The DOI matches its Crossref record; 11 of the 11 references it cites were found in a registry or an index.
Mutations in the gene encoding gap junction protein β-3 associated with autosomal dominant hearing impairment
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Citations
Cites
Connexin 26 mutations in hereditary non-syndromic sensorineural deafness
Kelsell, D. P., Dunlop, J., Stevens, H. P., Lench, N. J., Liang, J. N., Parry, G., Mueller, R. F., & Leigh, I. M. (1997) · Nature · doi:10.1038/387080a0 · Cited by 1,470
Connexin Mutations in X-Linked Charcot-Marie-Tooth Disease
Bergoffen, J., Scherer, S. S., Wang, S., Scott, M. O., Bone, L. J., Paul, D. L., Chen, K., Lensch, M. W., Chance, P. F., & Fischbeck, K. H. (1993) · Science · doi:10.1126/science.8266101 · Cited by 1,066
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
Elgoyhen, A. B., Johnson, D. S., Boulter, J., Vetter, D. E., & Heinemann, S. (1994) · Cell · doi:10.1016/0092-8674(94)90555-x · Cited by 899
Handbook of clinical audiology
Katz, J. L. (1978) · Cited by 604
Novel Mutations in the Connexin 26 Gene (GJB2) That Cause Autosomal Recessive (DFNB1) Hearing Loss
Kelley, P. M., Harris, D. J., Comer, B. C., Askew, J. W., Fowler, T., Smith, S. D., & Kimberling, W. J. (1998) · The American Journal of Human Genetics · doi:10.1086/301807 · Cited by 500
Genetic epidemiological studies of early‐onset deafness in the U.S. school‐age population
Marazita, M. L., Ploughman, L. M., Rawlings, B., Remington, E., Arnos, K. S., & Nance, W. E. (1993) · American Journal of Medical Genetics · doi:10.1002/ajmg.1320460504 · Cited by 452
Nonsyndromic hearing impairment: unparalleled heterogeneity.
Camp, G. V., Willems, P. J., & Smith, R. J. (1997) · PubMed · Cited by 334
Connexin 26 gene linked to a dominant deafness
Denoyelle, F., Lina-Granade, G., Plauchu, H., Bruzzone, R., Chaïb, H., Lévi-Acobas, F., Weil, D., & Petit, C. (1998) · Nature · doi:10.1038/30639 · Cited by 304
Handbook of Clinical Audiology (4th ed.)
Hayes, D. (1994) · Ear and Hearing · doi:10.1097/00003446-199412000-00011 · Cited by 240
Cited by
Neuronal KCNQ potassium channels:physislogy and role in disease
Jentsch, T. J. (2000) · Nature Reviews Neuroscience · doi:10.1038/35036198 · Cited by 849
Mutations in the Gene Encoding Tight Junction Claudin-14 Cause Autosomal Recessive Deafness DFNB29
Wilcox, E. R., Burton, Q. L., Naz, S., Riazuddin, S., Smith, T. N., Ploplis, B., Belyantseva, I., Ben-Yosef, T., Liburd, N. A., Morell, R. J., et al. (2001) · Cell · doi:10.1016/s0092-8674(01)00200-8 · Cited by 444
A genetic approach to understanding auditory function
Steel, K. P., & Kros, C. J. (2001) · Nature Genetics · doi:10.1038/84758 · Cited by 290
Mutations in GJB6 cause hidrotic ectodermal dysplasia
Lamartine, J., Munhoz Essenfelder, G., Kibar, Z., Lanneluc, I., Callouet, E., Laoudj, D., Lemaître, G., Hand, C., Hayflick, S. J., Zonana, J., et al. (2000) · Nature Genetics · doi:10.1038/79851 · Cited by 284
Targeted disruption of the Kcnq1 gene produces a mouse model of Jervell and Lange– Nielsen Syndrome
Casimiro, M. C., Knollmann, B. C., Ebert, S. N., Vary, J. C., Greene, A. E., Franz, M. R., Grinberg, A., Huang, S. P., & Pfeifer, K. (2001) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.041398998 · Cited by 261
Metadata
- Authors
- Xia., J.-H., Liu, C.-Y., Tang, B.-S., Pan, Q., Huang, L., Dai, H.-P., Zhang, B.-R., Xie, W., Hu, D.-X., Zheng, D., Shi, X.-L., Wang, D.-A., Xia, K., Yu, K.-P., Liao, X.-D., Feng, Y., Yang, Y.-F., Xiao, J.-Y., Xie, D.-H., & Huang, J.-Z.
- Venue
- Nature Genetics
- Published
- 1998-12-01
- Volume
- 20
- Issue
- 4
- Pages
- 370-373
- ISSN
- 1061-4036 (ISSN-L)
- 1546-1718
- DOI
- 10.1038/3845
- OpenAlex
- W2099041486
- Cited by
- 425
- References
- 11
- FWCI
- 23.14
- 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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- CoChat. (2026). Citation check: Mutations in the gene encoding gap junction protein β-3 associated with autosomal dominant hearing impairment. https://app.cochat.ai/papers/10.1038/3845
- The paper
- Xia., J.-H., Liu, C.-Y., Tang, B.-S., Pan, Q., Huang, L., Dai, H.-P., Zhang, B.-R., Xie, W., Hu, D.-X., Zheng, D., Shi, X.-L., Wang, D.-A., Xia, K., Yu, K.-P., Liao, X.-D., Feng, Y., Yang, Y.-F., Xiao, J.-Y., Xie, D.-H., & Huang, J.-Z. (1998). Mutations in the gene encoding gap junction protein β-3 associated with autosomal dominant hearing impairment. Nature Genetics. https://doi.org/10.1038/3845
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.
