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

C. Fridman

Department of Biology

Institute of Bioscience

University of São Paulo



Name/email consistency: high



  • Department of Biology, Institute of Bioscience, University of São Paulo, Brazil. 2000 - 2003


  1. Angelman syndrome associated with oculocutaneous albinism due to an intragenic deletion of the P gene. Fridman, C., Hosomi, N., Varela, M.C., Souza, A.H., Fukai, K., Koiffmann, C.P. Am. J. Med. Genet. A (2003) [Pubmed]
  2. Paternal UPD15: further genetic and clinical studies in four Angelman syndrome patients. Fridman, C., Varela, M.C., Kok, F., Diament, A., Koiffmann, C.P. Am. J. Med. Genet. (2000) [Pubmed]
  3. Origin of uniparental disomy 15 in patients with Prader-Willi or Angelman syndrome. Fridman, C., Koiffmann, C.P. Am. J. Med. Genet. (2000) [Pubmed]
  4. Prader-Willi syndrome: genetic tests and clinical findings. Fridman, C., Varela, M.C., Kok, F., Setian, N., Koiffmann, C.P. Genet. Test. (2000) [Pubmed]
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