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Mapping striate and extrastriate visual areas in human cerebral cortex.

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DeYoe, E A, Carman, G J, Bandettini, P, Glickman, S, Wieser, J, Cox, R, Miller, D, Neitz, J·1996·Proceedings of the National Academy of Sciences

DOI 10.1073/pnas.93.6.2382

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Abstract

Functional magnetic resonance imaging (fMRI) was used to identify and map the representation of the visual field in seven areas of human cerebral cortex and to identify at least two additional visually responsive regions. The cortical locations of neurons responding to stimulation along the vertical or horizontal visual field meridia were charted on three-dimensional models of the cortex and on unfolded maps of the cortical surface. These maps were used to identify the borders among areas that would be topographically homologous to areas V1, V2, V3, VP, and parts of V3A and V4 of the macaque monkey. Visually responsive areas homologous to the middle temporal/medial superior temporal area complex and unidentified parietal visual areas were also observed. The topography of the visual areas identified thus far is consistent with the organization in macaque monkeys. However, these and other findings suggest that human and simian cortical organization may begin to differ in extrastriate cortex at, or beyond, V3A and V4.

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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
Pathways for motion analysis: Cortical connections of the medial superior temporal and fundus of the superior temporal visual areas in the macaque
Boussaoud, D., Ungerleider, L. G., & Desimone, R. (1990) · Journal of Comparative Neurology · doi:10.1002/cne.902960311 · Cited by 634

Show all 2 references

Cortical Surface-Based Analysis
Dale, A. M., Fischl, B., & Sereno, M. I. (1999) · NeuroImage · doi:10.1006/nimg.1998.0395 · Cited by 10,910
The 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
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
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
The visual word form area
Cohen, L., Dehaene, S., Naccache, L., Lehéricy, S., Dehaene-Lambertz, G., Hénaff, M.-A., & Michel, F. (2000) · Brain · doi:10.1093/brain/123.2.291 · Cited by 1,954
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
Sensory gain control (amplification) as a mechanism of selective attention: electrophysiological and neuroimaging evidence
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
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
Electrophysiological studies of human face perception. I: Potentials generated in occipitotemporal cortex by face and non-face stimuli
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
Less 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
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
Self-citation
Comparative 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
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
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
Electrophysiological studies of human face perception. III: Effects of top-down processing on face-specific potentials
Puce, A. (1999) · Cerebral Cortex · doi:10.1093/cercor/9.5.445 · Cited by 422
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
Large-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
The large-scale neural network for spatial attention displays multifunctional overlap but differential asymmetry.
Kim, Y.-H., Gitelman, D. R., Nobre, A. C., Parrish, T. B., LaBar, K. S., & Mesulam, M.-M. (1999) · NeuroImage · doi:10.1006/nimg.1999.0408 · Cited by 316
The functional anatomy of attention to visual motion. A functional MRI study
Buchel, C. (1998) · Brain · doi:10.1093/brain/121.7.1281 · Cited by 303
Prior expectations bias sensory representations in visual cortex
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Negative BOLD differentiates visual imagery and perception
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Specializations of the granular prefrontal cortex of primates: Implications for cognitive processing
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Untitled work
Liddle (2001) · doi:10.1002/1097-0193(200102)12:2<100::aid-hbm1007>3.0.co;2-6

Authors: DeYoe, E. A., Carman, G. J., Bandettini, P., Glickman, S., Wieser, J., Cox, R., Miller, D., & Neitz, J.
Venue: Proceedings of the National Academy of Sciences
Publisher: Proceedings of the National Academy of Sciences
Published: 1996-03-19
Volume: 93
Issue: 6
Pages: 2382-2386
ISSN: 0027-8424 (ISSN-L)
1091-6490
DOI: 10.1073/pnas.93.6.2382
OpenAlex: W2142245130
Cited by: 1,046
References: 2
FWCI: 23.55
Type: journal article
Language: en
Open access: green

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Mapping striate and extrastriate visual areas in human cerebral cortex.

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