The DOI matches its Crossref record; 174 of the 179 references it cites were found in a registry or an index.
Visual field maps in human cortex.
Open accessAbstract
Much of the visual cortex is organized into visual field maps: nearby neurons have receptive fields at nearby locations in the image. Mammalian species generally have multiple visual field maps with each species having similar, but not identical, maps. The introduction of functional magnetic resonance imaging made it possible to identify visual field maps in human cortex, including several near (1) medial occipital (V1,V2,V3), (2) lateral occipital (LO-1,LO-2, hMT+), (3) ventral occipital (hV4, VO-1, VO-2), (4) dorsal occipital (V3A, V3B), and (5) posterior parietal cortex (IPS-0 to IPS-4). Evidence is accumulating for additional maps, including some in the frontal lobe. Cortical maps are arranged into clusters in which several maps have parallel eccentricity representations, while the angular representations within a cluster alternate in visual field sign. Visual field maps have been linked to functional and perceptual properties of the visual system at various spatial scales, ranging from the level of individual maps to map clusters to dorsal-ventral streams. We survey recent measurements of human visual field maps, describe hypotheses about the function and relationships between maps, and consider methods to improve map measurements and characterize the response properties of neurons comprising these maps.
Overview
Integrity signals
Registry
Cites
Statistics
Verification
Claims the paper makes
Claims other papers make about this one
Each is checked against this paper’s own text: does it say what the citing paper says it does?
In the citing paper
“It is likely that the developmental changes we document in the LOTS reflect increased sensitivity to visual inputs delivered through neighboring ventral visual areas such as hV4, VO1, and VO2 (Ben-Shachar et al., 2007; Wandell, Dumoulin, & Brewer, 2007).”
From The Development of Cortical Sensitivity to Visual Word Forms (2011) · cites this paper as Wandell et al., 2007
In the citing paper
“Hence, the circuits here provide no explanation for observed cortical maps [70],[71].”
From Towards a mathematical theory of cortical micro-circuits (2009) · cites this paper as [70]
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
The fusiform face area: a module in human extrastriate cortex specialized for face perception
Kanwisher, N., McDermott, J., & Chun, M. M. (1997) · The Journal of Neuroscience · doi:10.1523/jneurosci.17-11-04302.1997 · Cited by 7,738
Separate visual pathways for perception and action
Goodale, M. A., & Milner, A. D. (1992) · Trends in Neurosciences · doi:10.1016/0166-2236(92)90344-8 · Cited by 6,519
Measuring the thickness of the human cerebral cortex from magnetic resonance images
Fischl, B. R., & Dale, A. M. (2000) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.200033797 · Cited by 5,995
Ungerleider, L. G. (1982) · Medical Entomology and Zoology · Cited by 4,531
Ingle, D., Goodale, M. A., & Mansfield, R. J. W. (1982) · The MIT Press eBooks · Cited by 4,118
Ogawa, S., Tank, D. W., Menon, R., Ellermann, J. M., Kim, S. G., Merkle, H., & Ugurbil, K. (1992) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.89.13.5951 · Cited by 3,681
Automatic 3D intersubject registration of MR volumetric data in standardized Talairach space
Collins, D. L., Neelin, P., Peters, T. M., & Evans, A. C. (1994) · Journal of Computer Assisted Tomography · doi:10.1097/00004728-199403000-00005 · Cited by 3,431 · cited 2×
“…varied, and methods for placing a brain within a stereotaxic coordinate system, such as Talairach (Talairach and Tournoux, 1988) or MNI space (Collins et al., 1994), rarely provide spatial certainty within half a centimeter (Di Russo et al., 2002; Iaria and Petrides, 2007; Thompson et al.,…”
Milner, A. D., & Goodale, M. A. (2002) · The MIT Press eBooks · doi:10.7551/mitpress/7111.003.0023 · Cited by 3,345
MAGOUN, H. N. (1965) · The Journal of Nervous and Mental Disease · doi:10.1097/00005053-196504000-00011 · Cited by 2,932
Flagged first, then by citations
5 of the 179 references couldn’t be matched to a known paper.
Research works printed but not linked: 2
- Talbot, 1940, Arrangement of visual field on cat's cortex, Am. J. Physiol., 129, 477
- Talbot, 1942, A lateral localization in the cat's visual cortex, Fed. Proc., 1, 84
Cited by
Sorted by citations
Items 301–400 of 999
Matsuzaki, N., Juhász, C., & Asano, E. (2013) · Clinical Neurophysiology · doi:10.1016/j.clinph.2013.02.007 · Cited by 47
“Although functional specialization of these occipital regions has been extensively described in previous studies of humans and non-human primates (Wandell et al., 2007), functional connectivity across the human occipital regions (beyond anatomical connectivity) has not been fully understood.”
BackgroundCortical connective field estimates from resting state fMRI activity
Gravel, N., Harvey, B. M., Nordhjem, B. J. T., Haak, K. V., Dumoulin, S. O., Renken, R. J., Ćurĉić‐Blake, B., & Cornelissen, F. W. (2014) · Frontiers in Neuroscience · doi:10.3389/fnins.2014.00339 · Cited by 45
“The cortical surface was reconstructed at the white/gray matter boundary and rendered as a smoothed 3D mesh (Wandell et al., 2007).”
MethodGomez, J., Zhen, Z., & Weiner, K. S. (2019) · PLoS Biology · doi:10.1371/journal.pbio.3000362 · Cited by 49
Topographic numerosity maps cover subitizing and estimation ranges
Cai, Y., Hofstetter, S., van Dijk, J. A., Zuiderbaan, W., van der Zwaag, W., Harvey, B. M., & Dumoulin, S. O. (2021) · Nature Communications · doi:10.1038/s41467-021-23785-7 · Cited by 47
Probing principles of large‐scale object representation: Category preference and location encoding
Cichy, R. M., Sterzer, P., Heinzle, J., Elliott, L. T., Ramírez, F., & Haynes, J. (2012) · Human Brain Mapping · doi:10.1002/hbm.22020 · Cited by 46
“This result is expected for low-level visual areas that are retinotopically organized [Grill-Spector andMalach, 2004;Wandell et al., 2007].”
BackgroundMethodVisuospatial processing: A review from basic to current concepts
Trés, E. S., & Brucki, S. M. D. (2014) · Dementia & Neuropsychologia · doi:10.1590/s1980-57642014dn82000014 · Cited by 50
Jitsuishi, T., Hirono, S., Yamamoto, T., Kitajo, K., Iwadate, Y., & Yamaguchi, A. (2020) · Scientific Reports · doi:10.1038/s41598-020-57837-7 · Cited by 46
Inferior Occipital Gyrus Is Organized along Common Gradients of Spatial and Face-Part Selectivity
de Haas, B., Sereno, M. I., & Schwarzkopf, D. S. (2021) · Journal of Neuroscience · doi:10.1523/jneurosci.2415-20.2021 · Cited by 42
Imageless imagery in aphantasia revealed by early visual cortex decoding
Chang, S., Zhang, X., Cao, Y., Pearson, J., & Meng, M. (2025) · Current Biology · doi:10.1016/j.cub.2024.12.012 · Cited by 45
Spatial neglect and the neural coding of attentional priority
Ptak, R., & Fellrath, J. (2013) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2013.01.026 · Cited by 48
“There is strong evidence from monkey neurophysiology and functional brain imaging of the human brain for a spatiotopic organisation of higher visual areas of the dorsal stream, including at least four areas lying in the IPS (Andersen et al., 1997; Swisher et al., 2007; Wandell et al., 2007).”
BackgroundColor responsiveness argues against a dorsal component of human V4
Goddard, E., Mannion, D. J., McDonald, J. S., Solomon, S. G., & Clifford, C. W. G. (2011) · Journal of Vision · doi:10.1167/11.4.3 · Cited by 45
What cognitive sciences have to say about the impacts of nutritional labelling formats
Muller, L., & Prevost, M. (2016) · Journal of Economic Psychology · doi:10.1016/j.joep.2016.01.005 · Cited by 45
Neural architectures for stereo vision
Parker, A. J., Smith, J. E. T., & Krug, K. (2016) · Philosophical Transactions of the Royal Society B Biological Sciences · doi:10.1098/rstb.2015.0261 · Cited by 45
Sun, J.-W., Fan, R., Wang, Q., Wang, Q.-Q., Jia, X., & Ma, H. (2021) · Brain Research · doi:10.1016/j.brainres.2021.147299 · Cited by 47
The Scale of Functional Specialization within Human Prefrontal Cortex: Figure 1.
Gilbert, S. J., Henson, R. N., & Simons, J. S. (2010) · Journal of Neuroscience · doi:10.1523/jneurosci.3220-09.2010 · Cited by 46
Representation of Contralateral Visual Space in the Human Hippocampus
Silson, E. H., Zeidman, P., Knapen, T. H. J., & Baker, C. I. (2021) · Journal of Neuroscience · doi:10.1523/jneurosci.1990-20.2020 · Cited by 47
Tau follows principal axes of functional and structural brain organization in Alzheimer’s disease
Ottoy, J., Kang, M. S., Tan, J. X. M., Boone, L., de Wael, R. V., Park, B., Bezgin, G., Lussier, F. Z., Pascoal, T. A., Rahmouni, N., et al. (2024) · Nature Communications · doi:10.1038/s41467-024-49300-2 · Cited by 56
Neurophysiology of functional imaging
van Eijsden, P., Hyder, F., Rothman, D. L., & Shulman, R. G. (2008) · NeuroImage · doi:10.1016/j.neuroimage.2008.08.026 · Cited by 44
Visual Feature-Tolerance in the Reading Network
Rauschecker, A. M., Bowen, R. F., Perry, L. M., Kevan, A., Dougherty, R. F., & Wandell, B. A. (2011) · Neuron · doi:10.1016/j.neuron.2011.06.036 · Cited by 44
“The targetingmethod is important given the close proximity of area hMT+ to other visual areas (Wandell et al., 2007), as well as individual subject variability in hMT+ location in relation to skull (Sack et al.”
BackgroundThe Attentional Field Revealed by Single-Voxel Modeling of fMRI Time Courses
Puckett, A. M., & DeYoe, E. A. (2015) · Journal of Neuroscience · doi:10.1523/jneurosci.3754-14.2015 · Cited by 48
“…criteria described by a number of labs (Sereno et al., 1995, 2001; DeYoe et al., 1996; Engel et al., 1997; Pitzalis et al., 2006, 2010; Hansen et al., 2007; Swisher et al., 2007; Wandell et al., 2007; Amano et al., 2009; Arcaro et al., 2009; Silver and Kastner, 2009; Wandell and Winawer, 2011).”
BackgroundChou, K., Yang, F., Fuh, J., Kuo, C.-Y., Wang, Y.-H., Lirng, J.-F., Lin, Y., Wang, S., & Lin, C. (2016) · Cephalalgia · doi:10.1177/0333102416668657 · Cited by 44
“However, these occipital areas participate in visuospatial perception and localization (36).”
BackgroundUsing diffusion MRI to discriminate areas of cortical grey matter
Ganepola, T., Nagy, Z., Ghosh, A., Papadopoulo, T., Alexander, D. C., & Sereno, M. I. (2017) · NeuroImage · doi:10.1016/j.neuroimage.2017.12.046 · Cited by 44
“This is an open access article unde sample size, which was problematic given inter-subject variability of cytoarchitectonic boundaries but also within-area variation (Geyer et al., 2000, 1997; Orban et al., 2004; Sereno and Tootell, 2005; Wandell et al., 2007), (2) the unavoidable artefacts of the histological process…”
BackgroundIndividualized cognitive neuroscience needs 7T: Comparing numerosity maps at 3T and 7T MRI
Cai, Y., Hofstetter, S., van der Zwaag, W., Zuiderbaan, W., & Dumoulin, S. O. (2021) · NeuroImage · doi:10.1016/j.neuroimage.2021.118184 · Cited by 44
Grégoire, A., Deggouj, N., Dricot, L., Decat, M., & Kupers, R. C. (2022) · Frontiers in Neuroscience · doi:10.3389/fnins.2022.850245 · Cited by 43
“An estimated 30–40% of the cortical mantle is devoted to processing visual information, compared to only 8% for audition (Wandell et al., 2007).”
Schulte, T., Müller‐Oehring, E. M., Torsten Rohlfing, B., Pfefferbaum, A., & Sullivan, E. V. (2010) · Journal of Neuroscience · doi:10.1523/jneurosci.2160-10.2010 · Cited by 43
Progressive Thinning of Visual Cortex in Primary Open-Angle Glaucoma of Varying Severity
Yu, L., Xie, L., Dai, C., Xie, B., Liang, M., Zhao, L., Yin, X., & Wang, J. (2015) · PLoS ONE · doi:10.1371/journal.pone.0121960 · Cited by 43
Motion Direction Biases and Decoding in Human Visual Cortex
Wang, H. X., Merriam, E. P., Freeman, J., & Heeger, D. J. (2014) · Journal of Neuroscience · doi:10.1523/jneurosci.1034-14.2014 · Cited by 43
“…agreed that human primary visual cortex (V1) is analogous to monkey V1 and that human visual cortical area MT is analogous to monkey areas MT and MST. Activity in human MT , measured with fMRI, is greater for moving than static stimuli (Watson et al., 1993; Tootell et al., 1995; Huk et al., 2002).”
BackgroundAlnæs, D., Kaufmann, T., Richard, G., Duff, E. P., Sneve, M. H., Endestad, T., Nordvik, J. E., Andreassen, O. A., Smith, S. M., & Westlye, L. T. (2015) · NeuroImage · doi:10.1016/j.neuroimage.2015.01.026 · Cited by 45
“This differential coupling anddecoupling between the dorsal attention and visual nodes may reflect the fact that the objects were tracked predominantly in the central parts of the visual field, since the occipital pole is known to retinotopically represent the central parts of the visual field (Wandell et al., 2007).”
BackgroundMagnetoencephalographic signatures of visual form and motion binding
Aissani, C., Cottereau, B. R., Dumas, G., Paradis, A., & Lorenceau, J. (2011) · Brain Research · doi:10.1016/j.brainres.2011.05.051 · Cited by 42
Sun, P., Gardner, J. L., Costagli, M., Ueno, K., Waggoner, R. A., Tanaka, K., & Cheng, K. (2012) · Cerebral Cortex · doi:10.1093/cercor/bhs149 · Cited by 43
“The continuous and periodic stimulation paradigm offers the advantages of exhaustive coverage of a given stimulus space and effective separation of the stimulus-evoked response from an intrinsic noise (Engel et al. 1994; Kalatsky and Stryker 2003; Wandell et al. 2007; Engel 2011).”
InfluentialThe transition in the ventral stream from feature to real-world entity representations
Orban, G. A., Zhu, Q., & Vanduffel, W. (2014) · Frontiers in Psychology · doi:10.3389/fpsyg.2014.00695 · Cited by 46
“In summary, the retinotopic organization of occipital cortex is remarkably similar in human and non-human primates, more than initially appreciated (Wandell et al., 2007).”
BackgroundSpoken language comprehension activates the primary visual cortexPreprint
Seydell‐Greenwald, A., Wang, X., Newport, E. L., Bi, Y., & Striem-Amit, E. (2020) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2020.12.02.408765 · Cited by 43
“This appears to be a marked deviation from its function in sighted individuals, where V1 is involved in the processing of basic visual features (Hubel and Wiesel, 1962, 1968; Grill-Spector and Malach, 2004; Wandell et al., 2007a).”
BackgroundMethodTowards a psychodynamic neuroscience
Fotopoulou, A. (2012) · Oxford University Press eBooks · doi:10.1093/med/9780199600526.003.0003 · Cited by 42
Fabius, J. H., Fracasso, A., Acunzo, D. J., der Stigchel, S. V., & Melcher, D. (2020) · Journal of Neuroscience · doi:10.1523/jneurosci.1169-20.2020 · Cited by 42
“Given that the visual system is retinotopically organized (Wandell et al., 2007), this raises the question of how perceptual continuity is established.”
BackgroundLange, R., Kumagai, A., Weiss, S., Zaffke, K. B., Day, S., Wicker, D., Howson, A., Jayasundera, K. T., Smolinski, L., Hedlich, C., et al. (2021) · Journal of Patient-Reported Outcomes · doi:10.1186/s41687-020-00281-y · Cited by 33
“One possibility is that differences in functional impairments due to central and peripheral vision loss may be related to the processing of visual information that is believed to occur via two distinct “cortical streams,” the ventral and dorsal stream [56, 57].”
BackgroundFunctional Connectivity Patterns of Visual Cortex Reflect its Anatomical Organization
Genç, E., Schölvinck, M. L., Bergmann, J., Singer, W., & Kohler, A. (2015) · Cerebral Cortex · doi:10.1093/cercor/bhv175 · Cited by 40
Lv, X., Qiu, Y., Tian, J., Xie, C., Han, L., Su, H., Liu, Z., Peng, J., Lin, C., Wu, M., et al. (2012) · Liver International · doi:10.1111/liv.12096 · Cited by 42
“The lingual gyrus, middle occipital gyrus and middle temporal gyrus are intimately involved in visual information processing (19, 20) and modulation of topdown visuospatial selective attention (21).”
BackgroundHigh-resolution retinotopic maps estimated with magnetoencephalography
Nasiotis, K., Clavagnier, S., Baillet, S., & Pack, C. C. (2016) · NeuroImage · doi:10.1016/j.neuroimage.2016.10.017 · Cited by 42
“The sources that had foveal responses were clustered at the most posterior part of the cortex, and those with higher eccentricity were located more anteriorly, as expected from known retinotopic organization (Wandell et al., 2007).”
Population receptive field tuning properties of visual cortex during childhood
Dekker, T. M., Schwarzkopf, D. S., de Haas, B., Marko Nardini, A., & Sereno, M. I. (2019) · Developmental Cognitive Neuroscience · doi:10.1016/j.dcn.2019.01.001 · Cited by 41
Choi, S., Jeong, G., Kim, Y.-B., & Cho, Z. (2020) · NeuroImage · doi:10.1016/j.neuroimage.2020.117145 · Cited by 42
“area in the visual field map (Sereno et al., 1995; Wandell et al., 2007), while in the multi-modal parcellation from Human Connectome Project (HCP), it is located in themiddle temporal or occipital area (Glasser et al.”
BackgroundDivisive normalization unifies disparate response signatures throughout the human visual hierarchy
Aqil, M., Knapen, T. H. J., & Dumoulin, S. O. (2021) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.2108713118 · Cited by 45
“Next, we directly compare the four models’ performance across nine visual regions spanning the hierarchy of human visual cortex (V1, secondary visual cortex [V2], third visual cortex [V3], visual area 3AB [V3AB], human visual area V4 [hV4], lateral occipital [LO], temporal occipital [TO], ventral occipital [VO], and i…”
MethodConcepts in the Brain: The View From Cross-linguistic Diversity
Kemmerer, D. (2019) · doi:10.1093/oso/9780190682620.001.0001 · Cited by 42
Spatial patterns in tactile perception: Is there a tactile field?
Haggard, P., & Giovagnoli, G. (2011) · Acta Psychologica · doi:10.1016/j.actpsy.2011.03.001 · Cited by 43
Genç, E., Bergmann, J., Singer, W., & Kohler, A. (2013) · Cerebral Cortex · doi:10.1093/cercor/bht342 · Cited by 41
“To obtain phase-encoded retinotopic preference maps of our participants we presented rotating wedge and expanding ring stimuli that create spatial sequences of neural activity in visual cortex (Engel et al. 1994; Sereno et al. 1995; Wandell et al. 2007).”
BackgroundMethodA Hierarchy of Attentional Priority Signals in Human Frontoparietal Cortex
Liu, T., & Hou, Y. (2013) · Journal of Neuroscience · doi:10.1523/jneurosci.1780-13.2013 · Cited by 41
Characterizing the effects of feature salience and top-down attention in the early visual system
Poltoratski, S., Ling, S., McCormack, D. R., & Tong, F. (2017) · Journal of Neurophysiology · doi:10.1152/jn.00924.2016 · Cited by 45
“Cortical visual areas V1–hV4 were demarcated using standard retinotopy procedures, with the use of data acquired from separate scan sessions at 3T (Engel et al. 1997; Wandell et al. 2007).”
MethodDeep recurrent neural network reveals a hierarchy of process memory during dynamic natural vision
Shi, J., Wen, H., Zhang, Y., Han, K., & Liu, Z. (2018) · Human Brain Mapping · doi:10.1002/hbm.24006 · Cited by 39
“Both spatial and temporal information is processed by cascaded areas with increasing spatial receptive fields (Wandell et al., 2007) and temporal receptive windows (TRWs) (Hasson et al., 2008) along the visual hierarchy.”
BackgroundRecurrent processes support a cascade of hierarchical decisions
Gwilliams, L., & King, J.-R. (2020) · eLife · doi:10.7554/elife.56603 · Cited by 48
“…signals peaked in the early visual cortex (mean MNI [x = 27.59; y = 74.15; z = 1.07]), and propagated along the ventral and dorsal streams during the first 200 ms (Figure 2A, Video 2); confirming the retinotopic organization of the visual hierarchy (Hagler and Sereno, 2006; Wandell et al., 2007).”
BackgroundInfluentialSong, C., Schwarzkopf, D. S., Kanai, R., & Rees, G. E. (2011) · Journal of Neuroscience · doi:10.1523/jneurosci.0308-11.2011 · Cited by 43
“Due to the retinotopic organization of the early visual system, the upper and lower visual fields are represented by the ventral and dorsal portions, respectively, of areas V1–V3 (Wandell et al., 2007).”
BackgroundGlobal Order and Local Disorder in Brain Maps
Rothschild, G., & Mizrahi, A. (2015) · Annual Review of Neuroscience · doi:10.1146/annurev-neuro-071013-014038 · Cited by 39
Sabbah, N., Authié, C., Sanda, N., Mohand‐Saïd, S., Sahel, J., Safran, A. B., Habas, C., & Amedi, A. (2016) · NeuroImage · doi:10.1016/j.neuroimage.2016.04.056 · Cited by 39
Vernon, R. J. W., Gouws, A. D., Lawrence, S. J. D., Wade, A. R., & Morland, A. B. (2016) · Journal of Neuroscience · doi:10.1523/jneurosci.3603-15.2016 · Cited by 40
Shao, Y., Li, Q., Li, B., Lin, Q., Su, T., Shi, W., Zhu, P., Yuan, Q., Shu, Y., He, Y. Z., et al. (2019) · Molecular Medicine Reports · doi:10.3892/mmr.2019.10147 · Cited by 39
Orientation anisotropies in human primary visual cortex depend on contrast
Maloney, R. T., & Clifford, C. W. G. (2015) · NeuroImage · doi:10.1016/j.neuroimage.2015.06.034 · Cited by 40
“The definition of all ROIs (including V1) was based on separate retinotopic mapping scans performed prior to Experiments 1 and 2 for each subject using well-established phase-encoded designs (DeYoe et al., 1996; Engel et al., 1994, 1997; Larsson and Heeger, 2006; Wandell & Winawer, 2011; Wandell et al., 2007), and the…”
Learning to Discriminate Face Views
Bi, T., Chen, N., Weng, Q., He, D., & Fang, F. (2010) · Journal of Neurophysiology · doi:10.1152/jn.00286.2010 · Cited by 40
Zooming In and Zooming Out of the Attentional Focus: An fMRI Study
Chen, Q., Marshall, J. C., Weidner, R., & Fink, G. R. (2008) · Cerebral Cortex · doi:10.1093/cercor/bhn128 · Cited by 40
Cortical depth profiles in primary visual cortex for illusory and imaginary experiences
Bergmann, J., Petro, L. S., Abbatecola, C., Li, M. S., Morgan, A., & Muckli, L. F. (2024) · Nature Communications · doi:10.1038/s41467-024-45065-w · Cited by 39
Neural Representations of Contextual Guidance in Visual Search of Real-World Scenes
Preston, T. J., Guo, F., Das, K., Giesbrecht, B., & Eckstein, M. P. (2013) · Journal of Neuroscience · doi:10.1523/jneurosci.5840-12.2013 · Cited by 44
“The ability to decode coarse locations of contextually relevant regions of the image from activity in LOC and IPS is consistent with previous studies showing that these areas have a retinotopic organization (Wandell et al., 2007; Silver and Kastner, 2009).”
ResultIs orbital volume associated with eyeball and visual cortex volume in humans?
Pearce, E., & Bridge, H. (2013) · Annals of Human Biology · doi:10.3109/03014460.2013.815272 · Cited by 39
“The ‘‘gold standard’’ for identifying visual areas in human subjects is the use of retinotopic mapping, which relies on each visual area only having a single representation of space to functionally locate more than 10 visual areas (reviewed in Wandell et al., 2007).”
A Specialized Multi-Transmit Head Coil for High Resolution fMRI of the Human Visual Cortex at 7T
Sengupta, S., Roebroeck, A. F., Kemper, V. G., Poser, B. A., Zimmermann, J., Goebel, R., & Adriany, G. (2016) · PLoS ONE · doi:10.1371/journal.pone.0165418 · Cited by 39
“The frontal-open design of the 16 channel coil allowed for a visual angle was 29 ̊—extending into the subjects’ near-peripheral vision; for the 32 channel whole head coil the visual angle was 10 ̊—extending into the subjects’ central and paracentral vision [32]—as its viewing angle is limited due to the coil’s design.”
BackgroundBaldassarre, L., Pontil, M., & Mourão-Miranda, J. (2017) · Frontiers in Neuroscience · doi:10.3389/fnins.2017.00062 · Cited by 39
“The fist two regions are known to be involved in visual processing (e.g., Wandell et al., 2007) and Left culmen the last two have been associated with emotional processing (e.g., Etkin et. al., 2011).”
BackgroundTask-dependent enhancement of facial expression and identity representations in human cortex
Dobs, K., Schultz, J., Bülthoff, I., & Gardner, J. L. (2018) · NeuroImage · doi:10.1016/j.neuroimage.2018.02.013 · Cited by 43
“In a separate scanning session, we mapped early visual cortex for each subject using standard topographic mapping methodology (Wandell et al., 2007; Gardner et al., 2008).”
Poltoratski, S., Maier, A., Newton, A. T., & Tong, F. (2019) · Current Biology · doi:10.1016/j.cub.2019.04.068 · Cited by 40
The role of neural tuning in quantity perception
Tsouli, A., Harvey, B. M., Hofstetter, S., Cai, Y., van der Smagt, M. J., Pas, S. F. T., & Dumoulin, S. O. (2021) · Trends in Cognitive Sciences · doi:10.1016/j.tics.2021.10.004 · Cited by 39
Advances in spiral fMRI: A high-resolution study with single-shot acquisition
Kasper, L., Engel, M., Heinzle, J., Müller-Schrader, M., Graedel, N. N., Reber, J., Schmid, T., Barmet, C., Wilm, B. J., Stephan, K. E., et al. (2021) · NeuroImage · doi:10.1016/j.neuroimage.2021.118738 · Cited by 39
Neural structures and mechanisms involved in scene recognition: A review and interpretation
Sewards, T. V. (2010) · Neuropsychologia · doi:10.1016/j.neuropsychologia.2010.11.018 · Cited by 40
Cerebral Asymmetry of fMRI-BOLD Responses to Visual Stimulation
Hougaard, A., Jensen, B. H., Amin, F. M., Rostrup, E., Hoffmann, M. B., & Ashina, M. (2015) · PLoS ONE · doi:10.1371/journal.pone.0126477 · Cited by 41
“However, they are likely to be related to differential processing of information in the left and right hemifield, as many visual areas have been demonstrated to comprise a retinotopic map of the contralateral visual hemifield [30].”
BackgroundSomers, D. C., & Sheremata, S. (2013) · Wiley Interdisciplinary Reviews Cognitive Science · doi:10.1002/wcs.1230 · Cited by 41
Borders, map clusters, and supra-areal organization in visual cortex
Buckner, R. L., & Yeo, B. T. T. (2014) · NeuroImage · doi:10.1016/j.neuroimage.2013.12.036 · Cited by 38
“Beyond the V1/V2/V3 cluster, additional candidate map clusters are located near the human homologue of the middle temporal (MT) visual area, V3A/V3B, the ventral occipital (VO) complex, and the intraparietal sulcus (IPS) (Wandell et al., 2007)(Fig.”
Orientation Selectivity of Motion-Boundary Responses in Human Visual Cortex
Larsson, J. T., Heeger, D. J., & Landy, M. S. (2010) · Journal of Neurophysiology · doi:10.1152/jn.00400.2010 · Cited by 38
Jo, H. J., Saad, Z. S., Gotts, S. J., Martin, A. D., & Cox, R. W. (2012) · PLoS ONE · doi:10.1371/journal.pone.0048847 · Cited by 35
“Visual cortex in the depths of the calcarine sulcus in humans, shown here to exhibit fine-grained functional correspondency, is more involved in representing the horizontal meridian [66,67], potentially casting further doubt on the role of the callosum in mediating all of these functional relationships.”
BackgroundDifferential patterns of 2D location versus depth decoding along the visual hierarchy
Finlayson, N. J., Zhang, X., & Golomb, J. D. (2016) · NeuroImage · doi:10.1016/j.neuroimage.2016.12.039 · Cited by 38
“Both neurophysiology and functional neuroimaging studies have revealed a large number of regions in the brain sensitive to 2D visuo-spatial information: visual cortex is organized into topographic maps of 2D spatial location (Engel et al., 1994; Grill-Spector and Malach, 2004; Maunsell and Newsome, 1987; Sereno et al.…”
Kröger, A., Hof, K., Krick, C. M., Siniatchkin, M., Jarczok, T. A., Freitag, C. M., & Bender, S. (2014) · PLoS ONE · doi:10.1371/journal.pone.0088585 · Cited by 41
“The intraparietal sulcus which is located close to the dipole may also be indicated by the dipole, as it is involved in the detection of spatial relations [55,56] which is also important for biological motion detection.”
Backgroundvan der Hoorn, A., Renken, R. J., Leenders, K. L., & de Jong, B. M. (2014) · PLoS ONE · doi:10.1371/journal.pone.0095861 · Cited by 38
“An additional argument that ‘change’-related activations predominantly occurred in the peripheral visual field can be concluded from the anterior calcarine activation, which topologically represents the peripheral field [97,98].”
BackgroundNeural Pathways Conveying Novisual Information to the Visual Cortex
Qin, W., & Yu, C. (2013) · Neural Plasticity · doi:10.1155/2013/864920 · Cited by 43
“[2] B.”
Machado, A. R., Pereira, A. C., Ferreira, F. S., Ferreira, S., Quendera, B., Silva, E. D., & Castelo-Branco, M. S. (2017) · Scientific Reports · doi:10.1038/s41598-017-11317-7 · Cited by 37
Population Dynamics of Early Visual Cortex during Working Memory
Rahmati, M., Saber, G. T., & Curtis, C. E. (2017) · Journal of Cognitive Neuroscience · doi:10.1162/jocn_a_01196 · Cited by 37
“Visual area boundaries were drawn on retinotopic maps based on standard conventions (Wandell et al., 2007; Larsson & Heeger, 2006).”
MethodfMRI of the rod scotoma elucidates cortical rod pathways and implications for lesion measurements
Barton, B., & Brewer, A. A. (2015) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1423673112 · Cited by 37
“Artificial, reversible scotomas caused by stabilization of the stimulus on the retina are transient and most effective in the periphery (38), making them difficult to measure in early visual areas with fMRI because of the comparatively slow temporal resolution of fMRI and the relatively smaller amount of cortex devote…”
BackgroundHara, Y., Pestilli, F., & Gardner, J. L. (2014) · Frontiers in Computational Neuroscience · doi:10.3389/fncom.2014.00012 · Cited by 36
“In interleaved trials, the cues could point to one, two or four of the locations.”
BackgroundMethodRepresentation of Naturalistic Image Structure in the Primate Visual CortexPreprint
Movshon, J. A., & Simoncelli, E. P. (2014) · Cold Spring Harbor Symposia on Quantitative Biology · doi:10.1101/sqb.2014.79.024844 · Cited by 37
“We render the responses on a flattened map of the posterior pole of the cortex in a representative subject; the marked borders between visual areas were established in earlier topographic mapping studies using standard techniques (Wandell et al. 2007; Gardner et al. 2008).”
Continuous mapping of the cortical object vision pathway using traveling waves in object space
Goesaert, E., & de Beeck, H. O. (2009) · NeuroImage · doi:10.1016/j.neuroimage.2009.11.036 · Cited by 36
Donner, T. H., Sagi, D., Bonneh, Y. S., & Heeger, D. J. (2013) · Journal of Neuroscience · doi:10.1523/jneurosci.3388-12.2013 · Cited by 36
“Retinotopic maps in human visual cortex were measured using standard procedures (Wandell et al., 2007) to identify visual field maps corresponding to V1, V2, V3, and V4 in each individual subject following the conventions of Wandell et al. (Wandell et al., 2007).”
MethodHuman primary visual cortex (V1) is selective for second-order spatial frequency
Hallum, L. E., Landy, M. S., & Heeger, D. J. (2011) · Journal of Neurophysiology · doi:10.1152/jn.01007.2010 · Cited by 35
Visual Mapping Using Blood Oxygen Level Dependent Functional Magnetic Resonance Imaging
DeYoe, E. A., & Raut, R. V. (2014) · Neuroimaging Clinics of North America · doi:10.1016/j.nic.2014.08.001 · Cited by 38
An illusion predicted by V1 population activity implicates cortical topography in shape perception
Michel, M. M., Chen, Y., Geisler, W. S., & Seidemann, E. (2013) · Nature Neuroscience · doi:10.1038/nn.3517 · Cited by 35
The visual cortex and visual cognition in Huntington’s disease: An overview of current literature
Coppen, E. M., van der Grond, J., Hart, E. P., Lakke, E. A. J. F., & Roos, R. A. C. (2018) · Behavioural Brain Research · doi:10.1016/j.bbr.2018.05.019 · Cited by 37
“Visual field mapping using functional Magnetic Resonance Imaging (fMRI) showed that approximately 20–30% of the human brain is directly or indirectly involved in visual processing [3,4].”
Real-time decoding of the direction of covert visuospatial attention
Andersson, P. U., Ramsey, N. F., Raemaekers, M. A. H., Viergever, M. A., & Pluim, J. P. W. (2012) · Journal of Neural Engineering · doi:10.1088/1741-2560/9/4/045004 · Cited by 38
Real-Time Decoding of Brain Responses to Visuospatial Attention Using 7T fMRI
Andersson, P. U., Pluim, J. P. W., Siero, J. C. W., Klein, S., Viergever, M. A., & Ramsey, N. F. (2011) · PLoS ONE · doi:10.1371/journal.pone.0027638 · Cited by 38
“Topography of the visual field on the visual cortex has been elucidated in great detail [57].”
BackgroundNeural correlates of psychotic-like experiences during spiritual-trance state
Mainieri, A. G., Peres, J. F. P., Moreira-Almeida, A., Mathiak, K., Habel, U., & Kohn, N. (2017) · Psychiatry Research: Neuroimaging · doi:10.1016/j.pscychresns.2017.06.006 · Cited by 35
The Conceptual Format Debate and the Challenge from (Global) Supramodality
Calzavarini, F. (2021) · The British Journal for the Philosophy of Science · doi:10.1086/717564 · Cited by 39
Tosoni, A., Capotosto, P., Baldassarre, A., Spadone, S., & Sestieri, C. (2023) · Frontiers in Human Neuroscience · doi:10.3389/fnhum.2023.1250096 · Cited by 38
“Stimulus location and behavioral relevance in the DAN are coded within several retinotopic maps (Wandell et al., 2007; Silver and Kastner, 2009), updated by either endogenous or exogenous information (Kincade et al.”
Visual Field Map Organization in Human Visual Cortex
Alyssa, A., & Barto, B. (2012) · InTech eBooks · doi:10.5772/51914 · Cited by 36
“(and visual space) are also adjacent in cortex [12].”
BackgroundMethodResultInfluentialCytoarchitectonic mapping of attentional selection and reorienting in parietal cortex
Gillebert, C. R., Mantini, D., Peeters, R. R., Dupont, P. J., & Vandenberghe, R. R. (2012) · NeuroImage · doi:10.1016/j.neuroimage.2012.11.026 · Cited by 39
“Posterior IPS, also called IPS0 or IPS1, contains retinotopic representations of left and right visual field (Silver et al., 2005; Silver and Kastner, 2009; Swisher et al., 2007; Wandell et al., 2007).”
Lyon, D. C., & Connolly, J. D. (2011) · Proceedings of the Royal Society B Biological Sciences · doi:10.1098/rspb.2011.2048 · Cited by 35
Mapping the visual brain areas susceptible to phosphene induction through brain stimulation
Schaeffner, L. F., & Welchman, A. E. (2016) · Experimental Brain Research · doi:10.1007/s00221-016-4784-4 · Cited by 35
“The borders between functional areas were defined by the resulting angular maps (Wandell et al. 2007).”
BackgroundExploring structure and function of sensory cortex with 7 T MRI
Schluppeck, D., Sánchez-Panchuelo, R.-M., & Francis, S. (2017) · NeuroImage · doi:10.1016/j.neuroimage.2017.01.081 · Cited by 33
Structural reorganization of the early visual cortex following Braille training in sighted adults
Bola, Ł., Siuda-Krzywicka, K., Paplińska, M., Sumera, E., Zimmermann, M., Jednoróg, K., Marchewka, A., & Marcin Szwed, A. (2017) · Scientific Reports · doi:10.1038/s41598-017-17738-8 · Cited by 36
Time course of spatiotopic updating across saccades
Fabius, J., Fracasso, A., Nijboer, T., & van der Stigchel, S. (2019) · Proceedings of the National Academy of Sciences of the United States of America · doi:10.1073/pnas.1812210116 · Cited by 33
“However, given that the visual system is largely retinotopically organized (7), saccades repeatedly create temporal discontinuities and spatial instabilities in the retinotopic representations, posing a problem for continuity in visual processing.”
BackgroundGraded Size Sensitivity of Object-Exemplar–Evoked Activity Patterns Within Human LOC Subregions
Eger, E., Kell, C. A., & Kleinschmidt, A. K. (2008) · Journal of Neurophysiology · doi:10.1152/jn.90305.2008 · Cited by 34
Chang, Z., Bai, H., Zhang, L., Gupta, K., He, W., & Billinghurst, M. (2022) · Frontiers in Virtual Reality · doi:10.3389/frvir.2022.995090 · Cited by 35
“…lobe was proved to be related to selective attention (Behrmann et al., 2004) and occipital lobe was thought to be in charge of visual processing (Wandell et al., 2007), we expected to re fl ect this type of cognitive load with the signals captured from P3, P4, and Pz EEG sites located at…”
Metadata
- Authors
- Wandell, B. A., Dumoulin, S. O., & Brewer, A. A.
- Affiliations
- Stanford University (US)
- University of California, Irvine (US)
- Corresponding author
- Wandell, Brian A.
- Venue
- Neuron
- Publisher
- Elsevier BV
- Published
- 2007-10
- Volume
- 56
- Issue
- 2
- Pages
- 366-383
- ISSN
- 0896-6273 (ISSN-L)
- OpenAlex
- W2141073321
- Cited by
- 1,231
- References
- 179
- Citations by year
- 2026: 73 · 2025: 83 · 2024: 66 · 2023: 65 · 2022: 75 · 2021: 97 · 2020: 58 · 2019: 80 · 2018: 62 · 2017: 60 · 2016: 67 · 2015: 56 · 2014: 68 · 2013: 79 · 2012: 60
- FWCI
- 2.51
- Type
- journal article
- Language
- en
- Open access
- bronze
- doi.org
- Licence
- www.elsevier.com/tdm/userlicense/1.0/ (tdm)
- www.elsevier.com/legal/tdmrep-license (tdm)
- www.elsevier.com/open-access/userlicense/1.0/ (vor, 2152 d)
- doi.org/10.15223/policy-017 (stm-asf)
- doi.org/10.15223/policy-037 (stm-asf)
- doi.org/10.15223/policy-012 (stm-asf)
- doi.org/10.15223/policy-029 (stm-asf)
- doi.org/10.15223/policy-004 (stm-asf)
- Locations
- Neuron (publishedVersion)
- PubMed (publishedVersion)
- Funders
- Larry L. Hillblom Foundation
- National Eye Institute (RO1 EY03164)
- Topics
- Life Sciences › Neuroscience › Cognitive Neuroscience › Visual perception and processing mechanisms
- Life Sciences › Neuroscience › Cognitive Neuroscience › Face Recognition and Perception
- Physical Sciences › Computer Science › Computer Vision and Pattern Recognition › Visual Attention and Saliency Detection
- Keywords
- visual field maps, receptive fields, human visual cortex, lateral occipital cortex, posterior parietal cortex, functional MRI, visual system organization
- MeSH terms
- Animals, Brain Mapping, Humans, Magnetic Resonance Imaging, Models, Anatomic, Models, Neurological, Visual Cortex, Visual Fields
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