SINGLE-CELL RESPONSES IN STRIATE CORTEX OF KITTENS DEPRIVED OF VISION IN ONE EYE

Receptive fields, binocular interaction and functional architecture in the cat’s visual cortex

Hubel, D. H., & Wiesel, T. N. (1962) · The Journal of Physiology · doi:10.1113/jphysiol.1962.sp006837 · Cited by 13,680 · see citing works

Receptive fields of single neurones in the cat's striate cortex

Hubel, D. H., & Wiesel, T. N. (1959) · The Journal of Physiology · doi:10.1113/jphysiol.1959.sp006308 · Cited by 4,653 · 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

RECEPTIVE FIELDS OF CELLS IN STRIATE CORTEX OF VERY YOUNG, VISUALLY INEXPERIENCED KITTENS

Hubel, D. H., & Wiesel, T. N. (1963) · Journal of Neurophysiology · doi:10.1152/jn.1963.26.6.994 · Cited by 1,113 · see citing works

Shape and arrangement of columns in cat's striate cortex

Hubel, D. H., & Wiesel, T. N. (1963) · The Journal of Physiology · doi:10.1113/jphysiol.1963.sp007079 · Cited by 834 · see citing works

Single unit activity in striate cortex of unrestrained cats

Hubel, D. H. (1959) · The Journal of Physiology · doi:10.1113/jphysiol.1959.sp006238 · Cited by 578 · see citing works

EFFECT OF TOTAL ABSENCE OF FUNCTION ON THE OPTIC SYSTEM OF RABBITS

Goodman, L. (1932) · American Journal of Physiology-Legacy Content · doi:10.1152/ajplegacy.1932.100.1.46 · Cited by 66 · see citing works

The Effect of Light on the Appearance and Development of the Electroretinogram in Newborn Kittens

Zetterström, B. (1955) · Acta Physiologica Scandinavica · doi:10.1111/j.1748-1716.1955.tb01284.x · Cited by 63 · see citing works

Experimentell-anatomische Studien über die durch den Mangel optischer Reize veranlassten Entwicklungshemmungen im Occipitallappen des Hundes und der Katze

Berger, H. (1900) · European Archives of Psychiatry and Clinical Neuroscience · doi:10.1007/bf02114317 · Cited by 49 · see citing works

Interocular transfer of habits learned monocularly in visually naive and visually experienced cats.

Riesen, A. H., Kurke, M. I., & Mellinger, J. C. (1953) · Journal of Comparative and Physiological Psychology · doi:10.1037/h0057003 · Cited by 46 · see citing works

Interocular transfer of learning in visually naive and experienced infant chimpanzees.

Chow, K. L., & Nissen, H. W. (1955) · Journal of Comparative and Physiological Psychology · doi:10.1037/h0042364 · Cited by 33 · see citing works

Synaptic Activity and the Construction of Cortical Circuits

Katz, L. C., & Shatz, C. J. (1996) · Science · doi:10.1126/science.274.5290.1133 · Cited by 3,048 · see citing works

The period of susceptibility to the physiological effects of unilateral eye closure in kittens

Hubel, D. H., & Wiesel, T. N. (1970) · The Journal of Physiology · doi:10.1113/jphysiol.1970.sp009022 · Cited by 3,030 · see citing works

Theory for the development of neuron selectivity: orientation specificity and binocular interaction in visual cortex

Bienenstock, E., Cooper, L., & Munro, P. (1982) · The Journal of Neuroscience · doi:10.1523/jneurosci.02-01-00032.1982 · Cited by 2,896 · see citing works

Ferrier lecture. Functional architecture of macaque monkey visual cortex

Hubel, D. H., & Wiesel, T. N. (1977) · Proceedings of the Royal Society of London. Series B. Biological Sciences · doi:10.1098/rspb.1977.0085 · Cited by 2,608 · see citing works

Long-term in vivo imaging of experience-dependent synaptic plasticity in adult cortex

Trachtenberg, J. T., Chen, B. E., Knott, G. W., Feng, G., Sanes, J. R., Welker, E., & Svoboda, K. (2002) · Nature · doi:10.1038/nature01273 · Cited by 1,927 · see citing works

Neurotrophins and Neuronal Plasticity

Thoenen, H. (1995) · Science · doi:10.1126/science.270.5236.593 · Cited by 1,927 · see citing works

Experience and brain development

Greenough, W. T., Black, J. E., & Wallace, C. S. (1987) · Child Development · doi:10.2307/1130197 · Cited by 1,398 · see citing works

Critical period regulation

Hensch, T. K. (2004) · Annual Review of Neuroscience · doi:10.1146/annurev.neuro.27.070203.144327 · Cited by 1,300 · see citing works

Adolescence as a sensitive period of brain development

Fuhrmann, D., Knoll, L. J., & Blakemore, S.-J. (2015) · Trends in Cognitive Sciences · doi:10.1016/j.tics.2015.07.008 · Cited by 1,158 · see citing works

The development of ocular dominance columns in normal and visually deprived monkeys

Le Vay, S., Wiesel, T. N., & Hubel, D. H. (1980) · Journal of Comparative Neurology · doi:10.1002/cne.901910102 · Cited by 1,123 · see citing works

How the Timing and Quality of Early Experiences Influence the Development of Brain Architecture

Fox, S. E., Levitt, P., & Nelson, C. A. (2010) · Child Development · doi:10.1111/j.1467-8624.2009.01380.x · Cited by 1,088 · see citing works

Hippocampal GABAergic Inhibitory Interneurons

Pelkey, K. A., Chittajallu, R., Craig, M. T., Tricoire, L., Wester, J. C., & McBain, C. J. (2017) · Physiological Reviews · doi:10.1152/physrev.00007.2017 · Cited by 889 · see citing works

Postnatal development of the visual cortex and the influence of environment

Wiesel, T. N. (1982) · Nature · doi:10.1038/299583a0 · Cited by 978 · see citing works

Psychobiology of plasticity: Effects of training and experience on brain and behavior

Rosenzweig, M. R., & Bennett, E. L. (1996) · Behavioural Brain Research · doi:10.1016/0166-4328(95)00216-2 · Cited by 972 · see citing works

Local GABA Circuit Control of Experience-Dependent Plasticity in Developing Visual Cortex

Hensch, T. K., Fagiolini, M., Mataga, N., Stryker, M. P., Baekkeskov, S., & Kash, S. F. (1998) · Science · doi:10.1126/science.282.5393.1504 · Cited by 910 · see citing works

A Critical Period for Enhanced Synaptic Plasticity in Newly Generated Neurons of the Adult Brain

Ge, S., Yang, C.-H., Hsu, K.-S., Ming, G.-L., & Song, H. (2007) · Neuron · doi:10.1016/j.neuron.2007.05.002 · Cited by 927 · see citing works

Early experience alters brain function and structure

Als, H., Duffy, F. H., McAnulty, G. B., Rivkin, M. J., Vajapeyam, S., Mulkern, R. V., Warfield, S. K., Huppi, P. S., Butler, S. C., Conneman, N., et al. (2004) · Pediatrics · doi:10.1542/peds.113.4.846 · Cited by 890 · see citing works

Adolescence as a neurobiological critical period for the development of higher-order cognition

Larsen, B., & Luna, B. (2018) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2018.09.005 · Cited by 853 · see citing works

Modulation of visual cortical plasticity by acetylcholine and noradrenaline

Bear, M. F., & Singer, W. (1986) · Nature · doi:10.1038/320172a0 · Cited by 858 · see citing works

Elimination of synapses in the developing nervous system

Purves, D., & Lichtman, J. W. (1980) · Science · doi:10.1126/science.7414326 · Cited by 808 · 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

Patterned Activity, Synaptic Convergence, and the NMDA Receptor in Developing Visual Pathways

Constantine-Paton, M., Cline, H. T., & Debski, E. (1990) · Annual Review of Neuroscience · doi:10.1146/annurev.ne.13.030190.001021 · Cited by 784 · see citing works

Neural reorganization following sensory loss: the opportunity of change

Merabet, L. B., & Pascual-Leone, A. (2010) · Nature Reviews Neuroscience · doi:10.1038/nrn2758 · Cited by 751 · see citing works

Ocular dominance in layer IV of the cat's visual cortex and the effects of monocular deprivation.

Shatz, C. J., & Stryker, M. P. (1978) · The Journal of Physiology · doi:10.1113/jphysiol.1978.sp012421 · Cited by 691 · see citing works

Binocular impulse blockade prevents the formation of ocular dominance columns in cat visual cortex

Stryker, M., & Harris, W. (1986) · The Journal of Neuroscience · doi:10.1523/jneurosci.06-08-02117.1986 · Cited by 687 · see citing works

Development and plasticity of the primary visual cortex

Espinosa, J. S., & Stryker, M. P. (2012) · Neuron · doi:10.1016/j.neuron.2012.06.009 · Cited by 672 · see citing works

Experience-driven plasticity of visual cortex limited by myelin and nogo receptor

McGee, A. W., Yang, Y., Fischer, Q. S., Daw, N. W., & Strittmatter, S. M. (2005) · Science · doi:10.1126/science.1114362 · Cited by 643 · see citing works

Regulation of NMDA receptor subunit expression and its implications for LTD, LTP, and metaplasticity

Yashiro, K., & Philpot, B. D. (2008) · Neuropharmacology · doi:10.1016/j.neuropharm.2008.07.046 · Cited by 649 · 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

Compensatory plasticity and sensory substitution in the cerebral cortex

Rauschecker, J. P. (1995) · Trends in Neurosciences · doi:10.1016/0166-2236(95)93948-w · Cited by 590 · see citing works

Cerebral plasticity: windows of opportunity in the developing brain

Ismail, F. Y., Fatemi, A., & Johnston, M. V. (2017) · European Journal of Paediatric Neurology · doi:10.1016/j.ejpn.2016.07.007 · Cited by 572 · see citing works

Experience and the developing prefrontal cortex

Kolb, B., Mychasiuk, R., Muhammad, A., Li, Y., Frost, D. O., & Gibb, R. (2012) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1121251109 · Cited by 564 · see citing works

Retinal waves and visual system development

Wong, R. O. L. (1999) · Annual Review of Neuroscience · doi:10.1146/annurev.neuro.22.1.29 · Cited by 544 · see citing works

Experience leaves a lasting structural trace in cortical circuits

Hofer, S. B., Mrsic-Flogel, T. D., Bonhoeffer, T., & Hübener, M. (2009) · Nature · doi:10.1038/nature07487 · Cited by 514 · see citing works

Critical period regulation across multiple timescales

Reh, R. K., Dias, B. G., Nelson, C. A., Kaufer, D., Werker, J. F., Kolb, B., Levine, J. D., & Hensch, T. K. (2020) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1820836117 · Cited by 492 · see citing works

Microglial P2Y12 is necessary for synaptic plasticity in mouse visual cortex

Sipe, G. O., Lowery, Tremblay, M.-È., Kelly, E. A., Lamantia, C. E., & Majewska, A. K. (2016) · Nature Communications · doi:10.1038/ncomms10905 · Cited by 512 · see citing works

Experience-Dependent Transfer of Otx2 Homeoprotein into the Visual Cortex Activates Postnatal Plasticity

Sugiyama, S., Di Nardo, A. A., Aizawa, S., Matsuo, I., Volovitch, M., Prochiantz, A., & Hensch, T. K. (2008) · Cell · doi:10.1016/j.cell.2008.05.054 · Cited by 491 · see citing works

Single-cell analysis of experience-dependent transcriptomic states in the mouse visual cortex

Hrvatin, S., Hochbaum, D. R., Nagy, M. A., Cicconet, M., Robertson, K., Cheadle, L., Zilionis, R., Ratner, A., Borges-Monroy, R., Klein, A. M., et al. (2018) · Nature Neuroscience · doi:10.1038/s41593-017-0029-5 · Cited by 497 · see citing works

Apical dendritic spines of the visual cortex and light deprivation in the mouse

Valverde, P. (1967) · Experimental Brain Research · doi:10.1007/bf00237559 · Cited by 483 · see citing works

Npas4 regulates excitatory-inhibitory balance within neural circuits through cell-type-specific gene programs

Spiegel, I., Mardinly, A. R., Gabel, H. W., Bazinet, J. E., Couch, C. H., Tzeng, C. P., Harmin, D. A., & Greenberg, M. E. (2014) · Cell · doi:10.1016/j.cell.2014.03.058 · Cited by 416 · see citing works

Critical-Period Plasticity in the Visual Cortex

Levelt, C. N., & Hübener, M. (2012) · Annual Review of Neuroscience · doi:10.1146/annurev-neuro-061010-113813 · Cited by 402 · see citing works

Architectures of neuronal circuits

Luo, L. (2021) · Science · doi:10.1126/science.abg7285 · Cited by 390 · see citing works

Environment and Brain Plasticity: Towards an Endogenous Pharmacotherapy

Sale, A., Berardi, N., & Maffei, L. (2014) · Physiological Reviews · doi:10.1152/physrev.00036.2012 · Cited by 402 · see citing works

A disinhibitory microcircuit initiates critical-period plasticity in the visual cortex

Kuhlman, S. J., Olivas, N. D., Tring, E., Ikrar, T., Xu, X., & Trachtenberg, J. T. (2013) · Nature · doi:10.1038/nature12485 · Cited by 412 · see citing works

Communication Between the Synapse and the Nucleus in Neuronal Development, Plasticity, and Disease

Cohen, S., & Greenberg, M. E. (2008) · Annual Review of Cell and Developmental Biology · doi:10.1146/annurev.cellbio.24.110707.175235 · Cited by 400 · see citing works

The BCM theory of synapse modification at 30: interaction of theory with experiment

Cooper, L. N., & Bear, M. F. (2012) · Nature Reviews Neuroscience · doi:10.1038/nrn3353 · Cited by 395 · see citing works

Early Musical Training and White-Matter Plasticity in the Corpus Callosum: Evidence for a Sensitive Period

Steele, C. J., Bailey, J. A., Zatorre, R. J., & Penhune, V. B. (2013) · The Journal of Neuroscience · doi:10.1523/jneurosci.3578-12.2013 · Cited by 388 · see citing works

Memory for items and memory for relations in the procedural/declarative memory framework

Cohen, N. J., Poldrack, R. A., & Eichenbaum, H. (1997) · Memory · doi:10.1080/741941149 · Cited by 383 · see citing works

Plastic changes in the central auditory system after hearing loss, restoration of function, and during learning.

Syka, J. (2002) · Physiological Reviews · doi:10.1152/physrev.00002.2002 · Cited by 369 · see citing works

Persistent cortical plasticity by upregulation of chondroitin 6-sulfation

Miyata, S., Komatsu, Y., Yoshimura, Y., Taya, C., & Kitagawa, H. (2012) · Nature Neuroscience · doi:10.1038/nn.3023 · Cited by 365 · see citing works

Risk and resilience: genetic and environmental influences on development of the stress response

Gillespie, C. F., Phifer, J., Bradley, B., & Ressler, K. J. (2009) · Depression and Anxiety · doi:10.1002/da.20605 · Cited by 351 · see citing works

Enrich the environment to empower the brain

Sale, A., Berardi, N., & Maffei, L. (2009) · Trends in Neurosciences · doi:10.1016/j.tins.2008.12.004 · Cited by 341 · see citing works

Nurturing brain plasticity: Impact of environmental enrichment

Baroncelli, L., Braschi, C., Spolidoro, M., Begenisic, T., Sale, A., & Maffei, L. (2010) · Cell Death & Differentiation · doi:10.1038/cdd.2009.193 · Cited by 330 · see citing works

Distinct roles for spontaneous and visual activity in remodeling of the retinogeniculate synapse

Hooks, B. M., & Chen, C. (2006) · Neuron · doi:10.1016/j.neuron.2006.07.007 · Cited by 311 · see citing works

Massive restructuring of neuronal circuits during functional reorganization of adult visual cortex

Keck, T., Mrsic-Flogel, T. D., Vaz Afonso, M., Eysel, U. T., Bonhoeffer, T., & Hübener, M. (2008) · Nature Neuroscience · doi:10.1038/nn.2181 · Cited by 315 · see citing works

Ube3a is required for experience-dependent maturation of the neocortex

Yashiro, K., Riday, T. T., Condon, K. H., Roberts, A. C., Bernardo, D. R., Prakash, R., Weinberg, R. J., Ehlers, M. D., & Philpot, B. D. (2009) · Nature Neuroscience · doi:10.1038/nn.2327 · Cited by 328 · see citing works

Experience-dependent structural plasticity in the cortex

Fu, M., & Zuo, Y. (2011) · Trends in Neurosciences · doi:10.1016/j.tins.2011.02.001 · Cited by 322 · see citing works

Decreased Cortical Representation of Genital Somatosensory Field After Childhood Sexual Abuse

Heim, C. M., Mayberg, H. S., Mletzko, T., Nemeroff, C. B., & Pruessner, J. C. (2013) · American Journal of Psychiatry · doi:10.1176/appi.ajp.2013.12070950 · Cited by 318 · see citing works

Autism: A “Critical Period” Disorder?

LeBlanc, J. J., & Fagiolini, M. (2011) · Neural Plasticity · doi:10.1155/2011/921680 · Cited by 301 · see citing works

The location and function of NMDA receptors in cat and kitten visual cortex

Fox, K., Sato, H., & Daw, N. (1989) · The Journal of Neuroscience · doi:10.1523/jneurosci.09-07-02443.1989 · Cited by 307 · see citing works

Limitations on input as a basis for neural organization and perceptual development: A preliminary theoretical statement

Turkewitz, G., & Kenny, P. A. (1982) · Developmental Psychobiology · doi:10.1002/dev.420150408 · Cited by 304 · see citing works

Dendritic Spine Dynamics Are Regulated by Monocular Deprivation and Extracellular Matrix Degradation

Oray, S., Majewska, A., & Sur, M. (2004) · Neuron · doi:10.1016/j.neuron.2004.12.001 · Cited by 296 · see citing works

Loss of adaptive myelination contributes to methotrexate chemotherapy-related cognitive impairment

Geraghty, A. C., Gibson, E. M., Ghanem, R. A., Greene, J. J., Ocampo, A., Goldstein, A. K., Ni, L., Yang, T., Marton, R. M., Paşca, S. P., et al. (2019) · Neuron · doi:10.1016/j.neuron.2019.04.032 · Cited by 288 · see citing works

The neuro-environmental loop of plasticity: a cross-species analysis of parental effects on emotion circuitry development following typical and adverse caregiving

Callaghan, B. L., & Tottenham, N. (2016) · Neuropsychopharmacology · doi:10.1038/npp.2015.204 · Cited by 268 · see citing works

Sensory Deprivation Alters Aggrecan and Perineuronal Net Expression in the Mouse Barrel Cortex

McRae, P. A., Rocco, M. M., Kelly, G., Brumberg, J. C., & Matthews, R. T. (2007) · The Journal of Neuroscience · doi:10.1523/jneurosci.5425-06.2007 · Cited by 272 · see citing works

Excitatory-inhibitory balance and critical period plasticity in developing visual cortex

Hensch, T. K., & Fagiolini, M. (2005) · Progress in Brain Research · doi:10.1016/s0079-6123(04)47009-5 · Cited by 267 · see citing works

Toward Fulfilling the Promise of Molecular Medicine in Fragile X Syndrome

Krueger, D. D., & Bear, M. F. (2011) · Annual Review of Medicine · doi:10.1146/annurev-med-061109-134644 · Cited by 259 · see citing works

The critical period for ocular dominance plasticity in the Ferret's visual cortex

Issa, N. P., Trachtenberg, J. T., Chapman, B., Zahs, K. R., & Stryker, M. P. (1999) · The Journal of Neuroscience · doi:10.1523/jneurosci.19-16-06965.1999 · Cited by 243 · see citing works

Drawing Abilities in Williams Syndrome: A Case Study

Stiles, J. (2000) · Developmental Neuropsychology · doi:10.1207/s15326942dn1802_5 · Cited by 236 · see citing works

Gene expression changes and molecular pathways mediating activity-dependent plasticity in visual cortex

Tropea, D., Kreiman, G., Lyckman, A., Mukherjee, S., Yu, H., Horng, S., & Sur, M. (2006) · Nature Neuroscience · doi:10.1038/nn1689 · Cited by 226 · see citing works

The effect of dark rearing on the time course of the critical period in cat visual cortex

Mower, G. D. (1991) · Developmental Brain Research · doi:10.1016/0165-3806(91)90001-y · Cited by 220 · see citing works

Bidirectional plasticity in fast-spiking GABA circuits by visual experience

Yazaki-Sugiyama, Y., Kang, S., Câteau, H., Fukai, T., & Hensch, T. K. (2009) · Nature · doi:10.1038/nature08485 · Cited by 200 · 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

Targeting microglia for the treatment of Alzheimer’s Disease

Wes, P. D., Sayed, F. A., Bard, F., & Gan, L. (2016) · Glia · doi:10.1002/glia.22988 · Cited by 185 · see citing works

Modulation of Perineuronal Nets and Parvalbumin with Developmental Song Learning

Balmer, T. S., Carels, V. M., Frisch, J. L., & Nick, T. A. (2009) · The Journal of Neuroscience · doi:10.1523/jneurosci.2974-09.2009 · Cited by 181 · see citing works

Safety and Vision Outcomes of Subretinal Gene Therapy Targeting Cone Photoreceptors in Achromatopsia: A Nonrandomized Controlled Trial

Fischer, M. D., Michalakis, S., Wilhelm, B., Zobor, D., Muehlfriedel, R., Kohl, S., Weisschuh, N., Ochakovski, G. A., Klein, R., Schoen, C., et al. (2020) · JAMA Ophthalmology · doi:10.1001/jamaophthalmol.2020.1032 · Cited by 177 · see citing works

Recurrent network activity drives striatal synaptogenesis

Kozorovitskiy, Y., Saunders, A., Johnson, C. A., Lowell, B. B., & Sabatini, B. L. (2012) · Nature · doi:10.1038/nature11052 · Cited by 176 · see citing works

Environmental enrichment extends ocular dominance plasticity into adulthood and protects from stroke-induced impairments of plasticity

Greifzu, F., Pielecka-Fortuna, J., Kalogeraki, E., Krempler, K., Favaro, P. D., Schlüter, O. M., & Löwel, S. (2014) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1313385111 · Cited by 144 · see citing works

Interactions of the serotonin and circadian systems: nature and nurture in rhythms and blues

Ciarleglio, C. M., Resuehr, H. E. S., & McMahon, D. G. (2011) · Neuroscience · doi:10.1016/j.neuroscience.2011.09.036 · Cited by 151 · see citing works

Serotonin triggers a transient epigenetic mechanism that reinstates adult visual cortex plasticity in rats: Epigenetics of serotonin-induced adult cortical plasticity

Vetencourt, J. F. M., Tiraboschi, E., Spolidoro, M., Castrén, E., & Maffei, L. (2011) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.2010.07488.x · Cited by 138 · see citing works

Structural plasticity underlies experience-dependent functional plasticity of cortical circuits.

Wilbrecht, L., Holtmaat, A., Wright, N., Fox, K., & Svoboda, K. (2010) · The Journal of Neuroscience · doi:10.1523/jneurosci.6403-09.2010 · Cited by 138 · see citing works

Axonal dynamics of excitatory and inhibitory neurons in somatosensory cortex

Marik, S. A., Yamahachi, H., McManus, J. N. J., Szabo, G., & Gilbert, C. D. (2010) · PLoS Biology · doi:10.1371/journal.pbio.1000395 · Cited by 124 · see citing works

‘Visual’ Acuity of the Congenitally Blind Using Visual-to-Auditory Sensory Substitution

Striem-Amit, E., Guendelman, M., & Amedi, A. (2012) · PLoS ONE · doi:10.1371/journal.pone.0033136 · Cited by 117 · see citing works

Comparison of Plasticity<i>In Vivo</i>and<i>In Vitro</i>in the Developing Visual Cortex of Normal and Protein Kinase A RIβ-Deficient Mice

Hensch, T. K., Gordon, J. A., Brandon, E. P., McKnight, G. S., Idzerda, R. L., & Stryker, M. P. (1998) · The Journal of Neuroscience · doi:10.1523/jneurosci.18-06-02108.1998 · Cited by 117 · see citing works

Rapid eye movement sleep deprivation modifies expression of long-term potentiation in visual cortex of immature rats.

Shaffery, J. P., Sinton, C. M., Bissette, G., Roffwarg, H. P., & Marks, G. A. (2002) · Neuroscience · doi:10.1016/s0306-4522(01)00589-9 · Cited by 114 · 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

Cortical Plasticity, Excitatory–Inhibitory Balance, and Sensory Perception

Carcea, I., & Froemke, R. C. (2013) · Progress in Brain Research · doi:10.1016/b978-0-444-63327-9.00003-5 · Cited by 110 · see citing works

Molecular evidence for early activity-dependent development of hamster motor neurons

Kalb, R., & Hockfield, S. (1988) · The Journal of Neuroscience · doi:10.1523/jneurosci.08-07-02350.1988 · Cited by 102 · see citing works

Otx2-PNN interaction to regulate cortical plasticity

Bernard, C., & Prochiantz, A. (2016) · Neural Plasticity · doi:10.1155/2016/7931693 · Cited by 102 · see citing works

The man who feels two hearts: the different pathways of interoception.

Couto, B., Salles, A., Sedeño, L., Peradejordi, M., Barttfeld, P., Canales-Johnson, A., Dos Santos, Y. V., Huepe, D., Bekinschtein, T., Sigman, M., et al. (2014) · Social Cognitive and Affective Neuroscience · doi:10.1093/scan/nst108 · Cited by 97 · see citing works

Extensive childhood experience with Pokémon suggests eccentricity drives organization of visual cortex

Gomez, J., Barnett, M., & Grill-Spector, K. (2019) · Nature Human Behaviour · doi:10.1038/s41562-019-0592-8 · Cited by 81 · see citing works

Perineuronal nets and schizophrenia: The importance of neuronal coatings

Bitanihirwe, B. K. Y., & Woo, T.-U. W. (2014) · Neuroscience &amp; Biobehavioral Reviews · doi:10.1016/j.neubiorev.2014.03.018 · Cited by 95 · see citing works

Light reintroduction after dark exposure reactivates plasticity in adults via perisynaptic activation of MMP-9

Murase, S., Lantz, C. L., & Quinlan, E. M. (2017) · eLife · doi:10.7554/elife.27345 · Cited by 87 · see citing works

Critical period for the monocular deprivation effect in rats: Assessment with sweep visually evoked potentials

Guire, E. S., Lickey, M. E., & Gordon, B. (1999) · Journal of Neurophysiology · doi:10.1152/jn.1999.81.1.121 · Cited by 83 · see citing works

Environmental regulation of the neural epigenome

Caldji, C., Hellstrom, I. C., Zhang, T.-Y., Diorio, J., & Meaney, M. J. (2011) · FEBS Letters · doi:10.1016/j.febslet.2011.03.032 · Cited by 82 · see citing works

From brain formation to plasticity: Insights on Otx2 homeoprotein

Sugiyama, S., Prochiantz, A., & Hensch, T. K. (2009) · Development, Growth &amp; Differentiation · doi:10.1111/j.1440-169x.2009.01093.x · Cited by 77 · see citing works

New Targets for Prevention of Schizophrenia: Is It Time for Interventions in the Premorbid Phase?

Seidman, L. J., & Nordentoft, M. (2015) · Schizophrenia Bulletin · doi:10.1093/schbul/sbv050 · Cited by 65 · see citing works

Delayed maturation of fast-spiking interneurons is rectified by activation of the TrkB receptor in the mouse model of fragile X syndrome.

Nomura, T., Musial, T. F., Marshall, J. J., Zhu, Y., Remmers, C. L., Xu, J., Nicholson, D. A., & Contractor, A. (2017) · The Journal of Neuroscience · doi:10.1523/jneurosci.2893-16.2017 · Cited by 64 · see citing works

Maternal regulation of infant brain state

Sarro, E. C., Wilson, D. A., & Sullivan, R. M. (2014) · Current Biology · doi:10.1016/j.cub.2014.06.017 · Cited by 61 · see citing works

The Non-Benzodiazepine Hypnotic Zolpidem Impairs Sleep-Dependent Cortical Plasticity

(2008) · Sleep · doi:10.5665/sleep/31.10.1381 · Cited by 60 · see citing works

Combined meeting of the French Society of clinical neurophysiology, Belgian society of clinical neurophysiology and Belgian society of EMG and clinical neurophysiology

(1991) · Electroencephalography and Clinical Neurophysiology · doi:10.1016/0013-4694(91)90105-d

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de Weerd, A. (2004) · Clinical Neurophysiology · doi:10.1016/j.clinph.2004.03.001 · Cited by 7 · see citing works

Repetitive transcranial magnetic stimulation. Recommendations for the practice of clinical neurophysiology : guidelines of the international federation of clinical neurophysiology

Hallett, M. (1999) · Electroencephalography and Clinical Neurophysiology · Cited by 6 · see citing works

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(2019) · Clinical Neurophysiology Practice · doi:10.1016/j.cnp.2019.10.003

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(2000) · Supplements to Clinical neurophysiology · doi:10.1016/s1567-424x(09)x7004-2