The DOI matches its Crossref record; 24 of the 24 references it cites were found in a registry or an index.
Mutations in the human retinal degeneration slow (RDS) gene can cause either retinitis pigmentosa or macular dystrophy
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Citations
Cites
A point mutation of the rhodopsin gene in one form of retinitis pigmentosa
Dryja, T. P., McGee, T. L., Reichel, E., Hahn, L. B., Cowley, G. S., Yandell, D. W., Sandberg, M. A., & Berson, E. L. (1990) · Nature · doi:10.1038/343364a0 · Cited by 1,072
Standard for clinical electroretinography
Marmor, M. F., Arden, G. B., Nilsson, S.-E., Zrenner, E., & International Standardization Committee (1989) · Documenta Ophthalmologica · doi:10.1007/bf00154486 · Cited by 806
Self-citationMutations within the Rhodopsin Gene in Patients with Autosomal Dominant Retinitis Pigmentosa
Dryja, T. P., McGee, T. L., Hahn, L. B., Cowley, G. S., Olsson, J. E., Reichel, E., Sandberg, M. A., & Berson, E. L. (1990) · New England Journal of Medicine · doi:10.1056/nejm199011083231903 · Cited by 501
Mutations in the human retinal degeneration slow gene in autosomal dominant retinitis pigmentosa
Kajiwara, K., Hahn, L. B., Mukai, S., Travis, G. H., Berson, E. L., & Dryja, T. P. (1991) · Nature · doi:10.1038/354480a0 · Cited by 471
Rhodopsin mutations in autosomal dominant retinitis pigmentosa.
Sung, C. H., Davenport, C. M., Hennessey, J. C., Maumenee, I. H., Jacobson, S. G., Heckenlively, J. R., Nowakowski, R., Fishman, G., Gouras, P., & Nathans, J. (1991) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.88.15.6481 · Cited by 461
Rosenfeld, P. J., Cowley, G. S., McGee, T. L., Sandberg, M. A., Berson, E. L., & Dryja, T. P. (1992) · Nature Genetics · doi:10.1038/ng0692-209 · Cited by 422
Travis, G. H., Brennan, M. B., Danielson, P. E., Kozak, C. A., & Sutcliffe, J. G. (1989) · Nature · doi:10.1038/338070a0 · Cited by 400
A three-base-pair deletion in the peripherin–RDS gene in one form of retinitis pigmentosa
Farrar, G. J., Kenna, P., Jordan, S. A., Kumar-Singh, R., Humphries, M. M., Sharp, E. M., Sheils, D. M., & Humphries, P. (1991) · Nature · doi:10.1038/354478a0 · Cited by 388
Travis, G. H., Sutcliffe, J. G., & Bok, D. (1991) · Neuron · doi:10.1016/0896-6273(91)90122-g · Cited by 325
Arikawa, K., Molday, L. L., Molday, R. S., & Williams, D. S. (1992) · The Journal of cell biology · doi:10.1083/jcb.116.3.659 · Cited by 308
Cited by
Dark adaptation and the retinoid cycle of vision
Lamb, T. D., & Pugh, E. N. (2004) · Progress in Retinal and Eye Research · doi:10.1016/j.preteyeres.2004.03.001 · Cited by 725
Genetic Association of Apolipoprotein E with Age-Related Macular Degeneration
Klaver, C. C. W., Kliffen, M., van Duijn, C. M., Hofman, A., Cruts, M., Grobbee, D. E., van Broeckhoven, C., & de Jong, P. T. V. M. (1998) · The American Journal of Human Genetics · doi:10.1086/301901 · Cited by 498
Genome-Wide Scan for Autism Susceptibility Genes
Philippe, A., Martinez, M., Guilloud-Bataille, M., Gillberg, C., Rastam, M., Sponheim, E., Coleman, M., Zappella, M., Aschauer, H., Van Maldergem, L., et al. (1999) · Human Molecular Genetics · doi:10.1093/hmg/8.5.805 · Cited by 471
Prevalence of mutations causing retinitis pigmentosa and other inherited retinopathies
Sohocki, M. M., Daiger, S. P., Bowne, S. J., Rodriquez, J. A., Northrup, H., Heckenlively, J. R., Birch, D. G., Mintz-Hittner, H., Ruiz, R. S., Lewis, R. A., et al. (2001) · Human Mutation · doi:10.1002/1098-1004(2001)17:1<42::aid-humu5>3.0.co;2-k · Cited by 329
Sullivan, L. S., Bowne, S. J., Birch, D. G., Hughbanks-Wheaton, D., Heckenlively, J. R., Lewis, R. A., Garcia, C. A., Ruiz, R. S., Blanton, S. H., Northrup, H., et al. (2006) · Investigative Opthalmology & Visual Science · doi:10.1167/iovs.05-1443 · Cited by 284
Metadata
- Authors
- Wells, J., Wroblewski, J., Keen, J., Inglehearn, C., Jubb, C., Eckstein, A., Jay, M., Arden, G., Bhattacharya, S., Fitzke, F., & Bird, A.
- Venue
- Nature Genetics
- Published
- 1993-03
- Volume
- 3
- Issue
- 3
- Pages
- 213-218
- ISSN
- 1061-4036 (ISSN-L)
- 1546-1718
- OpenAlex
- W2021371090
- Cited by
- 438
- References
- 24
- FWCI
- 18.61
- 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.
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- This page
- CoChat. (2026). Citation check: Mutations in the human retinal degeneration slow (RDS) gene can cause either retinitis pigmentosa or macular dystrophy. https://app.cochat.ai/papers/10.1038/ng0393-213
- The paper
- Wells, J., Wroblewski, J., Keen, J., Inglehearn, C., Jubb, C., Eckstein, A., Jay, M., Arden, G., Bhattacharya, S., Fitzke, F., & Bird, A. (1993). Mutations in the human retinal degeneration slow (RDS) gene can cause either retinitis pigmentosa or macular dystrophy. Nature Genetics. https://doi.org/10.1038/ng0393-213
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.
