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Functional Analysis of V3A and Related Areas in Human Visual Cortex
Open accessAbstract
Using functional magnetic resonance imaging (fMRI) and cortical unfolding techniques, we analyzed the retinotopy, motion sensitivity, and functional organization of human area V3A. These data were compared with data from additional human cortical visual areas, including V1, V2, V3/VP, V4v, and MT (V5). Human V3A has a retinotopy that is similar to that reported previously in macaque: (1) it has a distinctive, continuous map of the contralateral hemifield immediately anterior to area V3, including a unique retinotopic representation of the upper visual field in superior occipital cortex; (2) in some cases the V3A foveal representation is displaced from and superior to the confluent foveal representations of V1, V2, V3, and VP; and (3) inferred receptive fields are significantly larger in human V3A, compared with those in more posterior areas such as V1. However, in other aspects human V3A appears quite different from its macaque counterpart: human V3A is relatively motion-selective, whereas human V3 is less so. In macaque, the situation is qualitatively reversed: V3 is reported to be prominently motion-selective, whereas V3A is less so. As in human and macaque MT, the contrast sensitivity appears quite high in human areas V3 and V3A.
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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
Time course EPI of human brain function during task activation
Bandettini, P. A., Wong, E. C., Hinks, R. S., Tikofsky, R. S., & Hyde, J. S. (1992) · Magnetic Resonance in Medicine · doi:10.1002/mrm.1910250220 · Cited by 1,935
Information processing in the primate visual system: an integrated systems perspective
Van Essen, D. C., Anderson, C. H., & Felleman, D. J. (1992) · Science · doi:10.1126/science.1734518 · Cited by 1,266
Boussaoud, D., Ungerleider, L. G., & Desimone, R. (1990) · Journal of Comparative Neurology · doi:10.1002/cne.902960311 · Cited by 634 · cited 4×
“On the basis of macaque data (Gattass et al., 1988; Boussaoud et al., 1990), one also might expect relatively large receptive fields in V4v, another human area near V3A.”
BackgroundInfluential
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-citationFischl, B. (2012) · NeuroImage · doi:10.1016/j.neuroimage.2012.01.021 · Cited by 9,526
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-citationIntersubject synchronization of cortical activity during natural vision
Hasson, U., Nir, Y., Levy, I., Fuhrmann, G., & Malach, R. (2004) · Science · doi:10.1126/science.1089506 · Cited by 1,839
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
Polymodal Motion Processing in Posterior Parietal and Premotor Cortex
Bremmer, F., Schlack, A., Shah, N. J., Zafiris, O., Kubischik, M., Hoffmann, K.-P., Zilles, K., & Fink, G. R. (2001) · Neuron · doi:10.1016/s0896-6273(01)00198-2 · Cited by 803
Neural Systems for Visual Orienting and Their Relationships to Spatial Working Memory
Corbetta, M., Kincade, J. M., & Shulman, G. L. (2002) · Journal of Cognitive Neuroscience · doi:10.1162/089892902317362029 · Cited by 698
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
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
The Predictive Value of Changes in Effective Connectivity for Human Learning
Büchel, C., Coull, J. T., & Friston, K. J. (1999) · Science · doi:10.1126/science.283.5407.1538 · Cited by 447
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-citationA Comparison of Visual and Auditory Motion Processing in Human Cerebral Cortex
Lewis, J. W. (2000) · Cerebral Cortex · doi:10.1093/cercor/10.9.873 · Cited by 381
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
Brain activity at rest: a multiscale hierarchical functional organization
Doucet, G., Naveau, M., Petit, L., Delcroix, N., Zago, L., Crivello, F., Jobard, G., Tzourio-Mazoyer, N., Mazoyer, B., Mellet, E., et al. (2011) · Journal of Neurophysiology · doi:10.1152/jn.00895.2010 · Cited by 319
Visual motion serves but is not under the purview of the dorsal pathway
Gilaie-Dotan, S. (2016) · Neuropsychologia · doi:10.1016/j.neuropsychologia.2016.07.018 · Cited by 325
Reading normal and degraded words: Contribution of the dorsal and ventral visual pathways.
Cohen, L., Dehaene, S., Vinckier, F., Jobert, A., & Montavont, A. (2008) · NeuroImage · doi:10.1016/j.neuroimage.2007.11.036 · Cited by 303
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
Dunn, A. K., Devor, A., Dale, A. M., & Boas, D. A. (2005) · NeuroImage · doi:10.1016/j.neuroimage.2005.04.024 · Cited by 285
Self-citationVisual 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
Konen, C. S., & Kastner, S. (2008) · The Journal of Neuroscience · doi:10.1523/jneurosci.1930-08.2008 · Cited by 221
Devlin, J. T., & Poldrack, R. A. (2007) · NeuroImage · doi:10.1016/j.neuroimage.2006.09.055 · Cited by 195
fMRI reveals a preference for near viewing in the human parieto-occipital cortex
Quinlan, D. J., & Culham, J. C. (2007) · NeuroImage · doi:10.1016/j.neuroimage.2007.02.029 · Cited by 155
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-citationDetection of fMRI activation using Cortical Surface Mapping
Andrade, A., Kherif, F., Mangin, J.-F., Worsley, K. J., Paradis, A., Simon, O., Dehaene, S., Bihan, D. L., & Poline, J. (2001) · Human Brain Mapping · doi:10.1002/1097-0193(200102)12:2<79::aid-hbm1005>3.0.co;2-i · Cited by 150
Waves of consciousness: ongoing cortical patterns during binocular rivalry
Cosmelli, D., David, O., Lachaux, J.-P., Martinerie, J., Garnero, L., Renault, B., & Varela, F. (2004) · NeuroImage · doi:10.1016/j.neuroimage.2004.05.008 · Cited by 131
Perceiving electrical stimulation of identified human visual areas
Murphey, D. K., Maunsell, J. H. R., Beauchamp, M. S., & Yoshor, D. (2009) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0804998106 · Cited by 109
Long-lasting crossmodal cortical reorganization triggered by brief postnatal visual deprivation
Collignon, O., Dormal, G., de Heering, A., Lepore, F., Lewis, T. L., & Maurer, D. (2015) · Current Biology · doi:10.1016/j.cub.2015.07.036 · Cited by 94
Ban, H., Yamamoto, H., Hanakawa, T., Urayama, S.-I., Aso, T., Fukuyama, H., & Ejima, Y. (2013) · The Journal of Neuroscience · doi:10.1523/jneurosci.1455-12.2013 · Cited by 80
A common neural substrate for processing scenes and egomotion-compatible visual motion
Sulpizio, V., Galati, G., Fattori, P., Galletti, C., & Pitzalis, S. (2020) · Brain Structure and Function · doi:10.1007/s00429-020-02112-8 · Cited by 59
Early visual cortex organization in autism: an fMRI study
Hadjikhani, N., Chabris, C. F., Joseph, R. M., Clark, J., McGrath, L., Aharon, I., Feczko, E., Tager-Flusberg, H., & Harris, G. J. (2004) · Neuroreport · doi:10.1097/00001756-200402090-00011 · Cited by 57
Self-citationBinkofski, F., Butler, A., Buccino, G., Heide, W., Fink, G., Freund, H.-J., & Seitz, R. J. (2003) · Experimental Brain Research · doi:10.1007/s00221-003-1594-2 · Cited by 29
Spatiotemporal integration of looming visual and tactile stimuli near the face
Huang, R., Chen, C., & Sereno, M. I. (2018) · Human Brain Mapping · doi:10.1002/hbm.23995 · Cited by 17
Self-citationSulpizio, V., Teghil, A., Pitzalis, S., & Boccia, M. (2024) · Brain Structure and Function · doi:10.1007/s00429-024-02790-8 · Cited by 7
The brain as image processor and generator: towards function-restoring brain-computer-interfaces
van Hoof, R. (2022) · doi:10.26481/dis.20220603rh · Cited by 1
Metadata
- Authors
- Tootell, R. B. H., Mendola, J. D., Hadjikhani, N. K., Ledden, P. J., Liu, A. K., Reppas, J. B., Sereno, M. I., & Dale, A. M.
- Venue
- The Journal of Neuroscience
- Publisher
- Society for Neuroscience
- Published
- 1997-09-15
- Volume
- 17
- Issue
- 18
- Pages
- 7060-7078
- ISSN
- 0270-6474 (ISSN-L)
- 1529-2401
- OpenAlex
- W2148675954
- Cited by
- 817
- References
- 4
- FWCI
- 19.44
- Type
- journal article
- Language
- en
- Open access
- hybrid
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