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

Monica Castro Varela

Centro de Estudos do Genoma Humano

Department of Biology

Institute of Biosciences

University of São Paulo



Name/email consistency: high



  • Centro de Estudos do Genoma Humano, Department of Biology, Institute of Biosciences, University of São Paulo, Brazil. 2004 - 2006


  1. A new case of interstitial 6q16.2 deletion in a patient with Prader-Willi-like phenotype and investigation of SIM1 gene deletion in 87 patients with syndromic obesity. Varela, M.C., Simões-Sato, A.Y., Kim, C.A., Bertola, D.R., De Castro, C.I., Koiffmann, C.P. Eur. J. Med. Genet (2006) [Pubmed]
  2. Impact of molecular mechanisms, including deletion size, on Prader-Willi syndrome phenotype: study of 75 patients. Varela, M.C., Kok, F., Setian, N., Kim, C.A., Koiffmann, C.P. Clin. Genet. (2005) [Pubmed]
  3. Phenotypic variability in Angelman syndrome: comparison among different deletion classes and between deletion and UPD subjects. Varela, M.C., Kok, F., Otto, P.A., Koiffmann, C.P. Eur. J. Hum. Genet. (2004) [Pubmed]
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