Cited by 127
Look at this: the neural correlates of initiating and responding to bids for joint attention
Redcay, E., Kleiner, M., & Saxe, R. (2012) · Frontiers in Human Neuroscience · doi:10.3389/fnhum.2012.00169 · Cited by 124
Dodell-Feder, D., Tully, L. M., Lincoln, S. H., & Hooker, C. I. (2014) · NeuroImage: Clinical · doi:10.1016/j.nicl.2013.11.006 · Cited by 119
Generalization of value in reinforcement learning by humans
Wimmer, G. E., Daw, N. D., & Shohamy, D. (2012) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.2012.08017.x · Cited by 111
Sensory experience during locomotion promotes recovery of function in adult visual cortex
Kaneko, M., & Stryker, M. P. (2014) · eLife · doi:10.7554/elife.02798 · Cited by 126
Central tendency effects in time interval reproduction in autism
Karaminis, T., Cicchini, G. M., Neil, L., Cappagli, G., Aagten-Murphy, D., Burr, D., & Pellicano, E. (2016) · Scientific Reports · doi:10.1038/srep28570 · Cited by 112
Vicarious reinforcement in rhesus macaques (Macaca Mulatta)
Chang, S. W. C., Winecoff, A. A., & Platt, M. L. (2011) · Frontiers in Neuroscience · doi:10.3389/fnins.2011.00027 · Cited by 124
“Stimuli were controlled by a computer running Matlab using PsychToolbox (Brainard, 1997; Pelli, 1997).”
MethodMethodological recommendations for a heartbeat detection-based measure of interoceptive sensitivity
Kleckner, I. R., Wormwood, J. B., Simmons, W. K., Barrett, L. F., & Quigley, K. S. (2015) · Psychophysiology · doi:10.1111/psyp.12503 · Cited by 124
Global motion perception deficits in autism are reflected as early as primary visual cortex
Robertson, C. E., Thomas, C., Kravitz, D. J., Wallace, G. L., Baron-Cohen, S., Martin, A., & Baker, C. I. (2014) · Brain · doi:10.1093/brain/awu189 · Cited by 122
Rapidly learned stimulus expectations alter perception of motion
Chalk, M., Seitz, A. R., & Series, P. (2010) · Journal of Vision · doi:10.1167/10.8.2 · Cited by 122
Gershman, S. J., Pesaran, B., & Daw, N. D. (2009) · The Journal of Neuroscience · doi:10.1523/jneurosci.2469-09.2009 · Cited by 118
Humans incorporate attention-dependent uncertainty into perceptual decisions and confidence
Denison, R. N., Adler, W. T., Carrasco, M., & Ma, W. J. (2018) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1717720115 · Cited by 122
Motion Silences Awareness of Visual Change
Suchow, J. W., & Alvarez, G. A. (2011) · Current Biology · doi:10.1016/j.cub.2010.12.019 · Cited by 121
Distinct cortical codes and temporal dynamics for conscious and unconscious percepts
Salti, M., Monto, S., Charles, L., King, J.-R., Parkkonen, L., & Dehaene, S. (2015) · eLife · doi:10.7554/elife.05652 · Cited by 121
Prior object-knowledge sharpens properties of early visual feature-detectors
Teufel, C., Dakin, S. C., & Fletcher, P. C. (2018) · Scientific Reports · doi:10.1038/s41598-018-28845-5 · Cited by 119
Lawrence, S. J., Norris, D. G., & de Lange, F. P. (2019) · eLife · doi:10.7554/elife.44422 · Cited by 95
Metadata
- Authors
- Brainard, D. H.
- Venue
- Spatial Vision
- Publisher
- Walter de Gruyter GmbH
- Published
- 1997
- Volume
- 10
- Issue
- 4
- Pages
- 433-436
- ISSN
- 0169-1015 (ISSN-L)
- 1568-5683
- OpenAlex
- W4294214781
- Cited by
- 19,702
- References
- 0
- FWCI
- 16.98
- Type
- journal article
- Language
- en
- Open access
- closed
About these checks
Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.
Statistics and arithmetic are recomputed, not judged.
Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.
What counts as a claim ›How we measure confidence ›How we check this ›
Are you an author, or do you see a problem with this page? Request a review
Data sources
Bibliographic data: Semantic Scholar, OpenAlex, Crossref.
Contains information from the Semantic Scholar Academic Graph Datasets, made available under the ODC Attribution License (ODC-BY 1.0).
Semantic Scholar’s data is described in: Kinney, R., et al. (2023). The Semantic Scholar Open Data Platform. arXiv:2301.10140.