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

Duygu Selcen

Department of Neurology

Mayo Clinic




Name/email consistency: high



  • Department of Neurology, Mayo Clinic, Rochester, USA. 2013
  • Department of Neurology and Neuromuscular Research Laboratory, Mayo Clinic, Rochester, MN 55905. 2003 - 2011
  • Department of Neurology, Division of Child Neurology and Neuromuscular Disease Research Laboratory, Mayo Clinic College of Medicine, Mayo Clinic, USA. 2010 - 2011
  • Children's Hospital of Michigan, Department of Pediatrics, Division of Neurology, Wayne State University, USA. 2000


  1. GFPT1-myasthenia: clinical, structural, and electrophysiologic heterogeneity. Selcen, D., Shen, X.M., Milone, M., Brengman, J., Ohno, K., Deymeer, F., Finkel, R., Rowin, J., Engel, A.G. Neurology (2013) [Pubmed]
  2. Reducing bodies and myofibrillar myopathy features in FHL1 muscular dystrophy. Selcen, D., Bromberg, M.B., Chin, S.S., Engel, A.G. Neurology (2011) [Pubmed]
  3. Myofibrillar myopathies. Selcen, D. Neuromuscul. Disord. (2011) [Pubmed]
  4. Myofibrillar myopathies. Selcen, D. Curr. Opin. Neurol. (2010) [Pubmed]
  5. Mutation in BAG3 causes severe dominant childhood muscular dystrophy. Selcen, D., Muntoni, F., Burton, B.K., Pegoraro, E., Sewry, C., Bite, A.V., Engel, A.G. Ann. Neurol. (2009) [Pubmed]
  6. Myofibrillar myopathies. Selcen, D. Curr. Opin. Neurol. (2008) [Pubmed]
  7. The Z-disk diseases. Selcen, D., Carpén, O. Adv. Exp. Med. Biol. (2008) [Pubmed]
  8. Mutations in ZASP define a novel form of muscular dystrophy in humans. Selcen, D., Engel, A.G. Ann. Neurol. (2005) [Pubmed]
  9. Myofibrillar myopathy: clinical, morphological and genetic studies in 63 patients. Selcen, D., Ohno, K., Engel, A.G. Brain (2004) [Pubmed]
  10. Mutations in myotilin cause myofibrillar myopathy. Selcen, D., Engel, A.G. Neurology (2004) [Pubmed]
  11. Are MuSK antibodies the primary cause of myasthenic symptoms?. Selcen, D., Fukuda, T., Shen, X.M., Engel, A.G. Neurology (2004) [Pubmed]
  12. Myofibrillar myopathy caused by novel dominant negative alpha B-crystallin mutations. Selcen, D., Engel, A.G. Ann. Neurol. (2003) [Pubmed]
  13. Otocerebral anomalies associated with topical tretinoin use. Selcen, D., Seidman, S., Nigro, M.A. Brain Dev. (2000) [Pubmed]
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