Relevant bibliographies by topics / Retinotopic

Academic literature on the topic 'Retinotopic'

Author: Grafiati
Published: 10 December 2022
Last updated: 28 January 2023

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Journal articles on the topic "Retinotopic"

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Yang, Zhiyong, David J. Heeger, and Eyal Seidemann. "Rapid and Precise Retinotopic Mapping of the Visual Cortex Obtained by Voltage-Sensitive Dye Imaging in the Behaving Monkey." Journal of Neurophysiology 98, no. 2 (August 2007): 1002–14. http://dx.doi.org/10.1152/jn.00417.2007.

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Retinotopy is a fundamental organizing principle of the visual cortex. Over the years, a variety of techniques have been used to examine it. None of these techniques, however, provides a way to rapidly characterize retinotopy, at the submillimeter range, in alert, behaving subjects. Voltage-sensitive dye imaging (VSDI) can be used to monitor neuronal population activity at high spatial and temporal resolutions. Here we present a VSDI protocol for rapid and precise retinotopic mapping in the behaving monkey. Two monkeys performed a fixation task while thin visual stimuli swept periodically at a high speed in one of two possible directions through a small region of visual space. Because visual space is represented systematically across the cortical surface, each moving stimulus produced a traveling wave of activity in the cortex that could be precisely measured with VSDI. The time at which the peak of the traveling wave reached each location in the cortex linked this location with its retinotopic representation. We obtained detailed retinotopic maps from a region of about 1 cm2 over the dorsal portion of areas V1 and V2. Retinotopy obtained during <4 min of imaging had a spatial precision of 0.11–0.19 mm, was consistent across experiments, and reliably predicted the locations of the response to small localized stimuli. The ability to rapidly obtain precise retinotopic maps in behaving monkeys opens the door for detailed analysis of the relationship between spatiotemporal dynamics of population responses in the visual cortex and perceptually guided behavior.
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Sayres, Rory, and Kalanit Grill-Spector. "Relating Retinotopic and Object-Selective Responses in Human Lateral Occipital Cortex." Journal of Neurophysiology 100, no. 1 (July 2008): 249–67. http://dx.doi.org/10.1152/jn.01383.2007.

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What is the relationship between retinotopy and object selectivity in human lateral occipital (LO) cortex? We used functional magnetic resonance imaging (fMRI) to examine sensitivity to retinal position and category in LO, an object-selective region positioned posterior to MT along the lateral cortical surface. Six subjects participated in phase-encoded retinotopic mapping experiments as well as block-design experiments in which objects from six different categories were presented at six distinct positions in the visual field. We found substantial position modulation in LO using standard nonobject retinotopic mapping stimuli; this modulation extended beyond the boundaries of visual field maps LO-1 and LO-2. Further, LO showed a pronounced lower visual field bias: more LO voxels represented the lower contralateral visual field, and the mean LO response was higher to objects presented below fixation than above fixation. However, eccentricity effects produced by retinotopic mapping stimuli and objects differed. Whereas LO voxels preferred a range of eccentricities lying mostly outside the fovea in the retinotopic mapping experiment, LO responses were strongest to foveally presented objects. Finally, we found a stronger effect of position than category on both the mean LO response, as well as the distributed response across voxels. Overall these results demonstrate that retinal position exhibits strong effects on neural response in LO and indicates that these position effects may be explained by retinotopic organization.
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Tu, Yanshuai, Duyan Ta, Zhong-Lin Lu, and Yalin Wang. "Topology-preserving smoothing of retinotopic maps." PLOS Computational Biology 17, no. 8 (August 2, 2021): e1009216. http://dx.doi.org/10.1371/journal.pcbi.1009216.

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Retinotopic mapping, i.e., the mapping between visual inputs on the retina and neuronal activations in cortical visual areas, is one of the central topics in visual neuroscience. For human observers, the mapping is obtained by analyzing functional magnetic resonance imaging (fMRI) signals of cortical responses to slowly moving visual stimuli on the retina. Although it is well known from neurophysiology that the mapping is topological (i.e., the topology of neighborhood connectivity is preserved) within each visual area, retinotopic maps derived from the state-of-the-art methods are often not topological because of the low signal-to-noise ratio and spatial resolution of fMRI. The violation of topological condition is most severe in cortical regions corresponding to the neighborhood of the fovea (e.g., < 1 degree eccentricity in the Human Connectome Project (HCP) dataset), significantly impeding accurate analysis of retinotopic maps. This study aims to directly model the topological condition and generate topology-preserving and smooth retinotopic maps. Specifically, we adopted the Beltrami coefficient, a metric of quasiconformal mapping, to define the topological condition, developed a mathematical model to quantify topological smoothing as a constrained optimization problem, and elaborated an efficient numerical method to solve the problem. The method was then applied to V1, V2, and V3 simultaneously in the HCP dataset. Experiments with both simulated and real retinotopy data demonstrated that the proposed method could generate topological and smooth retinotopic maps.
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Rajimehr, Reza, Natalia Y. Bilenko, Wim Vanduffel, and Roger B. H. Tootell. "Retinotopy versus Face Selectivity in Macaque Visual Cortex." Journal of Cognitive Neuroscience 26, no. 12 (December 2014): 2691–700. http://dx.doi.org/10.1162/jocn_a_00672.

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Retinotopic organization is a ubiquitous property of lower-tier visual cortical areas in human and nonhuman primates. In macaque visual cortex, the retinotopic maps extend to higher-order areas in the ventral visual pathway, including area TEO in the inferior temporal (IT) cortex. Distinct regions within IT cortex are also selective to specific object categories such as faces. Here we tested the topographic relationship between retinotopic maps and face-selective patches in macaque visual cortex using high-resolution fMRI and retinotopic face stimuli. Distinct subregions within face-selective patches showed either (1) a coarse retinotopic map of eccentricity and polar angle, (2) a retinotopic bias to a specific location of visual field, or (3) nonretinotopic selectivity. In general, regions along the lateral convexity of IT cortex showed more overlap between retinotopic maps and face selectivity, compared with regions within the STS. Thus, face patches in macaques can be subdivided into smaller patches with distinguishable retinotopic properties.
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Fitzgibbon, T., and B. E. Reese. "Organization of retinal ganglion cell axons in the optic fiber layer and nerve of fetal ferrets." Visual Neuroscience 13, no. 5 (September 1996): 847–61. http://dx.doi.org/10.1017/s095252380000910x.

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AbstractPrevious authors have hypothesized that retinotopic projections may be influenced by ‘preordering’ of the axons as they grow towards their targets. In some nonmammalian species, axons are reorganized at or near the optic nerve head to establish a retinotopic order. Data are ambiguous concerning the retinotopy of the mammalian retinal nerve fiber layer and whether fibers become reorganized at the optic nerve head. We have examined this question in fetal and newborn ferrets (Mustela putorius furo) by comparing the arrangement of axons in the retinal nerve fiber layer with that in the optic nerve. Dil or DiA crystals were implanted into fixed tissue in the innermost layers of the retinal periphery, or at a location midway between the periphery and the optic nerve head. Fluorescence labelling was examined in 100–200 μm Vibratome sections, or the eyecup and nerve were photooxidized and 1–2 μm longitudinal or transverse sections were examined. Regardless of fetal age, eccentricity or quadrant of the implant site, a segregation of labelled peripheral axons from unlabelled central ones was not detected within the nerve fiber layer. Axons coursed into the nerve head along the margin of their retinal quadrant of origin, often entering the optic nerve as a radial wedge, thus preserving a rough map of retinal circumference. However, peripheral axons were in no way restricted to the peripheral (nor central) portions of the nerve head or nerve, indicating that the optic axons do not establish a map of retinal eccentricity. Our results demonstrate that (1) the nerve fiber layer is retinotopic only with respect to circumferential position and (2) optic axons are not actively reorganized to establish a retinotopic ordering at the nerve head. The present results suggest that any degree of order present within the optic nerve is a passive consequence of combining the fascicles of the retinal nerve fiber layer; optic axons are not instructed to establish, nor constrained to maintain, a retinotopic order within the optic nerve.
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Noory, Babak, Michael H. Herzog, and Haluk Ogmen. "Retinotopy of visual masking and non-retinotopic perception during masking." Attention, Perception, & Psychophysics 77, no. 4 (March 14, 2015): 1263–84. http://dx.doi.org/10.3758/s13414-015-0844-2.

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Choung, Oh-hyeon, Marc Lauffs, Haluk Ögmen, and Michael Herzog. "How unconscious retinotopic processing influences conscious non-retinotopic perception." Journal of Vision 18, no. 10 (September 1, 2018): 292. http://dx.doi.org/10.1167/18.10.292.

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Lauffs, Marc M., Oh-Hyeon Choung, Haluk Öğmen, and Michael H. Herzog. "Unconscious retinotopic motion processing affects non-retinotopic motion perception." Consciousness and Cognition 62 (July 2018): 135–47. http://dx.doi.org/10.1016/j.concog.2018.03.007.

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STIRLING, R. V., S. A. DUNLOP, and L. D. BEAZLEY. "Electrophysiological evidence for transient topographic organization of retinotectal projections during optic nerve regeneration in the lizard, Ctenophorus ornatus." Visual Neuroscience 16, no. 4 (July 1999): 681–93. http://dx.doi.org/10.1017/s0952523899164083.

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In the lizard, Ctenophorus ornatus, anatomical studies have revealed that optic axons regenerate to visual centers within 2 months of nerve crush but that, from the outset, the regenerated projections lack topographic order (Beazley et al., 1997; Dunlop et al., 1997b). Here we assess the functional topography of the regenerated retinotectal projections by electrophysiological recording of extracellular multiunit responses to visual stimulation and by observing the lizards' ability to capture live prey. At the completion of the electrophysiology, DiI was applied locally to the retina and the topography of the tectal projection later assessed. Electrophysiology revealed that, at 2–4.2 months, responses were weak and habituated readily; no retinotopic order was detected. Between 4.5–6 months, responses were more reliable and the majority of lizards displayed a crude retinotopic order, especially in the ventro-temporal to dorso-nasal retinal axis. Although responses were variable between 6–9 months, they tended to be more reliable again thereafter. However, from 6–18 months, the projection consistently lacked topography with many retinal regions projecting to each tectal locus. Lizards, including those with electrophysiological evidence of crude retinotopy, were consistently unable to capture live prey using the experimental eye. Labelling with DiI confirmed the absence of anatomical retinotopy throughout. Taken together, the electrophysiological and anatomical data indicate that retinotopically appropriate axon terminals (or parts thereof) are transiently active whilst inappropriately located ones are silent. Presumably in lizard map-making cues fade with time and/or the mechanisms are lacking to stabilize and refine the ephemeral map. Moreover, the transient retinotopy is insufficient for useful visual function.
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Cavanagh, P., and A. O. Holcombe. "Non-retinotopic crowding." Journal of Vision 7, no. 9 (March 19, 2010): 338. http://dx.doi.org/10.1167/7.9.338.

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Dissertations / Theses on the topic "Retinotopic"

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Seidel, Dirk. "Retinotopic and spatiotopic accommodation responses in emmetropia and myopia." Thesis, Glasgow Caledonian University, 2003. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.289522.

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The incidence of myopia has been rising steadily over the last century. Today the prevalence of the condition ranges from under 1% in remote parts of the world to over 90% in some highly industrialised urban areas. The associated pathological risk factors in connection with the continuous increase in the number of myopic individuals have put increasing pressure on the health and social systems worldwide. The aetiology and course of the condition has therefore always been of interest to patients, ophthalmic practitioners and researchers alike. Reduced accommodation responses as a precursor to or even a cause of myopia have been proposed for a long time. Increased lags of accommodation found in myopes, causing a reduction in the quality of the retinal image, seem to support animal models, which have suggested that retinal defocus if present over longer periods of time can lead to the elongation of the globe. In this work different aspects of the accommodation response have been studied in emmetropes (EMM), early-onset (EOM) and late-onset myopes (LOM) under a variety of viewing conditions. The steady state accommodation response, the microfluctuations of accommodation and accommodation step responses of different magnitudes (1-dioptre and 2-dioptre steps) were examined for retinotopic (eye referenced) and spatiotopic (body-referenced) viewing conditions. Retinotopic conditions involved viewing targets in Badal systems. Spatiotopic viewing involved real targets presented in free space thus providing size and proximity cues to the accommodation controller. The free space targets were viewed monocularly and binocularly, which examined the importance of vergence accommodation for the different refractive groups. Steady state accommodation responses were found to be similar across the refractive groups for all viewing conditions. LOM subjects however, showed higher variability of their steady-state response in Badal systems but not in free space viewing. LOMs also demonstrated significantly greater microfluctuations of accommodation in the retinotopic condition, while the fluctuations were of similar magnitude for all groups for free space viewing. While EMMs and EOMs responded promptly and quickly to step changes in target vergence in both retinotopic and spatiotopic conditions, LOMs showed slower reaction and response times in the blur-only environment. Analysis of the response rate (percentage of step changes made for a given number of stimulus changes) revealed that some LOMs hesitated to adjust their accommodation to small step changes in target distance when only retinotopic cues were present. Real targets alleviated these differences between the groups and increased the LOMs response rate considerably. The minimum blur threshold of the accommodation controller was examined presenting sinusoidal stimuli of very small dioptric magnitude in a Badal system. Fourier analysis revealed that EMMs and EOMs responded to stimuli < 0.15 D while LOMs required stimuli > 0.3 D. Cross-correlating the findings of the different experiments showed that LOMs with inaccurate and more variable accommodation responses in retinotopic conditions improve substantially with the introduction of real world targets, whereas EMMs and EOMs with sufficient blur accommodation show no significant improvement. The findings indicate a deficient blur processing in LOMs but demonstrate that there are no significant differences in accommodation performance between emmetropes and myopes in real world conditions. The implications of the findings on the development and progression of myopia are discussed at the end of the thesis.
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Choi, Yu Wing. "Neuromorphic implementation of retinotopic arrays of orientation selective hypercolumns /." View Abstract or Full-Text, 2003. http://library.ust.hk/cgi/db/thesis.pl?ELEC%202003%20CHOIY.

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Cutts, Catherine Sarah. "The role of correlated activity in the developing retinotopic map." Thesis, University of Cambridge, 2016. https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.709507.

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Silson, Edward H. "Functional specialization & parallel processing within retinotopic subdivisions of lateral occipital cortex." Thesis, University of York, 2013. http://etheses.whiterose.ac.uk/4966/.

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This thesis aimed to probe the functional specializations present within several retinotopic divisions of human lateral occipital cortex (LO). The divisions of interest were LO1 and LO2, two neighbouring visual field maps that are found within object-selective LO; the posterior portion of a larger area referred to as the lateral occipital complex (LOC), and V5/MT, the well-known visual complex that is highly selective to visual motion. In order to seek out the causal roles played by these divisions in human visual perception, I used transcranial magnetic stimulation to temporarily disrupt neural processing within these areas, while observers performed visual tasks. The visual tasks I employed examined both spatial vision, through orientation and shape discriminations, and motion processing, through speed discrimination. The data revealed a number of double dissociations. A double dissociation was present between LO1 and V5/MT in the perceptions of orientation and speed. A similar pattern of results was present during orientation and speed discrimination of the same moving stimuli, although this effect was markedly weaker. Additionally, a double dissociation was present between LO1 and LO2 in the perceptions of static orientation and shape, respectively. These double dissociations suggest that LO1, LO2 and V5/MT exhibit functional specializations for orientation, shape and speed, respectively and moreover, perform these specialized roles largely independently of one another. It is unsurprising that I found evidence for parallel processing of motion and aspects of spatial processing because: (1) V5/MT has been shown to be a cluster of multiple visual field maps with a common foveal representation – a feature that has led to the idea that the maps within clusters perform related aspects of processing, but are independent of the processing undertaken in adjacent visual field map clusters like LO; (2) neuropsychological evidence, from studies of akinetopsia and visual form agnosia, points to a double dissociation in processing of motion and form and (3) there is evidence of parallel processing pathways from early visual areas and even subcortical structures to V5/MT. The parallel processing of orientation and shape in LO1 and LO2 is a novel and more surprising finding for the following reasons: (1) These visual field maps are adjacent maps within a single cluster and therefore, might be expected to perform a series of related and dependent roles and (2) shape, as defined here by curvature, could be seen as a property that is dependent on orientation processing. These findings therefore, point to an architecture whereby the extrastriate visual maps in LO sample visual information from antecedent visual areas in parallel, to extract higher order spatial statistics. Mutual retinotopic information and parallel processing not only reduces replicated information across maps but also, provides a common mechanism for communication between maps which exhibit different specializations. Importantly, the well-known category-selectivity of extrastriate regions, like LO, may simply emerge from patterns of unique and low-level visual computations, which encode category specific image statistics, performed by the individual visual field maps that subdivide these areas.
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Creutzfeldt, Claire. "The role of EphrinA for the retinotopic map formation in mouse visual cortex." Diss., lmu, 2003. http://nbn-resolving.de/urn:nbn:de:bvb:19-16896.

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Strang, Niall C. "Modulation of foveal image quality in myopia : investigation of spatiotopic and retinotopic factors." Thesis, Glasgow Caledonian University, 1995. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.261581.

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Gebhardt, Christoph [Verfasser], and M. [Akademischer Betreuer] Bastmeyer. "Development & Experimental Validation of a Novel Computational Model of Retinotopic Mapping = (Entwicklung und experimentelle Überprüfung eines neuen Computermodells der Entstehung retinotoper Karten) / Christoph Gebhardt. Betreuer: M. Bastmeyer." Karlsruhe : KIT-Bibliothek, 2011. http://d-nb.info/1014817838/34.

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Voyatzis, Sylvie. "Neural activity controls retinotopic projections in the superior collicul us by modulating axon retraction and cell survival." Paris 6, 2009. http://www.theses.fr/2009PA066311.

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L’activité spontanée joue un rôle important dans le développement des cartes retinotopiques. Nous avons utilisé un model de co-culture qui récapitule la mise en place de la carte retino-colliculaire afin de déterminer où l’activité agit. Nous avons démontré que l’activité neuronale est requise pour la rétraction des axones rétiniens induite par les éphrine-As. Elle nécessite l’entrée de calcium par des canaux calciques de type-L et des stocks internes de calcium. Nous avons déterminé que des fluctuations d’AMPc et de la PKA sont aussi essentielles. Nous avons cherché à montrer l’existence d’oscillations d’AMPc grâce à une technique d’imagerie basée sur le principe du FRET. Nous avons analysé la maturation des types cellulaires rétiniens au cours de la co-culture, afin de déterminer les circuits neuronaux sous-tendant l’émergence de l’activité spontanée. Nous avons analysé la mort cellulaire d’une population de CGR. Nous avons montré que la diminution du nombre de CGR avait lieu entre DIV4 et DIV7, correspondant à la période P0 à P3 : le pic de mort cellulaire développementale in vivo. Cette mort cellulaire dépend de la cible et de l’activité neuronale.
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Sayres, Rory. "Decoding fmri response patterns in visual cortex : effects of object category, identity, retinotopic position, and short-term experience /." May be available electronically:, 2007. http://proquest.umi.com/login?COPT=REJTPTU1MTUmSU5UPTAmVkVSPTI=&clientId=12498.

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Berman, Daniel. "From Photons to Photos: Mapping Functional and Organizational Properties of Human Visual Cortex with fMRI." The Ohio State University, 2015. http://rave.ohiolink.edu/etdc/view?acc_num=osu1422972281.

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Book chapters on the topic "Retinotopic"

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Lysne, Paige, and Yenisel Cruz-Almeida. "Retinotopic Mapping." In Encyclopedia of Clinical Neuropsychology, 3007–8. Cham: Springer International Publishing, 2018. http://dx.doi.org/10.1007/978-3-319-57111-9_9116.

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Lysne, Paige, and Yenisel Cruz-Almeida. "Retinotopic Mapping." In Encyclopedia of Clinical Neuropsychology, 1–2. Cham: Springer International Publishing, 2017. http://dx.doi.org/10.1007/978-3-319-56782-2_9116-2.

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Eglen, Stephen J. "Retinotopic Development, Models of." In Encyclopedia of Computational Neuroscience, 2631–33. New York, NY: Springer New York, 2015. http://dx.doi.org/10.1007/978-1-4614-6675-8_406.

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Eglen, Stephen J. "Retinotopic Development, Models of." In Encyclopedia of Computational Neuroscience, 1–4. New York, NY: Springer New York, 2014. http://dx.doi.org/10.1007/978-1-4614-7320-6_406-1.

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Ma, Libo. "Retinotopic Sparse Representation of Natural Images." In Advances in Cognitive Neurodynamics (II), 435–39. Dordrecht: Springer Netherlands, 2010. http://dx.doi.org/10.1007/978-90-481-9695-1_69.

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Antsiperov, Viacheslav, and Vladislav Kershner. "Retinotopic Image Encoding by Samples of Counts." In Lecture Notes in Computer Science, 52–75. Cham: Springer International Publishing, 2023. http://dx.doi.org/10.1007/978-3-031-24538-1_3.

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Alonso-Fernandez, Fernando, and Josef Bigun. "Periocular Recognition Using Retinotopic Sampling and Gabor Decomposition." In Computer Vision – ECCV 2012. Workshops and Demonstrations, 309–18. Berlin, Heidelberg: Springer Berlin Heidelberg, 2012. http://dx.doi.org/10.1007/978-3-642-33868-7_31.

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Tu, Yanshuai, Duyan Ta, Zhong-Lin Lu, and Yalin Wang. "Topological Receptive Field Model for Human Retinotopic Mapping." In Medical Image Computing and Computer Assisted Intervention – MICCAI 2021, 639–49. Cham: Springer International Publishing, 2021. http://dx.doi.org/10.1007/978-3-030-87234-2_60.

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Cline, Hollis T. "The Activity-Dependent Mechanism in the Development of the Refined Retinotopic Map." In The Visual System from Genesis to Maturity, 63–70. Boston, MA: Birkhäuser Boston, 1992. http://dx.doi.org/10.1007/978-1-4899-6726-8_5.

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Tu, Yanshuai, Duyan Ta, Zhong-Lin Lu, and Yalin Wang. "Optimizing Visual Cortex Parameterization with Error-Tolerant Teichmüller Map in Retinotopic Mapping." In Medical Image Computing and Computer Assisted Intervention – MICCAI 2020, 218–27. Cham: Springer International Publishing, 2020. http://dx.doi.org/10.1007/978-3-030-59728-3_22.

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Conference papers on the topic "Retinotopic"

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Tu, Yanshuai, Duyan Tal, Zhong-Lin Lu, and Yalin Wang. "Diffeomorphic Smoothing for Retinotopic Mapping." In 2020 IEEE 17th International Symposium on Biomedical Imaging (ISBI). IEEE, 2020. http://dx.doi.org/10.1109/isbi45749.2020.9098316.

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Keck, I. R., V. Fischer, A. M. Tome, and E. W. Lang. "Spatiotemporal ICA applied to retinotopic fMRI data." In 2010 32nd Annual International Conference of the IEEE Engineering in Medicine and Biology Society (EMBC 2010). IEEE, 2010. http://dx.doi.org/10.1109/iembs.2010.5627291.

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Chen, XiuXia, Zhen Zhang, and Ximing Shi. "A no-linear retinotopic mapping cognitive 2D model." In 2012 3rd International Conference on System Science, Engineering Design and Manufacturing Informatization (ICSEM). IEEE, 2012. http://dx.doi.org/10.1109/icssem.2012.6340843.

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White, Brian R., Benjamin W. Zeff, Bradley L. Schlaggar, Hamid Dehghani, and Joseph P. Culver. "Phase-Encoded Retinotopic Mapping in Humans with DOT." In Biomedical Optics. Washington, D.C.: OSA, 2008. http://dx.doi.org/10.1364/biomed.2008.bme3.

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Tu, Yanshuai, Duyan Ta, Xianfeng David Gu, Zhong-Lin Lu, and Yalin Wang. "Diffeomorphic Registration for Retinotopic Mapping Via Quasiconformal Mapping." In 2020 IEEE 17th International Symposium on Biomedical Imaging (ISBI). IEEE, 2020. http://dx.doi.org/10.1109/isbi45749.2020.9098386.

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Ko, H., R. H. Baran, and M. Arozullah. "Data compression and novelty filtering in retinotopic backpropagation networks." In 1991 IEEE International Joint Conference on Neural Networks. IEEE, 1991. http://dx.doi.org/10.1109/ijcnn.1991.170765.

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Ta, Duyan, Jie Shi, Brian Barton, Alyssa Brewer, Zhong-Lin Lu, and Yalin Wang. "Characterizing human retinotopic mapping with conformal geometry: a preliminary study." In SPIE Medical Imaging, edited by Sebastien Ourselin and Martin A. Styner. SPIE, 2014. http://dx.doi.org/10.1117/12.2043570.

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Chacon-Murguia, Mario I., Oscar Alejandro Chavez-Montes, and Juan A. Ramirez-Quintana. "Background modeling on depth video sequences using self-organizing retinotopic maps." In 2016 International Joint Conference on Neural Networks (IJCNN). IEEE, 2016. http://dx.doi.org/10.1109/ijcnn.2016.7727319.

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Aslin, Richard N., James Goodwin, Lauren Emberson, Holly Palmeri, and Andrew J. Berger. "Retinotopic mapping in infant visual cortex using near-infrared spectroscopy (NIRS)." In Frontiers in Optics. Washington, D.C.: OSA, 2012. http://dx.doi.org/10.1364/fio.2012.fw1c.4.

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Anqi Qiu, B. J. Rosenau, A. S. Greenberg, P. Barta, S. Yantis, and M. I. Miller. "Localizing Retinotopic fMRI Activation in Human Primary Visual Cortex via Dynamic Programming." In 2005 IEEE Engineering in Medicine and Biology 27th Annual Conference. IEEE, 2005. http://dx.doi.org/10.1109/iembs.2005.1616668.

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