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Borders of Multiple Visual Areas in Humans Revealed by Functional Magnetic Resonance Imaging
Abstract
The borders of human visual areas V1, V2, VP, V3, and V4 were precisely and noninvasively determined. Functional magnetic resonance images were recorded during phase-encoded retinal stimulation. This volume data set was then sampled with a cortical surface reconstruction, making it possible to calculate the local visual field sign (mirror image versus non-mirror image representation). This method automatically and objectively outlines area borders because adjacent areas often have the opposite field sign. Cortical magnification factor curves for striate and extrastriate cortical areas were determined, which showed that human visual areas have a greater emphasis on the center-of-gaze than their counterparts in monkeys. Retinotopically organized visual areas in humans extend anteriorly to overlap several areas previously shown to be activated by written words.
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Citations
Cites
Distributed hierarchical processing in the primate cerebral cortex
Felleman, D. J., & Van Essen, D. C. (1991) · Cerebral Cortex · doi:10.1093/cercor/1.1.1 · Cited by 7,783
Functional mapping of the human visual cortex by magnetic resonance imaging
Belliveau, J. W., Kennedy, D. N., McKinstry, R. C., Buchbinder, B. R., Weisskoff, R. M., Cohen, M. S., Vevea, J. M., Brady, T. J., & Rosen, B. R. (1991) · Science · doi:10.1126/science.1948051 · Cited by 1,883
Self-citationWord recognition in the human inferior temporal lobe
Nobre, A. C., Allison, T., & McCarthy, G. (1994) · Nature · doi:10.1038/372260a0 · Cited by 789
Cited by
Cortical Surface-Based Analysis
Dale, A. M., Fischl, B., & Sereno, M. I. (1999) · NeuroImage · doi:10.1006/nimg.1998.0395 · Cited by 10,910
Self-citationThe organization of the human cerebral cortex estimated by intrinsic functional connectivity
Thomas Yeo, B. T., Krienen, F. M., Sepulcre, J., Sabuncu, M. R., Lashkari, D., Hollinshead, M., Roffman, J. L., Smoller, J. W., Zöllei, L., Polimeni, J. R., et al. (2011) · Journal of Neurophysiology · doi:10.1152/jn.00338.2011 · Cited by 9,182
Fischl, B. (2012) · NeuroImage · doi:10.1016/j.neuroimage.2012.01.021 · Cited by 9,526
The organization of the human cerebellum estimated by intrinsic functional connectivity
Buckner, R. L., Krienen, F. M., Castellanos, A., Diaz, J. C., & Yeo, B. T. T. (2011) · Journal of Neurophysiology · doi:10.1152/jn.00339.2011 · Cited by 7,304
Cortical Surface-Based Analysis
Fischl, B., Sereno, M. I., & Dale, A. M. (1999) · NeuroImage · doi:10.1006/nimg.1998.0396 · Cited by 6,147
Self-citationLocal-global parcellation of the human cerebral cortex from intrinsic functional connectivity MRI
Schaefer, A., Kong, R., Gordon, E. M., Laumann, T. O., Zuo, X.-N., Holmes, A. J., Eickhoff, S. B., & Yeo, B. T. T. (2018) · Cerebral Cortex · doi:10.1093/cercor/bhx179 · Cited by 3,657
Mechanisms of visual attention in the human cortex
Ungerleider, S. K. A. L. G. (2000) · Annual Review of Neuroscience · doi:10.1146/annurev.neuro.23.1.315 · Cited by 2,159
Kosslyn, S. M., Ganis, G., & Thompson, W. L. (2001) · Nature Reviews Neuroscience · doi:10.1038/35090055 · Cited by 1,894
Dynamic Statistical Parametric Mapping
Dale, A. M., Liu, A. K., Fischl, B. R., Buckner, R. L., Belliveau, J. W., Lewine, J. D., & Halgren, E. (2000) · Neuron · doi:10.1016/s0896-6273(00)81138-1 · Cited by 1,787
Self-citationThe neural mechanisms of top-down attentional control
Hopfinger, J. B., Buonocore, M. H., & Mangun, G. R. (2000) · Nature Neuroscience · doi:10.1038/72999 · Cited by 1,876
Decoding the visual and subjective contents of the human brain
Kamitani, Y., & Tong, F. (2005) · Nature Neuroscience · doi:10.1038/nn1444 · Cited by 1,829
Human Brain Language Areas Identified by Functional Magnetic Resonance Imaging
Binder, J. R., Frost, J. A., Hammeke, T. A., Cox, R. W., Rao, S. M., & Prieto, T. (1997) · The Journal of Neuroscience · doi:10.1523/jneurosci.17-01-00353.1997 · Cited by 1,424
Visual field maps in human cortex.
Wandell, B. A., Dumoulin, S. O., & Brewer, A. A. (2007) · Neuron · doi:10.1016/j.neuron.2007.10.012 · Cited by 1,231
Overlapping mechanisms of attention and spatial working memory
Awh, E., & Jonides, J. (2001) · Trends in Cognitive Sciences · doi:10.1016/s1364-6613(00)01593-x · Cited by 1,229
Hillyard, S. A., Vogel, E. K., & Luck, S. J. (1998) · Philosophical Transactions of the Royal Society of London. Series B: Biological Sciences · doi:10.1098/rstb.1998.0281 · Cited by 1,201
The Human Connectome Project's neuroimaging approach
Glasser, M. F., Smith, S. M., Marcus, D. S., Andersson, J. L. R., Auerbach, E. J., Behrens, T. E. J., Coalson, T. S., Harms, M. P., Jenkinson, M., Moeller, S., et al. (2016) · Nature Neuroscience · doi:10.1038/nn.4361 · Cited by 1,090
The structural basis of inter-individual differences in human behaviour and cognition
Kanai, R., & Rees, G. (2011) · Nature reviews. Neuroscience · doi:10.1038/nrn3000 · Cited by 1,055
Reconstructing Visual Experiences from Brain Activity Evoked by Natural Movies
Nishimoto, S., Vu, A. T., Naselaris, T., Benjamini, Y., Yu, B., & Gallant, J. L. (2011) · Current Biology · doi:10.1016/j.cub.2011.08.031 · Cited by 933
Allison, T. (1999) · Cerebral Cortex · doi:10.1093/cercor/9.5.415 · Cited by 882
Topographic mapping of a hierarchy of temporal receptive windows using a narrated story
Lerner, Y., Honey, C. J., Silbert, L. J., & Hasson, U. (2011) · The Journal of Neuroscience · doi:10.1523/jneurosci.3684-10.2011 · Cited by 834
Smoothing and cluster thresholding for cortical surface-based group analysis of fMRI data
Hagler, D. J., Saygin, A. P., & Sereno, M. I. (2006) · NeuroImage · doi:10.1016/j.neuroimage.2006.07.036 · Cited by 752
Self-citationLess Is More: Expectation Sharpens Representations in the Primary Visual Cortex
Kok, P., Jehee, J. F. M., & de Lange, F. P. (2012) · Neuron · doi:10.1016/j.neuron.2012.04.034 · Cited by 798
Feature binding, attention and object perception
Treisman, A. (1998) · Philosophical Transactions of the Royal Society of London. Series B: Biological Sciences · doi:10.1098/rstb.1998.0284 · Cited by 754
A physiological correlate of the 'spotlight' of visual attention
Brefczynski, J. A., & DeYoe, E. A. (1999) · Nature Neuroscience · doi:10.1038/7280 · Cited by 723
Mapping of Contralateral Space in Retinotopic Coordinates by a Parietal Cortical Area in Humans
Sereno, M. I., Pitzalis, S., & Martinez, A. (2001) · Science · doi:10.1126/science.1063695 · Cited by 682
Self-citationComparative mapping of higher visual areas in monkeys and humans
Orban, G. A., Van Essen, D., & Vanduffel, W. (2004) · Trends in Cognitive Sciences · doi:10.1016/j.tics.2004.05.009 · Cited by 639
Visuo-haptic object-related activation in the ventral visual pathway
Amedi, A., Malach, R., Hendler, T., Peled, S., & Zohary, E. (2001) · Nature Neuroscience · doi:10.1038/85201 · Cited by 630
Eccentricity bias as an organizing principle for human high-order object areas
Hasson, U., Levy, I., Behrmann, M., Hendler, T., & Malach, R. (2002) · Neuron · doi:10.1016/s0896-6273(02)00662-1 · Cited by 578
Miyawaki, Y., Uchida, H., Yamashita, O., Sato, M.-A., Morito, Y., Tanabe, H. C., Sadato, N., & Kamitani, Y. (2008) · Neuron · doi:10.1016/j.neuron.2008.11.004 · Cited by 543
Neural decoding of visual imagery during sleep
Horikawa, T., Tamaki, M., Miyawaki, Y., & Kamitani, Y. (2013) · Science · doi:10.1126/science.1234330 · Cited by 498
When is early visual cortex activated during visual mental imagery?
Kosslyn, S. M., & Thompson, W. L. (2003) · Psychological Bulletin · doi:10.1037/0033-2909.129.5.723 · Cited by 515
Shape perception reduces activity in human primary visual cortex
Murray, S. O., Kersten, D., Olshausen, B. A., Schrater, P., & Woods, D. L. (2002) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.192579399 · Cited by 496
The topography of high-order human object areas
Malach, R., Levy, I., & Hasson, U. (2002) · Trends in Cognitive Sciences · doi:10.1016/s1364-6613(02)01870-3 · Cited by 459
Braun, A. R., Balkin, T. J., Wesensten, N. J., Gwadry, F., Carson, R. E., Varga, M., Baldwin, P., Belenky, G., & Herscovitch, P. (1998) · Science · doi:10.1126/science.279.5347.91 · Cited by 474
Attention reverses the effect of prediction in silencing sensory signals
Kok, P., Rahnev, D., Jehee, J. F. M., Lau, H. C., & de Lange, F. P. (2012) · Cerebral Cortex · doi:10.1093/cercor/bhr310 · Cited by 430
Visual mental imagery induces retinotopically organized activation of early visual areas
Slotnick, S. D., Thompson, W. L., & Kosslyn, S. M. (2005) · Cerebral Cortex · doi:10.1093/cercor/bhi035 · Cited by 458
Puce, A. (1999) · Cerebral Cortex · doi:10.1093/cercor/9.5.445 · Cited by 422
Cortical magnification within human primary visual cortex correlates with acuity thresholds
Duncan, R. O., & Boynton, G. M. (2003) · Neuron · doi:10.1016/s0896-6273(03)00265-4 · Cited by 385
A Primer on Pattern-Based Approaches to fMRI: Principles, Pitfalls, and Perspectives
Haynes, J.-D. (2015) · Neuron · doi:10.1016/j.neuron.2015.05.025 · Cited by 402
Re-evaluating the role of TPJ in attentional control: Contextual updating?
Geng, J. J., & Vossel, S. (2013) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2013.08.010 · Cited by 411
Vuilleumier, P., & Driver, J. (2007) · Philosophical Transactions of the Royal Society B Biological Sciences · doi:10.1098/rstb.2007.2092 · Cited by 397
Neuronal basis of contrast discrimination
Boynton, G. M., Demb, J. B., Glover, G. H., & Heeger, D. J. (1999) · Vision Research · doi:10.1016/s0042-6989(98)00113-8 · Cited by 391
Liu, A. K., Belliveau, J. W., & Dale, A. M. (1998) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.95.15.8945 · Cited by 384
Self-citationLarge-scale mirror-symmetry organization of human occipito-temporal object areas
Hasson, U., Harel, M., Levy, I., & Malach, R. (2003) · Neuron · doi:10.1016/s0896-6273(03)00144-2 · Cited by 336
Xiao, J., Liu, P., Wang, C. X., & Yang, G. W. (2017) · Progress in Materials Science · doi:10.1016/j.pmatsci.2017.02.004 · Cited by 352
Cortical Hierarchies Perform Bayesian Causal Inference in Multisensory Perception
Rohe, T., & Noppeney, U. (2015) · PLOS Biology · doi:10.1371/journal.pbio.1002073 · Cited by 344
Seeing it all: Convolutional network layers map the function of the human visual system
Eickenberg, M., Gramfort, A., Varoquaux, G., & Thirion, B. (2017) · NeuroImage · doi:10.1016/j.neuroimage.2016.10.001 · Cited by 338
A human parietal face area contains aligned head-centered visual and tactile maps
Sereno, M. I., & Huang, R.-S. (2006) · Nature Neuroscience · doi:10.1038/nn1777 · Cited by 322
Self-citationAttention modulates spatial priority maps in the human occipital, parietal and frontal cortices
Sprague, T. C., & Serences, J. T. (2013) · Nature Neuroscience · doi:10.1038/nn.3574 · Cited by 266
The pyramidal cell in cognition: a comparative study in human and monkey
Elston, G. N., Benavides-Piccione, R., & DeFelipe, J. (2001) · The Journal of Neuroscience · doi:10.1523/jneurosci.21-17-j0002.2001 · Cited by 317
Leung, H.-C., Gore, J. C., & Goldman-Rakic, P. S. (2002) · Journal of Cognitive Neuroscience · doi:10.1162/08989290260045882 · Cited by 314
Prior Expectations Evoke Stimulus Templates in the Primary Visual Cortex
Kok, P., Failing, M. F., & de Lange, F. P. (2014) · Journal of Cognitive Neuroscience · doi:10.1162/jocn_a_00562 · Cited by 293
Prior expectations bias sensory representations in visual cortex
Kok, P., Brouwer, G. J., van Gerven, M. A. J., & de Lange, F. P. (2013) · The Journal of Neuroscience · doi:10.1523/jneurosci.0742-13.2013 · Cited by 260
What Geometric Visual Hallucinations Tell Us about the Visual Cortex
Bressloff, P. C., Cowan, J. D., Golubitsky, M., Thomas, P. J., & Wiener, M. C. (2002) · Neural Computation · doi:10.1162/089976602317250861 · Cited by 290
Learning Strengthens the Response of Primary Visual Cortex to Simple Patterns
Furmanski, C. S., Schluppeck, D., & Engel, S. A. (2004) · Current Biology · doi:10.1016/j.cub.2004.03.032 · Cited by 286
Negative BOLD differentiates visual imagery and perception
Amedi, A., Malach, R., & Pascual-Leone, A. (2005) · Neuron · doi:10.1016/j.neuron.2005.10.032 · Cited by 271
Visual cortex activity in early and late blind people
Burton, H. (2003) · The Journal of Neuroscience · doi:10.1523/jneurosci.23-10-04005.2003 · Cited by 270
The Retinotopic Organization of Striate Cortex Is Well Predicted by Surface Topology
Benson, N. C., Butt, O. H., Datta, R., Radoeva, P. D., Brainard, D. H., & Aguirre, G. K. (2012) · Current Biology · doi:10.1016/j.cub.2012.09.014 · Cited by 227
fMRI Repetition Suppression: Neuronal Adaptation or Stimulus Expectation?
Larsson, J., & Smith, A. T. (2012) · Cerebral Cortex · doi:10.1093/cercor/bhr119 · Cited by 264
Imagery and perception share cortical representations of content and location
Cichy, R. M., Heinzle, J., & Haynes, J.-D. (2012) · Cerebral Cortex · doi:10.1093/cercor/bhr106 · Cited by 242
Zilles, K. (2002) · European Neuropsychopharmacology · doi:10.1016/s0924-977x(02)00108-6 · Cited by 244
Holmes, N., Leggett, J., Boto, E., Roberts, G., Hill, R. M., Tierney, T. M., Shah, V., Barnes, G. R., Brookes, M. J., & Bowtell, R. (2018) · NeuroImage · doi:10.1016/j.neuroimage.2018.07.028 · Cited by 250
Hof, P. R., Vogt, B. A., Bouras, C., & Morrison, J. H. (1997) · Vision Research · doi:10.1016/s0042-6989(96)00240-4 · Cited by 246
Functional Imaging of the Human Lateral Geniculate Nucleus and Pulvinar
Kastner, S., O'Connor, D. H., Fukui, M. M., Fehd, H. M., Herwig, U., & Pinsk, M. A. (2004) · Journal of Neurophysiology · doi:10.1152/jn.00553.2003 · Cited by 228
Topographic representation of the human body in the occipitotemporal cortex
Orlov, T., Makin, T. R., & Zohary, E. (2010) · Neuron · doi:10.1016/j.neuron.2010.09.032 · Cited by 236
Complete Pattern of Ocular Dominance Columns in Human Primary Visual Cortex
Adams, D. L., Sincich, L. C., & Horton, J. C. (2007) · The Journal of Neuroscience · doi:10.1523/jneurosci.2923-07.2007 · Cited by 212
Dissociation between Ventral and Dorsal fMRI Activation during Object and Action Recognition
Shmuelof, L., & Zohary, E. (2005) · Neuron · doi:10.1016/j.neuron.2005.06.034 · Cited by 227
Primary visual cortex activity along the apparent-motion trace reflects illusory perception
Muckli, L., Kohler, A., Kriegeskorte, N., & Singer, W. (2005) · PLoS Biology · doi:10.1371/journal.pbio.0030265 · Cited by 225
Konen, C. S., & Kastner, S. (2008) · The Journal of Neuroscience · doi:10.1523/jneurosci.1930-08.2008 · Cited by 221
Top-down effects on early visual processing in humans: A predictive coding framework
Rauss, K., Schwartz, S., & Pourtois, G. (2011) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2010.12.011 · Cited by 219
Child Development and Neuroscience.
Nelson, C. A., & Bloom, F. E. (1997) · Child Development · doi:10.1111/j.1467-8624.1997.tb01974.x · Cited by 236
Devlin, J. T., & Poldrack, R. A. (2007) · NeuroImage · doi:10.1016/j.neuroimage.2006.09.055 · Cited by 195
Functional connectivity of visual cortex in the blind follows retinotopic organization principles
Striem-Amit, E., Ovadia-Caro, S., Caramazza, A., Margulies, D. S., Villringer, A., & Amedi, A. (2015) · Brain · doi:10.1093/brain/awv083 · 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
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
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
Receptive fields in human visual cortex mapped with surface electrodes
Yoshor, D., Bosking, W. H., Ghose, G. M., & Maunsell, J. H. R. (2007) · Cerebral Cortex · doi:10.1093/cercor/bhl138 · Cited by 152
Primary visual cortex activation on the path of apparent motion is mediated by feedback from hMT+/V5
Sterzer, P., Haynes, J.-D., & Rees, G. (2006) · NeuroImage · doi:10.1016/j.neuroimage.2006.05.029 · Cited by 156
The human homologue of macaque area V6A
Pitzalis, S., Sereno, M. I., Committeri, G., Fattori, P., Galati, G., Tosoni, A., & Galletti, C. (2013) · NeuroImage · doi:10.1016/j.neuroimage.2013.06.026 · Cited by 154
Self-citationLarger extrastriate population receptive fields in autism spectrum disorders
Schwarzkopf, D. S., Anderson, E. J., de Haas, B., White, S. J., & Rees, G. (2014) · The Journal of Neuroscience · doi:10.1523/jneurosci.4416-13.2014 · Cited by 138
Beyond the Edges of a View: Boundary Extension in Human Scene-Selective Visual Cortex
Park, S., Intraub, H., Yi, D.-J., Widders, D., & Chun, M. M. (2007) · Neuron · doi:10.1016/j.neuron.2007.04.006 · Cited by 144
Localizing Pain Matrix and Theory of Mind networks with both verbal and non-verbal stimuli
Jacoby, N., Bruneau, E., Koster-Hale, J., & Saxe, R. (2016) · NeuroImage · doi:10.1016/j.neuroimage.2015.11.025 · Cited by 141
Flament, D., Ellermann, J. M., Kim, S.-G., Uǧurbil, K., & Ebner, T. J. (1996) · Human Brain Mapping · doi:10.1002/hbm.460040302 · Cited by 140
Attention gates visual coding in the human pulvinar
Fischer, J., & Whitney, D. (2012) · Nature Communications · doi:10.1038/ncomms2054 · Cited by 127
Mapping multisensory parietal face and body areas in humans
Huang, R.-S., Chen, C.-F., Tran, A. T., Holstein, K. L., & Sereno, M. I. (2012) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1207946109 · Cited by 131
Self-citationVisual memory and visual perception recruit common neural substrates
Slotnick, S. D. (2004) · Behavioral and Cognitive Neuroscience Reviews · doi:10.1177/1534582304274070 · Cited by 130
Correspondences between retinotopic areas and myelin maps in human visual cortex
Abdollahi, R. O., Kolster, H., Glasser, M. F., Robinson, E. C., Coalson, T. S., Dierker, D., Jenkinson, M., Van Essen, D. C., & Orban, G. A. (2014) · NeuroImage · doi:10.1016/j.neuroimage.2014.06.042 · Cited by 126
Neuroimaging of Language: Why Hasn't a Clearer Picture Emerged?
Fedorenko, E., & Kanwisher, N. (2009) · Language and Linguistics Compass · doi:10.1111/j.1749-818x.2009.00143.x · Cited by 117
Perceptual grouping and inverse fMRI activity patterns in human visual cortex
Fang, F., Kersten, D., & Murray, S. O. (2008) · Journal of Vision · doi:10.1167/8.7.2 · Cited by 122
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
Lawrence, S. J., Norris, D. G., & de Lange, F. P. (2019) · eLife · doi:10.7554/elife.44422 · Cited by 95
Wilson, S. M., Isenberg, A. L., & Hickok, G. (2009) · Human Brain Mapping · doi:10.1002/hbm.20782 · Cited by 110
Auditory attention activates peripheral visual cortex
Cate, A. D., Herron, T. J., Yund, E. W., Stecker, G. C., Rinne, T., Kang, X., Petkov, C. I., Disbrow, E. A., & Woods, D. L. (2009) · PLoS ONE · doi:10.1371/journal.pone.0004645 · Cited by 111
Fine-Grained Nociceptive Maps in Primary Somatosensory Cortex
Mancini, F., Haggard, P., Iannetti, G. D., Longo, M. R., & Sereno, M. I. (2012) · The Journal of Neuroscience · doi:10.1523/jneurosci.3059-12.2012 · Cited by 107
Self-citationSubjective confidence reflects representation of Bayesian probability in cortex
Geurts, L. S., Cooke, J. R. H., van Bergen, R. S., & Jehee, J. F. M. (2022) · Nature Human Behaviour · doi:10.1038/s41562-021-01247-w · Cited by 104
Bosking, W. H., Beauchamp, M. S., & Yoshor, D. (2017) · Annual Review of Vision Science · doi:10.1146/annurev-vision-111815-114525 · Cited by 93
Cholinergic Enhancement Reduces Spatial Spread of Visual Responses in Human Early Visual Cortex
Silver, M. A., Shenhav, A., & D'Esposito, M. (2008) · Neuron · doi:10.1016/j.neuron.2008.09.038 · Cited by 100
A cross-validated cytoarchitectonic atlas of the human ventral visual stream
Rosenke, M., Weiner, K. S., Barnett, M. A., Zilles, K., Amunts, K., Goebel, R., & Grill-Spector, K. (2018) · NeuroImage · doi:10.1016/j.neuroimage.2017.02.040 · Cited by 97
Cortical excitability controls the strength of mental imagery
Keogh, R., Bergmann, J., & Pearson, J. (2020) · eLife · doi:10.7554/elife.50232 · Cited by 94
Metadata
- Authors
- Sereno, M. I., Dale, A. M., Reppas, J. B., Kwong, K. K., Belliveau, J. W., Brady, T. J., Rosen, B. R., & Tootell, R. B. H.
- Venue
- Science
- Published
- 1995-05-12
- Volume
- 268
- Issue
- 5212
- Pages
- 889-893
- ISSN
- 0036-8075 (ISSN-L)
- 1095-9203
- OpenAlex
- W2093793583
- Cited by
- 2,658
- References
- 3
- FWCI
- 42.54
- Type
- journal article
- Language
- en
- Open access
- closed
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