The DOI matches its Crossref record; 23 of the 23 references it cites were found in a registry or an index.
Mutations in COL11A2 cause non-syndromic hearing loss (DFNA13)
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Citations
Cites
A low-viscosity epoxy resin embedding medium for electron microscopy
Spurr, A. R. (1969) · Journal of Ultrastructure Research · doi:10.1016/s0022-5320(69)90033-1 · Cited by 12,865
Genetic Epidemiology of Hearing Impairment
MORTON, N. E. (1991) · Annals of the New York Academy of Sciences · doi:10.1111/j.1749-6632.1991.tb19572.x · Cited by 944
Articular cartilage and osteoarthritis
Dziak, R. (1992) · Bone and Mineral · doi:10.1016/0169-6009(92)90848-8 · Cited by 843
Cartilage contains mixed fibrils of collagen types II, IX, and XI.
Mendler, M., Eich-Bender, S. G., Vaughan, L., Winterhalter, K. H., & Bruckner, P. (1989) · The Journal of cell biology · doi:10.1083/jcb.108.1.191 · Cited by 509
Fessler, J. H., & Fessler, L. I. (1978) · Annual Review of Biochemistry · doi:10.1146/annurev.bi.47.070178.001021 · Cited by 446
Autosomal dominant and recessive osteochondrodysplasias associated with the COL11A2 locus
Vikkula, M., Madman, E. C. M., Lui, V. C. H., Zhidkova, N. I., Tiller, G. E., Goldring, M. B., van Beersum, S. E. C., de Waal Malefijt, M. C., van den Hoogen, F. H. J., Ropers, H.-H., et al. (1995) · Cell · doi:10.1016/0092-8674(95)90493-x · Cited by 407
Self-citationA fibrillar collagen gene, Col11a1, is essential for skeletal morphogenesis
Li, Y., Lacerda, D. A., Warman, M. L., Beier, D. R., Yoshioka, H., Ninomiya, Y., Oxford, J. T., Morris, N. P., Andrikopoulos, K., Ramirez, F., et al. (1995) · Cell · doi:10.1016/0092-8674(95)90492-1 · Cited by 379
Nonsyndromic hearing impairment: unparalleled heterogeneity.
Camp, G. V., Willems, P. J., & Smith, R. J. (1997) · PubMed · Cited by 334
Self-citationGenetic Associations in Age-Related Hearing Thresholds
Gates, G. A., Couropmitree, N. N., & Myers, R. H. (1999) · Archives of Otolaryngology–Head & Neck Surgery · doi:10.1001/archotol.125.6.654 · Cited by 296
Cochlear pathology of long term neomycin induced deafness in cats
Leake, P. A., & Hradek, G. T. (1988) · Hearing Research · doi:10.1016/0378-5955(88)90018-4 · Cited by 277
Cited by
Initial sequencing and analysis of the human genome
International Human Genome Sequencing Consortium, Whitehead Institute for Biomedical Research, C. F. G. R., Lander, E. S., Linton, L. M., Birren, B., Nusbaum, C., Zody, M. C., Baldwin, J., Devon, K., Dewar, K., et al. (2001) · Nature · doi:10.1038/35057062 · Cited by 24,216
Metadata
- Authors
- McGuirt, W. T., Prasad, S. D., Griffith, A. J., Kunst, H. P. M., Green, G. E., Shpargel, K. B., Runge, C., Huybrechts, C., Mueller, R. F., Lynch, E., King, M.-C., Brunner, H. G., Cremers, C. W. R. J., Takanosu, M., Li, S.-W., Arita, M., Mayne, R., Prockop, D. J., Camp, G. V., & Smith, R. J. H.
- Venue
- Nature Genetics
- Published
- 1999-12
- Volume
- 23
- Issue
- 4
- Pages
- 413-419
- ISSN
- 1061-4036 (ISSN-L)
- 1546-1718
- OpenAlex
- W2140114390
- Cited by
- 265
- References
- 23
- FWCI
- 8.97
- 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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How to cite
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- This page
- CoChat. (2026). Citation check: Mutations in COL11A2 cause non-syndromic hearing loss (DFNA13). https://app.cochat.ai/papers/10.1038/70516
- The paper
- McGuirt, W. T., Prasad, S. D., Griffith, A. J., Kunst, H. P. M., Green, G. E., Shpargel, K. B., Runge, C., Huybrechts, C., Mueller, R. F., Lynch, E., King, M.-C., Brunner, H. G., Cremers, C. W. R. J., Takanosu, M., Li, S.-W., Arita, M., Mayne, R., Prockop, D. J., Camp, G. V., & Smith, R. J. H. (1999). Mutations in COL11A2 cause non-syndromic hearing loss (DFNA13). Nature Genetics. https://doi.org/10.1038/70516
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.
