Cited by 212Visual perception and processing mechanismsFace Recognition and PerceptionTactile and Sensory Interactions

The DOI matches its Crossref record; 75 of the 76 references it cites were found in a registry or an index.

Complete Pattern of Ocular Dominance Columns in Human Primary Visual Cortex

Open access

Adams, Daniel L., Sincich, Lawrence C., Horton, Jonathan C.·2007·The Journal of Neuroscience

DOI 10.1523/jneurosci.2923-07.2007PMC PMC6673158

Open this paper in CoChat — free account Open PDF

Abstract

The occipital lobes were obtained after death from six adult subjects with monocular visual loss. Flat-mounts were processed for cytochrome oxidase (CO) to reveal metabolic activity in the primary (V1) and secondary (V2) visual cortices. Mean V1 surface area was 2643 mm 2 (range, 1986–3477 mm 2 ). Ocular dominance columns were present in all cases, having a mean width of 863 μm. There were 78–126 column pairs along the V1 perimeter. Human column patterns were highly variable, but in at least one person they resembled a scaled-up version of macaque columns. CO patches in the upper layers were centered on ocular dominance columns in layer 4C, with one exception. In this individual, the columns in a local area resembled those present in the squirrel monkey, and no evidence was found for column/patch alignment. In every subject, the blind spot of the contralateral eye was conspicuous as an oval region without ocular dominance columns. It provided a precise landmark for delineating the central 15° of the visual field. A mean of 53.1% of striate cortex was devoted to the representation of the central 15°. This fraction was less than the proportion of striate cortex allocated to the representation of the central 15° in the macaque. Within the central 15°, each eye occupied an equal territory. Beyond this eccentricity, the contralateral eye predominated, occupying 63% of the cortex. In one subject, monocular visual loss began at age 4 months, causing shrinkage of ocular dominance columns. In V2, which had a larger surface area than V1, CO stripes were present but could not be classified as thick or thin.

The claims and statistics of this paper haven’t been checked yet.

Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.

Integrity signals

Registry

Crossref · 10.1523/jneurosci.2923-07.2007

Cites

75 of 75 references verified0 citation errors · 0 not checkable

Statistics

Claims the paper makes

The claims and statistics of this paper haven’t been checked yet.

Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.

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?

Self-check

Percentages, sums and reported differences re-computed from the paper’s own numbers.

The self-check needs the paper’s full text.

A Computational Approach to Edge Detection
Canny, J. (1986) · IEEE Transactions on Pattern Analysis and Machine Intelligence · doi:10.1109/tpami.1986.4767851 · Cited by 30,004
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 2,663
Ferrier lecture. Functional architecture of macaque monkey visual cortex
Hubel, D. H., & Wiesel, T. N. (1977) · Proceedings of the Royal Society of London. Series B. Biological Sciences · doi:10.1098/rspb.1977.0085 · Cited by 2,608
Changes in the visual system of monocularly sutured or enucleated cats demonstrable with cytochrome oxidase histochemistry
Wong‐Riley, M. T. T. (1979) · Brain Research · doi:10.1016/0006-8993(79)90728-5 · Cited by 1,853
Topography of ganglion cells in human retina
Curcio, C. A., & Allen, K. A. (1990) · The Journal of Comparative Neurology · doi:10.1002/cne.903000103 · Cited by 1,849
Plasticity of ocular dominance columns in monkey striate cortex
Hubel, D. H., Wiesel, T. N., LeVay, S., Barlow, H. B., & Gaze, R. M. (1977) · Philosophical transactions of the Royal Society of London. Series B, Biological sciences · doi:10.1098/rstb.1977.0050 · Cited by 1,629
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
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
The visual field representation in striate cortex of the macaque monkey: Asymmetries, anisotropies, and individual variability
Essen, D. C. V., Newsome, W. T., & Maunsell, J. H. R. (1984) · Vision Research · doi:10.1016/0042-6989(84)90041-5 · Cited by 938
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
Self-citation

Flagged first, then by citations

Show all 76 references

1 of the 76 references couldn’t be matched to a known paper.

Research works printed but not linked: 3

Brodmann, 1918, Individuelle Variationen der Sehsphäre und ihr Bedeutung für die Klinik der Hinterhauptschüsse, Allgz Psychiat (Berlin), 74, 564
Filimonoff, 1932, Über die Variabilität der Grosshirnrindenstruktur. Regio occipitalis beim erwachsenen Menschen, J Psychol Neurol, 44, 1
Popoff, 1927, Zur Kenntnis der Grösse der Area striate und die Methodik ihrer Ausmessung, J Psychol Neurol, 34, 238

Sorted by citations

Items 101–200 of 211

Accurate decoding of sub-TR timing differences in stimulations of sub-voxel regions from multi-voxel response patterns
Misaki, M., Luh, W., & Bandettini, P. A. (2012) · NeuroImage · doi:10.1016/j.neuroimage.2012.10.069 · Cited by 15
Barratt Impulsivity in Healthy Adults Is Associated with Higher Gray Matter Concentration in the Parietal Occipital Cortex that Represents Peripheral Visual Field
Ide, J. S., Tung, H. C., Yang, C.-T., Tseng, Y., & Li, C. R. (2017) · Frontiers in Human Neuroscience · doi:10.3389/fnhum.2017.00222 · Cited by 15
Mesoscale cortical mechanisms of perceptual conflict resolution in binocular rivalry
Qian, C., Zhang, Z., Chen, Z., de Hollander, G., Knapen, T. H. J., He, S., & Zhang, P. (2025) · Nature Human Behaviour · doi:10.1038/s41562-025-02320-4 · Cited by 18
Refined Frequency Doubling Perimetry Analysis Reaffirms Central Nervous System Control of Chronic Glaucomatous Neurodegeneration
Reilly, M. A., Villarreal, A., Maddess, T., & Sponsel, W. E. (2015) · Translational Vision Science & Technology · doi:10.1167/tvst.4.3.7 · Cited by 14
Neuronal composition of processing modules in human V1: laminar density for neuronal and non-neuronal populations and a comparison with macaque
García‐Marín, V., Kelly, J. G., & Hawken, M. J. (2023) · Cerebral Cortex · doi:10.1093/cercor/bhad512 · Cited by 14
Changes in Visual Cortex in Healthy Aging and Dementia
Brewer, A., & Barton, B. (2016) · InTech eBooks · doi:10.5772/64562 · Cited by 12
Dense, shape‐optimized posterior 32‐channel coil for submillimeter functional imaging of visual cortex at 3T
Farivar, R., Grigorov, F., van der Kouwe, A. J. W., Wald, L. L., & Keil, B. R. (2015) · Magnetic Resonance in Medicine · doi:10.1002/mrm.25815 · Cited by 13
Orientation pinwheels in primary visual cortex of a highly visual marsupial
Jung, Y. J., Almasi, A., Sun, S. H., Yunzab, M., Cloherty, S. L., Bauquier, S. H., Renfree, M. B., Hamish Meffin, A., & Ibbotson, M. R. (2022) · Science Advances · doi:10.1126/sciadv.abn0954 · Cited by 13
What has vision science taught us about functional MRI?
Himmelberg, M. M., Gardner, J. L., & Winawer, J. A. (2022) · NeuroImage · doi:10.1016/j.neuroimage.2022.119536 · Cited by 11
Adaptation and Neuronal Network in Visual Cortex
Bachatene, L., Bharmauria, V., & Molotchnikoff, S. (2012) · InTech eBooks · doi:10.5772/46011 · Cited by 12
Decoding eye-of-origin outside of awareness
Baker, D. H. (2016) · NeuroImage · doi:10.1016/j.neuroimage.2016.12.008 · Cited by 12
Revealing human ocular dominance columns using high-resolution functional magnetic resonance imaging
Cheng, K. (2011) · NeuroImage · doi:10.1016/j.neuroimage.2011.08.086 · Cited by 11
Population Models, Not Analyses, of Human Neuroscience Measurements
Gardner, J. L., & Merriam, E. P. (2021) · Annual Review of Vision Science · doi:10.1146/annurev-vision-093019-111124 · Cited by 9
Depth-dependent functional MRI responses to chromatic and achromatic stimuli throughout V1 and V2
Navarro, K. T., Sanchez, M. J., Engel, S. A., Olman, C. A., & Weldon, K. B. (2020) · NeuroImage · doi:10.1016/j.neuroimage.2020.117520 · Cited by 9
Micro-scale functional modules in the human temporal lobe
Chapeton, J. I., Wittig, J. H., Inati, S. K., & Zaghloul, K. A. (2022) · Nature Communications · doi:10.1038/s41467-022-34018-w · Cited by 10
Extrastriate Visual Cortex
Boyd, J. D., & Matsubara, J. A. (2011) · Elsevier eBooks · doi:10.1016/b978-0-323-05714-1.00031-5 · Cited by 10
Development of ocular dominance columns across rodents and other species: revisiting the concept of critical period plasticity
Takahata, T. (2024) · Frontiers in Neural Circuits · doi:10.3389/fncir.2024.1402700 · Cited by 10
Quantized visual awareness
Escobar, W. A. (2013) · Frontiers in Psychology · doi:10.3389/fpsyg.2013.00869 · Cited by 9
Modeling the electrical field created by mass neural activity
Privman, E., Malach, R., & Yeshurun, Y. (2013) · Neural Networks · doi:10.1016/j.neunet.2013.01.004 · Cited by 9
Patterns of Cortical Visual Field Defects From Embolic Stroke Explained by the Anastomotic Organization of Vascular Microlobules
Horton, J. C., & Adams, D. L. (2018) · Journal of Neuro-Ophthalmology · doi:10.1097/wno.0000000000000733 · Cited by 8
Self-citation
Autoencoding sensory substitution
Tóth, V., & Parkkonen, L. (2019) · Unpublished · doi:10.13140/rg.2.2.10576.87048 · Cited by 7
Investigating the human binocular visual system using multi-modal magnetic resonance imaging
Bridge, H., Ip, I. B., & Parker, A. J. (2023) · Perception · doi:10.1177/03010066231178664 · Cited by 7
Decoding of columnar-level organization across cortical depth using BOLD- and CBV-fMRI at 7 T
Haenelt, D., Chaimow, D., Schmidt, M. E., Nasr, S., Weiskopf, N., & Trampel, R. (2026) · Imaging Neuroscience · doi:10.1162/imag.a.1124 · Cited by 6
Theoretical Implications on Visual (Color) Representation and Cytochrome Oxidase Blobs
Bókkon, I., & Vimal, R. L. P. (2013) · Activitas Nervosa Superior · doi:10.1007/bf03379594 · Cited by 7
Electrophysiological evidence for a post-perceptual influence of global visual context on perceived orientation
Corbett, J. E., Enns, J. T., & Handy, T. C. (2009) · Brain Research · doi:10.1016/j.brainres.2009.07.038 · Cited by 7
After over 200 years, 7 T magnetic resonance imaging reveals the foliate structure of the human corpus callosum in vivo
Wiggins, C. J., Schäfer, A., Dhital, B., Bihan, D. L., & Turner, R. (2017) · British Journal of Radiology · doi:10.1259/bjr.20160906 · Cited by 6
Efficient allocation of attentional sensitivity gain in visual cortex reduces foveal sensitivity in visual search
Walshe, R. C., & Geisler, W. S. (2021) · Current Biology · doi:10.1016/j.cub.2021.10.011 · Cited by 8
Syllable processing is organized in discrete subregions of the human superior temporal gyrus
Cleary, D. R., Tchoe, Y., Bourhis, A. M., Dickey, C. W., Stedelin, B., Ganji, M., Lee, S., Lee, J., Siler, D. A., Brown, E. C., et al. (2024) · PLoS Biology · doi:10.1371/journal.pbio.3002774 · Cited by 6
Spatial scale and distribution of neurovascular signals underlying decoding of orientation and eye of origin from fMRI data
Larsson, J. T., Harrison, C., Jackson, J. B., Oh, S.-M., & Zeringyte, V. (2016) · Journal of Neurophysiology · doi:10.1152/jn.00590.2016 · Cited by 6
What We Have Learned about Human Primary Visual Cortex from High Resolution Functional Magnetic Resonance Imaging
Cheng, K. (2015) · Magnetic Resonance in Medical Sciences · doi:10.2463/mrms.2015-0008 · Cited by 6
A Global Orientation Map in the Primary Visual Cortex (V1): Could a Self Organizing Model Reveal Its Hidden Bias?
Philips, R. T., & Chakravarthy, V. S. (2017) · Frontiers in Neural Circuits · doi:10.3389/fncir.2016.00109 · Cited by 6
Attenuated and delayed neural activity in cortical microcircuitry of monocular processing and binocular interactions in human amblyopia
Wang, Y., Qian, C., Gao, Y., Zhou, Y., Zhang, X., Wen, W., & Zhang, P. (2025) · Imaging Neuroscience · doi:10.1162/imag_a_00561 · Cited by 6
Infants' visual system nonretinotopically integrates color signals along a motion trajectory
Yang, J., Watanabe, J., Kanazawa, S., Nishida, S., & Yamaguchi, M. K. (2015) · Journal of Vision · doi:10.1167/15.1.25 · Cited by 5
Cortical Representation of a Myopic Peripapillary Crescent
Adams, D. L., Economides, J. R., & Horton, J. C. (2016) · Ophthalmology · doi:10.1016/j.ophtha.2016.03.033 · Cited by 5
Self-citation
In vivo functional localization of the temporal monocular crescent representation in human primary visual cortex
Nasr, S., LaPierre, C., Vaughn, C. E., Witzel, T., Stockmann, J., & Polimeni, J. R. (2020) · NeuroImage · doi:10.1016/j.neuroimage.2020.116516 · Cited by 5
Empirical Evidence for Intraspecific Multiple Realization?
Strappini, F., Martelli, M., Cozzo, C., & Pace, E. D. (2020) · Frontiers in Psychology · doi:10.3389/fpsyg.2020.01676 · Cited by 6
Processing in the Primary Visual Cortex
Casagrande, V. A., & Marion, R. (2011) · Elsevier eBooks · doi:10.1016/b978-0-323-05714-1.00030-3 · Cited by 5
Distribution of cytochrome oxidase‐rich patches in human primary visual cortex
Marcondes, M., Rosa, M. G. P., Fiorani, M., Lima, B., & Gattass, R. (2018) · The Journal of Comparative Neurology · doi:10.1002/cne.24435 · Cited by 5
Layer Dependence of Monocular and Binocular Responses in Human Ocular Dominance Columns at 7T using VASO and BOLDPreprint
Akbari, A., Gati, J. S., Zeman, P., Liem, B., & Menon, R. S. (2023) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2023.04.06.535924 · Cited by 5
Analytic Model for Feature Maps in the Primary Visual Cortex
Liu, X., & Robinson, P. A. (2022) · Frontiers in Computational Neuroscience · doi:10.3389/fncom.2022.659316 · Cited by 4
Overall patterns of eye-specific retino-geniculo-cortical projections to layers III, IV, and VI in primary visual cortex of the greater galago (Otolemur crassicudatus), and correlation with cytochrome oxidase blobs
Olavarría, J. F., Qi, H., Takahata, T., & Kaas, J. H. (2022) · Visual Neuroscience · doi:10.1017/s0952523822000062 · Cited by 4
Factors influencing occlusion therapy in refractive amblyopia
Shetty, N., & Prathyusha, I. (2019) · The Journal of Medical Research · doi:10.31254/jmr.2019.5105 · Cited by 4
Effects of eye dominance (left vs. right) and cannabis use on intermanual coordination and negative symptoms in schizophrenia patients
Gorynia, I., Schwaiger, M., & Heinz, A. (2014) · European Archives of Psychiatry and Clinical Neuroscience · doi:10.1007/s00406-014-0503-y · Cited by 4
Evolution of Human Visual System Specializations
Orban, G. A. (2016) · Evolution of Nervous Systems · doi:10.1016/b978-0-12-804042-3.00117-2 · Cited by 4
1.2 Physiological Basis of the BOLD Signal
Goense, J. B. M., & Logothetis, N. K. (2010) · Oxford University Press eBooks · doi:10.1093/acprof:oso/9780195372731.003.0002 · Cited by 4
Using high-resolution functional MRI to differentiate impacts of strabismic and anisometropic amblyopia on evoked ocular dominance activity in humansPreprint
Nasr, S., Skerswetat, J., Gaier, E. D., Malladi, S. N., Kennedy, B., Tootell, R. B. H., Bex, P. J., & Hunter, D. G. (2024) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2024.02.11.579855 · Cited by 4
Temporal crescent syndrome caused by a lateral ventricular glioependymal cyst: case report
Yamaguchi, I., Pooh, K., Azumi, M., & Takagi, Y. (2020) · Journal of Neurosurgery Pediatrics · doi:10.3171/2020.3.peds2021 · Cited by 3
Effects of complete monocular deprivation in visuo-spatial memory
Cattaneo, Z., Merabet, L. B., Bhatt, E., & Vecchi, T. (2008) · Brain Research Bulletin · doi:10.1016/j.brainresbull.2008.05.009 · Cited by 3
Functional Imaging of the Human Visual System
Orban, G. A., & Ferri, S. (2016) · Neuromethods · doi:10.1007/978-1-4939-5611-1_18 · Cited by 3
Thalamocortical Interactions for Sensory Processing
Alonso, J. M., & Swadlow, H. A. (2017) · Oxford University Press eBooks · doi:10.1093/acrefore/9780190264086.013.112 · Cited by 3
Hierarchical cortical plasticity in congenital sight impairmentPreprint
Maimon-Mor, R. O., Farahbakhsh, M., Hedger, N., Rider, A. T., Anderson, E. J., Rees, G. E., Knapen, T. H. J., Michaelides, M., & Dekker, T. M. (2024) · eLife · doi:10.7554/elife.100404.1 · Cited by 3
How shape information is coded by V4 cortical response of macaque monkey
Liu, M., Chang, S., Chen, M., Li, P., Roe, A. W., & Hu, J. (2025) · Journal of Neurophysiology · doi:10.1152/jn.00520.2024 · Cited by 3
Extrastriate activity reflects the absence of local retinal input
Urale, P. W. B., Zhu, L., Gough, R., Arnold, D. H., & Schwarzkopf, D. S. (2023) · Consciousness and Cognition · doi:10.1016/j.concog.2023.103566 · Cited by 3
Cortical field maps across human sensory cortex
Brewer, A. A., & Barton, B. (2023) · Frontiers in Computational Neuroscience · doi:10.3389/fncom.2023.1232005 · Cited by 4
Optimal visual search with highly heuristic decision rules
Zhang, A., & Geisler, W. S. (2025) · Journal of Vision · doi:10.1167/jov.25.4.5 · Cited by 2
Single-cell RNA sequencing of adult primate neocortex reveals the regulatory dynamics of neural plasticity
Zhang, C. (2025) · American Journal of Translational Research · doi:10.62347/zeor5569 · Cited by 2
Functional MRI of the Visual System
Dumoulin, S. O. (2015) · Biological magnetic resonance · doi:10.1007/978-1-4899-7591-1_15 · Cited by 4
The Primary Visual Cortex
Skalicky, S. E. (2015) · Springer eBooks · doi:10.1007/978-981-287-846-5_14 · Cited by 2
The Visual Cortex
Meyer, M. A. (2016) · Springer eBooks · doi:10.1007/978-3-319-39581-4_12 · Cited by 2
Cloverleaf Clusters: A Common Macrostructural Organization across Human Visual and Auditory Cortex
Brewer, A. A., & Barton, B. (2018) · InTech eBooks · doi:10.5772/intechopen.77964 · Cited by 2
Perceptual size discrimination requires awareness and late visual areas: A continuous flash suppression and interocular transfer study
Peel, H. J., Sherman, J. A., Sperandio, I., Laycock, R., & Chouinard, P. A. (2018) · Consciousness and Cognition · doi:10.1016/j.concog.2018.11.012 · Cited by 3
Feasibility of functional magnetic resonance imaging of ocular dominance and orientation preference in primary visual cortex
de Oliveira, M. M., Pang, J. C. S., Robinson, P. A., Liu, X., & Schira, M. M. (2019) · PLoS Computational Biology · doi:10.1371/journal.pcbi.1007418 · Cited by 2
Symmetry Breaking and Pattern Selection in Models of Visual Development
Reichl, L. (2010) · doi:10.53846/goediss-2930 · Cited by 2
Interaction between visual perception and mental representations of imagery and memory in the early visual areas
Saad, E. (2015) · Työväentutkimus Vuosikirja · Cited by 2
Functional Imaging of the Human Visual System
Orban, G. A., & Ürgen, B. A. (2025) · Neuromethods · doi:10.1007/978-1-0716-4438-6_19 · Cited by 2
Cortical white matter: no longer a silent partner
Rockland, K. S., & Rushmore, J. (2026) · Frontiers in Neuroanatomy · doi:10.3389/fnana.2025.1726067 · Cited by 1
Retinal-Specificity of Sensory Eye Dominance and Its Learning-Induced Improvements
Kam, K. Y., & Chang, D. H. F. (2026) · Investigative Ophthalmology & Visual Science · doi:10.1167/iovs.67.4.44 · Cited by 1
12. Visual system architecture
Winawer, J. A., & Horiguchi, H. (2016) · CRC Press eBooks · doi:10.1201/9781315373034-13 · Cited by 1
The Expression Patterns of Cytochrome Oxidase and Immediate-Early Genes Show Absence of Ocular Dominance Columns in the Striate Cortex of Squirrel Monkeys Following Monocular Inactivation
Li, S., Yao, S., Zhou, Q., & Takahata, T. (2021) · Frontiers in Neuroanatomy · doi:10.3389/fnana.2021.751810 · Cited by 1
Impact of Monocular Retinal Lesions on Blob Size in Adult Human V1
Marcondes, M., Farias, M. F., Pary, L. F., Fiorani, M., Lima, B., Amorim, A. K. J., & Gattass, R. (2024) · Journal of Cognitive Neuroscience · doi:10.1162/jocn_a_02133 · Cited by 1
The causal involvement of the visual cortex in visual working memory remains uncertain
Grassi, P. R., Bannert, M. M., & Bartels, A. (2024) · Royal Society Open Science · doi:10.1098/rsos.231884 · Cited by 1
Selective Functional Connectivity between Ocular Dominance Columns in the Primary Visual Cortex
Aganj, I., & Nasr, S. (2024) · Lecture notes in computer science · doi:10.1007/978-3-031-73119-8_1 · Cited by 1
The Neurology of Vision
Sun, L. D. (2019) · Springer eBooks · doi:10.1007/978-3-030-10886-1_38 · Cited by 1
Functional magnetic resonance imaging
Bartels, A., Goense, J. B. M., & Logothetis, N. K. (2012) · Cambridge University Press eBooks · doi:10.1017/cbo9780511979958.011 · Cited by 1
Functional Imaging of the Human Visual System
Orban, G. A., & Kourtzi, Z. (2009) · Neuromethods · doi:10.1007/978-1-60327-919-2_17 · Cited by 1
Parametric Classifications of Cortical Organization
Jang, J., & Paik, S. (2022) · KAIST research series · doi:10.1007/978-981-19-0031-0_4 · Cited by 1
Abundance of Degrees of Freedom
(2008) · Springer eBooks · doi:10.1007/978-3-540-29678-2_19 · Cited by 1
Striate Cortex
Wong‐Riley, M. T. T. (2010) · The Corsini Encyclopedia of Psychology · doi:10.1002/9780470479216.corpsy0949 · Cited by 1
Pulse trains to percepts: A virtual patient describing the perceptual effects of human visual cortical stimulationPreprint
Fine, I., & Boynton, G. M. (2023) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2023.03.18.532424 · Cited by 1
The causal involvement of the visual cortex in visual working memory remains unclear: a comment on Phylactou et al., 2023Preprint
Grassi, P. R., Bannert, M. M., & Bartels, A. (2023) · doi:10.31234/osf.io/t3z7u · Cited by 1
Modular Phoneme Processing in Human Superior Temporal GyrusPreprint
Cleary, D. R., Tchoe, Y., Bourhis, A. M., Dickey, C. W., Stedelin, B., Ganji, M., Lee, S. H., Lee, J., Siler, D. A., Brown, E. C., et al. (2024) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2024.01.17.576120 · Cited by 1
Relating ECoG and the local field potential to underlying mechanisms
Vermaas, M. (2014) · Utrecht University Repository (Utrecht University)
Vision and Driving after Stroke
Smith, M. E. (2014) · White Rose eTheses Online (University of Leeds, The University of Sheffield, University of York)
From local constraints to global binocular motion perception
Heron, S. (2014) · Enlighten: Theses (The University of Glasgow)
Eficacia de la estimulación neurosensorial en ambliopías
Argilés, M. (2011) · LA Referencia (Red Federada de Repositorios Institucionales de Publicaciones Científicas)
Filling in at partially deafferented visual cortex
de Alvarenga, D. P., Couto, M. F., & Pessoa, V. F. (2008) · British Journal of Ophthalmology · doi:10.1136/bjo.2008.139683
Fine-scale spatial organization of face and object selectivity in the temporal lobe: Do fMRI, optical imaging, and electrophysiology agree
de Beeck, H. O. (2008)
Zur Funktion des Gehirns: Die Sehwelt
Müller, W. D. A., & Frings, S. (2009) · Springer-Lehrbuch · doi:10.1007/978-3-642-00462-9_23
Striate Cortex Functions
Adams, D. L., & Horton, J. C. (2008) · Springer eBooks · doi:10.1007/978-3-540-29678-2_5695 · Cited by 1
Self-citation
The role of sensory history and stimulus context in human time perception. Adaptive and integrative distortions of perceived duration
Fulcher, C. (2017) · Bradford Scholars (University of Bradford)
Clinical Study of Changes in Eye Dominance after Pseudophakic Conventional Monovision
Lee, M., & Shin, K. C. (2019) · Journal of the Korean Ophthalmological Society · doi:10.3341/jkos.2019.60.6.534
Static Automated Perimetry: Hand in Hand with the Neurologist
Eissa, I. M. (2019) · Archives in Neurology & Neuroscience · doi:10.33552/ann.2019.03.000565
Generalized neural field theory of cortical plasticity illustrated by an application to the linear phase of ocular dominance column formation in primary visual cortex
Yajadda, M. M. A., Robinson, P. A., & Henderson, J. A. (2021) · Biological Cybernetics · doi:10.1007/s00422-021-00901-w
Two interdigitated fine-scale channels for encoding motion and stereopsis within the human magnocellular streamPreprint
Kennedy, B., Bex, P. J., Hunter, D. G., & Nasr, S. (2022) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2022.04.20.488911
Overall patterns of eye-specific retino-geniculo-cortical projections to layers III, IV and VI in primary visual cortex of the prosimian galago, and correlation with cytochrome oxidase blobsPreprint
Olavarría, J. F., Qi, H., Takahata, T., & Kaas, J. H. (2022) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2022.06.08.495376
Mutual consistency of multiple visual feature maps constrains combined map topology
Liu, X., & Robinson, P. A. (2023) · Physical review. E · doi:10.1103/physreve.107.064401
Hierarchical cortical plasticity in congenital sight impairmentPreprint
Maimon-Mor, R. O., Farahbakhsh, M., Hedger, N., Rider, A. T., Anderson, E. J., Rees, G. E., Knapen, T. H. J., Michaelides, M., & Dekker, T. M. (2024) · eLife · doi:10.1101/2024.07.04.602138
Hierarchical cortical plasticity in congenital sight impairmentPreprint
Maimon-Mor, R. O., Farahbakhsh, M., Hedger, N., Rider, A. T., Anderson, E. J., Rees, G. E., Knapen, T. H. J., Michaelides, M., & Dekker, T. M. (2024) · eLife · doi:10.7554/elife.100404
Some Further Developments on a Neurobiologically-based Model for Color Sensations in Humans
Wu, C. Q. (2025) · Electronic Imaging · doi:10.2352/ei.2025.37.11.hvei-207 · Cited by 1
Three-dimensional ultrastructural differences between thalamic and non-thalamic recipient layers in macaque V1Preprint
García‐Marín, V., & Hawken, M. J. (2025) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2025.08.04.668334

Authors: Adams, D. L., Sincich, L. C., & Horton, J. C.
Affiliations: University of California, San Francisco (US)
Corresponding author: Horton, Jonathan C.
ORCID: Adams, Daniel L.
Sincich, Lawrence C.
Horton, Jonathan C.
Venue: The Journal of Neuroscience
Publisher: Society for Neuroscience
Published: 2007-09-26
Volume: 27
Issue: 39
Pages: 10391-10403
ISSN: 0270-6474 (ISSN-L)
1529-2401
DOI: 10.1523/jneurosci.2923-07.2007
PMC: PMC6673158
OpenAlex: W2041587140
Cited by: 212
References: 76
Citations by year: 2026: 7 · 2025: 12 · 2024: 13 · 2023: 11 · 2022: 14 · 2021: 9 · 2020: 12 · 2019: 13 · 2018: 7 · 2017: 17 · 2016: 12 · 2015: 13 · 2014: 8 · 2013: 8 · 2012: 13
FWCI: 5.38
Type: journal article
Language: en
Open access: hybrid
doi.org
Licence: cc-by-nc-sa
creativecommons.org/licenses/by-nc-sa/4.0/ (vor, 182 d)
Locations: Journal of Neuroscience (publishedVersion, cc-by-nc-sa)
Europe PMC (PubMed Central) (publishedVersion)
PubMed Central (publishedVersion)
PubMed (publishedVersion)
eScholarship (California Digital Library) (submittedVersion)
Iris (University of Trento) (submittedVersion)
Funders: National Eye Institute (EY02162, P30EY002162, R01EY010217)
Topics: Life Sciences › Neuroscience › Cognitive Neuroscience › Visual perception and processing mechanisms
Life Sciences › Neuroscience › Cognitive Neuroscience › Face Recognition and Perception
Life Sciences › Neuroscience › Cognitive Neuroscience › Tactile and Sensory Interactions
Keywords: ocular dominance columns, primary visual cortex, secondary visual cortex, cytochrome c oxidase, monocular visual loss, visual field representation, blind spots, column width, squirrel monkey
MeSH terms: Adult, Aged, Animals, Blindness, Cadaver, Electron Transport Complex IV, Humans, Macaca, Male, Visual Cortex, Visual Fields, Vision, Binocular, Vision, Monocular, Eye Enucleation, Dominance, Ocular

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

Complete Pattern of Ocular Dominance Columns in Human Primary Visual Cortex

Abstract

Overview

Integrity signals

Verification

Claims the paper makes

Claims other papers make about this one

Self-check

Citations

Cites

Cited by

Related

Metadata

Record

About these checks