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

Tuija Löppönen

University of Oulu



Name/email consistency: high



  • University of Oulu, Finland. 2004
  • Department of Clinical Genetics, Oulu University Hospital, Kajaanintie 50, FIN-90220 Oulu, Finland. 2003


  1. Childhood-onset osteoarthritis, tall stature, and sensorineural hearing loss associated with Arg75-Cys mutation in procollagen type II gene (COL2A1). Löppönen, T., Körkkö, J., Lundan, T., Seppänen, U., Ignatius, J., Kääriäinen, H. Arthritis Rheum. (2004) [Pubmed]
  2. Connexin 26 mutations and nonsyndromic hearing impairment in northern Finland. Löppönen, T., Väisänen, M.L., Luotonen, M., Allinen, M., Uusimaa, J., Lindholm, P., Mäki-Torkko, E., Väyrynen, M., Löppönen, H., Leisti, J. Laryngoscope (2003) [Pubmed]
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