Visual field maps in human cortex.

Wandell, Brian A.; Dumoulin, Serge O.; Brewer, Alyssa A.

doi:10.1016/j.neuron.2007.10.012

Cited by 1,231Visual perception and processing mechanismsFace Recognition and PerceptionVisual Attention and Saliency Detection

Visual field maps in human cortex.

Open access

Wandell, Brian A., Dumoulin, Serge O., Brewer, Alyssa A.·2007·Neuron

DOI 10.1016/j.neuron.2007.10.012

Open this paper in CoChat — free account Open PDF

Abstract

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.

Integrity signals

Registry

Crossref · 10.1016/j.neuron.2007.10.012

Cites

174 of 174 references verified0 citation errors · 0 not checkable

Statistics

Recomputing p-values needs the paper’s full text.

Claims the paper makes

We couldn’t retrieve this paper’s full text, so its claims and self-check weren’t run. The registry and citation checks still apply.

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?

LOTS developmental changes probably reflect greater sensitivity to visual input from nearby ventral areas like hV4, VO1, and VO2.
“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
The circuits derived in the paper provide no explanation for observed cortical maps.
“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]

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 · see citing works
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 · see citing works
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 · see citing works
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 5,789 · see citing works
Two cortical visual systems
Ungerleider, L. G. (1982) · Medical Entomology and Zoology · Cited by 4,139 · see citing works
Analysis of visual behavior
Ingle, D., Goodale, M. A., & Mansfield, R. J. W. (1982) · Medical Entomology and Zoology · Cited by 4,131 · see citing works
Intrinsic signal changes accompanying sensory stimulation: functional brain mapping with magnetic resonance imaging.
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 · see citing works
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× · see citing works
“…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.,…”
The Visual Brain in Action
Milner, A. D., & Goodale, M. A. (2002) · The MIT Press eBooks · doi:10.7551/mitpress/7111.003.0023 · Cited by 3,345 · see citing works
Thomas, Springfield, Illinois
MAGOUN, H. N. (1965) · The Journal of Nervous and Mental Disease · doi:10.1097/00005053-196504000-00011 · Cited by 2,931 · see citing works
Borders of Multiple Visual Areas in Humans Revealed by Functional Magnetic Resonance Imaging
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. (1995) · Science · doi:10.1126/science.7754376 · Cited by 2,658 · see citing works
RECEPTIVE FIELDS AND FUNCTIONAL ARCHITECTURE IN TWO NONSTRIATE VISUAL AREAS (18 AND 19) OF THE CAT
Hubel, D. H., & Wiesel, T. N. (1965) · Journal of Neurophysiology · doi:10.1152/jn.1965.28.2.229 · Cited by 2,615 · see citing works
Oxygenation‐sensitive contrast in magnetic resonance image of rodent brain at high magnetic fields
Ogawa, S., Lee, T., Nayak, A. S., & Glynn, P. (1990) · Magnetic Resonance in Medicine · doi:10.1002/mrm.1910140108 · Cited by 2,269 · see citing works
Fiber Tract–based Atlas of Human White Matter Anatomy
Wakana, S., Jiang, H., Nagae‐Poetscher, L. M., van Zijl, P. C. M., & Mori, S. (2004) · Radiology · doi:10.1148/radiol.2301021640 · Cited by 2,023 · see citing works
Tracking neuronal fiber pathways in the living human brain
Conturo, T. E., Lori, N. F., Cull, T. S., Akbudak, E., Snyder, A. Z., Shimony, J. S., McKinstry, R. C., Burton, H., & Raichle, M. E. (1999) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.96.18.10422 · Cited by 1,774 · see citing works
Object-related activity revealed by functional magnetic resonance imaging in human occipital cortex.
Malach, R., Reppas, J. B., Benson, R. R., Kwong, K. K., Jiang, H., Kennedy, W. A., Ledden, P. J., Brady, T. J., Rosen, B. R., & Tootell, R. B. H. (1995) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.92.18.8135 · Cited by 1,761 · see citing works
A direct demonstration of functional specialization in human visual cortex
Zeki, S., Watson, J. D. G., Lueck, C. J., Friston, K. J., Christopher Kennard, C., & Frackowiak, R. S. J. (1991) · Journal of Neuroscience · doi:10.1523/jneurosci.11-03-00641.1991 · Cited by 1,717 · see citing works
Retinotopic organization in human visual cortex and the spatial precision of functional MRI
Engel, S. A. (1997) · Cerebral Cortex · doi:10.1093/cercor/7.2.181 · Cited by 1,606 · see citing works
Fiber tract-based atlas of human white matter anatomy
Wakana, S. (2006) · Medical Entomology and Zoology · Cited by 1,544 · see citing works
Perceptual Organization
Pittenger, J. B., Kubovy, M., & Pomerantz, J. R. (1982) · The American Journal of Psychology · doi:10.2307/1422146 · Cited by 1,424 · see citing works
Functional analysis of human MT and related visual cortical areas using magnetic resonance imaging
Tootell, R. B. H., Reppas, J. B., Kwong, K. K., Malach, R., Born, R. T., Brady, T., Rosen, B. R., & Belliveau, J. (1995) · Journal of Neuroscience · doi:10.1523/jneurosci.15-04-03215.1995 · Cited by 1,412 · see citing works
Two Visual Systems
Schneider, G. E. (1969) · Science · doi:10.1126/science.163.3870.895 · Cited by 1,389 · see citing works
Area V5 of the Human Brain: Evidence from a Combined Study Using Positron Emission Tomography and Magnetic Resonance Imaging
Watson, J. D. G., Myers, R., Frackowiak, R. S. J., Hajnal, J. V., Woods, R. P., Mazziotta, J. C., Shipp, S. D., & Zeki, S. (1993) · Cerebral Cortex · doi:10.1093/cercor/3.2.79 · Cited by 1,235 · see citing works
Untitled work
(1995) · Medical Entomology and Zoology · Cited by 1,212 · see citing works
THE HUMAN VISUAL CORTEX
Kalanit Grill-spector, A., & Malach, R. (2004) · Annual Review of Neuroscience · doi:10.1146/annurev.neuro.27.070203.144220 · Cited by 1,191 · see citing works
Population receptive field estimates in human visual cortex
Dumoulin, S. O., & Wandell, B. A. (2007) · NeuroImage · doi:10.1016/j.neuroimage.2007.09.034 · Cited by 1,183 · see citing works
Cortex: Statistics and Geometry of Neuronal Connectivity
Braitenberg, V., & Schüz, A. (1998) · doi:10.1007/978-3-662-03733-1 · Cited by 1,178 · cited 2× · see citing works
“The Size and Location of Human Visual Cortex Each hemisphere of human cortex spans a surface area on the order of 1000 cm(2) (Van Essen, 2007) and ranges between 2–4 mm in thickness (Blinkov and Glezer, 1968; Braitenberg and Schüz, 1998; Fischl and Dale, 2000).”
The sensations produced by electrical stimulation of the visual cortex
Brindley, G. S., & Lewin, W. S. (1968) · The Journal of Physiology · doi:10.1113/jphysiol.1968.sp008519 · Cited by 1,170 · cited 2× · see citing works
“Experiments in human showed that stimulation of primary visual cortex gave rise to a sensation at the location corresponding to the visual field map representation (Brindley and Lewin, 1968).”
Background
Cortical sources of the early components of the visual evoked potential
Russo, F. D., Martı́nez, A., Sereno, M. I., Pitzalis, S., & Hillyard, S. A. (2001) · Human Brain Mapping · doi:10.1002/hbm.10010 · Cited by 1,170 · see citing works
Differential Processing of Objects under Various Viewing Conditions in the Human Lateral Occipital Complex
Kalanit Grill-spector, A., Kushnir, T., Edelman, S., Avidan, G., Itzchak, Y., & Malach, R. (1999) · Neuron · doi:10.1016/s0896-6273(00)80832-6 · Cited by 1,156 · see citing works
A Population-Average, Landmark- and Surface-based (PALS) atlas of human cerebral cortex
Van Essen, D. C. (2005) · NeuroImage · doi:10.1016/j.neuroimage.2005.06.058 · Cited by 1,151 · see citing works
The representation of the visual field on the cerebral cortex in monkeys
Daniel, P. M., & Whitteridge, D. (1961) · The Journal of Physiology · doi:10.1113/jphysiol.1961.sp006803 · Cited by 1,147 · see citing works
Mapping striate and extrastriate visual areas in human cerebral cortex.
DeYoe, E. A., Carman, G. J., Bandettini, P. A., Glickman, S., Wieser, J., Cox, R. W., Miller, D. A., & Jay Neitz, A. (1996) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.93.6.2382 · Cited by 1,047 · see citing works
The visual neurosciences
Chalupa, L. M., Werner, J. S., & Barnstable, C. J. (2004) · Cited by 1,020 · see citing works
fMRI of human visual cortex
Engel, S. A., Rumelhart, D. E., Wandell, B. A., Lee, A. T.-J., Glover, G. H., Chichilnisky, E. J., & Shadlen, M. N. (1994) · Nature · doi:10.1038/369525a0 · Cited by 977 · see citing works
Hierarchical organization and functional streams in the visual cortex
Van Essen, D. C., & Maunsell, J. H. R. (1983) · Trends in Neurosciences · doi:10.1016/0166-2236(83)90167-4 · Cited by 962 · see citing works
The field topography of ERG components in man—I. The photopic luminance response
Sutter, E. E., & Tran, D. (1992) · Vision Research · doi:10.1016/0042-6989(92)90235-b · Cited by 949 · see citing works
Two mechanisms of vision in primates
Trevarthen, C. (1968) · Psychological Research · doi:10.1007/bf00422717 · Cited by 917 · see citing works
Cortical microstimulation influences perceptual judgements of motion direction
Salzman, C. D., Britten, K. H., & Newsome, W. T. (1990) · Nature · doi:10.1038/346174a0 · Cited by 881 · see citing works
Functional Analysis of V3A and Related Areas in Human Visual Cortex
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. (1997) · Journal of Neuroscience · doi:10.1523/jneurosci.17-18-07060.1997 · Cited by 818 · see citing works
The retinotopic organization of area 17 (striate cortex) in the cat
Tusa, R. J., Palmer, L. A., & Rosenquist, A. C. (1978) · The Journal of Comparative Neurology · doi:10.1002/cne.901770204 · Cited by 736 · see citing works
The Representation of the Visual Field in Human Striate Cortex
Horton, J. C. (1991) · Archives of Ophthalmology · doi:10.1001/archopht.1991.01080060080030 · Cited by 715 · see citing works
The Retinotopy of Visual Spatial Attention
Tootell, R. B. H., Hadjikhani, N. K., Hall, E., Marrett, S., Vanduffel, W., Vaughan, J. T., & Dale, A. M. (1998) · Neuron · doi:10.1016/s0896-6273(00)80659-5 · Cited by 714 · see citing works
Center–periphery organization of human object areas
Levy, I., Hasson, U., Avidan, G., Hendler, T., & Malach, R. (2001) · Nature Neuroscience · doi:10.1038/87490 · Cited by 687 · see citing works
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 · see citing works
Visuotopic organization and extent of V3 and V4 of the macaque
Gattass, R., Sousa, A., & Gross, C. (1988) · The Journal of Neuroscience · doi:10.1523/jneurosci.08-06-01831.1988 · Cited by 676 · see citing works
Microstimulation in visual area MT: effects on direction discrimination performance
Salzman, C., Murasugi, C., Britten, K., & Newsome, W. (1992) · The Journal of Neuroscience · doi:10.1523/jneurosci.12-06-02331.1992 · Cited by 657 · see citing works
Brodmann's Areas 17 and 18 Brought into Stereotaxic Space—Where and How Variable?
Amunts, K., Maliković, A., Mohlberg, H., Schormann, T., & Zilles, K. (2000) · NeuroImage · doi:10.1006/nimg.1999.0516 · Cited by 640 · see citing works
Spatial mapping in the primate sensory projection: Analytic structure and relevance to perception
Schwartz, E. (1977) · Biological Cybernetics · doi:10.1007/bf01885636 · Cited by 629 · see citing works
Organization of visual inputs to the inferior temporal and posterior parietal cortex in macaques
Baizer, J. S., Ungerleider, L. G., & Desimone, R. (1991) · Journal of Neuroscience · doi:10.1523/jneurosci.11-01-00168.1991 · Cited by 626 · see citing works
Retinotopy and Functional Subdivision of Human Areas MT and MST
Huk, A. C., Dougherty, R. F., & Heeger, D. J. (2002) · Journal of Neuroscience · doi:10.1523/jneurosci.22-16-07195.2002 · Cited by 614 · see citing works
Topographical Variation of the Human Primary Cortices: Implications for Neuroimaging, Brain Mapping, and Neurobiology
Rademacher, J., Caviness, V. S., Steinmetz, H., & Galaburda, A. M. (1993) · Cerebral Cortex · doi:10.1093/cercor/3.4.313 · Cited by 612 · see citing works
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 · see citing works
Magnetic resonance imaging of blood vessels at high fields: In vivo and in vitro measurements and image simulation
Ogawa, S., & Lee, T. (1990) · Magnetic Resonance in Medicine · doi:10.1002/mrm.1910160103 · Cited by 565 · see citing works
Two Retinotopic Visual Areas in Human Lateral Occipital Cortex
Larsson, J. T., & Heeger, D. J. (2006) · Journal of Neuroscience · doi:10.1523/jneurosci.1657-06.2006 · Cited by 564 · see citing works
DISTURBANCES OF VISION BY CEREBRAL LESIONS
Holmes, G. (1918) · British Journal of Ophthalmology · doi:10.1136/bjo.2.7.353 · Cited by 552 · see citing works
Divide and conquer: A defense of functional localizers
Saxe, R., Brett, M., & Kanwisher, N. (2006) · NeuroImage · doi:10.1016/j.neuroimage.2005.12.062 · Cited by 544 · see citing works
Visual field representations and locations of visual areas V1/2/3 in human visual cortex
Dougherty, R. F., Koch, V. M., Brewer, A. A., Fischer, B., Jan Modersitzki, C., & Wandell, B. A. (2003) · Journal of Vision · doi:10.1167/3.10.1 · Cited by 538 · see citing works
A representation of the visual field in the caudal third of the middle tempral gyrus of the owl monkey (Aotus trivirgatus).
Allman, J., & Kaas, J. (1971) · Brain Research · doi:10.1016/0006-8993(71)90635-4 · Cited by 525 · see citing works
Retinotopy and color sensitivity in human visual cortical area V8
Hadjikhani, N. K., Liu, A. K., Dale, A. M., Cavanagh, P., & Tootell, R. B. H. (1998) · Nature Neuroscience · doi:10.1038/681 · Cited by 525 · see citing works
Bypassing V1: a direct geniculate input to area MT
Sincich, L. C., Park, K. F., Wohlgemuth, M. J., & Horton, J. C. (2004) · Nature Neuroscience · doi:10.1038/nn1318 · Cited by 496 · see citing works
Visual Motion Processing Investigated Using Contrast Agent-Enhanced fMRI in Awake Behaving Monkeys
Vanduffel, W., Fize, D., Mandeville, J. B., Nelissen, K., Hecke, P. V., Rosen, B. R., Tootell, R. B. H., & Orban, G. A. (2001) · Neuron · doi:10.1016/s0896-6273(01)00502-5 · Cited by 492 · see citing works
A New Anatomical Landmark for Reliable Identification of Human Area V5/MT: a Quantitative Analysis of Sulcal Patterning
Dumoulin, S. O. (2000) · Cerebral Cortex · doi:10.1093/cercor/10.5.454 · Cited by 483 · see citing works
Topographic Maps of Visual Spatial Attention in Human Parietal Cortex
Silver, M. A., Ress, D. B., & Heeger, D. J. (2005) · Journal of Neurophysiology · doi:10.1152/jn.01316.2004 · Cited by 482 · see citing works
Objective analysis of the topological organization of the primate cortical visual system
Young, M. P. (1992) · Nature · doi:10.1038/358152a0 · Cited by 466 · see citing works
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 · see citing works
Visual Topography of Human Intraparietal Sulcus
Swisher, J. D., Halko, M. A., Merabet, L. B., McMains, S. A., & Somers, D. C. (2007) · Journal of Neuroscience · doi:10.1523/jneurosci.0991-07.2007 · Cited by 456 · see citing works
Physiological Studies on Neural Mechanisms of Visual Localization and Discrimination
Talbot, S. A., & Marshall, W. H. (1941) · American Journal of Ophthalmology · doi:10.1016/s0002-9394(41)91363-6 · Cited by 451 · see citing works
Visual field maps and stimulus selectivity in human ventral occipital cortex
Brewer, A. A., Liu, J. V., Wade, A. R., & Wandell, B. A. (2005) · Nature Neuroscience · doi:10.1038/nn1507 · Cited by 430 · see citing works
A critique of functional localisers
Friston, K. J., Rotshtein, P., Geng, J. J., Sterzer, P., & Henson, R. N. (2006) · NeuroImage · doi:10.1016/j.neuroimage.2005.08.012 · Cited by 424 · see citing works
The topography and variability of the primary visual cortex in man
Stensaas, S. S., Eddington, D. K., & Dobelle, W. H. (1974) · Journal of neurosurgery · doi:10.3171/jns.1974.40.6.0747 · Cited by 420 · see citing works
Representation of central visual fields in prestriate cortex of monkey
Zeki, S. (1969) · Brain Research · doi:10.1016/0006-8993(69)90110-3 · Cited by 414 · see citing works
The Human Brain in Figures and Tables
Snider, R. S. (1969) · Neurology · doi:10.1212/wnl.19.7.714-a · Cited by 400 · see citing works
The position and topography of the human colour centre as revealed by functional magnetic resonance imaging
McKeefry, D. J. (1997) · Brain · doi:10.1093/brain/120.12.2229 · Cited by 386 · see citing works
Cortical structure predicts the pattern of corticocortical connections
Barbas, H. (1997) · Cerebral Cortex · doi:10.1093/cercor/7.7.635 · Cited by 382 · see citing works
Correlated Size Variations in Human Visual Cortex, Lateral Geniculate Nucleus, and Optic Tract
Andrews, T. J., Halpern, S. D., & Purves, D. (1997) · Journal of Neuroscience · doi:10.1523/jneurosci.17-08-02859.1997 · Cited by 380 · see citing works
The Processing of First- and Second-Order Motion in Human Visual Cortex Assessed by Functional Magnetic Resonance Imaging (fMRI)
Smith, A. T., Greenlee, M. W., Singh, K. D., Kraemer, F. M., & Hennig, J. (1998) · Journal of Neuroscience · doi:10.1523/jneurosci.18-10-03816.1998 · Cited by 370 · see citing works
Retinotopic organization of human visual cortex mapped with positron- emission tomography
Fox, P. T., Miezin, F. M., Allman, J. M., Essen, D. C. V., & Raichle, M. E. (1987) · Journal of Neuroscience · doi:10.1523/jneurosci.07-03-00913.1987 · Cited by 364 · see citing works
Estimating Receptive Field Size from fMRI Data in Human Striate and Extrastriate Visual Cortex
Smith, A. T. (2001) · Cerebral Cortex · doi:10.1093/cercor/11.12.1182 · Cited by 357 · see citing works
Inverse retinotopy: Inferring the visual content of images from brain activation patterns
Thirion, B., Duchesnay, É., Hubbard, E. M., Dubois, J., Poline, J., Bihan, D. L., & Dehaene, S. (2006) · NeuroImage · doi:10.1016/j.neuroimage.2006.06.062 · Cited by 356 · see citing works
Exploring the Thalamus
(2001) · Elsevier eBooks · doi:10.1016/b978-0-12-305460-9.x5013-8 · Cited by 355 · see citing works
Evolution of Nervous Systems
Hirth, F., & Reichert, H. (2007) · Cited by 355 · see citing works
Three-dimensional statistical analysis of sulcal variability in the human brain
Thompson, P. M., Schwartz, C., Lin, R. T., Khan, A. A., & Toga, A. W. (1996) · The Journal of Neuroscience · doi:10.1523/jneurosci.16-13-04261.1996 · Cited by 346 · see citing works
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 · see citing works
Laminar distribution of neurons in extrastriate areas projecting to visual areas V1 and V4 correlates with the hierarchical rank and indicates the operation of a distance rule
Barone, P., Batardiere, A., Knoblauch, K., & Kennedy, H. (2000) · The Journal of Neuroscience · doi:10.1523/jneurosci.20-09-03263.2000 · Cited by 300 · see citing works
The cerebral cortex
CARPENTER, M. B. (1976) · Cited by 295 · see citing works
PROJECTION OF THE RETINA ON TO STRIATE AND PRESTRIATE CORTEX IN THE SQUIRREL MONKEY, SAIMIRI SCIUREUS
Cowey, A. (1964) · Journal of Neurophysiology · doi:10.1152/jn.1964.27.3.366 · Cited by 293 · see citing works
Modulation of Sensory Suppression: Implications for Receptive Field Sizes in the Human Visual Cortex
Kästner, S., Weerd, P. D., Pinsk, M. A., Elizondo, M. I., Desimone, R., & Ungerleider, L. G. (2001) · Journal of Neurophysiology · doi:10.1152/jn.2001.86.3.1398 · Cited by 289 · see citing works
Distinguishing Subregions of the Human MT+ Complex Using Visual Fields and Pursuit Eye Movements
Dukelow, S. P., DeSouza, J. F. X., Culham, J. C., van den Berg, A. V., Menon, R. S., & Vilis, T. (2001) · Journal of Neurophysiology · doi:10.1152/jn.2001.86.4.1991 · Cited by 289 · see citing works
Visual field map clusters in human cortex
Wandell, B. A., Brewer, A. A., & Dougherty, R. F. (2005) · Philosophical Transactions of the Royal Society B Biological Sciences · doi:10.1098/rstb.2005.1628 · Cited by 284 · see citing works
Wide-Field Retinotopy Defines Human Cortical Visual Area V6
Pitzalis, S., Galletti, C., Huang, R., Patria, F., Committeri, G., Galati, G., Fattori, P., & Sereno, M. I. (2006) · Journal of Neuroscience · doi:10.1523/jneurosci.0178-06.2006 · Cited by 271 · see citing works
Efficient Design of Event-Related fMRI Experiments Using M-Sequences
Buračas, G. T., & Boynton, G. M. (2002) · NeuroImage · doi:10.1006/nimg.2002.1116 · Cited by 271 · see citing works
Topographic Organization for Delayed Saccades in Human Posterior Parietal Cortex
Schluppeck, D., Glimcher, P. W., & Heeger, D. J. (2005) · Journal of Neurophysiology · doi:10.1152/jn.01290.2004 · Cited by 263 · see citing works
Where is 'Dorsal V4' in Human Visual Cortex? Retinotopic, Topographic and Functional Evidence
Tootell, R. B. H. (2001) · Cerebral Cortex · doi:10.1093/cercor/11.4.298 · Cited by 255 · see citing works
Anatomical Evidence for MT and Additional Cortical Visual Areas in Humans
Tootell, R. B. H., & Taylor, J. B. (1995) · Cerebral Cortex · doi:10.1093/cercor/5.1.39 · Cited by 253 · see citing works
Functional measurements of human ventral occipital cortex: retinotopy and colour
Wade, A. R., Brewer, A. A., Rieger, J. W., & Wandell, B. A. (2002) · Philosophical Transactions of the Royal Society B Biological Sciences · doi:10.1098/rstb.2002.1108 · Cited by 253 · see citing works
The cortical deficit in humans with strabismic amblyopia
Barnes, G. R., Hess, R. F., Dumoulin, S. O., Achtman, R. L., & Pike, G. B. (2001) · The Journal of Physiology · doi:10.1111/j.1469-7793.2001.0281b.x · Cited by 250 · see citing works
Visual Field Defects After Penetrating Missile Wounds of the Brain.
(1962) · Archives of Ophthalmology · doi:10.1001/archopht.1962.00960020113017 · Cited by 248 · see citing works
High‐resolution MRI reflects myeloarchitecture and cytoarchitecture of human cerebral cortex
Eickhoff, S. B., Walters, N. B., Schleicher, A., Kril, J. J., Egan, G. F., Zilles, K., Watson, J. D. G., & Amunts, K. (2004) · Human Brain Mapping · doi:10.1002/hbm.20082 · Cited by 243 · see citing works
Orientation-Selective Adaptation to First- and Second-Order Patterns in Human Visual Cortex
Larsson, J. T., Landy, M. S., & Heeger, D. J. (2005) · Journal of Neurophysiology · doi:10.1152/jn.00668.2005 · Cited by 236 · see citing works
Spatial maps in frontal and prefrontal cortex
Hagler, D. J., & Sereno, M. I. (2005) · NeuroImage · doi:10.1016/j.neuroimage.2005.08.058 · Cited by 235 · see citing works
Brain maps, great and small: lessons from comparative studies of primate visual cortical organization
Rosa, M. G. P., & Tweedale, R. (2005) · Philosophical Transactions of the Royal Society B Biological Sciences · doi:10.1098/rstb.2005.1626 · Cited by 230 · see citing works
Sensitivity to optic flow in human cortical areas MT and MST
Smith, A. T., Wall, M. B., Williams, A. L., & Singh, K. D. (2006) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.2005.04526.x · Cited by 229 · see citing works
Functional Demarcation of a Border Between Areas V6 and V6A in the Superior Parietal Gyrus of the Macaque Monkey
Galletti, C., Fattori, P., Battaglini, P. P., Shipp, S. D., & Zeki, S. (1996) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.1996.tb01165.x · Cited by 229 · see citing works
The cortical visual area V6: brain location and visual topography
Galletti, C., Fattori, P., Gamberini, M., & Kutz, D. F. (1999) · European Journal of Neuroscience · doi:10.1046/j.1460-9568.1999.00817.x · Cited by 225 · see citing works
Visual Areas in Macaque Cortex Measured Using Functional Magnetic Resonance Imaging
Brewer, A. A., Press, W., Logothetis, N. K., & Wandell, B. A. (2002) · Journal of Neuroscience · doi:10.1523/jneurosci.22-23-10416.2002 · Cited by 219 · see citing works
Functional topographic mapping of the cortical ribbon in human vision with conventional MRI scanners
Schneider, W., Noll, D. C., & Cohen, J. D. (1993) · Nature · doi:10.1038/365150a0 · Cited by 214 · see citing works
LOCALIZATION OF FUNCTION IN THE CEREBRAL CORTEX: PAST, PRESENT AND FUTURE
Phillips, C. G., Zeki, S., & Barlow, H. B. (1984) · Brain · doi:10.1093/brain/107.1.328 · Cited by 209 · see citing works
Perceptual-cognitive universals as reflections of the world
Shepard, R. N. (2001) · Behavioral and Brain Sciences · doi:10.1017/s0140525x01000012 · Cited by 209 · see citing works
fMRI Retinotopic Mapping—Step by Step
Warnking, J. M. (2002) · NeuroImage · doi:10.1006/nimg.2002.1304 · Cited by 208 · see citing works
Topographic Maps in Human Frontal Cortex Revealed in Memory-Guided Saccade and Spatial Working-Memory Tasks
Kästner, S., DeSimone, K., Konen, C. S., Szczepanski, S. M., Weiner, K. S., & Schneider, K. A. (2007) · Journal of Neurophysiology · doi:10.1152/jn.00010.2007 · Cited by 203 · see citing works
Contrast Adaptation and Representation in Human Early Visual Cortex
Gardner, J. L., Sun, P., Waggoner, R. A., Ueno, K., Tanaka, K., & Cheng, K. (2005) · Neuron · doi:10.1016/j.neuron.2005.07.016 · Cited by 202 · see citing works
Organization of visual areas in macaque and human cerebral cortex
Essen, D. C. V. (2003) · Medical Entomology and Zoology · Cited by 202 · see citing works
Anatomical and physiological asymmetries related to visual areas V3 and VP in macaque extrastriate cortex
Burkhalter, A., Felleman, D. J., Newsome, W. T., & Essen, D. C. V. (1986) · Vision Research · doi:10.1016/0042-6989(86)90071-4 · Cited by 200 · see citing works
Functional organization of human occipital-callosal fiber tracts
Dougherty, R. F., Ben‐Shachar, M., Bammer, R., Brewer, A. A., & Wandell, B. A. (2005) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0500003102 · Cited by 200 · see citing works
Visual areas and spatial summation in human visual cortex
Press, W., Brewer, A. A., Dougherty, R. F., Wade, A. R., & Wandell, B. A. (2001) · Vision Research · doi:10.1016/s0042-6989(01)00074-8 · Cited by 194 · see citing works
Parietal and superior frontal visuospatial maps activated by pointing and saccades
Hagler, D. J., Riecke, L., & Sereno, M. I. (2007) · NeuroImage · doi:10.1016/j.neuroimage.2007.01.033 · Cited by 182 · see citing works
VISUAL AREAS I AND II OF CEREBRAL CORTEX OF RABBIT
Thompson, J. M., Woolsey, C. N., & Talbot, S. A. (1950) · Journal of Neurophysiology · doi:10.1152/jn.1950.13.4.277 · Cited by 182 · see citing works
Ventral visual cortex in humans: Cytoarchitectonic mapping of two extrastriate areas
Rottschy, C., Eickhoff, S. B., Schleicher, A., Mohlberg, H., Kujovic, M., Zilles, K., & Amunts, K. (2007) · Human Brain Mapping · doi:10.1002/hbm.20348 · Cited by 173 · see citing works
Reorganization of human cortical maps caused by inherited photoreceptor abnormalities
Baseler, H. A., Brewer, A. A., Sharpe, L. T., Morland, A. B., Jägle, H., & Wandell, B. A. (2002) · Nature Neuroscience · doi:10.1038/nn817 · Cited by 172 · see citing works
Topographic Organization in and near Human Visual Area V4
Hansen, K. A., Kay, K., & Gallant, J. L. (2007) · Journal of Neuroscience · doi:10.1523/jneurosci.2991-07.2007 · Cited by 170 · see citing works
Spatiotopic selectivity of BOLD responses to visual motion in human area MT
d’Avossa, G., Tosetti, M., Crespi, S. A., Biagi, L., Burr, D. C., & Morrone, M. C. (2006) · Nature Neuroscience · doi:10.1038/nn1824 · Cited by 166 · see citing works
The Retinotopic Organization of Primate Dorsal V4 and Surrounding Areas: A Functional Magnetic Resonance Imaging Study in Awake Monkeys
Fize, D., Vanduffel, W., Nelissen, K., Denys, K., d'Hotel, C. C., Faugeras, O. D., & Orban, G. A. (2003) · Journal of Neuroscience · doi:10.1523/jneurosci.23-19-07395.2003 · Cited by 165 · see citing works
The Encyclopedia of life sciences
(2002) · Choice Reviews Online · doi:10.5860/choice.39-6158 · Cited by 165 · see citing works
Combined Activation and Deactivation of Visual Cortex During Tactile Sensory Processing
Merabet, L. B., Swisher, J. D., McMains, S. A., Halko, M. A., Amedi, A., Pascual‐Leone, Á., & Somers, D. C. (2006) · Journal of Neurophysiology · doi:10.1152/jn.00806.2006 · Cited by 158 · see citing works
Real-Time Optical Mapping of Neuronal Activity: From Single Growth Cones to the Intact Mammalian Brain
Grinvald, A. (1985) · Annual Review of Neuroscience · doi:10.1146/annurev.ne.08.030185.001403 · Cited by 155 · see citing works
Cortical visual areas in monkeys: location, topography, connections, columns, plasticity and cortical dynamics
Gattass, R., Nascimento‐Silva, S., Soares, J. G. M., Lima, B., Jansen, A. K., DIOGO, A. C. M., Farias, M. F., Marcondes, E. P. B. M., Mariani, O. S. C., Azzi, J. C. B., et al. (2005) · Philosophical Transactions of the Royal Society B Biological Sciences · doi:10.1098/rstb.2005.1629 · Cited by 155 · see citing works
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 · see citing works
Topographic Organization of Human Visual Areas in the Absence of Input from Primary Cortex
Baseler, H. A., Morland, A. B., & Wandell, B. A. (1999) · Journal of Neuroscience · doi:10.1523/jneurosci.19-07-02619.1999 · Cited by 141 · see citing works
Convergent input from the striate cortex (area 17) to the cortex of the superior temporal sulcus in the rhesus monkey
Zeki, S. (1971) · Brain Research · doi:10.1016/0006-8993(71)90665-2 · Cited by 140 · see citing works
Retinotopic mapping of the visual cortex using functional magnetic resonance imaging in a patient with central scotomas from atrophic macular degeneration
Sunness, J. S., Liu, T., & Yantis, S. (2004) · Ophthalmology · doi:10.1016/j.ophtha.2003.12.050 · Cited by 135 · see citing works
A motion area in human visual cortex.
Orban, G. A., Dupont, P. J., Bruyn, B. D., Vogels, R., Vandenberghe, R. R., & Mortelmans, L. (1995) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.92.4.993 · Cited by 133 · see citing works
Die Sehstörungen bei Schußverletzungen der kortikalen Sehsphäre : nach Beobachtungen an Verwundeten der letzten japanischen Kriege
Inouye, T. (1909) · W. Engelmann eBooks · Cited by 130 · see citing works
Two-Dimensional Mapping of the Central and Parafoveal Visual Field to Human Visual Cortex
Schira, M. M., Wade, A. R., & Tyler, C. W. (2007) · Journal of Neurophysiology · doi:10.1152/jn.00972.2006 · Cited by 125 · see citing works
Independent anatomical and functional measures of the V1/V2 boundary in human visual cortex
Bridge, H., Clare, S., Jenkinson, M., Jezzard, P., Parker, A. J., & Matthews, P. M. (2005) · Journal of Vision · doi:10.1167/5.2.1 · Cited by 125 · see citing works
Human MST But Not MT Responds to Tactile Stimulation
Beauchamp, M. S., Yasar, N. E., Kishan, N., & Ro, T. (2007) · Journal of Neuroscience · doi:10.1523/jneurosci.0754-07.2007 · Cited by 118 · see citing works
Specializations for Chromatic and Temporal Signals in Human Visual Cortex
Liu, J. V., & Wandell, B. A. (2005) · Journal of Neuroscience · doi:10.1523/jneurosci.4206-04.2005 · Cited by 117 · see citing works
Evidence for a Modified V3 with Dorsal and Ventral Halves in Macaque Monkeys
Lyon, D. C., & Kaas, J. H. (2002) · Neuron · doi:10.1016/s0896-6273(02)00580-9 · Cited by 112 · see citing works
LOCALIZATION OF FUNCTION IN THE CEREBRAL CORTEX
Jefferson, G. (1950) · British Medical Bulletin · doi:10.1093/oxfordjournals.bmb.a073626 · Cited by 102 · see citing works
Improbable areas in the visual brain
Zeki, S. (2002) · Trends in Neurosciences · doi:10.1016/s0166-2236(02)00008-5 · Cited by 95 · see citing works
Retinotopic Maps in Human Prestriate Visual Cortex: The Demarcation of Areas V2 and V3
Shipp, S. D., Watson, J. D. G., Frackowiak, R. S. J., & Zeri, S. (1995) · NeuroImage · doi:10.1006/nimg.1995.1015 · Cited by 92 · see citing works
Human V5/MT+: comparison of functional and cytoarchitectonic data
Wilms, M., Eickhoff, S. B., Specht, K., Amunts, K., Shah, N. J., Maliković, A., & Fink, G. R. (2005) · Anatomy and Embryology · doi:10.1007/s00429-005-0064-y · Cited by 90 · see citing works
Beyond retinotopic mapping: the spatial representation of objects in the human lateral occipital complex
McKyton, A., & Zohary, E. (2007) · Cerebral Cortex · doi:10.1093/cercor/bhl027 · Cited by 88 · cited 3× · see citing works
“It may be, however, that responses in retinotopic maps can be influenced by eye position (DeSouza et al., 2002; McKyton and Zohary, 2007).”
Parametric reverse correlation reveals spatial linearity of retinotopic human V1 BOLD response
Hansen, K. A., David, S. V., & Gallant, J. L. (2004) · NeuroImage · doi:10.1016/j.neuroimage.2004.05.012 · Cited by 87 · see citing works
Surface‐Based Atlases of Cerebellar Cortex in the Human, Macaque, and Mouse
Essen, D. C. V. (2002) · Annals of the New York Academy of Sciences · doi:10.1111/j.1749-6632.2002.tb07588.x · Cited by 85 · see citing works
Orientation-Selective Adaptation to Illusory Contours in Human Visual Cortex
Montaser‐Kouhsari, L., Landy, M. S., Heeger, D. J., & Larsson, J. T. (2007) · Journal of Neuroscience · doi:10.1523/jneurosci.4173-06.2007 · Cited by 83 · see citing works
Parallelism and Functional Specialization in Human Visual CortexPreprint
Zeki, S. M. (1990) · Cold Spring Harbor Symposia on Quantitative Biology · doi:10.1101/sqb.1990.055.01.062 · Cited by 82 · see citing works
Multifocal fMRI mapping of visual cortical areas
Vanni, S., Henriksson, L., & James, A. C. (2005) · NeuroImage · doi:10.1016/j.neuroimage.2005.01.046 · Cited by 80 · see citing works
Linking retinotopic fMRI mapping and anatomical probability maps of human occipital areas V1 and V2
Wohlschläger, A., Specht, K., Lie, C., Mohlberg, H., Wohlschläger, A., Bente, K., Pietrzyk, U., Stöcker, T., Zilles, K., Amunts, K., et al. (2005) · NeuroImage · doi:10.1016/j.neuroimage.2005.01.021 · Cited by 79 · see citing works
Estimating linear cortical magnification in human primary visual cortex via dynamic programming
Qiu, A., Tamber-Rosenau, B. J., Greenberg, A. S., Hurdal, M. K., Barta, P. E., Yantis, S., & Miller, M. I. (2006) · NeuroImage · doi:10.1016/j.neuroimage.2005.11.049 · Cited by 79 · see citing works
ON THE VISUAL PATH AND CENTRE
Henschen, S. E. (1893) · Brain · doi:10.1093/brain/16.1-2.170 · Cited by 78 · see citing works
Abnormal retinotopic representations in human visual cortex revealed by fMRI
Morland, A. B., Baseler, H. A., Hoffmann, M. B., Sharpe, L. T., & Wandell, B. A. (2001) · Acta Psychologica · doi:10.1016/s0001-6918(01)00025-7 · Cited by 76 · see citing works
Extended Concepts of Occipital Retinotopy
Tyler, C. W., Likova, L. T., Chen, C., Kontsevich, L. L., Schira, M. M., & Wade, A. R. (2005) · Current Medical Imaging Formerly Current Medical Imaging Reviews · doi:10.2174/157340505774574772 · Cited by 67 · see citing works
The projections to the superior temporal sulcus from areas 17 and 18 in the rhesus monkey
Zeki, S. (1976) · Proceedings of the Royal Society B Biological Sciences · doi:10.1098/rspb.1976.0040 · Cited by 67 · see citing works
Automatic volumetric segmentation of human visual retinotopic cortex
Dumoulin, S. O., Hoge, R. D., Baker, C. L., Hess, R. F., Achtman, R. L., & Evans, A. C. (2003) · NeuroImage · doi:10.1016/s1053-8119(02)00058-7 · Cited by 66 · see citing works
Gordon Holmes, the cortical retina, and the wounds of war
Fishman, R. S. (1997) · Documenta Ophthalmologica · doi:10.1007/bf02569044 · Cited by 66 · see citing works
The fidelity of the cortical retinotopic map in human amblyopia
Li, X., Dumoulin, S. O., Mansouri, B., & Hess, R. F. (2007) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.2007.05356.x · Cited by 57 · see citing works
Eye Position Signals Modulate Early Dorsal and Ventral Visual Areas
DeSouza, J. F. X. (2002) · Cerebral Cortex · doi:10.1093/cercor/12.9.991 · Cited by 56 · see citing works
Visual Function and Brain Organization in Non-decussating Retinal-Fugal Fibre Syndrome
Victor, J. D. (2000) · Cerebral Cortex · doi:10.1093/cercor/10.1.2 · Cited by 55 · see citing works
The V1–V2–V3 complex: quasiconformal dipole maps in primate striate and extra-striate cortex
Balasubramanian, M., Polimeni, J. R., & Schwartz, E. L. (2002) · Neural Networks · doi:10.1016/s0893-6080(02)00094-1 · Cited by 55 · see citing works
Occipital sulci of the human brain: Variability and probability maps
Iaria, G., & Petrides, M. (2007) · The Journal of Comparative Neurology · doi:10.1002/cne.21254 · Cited by 52 · see citing works
Localization of the Human Cortical Visual Area MT Based on Computer Aided Histological Analysis
Annese, J., Gazzaniga, M. S., & Toga, A. W. (2004) · Cerebral Cortex · doi:10.1093/cercor/bhh205 · Cited by 50 · see citing works
High-resolution MRI: in vivo histology?
Bridge, H., & Clare, S. (2005) · Philosophical Transactions of the Royal Society B Biological Sciences · doi:10.1098/rstb.2005.1777 · Cited by 49 · see citing works
Independent anatomical and functional measures of the V1/V2 boundary in human visual cortex.
Bridge, H., Clare, S., Jenkinson, M., Jezzard, P., Parker, A. J., & Matthews, P. M. (2005) · Journal of Visualization · Cited by 48 · see citing works
Representation of Head-Centric Flow in the Human Motion Complex
Goossens, J., Dukelow, S. P., Menon, R. S., Vilis, T., & van den Berg, A. V. (2006) · Journal of Neuroscience · doi:10.1523/jneurosci.0730-06.2006 · Cited by 47 · see citing works
Visual Cortex in Humans
Wandell, B. A., Dumoulin, S. O., & Brewer, A. A. (2009) · Elsevier eBooks · doi:10.1016/b978-008045046-9.00241-2 · Cited by 40 · see citing works
fMRI of peripheral visual field representation
Stenbacka, L., & Vanni, S. (2007) · Clinical Neurophysiology · doi:10.1016/j.clinph.2007.01.023 · Cited by 33 · see citing works
Visual Field Defects after Penetrating Missile Wounds of the Brain
Zeigler, H. P., Teuber, H., Battersby, W. S., & Bender, M. B. (1961) · The American Journal of Psychology · doi:10.2307/1419762 · Cited by 30 · see citing works
Neurofilament protein expression in the geniculostriate pathway of a New World monkey (Callithrix jacchus)
Bourne, J. A., & Rosa, M. G. P. (2003) · Experimental Brain Research · doi:10.1007/s00221-003-1397-5 · Cited by 27 · see citing works
Interindividual and interspecies variations of the extrastriate visual cortex
Ejima, Y., Takahashi, S., Yamamoto, H., Fukunaga, M., Tanaka, C., Ebisu, T., & Umeda, M. (2003) · Neuroreport · doi:10.1097/00001756-200308260-00008 · Cited by 27 · see citing works
Computational Neuroimaging : Color Signals in the Visual Pathways
Wandell, B. A., Dumoulin, S. O., & Brewer, A. A. (2006) · 神経眼科 = Neuro-ophthalmology Japan · Cited by 8 · see citing works
Neocortical neuron number in humans: Effect of sex and age
(1997) · doi:10.1002/(sici)1096-9861(19970728)384:2
Untitled work
Bush (1998) · doi:10.1002/(sici)1097-0193(1998)6:4
Auditory and visual word processing studied with fMRI
(1999) · doi:10.1002/(sici)1097-0193(1999)7:1

Flagged first, then by citations

5 of the 179 references couldn’t be matched to a known paper.

Sorted by citations

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 · see citing works
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 · see citing works
Local-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 · see citing works
“Intriguingly, LO1 and LO2, which are in the same visual field map clusters (Wandell et al. 2007), appeared to be grouped together, although also fractionated, possibly also based on visual eccentricity organization (c.”
Background
Identifying natural images from human brain activity
Kay, K., Naselaris, T., Prenger, R., & Gallant, J. L. (2008) · Nature · doi:10.1038/nature06713 · Cited by 1,272 · see citing works
The ventral visual pathway: an expanded neural framework for the processing of object quality
Kravitz, D. J., Saleem, K. S., Baker, C. I., Ungerleider, L. G., & Mishkin, M. (2012) · Trends in Cognitive Sciences · doi:10.1016/j.tics.2012.10.011 · Cited by 1,154 · see citing works
Steady-state visually evoked potentials: Focus on essential paradigms and future perspectives
Vialatte, F.-B., Maurice, M., Dauwels, J., & Cichocki, A. (2010) · Progress in Neurobiology · doi:10.1016/j.pneurobio.2009.11.005 · Cited by 1,066 · see citing works
The Distributed Nature of Working Memory
Christophel, T. B., Klink, P. C., Spitzer, B., Roelfsema, P. R., & Haynes, J.-D. (2017) · Trends in Cognitive Sciences · doi:10.1016/j.tics.2016.12.007 · Cited by 882 · see citing works
The evolution of distributed association networks in the human brain
Buckner, R. L., & Krienen, F. M. (2013) · Trends in Cognitive Sciences · doi:10.1016/j.tics.2013.09.017 · Cited by 836 · see citing works
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 · see citing works
“The spatial receptive fields of individual voxels were spatially localized (Figures 2F and 2G, left) and were organized retinotopically (Figures 2H and 2I), as reported in previous fMRI studies [12, 19–23].”
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 · see citing works
Alpha-Beta and Gamma Rhythms Subserve Feedback and Feedforward Influences among Human Visual Cortical Areas
Michalareas, G., Vezoli, J., van Pelt, S., Schoffelen, J.-M., Kennedy, H., & Fries, P. (2016) · Neuron · doi:10.1016/j.neuron.2015.12.018 · Cited by 696 · see citing works
“Therein, they are jointly referred to as the “V3A complex” and they represent the same cortical areas previously referred to as V3A and V3B (Wandell et al., 2007).”
Probabilistic Maps of Visual Topography in Human Cortex
Wang, L., Mruczek, R. E. B., Arcaro, M. J., & Kästner, S. (2014) · Cerebral Cortex · doi:10.1093/cercor/bhu277 · Cited by 714 · see citing works
“Higher order regions with larger receptive fields, such as TO1/2, VO1/2, and PHC1/2, are better identified using a longer stimulus cycle (40 or 64 s), thinner wedges (45°), and typically require a longer scan session (Wandell et al. 2007; Kolster et al. 2010).”
Background
A Hierarchy of Time-Scales and the Brain
Kiebel, S. J., Daunizeau, J., & Friston, K. J. (2008) · PLoS Computational Biology · doi:10.1371/journal.pcbi.1000209 · Cited by 694 · see citing works
Hierarchy of transcriptomic specialization across human cortex captured by structural neuroimaging topography
Burt, J. B., Demirtaş, M., Eckner, W. J., Navejar, N. M., Ji, J. L., Martin, W. J., Bernacchia, A., Anticevic, A., & Murray, J. D. (2018) · Nature Neuroscience · doi:10.1038/s41593-018-0195-0 · Cited by 657 · see citing works
Shared memories reveal shared structure in neural activity across individuals
Chen, J., Leong, Y. C., Honey, C. J., Yong, C. H., Norman, K. A., & Hasson, U. (2017) · Nature Neuroscience · doi:10.1038/nn.4450 · Cited by 645 · see citing works
“The well-studied spatial organization of sensory responses takes the form of “topographic maps” in the brain, e.g., retinotopic or tonotopic maps of visual or auditory features, which are preserved across individuals 36–38 .”
Parcellations and Hemispheric Asymmetries of Human Cerebral Cortex Analyzed on Surface-Based Atlases
Van Essen, D. C., Glasser, M. F., Dierker, D. L., Harwell, J., & Coalson, T. (2012) · Cerebral Cortex · doi:10.1093/cercor/bhr291 · Cited by 616 · see citing works
“6A).”
Background
The Frontoparietal Attention Network of the Human Brain: Action, Saliency, and a Priority Map of the Environment
Ptak, R. (2012) · The Neuroscientist · doi:10.1177/1073858411409051 · Cited by 597 · see citing works
Decoding and Reconstructing Color from Responses in Human Visual Cortex
Brouwer, G. J., & Heeger, D. J. (2009) · Journal of Neuroscience · doi:10.1523/jneurosci.3577-09.2009 · Cited by 586 · see citing works
High-field fMRI unveils orientation columns in humans
Yacoub, E. S., Harel, N., & Uǧurbil, K. (2008) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0804110105 · Cited by 564 · see citing works
Topographic maps in human frontal and parietal cortex
Silver, M. A., & Kästner, S. (2009) · Trends in Cognitive Sciences · doi:10.1016/j.tics.2009.08.005 · Cited by 549 · see citing works
Surface-Based and Probabilistic Atlases of Primate Cerebral Cortex
Essen, D. C. V., & Dierker, D. L. (2007) · Neuron · doi:10.1016/j.neuron.2007.10.015 · Cited by 551 · see citing works
Neuronal Synchronization along the Dorsal Visual Pathway Reflects the Focus of Spatial Attention
Siegel, M., Donner, T. H., Oostenveld, R., Fries, P., & Engel, A. K. (2008) · Neuron · doi:10.1016/j.neuron.2008.09.010 · Cited by 487 · see citing works
Evolution of opsins and phototransduction
Shichida, Y., & Matsuyama, T. (2009) · Philosophical Transactions of the Royal Society B Biological Sciences · doi:10.1098/rstb.2009.0051 · Cited by 473 · see citing works
A Real-World Size Organization of Object Responses in Occipitotemporal Cortex
Konkle, T., & Oliva, A. (2012) · Neuron · doi:10.1016/j.neuron.2012.04.036 · Cited by 444 · see citing works
“Object-responsive cortex anterior to early visual areas was originally thought to be nonretinotopic; however, there are nowmany well-documented retinotopic maps extending along dorsal and ventral streams (e.g., for reviews, see Wandell et al., 2007; Silver and Kastner, 2009).”
Background
Towards a mathematical theory of cortical micro-circuits
George, D., & Hawkins, J. (2009) · PLoS Computational Biology · doi:10.1371/journal.pcbi.1000532 · Cited by 404 · see citing works
Imaging retinotopic maps in the human brain
Wandell, B. A., & Winawer, J. A. (2010) · Vision Research · doi:10.1016/j.visres.2010.08.004 · Cited by 376 · see citing works
The Retinotopic Organization of the Human Middle Temporal Area MT/V5 and Its Cortical Neighbors
Kolster, H., Peeters, R. R., & Orban, G. A. (2010) · Journal of Neuroscience · doi:10.1523/jneurosci.2069-10.2010 · Cited by 363 · see citing works
Preserved Functional Specialization for Spatial Processing in the Middle Occipital Gyrus of the Early Blind
Renier, L. A., Anurova, I., Volder, A. D., Carlson, S., VanMeter, J. W., & Rauschecker, J. P. (2010) · Neuron · doi:10.1016/j.neuron.2010.09.021 · Cited by 355 · see citing works
Enhanced visual functioning in autism: An ALE meta-analysis
Samson, F., Mottron, L., Soulières, I., & Zeffiro, T. A. (2012) · Human Brain Mapping · doi:10.1002/hbm.21307 · Cited by 351 · see citing works
“In inferotemporal, occipital, and inferior parietal regions, more voxels showed higher ALE values in autistics than in non-autistics in areas subserving integration of local visual features, manipulation of visual features, object recognition and object identification [Wandell et al., 2007].”
Background
Retinotopic Organization of Human Ventral Visual Cortex
Arcaro, M. J., McMains, S. A., Singer, B. D., & Kästner, S. (2009) · Journal of Neuroscience · doi:10.1523/jneurosci.2807-09.2009 · Cited by 348 · see citing works
Using high-resolution quantitative mapping of R1 as an index of cortical myelination
Lutti, A., Dick, F., Sereno, M. I., & Weiskopf, N. (2014) · NeuroImage · doi:10.1016/j.neuroimage.2013.06.005 · Cited by 346 · see citing works
“This has been an extremely productive approach, and has shown that much of the cortex is tiled with maps (Graziano and Aflalo, 2007; Schreiner and Winer, 2007; Wandell et al., 2007).”
Topography and Areal Organization of Mouse Visual Cortex
Garrett, M., Nauhaus, I., Marshel, J. H., & Callaway, E. (2014) · Journal of Neuroscience · doi:10.1523/jneurosci.1124-14.2014 · Cited by 314 · see citing works
“However, the possibility remains that two distinct visual field representations could have the same visual field sign and share a border, as is the case for some adjacent regions in humans (Larsson and Heeger, 2006; Wandell et al., 2007).”
BackgroundMethodInfluential
A functional and perceptual signature of the second visual area in primates
Freeman, J., Ziemba, C. M., Heeger, D. J., Simoncelli, E. P., & Movshon, J. A. (2013) · Nature Neuroscience · doi:10.1038/nn.3402 · Cited by 341 · see citing works
When size matters: attention affects performance by contrast or response gain
Herrmann, K., Montaser‐Kouhsari, L., Carrasco, M., & Heeger, D. J. (2010) · Nature Neuroscience · doi:10.1038/nn.2669 · Cited by 329 · see citing works
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 · see citing works
“25 Many parts of the human and primate visual cortices exhibit retinotopic organization 26 in so-called visual field maps: The image presented to the retina is kept topographically 27 intact in the next processing steps on the cortical surface [6].”
BackgroundResult
Flexible cognitive resources: competitive content maps for attention and memory
Franconeri, S., Alvarez, G. A., & Cavanagh, P. (2013) · Trends in Cognitive Sciences · doi:10.1016/j.tics.2013.01.010 · Cited by 336 · see citing works
Functional specialization for auditory–spatial processing in the occipital cortex of congenitally blind humans
Collignon, O., Vandewalle, G., Voss, P., Albouy, G., Charbonneau, G., Lassonde, M. C., & Leporé, F. (2011) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1013928108 · Cited by 322 · see citing works
The Relationship between Cortical Magnification Factor and Population Receptive Field Size in Human Visual Cortex: Constancies in Cortical Architecture
Harvey, B. M., & Dumoulin, S. O. (2011) · Journal of Neuroscience · doi:10.1523/jneurosci.2572-11.2011 · Cited by 311 · see citing works
“Using fMRI, the CMF (Sereno et al., 1995; DeYoe et al., 1996; Dougherty et al., 2003; Wandell et al., 2007) and aggregate RF within an fMRI recording site (pRF) can be routinely determined (Dumoulin and Wandell, 2008; Kay et al.”
BackgroundMethodInfluential
Neural Encoding and Decoding with Deep Learning for Dynamic Natural Vision
Wen, H., Shi, J., Zhang, Y., Lu, K., Cao, J., & Liu, Z. (2017) · Cerebral Cortex · doi:10.1093/cercor/bhx268 · Cited by 297 · see citing works
“The human visual cortex may use a deeper hierarchy, than the 8-layer CNN in this study, spanning >20 visual areas (Wandell et al. 2007), and thus it may be better explained by deeper CNNs (Simonyan and Ziserman”
MethodResult
fMRI Repetition Suppression: Neuronal Adaptation or Stimulus Expectation?
Larsson, J., & Smith, A. T. (2012) · Cerebral Cortex · doi:10.1093/cercor/bhr119 · Cited by 264 · see citing works
“We used the nomenclature and scheme for defining visual areas of Wandell et al. (2007) and Larsson and Heeger (2006); however, the conclusions of the study do not depend on the particular parcellation scheme used.”
Method
Connectivity‐based parcellation: Critique and implications
Eickhoff, S. B., Thirion, B., Varoquaux, G. P., & Bzdok, D. (2015) · Human Brain Mapping · doi:10.1002/hbm.22933 · Cited by 267 · see citing works
“, a low-level region) contains functional gradients related to retinotopy [Wandell et al., 2007].”
Background
Mapping hV4 and ventral occipital cortex: The venous eclipse
Winawer, J. A., Horiguchi, H., Sayres, R., Amano, K., & Wandell, B. A. (2010) · Journal of Vision · doi:10.1167/10.5.1 · Cited by 270 · see citing works
Correction of Distortion in Flattened Representations of the Cortical Surface Allows Prediction of V1-V3 Functional Organization from Anatomy
Benson, N. C., Butt, O. H., Brainard, D. H., & Aguirre, G. K. (2014) · PLoS Computational Biology · doi:10.1371/journal.pcbi.1003538 · Cited by 222 · see citing works
Mapping the Human Cortical Surface by Combining Quantitative T1 with Retinotopy†
Sereno, M. I., Lutti, A., Weiskopf, N., & Dick, F. (2012) · Cerebral Cortex · doi:10.1093/cercor/bhs213 · Cited by 261 · see citing works
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 · see citing works
Orientation Decoding Depends on Maps, Not Columns
Freeman, J., Brouwer, G. J., Heeger, D. J., & Merriam, E. P. (2011) · Journal of Neuroscience · doi:10.1523/jneurosci.5160-10.2011 · Cited by 256 · see citing works
The myeloarchitectonic studies on the human cerebral cortex of the Vogt–Vogt school, and their significance for the interpretation of functional neuroimaging data
Nieuwenhuys, R. (2012) · Brain Structure and Function · doi:10.1007/s00429-012-0460-z · Cited by 252 · see citing works
“Physiological studies have shown that the preoccipital region harbours a large number of functional areas (see: Wandell et al. 2007).”
Background
Microstructural Parcellation of the Human Cerebral Cortex – From Brodmann's Post-Mortem Map to in vivo Mapping with High-Field Magnetic Resonance Imaging
Geyer, S., Weiß, M., Reimann, K., Lohmann, G., & Turner, R. (2011) · Frontiers in Human Neuroscience · doi:10.3389/fnhum.2011.00019 · Cited by 247 · see citing works
Mid-level visual features underlie the high-level categorical organization of the ventral stream
Long, B., Yu, C.-P., & Konkle, T. (2018) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1719616115 · Cited by 245 · see citing works
Neural representations of faces and limbs neighbor in human high-level visual cortex: evidence for a new organization principle
Weiner, K. S., & Kalanit Grill-spector, A. (2011) · Psychological Research · doi:10.1007/s00426-011-0392-x · Cited by 237 · see citing works
Anatomy of the visual word form area: Adjacent cortical circuits and long-range white matter connections
Yeatman, J. D., Rauschecker, A. M., & Wandell, B. A. (2012) · Brain and Language · doi:10.1016/j.bandl.2012.04.010 · Cited by 239 · see citing works
“Retinotopic areas were defined by angle reversals (Wandell & Winawer, 2010; Wandell et al., 2007).”
Computational neuroimaging and population receptive fields
Wandell, B. A., & Winawer, J. A. (2015) · Trends in Cognitive Sciences · doi:10.1016/j.tics.2015.03.009 · Cited by 240 · see citing works
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 · see citing works
An extended retinotopic map of mouse cortex
Zhuang, J., Ng, L., Williams, D., Valley, M. T., Li, Y., Garrett, M., & Waters, J. (2017) · eLife · doi:10.7554/elife.18372 · Cited by 234 · see citing works
The Human Connectome Project 7 Tesla retinotopy dataset: Description and population receptive field analysis
Benson, N. C., Jamison, K. W., Arcaro, M. J., Vu, A. T., Glasser, M. F., Coalson, T. S., Essen, D. C. V., Yacoub, E. S., Uǧurbil, K., Winawer, J. A., et al. (2018) · Journal of Vision · doi:10.1167/18.13.23 · Cited by 233 · see citing works
“…investigations of the properties of visual cortex (Abdollahi et al., 2014; Benson, Butt, Brainard, & Aguirre, 2014; Wang, Mruczek, Arcaro, & Kastner, 2015; for a review, see Silver & Kastner, 2009; Tootell, Dale, Sereno, & Malach, 1996; Wandell, Dumoulin, & Brewer, 2007; Wandell & Winawer, 2011).”
Neural Plasticity: The Biological Substrate For Neurorehabilitation
Warraich, Z., & Kleim, J. A. (2010) · PM&R · doi:10.1016/j.pmrj.2010.10.016 · Cited by 227 · see citing works
Mapping Human Somatosensory Cortex in Individual Subjects With 7T Functional MRI
Sánchez-Panchuelo, R.-M., Francis, S., Bowtell, R. W., & Schluppeck, D. (2010) · Journal of Neurophysiology · doi:10.1152/jn.01017.2009 · Cited by 228 · see citing works
Mixed-norm estimates for the M/EEG inverse problem using accelerated gradient methods
Gramfort, A., Kowalski, M., & Hämäläinen, M. (2012) · Physics in Medicine and Biology · doi:10.1088/0031-9155/57/7/1937 · Cited by 224 · see citing works
“The diﬀerent body parts are mapped to locations at S1 and a location in the visual ﬁeld maps to an area at V1 This later is known as the retinotopic organization of V1 (Wandell et al. 2007).”
Ultra-high field MRI: Advancing systems neuroscience towards mesoscopic human brain function
Dumoulin, S. O., Fracasso, A., van der Zwaag, W., Siero, J. C. W., & Petridou, N. (2017) · NeuroImage · doi:10.1016/j.neuroimage.2017.01.028 · Cited by 216 · see citing works
“MARK by their topographic organization or their functional specialization, and each area is believed to support a specific function or computation (Dumoulin, 2015; Grill-Spector and Malach, 2004; Op de Beeck et al., 2008; Tootell et al., 1996; Vanduffel et al., 2014; Wandell et al., 2007).”
Anatomy and White Matter Connections of the Lingual Gyrus and Cuneus
Palejwala, A. H., Dadario, N. B., Young, I. M., O’Connor, K. P., Briggs, R. G., Conner, A. K., OʼDonoghue, D. L., & Sughrue, M. E. (2021) · World Neurosurgery · doi:10.1016/j.wneu.2021.04.050 · Cited by 223 · see citing works
Impact of blindness onset on the functional organization and the connectivity of the occipital cortex
Collignon, O., Dormal, G., Albouy, G., Vandewalle, G., Voss, P., Phillips, C. L. M., & Leporé, F. (2013) · Brain · doi:10.1093/brain/awt176 · Cited by 218 · see citing works
“Such conceptions recently appeared in studies investigating adults with amblyopia suggesting that the original model of a fixed critical period for plasticity may have exceptions, putatively through latent synapses capable of re-expression in adults (Bavelier et al., 2010; Hess et al., 2010).”
Background
The neural bases of spatial frequency processing during scene perception
Kauffmann, L., RamanoÃ«l, S., & Peyrin, C. (2014) · Frontiers in Integrative Neuroscience · doi:10.3389/fnint.2014.00037 · Cited by 210 · see citing works
“We first identified scene-selective regions using a localizer adapted from previous studies (Epstein and Kanwisher, 1998; Epstein et al., 2003; Bar et al., 2008b; Walther et al., 2009) in which participants viewed gray-scale photographs of scenes, faces and common objects.”
Method
The Processing of Three-Dimensional Shape from Disparity in the Human Brain
Georgieva, S. S., Peeters, R. R., Kolster, H., Todd, J. T., & Orban, G. A. (2009) · Journal of Neuroscience · doi:10.1523/jneurosci.4753-08.2009 · Cited by 209 · see citing works
Categorical Clustering of the Neural Representation of Color
Brouwer, G. J., & Heeger, D. J. (2013) · Journal of Neuroscience · doi:10.1523/jneurosci.2472-13.2013 · Cited by 209 · see citing works
“We adopted the convention of defining V4v, VO1, and VO2 as adjacent visual cortical areas on the ventral surface of the occipital lobe, each with a representation of the entire contralateral hemifield (Brewer et al., 2005; Wandell et al., 2007).”
Method
Plasticity and stability of visual field maps in adult primary visual cortex
Wandell, B. A., & Smirnakis, S. M. (2009) · Nature reviews. Neuroscience · doi:10.1038/nrn2741 · Cited by 204 · see citing works
Prioritized Maps of Space in Human Frontoparietal Cortex
Jerde, T. A., Merriam, E. P., Riggall, A. C., Hedges, J. H., & Curtis, C. E. (2012) · Journal of Neuroscience · doi:10.1523/jneurosci.3810-12.2012 · Cited by 208 · see citing works
“In human cortex, fMRI studies have identified 12 topographic maps in visual cortex that provide an orderly tiling of visual space (Wandell et al., 2007).”
Background
The Development of Cortical Sensitivity to Visual Word Forms
Ben-Shachar, M., Dougherty, R. F., Deutsch, G. K., & Wandell, B. A. (2011) · Journal of Cognitive Neuroscience · doi:10.1162/jocn.2011.21615 · Cited by 190 · see citing works
Classification of Hand Movements From EEG Using a Deep Attention-Based LSTM Network
Zhang, G., Davoodnia, V., Sepas‐Moghaddam, A., Zhang, Y., & Etemad, A. (2019) · IEEE Sensors Journal · doi:10.1109/jsen.2019.2956998 · Cited by 201 · see citing works
“Moreover, the information flow in the parietal-occipital and occipital regions were also consistent with the activities reported in [41].”
BackgroundResult
Large-scale remapping of visual cortex is absent in adult humans with macular degeneration
Baseler, H. A., Gouws, A. D., Haak, K. V., Racey, C., Crossland, M. D., Tufail, A., Rubin, G. S., Cornelissen, F. W., & Morland, A. B. (2011) · Nature Neuroscience · doi:10.1038/nn.2793 · Cited by 193 · see citing works
“2793" language="eng" relation="no"> The human brain contains maps of the retina on the surface of the occipital lobe”
Background
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 · see citing works
“…phase-encoded retinotopic mapping protocol, with eccentricity and polar mapping of ring and wedge stimuli, respectively, to measure visual retinotopic mapping (Engel et al., 1994; Sereno et al., 1995; Wandell et al., 2007b; Wandell and Winawer, 2011), delivered during two separate experiments.”
BackgroundMethodInfluential
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 · see citing works
Overlearning hyperstabilizes a skill by rapidly making neurochemical processing inhibitory-dominant
Shibata, K., Sasaki, Y., Bang, J. W., Walsh, E. G., Machizawa, M. G., Tamaki, M., Chang, L.-H., & Watanabe, T. (2017) · Nature Neuroscience · doi:10.1038/nn.4490 · Cited by 184 · see citing works
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 · see citing works
“Freesurfer was used to delineate the visual areas using standard retinotopic mapping procedures (Sereno et al., 1995; DeYoe et al., 1996; Engel et al., 1997; Wandell et al., 2007).”
Method
Hexadirectional coding of visual space in human entorhinal cortex
Nau, M., Navarro Schröder, T., Bellmund, J. L. S., & Doeller, C. F. (2018) · Nature Neuroscience · doi:10.1038/s41593-017-0050-8 · Cited by 182 · see citing works
High temporal resolution decoding of object position and category
Carlson, T. A., Hogendoorn, H., Ryota Kanai, C., Mesík, J., & Turret, J. (2011) · Journal of Vision · doi:10.1167/11.10.9 · Cited by 190 · see citing works
Attentional Enhancement via Selection and Pooling of Early Sensory Responses in Human Visual Cortex
Pestilli, F., Carrasco, M., Heeger, D. J., & Gardner, J. L. (2011) · Neuron · doi:10.1016/j.neuron.2011.09.025 · Cited by 190 · see citing works
Olfactory Maps in the Brain
Murthy, V. N. (2011) · Annual Review of Neuroscience · doi:10.1146/annurev-neuro-061010-113738 · Cited by 175 · see citing works
“…of the sensory surface to higher brain regions; for example, neighboring points in visual space activate neighboring points on the retina, and this relation is preserved through several subsequent stages of processing (Knierim & Van Essen 1992, Talbot & Marshall 1941, Wandell et al. 2007).”
Background
The Foveal Confluence in Human Visual Cortex
Schira, M. M., Tyler, C. W., Breakspear, M. J., & Špehar, B. (2009) · Journal of Neuroscience · doi:10.1523/jneurosci.1760-09.2009 · Cited by 176 · see citing works
Attraction of Position Preference by Spatial Attention throughout Human Visual Cortex
Klein, B. P., Harvey, B. M., & Dumoulin, S. O. (2014) · Neuron · doi:10.1016/j.neuron.2014.08.047 · Cited by 175 · see citing works
“ROIbordersweredeﬁnedfollowingrever-salsinthepolarangleandeccentricityprogressions(Serenoetal.,1995;Wan-dell et al., 2007), and ROIs were identiﬁed following published descriptions of their relative locations (Arcaro et al., 2011; DeYoe et al., 1996; Engel et al., 1997; Wandell et al., 2007).”
A Major Human White Matter Pathway Between Dorsal and Ventral Visual Cortex
Takemura, H., Rokem, A., Winawer, J. A., Yeatman, J. D., Wandell, B. A., & Pestilli, F. (2015) · Cerebral Cortex · doi:10.1093/cercor/bhv064 · Cited by 173 · see citing works
“Several theories have been proposed to characterize the organization of these visual field maps (Wandell et al. 2007).”
Background
Asynchronous Broadband Signals Are the Principal Source of the BOLD Response in Human Visual Cortex
Winawer, J. A., Kay, K., Foster, B. L., Rauschecker, A. M., Parvizi, J., & Wandell, B. A. (2013) · Current Biology · doi:10.1016/j.cub.2013.05.001 · Cited by 169 · see citing works
“Spatial position and size are important properties of visual encoding, reflected in the multiplicity of visual field maps tiling the cortex [3, 4].”
High-density diffuse optical tomography for imaging human brain function
Wheelock, M. D., Culver, J. P., & Eggebrecht, A. T. (2019) · Review of Scientific Instruments · doi:10.1063/1.5086809 · Cited by 169 · see citing works
Visual Field Map Clusters in Macaque Extrastriate Visual Cortex
Kolster, H., Mandeville, J. B., Arsenault, J. T., Ekstrom, L. B., Wald, L. L., & Vanduffel, W. (2009) · Journal of Neuroscience · doi:10.1523/jneurosci.0518-09.2009 · Cited by 168 · see citing works
Relating Retinotopic and Object-Selective Responses in Human Lateral Occipital Cortex
Sayres, R., & Kalanit Grill-spector, A. (2008) · Journal of Neurophysiology · doi:10.1152/jn.01383.2007 · Cited by 167 · see citing works
Similarity-Based Fusion of MEG and fMRI Reveals Spatio-Temporal Dynamics in Human Cortex During Visual Object Recognition
Cichy, R. M., Pantazis, D., & Oliva, A. (2016) · Cerebral Cortex · doi:10.1093/cercor/bhw135 · Cited by 161 · see citing works
“Both streams consist of multiple brain regions (Felleman and Van Essen 1991; Grill-Spector and Malach 2004; Wandell et al. 2007; Op de Beeck et al. 2008; Grill-Spector and Weiner 2014) that encode different aspects of the visual input in neuronal population codes (Haxby et al.”
Background
Spatial frequency tuning in human retinotopic visual areas
Henriksson, L., Nurminen, L., Hyvärinen, A., & Vanni, S. (2008) · Journal of Vision · doi:10.1167/8.10.5 · Cited by 172 · see citing works
Future trends in Neuroimaging: Neural processes as expressed within real-life contexts
Hasson, U., & Honey, C. J. (2012) · NeuroImage · doi:10.1016/j.neuroimage.2012.02.004 · Cited by 165 · see citing works
“One very productive line of research, for example, is the mapping of retinotopic areas in the visual system, which has revealed many new retinotopic areas (Arcaro et al., 2009; Engel et al., 1997a; Larsson and Heeger, 2006; Sereno et al., 1995; Silver and Kastner, 2009;Wandell et al., 2007).”
Background
Not one extrastriate body area: Using anatomical landmarks, hMT+, and visual field maps to parcellate limb-selective activations in human lateral occipitotemporal cortex
Weiner, K. S., & Kalanit Grill-spector, A. (2011) · NeuroImage · doi:10.1016/j.neuroimage.2011.03.041 · Cited by 162 · see citing works
Higher-Order Areas of the Mouse Visual Cortex
Glickfeld, L. L., & Olsen, S. R. (2017) · Annual Review of Vision Science · doi:10.1146/annurev-vision-102016-061331 · Cited by 162 · see citing works
Bringing the real world into the fMRI scanner: Repetition effects for pictures versus real objects
Snow, J. C., Pettypiece, C. E., Figley, T. D., McLean, A. D., Stroman, P. W., Goodale, M. A., & Culham, J. C. (2011) · Scientific Reports · doi:10.1038/srep00130 · Cited by 160 · see citing works
“Similar activation was also evident within ‘dorsal stream object areas’, extending from the expected location of anterior V3, dorsally into the intraparietal sulcus (IPS) anterior to the expected location of IPS-”
Background
Lesion evidence for the critical role of the intraparietal sulcus in spatial attention
Gillebert, C. R., Mantini, D., Thijs, V., Sunaert, S. G., Dupont, P. J., & Vandenberghe, R. R. (2011) · Brain · doi:10.1093/brain/awr085 · Cited by 154 · see citing works
Larger 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 · see citing works
“We further delineated V4 and V3A as full hemifield representations adjacent to the ventral and dorsal portions, respectively, of V3 (Wandell et al., 2007).”
Background
Dissociated α-Band Modulations in the Dorsal and Ventral Visual Pathways in Visuospatial Attention and Perception
Capilla, A., Schoffelen, J., Paterson, G., Thut, G., & Groß, J. (2012) · Cerebral Cortex · doi:10.1093/cercor/bhs343 · Cited by 147 · see citing works
Short-Term Memory for Space and Time Flexibly Recruit Complementary Sensory-Biased Frontal Lobe Attention Networks
Michalka, S., Kong, L., Rosen, M. L., Shinn‐Cunningham, B. G., & Somers, D. C. (2015) · Neuron · doi:10.1016/j.neuron.2015.07.028 · Cited by 149 · see citing works
“…information—the retina records spatial information with high precision, and over 20 cortical areas exhibit visuospatial maps (Swisher et al., 2007; Wandell et al., 2007; Silver and Kastner, 2009); however, the timing of visual responses is sluggish and is influenced by nontemporal stimulus…”
Transformation from image-based to perceptual representation of materials along the human ventral visual pathway
Hiramatsu, C., Goda, N., & Komatsu, H. (2011) · NeuroImage · doi:10.1016/j.neuroimage.2011.04.056 · Cited by 148 · see citing works
“Retinotopic areas, V1, V2, V3, V4, V3A, and V3B, were delineated based on retinotopy obtained from the retinotopic mapping experiment (Wandell et al., 2007), and neighboring areas were combined because of the relatively small size of each area for the subsequent analyses.”
Background
Modeling center-surround configurations in population receptive fields using fMRI
Zuiderbaan, W., Harvey, B. M., & Dumoulin, S. O. (2012) · Journal of Vision · doi:10.1167/12.3.10 · Cited by 149 · see citing works
Laminar Organization of Working Memory Signals in Human Visual Cortex
Lawrence, S. J. D., van Mourik, T., Kok, P., Koopmans, P. J., Norris, D. G., & de Lange, F. P. (2018) · Current Biology · doi:10.1016/j.cub.2018.08.043 · Cited by 146 · see citing works
Extensive sampling for complete models of individual brains
Naselaris, T., Allen, E., & Kay, K. (2021) · Current Opinion in Behavioral Sciences · doi:10.1016/j.cobeha.2020.12.008 · Cited by 140 · see citing works
“com such as retinotopic organization [40] and face-selectivity [41]—not only generalize across individuals, but for the most part generalize across species [42,43].”
Background
Cortical plasticity and preserved function in early blindness
Renier, L., De Volder, A. G., & Rauschecker, J. P. (2014) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2013.01.025 · Cited by 144 · see citing works
“As the MOG is part of the visual dorsal stream in sighted individuals (Dumoulin et al., 2000; Wandell et al., 2007), and considering that this region was recruited by similar tasks in vision in a control experiment in a separate group, it follows that specialized brain regions develop their computational functions ind…”
Background
The neurobiological basis of seeing words
Wandell, B. A. (2011) · Annals of the New York Academy of Sciences · doi:10.1111/j.1749-6632.2010.05954.x · Cited by 142 · see citing works

Authors: Wandell, B. A., Dumoulin, S. O., & Brewer, A. A.
Affiliations: Stanford University (US)
University of California, Irvine (US)
Corresponding author: Wandell, Brian A.
ORCID: Wandell, Brian A.
Dumoulin, Serge O.
Brewer, Alyssa A.
Venue: Neuron
Publisher: Elsevier BV
Published: 2007-10
Volume: 56
Issue: 2
Pages: 366-383
ISSN: 0896-6273 (ISSN-L)
DOI: 10.1016/j.neuron.2007.10.012
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

Visual field maps in human cortex.

Abstract

Integrity signals

Claims the paper makes

Claims other papers make about this one

Cites

Cited by

Related

Record

About these checks