Effects of retinal ganglion cell loss on magno-, parvo-, koniocellular pathways in the lateral geniculate nucleus and visual cortex in glaucoma

Changes in the visual system of monocularly sutured or enucleated cats demonstrable with cytochrome oxidase histochemistry

Wong‐Riley, M. T. T. (1979) · Brain Research · doi:10.1016/0006-8993(79)90728-5 · Cited by 1,853 · see citing works

Anatomy and physiology of a color system in the primate visual cortex

Livingstone, M. S., & Hubel, D. H. (1984) · Journal of Neuroscience · doi:10.1523/jneurosci.04-01-00309.1984 · Cited by 1,637 · see citing works

Optic Nerve Damage in Human Glaucoma

Quigley, H. A. (1982) · Archives of Ophthalmology · doi:10.1001/archopht.1982.01030030137016 · Cited by 1,177 · see citing works

Stereological methods for estimating the total number of neurons and synapses: issues of precision and bias

West, M. J. (1999) · Trends in Neurosciences · doi:10.1016/s0166-2236(98)01362-9 · Cited by 814 · see citing works

Retinal ganglion cells that project to the dorsal lateral geniculate nucleus in the macaque monkey

Perry, V. H., Oehler, R., & Cowey, A. (1984) · Neuroscience · doi:10.1016/0306-4522(84)90006-x · Cited by 717 · see citing works

The origin of efferent pathways from the primary visual cortex, area 17, of the macaque monkey as shown by retrograde transport of horseradish peroxidase

Lund, J. S., Lund, R. D., Hendrickson, A. E., Milam, A. H., & Fuchs, A. F. (1975) · The Journal of Comparative Neurology · doi:10.1002/cne.901640303 · Cited by 681 · see citing works

Biochemical and immunochemical evidence that the "major postsynaptic density protein" is a subunit of a calmodulin-dependent protein kinase.

Kennedy, M. B., Bennett, M. K., & Erondu, N. E. (1983) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.80.23.7357 · Cited by 610 · see citing works

The Koniocellular Pathway in Primate Vision

Hendry, S. H. C., & Reid, R. C. (2000) · Annual Review of Neuroscience · doi:10.1146/annurev.neuro.23.1.127 · Cited by 591 · see citing works

Contemporary Research Methods in Neuroanatomy

(1970) · Springer eBooks · doi:10.1007/978-3-642-85986-1 · Cited by 586 · see citing works

Functional specificity of lateral geniculate nucleus laminae of the rhesus monkey

Schiller, P. H., & Malpeli, J. G. (1978) · Journal of Neurophysiology · doi:10.1152/jn.1978.41.3.788 · Cited by 548 · see citing works

Experimental Brain Injury Induces Regionally Distinct Apoptosis during the Acute and Delayed Post-Traumatic Period

Conti, A., Raghupathi, R., Trojanowski, J., & McIntosh, T. (1998) · Journal of Neuroscience · doi:10.1523/jneurosci.18-15-05663.1998 · Cited by 543 · see citing works

CaMKII regulates the frequency-response function of hippocampal synapses for the production of both LTD and LTP

Mayford, M. R., Wang, J., Kandel, E. R., & O’Dell, T. J. (1995) · Cell · doi:10.1016/0092-8674(95)90009-8 · Cited by 523 · see citing works

Anterograde and Retrograde Transneuronal Degeneration in the Central and Peripheral Nervous System

Cowan, W. M. (1970) · Springer eBooks · doi:10.1007/978-3-642-85986-1_11 · Cited by 461 · see citing works

Retinal ganglion cells that project to the superior colliculus and pretectum in the macaque monkey

Perry, V. H., & Cowey, A. (1984) · Neuroscience · doi:10.1016/0306-4522(84)90007-1 · Cited by 456 · see citing works

Mechanisms of optic nerve damage in primary open angle glaucoma

Fechtner, R. D., & Weinreb, R. N. (1994) · Survey of Ophthalmology · doi:10.1016/s0039-6257(05)80042-6 · Cited by 433 · see citing works

Functions of the colour-opponent and broad-band channels of the visual system

Schiller, P. H., Logothetis, N. K., & Charles, E. R. (1990) · Nature · doi:10.1038/343068a0 · Cited by 417 · see citing works

Cytochrome oxidase patches: a new cytoarchitectonic feature of monkey visual cortex

Horton, J. C. (1984) · Philosophical transactions of the Royal Society of London. Series B, Biological sciences · doi:10.1098/rstb.1984.0021 · Cited by 407 · see citing works

Differential Calcium Binding Protein Immunoreactivity Distinguishes Classes of Relay Neurons in Monkey Thalamic Nuclei

Jones, E. G., & Hendry, S. H. C. (1989) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.1989.tb00791.x · Cited by 385 · see citing works

Evidence that the major postsynaptic density protein is a component of a Ca2+/calmodulin-dependent protein kinase.

Kelly, P., McGuinness, T. L., & Greengard, P. (1984) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.81.3.945 · Cited by 384 · see citing works

A third parallel visual pathway to primate area V1

Casagrande, V. A. (1994) · Trends in Neurosciences · doi:10.1016/0166-2236(94)90065-5 · Cited by 337 · see citing works

Anatomical Organization Of Macaque Monkey Striate Visual Cortex

Lund, J. S. (1988) · Annual Review of Neuroscience · doi:10.1146/annurev.ne.11.030188.001345 · Cited by 336 · see citing works

Evidence that Blue‐on Cells are Part of the Third Geniculocortical Pathway in Primates

Martin, P. R., White, A. J. R., Goodchild, A. K., Wilder, H. D., & Sefton, A. E. (1997) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.1997.tb01509.x · Cited by 328 · see citing works

Synapse-specific localization of NMDA and GABAA receptor subunits revealed by antigen-retrieval immunohistochemistry

Fritschy, J., Weinmann, O., Wenzel, A., & Benke, D. (1998) · The Journal of Comparative Neurology · doi:10.1002/(sici)1096-9861(19980112)390:2 · Cited by 321 · see citing works

Evidence that Alzheimer’s disease is a microvascular disorder: the role of constitutive nitric oxide

de la Torre, J. C., & Stefano, G. B. (2000) · Brain Research Reviews · doi:10.1016/s0165-0173(00)00043-6 · Cited by 307 · see citing works

Loss of Neurons in Magnocellular and Parvocellular Layers of the Lateral Geniculate Nucleus in Glaucoma

Yücel, Y. H. (2000) · Archives of Ophthalmology · doi:10.1001/archopht.118.3.378 · Cited by 305 · see citing works

A Neurochemically Distinct Third Channel in the Macaque Dorsal Lateral Geniculate Nucleus

Hendry, S. H. C., & Yoshioka, T. (1994) · Science · doi:10.1126/science.8160015 · Cited by 297 · see citing works

The Neuropathological and Behavioral Consequences of Intraspinal Microglial/Macrophage Activation

Popovich, P. G., Guan, Z., McGaughy, V. M., Fisher, L. C., Hickey, W. F., & Basso, D. M. (2002) · Journal of Neuropathology & Experimental Neurology · doi:10.1093/jnen/61.7.623 · Cited by 295 · see citing works

Experimental glaucoma in the rhesus monkey.

Gaasterland, D., & Kupfer, C. (1974) · PubMed · Cited by 269 · see citing works

Experimental glaucoma and cell size, density, and number in the primate lateral geniculate nucleus.

Weber, A. J., Chen, H., Hubbard, W. C., & Kaufman, P. L. P. (2000) · PubMed · Cited by 265 · see citing works

Progression of Early Glaucomatous Visual Field Loss as Detected by Blue-on-Yellow and Standard White-on-White Automated Perimetry

Johnson, C. A. (1993) · Archives of Ophthalmology · doi:10.1001/archopht.1993.01090050085035 · Cited by 233 · see citing works

Identification of the Major Postsynaptic Density Protein as Homologous with the Major Calmodulin‐Binding Subunit of a Calmodulin‐Dependent Protein Kinase

Goldenring, J. R., McGuire, J. S., & DeLorenzo, R. J. (1984) · Journal of Neurochemistry · doi:10.1111/j.1471-4159.1984.tb12713.x · Cited by 219 · see citing works

Atrophy of relay neurons in magno- and parvocellular layers in the lateral geniculate nucleus in experimental glaucoma.

Yücel, Y. H., Zhang, Q., Weinreb, R. N., Kaufman, P. L., & Gupta, N. (2001) · PubMed · Cited by 214 · see citing works

Visual function-specific perimetry for indirect comparison of different ganglion cell populations in glaucoma.

Sample, P. A., Bosworth, C. F., Blumenthal, E. Z., Girkin, C. A., & Weinreb, R. N. (2000) · PubMed · Cited by 206 · see citing works

Circuitry for color coding in the primate retina.

Dacey, D. M. (1996) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.93.2.582 · Cited by 204 · see citing works

Transneuronal cell degeneration in the lateral geniculate nucleus of the macaque monkey.

Matthews, M. R., Cowan, W. M., & Powell, T. P. S. (1960) · PubMed · Cited by 200 · see citing works

CaMKII regulates the density of central glutamatergic synapses in vivo

Rongo, C., & Kaplan, J. M. (1999) · Nature · doi:10.1038/46065 · Cited by 189 · see citing works

Lateral Geniculate Nucleus in Glaucoma

Chaturvedi, N., Hedley‐Whyte, E. T., & Dreyer, E. B. (1993) · American Journal of Ophthalmology · doi:10.1016/s0002-9394(14)71283-8 · Cited by 186 · see citing works

CHANGES IN SIZES OF CORTICAL AND LOWER MOTOR NEURONS IN AMYOTROPHIC LATERAL SCLEROSIS

Kiernan, J. A., & Hudson, A. J. (1991) · Brain · doi:10.1093/brain/114.2.843 · Cited by 186 · see citing works

The role of calcium–calmodulin kinase II in three forms of synaptic plasticity

Stevens, C. F., Tonegawa, S., & Wang, Y. (1994) · Current Biology · doi:10.1016/s0960-9822(00)00153-6 · Cited by 182 · see citing works

Short-wavelength Color Visual Fields in Glaucoma Suspects at Risk

Sample, P. A., Taylor, J. D. N., Martinez, G. A., Lusky, M., & Weinreb, R. N. (1993) · American Journal of Ophthalmology · doi:10.1016/s0002-9394(14)73928-5 · Cited by 171 · see citing works

Neuron atrophy during aging: programmed or sporadic?

Finch, C. E. (1993) · Trends in Neurosciences · doi:10.1016/0166-2236(93)90134-8 · Cited by 166 · see citing works

A comparison of koniocellular, magnocellular and parvocellular receptive field properties in the lateral geniculate nucleus of the owl monkey (Aotus trivirgatus)

Xu, X., Ichida, J. M., Allison, J. D., Boyd, J. D., Bonds, A. B., & Casagrande, V. A. (2001) · The Journal of Physiology · doi:10.1111/j.1469-7793.2001.0203j.x · Cited by 162 · see citing works

Functional mapping in the human brain using high magnetic fields

Uǧurbil, K., Hu, X. P., Chen, W., Zhu, X.-H., Kim, S., & Georgopoulos, A. P. (1999) · Philosophical Transactions of the Royal Society B Biological Sciences · doi:10.1098/rstb.1999.0474 · Cited by 153 · see citing works

On the neurons and synapses of the lateral geniculate nucleus of the monkey, and the effects of eye enucleation

Vay, S. L. (1971) · Cell and Tissue Research · doi:10.1007/bf00968547 · Cited by 131 · see citing works

Laminar organization of geniculocortical projections in Galago senegalensis and Aotus trivirgatus

DIAMOND, I. T., Conley, M., Itoh, K., & Fitzpatrick, D. (1985) · The Journal of Comparative Neurology · doi:10.1002/cne.902420408 · Cited by 118 · 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

Transneuronal Degeneration in the Spread of Alzheimer's Disease Pathology: Immunohistochemical Evidence for the Transmission of Tau Hyperphosphorylation

Su, J. H., Deng, G., & Cotman, C. W. (1997) · Neurobiology of Disease · doi:10.1006/nbdi.1997.0164 · Cited by 96 · see citing works

Comparison of Conventional and High-Pass Resolution Perimetry in a Prospective Study of Patients With Glaucoma and Healthy Controls

Chauhan, B. C. (1999) · Archives of Ophthalmology · doi:10.1001/archopht.117.1.24 · Cited by 96 · see citing works

Frequency Doubling Technology Perimetry Using a 24-2 Stimulus Presentation Pattern

Johnson, C. A., Cioffi, G. A., & Buskirk, E. M. V. (1999) · Optometry and Vision Science · doi:10.1002/j.1538-9235.1999.tb05474.x · Cited by 94 · see citing works

The distribution and morphology of LGN K pathway axons within the layers and CO blobs of owl monkey V1

Ding, Y., & Casagrande, V. A. (1997) · Visual Neuroscience · doi:10.1017/s0952523800012657 · Cited by 93 · see citing works

Distribution of calcium‐binding proteins within the parallel visual pathways of a primate (Galago crassicaudatus)

Johnson, J., & Casagrande, V. A. (1995) · The Journal of Comparative Neurology · doi:10.1002/cne.903560208 · Cited by 92 · see citing works

Glaucoma in primates: cytochrome oxidase reactivity in parvo- and magnocellular pathways.

Crawford, M. L. J., Harwerth, R. S., Smith, E. L., Shen, F., & Carter‐Dawson, L. D. (2000) · PubMed · Cited by 90 · see citing works

Parameters affecting the loss of ganglion cells of the retina following ablations of striate cortex in primates

Weller, R. E., & Kaas, J. H. (1989) · Visual Neuroscience · doi:10.1017/s0952523800005514 · Cited by 88 · see citing works

Quantitative studies of transneuronal atrophy in the dorsal lateral geniculate nucleus of cats and kittens

Guillery, R. W. (1973) · The Journal of Comparative Neurology · doi:10.1002/cne.901490403 · Cited by 86 · see citing works

Neuronal chemistry and functional organization in the primate visual system

Hendry, S. H. C., & Calkins, D. J. (1998) · Trends in Neurosciences · doi:10.1016/s0166-2236(98)01245-4 · Cited by 84 · see citing works

Short-wavelength automated perimetry: it's role in the clinic and for understanding ganglion cell function.

Sample, P. (2000) · Progress in retinal and eye research · doi:10.1016/s1350-9462(00)00001-x · Cited by 83 · see citing works

Laser-Induced Primate Glaucoma

Radius, R. L. (1984) · Archives of Ophthalmology · doi:10.1001/archopht.1984.01040031377031 · Cited by 83 · see citing works

Experimental glaucoma in primates: changes in cytochrome oxidase blobs in V1 cortex.

Crawford, M. L. J., Harwerth, R. S., Smith, E. L., Mills, S., & Ewing, B. (2001) · PubMed · Cited by 82 · see citing works

Organization of the primate circadian system.

Moore, R. Y. (1993) · PubMed · Cited by 81 · see citing works

Magnocellular and parvocellular visual pathways are both affected in a macaque monkey model of glaucoma

Vickers, J. C., Hof, P., Schumer, R., Wang, R.-F., Podos, S., & Morrison, J. (1997) · Australian and New Zealand Journal of Ophthalmology · doi:10.1111/j.1442-9071.1997.tb01400.x · Cited by 78 · see citing works

Transneuronal retrograde degeneration of retinal ganglion cells following restricted lesions of striate cortex in the monkey

Johnson, H. L., & Cowey, A. (2000) · Experimental Brain Research · doi:10.1007/s002210000384 · Cited by 77 · see citing works

FURTHER OBSERVATIONS ON TRANSNEURONAL DEGENERATION IN THE LATERAL GENICULATE NUCLEUS OF THE MACAQUE MONKEY.

Matthews, M. R. (1964) · PubMed · Cited by 64 · see citing works

Responses to chromatic and luminance contrast in glaucoma: a psychophysical and electrophysiological study

Porciatti, V., Bartolo, E. D., Nardi, M., & Fiorentini, A. (1997) · Vision Research · doi:10.1016/s0042-6989(97)00018-7 · Cited by 62 · see citing works

Anatomical pathways for color vision in the human retina

Kolb, H. (1991) · Visual Neuroscience · doi:10.1017/s0952523800010944 · Cited by 61 · see citing works

The interneuronal nature of GABAergic neurons in the lateral geniculate nucleus of the rhesus monkey: a combined HRP and GABA-immunocytochemical study

Montero, V. M. (1986) · Experimental Brain Research · doi:10.1007/bf00340502 · Cited by 59 · see citing works

Impaired visual function in glaucoma

Parisi, V. (2001) · Clinical Neurophysiology · doi:10.1016/s1388-2457(00)00525-3 · Cited by 53 · see citing works

Early Magnocellular Loss in Glaucoma Demonstrated Using the Pseudorandomly Stimulated Flash Visual Evoked Potential

Klistorner, A. I., & Graham, S. L. (1999) · Journal of Glaucoma · doi:10.1097/00061198-199904000-00010 · Cited by 52 · see citing works

The Glenn A. Fry Award Lecture: Early Losses of Visual Function in Glaucoma

Johnson, C. A. (1995) · Optometry and Vision Science · doi:10.1002/j.1538-9235.1995.tb03888.x · Cited by 50 · see citing works

Histomorphometric Analysis of Optic Nerve Changes in Experimental Glaucoma

cel, Y. H. Y., KALICHMAN, M. W., Mizisin, A. P., Powell, H. C., & Weinreb, R. N. (1999) · Journal of Glaucoma · doi:10.1097/00061198-199902000-00009 · Cited by 46 · see citing works

Monitoring glaucoma progression with visual evoked potentials of the blue-sensitive pathway.

Horn, F. K., Jonas, J. B., Budde, W. M., Jünemann, A., Mardin, C. Y., & Korth, M. J. (2002) · PubMed · Cited by 43 · see citing works

Retinal ganglion cell degeneration following loss of postsynaptic target neurons in the dorsal lateral geniculate nucleus of the adult cat

Pearson, H. E., & Stoffler, D. J. (1992) · Experimental Neurology · doi:10.1016/0014-4886(92)90164-l · Cited by 43 · see citing works

Atrophy and Degeneration of Ganglion Cells in Central Retina Following Loss of Postsynaptic Target Neurons in the Dorsal Lateral Geniculate Nucleus of the Adult Cat

Pearson, H. E., & Thompson, T. P. (1993) · Experimental Neurology · doi:10.1006/exnr.1993.1012 · Cited by 38 · see citing works

The effects of partial retinal lesions on activity and size of cells in the dorsal lateral geniculate nucleus

Eysel, U. T., & WOLFHARD, U. F. (1984) · The Journal of Comparative Neurology · doi:10.1002/cne.902290214 · Cited by 37 · see citing works

Glaucoma and the Brain

Gupta, N., & cel, Y. H. Y. (2001) · Journal of Glaucoma · doi:10.1097/00061198-200110001-00011 · Cited by 37 · see citing works

Detection of Visual Dysfunction in Optic Atrophy by Functional Magnetic Resonance Imaging During Monocular Visual Stimulation

Miki, A., Nakajima, T., Takagi, M., Shirakashi, M., & Abe, H. (1996) · American Journal of Ophthalmology · doi:10.1016/s0002-9394(14)72067-7 · Cited by 35 · see citing works

Contribution of the Superior Colliculus and the Mesencephalic Reticular Formation to Gaze Control

Waitzman, D. M., Pathmanathan, J. S., Presnell, R., Ayers, A. S., & DePalma-Bowles, S. (2002) · Annals of the New York Academy of Sciences · doi:10.1111/j.1749-6632.2002.tb02813.x · Cited by 32 · see citing works

Responses of retinal ganglion cells to eyeball deformation: A neurophysiological basis for “pressure phosphenes”

Grüsser, O. ‐., Grüsser‐Cornehls, U., Kusel, R., & Przybyszewski, A. W. (1989) · Vision Research · doi:10.1016/0042-6989(89)90123-5 · Cited by 32 · see citing works

Glial cell types, lineages, and response to injury in rat and fish: Implications for regeneration

Sivron, T., & Schwartz, M. (1995) · Glia · doi:10.1002/glia.440130302 · Cited by 32 · see citing works

Demonstration of ocular dominance columns in Nissl-stained sections of monkey visual cortex following enucleation

Haseltine, E. C., DeBruyn, E. J., & Casagrande, V. A. (1979) · Brain Research · doi:10.1016/0006-8993(79)90878-3 · Cited by 30 · see citing works

THE DISTRIBUTION OF CELL SIZE IN THE LATERAL GENICULATE NUCLEUS OF MAN FOLLOWING TRANSNEUUONAL CELL ATROPHY

KUOFER, C. (1965) · Journal of Neuropathology & Experimental Neurology · doi:10.1097/00005072-196510000-00008 · Cited by 28 · see citing works

Cortical Synaptic Arrangements of the Third Visual Pathway in Three Primate Species:Macaca mulatta, Saimiri sciureus, andAotus trivirgatus

Shostak, Y., Ding, Y., Mavity‐Hudson, J., & Casagrande, V. A. (2002) · Journal of Neuroscience · doi:10.1523/jneurosci.22-07-02885.2002 · Cited by 26 · see citing works

Macaque accessory optic system: I. Definition of the medial terminal nucleus

Cooper, H. M., Baleydier, C., & Magnin, M. (1990) · The Journal of Comparative Neurology · doi:10.1002/cne.903020215 · Cited by 23 · see citing works

Lateral Geniculate Nucleus in Glaucoma

Weinreb, R. N., Lindsey, J. D., & Sample, P. A. (1994) · American Journal of Ophthalmology · doi:10.1016/s0002-9394(14)72863-6 · Cited by 22 · see citing works

Properties of high‐pass resolution perimetry targets

Frisén, L., & Nikolajeff, F. K. (1993) · Acta Ophthalmologica · doi:10.1111/j.1755-3768.1993.tb07142.x · Cited by 22 · see citing works

The mystery of the visual system K pathway

Casagrande, V. A. (1999) · The Journal of Physiology · doi:10.1111/j.1469-7793.1999.0630s.x · Cited by 20 · see citing works

Functional Assessment of Glaucoma

Sample, P. A., & Johnson, C. A. (2001) · Journal of Glaucoma · doi:10.1097/00061198-200110001-00018 · Cited by 16 · see citing works

Employing following eye movements to discriminate normal from glaucoma subjects

Severt, W., Maddess, T., & Ibbotson, M. R. (2000) · Clinical and Experimental Ophthalmology · doi:10.1046/j.1442-9071.2000.00295.x · Cited by 9 · see citing works

Lateral Geniculate Nucleus in Glaucoma

Spaeth, G. L. (1995) · American Journal of Ophthalmology · doi:10.1016/s0002-9394(14)73831-0 · Cited by 5 · see citing works

Cortical consequences of elevated intraocular pressure in a primate model of glaucoma

Lam, D. Y. (2009) · cIRcle (University of British Columbia) · doi:10.14288/1.0090079 · Cited by 3 · see citing works

Primary open-angle glaucoma

Weinreb, R. N., & Khaw, P. T. (2004) · The Lancet · doi:10.1016/s0140-6736(04)16257-0 · Cited by 2,227 · see citing works

The optic nerve head as a biomechanical structure: a new paradigm for understanding the role of IOP-related stress and strain in the pathophysiology of glaucomatous optic nerve head damage

Burgoyne, C. F., Downs, J. C., Bellezza, A. J., Suh, J.-K. F., & Hart, R. T. (2004) · Progress in Retinal and Eye Research · doi:10.1016/j.preteyeres.2004.06.001 · Cited by 1,142 · see citing works

The molecular basis of retinal ganglion cell death in glaucoma

Almasieh, M., Wilson, A. M., Morquette, B., Vargas, J. L. C., & Polo, A. D. (2011) · Progress in Retinal and Eye Research · doi:10.1016/j.preteyeres.2011.11.002 · Cited by 974 · see citing works

Oxidative stress in glaucomatous neurodegeneration: Mechanisms and consequences

Tezel, G. (2006) · Progress in Retinal and Eye Research · doi:10.1016/j.preteyeres.2006.07.003 · Cited by 728 · see citing works

The role of microglia in retinal neurodegeneration: Alzheimer’s disease, parkinson, and glaucoma.

Ramirez, A. I., de Hoz, R., Salobrar-Garcia, E., Salazar, J. J., Rojas, B., Ajoy, D., López-Cuenca, I., Rojas, P., Triviño, A., & Ramírez, J. M. (2017) · Frontiers in Aging Neuroscience · doi:10.3389/fnagi.2017.00214 · Cited by 466 · see citing works

Human glaucoma and neural degeneration in intracranial optic nerve, lateral geniculate nucleus, and visual cortex

Gupta, N. (2006) · British Journal of Ophthalmology · doi:10.1136/bjo.2005.086769 · Cited by 434 · see citing works

Glaucoma as a neurodegenerative disease

Gupta, N., & Yücel, Y. H. (2007) · Current Opinion in Ophthalmology · doi:10.1097/icu.0b013e3280895aea · Cited by 423 · see citing works

A biomechanical paradigm for axonal insult within the optic nerve head in aging and glaucoma

Burgoyne, C. F. (2010) · Experimental Eye Research · doi:10.1016/j.exer.2010.09.005 · Cited by 393 · see citing works

Ophthalmic drug discovery: novel targets and mechanisms for retinal diseases and glaucoma

Zhang, K., Zhang, L., & Weinreb, R. N. (2012) · Nature Reviews Drug Discovery · doi:10.1038/nrd3745 · Cited by 316 · see citing works

Critical pathogenic events underlying progression of neurodegeneration in glaucoma

Calkins, D. J. (2012) · Progress in Retinal and Eye Research · doi:10.1016/j.preteyeres.2012.07.001 · Cited by 305 · see citing works

Mechanical Environment of the Optic Nerve Head in Glaucoma

Downs, J. C., Roberts, M. D., & Burgoyne, C. F. (2008) · Optometry and Vision Science · doi:10.1097/opx.0b013e31817841cb · Cited by 252 · see citing works

Atrophy of the lateral geniculate nucleus in human glaucoma detected by magnetic resonance imaging

Gupta, N., Greenberg, G., de Tilly, L. N., Gray, B., Polemidiotis, M., & Yucel, Y. H. (2008) · British Journal of Ophthalmology · doi:10.1136/bjo.2008.138172 · Cited by 218 · see citing works

Changes in cortical grey matter density associated with long-standing retinal visual field defects

Boucard, C. C., Hernowo, A. T., Maguire, R. P., Jansonius, N. M., Roerdink, J. B. T. M., Hooymans, J. M. M., & Cornelissen, F. W. (2009) · Brain · doi:10.1093/brain/awp119 · Cited by 214 · see citing works

Premise and Prediction???How Optic Nerve Head Biomechanics Underlies the Susceptibility and Clinical Behavior of the Aged Optic Nerve Head

Burgoyne, C. F., & Downs, J. C. (2008) · Journal of Glaucoma · doi:10.1097/ijg.0b013e31815a343b · Cited by 213 · see citing works

Risk assessment in the management of patients with ocular hypertension

Weinreb, R. N., Friedman, D. S., Fechtner, R. D., Cioffi, G. A., Coleman, A. L., Girkin, C. A., Liebmann, J. M., Singh, K., Wilson, M. R., Wilson, R., et al. (2004) · American Journal of Ophthalmology · doi:10.1016/j.ajo.2004.04.054 · Cited by 204 · see citing works

Diagnostic Tools for Glaucoma Detection and Management

Sharma, P., Sample, P. A., Zangwill, L. M., & Schuman, J. S. (2008) · Survey of Ophthalmology · doi:10.1016/j.survophthal.2008.08.003 · Cited by 199 · see citing works

Aging and ocular tissue stiffness in glaucoma

Liu, B., McNally, S., Kilpatrick, J. I., Jarvis, S., & O'Brien, C. J. (2017) · Survey of Ophthalmology · doi:10.1016/j.survophthal.2017.06.007 · Cited by 175 · see citing works

A Sick Eye in a Sick Body? Systemic Findings in Patients with Primary Open-angle Glaucoma

Pache, M., & Flammer, J. (2006) · Survey of Ophthalmology · doi:10.1016/j.survophthal.2006.02.008 · Cited by 172 · see citing works

Spectral domain optical coherence tomography for glaucoma (an AOS thesis).

Schuman, J. S. (2008) · PubMed Central · Cited by 168 · see citing works

Presence and Risk Factors for Glaucoma in Patients with Diabetes

Song, B. J., Aiello, L. P., & Pasquale, L. R. (2016) · Current Diabetes Reports · doi:10.1007/s11892-016-0815-6 · Cited by 164 · see citing works

Alzheimers Disease and Retinal Neurodegeneration

Guo, L., Duggan, J., & Cordeiro, M. F. (2010) · Current Alzheimer Research · doi:10.2174/156720510790274491 · Cited by 161 · see citing works

Oxidative Stress in Glaucoma: A Burden of Evidence

Kumar, D. M., & Agarwal, N. A. (2007) · Journal of Glaucoma · doi:10.1097/01.ijg.0000243480.67532.1b · Cited by 159 · see citing works

Update on the Pattern Electroretinogram in Glaucoma

Bach, M., & Hoffmann, M. B. (2008) · Optometry and Vision Science · doi:10.1097/opx.0b013e318177ebf3 · Cited by 153 · see citing works

The Novel Rho Kinase (ROCK) Inhibitor K-115: A New Candidate Drug for Neuroprotective Treatment in Glaucoma

Yamamoto, K. T., Maruyama, K., Himori, N., Omodaka, K., Yokoyama, Y., Shiga, Y., Morin, R., & Nakazawa, T. (2014) · Investigative Ophthalmology & Visual Science · doi:10.1167/iovs.13-13842 · Cited by 151 · see citing works

Gonadal Hormones and Retinal Disorders: A Review

Nuzzi, R., Scalabrin, S., Becco, A., & Panzica, G. (2018) · Frontiers in Endocrinology · doi:10.3389/fendo.2018.00066 · Cited by 151 · see citing works

Retinal changes in Alzheimer's disease— integrated prospects of imaging, functional and molecular advances

Gupta, V. B., Chitranshi, N., den Haan, J., Mirzaei, M., You, Y., Lim, J. K. H., Basavarajappa, D. K., Godinez, A., Angelantonio, S. D., Sachdev, P. S., et al. (2020) · Progress in Retinal and Eye Research · doi:10.1016/j.preteyeres.2020.100899 · Cited by 143 · see citing works

Light induced cytosolic drug delivery from liposomes with gold nanoparticles

Lajunen, T., Viitala, L., Kontturi, L.-S., Laaksonen, T., Liang, H., Vuorimaa, E., Viitala, T., Guével, X. L., Yliperttula, M. L., Murtomäki, L. S., et al. (2015) · Journal of Controlled Release · doi:10.1016/j.jconrel.2015.02.028 · Cited by 138 · see citing works

Retinal tau pathology in human glaucomas

Gupta, N., Fong, J., Ang, L. C., & Yücel, Y. H. (2008) · Canadian Journal of Ophthalmology · doi:10.3129/i07-185 · Cited by 134 · see citing works

Critical role of Nrf2 in oxidative stress‐induced retinal ganglion cell death

Himori, N., Yamamoto, K. T., Maruyama, K., Ryu, M., Taguchi, K., Yamamoto, M. P., & Nakazawa, T. (2013) · Journal of Neurochemistry · doi:10.1111/jnc.12325 · Cited by 132 · see citing works

Clinical Ability of Pattern Electroretinograms and Visual Evoked Potentials in Detecting Visual Dysfunction in Ocular Hypertension and Glaucoma

Parisi, V., Miglior, S., Manni, G., Centofanti, M., & Bucci, M. G. (2006) · Ophthalmology · doi:10.1016/j.ophtha.2005.10.044 · Cited by 132 · see citing works

Resting-state functional MRI: Functional connectivity analysis of the visual cortex in primary open-angle glaucoma patients

Dai, H., Morelli, J. N., Ai, F., Yin, D., Hu, C., Xu, D., & Li, Y. (2012) · Human Brain Mapping · doi:10.1002/hbm.22079 · Cited by 130 · see citing works

Retinotopic organization of primary visual cortex in glaucoma: Comparing fMRI measurements of cortical function with visual field loss

Duncan, R. O., Sample, P. A., Weinreb, R. N., Bowd, C., & Zangwill, L. M. (2006) · Progress in Retinal and Eye Research · doi:10.1016/j.preteyeres.2006.10.001 · Cited by 130 · see citing works

Glaucoma of the brain: a disease model for the study of transsynaptic neural degeneration

Yücel, Y. H., & Gupta, N. (2008) · Progress in brain research · doi:10.1016/s0079-6123(08)01132-1 · Cited by 129 · see citing works

Glaucoma and the brain: Trans-synaptic degeneration, structural change, and implications for neuroprotection

Lawlor, M., Danesh-Meyer, H. V., Levin, L. A., Davagnanam, I., Vita, E. D., & Plant, G. T. (2017) · Survey of Ophthalmology · doi:10.1016/j.survophthal.2017.09.010 · Cited by 123 · see citing works

Chronic ocular hypertension induces dendrite pathology in the lateral geniculate nucleus of the brain

Gupta, N., Ly, T., Zhang, Q., Kaufman, P. L., Weinreb, R. N., & Yücel, Y. H. (2007) · Experimental Eye Research · doi:10.1016/j.exer.2006.09.013 · Cited by 122 · see citing works

Deformation of the Normal Monkey Optic Nerve Head Connective Tissue after Acute IOP Elevation within 3-D Histomorphometric Reconstructions

Yang, H., Downs, J. C., Sigal, I. A., Roberts, M. D., Thompson, H. W., & Burgoyne, C. F. (2009) · Investigative Ophthalmology & Visual Science · doi:10.1167/iovs.09-3410 · Cited by 122 · see citing works

Voxel-Based Morphometry and Diffusion Tensor Imaging of the Optic Pathway in Primary Open-Angle Glaucoma: A Preliminary Study

Zikou, A. K., Kitsos, G., Tzarouchi, L. C., Astrakas, L. G., Alexiou, G. Α., & Argyropoulou, M. I. (2011) · American Journal of Neuroradiology · doi:10.3174/ajnr.a2714 · Cited by 118 · see citing works

Memantine Protects Neurons From Shrinkage in the Lateral Geniculate Nucleus in Experimental Glaucoma

Yücel, Y. H. (2006) · Archives of Ophthalmology · doi:10.1001/archopht.124.2.217 · Cited by 117 · see citing works

Identifying Glaucomatous Vision Loss with Visual-Function–Specific Perimetry in the Diagnostic Innovations in Glaucoma Study

Sample, P. A., Medeiros, F. A., Racette, L., Pascual, J. P., Boden, C., Zangwill, L. M., Bowd, C., & Weinreb, R. N. (2006) · Investigative Ophthalmology & Visual Science · doi:10.1167/iovs.05-1546 · Cited by 114 · see citing works

Transneuronal Retrograde Degeneration of the Retinal Ganglion Cells in Patients with Cerebral Infarction

Park, H.-Y. L., Park, Y. G., Cho, A.-H., & Park, C. K. (2013) · Ophthalmology · doi:10.1016/j.ophtha.2012.11.021 · Cited by 111 · see citing works

Effects of Coenzyme Q10 in Conjunction With Vitamin E on Retinal-evoked and Cortical-evoked Responses in Patients With Open-angle Glaucoma

Parisi, V., Centofanti, M., Gandolfi, S., Marangoni, D., Rossetti, L. M., Tanga, L., Tardini, M., Traina, S., Ungaro, N., Vetrugno, M., et al. (2012) · Journal of Glaucoma · doi:10.1097/ijg.0b013e318279b836 · Cited by 111 · see citing works

Neuroprotective agents in the management of glaucoma

Nucci, C., Martucci, A., Giannini, C., Morrone, L. A., Bagetta, G., & Mancino, R. (2018) · Eye · doi:10.1038/s41433-018-0050-2 · Cited by 111 · see citing works

Alzheimer’s Disease and Glaucoma: Mechanistic Similarities and Differences

Ghiso, J. A. (2013) · Journal of Glaucoma · doi:10.1097/ijg.0b013e3182934af6 · Cited by 107 · see citing works

The Pathogenesis of Glaucoma in the Interplay with the Immune System

Rieck, J. (2013) · Investigative Ophthalmology & Visual Science · doi:10.1167/iovs.12-9781 · Cited by 104 · see citing works

Retinal ganglion cell protection by 17‐β‐estradiol in a mouse model of inherited glaucoma

Zhou, X., Li, F., Ge, J., Sarkisian, S. R., Tomita, H., Zaharia, A., Chodosh, J., & Cao, W. (2007) · Developmental Neurobiology · doi:10.1002/dneu.20373 · Cited by 105 · see citing works

Detection of Optic Nerve Head Neural Canal Opening within Histomorphometric and Spectral Domain Optical Coherence Tomography Data Sets

Strouthidis, N. G., Yang, H., Fortune, B. A., Downs, J. C., & Burgoyne, C. F. (2009) · Investigative Ophthalmology & Visual Science · doi:10.1167/iovs.08-2302 · Cited by 103 · see citing works

Neuroinflammation in Primary Open-Angle Glaucoma

Vernazza, S., Tirendi, S., Bassi, A. M., Traverso, C. E., & Saccà, S. C. (2020) · Journal of Clinical Medicine · doi:10.3390/jcm9103172 · Cited by 104 · see citing works

Detection of early neuron degeneration and accompanying glial responses in the visual pathway in a rat model of acute intraocular hypertension

Zhang, S., Wang, H., Lu, Q., Qing, G., Wang, N., Wang, Y., Li, S., Yang, D., & Yan, F. (2009) · Brain Research · doi:10.1016/j.brainres.2009.09.029 · Cited by 99 · see citing works

Automated Morphometry of the Visual Pathway in Primary Open-Angle Glaucoma

Hernowo, A. T., Boucard, C. C., Jansonius, N. M., Hooymans, J. M. M., & Cornelissen, F. W. (2011) · Investigative Ophthalmology & Visual Science · doi:10.1167/iovs.10-5682 · Cited by 100 · see citing works

Selective magnetization transfer ratio decrease in the visual cortex following optic neuritis.

Audoin, B., Fernando, K., Swanton, J., Thompson, A., Plant, G., & Miller, D. H. (2006) · Brain : a journal of neurology · doi:10.1093/brain/awl039 · Cited by 103 · see citing works

Shared and Differential Retinal Responses against Optic Nerve Injury and Ocular Hypertension

Vidal‐Sanz, M., Galindo‐Romero, C., Valiente‐Soriano, F. J., Nadal-Nicolás, F. M., Ortín-Martínez, A., Rovere, G., Salinas‐Navarro, M., Lucas‐Ruiz, F., Sánchez-Migallón, M. C., Sobrado‐Calvo, P., et al. (2017) · Frontiers in Neuroscience · doi:10.3389/fnins.2017.00235 · Cited by 97 · see citing works

Age-related changes in the visual pathways: blame it on the axon

Calkins, D. J. (2013) · Investigative Opthalmology & Visual Science · doi:10.1167/iovs.13-12784 · Cited by 96 · see citing works

Optic neuropathies: characteristic features and mechanisms of retinal ganglion cell loss

You, Y., Gupta, V., Li, J. C., Klistorner, A. I., & Graham, S. L. (2013) · Reviews in the Neurosciences · doi:10.1515/revneuro-2013-0003 · Cited by 96 · see citing works

Animal Toxins as Therapeutic Tools to Treat Neurodegenerative Diseases

de Souza, J. M., Gonçalves, B. D. C., Gomez, M. V., Vieira, L. B., & Ribeiro, F. M. (2018) · Frontiers in Pharmacology · doi:10.3389/fphar.2018.00145 · Cited by 94 · see citing works

Treatment with citicoline eye drops enhances retinal function and neural conduction along the visual pathways in open angle glaucoma

Parisi, V., Centofanti, M., Ziccardi, L., Tanga, L., Michelessi, M., Roberti, G., & Manni, G. (2015) · Graefe s Archive for Clinical and Experimental Ophthalmology · doi:10.1007/s00417-015-3044-9 · Cited by 94 · see citing works

Evidence of the neuroprotective role of citicoline in glaucoma patients

Parisi, V., Coppola, G., Centofanti, M., Oddone, F., Angrisani, A. M., Ziccardi, L., Ricci, B., Quaranta, L., & Manni, G. (2008) · Progress in brain research · doi:10.1016/s0079-6123(08)01137-0 · Cited by 92 · see citing works

Retinal Structures and Visual Cortex Activity are Impaired Prior to Clinical Vision Loss in Glaucoma

Murphy, M. C., Conner, I. P., Teng, C. Y., Lawrence, J. D., Safiullah, Z. N., Wang, B., Bilonick, R. A., Kim, S., Wollstein, G., Schuman, J. S., et al. (2016) · Scientific Reports · doi:10.1038/srep31464 · Cited by 89 · see citing works

Neuroprotective effects of intravitreally transplanted adipose tissue and bone marrow–derived mesenchymal stem cells in an experimental ocular hypertension model

Emre, E., Yüksel, N., Duruksu, G., Pirhan, D., Subaşı, C., Erman, G., & Karaöz, E. (2015) · Cytotherapy · doi:10.1016/j.jcyt.2014.12.005 · Cited by 89 · see citing works

Evaluation of the retina and optic nerve in a rat model of chronic glaucoma using in vivo manganese-enhanced magnetic resonance imaging

Chan, K. C., Fu, Q., Hui, E. S. K., So, K., & Wu, E. X. (2008) · NeuroImage · doi:10.1016/j.neuroimage.2008.01.002 · Cited by 89 · see citing works

The Morphological Difference Between Glaucoma and Other Optic Neuropathies

Burgoyne, C. F. (2015) · Journal of Neuro-Ophthalmology · doi:10.1097/wno.0000000000000289 · Cited by 89 · see citing works

Pattern electroretinogram in glaucoma

Ventura, L. M., & Porciatti, V. (2006) · Current Opinion in Ophthalmology · doi:10.1097/01.icu.0000193082.44938.3c · Cited by 88 · see citing works

Electrophysiological Assessment of Glaucomatous Visual Dysfunction During Treatment with Cytidine-5′-diphosphocholine (citicoline): A Study of 8 years of Follow-up

Parisi, V. (2005) · Documenta Ophthalmologica · doi:10.1007/s10633-005-7348-7 · Cited by 87 · see citing works

Primate Glaucoma Models

Rasmussen, C. A., & Kaufman, P. L. (2005) · Journal of Glaucoma · doi:10.1097/01.ijg.0000169409.01635.bc · Cited by 87 · see citing works

Retinal ganglion cell repopulation for vision restoration in optic neuropathy: a roadmap from the RReSTORe Consortium

Soucy, J. R., Aguzzi, E. A., Cho, J. Y., Gilhooley, M. J., Keuthan, C. J., Luo, Z., Monavarfeshani, A., Saleem, M. A., Wang, X., Wohlschlegel, J., et al. (2023) · Molecular Neurodegeneration · doi:10.1186/s13024-023-00655-y · Cited by 82 · see citing works

Use of calcium channel blockers for glaucoma

Araie, M., & Mayama, C. (2010) · Progress in Retinal and Eye Research · doi:10.1016/j.preteyeres.2010.09.002 · Cited by 86 · see citing works

Reconnecting Eye to Brain

Crair, M. C., & Mason, C. A. (2016) · Journal of Neuroscience · doi:10.1523/jneurosci.1711-16.2016 · Cited by 86 · see citing works

The value of visual field testing in the era of advanced imaging: clinical and psychophysical perspectives

Phu, J., Khuu, S. K., Yapp, M., Assaad, N. N., Hennessy, M., & Kalloniatis, M. (2017) · Clinical and Experimental Optometry · doi:10.1111/cxo.12551 · Cited by 86 · see citing works

Neurodegeneration and Neuroprotection in Glaucoma.

Gauthier, A. C., & Liu, J. (2016) · Europe PMC (PubMed Central) · Cited by 85 · see citing works

Glaucoma as Neurodegeneration in the Brain

Chan, J. W., Chan, N. C. Y., & Sadun, A. A. (2021) · Eye and Brain · doi:10.2147/eb.s293765 · Cited by 91 · see citing works

The Outflow Pathway: A Tissue With Morphological and Functional Unity

Saccà, S. C., Gandolfi, S., Bagnis, A., Manni, G., Damonte, G., Traverso, C. E., & Izzotti, A. (2016) · Journal of Cellular Physiology · doi:10.1002/jcp.25305 · Cited by 83 · see citing works

Functional MRI Signal Changes in Primary Visual Cortex Corresponding to the Central Normal Visual Field of Patients with Primary Open-Angle Glaucoma

Qing, G., Zhang, S., Wang, B., & Wang, N. (2010) · Investigative Ophthalmology & Visual Science · doi:10.1167/iovs.09-4834 · Cited by 80 · see citing works

Progressive Degeneration of Retinal and Superior Collicular Functions in Mice With Sustained Ocular Hypertension

Chen, H., Zhao, Y., Liu, M., Feng, L., Puyang, Z., Yi, J., Liang, P., Zhang, H. F., Cang, J., Troy, J. B., et al. (2015) · Investigative Ophthalmology & Visual Science · doi:10.1167/iovs.14-15691 · Cited by 80 · see citing works

Drug delivery devices for retinal diseases

Kaji, H., Nagai, N., Nishizawa, M., & Abe, T. (2017) · Advanced Drug Delivery Reviews · doi:10.1016/j.addr.2017.07.002 · Cited by 81 · see citing works

Variability of serum oxidative stress biomarkers relative to biochemical data and clinical parameters of glaucoma patients.

Engin, K. N., Yemisci, B., Yiğit, U., Ağaçhan, A., & Coşkun, C. (2010) · PubMed Central · Cited by 79 · see citing works

Is Estrogen a Therapeutic Target for Glaucoma?

Dewundara, S., Wiggs, J. L., Sullivan, D. A., & Pasquale, L. R. (2016) · Seminars in Ophthalmology · doi:10.3109/08820538.2015.1114845 · Cited by 79 · see citing works

What Changes Can We Expect in the Brain of Glaucoma Patients?

Gupta, N., & Yücel, Y. H. (2007) · Survey of Ophthalmology · doi:10.1016/j.survophthal.2007.08.006 · Cited by 78 · see citing works

Retinal Ganglion Cell Functional Plasticity and Optic Neuropathy

Porciatti, V., & Ventura, L. M. (2012) · Journal of Neuro-Ophthalmology · doi:10.1097/wno.0b013e3182745600 · Cited by 76 · see citing works

Riluzole- and Resveratrol-Induced Delay of Retinal Ganglion Cell Death in an Experimental Model of Glaucoma

Pirhan, D., Yüksel, N., Emre, E., Cengiz, A., & Yıldız, D. K. (2015) · Current Eye Research · doi:10.3109/02713683.2015.1004719 · Cited by 76 · see citing works

Brain involvement in glaucoma: advanced neuroimaging for understanding and monitoring a new target for therapy

Nucci, C., Martucci, A., Cesareo, M., Mancino, R., Russo, R., Bagetta, G., Cerulli, L., & Garaci, F. G. (2012) · Current Opinion in Pharmacology · doi:10.1016/j.coph.2012.08.004 · Cited by 75 · see citing works

The connective tissue phenotype of glaucomatous cupping in the monkey eye - Clinical and research implications

Yang, H., Reynaud, J. F., Lockwood, H., Williams, G. A., Hardin, C., Reyes, L., Stowell, C., Gardiner, S. K., & Burgoyne, C. F. (2017) · Progress in Retinal and Eye Research · doi:10.1016/j.preteyeres.2017.03.001 · Cited by 74 · see citing works

Morphological changes in the visual pathway induced by experimental glaucoma in Japanese monkeys

Ito, Y., Shimazawa, M., Chen, Y., Tsuruma, K., Yamashima, T., Araie, M., & Hara, H. (2009) · Experimental Eye Research · doi:10.1016/j.exer.2009.03.013 · Cited by 74 · see citing works

Diffusion tensor magnetic resonance imaging reveals visual pathway damage that correlates with clinical severity in glaucoma

Chen, Z., Lin, F., Wang, J., Li, Z., Dai, H., Mu, K., Ge, J., & Zhang, H. (2012) · Clinical and Experimental Ophthalmology · doi:10.1111/j.1442-9071.2012.02832.x · Cited by 74 · see citing works

Psychophysical Measurement of Neural Adaptation Abnormalities in Magnocellular and Parvocellular Pathways in Glaucoma

McKendrick, A. M., Badcock, D. R., & Morgan, W. H. (2004) · Investigative Ophthalmology & Visual Science · doi:10.1167/iovs.03-1225 · Cited by 74 · see citing works

Interconnection Between Brain and Retinal Neurodegenerations

Jindal, V. (2014) · Molecular Neurobiology · doi:10.1007/s12035-014-8733-6 · Cited by 74 · see citing works

Assessment of Lateral Geniculate Nucleus Atrophy with 3T MR Imaging and Correlation with Clinical Stage of Glaucoma

Dai, H., Mu, K., Qi, J., Wang, C. Y., Zhu, W., Xia, L. M., Chen, Z. Q., Zhang, H., Ai, F., & Morelli, J. N. (2011) · American Journal of Neuroradiology · doi:10.3174/ajnr.a2486 · Cited by 73 · see citing works

Evidence for Widespread Structural Brain Changes in Glaucoma: A Preliminary Voxel-Based MRI Study

Williams, A. L., Lackey, J., Wizov, S. S., Chia, T. M. T., Gatla, S., Moster, M. L., Sergott, R. C., Spaeth, G. L., & Lai, S. (2013) · Investigative Ophthalmology & Visual Science · doi:10.1167/iovs.13-11776 · Cited by 72 · see citing works

Estrogen has a neuroprotective effect on axotomized RGCs through ERK signal transduction pathway

Nakazawa, T., Takahashi, H., & Shimura, M. (2006) · Brain Research · doi:10.1016/j.brainres.2006.03.084 · Cited by 71 · see citing works

Molecular complexity of primary open angle glaucoma: current concepts

Ray, K., & Mookherjee, S. (2009) · Journal of Genetics · doi:10.1007/s12041-009-0065-3 · Cited by 70 · see citing works

Reduced Cortical Thickness in Primary Open-Angle Glaucoma and Its Relationship to the Retinal Nerve Fiber Layer Thickness

Yu, L., Xie, B., Yin, X., Liang, M., Evans, A. C., Wang, J., & Dai, C. (2013) · PLoS ONE · doi:10.1371/journal.pone.0073208 · Cited by 70 · see citing works

Ischemia Results 3 Months Later in Altered ERG, Degeneration of Inner Layers, and Deafferented Tectum: Neuroprotection with Brimonidine

Mayor-Torroglosa, S., de la Villa, P., Rodrı́guez, M. E., Lafuente, M. P., Avilés‐Trigueros, M., ́s, A. G. ́.-A., de Imperial, J. M., ́rez, M. ́. P. V.-P., & Vidal‐Sanz, M. (2005) · Investigative Ophthalmology & Visual Science · doi:10.1167/iovs.05-0392 · Cited by 68 · see citing works

Retinal neurodegeneration in experimental glaucoma

Vidal‐Sanz, M., Valiente‐Soriano, F. J., Ortín-Martínez, A., Nadal-Nicolás, F. M., Jiménez-López, M., Salinas‐Navarro, M., Alarcón-Martínez, L., García‐Ayuso, D., Avilés‐Trigueros, M., Agudo‐Barriuso, M., et al. (2015) · Progress in brain research · doi:10.1016/bs.pbr.2015.04.008 · Cited by 68 · see citing works

Proton magnetic resonance spectroscopy revealed choline reduction in the visual cortex in an experimental model of chronic glaucoma

Chan, K. C., So, K., & Wu, E. X. (2008) · Experimental Eye Research · doi:10.1016/j.exer.2008.10.002 · Cited by 66 · see citing works

Ocular Drug Delivery for Glaucoma Management

Gooch, N., Molokhia, S. A., Condie, R. M., Burr, R. M., Archer, B. J., Ambati, B. K., & Wirostko, B. M. (2012) · Pharmaceutics · doi:10.3390/pharmaceutics4010197 · Cited by 66 · see citing works

Sex Hormones and Optic Nerve Disorders: A Review

Nuzzi, R., Scalabrin, S., Becco, A., & Panzica, G. (2019) · Frontiers in Neuroscience · doi:10.3389/fnins.2019.00057 · Cited by 66 · see citing works

Simultaneous Comparison of Relative Damage to Chromatic Pathways in Ocular Hypertension and Glaucoma: Correlation with Clinical Measures

Castelo-Branco, M. S., Faria, P., Forjaz, V., Kozák, L. R., & Azevedo, H. (2004) · Investigative Ophthalmology & Visual Science · doi:10.1167/iovs.03-0815 · Cited by 65 · see citing works

Retinotopic Organization of Primary Visual Cortex in Glaucoma: A Method for Comparing Cortical Function with Damage to the Optic Disk

Duncan, R. O., Sample, P. A., Weinreb, R. N., Bowd, C., & Zangwill, L. M. (2007) · Investigative Ophthalmology & Visual Science · doi:10.1167/iovs.06-0773 · Cited by 63 · see citing works

Selective reduction of fMRI responses to transient achromatic stimuli in the magnocellular layers of the LGN and the superficial layer of the SC of early glaucoma patients

Zhang, P., Wen, W., Sun, X., & He, S. (2015) · Human Brain Mapping · doi:10.1002/hbm.23049 · Cited by 63 · see citing works

Strategies to improve early diagnosis in glaucoma

Tatham, A. J., Medeiros, F. A., Zangwill, L. M., & Weinreb, R. N. (2015) · Progress in brain research · doi:10.1016/bs.pbr.2015.03.001 · Cited by 63 · see citing works

Brain‐Derived Neurotrophic Factor as a Biomarker in Primary Open‐Angle Glaucoma

Ghaffariyeh, A., Honarpisheh, N., Heidari, M. H., Puyan, S., & Abasov, F. (2010) · Optometry and Vision Science · doi:10.1097/opx.0b013e3181fc329f · Cited by 61 · see citing works

Wallerian and trans-synaptic degeneration contribute to optic radiation damage in multiple sclerosis: a diffusion tensor MRI study

Rocca, M. A., Mesaroš, Š., Preziosa, P., Pagani, E., Stošić-Opinćal, T., Dujmović, I., Drulovic, J. S., & Filippi, M. (2013) · Multiple Sclerosis Journal · doi:10.1177/1352458513485146 · Cited by 60 · see citing works

Brain Changes in Glaucoma

Gupta, N., & Yücel, Y. H. (2003) · European Journal of Ophthalmology · doi:10.1177/112067210301303s06 · Cited by 89 · see citing works

Central Nervous System Changes in Glaucoma

Yücel, Y. H. (2013) · Journal of Glaucoma · doi:10.1097/ijg.0b013e3182934a55 · Cited by 23 · see citing works

Loss of Neurons in Magnocellular and Parvocellular Layers of the Lateral Geniculate Nucleus in Glaucoma

Yücel, Y. H. (2000) · Archives of Ophthalmology · doi:10.1001/archopht.118.3.378 · Cited by 305 · see citing works

Impact de la pathologie glaucomateuse sur les voies visuelles centrales et les structures circadiennes

Chiquet, C., Drouyer, E., WoldeMussie, E., Ruíz, G., Wheeler, L. A., Denis, P., Cooper, H. M., & Romanet, J. P. (2006) · Journal Français d Ophtalmologie · doi:10.1016/s0181-5512(06)73858-x · Cited by 8 · see citing works

Lateral Geniculate Nucleus in Glaucoma

Chaturvedi, N., Hedley‐Whyte, E. T., & Dreyer, E. B. (1993) · American Journal of Ophthalmology · doi:10.1016/s0002-9394(14)71283-8 · Cited by 186 · see citing works