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

Christopher J. Klein

Department of Neurology

Division of Peripheral Nerve Diseases

Mayo Clinic




Name/email consistency: high



  • Department of Neurology, Division of Peripheral Nerve Diseases, Mayo Clinic, Rochester, USA. 2002 - 2013
  • 200 First Street SW, Rochester, MN 55905. 2011
  • Mayo Clinic, 200 First St SW, Mayo Clinic, Rochester. 2011


  1. DNMT1 mutation hot spot causes varied phenotypes of HSAN1 with dementia and hearing loss. Klein, C.J., Bird, T., Ertekin-Taner, N., Lincoln, S., Hjorth, R., Wu, Y., Kwok, J., Mer, G., Dyck, P.J., Nicholson, G.A. Neurology (2013) [Pubmed]
  2. TRPV4 mutations and cytotoxic hypercalcemia in axonal Charcot-Marie-Tooth neuropathies. Klein, C.J., Shi, Y., Fecto, F., Donaghy, M., Nicholson, G., McEntagart, M.E., Crosby, A.H., Wu, Y., Lou, H., McEvoy, K.M., Siddique, T., Deng, H.X., Dyck, P.J. Neurology (2011) [Pubmed]
  3. Mass spectrometric-based proteomic analysis of amyloid neuropathy type in nerve tissue. Klein, C.J., Vrana, J.A., Theis, J.D., Dyck, P.J., Dyck, P.J., Spinner, R.J., Mauermann, M.L., Bergen, H.R., Zeldenrust, S.R., Dogan, A. Arch. Neurol. (2011) [Pubmed]
  4. Meralgia paresthetica: Relation to obesity, advanced age, and diabetes mellitus. Parisi, T.J., Mandrekar, J., Dyck, P.J., Klein, C.J. Neurology (2011) [Pubmed]
  5. Large kindred evaluation of mitofusin 2 novel mutation, extremes of neurologic presentations, and preserved nerve mitochondria. Klein, C.J., Kimmel, G.W., Pittock, S.J., Engelstad, J.E., Cunningham, J.M., Wu, Y., Dyck, P.J. Arch. Neurol. (2011) [Pubmed]
  6. SEPT9 mutations and a conserved 17q25 sequence in sporadic and hereditary brachial plexus neuropathy. Klein, C.J., Wu, Y., Cunningham, J.M., Windebank, A.J., Dyck, P.J., Friedenberg, S.M., Klein, D.M., Dyck, P.J. Arch. Neurol. (2009) [Pubmed]
  7. The inherited neuropathies. Klein, C.J. Neurol. Clin (2007) [Pubmed]
  8. Genetic testing in inherited peripheral neuropathies. Klein, C.J., Dyck, P.J. J. Peripher. Nerv. Syst. (2005) [Pubmed]
  9. SPTLC1 and RAB7 mutation analysis in dominantly inherited and idiopathic sensory neuropathies. Klein, C.J., Wu, Y., Kruckeberg, K.E., Hebbring, S.J., Anderson, S.A., Cunningham, J.M., Dyck, P.J., Klein, D.M., Thibodeau, S.N., Dyck, P.J. J. Neurol. Neurosurg. Psychiatr. (2005) [Pubmed]
  10. Adult polyglucosan body disease: case description of an expanding genetic and clinical syndrome. Klein, C.J., Boes, C.J., Chapin, J.E., Lynch, C.D., Campeau, N.G., Dyck, P.J., Dyck, P.J. Muscle. Nerve (2004) [Pubmed]
  11. Pathology and molecular genetics of inherited neuropathy. Klein, C.J. J. Neurol. Sci. (2004) [Pubmed]
  12. The gene for HMSN2C maps to 12q23-24: a region of neuromuscular disorders. Klein, C.J., Cunningham, J.M., Atkinson, E.J., Schaid, D.J., Hebbring, S.J., Anderson, S.A., Klein, D.M., Dyck, P.J., Litchy, W.J., Thibodeau, S.N., Dyck, P.J. Neurology (2003) [Pubmed]
  13. Inflammation and neuropathic attacks in hereditary brachial plexus neuropathy. Klein, C.J., Dyck, P.J., Friedenberg, S.M., Burns, T.M., Windebank, A.J., Dyck, P.J. J. Neurol. Neurosurg. Psychiatr. (2002) [Pubmed]
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