Learning to see again: biological constraints on cortical plasticity and the implications for sight restoration technologies

Image quality assessment: from error visibility to structural similarity

Wang, Z., Bovik, A. C., Sheikh, H. R., & Simoncelli, E. P. (2004) · IEEE Transactions on Image Processing · doi:10.1109/tip.2003.819861 · Cited by 57,892 · see citing works

Untitled work

(1966) · Medical Entomology and Zoology · Cited by 10,293 · see citing works

Signal detection theory and psychophysics

Ingleby, D. (1967) · Journal of Sound and Vibration · doi:10.1016/0022-460x(67)90197-6 · Cited by 8,616 · see citing works

Critical period plasticity in local cortical circuits

Hensch, T. K. (2005) · Nature Reviews Neuroscience · doi:10.1038/nrn1787 · Cited by 2,323 · see citing works

Untitled work

Hochstein (2002) · doi:10.1016/s0896-6273(02)01091-7 · Cited by 1,397 · see citing works

EFFECTS OF VISUAL DEPRIVATION ON MORPHOLOGY AND PHYSIOLOGY OF CELLS IN THE CAT'S LATERAL GENICULATE BODY

Wiesel, T. N., & Hubel, D. H. (1963) · Journal of Neurophysiology · doi:10.1152/jn.1963.26.6.978 · Cited by 1,291 · see citing works

Evidence for striatal dopamine release during a video game

Koepp, M. J., Gunn, R. N., Lawrence, A. D., Cunningham, V. J., Dagher, A., Jones, T., Brooks, D. J., Bench, C. J., & Grasby, P. M. (1998) · Nature · doi:10.1038/30498 · Cited by 1,279 · see citing works

Plasticity in the frequency representation of primary auditory cortex following discrimination training in adult owl monkeys

Recanzone, G., Schreiner, C., & Merzenich, M. (1993) · The Journal of Neuroscience · doi:10.1523/jneurosci.13-01-00087.1993 · Cited by 1,266 · see citing works

The influence of improvement in one mental function upon the efficiency of other functions. (I).

Woodworth, R. S., & Thorndike, E. L. (1901) · Psychological Review · doi:10.1037/h0074898 · Cited by 1,223 · see citing works

BDNF Regulates the Maturation of Inhibition and the Critical Period of Plasticity in Mouse Visual Cortex

Huang, Z. J., Kirkwood, A., Pizzorusso, T., Porciatti, V., Morales, B., Bear, M. F., Maffei, L., & Tonegawa, S. (1999) · Cell · doi:10.1016/s0092-8674(00)81509-3 · Cited by 1,198 · see citing works

Playing an Action Video Game Reduces Gender Differences in Spatial Cognition

Feng, J., Spence, I., & Pratt, J. (2007) · Psychological Science · doi:10.1111/j.1467-9280.2007.01990.x · Cited by 1,155 · see citing works

Cross-modal plasticity: where and how?

Bavelier, D., & Neville, H. J. (2002) · Nature Reviews Neuroscience · doi:10.1038/nrn848 · Cited by 1,040 · see citing works

The reverse hierarchy theory of visual perceptual learning

Ahissar, M., & Hochstein, S. (2004) · Trends in Cognitive Sciences · doi:10.1016/j.tics.2004.08.011 · Cited by 1,005 · see citing works

The antidepressant fluoxetine restores plasticity in the adult visual cortex

Vetencourt, J. F. M., Sale, A., Viegi, A., Baroncelli, L., De Pasquale, R., F. O'Leary, O., Castrén, E., & Maffei, L. (2008) · Science · doi:10.1126/science.1150516 · Cited by 890 · see citing works

Receptive field dynamics in adult primary visual cortex

Gilbert, C. D., & Wiesel, T. N. (1992) · Nature · doi:10.1038/356150a0 · Cited by 871 · see citing works

Practising orientation identification improves orientation coding in V1 neurons

Schoups, A., Vogels, R., Qian, N., & Orban, G. (2001) · Nature · doi:10.1038/35087601 · Cited by 856 · see citing works

Task difficulty and the specificity of perceptual learning

Ahissar, M., & Hochstein, S. (1997) · Nature · doi:10.1038/387401a0 · Cited by 823 · see citing works

Subretinal electronic chips allow blind patients to read letters and combine them to words

Zrenner, E., Bartz-Schmidt, K. U., Benav, H., Besch, D., Bruckmann, A., Gabel, V.-P., Gekeler, F., Greppmaier, U., Harscher, A., Kibbel, S., et al. (2011) · Proceedings of the Royal Society B: Biological Sciences · doi:10.1098/rspb.2010.1747 · Cited by 819 · see citing works

Parallel processing strategies of the primate visual system

Nassi, J. J., & Callaway, E. M. (2009) · Nature Reviews Neuroscience · doi:10.1038/nrn2619 · Cited by 802 · see citing works

Critical periods in speech perception: New directions

Werker, J. F., & Hensch, T. K. (2015) · Annual Review of Psychology · doi:10.1146/annurev-psych-010814-015104 · Cited by 774 · see citing works

EXTENT OF RECOVERY FROM THE EFFECTS OF VISUAL DEPRIVATION IN KITTENS

Wiesel, T. N., & Hubel, D. H. (1965) · Journal of Neurophysiology · doi:10.1152/jn.1965.28.6.1060 · Cited by 704 · see citing works

Organization of visual pathways in normal and visually deprived cats.

Sherman, S. M., & Spear, P. D. (1982) · Physiological Reviews · doi:10.1152/physrev.1982.62.2.738 · Cited by 704 · see citing works

Interim results from the international trial of Second Sight's visual prosthesis

Humayun, M. S., Dorn, J. D., da Cruz, L., Dagnelie, G., Sahel, J.-A., Stanga, P. E., Cideciyan, A. V., Duncan, J. L., Eliott, D., Filley, E., et al. (2012) · Ophthalmology · doi:10.1016/j.ophtha.2011.09.028 · Cited by 700 · see citing works

The Neural Basis of Perceptual Learning

Gilbert, C. D., Sigman, M., & Crist, R. E. (2001) · Neuron · doi:10.1016/s0896-6273(01)00424-x · Cited by 688 · see citing works

Balancing Plasticity/Stability Across Brain Development

Takesian, A. E., & Hensch, T. K. (2013) · Progress in Brain Research · doi:10.1016/b978-0-444-63327-9.00001-1 · Cited by 667 · see citing works

Reorganization of Retinotopic Cortical Maps in Adult Mammals After Lesions of the Retina

Kaas, J. H., Krubitzer, L. A., Chino, Y. M., Langston, A., Polley, E. H., & Blair, N. P. (1990) · Science · doi:10.1126/science.2326637 · Cited by 647 · see citing works

Mechanisms underlying development of visual maps and receptive fields

Huberman, A. D., Feller, M. B., & Chapman, B. (2008) · Annual Review of Neuroscience · doi:10.1146/annurev.neuro.31.060407.125533 · Cited by 628 · see citing works

Axonal sprouting accompanies functional reorganization in adult cat striate cortex

Darian‐Smith, C., & Gilbert, C. D. (1994) · Nature · doi:10.1038/368737a0 · Cited by 601 · see citing works

Removing brakes on adult brain plasticity: From molecular to behavioral interventions

Bavelier, D., Levi, D. M., Li, R. W., Dan, Y., & Hensch, T. K. (2010) · The Journal of Neuroscience · doi:10.1523/jneurosci.4812-10.2010 · Cited by 589 · see citing works

Adler's physiology of the eye

Levin, L. A., NILSSON, S. F. E., Hoeve, J. N. V., Wu, S. M.-S., Kaufman, P. L., & Alm, A. (2011) · Andalas University Repository (Andalas University) · Cited by 578 · see citing works

Visual categorization shapes feature selectivity in the primate temporal cortex

Sigala, N., & Logothetis, N. K. (2002) · Nature · doi:10.1038/415318a · Cited by 559 · see citing works

Perceptual Learning Directs Auditory Cortical Map Reorganization through Top-Down Influences

Polley, D. B., Steinberg, E. E., & Merzenich, M. M. (2006) · Journal of Neuroscience · doi:10.1523/jneurosci.3771-05.2006 · Cited by 551 · see citing works

Information-limiting correlations

Moreno‐Bote, R., Beck, J. M., Kanitscheider, I., Pitkow, X., Latham, P. E., & Pouget, A. (2014) · Nature Neuroscience · doi:10.1038/nn.3807 · Cited by 541 · see citing works

Perceptual learning reflects external noise filtering and internal noise reduction through channel reweighting

Dosher, B. A., & Lu, Z. (1998) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.95.23.13988 · Cited by 527 · see citing works

Perceptual learning and top-down influences in primary visual cortex

Li, W., Piëch, V., & Gilbert, C. D. (2004) · Nature Neuroscience · doi:10.1038/nn1255 · Cited by 474 · see citing works

Artificial vision with wirelessly powered subretinal electronic implant alpha-IMS

Stingl, K., Bartz-Schmidt, K. U., Besch, D., Braun, A., Bruckmann, A., Gekeler, F., Greppmaier, U., Hipp, S., Hörtdörfer, G., Kernstock, C., et al. (2013) · Proceedings of the Royal Society B: Biological Sciences · doi:10.1098/rspb.2013.0077 · Cited by 473 · see citing works

Perceptual learning in Vision Research

Sagi, D. (2010) · Vision Research · doi:10.1016/j.visres.2010.10.019 · Cited by 435 · see citing works

The Effect of Perceptual Learning on Neuronal Responses in Monkey Visual Area V4

Yang, T., & Maunsell, J. H. R. (2004) · The Journal of Neuroscience · doi:10.1523/jneurosci.4442-03.2004 · Cited by 427 · see citing works

Retinotopic map refinement requires spontaneous retinal waves during a brief critical period of development

McLaughlin, T., Torborg, C. L., Feller, M. B., & O'Leary, D. D. M. (2003) · Neuron · doi:10.1016/s0896-6273(03)00790-6 · Cited by 422 · see citing works

Complete Transfer of Perceptual Learning across Retinal Locations Enabled by Double Training

Xiao, L.-Q., Zhang, J.-Y., Wang, R., Klein, S. A., Levi, D. M., & Yu, C. (2008) · Current Biology · doi:10.1016/j.cub.2008.10.030 · Cited by 414 · see citing works

Applications of prism adaptation: a tutorial in theory and method

Redding, G. M., Rossetti, Y., & Wallace, B. (2005) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2004.12.004 · Cited by 413 · see citing works

Visual Neural Development

Movshon, J. A., & Sluyters, R. C. V. (1981) · Annual Review of Psychology · doi:10.1146/annurev.ps.32.020181.002401 · Cited by 410 · see citing works

Vision without inversion of the retinal image.

Stratton, G. M. (1897) · Psychological Review · doi:10.1037/h0071173 · Cited by 406 · see citing works

Stereopsis and amblyopia: A mini-review

Levi, D. M., Knill, D. C., & Bavelier, D. (2015) · Vision Research · doi:10.1016/j.visres.2015.01.002 · Cited by 405 · see citing works

Otx2 Binding to Perineuronal Nets Persistently Regulates Plasticity in the Mature Visual Cortex

Beurdeley, M., Spatazza, J., Lee, H. H. C., Sugiyama, S., Bernard, C., Di Nardo, A. A., Hensch, T. K., & Prochiantz, A. (2012) · Journal of Neuroscience · doi:10.1523/jneurosci.0394-12.2012 · Cited by 398 · see citing works

Neural correlates of perceptual learning: A functional MRI study of visual texture discrimination

Schwartz, S., Maquet, P., & Frith, C. (2002) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.242414599 · Cited by 388 · see citing works

Subretinal visual implant alpha IMS - clinical trial interim report

Stingl, K., Bartz-Schmidt, K. U., Besch, D., Chee, C. K., Cottriall, C. L., Gekeler, F., Groppe, M., Jackson, T. L., MacLaren, R. E., Koitschev, A., et al. (2015) · Vision Research · doi:10.1016/j.visres.2015.03.001 · Cited by 387 · see citing works

Role of striate cortex and superior colliculus in visual guidance of saccadic eye movements in monkeys

Mohler, C. W., & Wurtz, R. H. (1977) · Journal of Neurophysiology · doi:10.1152/jn.1977.40.1.74 · Cited by 383 · see citing works

Congenital stationary night blindness: An analysis and update of genotype–phenotype correlations and pathogenic mechanisms

Zeitz, C., Robson, A. G., & Audo, I. S. (2014) · Progress in Retinal and Eye Research · doi:10.1016/j.preteyeres.2014.09.001 · Cited by 377 · see citing works

Visual behaviour mediated by retinal projections directed to the auditory pathway

von Melchner, L., Pallas, S. L., & Sur, M. (2000) · Nature · doi:10.1038/35009102 · Cited by 371 · see citing works

Learning to see: experience and attention in primary visual cortex

Crist, R. E., Li, W., & Gilbert, C. D. (2001) · Nature Neuroscience · doi:10.1038/87470 · Cited by 364 · see citing works

Microstimulation of inferotemporal cortex influences face categorization

Afraz, S.-R., Kiani, R., & Esteky, H. (2006) · Nature · doi:10.1038/nature04982 · Cited by 363 · see citing works

The Argus II epiretinal prosthesis system allows letter and word reading and long-term function in patients with profound vision loss

da Cruz, L., Coley, B. F., Dorn, J., Merlini, F., Filley, E., Christopher, P., Chen, F. K., Wuyyuru, V., Sahel, J., Stanga, P., et al. (2013) · British Journal of Ophthalmology · doi:10.1136/bjophthalmol-2012-301525 · Cited by 359 · see citing works

Five-year safety and performance results from the argus II retinal prosthesis system clinical trial.

da Cruz, L., Dorn, J. D., Humayun, M. S., Dagnelie, G., Handa, J., Barale, P.-O., Sahel, J.-A., Stanga, P. E., Hafezi, F., Safran, A. B., et al. (2016) · Ophthalmology · doi:10.1016/j.ophtha.2016.06.049 · Cited by 359 · see citing works

Age in the development of closure ability in children.

Mooney, C. M. (1957) · Canadian Journal of Psychology/Revue Canadienne de Psychologie · doi:10.1037/h0083717 · Cited by 348 · see citing works

Photovoltaic restoration of sight with high visual acuity

Lorach, H., Goetz, G., Smith, R., Lei, X., Mandel, Y., Kamins, T. I., Mathieson, K., Huie, P., Harris, J. S., Sher, A., et al. (2015) · Nature Medicine · doi:10.1038/nm.3851 · Cited by 341 · see citing works

First-in-human trial of a novel suprachoroidal retinal prosthesis

Ayton, L. N., Blamey, P. J., Guymer, R. H., Luu, C. D., Nayagam, D. A. X., Sinclair, N. C., Shivdasani, M. N., Yeoh, J., McCombe, M. F., Briggs, R. J., et al. (2014) · PLoS ONE · doi:10.1371/journal.pone.0115239 · Cited by 333 · see citing works

Effects of Shape-Discrimination Training on the Selectivity of Inferotemporal Cells in Adult Monkeys

Kobatake, E., Wang, G., & Tanaka, K. (1998) · Journal of Neurophysiology · doi:10.1152/jn.1998.80.1.324 · Cited by 329 · see citing works

The Dynamics of Perceptual Learning: An Incremental Reweighting Model.

Petrov, A. A., Dosher, B. A., & Lu, Z. (2005) · Psychological Review · doi:10.1037/0033-295x.112.4.715 · Cited by 313 · see citing works

Physiological Correlates of Perceptual Learning in Monkey V1 and V2

Ghose, G. M., Yang, T., & Maunsell, J. H. R. (2002) · Journal of Neurophysiology · doi:10.1152/jn.00690.2001 · Cited by 310 · see citing works

Long-term deprivation affects visual perception and cortex

Fine, I., Wade, A. R., Brewer, A. A., May, M. G., Goodman, D. F., Boynton, G. M., Wandell, B. A., & MacLeod, D. I. A. (2003) · Nature Neuroscience · doi:10.1038/nn1102 · Cited by 309 · see citing works

Topographic reorganization in the striate cortex of the adult cat and monkey is cortically mediated

Darian‐Smith, C., & Gilbert, C. (1995) · Journal of Neuroscience · doi:10.1523/jneurosci.15-03-01631.1995 · Cited by 306 · see citing works

Video-Game Play Induces Plasticity in the Visual System of Adults with Amblyopia

Li, R. W., Ngo, C. V., Nguyen, J., & Levi, D. M. (2011) · PLoS Biology · doi:10.1371/journal.pbio.1001135 · Cited by 305 · see citing works

Learning Strengthens the Response of Primary Visual Cortex to Simple Patterns

Furmanski, C. S., Schluppeck, D., & Engel, S. A. (2004) · Current Biology · doi:10.1016/j.cub.2004.03.032 · Cited by 286 · see citing works

Reorganization of Visual Processing in Macular Degeneration

Baker, C. I., Eli Peli, A., Knouf, N. A., & Kanwisher, N. (2005) · Journal of Neuroscience · doi:10.1523/jneurosci.3476-04.2005 · Cited by 285 · see citing works

Developmental mechanisms of topographic map formation and alignment

Cang, J., & Feldheim, D. A. (2013) · Annual Review of Neuroscience · doi:10.1146/annurev-neuro-062012-170341 · Cited by 275 · see citing works

Frequency discrimination training engaging a restricted skin surface results in an emergence of a cutaneous response zone in cortical area 3a

Recanzone, G. H., Merzenich, M. M., & Jenkins, W. M. (1992) · Journal of Neurophysiology · doi:10.1152/jn.1992.67.5.1057 · Cited by 268 · see citing works

Retinal Remodeling in Inherited Photoreceptor Degenerations

Marc, R. E., & Jones, B. W. (2003) · Molecular Neurobiology · doi:10.1385/mn:28:2:139 · Cited by 258 · see citing works

Dynamic Changes in Brain Activity during Prism Adaptation

Luauté, J., Schwartz, S., Rossetti, Y., Spiridon, M., Gilles Rode, A., Dominique Boisson, A., & Vuilleumier, P. O. (2009) · Journal of Neuroscience · doi:10.1523/jneurosci.3054-08.2009 · Cited by 245 · see citing works

Comparing perceptual learning across tasks: A review

Fine, I., & Jacobs, R. A. (2002) · Journal of Vision · doi:10.1167/2.2.5 · Cited by 242 · see citing works

Optogenetic therapy for retinitis pigmentosa

Busskamp, V., Picaud, S. A., Sahel, J., & Roska, B. (2011) · Gene Therapy · doi:10.1038/gt.2011.155 · Cited by 237 · see citing works

Rule-Based Learning Explains Visual Perceptual Learning and Its Specificity and Transfer

Zhang, J.-Y., Zhang, G., Xiao, L.-Q., Klein, S. A., Levi, D. M., & Yu, C. (2010) · Journal of Neuroscience · doi:10.1523/jneurosci.0704-10.2010 · Cited by 236 · see citing works

Visual hallucinations as release phenomena

Cogan, D. G. (1973) · Graefe s Archive for Clinical and Experimental Ophthalmology · doi:10.1007/bf00407835 · Cited by 234 · see citing works

Critical Period Mechanisms in Developing Visual Cortex

Hensch, T. K. (2005) · Current topics in developmental biology/Current Topics in Developmental Biology · doi:10.1016/s0070-2153(05)69008-4 · Cited by 226 · see citing works

Artificial vision: needs, functioning, and testing of a retinal electronic prosthesis

Chader, G. J., Weiland, J. D., & Humayun, M. S. (2009) · Progress in brain research · doi:10.1016/s0079-6123(09)17522-2 · Cited by 226 · see citing works

Electrical stimulation of the left and right human fusiform gyrus causes different effects in conscious face perception

Rangarajan, V., Hermes, D., Foster, B. L., Weiner, K. S., Jacques, C., Grill-Spector, K., & Parvizi, J. (2014) · Journal of Neuroscience · doi:10.1523/jneurosci.0527-14.2014 · Cited by 226 · see citing works

Cerebral visual motion blindness: transitory akinetopsia induced by transcranial magnetic stimulation of human area V5

Beckers, G., & Hömberg, V. (1992) · Proceedings of the Royal Society B Biological Sciences · doi:10.1098/rspb.1992.0100 · Cited by 226 · see citing works

Lack of long-term cortical reorganization after macaque retinal lesions

Smirnakis, S. M., Brewer, A. A., Schmid, M. C., Tolias, A. S., Schüz, A., Augath, M. A., INHOFFEN, W., Wandell, B. A., & Logothetis, N. K. (2005) · Nature · doi:10.1038/nature03495 · Cited by 220 · see citing works

Role of emergent neural activity in visual map development

Ackman, J. B., & Crair, M. C. (2014) · Current Opinion in Neurobiology · doi:10.1016/j.conb.2013.11.011 · Cited by 219 · 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

Progressive improvement in discriminative abilities in adult owl monkeys performing a tactile frequency discrimination task

Recanzone, G. H., Jenkins, W. M., Hradek, G. T., & Merzenich, M. M. (1992) · Journal of Neurophysiology · doi:10.1152/jn.1992.67.5.1015 · Cited by 215 · see citing works

Experience-Dependent Plasticity in Adult Visual Cortex

Karmarkar, U. R., & Dan, Y. (2006) · Neuron · doi:10.1016/j.neuron.2006.11.001 · Cited by 208 · see citing works

Abnormal Functional Organization in the Dorsal Lateral Geniculate Nucleus of Mice Lacking the β2 Subunit of the Nicotinic Acetylcholine Receptor

Grubb, M. S., Rossi, F. M., Changeux, J.-P., & Thompson, I. D. (2003) · Neuron · doi:10.1016/s0896-6273(03)00789-x · Cited by 208 · see citing works

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

Learning-induced plasticity in animal and human auditory cortex

Ohl, F. W., & Scheich, H. (2005) · Current Opinion in Neurobiology · doi:10.1016/j.conb.2005.07.002 · Cited by 196 · see citing works

Demonstration of artificial visual percepts generated through thalamic microstimulation

Pezaris, J. S., & Reid, R. C. (2007) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0608563104 · Cited by 195 · see citing works

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

Rapid axonal sprouting and pruning accompany functional reorganization in primary visual cortex

Yamahachi, H., Marik, S. A., McManus, J. N. J., Denk, W., & Gilbert, C. D. (2009) · Neuron · doi:10.1016/j.neuron.2009.11.026 · Cited by 193 · see citing works

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

Perceptual learning in contrast discrimination and the (minimal) role of context

Yu, C., Klein, S. A., & Levi, D. M. (2004) · Journal of Vision · doi:10.1167/4.3.4 · Cited by 192 · see citing works

Red‐shifted channelrhodopsin stimulation restores light responses in blind mice, macaque retina, and human retina

Sengupta, A., Chaffiol, A., Macé, É., Caplette, R., Desrosiers, M., Lampič, M., Forster, V., Marre, O., Lin, J. Y., Sahel, J., et al. (2016) · EMBO Molecular Medicine · doi:10.15252/emmm.201505699 · Cited by 180 · see citing works

The detection of motion by blind subjects with the epiretinal 60-electrode (Argus II) retinal prosthesis

Dorn, J. D., Ahuja, A. K., Caspi, A., da Cruz, L., Dagnelie, G., Sahel, J.-A., Greenberg, R. J., McMahon, M. J., & Argus II Study Group, F. T. (2013) · JAMA Ophthalmology · doi:10.1001/2013.jamaophthalmol.221 · Cited by 177 · see citing works

Context-enabled learning in the human visual system

Adini, Y., Sagi, D., & Tsodyks, M. V. (2002) · Nature · doi:10.1038/415790a · Cited by 175 · see citing works

Three remarks on perceptual learning

Mollon, J. D., & Danilova, M. V. (1996) · Spatial Vision · doi:10.1163/156856896x00051 · Cited by 175 · 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

Ephrin-As Guide the Formation of Functional Maps in the Visual Cortex

Cang, J., Kaneko, M., Yamada, J., Woods, G., Stryker, M. P., & Feldheim, D. A. (2005) · Neuron · doi:10.1016/j.neuron.2005.10.026 · Cited by 171 · see citing works

Perceptual image quality assessment using a normalized Laplacian pyramid

Laparra, V., Ballé, J., Berardino, A., & Simoncelli, E. P. (2016) · Electronic Imaging · doi:10.2352/issn.2470-1173.2016.16.hvei-103 · Cited by 166 · see citing works

Improving Reading Speed for People with Central Vision Loss through Perceptual Learning

Chung, S. T. L. (2010) · Investigative Ophthalmology & Visual Science · doi:10.1167/iovs.10-6034 · Cited by 160 · see citing works

Perceptual Learning Selectively Refines Orientation Representations in Early Visual Cortex

Jehee, J. F. M., Ling, S., Swisher, J. D., van Bergen, R. S., & Tong, F. (2012) · Journal of Neuroscience · doi:10.1523/jneurosci.6112-11.2012 · Cited by 156 · see citing works

Ionotropic and metabotropic glutamate receptors show unique postsynaptic, presynaptic, and glial localizations in the dorsal cochlear nucleus

Petralia, R. S., Wang, Y., Zhao, H.-M., & Wenthold, R. J. (1996) · The Journal of Comparative Neurology · doi:10.1002/(sici)1096-9861(19960826)372:3 · Cited by 156 · see citing works

Valproate reopens critical-period learning of absolute pitch

Gervain, J., Vines, B. W., Chen, L. M., Seo, R. J., Hensch, T. K., Werker, J. F., & Young, A. H. (2013) · Frontiers in Systems Neuroscience · doi:10.3389/fnsys.2013.00102 · Cited by 151 · see citing works

Optogenetic Vision Restoration Using Rhodopsin for Enhanced Sensitivity

Gaub, B. M., Berry, M. H., Holt, A., Isacoff, E. Y., & Flannery, J. G. (2015) · Molecular Therapy · doi:10.1038/mt.2015.121 · Cited by 148 · see citing works

Genotype and Phenotype of 101 Dutch Patients with Congenital Stationary Night Blindness

Bijveld, M. M. C., Florijn, R. J., Bergen, A. A. B., van den Born, L. I., Kamermans, M., Wenniger-Prick, L. J. J. M. M. D. B., Riemslag, F. C. C., van Schooneveld, M. J., Kappers, A. M. L., & van Genderen, M. M. (2013) · Ophthalmology · doi:10.1016/j.ophtha.2013.03.002 · Cited by 146 · see citing works

Identification of OTX2 as a Medulloblastoma Oncogene Whose Product can be Targeted by All-Trans Retinoic Acid

Di, C., Liao, S., Adamson, D. C., Parrett, T. J., Broderick, D. K., Shi, Q., Christoph Lengauer, C., Cummins, J. M., Velculescu, V. E., Fults, D. W., et al. (2005) · Cancer Research · doi:10.1158/0008-5472.919.65.3 · Cited by 144 · see citing works

V1 Projection Zone Signals in Human Macular Degeneration Depend on Task, not Stimulus

Masuda, Y., Dumoulin, S. O., Nakadomari, S., & Wandell, B. A. (2008) · Cerebral Cortex · doi:10.1093/cercor/bhm256 · Cited by 144 · see citing works

Perceptual learning in vernier acuity: What is learned?

Saarinen, J. K. S., & Levi, D. M. (1995) · Vision Research · doi:10.1016/0042-6989(94)00141-8 · Cited by 143 · see citing works

Effects of perceptual learning on primary visual cortex activity in humans

Pourtois, G., Rauss, K. S., Vuilleumier, P. O., & Schwartz, S. (2007) · Vision Research · doi:10.1016/j.visres.2007.10.027 · Cited by 138 · see citing works

New concepts concerning the neural mechanisms of amblyopia and their clinical implications

WONG, A. M. F. (2012) · Canadian Journal of Ophthalmology · doi:10.1016/j.jcjo.2012.05.002 · Cited by 138 · see citing works

A quantitative measure for short-term cortical plasticity in human vision

Kapadia, M., Gilbert, C., & Westheimer, G. (1994) · Journal of Neuroscience · doi:10.1523/jneurosci.14-01-00451.1994 · Cited by 137 · see citing works

The filling-in process in patients with retinal scotomata

Gerrits, H. J. M., & Timmerman, G. J. M. E. N. (1969) · Vision Research · doi:10.1016/0042-6989(69)90092-3 · Cited by 135 · see citing works

Organization of the Visual Cortex in Human Albinism

Hoffmann, M. B., Tolhurst, D. J., Moore, A. T., & Morland, A. B. (2003) · Journal of Neuroscience · doi:10.1523/jneurosci.23-26-08921.2003 · Cited by 135 · see citing works

Visual Motion Area MT+/V5 Responds to Auditory Motion in Human Sight-Recovery Subjects

Sàenz, M., Lewis, L. B., Huth, A. G., Fine, I., & Christof Koch, A. (2008) · Journal of Neuroscience · doi:10.1523/jneurosci.0803-08.2008 · Cited by 134 · see citing works

Reorganization of visual processing in macular degeneration: Replication and clues about the role of foveal loss

Baker, C. I., Dilks, D. D., Eli Peli, A., & Kanwisher, N. (2008) · Vision Research · doi:10.1016/j.visres.2008.05.020 · Cited by 133 · see citing works

Effect of dark-rearing on experimental myopia in monkeys.

Raviola, E., & Wiesel, T. N. (1978) · PubMed · Cited by 132 · see citing works

Can visual function be restored in patients with homonymous hemianopia?

Pambakian, A., & Kennard, C. (1997) · British Journal of Ophthalmology · doi:10.1136/bjo.81.4.324 · Cited by 132 · see citing works

The “EyeCane”, a new electronic travel aid for the blind: Technology, behavior & swift learning

Maidenbaum, S., Hanassy, S., Abboud, S., Buchs, G., Chebat, D., Levy‐Tzedek, S., & Amedi, A. (2014) · Restorative Neurology and Neuroscience · doi:10.3233/rnn-130351 · Cited by 129 · see citing works

Visual Parsing After Recovery From Blindness

Ostrovsky, Y., Meyers, E. M., Ganesh, S., Mathur, U., & Sinha, P. (2009) · Psychological Science · doi:10.1111/j.1467-9280.2009.02471.x · Cited by 125 · see citing works

Holistic Processing of Faces: Learning Effects with Mooney Faces

Latinus, M., & Taylor, M. J. (2005) · Journal of Cognitive Neuroscience · doi:10.1162/0898929055002490 · Cited by 124 · see citing works

Reorganization of Visual Processing in Macular Degeneration Is Not Specific to the “Preferred Retinal Locus”

Dilks, D. D., Baker, C. I., Eli Peli, A., & Kanwisher, N. (2009) · Journal of Neuroscience · doi:10.1523/jneurosci.5258-08.2009 · Cited by 117 · see citing works

Monocular Core Zones and Binocular Border Strips in Primate Striate Cortex Revealed by the Contrasting Effects of Enucleation, Eyelid Suture, and Retinal Laser Lesions on Cytochrome Oxidase Activity

Horton, J. C., & Hocking, D. R. (1998) · Journal of Neuroscience · doi:10.1523/jneurosci.18-14-05433.1998 · Cited by 114 · see citing works

Early Specification of the Hierarchical Organization of Visual Cortical Areas in the Macaque Monkey

Batardière, A. (2002) · Cerebral Cortex · doi:10.1093/cercor/12.5.453 · Cited by 113 · see citing works

Filling-in of retinal scotomas

Zur, D., & Ullman, S. (2003) · Vision Research · doi:10.1016/s0042-6989(03)00038-5 · Cited by 113 · see citing works

The Puzzle of Visual Development: Behavior and Neural Limits

Kiorpes, L. (2016) · The Journal of Neuroscience · doi:10.1523/jneurosci.2937-16.2016 · Cited by 112 · see citing works

Characterizing the development of visual search expertise in pathology residents viewing whole slide images

Krupinski, E. A., Graham, A. R., & Weinstein, R. S. (2012) · Human Pathology · doi:10.1016/j.humpath.2012.05.024 · Cited by 110 · see citing works

Perceiving electrical stimulation of identified human visual areas

Murphey, D. K., Maunsell, J. H. R., Beauchamp, M. S., & Yoshor, D. (2009) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0804998106 · Cited by 109 · see citing works

Prolonged Perceptual Learning of Positional Acuity in Adult Amblyopia: Perceptual Template Retuning Dynamics

Li, R. W., Klein, S. A., & Levi, D. M. (2008) · Journal of Neuroscience · doi:10.1523/jneurosci.4271-08.2008 · Cited by 108 · see citing works

Development of pattern vision following early and extended blindness

Kalia, A., Lesmes, L. A., Dorr, M., Gandhi, T., Chatterjee, G., Ganesh, S., Bex, P. J., & Sinha, P. (2014) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1311041111 · Cited by 106 · see citing works

Form representation in monkey inferotemporal cortex is virtually unaltered by free viewing

DiCarlo, J. J., & Maunsell, J. H. R. (2000) · Nature Neuroscience · doi:10.1038/77722 · Cited by 102 · see citing works

One-Year Outcome of 49-Channel Suprachoroidal–Transretinal Stimulation Prosthesis in Patients With Advanced Retinitis Pigmentosa

Fujikado, T., Kamei, M., Sakaguchi, H., Kanda, H., Endo, T., Hirota, M., Morimoto, T., Nishida, K., Kishima, H., Terasawa, Y., et al. (2016) · Investigative Opthalmology & Visual Science · doi:10.1167/iovs.16-20367 · Cited by 101 · see citing works

Navigation using sensory substitution in real and virtual mazes

Chebat, D.-R., Maidenbaum, S., & Amedi, A. (2015) · PLOS ONE · doi:10.1371/journal.pone.0126307 · Cited by 99 · see citing works

Human Adult Cortical Reorganization and Consequent Visual Distortion

Dilks, D. D., Serences, J. T., Tamber-Rosenau, B. J., Yantis, S., & McCloskey, M. E. (2007) · Journal of Neuroscience · doi:10.1523/jneurosci.2650-07.2007 · Cited by 97 · see citing works

Brightness as a Function of Current Amplitude in Human Retinal Electrical Stimulation

Greenwald, S. H., Horsager, A., Humayun, M. S., Greenberg, R. J., McMahon, M. J., & Fine, I. (2009) · Investigative Ophthalmology & Visual Science · doi:10.1167/iovs.08-2897 · Cited by 95 · see citing works

Performance of real‐world functional vision tasks by blind subjects improves after implantation with the Argus® II retinal prosthesis system

Dagnelie, G., Christopher, P., Arditi, A. R., da Cruz, L., Duncan, J. L., Ho, A. C., de Koo, L. C. O., Sahel, J., Stanga, P. E., Thumann, G., et al. (2016) · Clinical and Experimental Ophthalmology · doi:10.1111/ceo.12812 · Cited by 93 · see citing works

Bilateral visual field maps in a patient with only one hemisphere

Muckli, L. F., Naumer, M. J., & Singer, W. (2009) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0809688106 · Cited by 90 · see citing works

Striate cortex lesions and visual acuity of the rhesus monkey.

Weiskrantz, L., & Cowey, A. (1963) · Journal of Comparative and Physiological Psychology · doi:10.1037/h0043778 · Cited by 85 · see citing works

Task relevancy and demand modulate double-training enabled transfer of perceptual learning

Wang, R., Zhang, J.-Y., Klein, S. A., Levi, D. M., & Yu, C. (2011) · Vision Research · doi:10.1016/j.visres.2011.07.019 · Cited by 85 · see citing works

Increasing Accessibility to the Blind of Virtual Environments, Using a Virtual Mobility Aid Based On the "EyeCane": Feasibility Study

Maidenbaum, S., Levy‐Tzedek, S., Chebat, D., & Amedi, A. (2013) · PLoS ONE · doi:10.1371/journal.pone.0072555 · Cited by 84 · see citing works

Plasticity and Stability of the Visual System in Human Achiasma

Hoffmann, M. B., Kaule, F. R., Levin, N., Masuda, Y., Kumar, A., Gottlob, I., Horiguchi, H., Dougherty, R. F., Stadler, J., Wolynski, B., et al. (2012) · Neuron · doi:10.1016/j.neuron.2012.05.026 · Cited by 84 · see citing works

Phosphene induction by microstimulation of macaque V1

Tehovnik, E. J., & Slocum, W. M. (2007) · Brain Research Reviews · doi:10.1016/j.brainresrev.2006.11.001 · Cited by 83 · see citing works

Retinal prostheses: progress toward the next generation implants

Ghezzi, D. (2015) · Frontiers in Neuroscience · doi:10.3389/fnins.2015.00290 · Cited by 83 · see citing works

The Argus II Retinal Prosthesis: 12-Month Outcomes from a Single-Study Center

Rizzo, S., Belting, C., Cinelli, L., Allegrini, L., Genovesi-Ebert, F., Barca, F., & Bartolo, E. D. (2014) · American Journal of Ophthalmology · doi:10.1016/j.ajo.2014.02.039 · Cited by 83 · see citing works

Developmental Remodeling of Primate Visual Cortical Pathways

Barone, P., Dehay, C., Berland, M., Bullier, J., & Kennedy, H. (1995) · Cerebral Cortex · doi:10.1093/cercor/5.1.22 · Cited by 82 · see citing works

Therapeutic potential of valproic acid for retinitis pigmentosa

Clemson, C., Tzekov, R. T., Krebs, M. P., Checchi, J., Bigelow, C., & Kaushal, S. (2010) · British Journal of Ophthalmology · doi:10.1136/bjo.2009.175356 · Cited by 82 · see citing works

Relearning to See in Cortical Blindness

Melnick, M. D., Tadin, D., & Huxlin, K. R. (2015) · The Neuroscientist · doi:10.1177/1073858415621035 · Cited by 82 · see citing works

Advances in auditory prostheses

Shannon, R. V. (2011) · Current Opinion in Neurology · doi:10.1097/wco.0b013e32834ef878 · Cited by 81 · see citing works

The limits of shape recognition following late emergence from blindness

McKyton, A., Ben-Zion, I., Doron, R., & Zohary, E. (2015) · Current Biology · doi:10.1016/j.cub.2015.06.040 · Cited by 79 · see citing works

Learning Increases Stimulus Salience in Anterior Inferior Temporal Cortex of the Macaque

Jagadeesh, B., Chelazzi, L., Mishkin, M., & Desimone, R. (2001) · Journal of Neurophysiology · doi:10.1152/jn.2001.86.1.290 · Cited by 76 · see citing works

Advances in gene therapy technologies to treat retinitis pigmentosa

Petrs‐Silva, H., & Linden, R. (2013) · Clinical ophthalmology · doi:10.2147/opth.s38041 · Cited by 75 · see citing works

Pixium Vision: First Clinical Results and Innovative Developments

Hornig, R., Dapper, M., Joliff, E. L., Hill, R. G., Ishaque, K., Posch, C., Benosman, R. B., Mer, Y. L., Sahel, J., & Picaud, S. A. (2016) · Springer eBooks · doi:10.1007/978-3-319-41876-6_8 · Cited by 73 · see citing works

Microstimulation Reveals Limits in Detecting Different Signals from a Local Cortical Region

Ni, A. M., & Maunsell, J. H. R. (2010) · Current Biology · doi:10.1016/j.cub.2010.02.065 · Cited by 73 · see citing works

Minimizing biases in estimating the reorganization of human visual areas with BOLD retinotopic mapping

Binda, P., Thomas, J. M., Boynton, G. M., & Fine, I. (2013) · Journal of Vision · doi:10.1167/13.7.13 · Cited by 70 · see citing works

Visual BOLD Response in Late Blind Subjects with Argus II Retinal Prosthesis

Castaldi, E., Cicchini, G. M., Cinelli, L., Biagi, L., Rizzo, S., & Morrone, M. C. (2016) · PLoS Biology · doi:10.1371/journal.pbio.1002569 · Cited by 69 · see citing works

Broad-based visual benefits from training with an integrated perceptual-learning video game

Deveau, J., Lovcik, G., & Seitz, A. R. (2014) · Vision Research · doi:10.1016/j.visres.2013.12.015 · Cited by 67 · see citing works

Resting-State Retinotopic Organization in the Absence of Retinal Input and Visual Experience

Bock, A., Binda, P., Benson, N. C., Bridge, H., Watkins, K. E., & Fine, I. (2015) · Journal of Neuroscience · doi:10.1523/jneurosci.4715-14.2015 · Cited by 66 · see citing works

Vernier perceptual learning transfers to completely untrained retinal locations after double training: A "piggybacking" effect

Wang, R., Zhang, J.-Y., Klein, S. A., Levi, D. M., & Yu, C. (2014) · Journal of Vision · doi:10.1167/14.13.12 · Cited by 66 · see citing works

Rewiring the adult brain

Calford, M. B., Chino, Y. M., Das, A., Eysel, U. T., Gilbert, C. D., Heinen, S. J., Kaas, J. H., & Ullman, S. (2005) · Nature · doi:10.1038/nature04359 · Cited by 65 · see citing works

Cortical Reorganization after Long-Term Adaptation to Retinal Lesions in Humans

Chung, S. T. L. (2013) · Journal of Neuroscience · doi:10.1523/jneurosci.2764-13.2013 · Cited by 65 · see citing works

Upright Vision and the Retinal Image.

Stratton, G. M. (1897) · Psychological Review · doi:10.1037/h0064110 · Cited by 65 · see citing works

Cholinergic Enhancement Increases the Effects of Voluntary Attention but Does Not Affect Involuntary Attention

Rokem, A., Landau, A. N., Garg, D., Prinzmetal, W., & Silver, M. A. (2010) · Neuropsychopharmacology · doi:10.1038/npp.2010.118 · Cited by 65 · see citing works

A Lack of Experience-Dependent Plasticity After More Than a Decade of Recovered Sight

Huber, E., Webster, J. M., Brewer, A. A., MacLeod, D. I. A., Wandell, B. A., Boynton, G. M., Wade, A. R., & Fine, I. (2015) · Psychological Science · doi:10.1177/0956797614563957 · Cited by 63 · see citing works

Djourno, Eyries, and the First Implanted Electrical Neural Stimulator to Restore Hearing

Eisen, M. D. (2003) · Otology & Neurotology · doi:10.1097/00129492-200305000-00025 · Cited by 61 · see citing works

Living with cochlear implants: experiences of 17 adult patients in Sweden

Hallberg, L. R. ‐., & Ringdahl, A. (2004) · International Journal of Audiology · doi:10.1080/14992020400050016 · Cited by 59 · see citing works

Orientation tuning for disparity defined edges in Macaque V2

Bredfeldt, C. E., & Cumming, B. G. (2004) · Journal of Vision · doi:10.1167/4.8.169 · Cited by 59 · see citing works

Homeoprotein Signaling in Development, Health, and Disease: A Shaking of Dogmas Offers Challenges and Promises from Bench to Bed

Spatazza, J., Lullo, E. D., Joliot, A., Dupont, E., Moya, K. L., & Prochiantz, A. (2013) · Pharmacological Reviews · doi:10.1124/pr.112.006577 · Cited by 58 · see citing works

Contrast masking effects change with practice

Dorais, A., & Sagi, D. (1997) · Vision Research · doi:10.1016/s0042-6989(96)00329-x · Cited by 57 · see citing works

Development of a surgical procedure for implantation of a prototype suprachoroidal retinal prosthesis

Saunders, A. L., Williams, C. E., Heriot, W. J., Briggs, R., Yeoh, J., Nayagam, D. A. X., McCombe, M. F., Villalobos, J., Burns, O., Luu, C. D., et al. (2013) · Clinical and Experimental Ophthalmology · doi:10.1111/ceo.12287 · Cited by 56 · see citing works

Task-Dependent V1 Responses in Human Retinitis Pigmentosa

Masuda, Y., Horiguchi, H., Dumoulin, S. O., Furuta, A., Miyauchi, S., Nakadomari, S., & Wandell, B. A. (2010) · Investigative Ophthalmology & Visual Science · doi:10.1167/iovs.09-4775 · Cited by 56 · see citing works

Pulse trains to percepts: the challenge of creating a perceptually intelligible world with sight recovery technologies

Fine, I., & Boynton, G. M. (2015) · Philosophical Transactions of the Royal Society B: Biological Sciences · doi:10.1098/rstb.2014.0208 · Cited by 55 · see citing works

Primary visual cortical remapping in patients with inherited peripheral retinal degeneration

Ferreira, S., Pereira, A. C., Quendera, B., Reis, A., Silva, E. D., & Castelo-Branco, M. S. (2016) · NeuroImage Clinical · doi:10.1016/j.nicl.2016.12.013 · Cited by 55 · see citing works

The benefits of cholinergic enhancement during perceptual learning are long-lasting

Rokem, A., & Silver, M. A. (2013) · Frontiers in Computational Neuroscience · doi:10.3389/fncom.2013.00066 · Cited by 53 · see citing works

Evolution of the circuitry for conscious color vision in primates

Jay Neitz, A., & Neitz, M. (2016) · Eye · doi:10.1038/eye.2016.257 · Cited by 52 · see citing works

What are the mechanisms of photoreceptor adaptation?

Bownds, M. D., & Arshavsky, V. Y. (1995) · Behavioral and Brain Sciences · doi:10.1017/s0140525x00039170 · Cited by 51 · see citing works

Worldwide Argus II implantation: recommendations to optimize patient outcomes

Ghodasra, D. H., Chen, A., Arévalo, J. F., Birch, D. G., Branham, K. E. H., Coley, B., Dagnelie, G., de Juan, E., Devenyi, R. G., Dorn, J. D., et al. (2016) · BMC Ophthalmology · doi:10.1186/s12886-016-0225-1 · Cited by 50 · see citing works

Neurobiological hypothesis of color appearance and hue perception

Schmidt, B. P., Neitz, M., & Neitz, J. (2014) · Journal of the Optical Society of America A · doi:10.1364/josaa.31.00a195 · Cited by 49 · see citing works

Catch-up saccades in head-unrestrained conditions reveal that saccade amplitude is corrected using an internal model of target movement

Daye, P. M., Blohm, G., & Lefèvre, P. (2014) · Journal of Vision · doi:10.1167/14.1.12 · Cited by 49 · see citing works

Sensory and cognitive influences on the training-related improvement of reading speed in peripheral vision

He, Y., Legge, G. E., & Yu, D. (2013) · Journal of Vision · doi:10.1167/13.7.14 · Cited by 47 · see citing works

Cortical and subcortical connections of V1 and V2 in early postnatal macaque monkeys

Baldwin, M. K. L., Kaskan, P. M., Zhang, B., Chino, Y. M., & Kaas, J. H. (2011) · The Journal of Comparative Neurology · doi:10.1002/cne.22732 · Cited by 47 · see citing works

Is peripheral visual acuity susceptible to perceptual learning in the adult?

Westheimer, G. (2001) · Vision Research · doi:10.1016/s0042-6989(00)00245-5 · Cited by 47 · see citing works

Spatial frequency masking and Weber's Law

Swift, D. J., & Smith, R. A. (1983) · Vision Research · doi:10.1016/0042-6989(83)90124-4 · Cited by 47 · see citing works

Large-Scale Axonal Reorganization of Inhibitory Neurons following Retinal Lesions

Marik, S. A., Yamahachi, H., Borgloh, S. M. Z. A., & Gilbert, C. D. (2014) · Journal of Neuroscience · doi:10.1523/jneurosci.4345-13.2014 · Cited by 45 · see citing works

Responsiveness of cat area 17 after monocular inactivation: limitation of topographic plasticity in adult cortex.

Rosa, M. G. P., Schmid, L. M., & Calford, M. B. (1995) · The Journal of Physiology · doi:10.1113/jphysiol.1995.sp020543 · Cited by 42 · see citing works

Visual function before and after the removal of bilateral congenital cataracts in adulthood

Fine, I., Smallman, H. S., Doyle, P. G., & MacLeod, D. I. A. (2002) · Vision Research · doi:10.1016/s0042-6989(01)00266-8 · Cited by 41 · see citing works

Perceptual learning for a pattern discrimination task

Fine, I., & Jacobs, R. A. (2000) · Vision Research · doi:10.1016/s0042-6989(00)00163-2 · Cited by 41 · see citing works

Fluoxetine and serotonin facilitate attractive-adaptation-induced orientation plasticity in adult cat visual cortex

Bachatene, L., Bharmauria, V., Cattan, S., & Molotchnikoff, S. (2013) · European Journal of Neuroscience · doi:10.1111/ejn.12206 · Cited by 39 · see citing works

Visual activity and cortical rewiring: activity-dependent plasticity of cortical networks

Horng, S. H., & Sur, M. (2006) · Progress in brain research · doi:10.1016/s0079-6123(06)57001-3 · Cited by 38 · see citing works

The geometric structure of color

Logvinenko, A. D. (2015) · Journal of Vision · doi:10.1167/15.1.16 · Cited by 37 · see citing works

One Picture Is Worth at Least a Million Neurons

Levy, I., Hasson, U., & Malach, R. (2004) · Current Biology · doi:10.1016/j.cub.2004.05.045 · Cited by 36 · see citing works

Adaptation, perceptual learning, and plasticity of brain functions

Horton, J. C., Fahle, M. W., Mulder, T. W., & Trauzettel‐Klosinski, S. (2017) · Graefe s Archive for Clinical and Experimental Ophthalmology · doi:10.1007/s00417-016-3580-y · Cited by 36 · see citing works

“The world is upside down” – The Innsbruck Goggle Experiments of Theodor Erismann (1883–1961) and Ivo Kohler (1915–1985)

Sachse, P., Beermann, U., Martini, M., Maran, T. K., Domeier, M., & Furtner, M. R. (2017) · Cortex · doi:10.1016/j.cortex.2017.04.014 · Cited by 36 · see citing works

Higher-contrast requirements for recognizing low-pass-filtered letters

Kwon, M., & Legge, G. E. (2013) · Journal of Vision · doi:10.1167/13.1.13 · Cited by 36 · see citing works

Perception of Graphical Virtual Environments by Blind Users via Sensory Substitution

Maidenbaum, S., Buchs, G., Abboud, S., Lavi‐Rotbain, O., & Amedi, A. (2016) · PLoS ONE · doi:10.1371/journal.pone.0147501 · Cited by 34 · see citing works

Long-term follow-up for efficacy and safety of treatment of retinitis pigmentosa with valproic acid

Bhalla, S., Joshi, D. D., Bhullar, S. S., Kasuga, D. T., Park, Y., & Kay, C. N. (2013) · British Journal of Ophthalmology · doi:10.1136/bjophthalmol-2013-303084 · Cited by 32 · see citing works

Efficacy of valproic acid for retinitis pigmentosa patients: a pilot study

Iraha, S., Hirami, Y., Ota, S., Sunagawa, G. A., Mandai, M., Tanihara, H., Takahashi, M., & Kurimoto, Y. (2016) · Clinical ophthalmology · doi:10.2147/opth.s109995 · Cited by 32 · see citing works

Plasticity, and Its Limits, in Adult Human Primary Visual Cortex

Haak, K. V., Haak, K. V., Morland, A. B., Haak, K. V., Morland, A. B., & Engel, S. A. (2015) · Multisensory Research · doi:10.1163/22134808-00002496 · Cited by 31 · see citing works

Confidence-based integrated reweighting model of task-difficulty explains location-based specificity in perceptual learning

Talluri, B. C., Hung, S.-C., Seitz, A. R., & Seriès, P. (2015) · Journal of Vision · doi:10.1167/15.10.17 · Cited by 31 · see citing works

Valproic acid treatment may be harmful in non-dominant forms of retinitis pigmentosa: Table 1

Sisk, R. A. (2012) · British Journal of Ophthalmology · doi:10.1136/bjophthalmol-2012-301950 · Cited by 30 · see citing works

Optimization of perceptual learning: Effects of task difficulty and external noise in older adults

DeLoss, D. J., Watanabe, T., & Andersen, G. J. (2013) · Vision Research · doi:10.1016/j.visres.2013.11.003 · Cited by 30 · see citing works

Rehabilitation Approaches in Macular Degeneration Patients

Maniglia, M., Cottereau, B. R., Soler, V. J., & Trotter, Y. (2016) · Frontiers in Systems Neuroscience · doi:10.3389/fnsys.2016.00107 · Cited by 30 · see citing works

Cholinergic Potentiation Improves Perceptual-Cognitive Training of Healthy Young Adults in Three Dimensional Multiple Object Tracking

Chamoun, M., Huppé‐Gourgues, F., Legault, I., Rosa‐Neto, P., Dumbrava, D., Faubert, J., & Vaucher, E. (2017) · Frontiers in Human Neuroscience · doi:10.3389/fnhum.2017.00128 · Cited by 29 · see citing works

Gamut relativity: A new computational approach to brightness and lightness perception

Vladusich, T. (2013) · Journal of Vision · doi:10.1167/13.1.14 · Cited by 29 · see citing works

The Argus® II Retinal Prosthesis System

Luo, Y. H.-L., & da Cruz, L. (2016) · Progress in Retinal and Eye Research · doi:10.1016/j.preteyeres.2015.09.003 · Cited by 351 · see citing works

Dynamic Stimulation of Visual Cortex Produces Form Vision in Sighted and Blind Humans

Beauchamp, M. S., Oswalt, D., Sun, P., Foster, B. L., Magnotti, J. F., Niketeghad, S., Pouratian, N., Bosking, W. H., & Yoshor, D. (2020) · Cell · doi:10.1016/j.cell.2020.04.033 · Cited by 257 · see citing works

An update on retinal prostheses

Ayton, L. N., Barnes, N., Dagnelie, G., Fujikado, T., Goetz, G., Hornig, R., Jones, B. W., Muqit, M. M. K., Rathbun, D. L., Stingl, K., et al. (2020) · Clinical Neurophysiology · doi:10.1016/j.clinph.2019.11.029 · Cited by 223 · see citing works

Advances in retinal prosthesis systems

Bloch, E., Luo, Y., & da Cruz, L. (2019) · Therapeutic Advances in Ophthalmology · doi:10.1177/2515841418817501 · Cited by 201 · see citing works

Neuroplasticity in adult human visual cortex

Castaldi, E., Lunghi, C., & Morrone, M. C. (2020) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2020.02.028 · Cited by 161 · see citing works

A model of ganglion axon pathways accounts for percepts elicited by retinal implants

Beyeler, M., Nanduri, D., Weiland, J. D., Rokem, A., Boynton, G. M., & Fine, I. (2019) · Scientific Reports · doi:10.1038/s41598-019-45416-4 · Cited by 143 · see citing works

Development of visual Neuroprostheses: trends and challenges.

Fernandez, E. (2018) · Bioelectronic Medicine · doi:10.1186/s42234-018-0013-8 · Cited by 114 · see citing works

Photovoltaic retinal prosthesis restores high-resolution responses to single-pixel stimulation in blind retinas

Chenais, N. A. L., Airaghi Leccardi, M. J. I., & Ghezzi, D. (2021) · Communications Materials · doi:10.1038/s43246-021-00133-2 · Cited by 110 · see citing works

Optogenetic restoration of retinal ganglion cell activity in the living primate

McGregor, J. E., Godat, T., Dhakal, K. R., Parkins, K., Strazzeri, J. M., Bateman, B. A., Fischer, W. S., Williams, D. R., & Merigan, W. H. (2020) · Nature Communications · doi:10.1038/s41467-020-15317-6 · Cited by 78 · see citing works

Harmonization of Outcomes and Vision Endpoints in Vision Restoration Trials: Recommendations from the International HOVER Taskforce

Ayton, L. N., Rizzo, J. F., Bailey, I. L., Colenbrander, A., Dagnelie, G., Geruschat, D. R., Hessburg, P. C., McCarthy, C. D., Petoe, M. A., Rubin, G. S., et al. (2020) · Translational Vision Science & Technology · doi:10.1167/tvst.9.8.25 · Cited by 75 · see citing works

Visual prosthesis: interfacing stimulating electrodes with retinal neurons to restore vision.

Barriga-Rivera, A., Bareket, L., Goding, J., Aregueta-Robles, U. A., & Suaning, G. J. (2017) · Frontiers in Neuroscience · doi:10.3389/fnins.2017.00620 · Cited by 73 · see citing works

Semantic and structural image segmentation for prosthetic vision

Sanchez-Garcia, M., Martinez-Cantin, R., & Guerrero, J. J. (2020) · PLOS ONE · doi:10.1371/journal.pone.0227677 · Cited by 62 · see citing works

pulse2percept: A Python-based simulation framework for bionic vision

Beyeler, M., Boynton, G., Fine, I., & Rokem, A. (2017) · Proceedings of the 16th Python in Science Conference · doi:10.25080/shinma-7f4c6e7-00c · Cited by 56 · see citing works

Deep Learning–Based Scene Simplification for Bionic Vision

Han, N., Srivastava, S., Xu, A., Klein, D., & Beyeler, M. (2021) · Augmented Humans Conference 2021 · doi:10.1145/3458709.3458982 · Cited by 45 · see citing works

Advances in visual prostheses: engineering and biological challenges

Borda, E., & Ghezzi, D. (2022) · Progress in Biomedical Engineering · doi:10.1088/2516-1091/ac812c · Cited by 44 · see citing works

Toward Long-Term Communication With the Brain in the Blind by Intracortical Stimulation: Challenges and Future Prospects

Fernández, E., Alfaro, A., & González-López, P. (2020) · Frontiers in Neuroscience · doi:10.3389/fnins.2020.00681 · Cited by 35 · see citing works

Brain (re)organization following visual loss

Voss, P. (2018) · Wiley Interdisciplinary Reviews Cognitive Science · doi:10.1002/wcs.1468 · Cited by 39 · see citing works

Towards a <i>Smart Bionic Eye</i> : AI-powered artificial vision for the treatment of incurable blindness

Beyeler, M., & Sanchez-Garcia, M. (2022) · Journal of Neural Engineering · doi:10.1088/1741-2552/aca69d · Cited by 34 · see citing works

Virtual reality simulation of epiretinal stimulation highlights the relevance of the visual angle in prosthetic vision

Thorn, J. T., Migliorini, E., & Ghezzi, D. (2020) · Journal of Neural Engineering · doi:10.1088/1741-2552/abb5bc · Cited by 34 · see citing works

The argus ii retinal prosthesis system

Bloch, E., & da Cruz, L. (2020) · Prosthesis · doi:10.5772/intechopen.84947 · Cited by 31 · see citing works

Simulation of visual perception and learning with a retinal prosthesis

Golden, J. R., Erickson-Davis, C. R., Cottaris, N. P., Parthasarathy, N., Rieke, F. M., Brainard, D. H., Wandell, B. A., & Chichilnisky, E. J. (2018) · Journal of Neural Engineering · doi:10.1088/1741-2552/aaf270 · Cited by 29 · see citing works

Optimization of visual information presentation for visual prosthesis

Guo, F., Yang, Y., & Gao, Y. (2018) · International Journal of Biomedical Imaging · doi:10.1155/2018/3198342 · Cited by 27 · see citing works

A computational model of phosphene appearance for epiretinal prostheses

Granley, J., & Beyeler, M. (2021) · 2021 43rd Annual International Conference of the IEEE Engineering in Medicine &amp; Biology Society (EMBC) · doi:10.1109/embc46164.2021.9629663 · Cited by 27 · see citing works

Cortical visual mapping following ocular gene augmentation therapy for achromatopsia

McKyton, A., Averbukh, E., Marks-Ohana, D., Levin, N., & Banin, E. (2021) · Journal of Neuroscience · doi:10.1523/jneurosci.3222-20.2021 · Cited by 27 · see citing works

Implications of Neural Plasticity in Retinal Prosthesis

Caravaca-Rodriguez, D., Gaytan, S. P., Suaning, G. J., & Barriga‐Rivera, A. (2022) · Investigative Ophthalmology & Visual Science · doi:10.1167/iovs.63.11.11 · Cited by 27 · see citing works

pulse2percept: A Python-based simulation framework for bionic visionPreprint

Beyeler, M., Boynton, G. M., Fine, I., & Rokem, A. (2017) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/148015 · Cited by 27 · see citing works

The Relative Importance of Depth Cues and Semantic Edges for Indoor Mobility Using Simulated Prosthetic Vision in Immersive Virtual Reality

Rasla, A., & Beyeler, M. (2022) · ACM Symposium on Virtual Reality Software and Technology (VRST) · doi:10.1145/3562939.3565620 · Cited by 22 · see citing works

Optogenetic therapy restores retinal activity in primate for at least a year following photoreceptor ablation

McGregor, J. E., Kunala, K., Xu, Z., Murphy, P. J., Godat, T., Strazzeri, J. M., Bateman, B. A., Fischer, W. S., Parkins, K., Chu, C. J., et al. (2021) · Molecular Therapy · doi:10.1016/j.ymthe.2021.09.014 · Cited by 21 · see citing works

Immersive Virtual Reality Simulations of Bionic Vision

Kasowski, J., & Beyeler, M. (2022) · Augmented Humans 2022 · doi:10.1145/3519391.3522752 · Cited by 18 · see citing works

Theoretical analysis of optogenetic spiking with ChRmine, bReaChES and CsChrimson-expressing neurons for retinal prostheses

Bansal, H., Gupta, N., & Roy, S. (2021) · Journal of Neural Engineering · doi:10.1088/1741-2552/ac1175 · Cited by 21 · see citing works

Neurophysiological and medical considerations for better-performing microelectronic retinal prostheses

Im, M., & Kim, S. (2020) · Journal of Neural Engineering · doi:10.1088/1741-2552/ab8ca9 · Cited by 20 · see citing works

Advances in neuroscience, not devices, will determine the effectiveness of visual prostheses

Abbasi, B., & Rizzo, J. F. (2021) · Seminars in Ophthalmology · doi:10.1080/08820538.2021.1887902 · Cited by 19 · see citing works

Artificial Retina: A Future Cellular-Resolution Brain-Machine Interface

Muratore, D. G., & Chichilnisky, E. J. (2020) · The frontiers collection · doi:10.1007/978-3-030-18338-7_24 · Cited by 19 · see citing works

Improving the spatial resolution of artificial vision using midget retinal ganglion cell populations modeled at the human fovea

Italiano, M. L., Guo, T., Lovell, N. H., & Tsai, D. (2022) · Journal of Neural Engineering · doi:10.1088/1741-2552/ac72c2 · Cited by 16 · see citing works

Aligning Visual Prosthetic Development With Implantee Needs

Nadolskis, L., Turkstra, L. M., Larnyo, E., & Beyeler, M. (2024) · Translational Vision Science & Technology · doi:10.1167/tvst.13.11.28 · Cited by 16 · see citing works

Creation of virtual channels in the retina using synchronous and asynchronous stimulation—a modelling study

Song, X., Guo, T., Shivdasani, M. N., Dokos, S., Lovell, N. H., Li, X., Qiu, S., Li, T., Zheng, S., & Li, L. (2020) · Journal of Neural Engineering · doi:10.1088/1741-2552/abc3a9 · Cited by 16 · see citing works

Modeling the Improved Visual Acuity Using Photodiode Based Retinal Implants Featuring Fractal Electrodes

Watterson, W. J., Montgomery, R. D., & Taylor, R. P. (2018) · Frontiers in Neuroscience · doi:10.3389/fnins.2018.00277 · Cited by 16 · see citing works

Neurophysiological considerations for visual implants

Meikle, S. J., & Wong, Y. T. (2022) · Brain Structure and Function · doi:10.1007/s00429-021-02417-2 · Cited by 15 · see citing works

Human-in-the-loop optimization of visual prosthetic stimulation

Fauvel, T., & Chalk, M. (2022) · Journal of Neural Engineering · doi:10.1088/1741-2552/ac7615 · Cited by 15 · see citing works

Axonal stimulation affects the linear summation of single-point perception in three Argus II users

Hou, Y., Nanduri, D., Granley, J., Weiland, J. D., & Beyeler, M. (2024) · Journal of Neural Engineering · doi:10.1088/1741-2552/ad31c4 · Cited by 14 · see citing works

A model of ganglion axon pathways accounts for percepts elicited by retinal implants

Beyeler, M., Nanduri, D., Weiland, J. D., Rokem, A., Boynton, G. M., & Fine, I. (2018) · doi:10.1101/453035 · Cited by 13 · see citing works

Individual variability of neural computations in the primate retina

Shah, N. P., Brackbill, N., Samarakoon, R., Rhoades, C. E., Kling, A., Sher, A., Litke, A. M., Singer, Y., Shlens, J., & Chichilnisky, E. J. (2021) · Neuron · doi:10.1016/j.neuron.2021.11.026 · Cited by 12 · see citing works

An optimized content-aware image retargeting method: toward expanding the perceived visual field of the high-density retinal prosthesis recipients

Li, H., Zeng, Y., Lu, Z., Cao, X., Su, X., Sui, X., Wang, J., & Chai, X. (2017) · Journal of Neural Engineering · doi:10.1088/1741-2552/aa966d · Cited by 11 · see citing works

Biophysical model of axonal stimulation in epiretinal visual prostheses

Beyeler, M. (2019) · International IEEE/EMBS Conference on Neural Engineering · doi:10.1109/ner.2019.8716969 · Cited by 11 · see citing works

Optogenetic activation of visual thalamus generates artificial visual percepts

Wang, J., Azimi, H., Zhao, Y., Kaeser, M., Sánchez, P. V., Vázquez‐Guardado, A., Rogers, J. A., Harvey, M., & Rainer, G. (2023) · eLife · doi:10.7554/elife.90431 · Cited by 10 · see citing works

Raising the stakes for cortical visual prostheses

Beauchamp, M. S., Bosking, W. H., Oswalt, D. N., & Yoshor, D. (2021) · Journal of Clinical Investigation · doi:10.1172/jci154983 · Cited by 9 · see citing works

Prospects of Optogenetic Prosthesis of the Degenerative Retina of the Eye

Оstrovsky, М. А., & Kirpichnikov, M. P. (2019) · Biochemistry (Moscow) · doi:10.1134/s0006297919050031 · Cited by 9 · see citing works

Restoring vision at the fovea

McGregor, J. E. (2019) · Current Opinion in Behavioral Sciences · doi:10.1016/j.cobeha.2019.10.003 · Cited by 9 · see citing works

Towards Immersive Virtual Reality Simulations of Bionic Vision

Kasowski, J., Wu, N., & Beyeler, M. (2021) · Augmented Humans International Conference (AHs) · doi:10.1145/3458709.3459003 · Cited by 9 · see citing works

Explainable machine learning predictions of perceptual sensitivity for retinal prostheses

Pogoncheff, G., Hu, Z., Rokem, A., & Beyeler, M. (2024) · Journal of Neural Engineering · doi:10.1088/1741-2552/ad310f · Cited by 9 · see citing works

Hybrid Neural Autoencoders for Stimulus Encoding in Visual and Other Sensory Neuroprostheses.

Granley, J., Relic, L., & Beyeler, M. (2022) · PubMed · Cited by 8 · see citing works

Biologically-inspired image processing in computational retina models

Melanitis, N., & Nikita, K. S. (2019) · Computers in Biology and Medicine · doi:10.1016/j.compbiomed.2019.103399 · Cited by 8 · see citing works

Residual contrast response in primary visual cortex of rats with inherited retinal degeneration

Chen, K. G., Hou, B., Zhao, Y., Yuan, P., Yao, D., & Chan, L. L. H. (2020) · Vision Research · doi:10.1016/j.visres.2020.08.007 · Cited by 8 · see citing works

Greedy Optimization of Electrode Arrangement for Epiretinal Prostheses

Bruce, A., & Beyeler, M. (2022) · Lecture notes in computer science · doi:10.1007/978-3-031-16449-1_57 · Cited by 8 · see citing works

Cross-task perceptual learning of object recognition in simulated retinal implant perception

Wang, L., Sharifian, F., Napp, J., Nath, C., & Pollmann, S. (2018) · Journal of Vision · doi:10.1167/18.13.22 · Cited by 8 · see citing works

Short pulses of epiretinal prostheses evoke network-mediated responses in retinal ganglion cells by stimulating presynaptic neurons

Roh, H., Otgondemberel, Y., & Im, M. (2022) · Journal of Neural Engineering · doi:10.1088/1741-2552/ac8ed7 · Cited by 7 · see citing works

Sensory augmentation to aid training with retinal prostheses

Kvansakul, J. G. S., Hamilton, L. H. W., Ayton, L. N., McCarthy, C. D., & Petoe, M. A. (2020) · Journal of Neural Engineering · doi:10.1088/1741-2552/ab9e1d · Cited by 7 · see citing works

Optogenetics and Vision

Kirpichnikov, M. P., & Оstrovsky, М. А. (2019) · Herald of the Russian Academy of Sciences · doi:10.1134/s1019331619010039 · Cited by 7 · see citing works

Linking Multi-Modal MRI to Clinical Measures of Visual Field Loss After Stroke

Beh, A., McGraw, P. V., Webb, B. S., & Schluppeck, D. (2022) · Frontiers in Neuroscience · doi:10.3389/fnins.2021.737215 · Cited by 6 · see citing works

NDE 4.0: Image and Sound Recognition

Hayes, K., & Rajput, A. (2022) · Springer eBooks · doi:10.1007/978-3-030-73206-6_26 · Cited by 5 · see citing works

Learning to see after early and extended blindness: A scoping review

May, E., Arach, P., Kishiki, E., Geneau, R., Maehara, G., Sukhai, M. A., & Hamm, L. M. (2022) · Frontiers in Psychology · doi:10.3389/fpsyg.2022.954328 · Cited by 5 · see citing works

Spatiotemporal Pixelization to Increase the Recognition Score of Characters for Retinal Prostheses

Kim, H.-S., & Park, K. S. (2017) · Sensors · doi:10.3390/s17102439 · Cited by 5 · see citing works

Proceedings of the 16th Python in Science Conference

(2017) · doi:10.25080/shinma-7f4c6e7-000 · Cited by 5 · see citing works

Deep Learning--Based Scene Simplification for Bionic Vision

Han, N., Srivastava, S., Xu, A., Klein, D., & Beyeler, M. (2021) · arXiv · doi:10.48550/arxiv.2102.00297 · Cited by 4 · see citing works

Learning to see again: Perceptual learning of simulated abnormal on- off-cell population responses in sighted individuals

Esquenazi, R., Meier, K., Beyeler, M., Boynton, G. M., & Fine, I. (2021) · Journal of Vision · doi:10.1167/jov.21.13.10 · Cited by 4 · see citing works

An infrared image‐enhancement algorithm in simulated prosthetic vision: Enlarging working environment of future retinal prostheses

Liang, J., Li, H., Chen, J., Zhai, Z., Wang, J., Di, L., & Chai, X. (2022) · Artificial Organs · doi:10.1111/aor.14247 · Cited by 4 · see citing works

TACTILE EDGES AND MOTION VIA PATTERNED MICROSTIMULATION OF THE HUMAN CORTEXPreprint

Valle, G., Alamari, A. H., Lienkämper, R., Downey, J. E., Sobinov, A. R., Endsley, L. J., Prasad, D., Boninger, M. L., Collinger, J. L., Warnke, P. C., et al. (2024) · medRxiv · doi:10.1101/2024.05.06.24306627 · Cited by 4 · see citing works

Retinal Phosphenes Induced by Transorbital Electrical Stimulation: Influence of Light Adaptation, Electrode Montage, and View Direction

Hunold, A., Ortega, D., Freitag, S., Link, D., Antal, A., Klee, S., & Haueisen, J. (2025) · Life · doi:10.3390/life15050820 · Cited by 3 · see citing works

Simulated prosthetic vision confirms checkerboard as an effective raster pattern for epiretinal implants

Kasowski, J., Varshney, A., Sadeghi, R., & Beyeler, M. (2025) · Journal of Neural Engineering · doi:10.1088/1741-2552/adecc4 · Cited by 3 · see citing works

Bionic Vision as Neuroadaptive XR: Closed-Loop Perceptual Interfaces for Neurotechnology

Beyeler, M. J. (2025) · IEEE International Symposium on Mixed and Augmented Reality Adjunct (ISMAR-Adjunct) · doi:10.1109/ismar-adjunct68609.2025.00034 · Cited by 4 · see citing works

Sight restoration reverses blindness-induced cross-modal functional connectivity changes between the visual and somatosensory cortex at rest

Nadvar, N., Stiles, N. R. B., Choupan, J., Patel, V. R., Ameri, H., Shi, Y., Liu, Z., Jonides, J. J., & Weiland, J. D. (2022) · Frontiers in Neuroscience · doi:10.3389/fnins.2022.902866 · Cited by 3 · see citing works

Spatiotemporal Pixelization to Increase the Recognition Score of Characters for Retinal Prostheses

Kim, H.-S., & Park, K. S. (2017) · Sensors · doi:10.3390/s17112439 · Cited by 3 · see citing works

RASPV: A Robotics Framework for Augmented Simulated Prosthetic Vision

Pérez-Yus, A., Santos-Villafranca, M., Tomas-Barba, J., Bermúdez-Cameo, J., Montano-Oliván, L., Nicolás, G. L., & Guerrero, J. J. (2024) · IEEE Access · doi:10.1109/access.2024.3357400 · Cited by 3 · see citing works

Human-in-the-loop optimization of visual prosthetic stimulation

Fauvel, T., & Chalk, M. (2021) · doi:10.1101/2021.11.24.469867 · Cited by 15 · see citing works

Navigational outcomes with a depth-based vision processing algorithm in a second-generation suprachoroidal retinal prosthesis

Moussallem, L., Lombardi, L., McGuinness, M. B., Kolic, M., Baglin, E. K., Jin, R., Habili, N., Kvansakul, J. G. S., Titchener, S. A., Abbott, C. J., et al. (2025) · Journal of Neural Engineering · doi:10.1088/1741-2552/adc83a · Cited by 2 · see citing works

Clinical effect of strabismus correction combined with visual training on children with intermittent exotropia

Guo, B. Z., Liu, Y., Cai, W., Suo, Q., & Su, H. (2025) · Medicine · doi:10.1097/md.0000000000043060 · Cited by 2 · see citing works

Imaging Electrical Activity of Retinal Ganglion Cells with Fluorescent Voltage and Calcium Indicator Proteins in Retinal Degenerative rd1 Blind Mice

Jung, Y., Lee, S., Rhee, J. K., Lee, C. E., Baker, B. J., & Song, Y. (2025) · ACS Chemical Neuroscience · doi:10.1021/acschemneuro.5c00740 · Cited by 2 · see citing works

Seeking after the Glitter of Intelligence in the Base Metal of Computing: The Scope and Limits of Computational Models in Researching Cognitive Phenomena

Kolenik, T. (2018) · Interdisciplinary Description of Complex Systems · doi:10.7906/indecs.16.4.3 · Cited by 2 · see citing works

A scalable data transmission scheme for implantable optogenetic visual prostheses

Hou, Z., Al‐Atabany, W., Farag, R., Vuong, Q. C., Mokhov, A., & Degenaar, P. A. (2020) · Journal of Neural Engineering · doi:10.1088/1741-2552/abaf2e · Cited by 2 · see citing works

Cross-modal activation of the primary visual cortex by auditory stimulation in RCS rats: considerations in visual prosthesis

Caravaca-Rodriguez, D., Suaning, G. J., & Barriga‐Rivera, A. (2022) · Annual International Conference of the IEEE Engineering in Medicine and Biology Society (EMBC) · doi:10.1109/embc48229.2022.9871504 · Cited by 2 · see citing works

Commentary: Detailed Visual Cortical Responses Generated by Retinal Sheet Transplants in Rats With Severe Retinal Degeneration

Beyeler, M. (2019) · Frontiers in Neuroscience · doi:10.3389/fnins.2019.00471 · Cited by 2 · see citing works

Training-induced changes in population receptive field properties in visual cortex: Impact of eccentric vision training on population receptive field properties and the crowding effect

Malania, M., Lin, Y.-S., Hörmandinger, C., Werner, J. S., Greenlee, M. W., & Plank, T. (2024) · Journal of Vision · doi:10.1167/jov.24.5.7 · Cited by 1 · see citing works

Visual–tactile shape perception in Argus II Participants: The impact of prolonged device use and blindness on performance

Saltzmann, S. M., & Stiles, N. R. B. (2025) · Journal of Vision · doi:10.1167/jov.25.12.19 · Cited by 1 · see citing works

Neural population dynamics of direct electrical stimulation of neocortex

Hickman, J. L., Hughes, G., Sahai, E., Miles, M., & Denman, D. J. (2026) · Cell Reports · doi:10.1016/j.celrep.2026.117420 · Cited by 1 · see citing works

Fuzzing the brain: automated stress testing for the safety of ML-driven neurostimulation

Downing, M., Peng, M., Granley, J., Beyeler, M., & Bultan, T. (2026) · Journal of Neural Engineering · doi:10.1088/1741-2552/ae4927 · Cited by 1 · see citing works

Wide-angle simulated artificial vision enhances spatial navigation and object interaction in a naturalistic environment

Hinrichs, S., Placidet, L., Duret, A., Authié, C., Arleo, A., & Ghezzi, D. (2024) · Journal of Neural Engineering · doi:10.1088/1741-2552/ad8b6f · Cited by 1 · see citing works

Modeling fixational eye movement for the vision prosthesis

Rizzo, R., & Seo, J. M. (2019) · Annual International Conference of the IEEE Engineering in Medicine and Biology Society (EMBC) · doi:10.1109/embc.2019.8857015

Editorial: A Conversation With the Brain: Can We Speak Its Language?

Barriga‐Rivera, A., Guo, T., Hayashida, Y., & Suaning, G. J. (2020) · Frontiers in Neuroscience · doi:10.3389/fnins.2020.00794

A Conversation With the Brain: Can We Speak Its Language?

(2020) · Frontiers research topics · doi:10.3389/978-2-88966-067-4

On the potential role of retinal sheet transplants for sight restorationPreprint

Beyeler, M. (2019) · doi:10.31219/osf.io/temqd

Simulador inmersivo de visión protésica modelando estímulos espacio-temporales

Santos-Villafranca, M., Tomas-Barba, J., Pérez-Yus, A., Bermúdez-Cameo, J., & Guerrero, J. (2023) · doi:10.17979/spudc.9788497498609.879

NDE 4.0: Image and Sound Recognition

Hayes, K., & Rajput, A. (2025) · Springer eBooks · doi:10.1007/978-3-030-48200-8_26-2

Wide visual angle enhances social interaction in a realistic virtual reality environment under simulated artificial visionPreprint

Hinrichs, S., Tisserand, Y., Scialom, E., & Ghezzi, D. (2025) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2025.03.27.645647

Neural Gain Modulation Propagates from Posterior to Anterior Brain Regions to Optimize Orientation Perception in Chronic AstigmatismPreprint

Son, S., Kang, H.-G., Kim, H. R., Shim, W. M., & Lee, J. (2025) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2025.04.13.648557

NDE 4.0: Image and Sound Recognition

Hayes, K., & Rajput, A. (2025) · Springer eBooks · doi:10.1007/978-3-031-84477-5_26

Intact early visual representations, not phosphene-adapted features, account for human perceptual behavior with retinal prosthesesPreprint

Skaza, J., Murlidaran, S., Varshney, A., Wen, Z., Eckstein, M. P., & Beyeler, M. (2025) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2025.06.23.660990

Dynamic neural compensation for distorted orientation perception in chronic astigmatism

Son, S., Kang, H.-G., Kim, H. R., Shim, W. M., & Lee, J. (2025) · iScience · doi:10.1016/j.isci.2025.113518

Are artificial retinas merely an approach to recover sight, or are they a tool of augmented reality beyond natural eyes in blind people?

Zhao, Z., & Asakawa, T. (2025) · BioScience Trends · doi:10.5582/bst.2025.01341

Static or Temporal? Semantic Scene Simplification to Aid Wayfinding in Immersive Simulations of Bionic Vision

Kasowski, J., Varshney, A., & Beyeler, M. (2025) · ACM Symposium on Virtual Reality Software and Technology (VRST) · doi:10.1145/3756884.3766003

Neuromorphic sensory substitution with an asynchronous tactile belt for unsighted people : from design to clinical trials

Arth, K. (2018) · doi:10.70675/d5697db0z82e1z4b25z81c7zf85e85367636

From Visual Plasticity to the Bionic Eye

Buss, S. S. (2016) · Einstein Journal of Biology and Medicine · doi:10.23861/ejbm20112725

Cortical Plasticity and Reorganization in Severe Vision Loss

Fernández, E., & Merabet, L. B. (2011) · Springer eBooks · doi:10.1007/978-1-4419-0754-7_4 · Cited by 4 · see citing works

Neuroplasticity in adult human visual cortex

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