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Journal articles on the topic 'Visual Cortex'

Author: Grafiati

Published: 4 June 2021

Last updated: 25 July 2025

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1

Miller, K. D. "= Visual Cortex." Science 330, no. 6007 (2010): 1059–60. http://dx.doi.org/10.1126/science.1198857.

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2

Wlesel, Torsten N., and Charles D. Gilbert. "Visual cortex." Trends in Neurosciences 9 (January 1986): 509–12. http://dx.doi.org/10.1016/0166-2236(86)90161-x.

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3

Prakaash Banga, Ved. "Unique Location of Visual Cortex." Journal of Ophthalmology & Clinical Research 9, no. 2 (2025): 01–02. https://doi.org/10.33140/jocr.09.02.01.

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Importance of Eyes among Five Sense Organs There are five sense organs, touch is sensed by skin ,sound by the ears,smell by the nose, taste by the tongue and vision by the eyes. It is through the eyes only that we perceive about 80% information of the surroundings, the remaining four are only responsible for 20% information of the surroundings. The eyes are the most vital sense organs, but their even more important role lies in expressing emotions. How they instantly convey love or anger has never been a focus in ophthalmology, even though no other sense organ can express human feelings in the

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4

Kaufman, K. J. "The Cerebral Cortex: Visual Cortex." Archives of Ophthalmology 104, no. 8 (1986): 1141. http://dx.doi.org/10.1001/archopht.1986.01050200047040.

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5

Cowey, A. "Cerebral Cortex, Vol. 3, Visual Cortex." Neuroscience 19, no. 3 (1986): 1023. http://dx.doi.org/10.1016/0306-4522(86)90314-3.

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6

Hughes, John R. "Cerebral cortex. Vol. 3. Visual cortex." Electroencephalography and Clinical Neurophysiology 63, no. 4 (1986): 392. http://dx.doi.org/10.1016/0013-4694(86)90029-5.

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7

Taira, Masato, and Narumi Katsuyama. "Visual association cortex." Journal of Japan Society for Fuzzy Theory and Intelligent Informatics 18, no. 3 (2006): 377–82. http://dx.doi.org/10.3156/jsoft.18.3_377.

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8

Tusa, Ronald J. "The Visual Cortex." American Journal of EEG Technology 26, no. 3 (1986): 135–43. http://dx.doi.org/10.1080/00029238.1986.11080198.

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9

Hübener, Mark. "Mouse visual cortex." Current Opinion in Neurobiology 13, no. 4 (2003): 413–20. http://dx.doi.org/10.1016/s0959-4388(03)00102-8.

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10

Tong, Frank. "Primary visual cortex and visual awareness." Nature Reviews Neuroscience 4, no. 3 (2003): 219–29. http://dx.doi.org/10.1038/nrn1055.

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11

Beltramo, Riccardo, and Massimo Scanziani. "A collicular visual cortex: Neocortical space for an ancient midbrain visual structure." Science 363, no. 6422 (2019): 64–69. http://dx.doi.org/10.1126/science.aau7052.

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Visual responses in the cerebral cortex are believed to rely on the geniculate input to the primary visual cortex (V1). Indeed, V1 lesions substantially reduce visual responses throughout the cortex. Visual information enters the cortex also through the superior colliculus (SC), but the function of this input on visual responses in the cortex is less clear. SC lesions affect cortical visual responses less than V1 lesions, and no visual cortical area appears to entirely rely on SC inputs. We show that visual responses in a mouse lateral visual cortical area called the postrhinal cortex are inde

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12

La Chioma, Alessandro, and Mark Hübener. "Visual Cortex: Binocular Matchmaking." Current Biology 31, no. 4 (2021): R197—R199. http://dx.doi.org/10.1016/j.cub.2020.12.011.

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13

Grill-Spector, Kalanit, and Rafael Malach. "THE HUMAN VISUAL CORTEX." Annual Review of Neuroscience 27, no. 1 (2004): 649–77. http://dx.doi.org/10.1146/annurev.neuro.27.070203.144220.

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14

Stern, Peter. "Another primary visual cortex." Science 363, no. 6422 (2019): 39.16–41. http://dx.doi.org/10.1126/science.363.6422.39-p.

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15

Snodderly, M. "Awakening the visual cortex." Journal of Vision 3, no. 12 (2010): 15. http://dx.doi.org/10.1167/3.12.15.

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16

Martin, K. "Microcircuits in visual cortex." Current Opinion in Neurobiology 12, no. 4 (2002): 418–25. http://dx.doi.org/10.1016/s0959-4388(02)00343-4.

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17

Mante, Valerio, and Matteo Carandini. "Visual Cortex: Seeing Motion." Current Biology 13, no. 23 (2003): R906—R908. http://dx.doi.org/10.1016/j.cub.2003.11.010.

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18

Poggio, Tomaso, and Thomas Serre. "Models of visual cortex." Scholarpedia 8, no. 4 (2013): 3516. http://dx.doi.org/10.4249/scholarpedia.3516.

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19

Jha, Vidyapati, Bineet Gupta, and Yogesh Pal. "MOONLIGHT AND VISUAL CORTEX." International Journal of Advanced Research 7, no. 10 (2019): 541–43. http://dx.doi.org/10.21474/ijar01/9863.

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20

Zeki, Semir. "The visual association cortex." Current Opinion in Neurobiology 3, no. 2 (1993): 155–59. http://dx.doi.org/10.1016/0959-4388(93)90203-b.

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21

Zeng, Hang, Gereon R. Fink, and Ralph Weidner. "Visual Size Processing in Early Visual Cortex Follows Lateral Occipital Cortex Involvement." Journal of Neuroscience 40, no. 22 (2020): 4410–17. http://dx.doi.org/10.1523/jneurosci.2437-19.2020.

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22

van den Hurk, Job, Marc Van Baelen, and Hans P. Op de Beeck. "Development of visual category selectivity in ventral visual cortex does not require visual experience." Proceedings of the National Academy of Sciences 114, no. 22 (2017): E4501—E4510. http://dx.doi.org/10.1073/pnas.1612862114.

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To what extent does functional brain organization rely on sensory input? Here, we show that for the penultimate visual-processing region, ventral-temporal cortex (VTC), visual experience is not the origin of its fundamental organizational property, category selectivity. In the fMRI study reported here, we presented 14 congenitally blind participants with face-, body-, scene-, and object-related natural sounds and presented 20 healthy controls with both auditory and visual stimuli from these categories. Using macroanatomical alignment, response mapping, and surface-based multivoxel pattern anal

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23

Schoups, Aniek A., and Ira B. Black. "Visual Experience Specifically Regulates Synaptic Molecules in Rat Visual Cortex." Journal of Cognitive Neuroscience 3, no. 3 (1991): 252–57. http://dx.doi.org/10.1162/jocn.1991.3.3.252.

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To study environmental modulation of synaptic molecular structure, the major postsynaptic density protein (mPSDp) from rat visual cortex was monitored. This membrane component, a Ca2+/calmodulin-dependent protein kinase subunit, was measured during normal postnatal development and after visual deprivation. Total synaptic membrane (SM) protein was used as an index of synapses as a whole. During the first 2 postnatal months, total SM protein in the visual cortex increased 32–fold. In contrast, the mPSDp increased 455–fold, indicating that different molecular components of the cortical synapse de

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24

Xie, Kei, and Bert Zhang. "Causal Role for Visual Cortex in Processing Visual Semantics." Communications in Humanities Research 55, no. 1 (2025): 27–33. https://doi.org/10.54254/2753-7064/2024.21047.

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This article reviewed previous studies testing for the causal or correlational relationship between modality-specific brain regions (e.g. motor cortex) and processing of corresponding perceptual-motor semantics. The proposed experiment aimed to investigate the functional role of visual cortex in understanding visual-associated words by studying the selective effect of transcranial direct current stimulation (tDCS) to primary visual cortex on response time (RT) to visual-associated words in lexical decision task. Participants will receive either sham or true anodal-tDCS, then perform the audito

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25

Chen, Ling-Chia, Pascale Sandmann, Jeremy D. Thorne, Martin G. Bleichner, and Stefan Debener. "Cross-Modal Functional Reorganization of Visual and Auditory Cortex in Adult Cochlear Implant Users Identified with fNIRS." Neural Plasticity 2016 (2016): 1–13. http://dx.doi.org/10.1155/2016/4382656.

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Cochlear implant (CI) users show higher auditory-evoked activations in visual cortex and higher visual-evoked activation in auditory cortex compared to normal hearing (NH) controls, reflecting functional reorganization of both visual and auditory modalities. Visual-evoked activation in auditory cortex is a maladaptive functional reorganization whereas auditory-evoked activation in visual cortex is beneficial for speech recognition in CI users. We investigated their joint influence on CI users’ speech recognition, by testing 20 postlingually deafened CI users and 20 NH controls with functional

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26

Qin, Wen, and Chunshui Yu. "Neural Pathways Conveying Novisual Information to the Visual Cortex." Neural Plasticity 2013 (2013): 1–14. http://dx.doi.org/10.1155/2013/864920.

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The visual cortex has been traditionally considered as a stimulus-driven, unimodal system with a hierarchical organization. However, recent animal and human studies have shown that the visual cortex responds to non-visual stimuli, especially in individuals with visual deprivation congenitally, indicating the supramodal nature of the functional representation in the visual cortex. To understand the neural substrates of the cross-modal processing of the non-visual signals in the visual cortex, we firstly showed the supramodal nature of the visual cortex. We then reviewed how the nonvisual signal

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27

Joo, Sung Jun. "Reaction Times to Predictable Visual Patterns Reflect Neural Responses in Early Visual Cortex." Korean Society for Emotion and Sensibility 24, no. 2 (2021): 57–64. http://dx.doi.org/10.14695/kjsos.2021.24.2.57.

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28

Ciaramitaro, V. M., and G. M. Boynton. "Visual-auditory spatial attention in human visual cortex." Journal of Vision 5, no. 8 (2010): 171. http://dx.doi.org/10.1167/5.8.171.

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29

Feng, W., V. S. Stormer, A. Martinez, J. J. McDonald, and S. A. Hillyard. "Sounds Activate Visual Cortex and Improve Visual Discrimination." Journal of Neuroscience 34, no. 29 (2014): 9817–24. http://dx.doi.org/10.1523/jneurosci.4869-13.2014.

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30

Sengpiel, Frank, and Mark Hübener. "Visual perception: Spotlight on the primary visual cortex." Current Biology 9, no. 9 (1999): R318—R321. http://dx.doi.org/10.1016/s0960-9822(99)80202-4.

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31

Silvanto, Juha. "Is primary visual cortex necessary for visual awareness?" Trends in Neurosciences 37, no. 11 (2014): 618–19. http://dx.doi.org/10.1016/j.tins.2014.09.006.

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32

Goda, Naokazu, Takuya Harada, Tadashi Ogawa, et al. "Influence of visual saliency in monkey visual cortex." Neuroscience Research 58 (January 2007): S96. http://dx.doi.org/10.1016/j.neures.2007.06.1125.

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33

Goldstein, Laura H., and David A. Oakley. "Visual discrimination in the absence of visual cortex." Behavioural Brain Research 24, no. 3 (1987): 181–93. http://dx.doi.org/10.1016/0166-4328(87)90056-8.

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34

Switkes, Eugene, David Rose, and Vernon G. Dobson. "Models of the Visual Cortex." American Journal of Psychology 101, no. 2 (1988): 304. http://dx.doi.org/10.2307/1422844.

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35

Froudarakis, Emmanouil, Paul G. Fahey, Jacob Reimer, Stelios M. Smirnakis, Edward J. Tehovnik, and Andreas S. Tolias. "The Visual Cortex in Context." Annual Review of Vision Science 5, no. 1 (2019): 317–39. http://dx.doi.org/10.1146/annurev-vision-091517-034407.

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In this article, we review the anatomical inputs and outputs to the mouse primary visual cortex, area V1. Our survey of data from the Allen Institute Mouse Connectivity project indicates that mouse V1 is highly interconnected with both cortical and subcortical brain areas. This pattern of innervation allows for computations that depend on the state of the animal and on behavioral goals, which contrasts with simple feedforward, hierarchical models of visual processing. Thus, to have an accurate description of the function of V1 during mouse behavior, its involvement with the rest of the brain c

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36

PARKER, A. J., and M. J. HAWKEN. "Hyperacuity and the visual cortex." Nature 326, no. 6108 (1987): 105–6. http://dx.doi.org/10.1038/326105b0.

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37

SWINDALE, N. V., and M. S. CYNADER. "Hyperacuity and the visual cortex." Nature 326, no. 6108 (1987): 106. http://dx.doi.org/10.1038/326106a0.

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38

Beltramo, Riccardo. "A new primary visual cortex." Science 370, no. 6512 (2020): 46.2–46. http://dx.doi.org/10.1126/science.abe1482.

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39

Gilbert, C. D., J. A. Hirsch, and T. N. Wiesel. "Lateral Interactions in Visual Cortex." Cold Spring Harbor Symposia on Quantitative Biology 55 (January 1, 1990): 663–77. http://dx.doi.org/10.1101/sqb.1990.055.01.063.

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40

Stern, Peter. "Rethinking primary visual cortex function." Science 364, no. 6447 (2019): 1247.14–1249. http://dx.doi.org/10.1126/science.364.6447.1247-n.

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41

Chan, Jane W. "The Cat Primary Visual Cortex." Journal of Neuro-Ophthalmology 26, no. 1 (2006): 70. http://dx.doi.org/10.1097/01.wno.0000206242.42410.de.

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42

Ozdemir, Aysegul, and Peter M. Black. "Mapping of Human Visual Cortex." Neurosurgery Quarterly 15, no. 2 (2005): 65–71. http://dx.doi.org/10.1097/01.wnq.0000155121.49959.2c.

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43

Wolf, F., H. U. Bauer, K. Pawelzik, and T. Geisel. "Organization of the visual cortex." Nature 382, no. 6589 (1996): 306. http://dx.doi.org/10.1038/382306a0.

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44

Bonhoeffer, Tobias, and Imke Gödecke. "Organization of the visual cortex." Nature 382, no. 6589 (1996): 306–7. http://dx.doi.org/10.1038/382306b0.

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45

Whalley, Katherine. "Networking in the visual cortex." Nature Reviews Neuroscience 12, no. 6 (2011): 306. http://dx.doi.org/10.1038/nrn3041.

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46

Downing, P. E., A. W. Y. Chan, M. V. Peelen, C. M. Dodds, and N. Kanwisher. "Domain Specificity in Visual Cortex." Cerebral Cortex 16, no. 10 (2005): 1453–61. http://dx.doi.org/10.1093/cercor/bhj086.

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47

Jain, Rishabh, Rachel Millin, and Bartlett W. Mel. "Multimap formation in visual cortex." Journal of Vision 15, no. 16 (2015): 3. http://dx.doi.org/10.1167/15.16.3.

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48

Maringer, Russell. "FMRI OF AMBLYOPIC VISUAL CORTEX." Optometry and Vision Science 79, Supplement (2002): 217. http://dx.doi.org/10.1097/00006324-200212001-00410.

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49

Heeger, David J., Geoffrey M. Boynton, Jonathan B. Demb, Eyal Seidemann, and William T. Newsome. "Motion Opponency in Visual Cortex." Journal of Neuroscience 19, no. 16 (1999): 7162–74. http://dx.doi.org/10.1523/jneurosci.19-16-07162.1999.

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50

Carandini, Matteo. "Visual cortex: Fatigue and adaptation." Current Biology 10, no. 16 (2000): R605—R607. http://dx.doi.org/10.1016/s0960-9822(00)00637-0.

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