The DOI matches its Crossref record; 59 of the 59 references it cites were found in a registry or an index.
Colour vision deficiency
Overview
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Citations
Cites
(1992) · Applied Ergonomics · doi:10.1016/0003-6870(92)90338-v · Cited by 7,112
Molecular Genetics of Human Color Vision: The Genes Encoding Blue, Green, and Red Pigments
Nathans, J., Thomas, D., & Hogness, D. S. (1986) · Science · doi:10.1126/science.2937147 · Cited by 1,721
Molecular Genetics of Inherited Variation in Human Color Vision
Nathans, J., Piantanida, T. P., Eddy, R. L., Shows, T. B., & Hogness, D. S. (1986) · Science · doi:10.1126/science.3485310 · Cited by 781
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 588
“Tho’ she kneel’d in that place where they grew…” The uses and origins of primate colour vision
Mollon, J. D. (1989) · Journal of Experimental Biology · doi:10.1242/jeb.146.1.21 · Cited by 571
Human visual pigments: microspectrophotometric results from the eyes of seven persons
Dartnall, H. J. A., Bowmaker, J. K., & Mollon, J. D. (1983) · Proceedings of the Royal Society of London. Series B. Biological Sciences · doi:10.1098/rspb.1983.0091 · Cited by 496
The machinery of colour vision
Solomon, S. G., & Lennie, P. (2007) · Nature Reviews Neuroscience · doi:10.1038/nrn2094 · Cited by 434
Spectral tuning of pigments underlying red–green color vision
Neitz, M., Neitz, J., & Jacobs, G. H. (1991) · Science · doi:10.1126/science.1903559 · Cited by 382
Kohl, S., Marx, T., Giddings, I., Jägle, H., Jacobson, S. G., Apfelstedt-Sylla, E., Zrenner, E., Sharpe, L. T., & Wissinger, B. (1998) · Nature Genetics · doi:10.1038/935 · Cited by 340
The cone dysfunction syndromes: Table 1
Aboshiha, J., Dubis, A. M., Carroll, J., Hardcastle, A. J., & Michaelides, M. (2016) · British Journal of Ophthalmology · doi:10.1136/bjophthalmol-2014-306505 · Cited by 314
Cited by
Fakorede, S. T., Akpan, L. G., Adekoya, K. O., & Oboh, B. (2022) · Egyptian Journal of Medical Human Genetics · doi:10.1186/s43042-022-00287-9 · Cited by 22
Metadata
- Authors
- Simunovic, M. P.
- Venue
- Eye
- Published
- 2009-11-20
- Volume
- 24
- Issue
- 5
- Pages
- 747-755
- ISSN
- 0078-5334 (ISSN-L)
- 0950-222X
- 1476-5454
- OpenAlex
- W1976542445
- Cited by
- 276
- References
- 59
- FWCI
- 0.72
- Type
- journal article
- Language
- en
- Open access
- closed
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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.
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How to cite
Cite CoChat for the checks on this page, and the paper for its own findings.
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- CoChat. (2026). Citation check: Colour vision deficiency. https://app.cochat.ai/papers/10.1038/eye.2009.251
- The paper
- Simunovic, M. P. (2010). Colour vision deficiency. Eye. https://doi.org/10.1038/eye.2009.251
Data sources
Bibliographic data: Semantic Scholar, OpenAlex, Crossref.
Contains information from the Semantic Scholar Academic Graph Datasets, made available under the ODC Attribution License (ODC-BY 1.0).
Semantic Scholar’s data is described in: Kinney, R., et al. (2023). The Semantic Scholar Open Data Platform. arXiv:2301.10140.
