Cited by 384Glaucoma and retinal disordersVisual perception and processing mechanismsDrug-Induced Ocular Toxicity

The DOI matches its Crossref record; 89 of the 90 references it cites were found in a registry or an index.

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

Yücel, Y·2003·Progress in Retinal and Eye Research

Open this paper in CoChat — free account

Abstract

Glaucoma is a leading cause of world blindness, and retinal ganglion cell death is its pathological hallmark. There is accumulating evidence that glaucomatous damage extends from retinal ganglion cells to vision centers in the brain. In an experimental primate model of unilateral glaucoma, degenerative changes are observed in magnocellular, parvocellular, and koniocellular pathways in the lateral geniculate nucleus, and these changes are presented in relation to intraocular pressure and the severity of optic nerve damage. Neuropathological findings are also present in lateral geniculate nucleus layers driven by the unaffected fellow eye. Finally, there is information on changes in the visual cortex in relation to varying degrees of retinal ganglion cell loss. The implications of these findings for refining concepts regarding the pathobiology of progression, and the detection and treatment of glaucoma, are discussed.

Integrity signals

Registry

Crossref · 10.1016/s1350-9462(03)00026-0

Cites

89 of 89 references verified0 citation errors · 0 not checkable

Statistics

Recomputing p-values needs the paper’s full text.

Claims the paper makes

This paper’s full text isn’t openly available, so its claims and self-check weren’t run. The registry and citation checks still apply.

Claims other papers make about this one

Each is checked against this paper’s own text: does it say what the citing paper says it does?

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
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
Optic Nerve Damage in Human Glaucoma
Quigley, H. A. (1982) · Archives of Ophthalmology · doi:10.1001/archopht.1982.01030030137016 · Cited by 1,177
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 820
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
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
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 614
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
Contemporary Research Methods in Neuroanatomy
(1970) · Springer eBooks · doi:10.1007/978-3-642-85986-1 · Cited by 587
CaMKII regulates the frequency-response function of hippocampal synapses for the production of both LTD and LTP.
Mayford, M., Wang, J., Kandel, E., & O'Dell, T. (1995) · Cell · doi:10.1016/0092-8674(95)90009-8 · Cited by 552

Show all 90 references

Sorted by citations

Items 301–378 of 378

High-fat Western diet induces retinal and metabolic alterations in APOE3 and APOE4 knock-in mice
Abhyankar, S. D., Luo, Q., Hartman, G. D., Mahajan, N. S., Corson, T. W., Oblak, A. L., Lamb, B. T., & Bhatwadekar, A. D. (2026) · Scientific Reports · doi:10.1038/s41598-025-34776-9 · Cited by 3
Unlocking the potential of histone deacetylase inhibitors in combatting age-related retinal degenerative diseases
Liu, B., Wang, M., Pu, N., Wang, J., Fan, W., Qu, C., Wu, H., Song, Z., & Tao, Y. (2025) · Ageing Research Reviews · doi:10.1016/j.arr.2025.102788 · Cited by 3
Imaging the visual system: from the eye to the brain
Thompson, B. S., Read, S. A., Dumoulin, S. O., Elsner, A. E., Porter, J., & Roorda, A. (2016) · Ophthalmic and Physiological Optics · doi:10.1111/opo.12298 · Cited by 4
Beeinträchtigung der Sehbahn bei Glaukomen
Schmidt, M. A., Engelhorn, T., Dörfler, A., & Michelson, G. (2019) · Klinische Monatsblätter für Augenheilkunde · doi:10.1055/a-0762-0822 · Cited by 3
Impact of cerebral hypoperfusion–reperfusion on optic nerve integrity and visual function in the DBA/2J mouse model of glaucoma
Fraenkl, S. A., Simon, Q., Yücel, Y. H., Gupta, N., Wittwer, V. V., Frueh, B. E., & Tschanz, S. A. (2022) · BMJ Open Ophthalmology · doi:10.1136/bmjophth-2022-001078 · Cited by 3
Self-citation
Glaucoma Drainage Devices
Cullen, C. L. (2007) · Humana Press eBooks · doi:10.1007/978-1-59745-449-0_12 · Cited by 3
Clinical Cupping: Laminar and Prelaminar Components
Burgoyne, C. F., Yang, H., & Downs, J. C. (2010) · Springer eBooks · doi:10.1007/978-0-387-76700-0_16 · Cited by 3
Cluster Analysis of Glaucoma Patients Using the Retinal Nerve Fiber Layer Thickness of the Optic Nerve and DTI Parameters of the Optic Radiation
Michelson, G., Wärntges, S., & Engelhorn, T. (2012) · Journal of Clinical & Experimental Ophthalmology · doi:10.4172/2155-9570.s4-001 · Cited by 3
Color Reflectivity Discretization Analysis of OCT Images in the Detection of Glaucomatous Nerve Fiber Layer Defects
Shah, S. B., García, A., Leiby, B. E., Cox, L., Katz, L. J., & Myers, J. S. (2016) · Journal of Glaucoma · doi:10.1097/ijg.0000000000000363 · Cited by 3
Magnetization transfer imaging reveals geniculocalcarine and striate area degeneration in primary glaucoma: a preliminary study
Zhang, Y., Liang, W., Wu, G., Zhang, X., & Wen, G. (2016) · Acta Radiologica Open · doi:10.1177/2058460116666876 · Cited by 3
Electrophysiological evaluation in normal-tension glaucoma suspects: a pilot study
Messenio, D., Marano, G., & Biganzoli, E. M. (2017) · Modeling and Artificial Intelligence in Ophthalmology · doi:10.35119/maio.v1i3.33 · Cited by 3
Caffeine abrogates oxidative stress imbalance: Its implication on lateral geniculate nucleus and visual cortex following hyaluronic acid exposure
Adekeye, A. O., Fafure, A. A., Jeje-Pius, S. T., Asuquo, D. O., Sanya, J. O., & Ogundipe, L. O. (2021) · Journal of Chemical Neuroanatomy · doi:10.1016/j.jchemneu.2021.101996 · Cited by 3
Visual cortex damage in a ferret model of ocular hypertension
Fujishiro, T., Honjo, M., Kawasaki, H., & Aihara, M. (2022) · Japanese Journal of Ophthalmology · doi:10.1007/s10384-022-00901-8 · Cited by 3
Optic Nerve: The Glaucomatous Optic Nerve
Burgoyne, C. F. (2009) · Springer eBooks · doi:10.1007/978-3-540-68240-0_1 · Cited by 3
New magnetic resonance imaging techniques identify cortical changes in glaucoma
Graham, S. L., & Klistorner, A. I. (2013) · Clinical and Experimental Ophthalmology · doi:10.1111/ceo.12043 · Cited by 3
Neuro-imaging of visual field defects
Boucard, C. C. (2006) · University of Groningen research database (University of Groningen / Centre for Information Technology) · Cited by 3
Functional Magnetic Resonance Imaging (fMRI) of the Visual Cortex with Wide-View Retinotopic Stimulation
Galenchik-Chan, A., Chernoff, D., Zhou, W., Duong, T. Q., & Muir, E. R. (2023) · Journal of Visualized Experiments · doi:10.3791/65597 · Cited by 2
Glaucoma‐inducing retinal ganglion cell degeneration alters diurnal rhythm of key molecular components of the central clock and locomotor activity in mice
Barsanele, P. S., de Assis, L. V. M., da Silva, J. E., Furtado, E. M. D. O., Fernandes, P., Cipolla‐Neto, J., Poletini, M. O., & Moraes, M. N. (2024) · The FASEB Journal · doi:10.1096/fj.202401105r · Cited by 2
Anterograde degeneration along the visual pathway following optic nerve injury: a review
Chapelle, A.-C. (2025) · Frontiers in Neurology · doi:10.3389/fneur.2025.1623798 · Cited by 1
Brain Activations in fMRI induced by Color Stimulation in Patients with Normotensive Glaucoma
Lešták, J. (2012) · Journal of Clinical & Experimental Ophthalmology · doi:10.4172/2155-9570.1000250 · Cited by 2
Management of Normal-Tension Glaucoma
Araie, M. (2014) · Elsevier eBooks · doi:10.1016/b978-0-7020-5193-7.00043-1 · Cited by 2
Increased resistance to oxidative DNA damage of trabecular meshwork cells byE. coli FPGgene transfection
Foresta, M., Fròsina, G., Saccà, S. C., Cartiglia, C., Longobardi, M. G., & Izzotti, A. (2011) · Free Radical Research · doi:10.3109/10715762.2011.579122 · Cited by 2
Central nervous system changes in glaucoma
Yücel, Y. H., & Gupta, N. (2010) · Elsevier eBooks · doi:10.1016/b978-0-7020-2983-7.00026-7 · Cited by 2
Self-citation
Amlodipine Attenuates Carrageenan-induced Oxidative Stress Targeting Transsynaptic Neuronal Damage by Promoting Survival of Retinal Ganglion Cells in Adult Zebrafish ( Danio rerio)
Nanda, A., Aparna, S., Sahoo, R. N., & Patri, M. (2024) · Annals of Neurosciences · doi:10.1177/09727531241246671 · Cited by 2
RECENT DEVELOPMENTS IN AUTOMATED PERIMETRY
Ghoncheh, M., Beygi, M. H. M., Nilforoushan, N., & Sepehr, R. (2008) · مجله چشم‌پزشکی بینا · Cited by 2
Relationship between Binocular Visual Function and Quality of Life in Bilateral Normal Tension Glaucoma Patients
Park, H. H., & Chun, Y. S. (2017) · Journal of the Korean Ophthalmological Society · doi:10.3341/jkos.2017.58.2.171 · Cited by 2
Optic Neuropathy and Ganglion Cell Degeneration in Glaucoma
Chen, D. F., & Cho, K. (2008) · Humana Press eBooks · doi:10.1007/978-1-59745-373-8_22 · Cited by 2
Independent patterns of damage within magno-, parvo- and koniocellular pathways in Parkinson's disease (Silva MF et al. Brain 2005; 128: 2260-2271)
Gaynes, B. I. (2006) · Brain · doi:10.1093/brain/awl292 · Cited by 2
Extraction of three-dimensional shapes in glaucoma patients in response to monocular depth cues
Sawamura, H., Asaoka, R., Murata, H., Ando, E., & Gillebert, C. R. (2024) · Japanese Journal of Ophthalmology · doi:10.1007/s10384-024-01054-6 · Cited by 1
The Relationship Between MRI-Measured Structure of the Visual Cortex and Visual Function in Patients With Glaucoma
Yamada, A., Tatewaki, Y., Omodaka, K., Matsudaira, I. Y., Taki, Y., & Nakazawa, T. (2025) · Journal of Glaucoma · doi:10.1097/ijg.0000000000002614 · Cited by 1
Optic Nerve Head Spatial Transcriptomic Change in Nonhuman Primate Early Experimental Glaucoma
Williams, G. A., Lee, J., Zangirolani, G. M., Reynaud, J. F., Yang, H., Marsh‐Armstrong, N., Burgoyne, C. F., & Chaudhary, P. (2026) · Investigative Ophthalmology & Visual Science · doi:10.1167/iovs.67.3.22 · Cited by 1
Differential diagnosis of optic neuropathy in patients with CNS diseases and normal tension glaucoma
Serova, N. (2019) · Ophthalmology Reports · doi:10.17816/ov2019173-76 · Cited by 1
Benefits of Explorative Saccade Training in Patients with Advanced Glaucomatous Visual Field Defects—A Randomized, Placebo-Controlled Study
Ferrand, N., Trauzettel‐Klosinski, S., Blumenstock, G., Voykov, B., & Kuester-Gruber, S. (2025) · Journal of Clinical Medicine · doi:10.3390/jcm14092876 · Cited by 1
Differential Impact of Retinal Lesions on Visual Responses of LGN X and Y Cells
Yang, J., Huxlin, K. R., & Briggs, F. (2025) · Journal of Neuroscience · doi:10.1523/jneurosci.0436-25.2025 · Cited by 1
Adaptive Changes in the Retina and Central Visual Areas in Glaucoma
Sansar, C., Li, J., & Vecino, E. (2011) · InTech eBooks · doi:10.5772/19787 · Cited by 1
A New Approach to Assess Early Progressive Loss Across Multiple Visual Channels In the Natural History of Glaucoma
Mateus, C., Raimundo, M., Oliveiros, B., Faria, P., Reis, A., & Castelo-Branco, M. S. (2015) · Journal of Glaucoma · doi:10.1097/ijg.0000000000000226 · Cited by 1
Changes in brain glucose metabolism following traumatic optic neuropathy in rats
Kim, K., Choi, H.-Y., Pak, K., & Jeon, H. (2020) · All Life · doi:10.1080/26895293.2020.1861110 · Cited by 1
Glaucoma as a Neurodegenerative Disease
Chan, N. C. Y., & Chan, J. W. (2021) · Advances in Ophthalmology and Optometry · doi:10.1016/j.yaoo.2021.05.003 · Cited by 1
Modifying treatment of degenerative retinal diseases. Part 2. Conditioning therapy techniques and the problem of maximizing retinal plasticity
Neroeva, N. V., Зуева, М. В., Катаргина, Л. А., Kotelin, V. I., Zhuravleva, A. N., Цапенко, И. В., & Fadeev, D. V. (2023) · Russian Ophthalmological Journal · doi:10.21516/2072-0076-2023-16-3-165-172 · Cited by 1
Factors in the development of refractory primary open-angle glaucoma (part 2)
Евгеньевич, Ф. Н., & Kuroyedov, А. V. (2023) · National Journal glaucoma · doi:10.53432/2078-4104-2023-22-4-68-79 · Cited by 1
Transorbital Alternating Current Stimulation in Glaucoma: State of the Art from Neurophysiological Bases to Clinical Practice
Granata, G., Delicati, S., & Falsini, B. (2024) · Optics · doi:10.3390/opt5030026 · Cited by 1
Amlodipine protects the retinal ganglionic cell damage maintaining intra ocular pressure by regulating the biological activities of carrageenan like red algae: an in vivo and in-silico study
Nanda, A., Choudhary, N., & Patri, M. (2025) · In Silico Pharmacology · doi:10.1007/s40203-025-00381-x · Cited by 1
Glaucoma: Mechanisms of Neurodegeneration
Wareham, L. K., Cooper, M., & Calkins, D. J. (2020) · Elsevier eBooks · doi:10.1016/b978-0-12-809324-5.24202-8 · Cited by 1
Optic Nerve: The Glaucomatous Optic Nerve
Burgoyne, C. F. (2016) · Springer eBooks · doi:10.1007/978-3-662-49042-6_1 · Cited by 1
Biomechanics of the Optic Nerve
Liu, T., Sheng, J., Fan, Y., & Wang, X. (2022) · Springer eBooks · doi:10.1007/978-981-16-4269-2_5 · Cited by 1
Desenvolvimento da sensibilidade ao contraste de luminância espacial e temporal
Moreira, S. M. C. F. (2010) · doi:10.11606/d.47.2010.tde-21102010-110538 · Cited by 1
Reply to "Letter to the Editor: Independent patterns of damage within magno-, parvo- and koniocellular pathways in Parkinson's disease (Silva MF et al. Brain 2005; 128: 2260-2271)." Concomitant impairment of multiple visual pathways in Parkinson's disease
Castelo-Branco, M. S., Silva, M. F., Januário, C., & Freire, A. (2006) · Brain · doi:10.1093/brain/awl293 · Cited by 1
J.E. Dowling, & J.D. Dowling (2016). Vision—How It Works and What can Go Wrong
Bach, M. (2017) · Perception · doi:10.1177/0301006617706280 · Cited by 1
Effects of short-term IOP elevation on receptive field properties of cat LGN cells
Tao, L. (2004) · Chinese Science Bulletin · doi:10.1360/04wc0070 · Cited by 1
Valor preditivo da topografia de disco óptico para o desenvolvimento de glaucoma
de Alencar, L. P. M. (2011) · doi:10.11606/t.5.2011.tde-07102011-114405
Temporal processing in auditory and visual systems: evidence of wider central nervous system involvement in glaucoma
O’Hare, F. (2011) · Minerva Access (University of Melbourne)
How much is the brain involved in glaucoma?
Alm, A. (2006) · British Journal of Ophthalmology · doi:10.1136/bjo.2006.090167
Glokom ve Oküler Hipertansiyon Hastalarında Humphrey Matriks Perimetrisi ve Standart Otomatik Perimetrinin SITA Stratejisi ile Elde Edilen Görme Alanı Sonuçlarının Karşılaştırılması
Yılmaz, P. T., Bozkurt, B., & Irkec, M. T. (2011) · Turkish Journal of Ophthalmology · doi:10.4274/tjo.41.20
WHAT IS GLAUCOMA: CLINICALLY, FUNCTIONALLY, PATHOLOGICALLY?
Questions, C., Rasmussen, C. A., & Kaufman, P. L. (2015)
Long Term Transneuronal Retrograde Degeneration of the Retinal Ganglion Cells in Patients with Cerebral Infarction
YILDIZ, A. A., Yıldız, A. M., Acar, Z., Güven, D., Olgun, A., & Şendül, S. Y. (2016) · Turkiye Klinikleri Journal of Ophthalmology · doi:10.5336/ophthal.2015-47455
Opportunities for the Development of Newer Drugs for Ocular Use
Bhardwaj, R. (2016) · Springer eBooks · doi:10.1007/978-3-319-25498-2_2
Analysis of Ganglion Cell Complex in Various Stages of Primary Open Angle Glaucoma
Singh, L. J., Bundela, R., Rathore, S. S., Ahmad, L., & Bb, L. (2016) · International Journal of Medical Research Professionals · doi:10.21276/ijmrp.2016.2.3.022
Stem Cells
Johnson, T. V., & Martin, K. R. G. (2014) · Elsevier eBooks · doi:10.1016/b978-0-7020-5193-7.00063-7
Primary Open-Angle Glaucoma, Trans-Lamina Cribrosa Pressure Difference, and Central Nerve System
Fan, N., Liu, G., Zhang, X., & Liu, X. (2019) · Advances in visual science and eye diseases · doi:10.1007/978-981-13-2137-5_5
Influência do posicionamento relativo entre a fóvea e a cabeça do nervo óptico sobre o campo visual central de pacientes com glaucoma
Matos, A. G. (2019) · doi:10.11606/t.17.2019.tde-15022019-163957
Glaucomatous Injury of Central Nerve System: The Role of Neuroimaging Technology in the Understanding of Disease
Zhang, S., Qing, G., Wang, H., Chen, W., Zhang, C., Wang, N., & Gan, J. (2019) · Advances in visual science and eye diseases · doi:10.1007/978-981-13-7896-6_7
Understanding Primary Open-Angle Glaucoma from the Perspective Beyond Ophthalmology
Wang, N., Liu, X., & Yang, D. (2019) · Advances in visual science and eye diseases · doi:10.1007/978-981-13-7896-6_2
Glaucomatous Injury of Central Nerve System
Chen, W., Zhang, S., Wang, N., Zhang, C., Zhang, Q., & Gan, J. (2019) · Advances in visual science and eye diseases · doi:10.1007/978-981-13-7896-6_6
Quantification of Macular Ellipsoid Zone Intensity in Glaucoma Patients
하아늘 (2019)
Psychophysiology of Glaucoma
Johnson, C. A., & Demirel, S. (2008) · Humana Press eBooks · doi:10.1007/978-1-59745-373-8_29
Performance na condução de automóvel por pacientes portadores de glaucoma primário de ângulo aberto: atenção dividida e discriminação de objetos
Ogata, N. G. (2020) · Digital Library of Theses and Dissertations (Universidade de São Paulo) · doi:10.11606/t.5.2020.tde-09062021-130628
Clinical evaluation of the eye-to-visual-pathway integrity of glaucomatous neurodegeneration using 1.5T MR imaging: The integrity of glaucomatous neurodegeneration
Engin, K. N., Yiğit, U., Bayramoğlu, S. T., Güner, N. T., Özyurt, O., Kutlay, T., Ağaçhan, A., & Penbe, Ç. (2022) · International Journal of Clinical and Experimental Ophthalmology · doi:10.29328/journal.ijceo.1001042
Avaliação dos polimorfismos E2, E3 e E4 no gene APOE em relação à etiologia do glaucoma primário de ângulo aberto em uma amostra da população brasileira
Occhiutto, M. L. (2021) · doi:10.47749/t/unicamp.2021.1166296
Impact of trace elements and risk factor for glaucoma pathogenesis
Choudhari, J., & Chaterjee, T. (2023) · MGM Journal of Medical Sciences · doi:10.4103/mgmj.mgmj_253_22
Pathogenese der Glaukome
Tamm, E. R. (2024) · Springer Reference Medizin · doi:10.1007/978-3-662-65929-8_1-1
Pathogenese der Glaukome
Tamm, E. R. (2025) · Springer Reference Medizin · doi:10.1007/978-3-662-65823-9_1
Efficacy of Chronic Non-Psychedelic Psilocybin on Visual Recovery in a Mouse Model of Occipital StrokePreprint
Nasini, S., Barzon, B., Tidei, S., Casile, A., Cambiaghi, M., Martin, S. D., Mattarei, A., Battelli, L., Bolognini, N., Marzoli, S. B., et al. (2025) · SSRN Electronic Journal · doi:10.2139/ssrn.5348341
Comparison of Dorzolamide and Netarsudil on Intraocular Pressure and Ocular Perfusion in Early Glaucoma
Angmo, D., Jain, V., Warjri, G. B., Sharma, N., Azad, S. V., & Dada, T. (2025) · Journal of Glaucoma · doi:10.1097/ijg.0000000000002615
Retinal Ganglion Cell Diversity in Disease: Clinical Implications and Type-Specific Evaluation
Makam, R., Rider, A. T., Yu‐Wai‐Man, P., & Gilhooley, M. J. (2025) · Journal of Neuro-Ophthalmology · doi:10.1097/wno.0000000000002381
Three-dimensional optical coherence tomography imaging of the optic nerve head
Strouthidis, N. G. (2012) · UCL Discovery (University College London)
Special considerations in low-tension glaucoma
Krupin, T. (2007) · Canadian Journal of Ophthalmology · doi:10.3129/can.j.ophthalmol.i07-043
Ocular diagnostics and occipital neurovascular coupling in ocular hypertension and open angle glaucoma
Messenio, D., Luconi, E., Re, R., Boracchi, P., Colombo, R., Riva, E., Spinelli, L., Contini, D., Cubeddu, R., Biganzoli, E. M., et al. (2025) · Frontiers in Neuroscience · doi:10.3389/fnins.2025.1689655
Effects of Treatment with Citicoline Plus Nicotinamide Oral Solution on Retinal Ganglion Cells and Visual Pathways in Glaucomatous Impairment
Parisi, V., Romano, D., Aminoleslami, A. A., Ziccardi, L., Prandini, R., Martella, S., & Rossetti, L. M. (2026) · Pharmaceuticals · doi:10.3390/ph19081179

Authors: Yücel, Y.
Affiliations: St. Michael's Hospital (CA)
Corresponding author: Yücel, Y
Venue: Progress in Retinal and Eye Research
Publisher: Elsevier BV
Published: 2003-07
Volume: 22
Issue: 4
Pages: 465-481
ISSN: 1350-9462 (ISSN-L)
DOI: 10.1016/s1350-9462(03)00026-0
OpenAlex: W1964207930
Cited by: 384
References: 90
Citations by year: 2026: 3 · 2025: 21 · 2024: 13 · 2023: 9 · 2022: 12 · 2021: 19 · 2020: 17 · 2019: 18 · 2018: 17 · 2017: 17 · 2016: 20 · 2015: 33 · 2014: 14 · 2013: 20 · 2012: 25
FWCI: 12.36
Type: journal article
Language: en
Open access: closed
Licence: www.elsevier.com/tdm/userlicense/1.0/ (tdm)
Locations: Progress in Retinal and Eye Research (publishedVersion)
PubMed (publishedVersion)
Funders: National Eye Institute (R01EY002698, EY02698)
Topics: Health Sciences › Medicine › Ophthalmology › Glaucoma and retinal disorders
Life Sciences › Neuroscience › Cognitive Neuroscience › Visual perception and processing mechanisms
Health Sciences › Medicine › Ophthalmology › Drug-Induced Ocular Toxicity
Keywords: glaucoma, retinal ganglion cell death, lateral geniculate nucleus, visual cortex, magnocellular pathway, parvocellular pathway, koniocellular pathway, intraocular pressure, optic nerve injury
MeSH terms: Animals, Geniculate Bodies, Glaucoma, Humans, Nerve Degeneration, Optic Nerve, Retinal Ganglion Cells, Visual Cortex, Visual Pathways, Cell Death

About these checks

Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.

Statistics and arithmetic are recomputed, not judged.

Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.

What counts as a claim ›How we measure confidence ›How we check this ›

Are you an author, or do you see a problem with this page? Request a review

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

Abstract

Overview

Integrity signals

Verification

Claims the paper makes

Claims other papers make about this one

Citations

Cites

Cited by

Related

Metadata

Record

About these checks