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

Peter Hedera

Department of Neurology

Vanderbilt University


TN 37232-8552



Name/email consistency: high



  • Department of Neurology, Vanderbilt University, Nashville, TN 37232-8552, USA. 2004 - 2010
  • Department of Pediatrics, Division of Genetics, University of Michigan, 1500 E. Medical Center Drive, USA. 2003
  • Department of Neurology, University of Michigan, Ann Arbor, USA. 2003


  1. Rotigotine adverse effects affecting patient's sexual partner. Hedera, P. Clin. Neuropharmacol (2010) [Pubmed]
  2. Positive family history of essential tremor influences the motor phenotype of Parkinson's disease. Hedera, P., Fang, J.Y., Phibbs, F., Cooper, M.K., Charles, P.D., Davis, T.L. Mov. Disord. (2009) [Pubmed]
  3. Myelopolyneuropathy and pancytopenia due to copper deficiency and high zinc levels of unknown origin II. The denture cream is a primary source of excessive zinc. Hedera, P., Peltier, A., Fink, J.K., Wilcock, S., London, Z., Brewer, G.J. Neurotoxicology (2009) [Pubmed]
  4. Familial mesial temporal lobe epilepsy maps to chromosome 4q13.2-q21.3. Hedera, P., Blair, M.A., Andermann, E., Andermann, F., D'Agostino, D., Taylor, K.A., Chahine, L., Pandolfo, M., Bradford, Y., Haines, J.L., Abou-Khalil, B. Neurology (2007) [Pubmed]
  5. Identification of a novel locus for febrile seizures and epilepsy on chromosome 21q22. Hedera, P., Ma, S., Blair, M.A., Taylor, K.A., Hamati, A., Bradford, Y., Abou-Khalil, B., Haines, J.L. Epilepsia (2006) [Pubmed]
  6. Autosomal dominant lateral temporal epilepsy: two families with novel mutations in the LGI1 gene. Hedera, P., Abou-Khalil, B., Crunk, A.E., Taylor, K.A., Haines, J.L., Sutcliffe, J.S. Epilepsia (2004) [Pubmed]
  7. Novel mutation in the SPG3A gene in an African American family with an early onset of hereditary spastic paraplegia. Hedera, P., Fenichel, G.M., Blair, M., Haines, J.L. Arch. Neurol. (2004) [Pubmed]
  8. Juberg-Hayward syndrome: report of a new patient with severe phenotype and novel clinical features. Hedera, P., Innis, J.W. Am. J. Med. Genet. A (2003) [Pubmed]
  9. Myelopolyneuropathy and pancytopenia due to copper deficiency and high zinc levels of unknown origin: further support for existence of a new zinc overload syndrome. Hedera, P., Fink, J.K., Bockenstedt, P.L., Brewer, G.J. Arch. Neurol. (2003) [Pubmed]
  10. The second kindred with autosomal dominant distal myopathy linked to chromosome 14q: genetic and clinical analysis. Hedera, P., Petty, E.M., Bui, M.R., Blaivas, M., Fink, J.K. Arch. Neurol. (2003) [Pubmed]
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