The DOI matches its Crossref record; 57 of the 57 references it cites were found in a registry or an index.
A genetic approach to understanding auditory function
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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
Prestin is the motor protein of cochlear outer hair cells
Zheng, J., Shen, W., He, D. Z. Z., Long, K. B., Madison, L. D., & Dallos, P. (2000) · Nature · doi:10.1038/35012009 · Cited by 1,344
Pendred syndrome is caused by mutations in a putative sulphate transporter gene (PDS)
Everett, L. A., Glaser, B., Beck, J. C., Idol, J. R., Buchs, A., Heyman, M., Adawi, F., Hazani, E., Nassir, E., Baxevanis, A. D., et al. (1997) · Nature Genetics · doi:10.1038/ng1297-411 · Cited by 1,144
Defective myosin VIIA gene responsible for Usher syndrome type IB
Well, D., Blanchard, S., Kaplan, J., Guilford, P., Gibson, F., Walsh, J., Mburu, P., Varela, A., Levilliers, J., Weston, M. D., et al. (1995) · Nature · doi:10.1038/374060a0 · Cited by 1,068
Self-citationCongenital Deafness and Sinoatrial Node Dysfunction in Mice Lacking Class D L-Type Ca2+ Channels
Platzer, J., Engel, J., Schrott-Fischer, A., Stephan, K., Bova, S., Chen, H., Zheng, H., & Striessnig, J. (2000) · Cell · doi:10.1016/s0092-8674(00)00013-1 · Cited by 932
Kubisch, C., Schroeder, B. C., Friedrich, T., Lütjohann, B., El-Amraoui, A., Marlin, S., Petit, C., & Jentsch, T. J. (1999) · Cell · doi:10.1016/s0092-8674(00)80556-5 · Cited by 867
Neuronal KCNQ potassium channels:physislogy and role in disease
Jentsch, T. J. (2000) · Nature Reviews Neuroscience · doi:10.1038/35036198 · Cited by 849
A Drosophila Mechanosensory Transduction Channel
Walker, R. G., Willingham, A. T., & Zuker, C. S. (2000) · Science · doi:10.1126/science.287.5461.2229 · Cited by 696
Karet, F. E., Finberg, K. E., Nelson, R. D., Nayir, A., Mocan, H., Sanjad, S. A., Rodriguez-Soriano, J., Santos, F., Cremers, C. W. R. J., Pietro, A. D., et al. (1999) · Nature Genetics · doi:10.1038/5022 · Cited by 695
A type VII myosin encoded by the mouse deafness gene shaker-1
Gibson, F., Walsh, J., Mburu, P., Varela, A., Brown, K. A., Antonio, M., Beisel, K. W., Steel, K. P., & Brown, S. D. M. (1995) · Nature · doi:10.1038/374062a0 · Cited by 683
Self-citation
Cited by
Trp ion channels and temperature sensation
Dhaka, A., Viswanath, V., & Patapoutian, A. (2006) · Annual Review of Neuroscience · doi:10.1146/annurev.neuro.29.051605.112958 · Cited by 782
Deafness and renal tubular acidosis in mice lacking the K-Cl co-transporter Kcc4
Boettger, T., Hübner, C. A., Maier, H., Rust, M. B., Beck, F. X., & Jentsch, T. J. (2002) · Nature · doi:10.1038/416874a · Cited by 414
Evolutionary Biology of Animal Cognition
Dukas, R. (2004) · Annual Review of Ecology, Evolution, and Systematics · doi:10.1146/annurev.ecolsys.35.112202.130152 · Cited by 357
Maassen, J. A., Jahangir Tafrechi, R. S., Janssen, G. M. C., Raap, A. K., Lemkes, H. H., & ’t Hart, L. M. (2006) · Endocrinology and Metabolism Clinics of North America · doi:10.1016/j.ecl.2006.02.014 · Cited by 33
Metadata
- Authors
- Steel, K. P., & Kros, C. J.
- Venue
- Nature Genetics
- Published
- 2001-02
- Volume
- 27
- Issue
- 2
- Pages
- 143-149
- ISSN
- 1061-4036 (ISSN-L)
- 1546-1718
- OpenAlex
- W1559668616
- Cited by
- 290
- References
- 57
- FWCI
- 18.61
- Type
- journal article
- Language
- en
- Open access
- closed
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- Steel, K. P., & Kros, C. J. (2001). A genetic approach to understanding auditory function. Nature Genetics. https://doi.org/10.1038/84758
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.
