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

Yoshiyuki Okano

Department of Pediatrics

Osaka City University Graduate School of Medicine

Osaka 545-8585



Name/email consistency: high



  • Department of Pediatrics, Osaka City University Graduate School of Medicine, Osaka 545-8585, Japan. 1998 - 2007


  1. Effects of tetrahydrobiopterin and phenylalanine on in vivo human phenylalanine hydroxylase by phenylalanine breath test. Okano, Y., Takatori, K., Kudo, S., Sakaguchi, T., Asada, M., Kajiwara, M., Yamano, T. Mol. Genet. Metab. (2007) [Pubmed]
  2. In vivo studies of phenylalanine hydroxylase by phenylalanine breath test: diagnosis of tetrahydrobiopterin-responsive phenylalanine hydroxylase deficiency. Okano, Y., Hase, Y., Kawajiri, M., Nishi, Y., Inui, K., Sakai, N., Tanaka, Y., Takatori, K., Kajiwara, M., Yamano, T. Pediatr. Res. (2004) [Pubmed]
  3. A genetic factor for age-related cataract: identification and characterization of a novel galactokinase variant, "Osaka," in Asians. Okano, Y., Asada, M., Fujimoto, A., Ohtake, A., Murayama, K., Hsiao, K.J., Choeh, K., Yang, Y., Cao, Q., Reichardt, J.K., Niihira, S., Imamura, T., Yamano, T. Am. J. Hum. Genet. (2001) [Pubmed]
  4. Two novel glucose-6-phosphate dehydrogenase variants found in newborn mass-screening for galactosaemia. Okano, Y., Fujimoto, A., Miyagi, T., Hirono, A., Miwa, S., Niihira, S., Hirokawa, H., Yamano, Y. Eur. J. Pediatr. (2001) [Pubmed]
  5. Molecular characterization of phenylketonuria in Japanese patients. Okano, Y., Asada, M., Kang, Y., Nishi, Y., Hase, Y., Oura, T., Isshiki, G. Hum. Genet. (1998) [Pubmed]
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