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Hoffmann, R. A wiki for the life sciences where authorship matters. Nature Genetics (2008)

Kei Kamide

Division of Hypertension and Nephrology

Research Institute

National Cardiovascular Center




Name/email consistency: high



  • Division of Hypertension and Nephrology, Research Institute, National Cardiovascular Center, Suita, Japan. 2004 - 2009
  • Department of Geriatric Medicine, Osaka University Graduate School of Medicine, Suita, Japan. 2004


  1. Genetic polymorphisms of L-type calcium channel alpha1C and alpha1D subunit genes are associated with sensitivity to the antihypertensive effects of L-type dihydropyridine calcium-channel blockers. Kamide, K., Yang, J., Matayoshi, T., Takiuchi, S., Horio, T., Yoshii, M., Miwa, Y., Yasuda, H., Yoshihara, F., Nakamura, S., Nakahama, H., Miyata, T., Kawano, Y. Circ. J. (2009) [Pubmed]
  2. Protein tyrosine kinase 2beta as a candidate gene for hypertension. Kamide, K., Kokubo, Y., Fukuhara, S., Hanada, H., Yang, J., Kada, A., Nagura, J., Takiuchi, S., Horio, T., Kawano, Y., Okayama, A., Tomoike, H., Miyata, T. Pharmacogenet. Genomics (2007) [Pubmed]
  3. Association of genetic polymorphisms of ACADSB and COMT with human hypertension. Kamide, K., Kokubo, Y., Yang, J., Matayoshi, T., Inamoto, N., Takiuchi, S., Horio, T., Miwa, Y., Yoshii, M., Tomoike, H., Tanaka, C., Banno, M., Okuda, T., Kawano, Y., Miyata, T. J. Hypertens. (2007) [Pubmed]
  4. Genetic variations of HSD11B2 in hypertensive patients and in the general population, six rare missense/frameshift mutations. Kamide, K., Kokubo, Y., Hanada, H., Nagura, J., Yang, J., Takiuchi, S., Tanaka, C., Banno, M., Miwa, Y., Yoshii, M., Matayoshi, T., Yasuda, H., Horio, T., Okayama, A., Tomoike, H., Kawano, Y., Miyata, T. Hypertens. Res. (2006) [Pubmed]
  5. Hypertension susceptibility genes on chromosome 2p24-p25 in a general Japanese population. Kamide, K., Kokubo, Y., Yang, J., Tanaka, C., Hanada, H., Takiuchi, S., Inamoto, N., Banno, M., Kawano, Y., Okayama, A., Tomoike, H., Miyata, T. J. Hypertens. (2005) [Pubmed]
  6. A novel missense mutation, F826Y, in the mineralocorticoid receptor gene in Japanese hypertensives: its implications for clinical phenotypes. Kamide, K., Yang, J., Kokubo, Y., Takiuchi, S., Miwa, Y., Horio, T., Tanaka, C., Banno, M., Nagura, J., Okayama, A., Tomoike, H., Kawano, Y., Miyata, T. Hypertens. Res. (2005) [Pubmed]
  7. Insulin-mediated regulation of the endothelial renin-angiotensin system and vascular cell growth. Kamide, K., Rakugi, H., Nagai, M., Takiuchi, S., Matsukawa, N., Higaki, J., Kawano, Y., Ogihara, T., Tuck, M.L. J. Hypertens. (2004) [Pubmed]
  8. Three novel missense mutations of WNK4, a kinase mutated in inherited hypertension, in Japanese hypertensives: implication of clinical phenotypes. Kamide, K., Takiuchi, S., Tanaka, C., Miwa, Y., Yoshii, M., Horio, T., Mannami, T., Kokubo, Y., Tomoike, H., Kawano, Y., Miyata, T. Am. J. Hypertens. (2004) [Pubmed]
  9. Six missense mutations of the epithelial sodium channel beta and gamma subunits in Japanese hypertensives. Kamide, K., Tanaka, C., Takiuchi, S., Miwa, Y., Yoshii, M., Horio, T., Kawano, Y., Miyata, T. Hypertens. Res. (2004) [Pubmed]
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