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Positional cloning of a novel potassium channel gene: KVLQT1 mutations cause cardiac arrhythmias
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Citations
Cited by
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Priori, S. G., Wilde, A. A., Horie, M., Cho, Y., Behr, E. R., Berul, C., Blom, N., Brugada, J., Chiang, C.-E., Huikuri, H., et al. (2013) · Heart Rhythm · doi:10.1016/j.hrthm.2013.05.014 · Cited by 1,942
Self-citationA novel potassium channel gene, KCNQ2, is mutated in an inherited epilepsy of newborns
Singh, N. A., Charlier, C., Stauffer, D., DuPont, B. R., Leach, R. J., Melis, R., Ronen, G. M., Bjerre, I., Quattlebaum, T., Murphy, J. V., et al. (1998) · Nature Genetics · doi:10.1038/ng0198-25 · Cited by 1,199
Zipes, D. P., Camm, A. J., Borggrefe, M., Buxton, A. E., Chaitman, B., Fromer, M., Gregoratos, G., Klein, G., Moss, A. J., Myerburg, R. J., et al. (2006) · Circulation · doi:10.1161/circulationaha.106.178233 · Cited by 1,080
Self-citationAntzelevitch, C., Pollevick, G. D., Cordeiro, J. M., Casis, O., Sanguinetti, M. C., Aizawa, Y., Guerchicoff, A., Pfeiffer, R., Oliva, A., Wollnik, B., et al. (2007) · Circulation · doi:10.1161/circulationaha.106.668392 · Cited by 933
Variants in KCNQ1 are associated with susceptibility to type 2 diabetes mellitus
Yasuda, K., Miyake, K., Horikawa, Y., Hara, K., Osawa, H., Furuta, H., Hirota, Y., Mori, H., Jonsson, A., Sato, Y., et al. (2008) · Nature Genetics · doi:10.1038/ng.207 · Cited by 776
Zhang, H., Craciun, L. C., Mirshahi, T., Rohács, T., Lopes, C. M. B., Jin, T., & Logothetis, D. E. (2003) · Neuron · doi:10.1016/s0896-6273(03)00125-9 · Cited by 523
Inherited disorders of voltage-gated sodium channels
George, A. L. (2005) · Journal of Clinical Investigation · doi:10.1172/jci25505 · Cited by 365
Gu, N., Vervaeke, K., Hu, H., & Storm, J. F. (2005) · The Journal of Physiology · doi:10.1113/jphysiol.2005.086835 · Cited by 363
Cooper, E. C., Harrington, E., Jan, Y. N., & Jan, L. Y. (2001) · The Journal of Neuroscience · doi:10.1523/jneurosci.21-24-09529.2001 · Cited by 305
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Neely, G. G., Kuba, K., Cammarato, A., Isobe, K., Amann, S., Zhang, L., Murata, M., Elmén, L., Gupta, V., Arora, S., et al. (2010) · Cell · doi:10.1016/j.cell.2010.02.023 · Cited by 213
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Asahara, S.-I., Etoh, H., Inoue, H., Teruyama, K., Shibutani, Y., Ihara, Y., Kawada, Y., Bartolome, A., Hashimoto, N., Matsuda, T., et al. (2015) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1422104112 · Cited by 63
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Andersen, M. N., Krzystanek, K., Petersen, F., Bomholtz, S. H., Olesen, S.-P., Abriel, H., Jespersen, T., & Rasmussen, H. B. (2013) · Journal of Biological Chemistry · doi:10.1074/jbc.m113.525931 · Cited by 30
Li, Y., Hof, T., Baldwin, T. A., Chen, L., Kass, R. S., & Dessauer, C. W. (2019) · Cells · doi:10.3390/cells8090981 · Cited by 27
Long QT syndrome patients may faint due to neurocardiogenic syncope
Toft, E. (2003) · Europace · doi:10.1016/s1099-5129(03)00083-7 · Cited by 25
Lemke, J., Gollasch, M., Tsvetkov, D., & Schulig, L. (2025) · Expert Opinion on Drug Discovery · doi:10.1080/17460441.2024.2438226 · Cited by 6
“In humans, mutations in all five Kcnq genes were described to cause disease phenotypes including long QT syndrome (K V 7.1) [17], epileptic encephalopathy (K V 7.2/3) [18,19], deafness (K V 7.4) [20] and complex central nervous system symptoms like intellectual disability and epileptic…”
InfluentialSex differences in potassium regulation: evidence, molecular mechanisms and clinical implications
Al-Qusairi, L. (2026) · Biology of Sex Differences · doi:10.1186/s13293-026-00862-4 · Cited by 3
Metadata
- Authors
- Wang, Q., Curran, M. E., Splawski, I., Burn, T. C., Millholland, J. M., VanRaay, T. J., Shen, J., Timothy, K. W., Vincent, G. M., de Jager, T., Schwartz, P. J., Towbin, J. A., Moss, A. J., Atkinson, D. L., Landes, G. M., Connors, T. D., & Keating, M. T.
- Venue
- Nature Genetics
- Published
- 1996-01
- Volume
- 12
- Issue
- 1
- Pages
- 17-23
- ISSN
- 1061-4036 (ISSN-L)
- 1546-1718
- OpenAlex
- W1991662012
- Cited by
- 1,759
- References
- 0
- FWCI
- 82.12
- Type
- journal article
- Language
- en
- Open access
- closed
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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.