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

Felix B. Müller

Department of Dermatology

University of Cologne

Kerpener Str. 62

50937 Köln



Name/email consistency: high



  • Department of Dermatology, University of Cologne, Kerpener Str. 62, 50937 Köln, Germany. 2005 - 2006


  1. A human keratin 10 knockout causes recessive epidermolytic hyperkeratosis. Müller, F.B., Huber, M., Kinaciyan, T., Hausser, I., Schaffrath, C., Krieg, T., Hohl, D., Korge, B.P., Arin, M.J. Hum. Mol. Genet. (2006) [Pubmed]
  2. Novel and recurrent mutations in keratin KRT5 and KRT14 genes in epidermolysis bullosa simplex: implications for disease phenotype and keratin filament assembly. Müller, F.B., Küster, W., Wodecki, K., Almeida, H., Bruckner-Tuderman, L., Krieg, T., Korge, B.P., Arin, M.J. Hum. Mutat. (2006) [Pubmed]
  3. A novel compound heterozygous mutation in Werner syndrome results in WRN transcript decay. Müller, F.B., Tsianakas, A., Kuwert, C., Korge, B.P., Hunzelmann, N. Br. J. Dermatol. (2005) [Pubmed]
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