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

Neil S. Gordon





Name/email consistency: high



  • Huntlywood, Wilmslow, UK. 2005 - 2010
  • Royal Manchester Children's Hospital, Huntlywood, 3 Styal Road, Wilmslow SK9 4AE, UK. 2009
  • Wilmslow, Cheshire, UK. 2009
  • Children's Hospitals, Manchester, UK. 2008
  • Huntlywood, 3 Styal Road, Wilmslow SK9 4AE, UK. 2002 - 2008
  • Wilmslow, UK. 2003


  1. Guanidinoacetate methyltransferase deficiency (GAMT). Gordon, N. Brain Dev. (2010) [Pubmed]
  2. Cerebral folate deficiency. Gordon, N. Dev. Med. Child. Neurol (2009) [Pubmed]
  3. Sydenham's chorea, and its complications affecting the nervous system. Gordon, N. Brain Dev. (2009) [Pubmed]
  4. Spontaneous intracranial hypotension. Gordon, N. Dev. Med. Child. Neurol (2009) [Pubmed]
  5. Segawa's disease: dopa-responsive dystonia. Gordon, N. Int. J. Clin. Pract. (2008) [Pubmed]
  6. Wiring of the brain. Gordon, N. Eur. J. Paediatr. Neurol. (2008) [Pubmed]
  7. Sjögren-Larsson syndrome. Gordon, N. Dev. Med. Child. Neurol (2007) [Pubmed]
  8. Glutaric aciduria types I and II. Gordon, N. Brain Dev. (2006) [Pubmed]
  9. Idiopathic intracranial hypertension. Gordon, N.S. Eur. J. Paediatr. Neurol. (2006) [Pubmed]
  10. Alpers syndrome: progressive neuronal degeneration of children with liver disease. Gordon, N. Dev. Med. Child. Neurol (2006) [Pubmed]
  11. Acyl-CoA dehydrogenase deficiency: varieties with neurological involvement. Gordon, N. Dev. Med. Child. Neurol (2005) [Pubmed]
  12. Focal dystonia, with special reference to writer's cramp. Gordon, N.S. Int. J. Clin. Pract. (2005) [Pubmed]
  13. Unexpected development of artistic talents. Gordon, N. Postgrad. Med. J (2005) [Pubmed]
  14. The neurology of sign language. Gordon, N. Brain Dev. (2004) [Pubmed]
  15. Succinic semialdehyde dehydrogenase deficiency (SSADH) (4-hydroxybutyric aciduria, gamma-hydroxybutyric aciduria). Gordon, N. Eur. J. Paediatr. Neurol. (2004) [Pubmed]
  16. Giant axonal neuropathy. Gordon, N. Dev. Med. Child. Neurol (2004) [Pubmed]
  17. Ornithine transcarbamylase deficiency: a urea cycle defect. Gordon, N. Eur. J. Paediatr. Neurol. (2003) [Pubmed]
  18. Glycogenosis type V or McArdle's disease. Gordon, N. Dev. Med. Child. Neurol (2003) [Pubmed]
  19. Glucose transporter type1 (GLUT-1) deficiency. Gordon, N., Newton, R.W. Brain Dev. (2003) [Pubmed]
  20. Alexander disease. Gordon, N. Eur. J. Paediatr. Neurol. (2003) [Pubmed]
  21. Sleep apnoea in infancy and childhood. Considering two possible causes: obstruction and neuromuscular disorders. Gordon, N. Brain Dev. (2002) [Pubmed]
  22. Stuttering: incidence and causes. Gordon, N. Dev. Med. Child. Neurol (2002) [Pubmed]
  23. Worster-drought and congenital bilateral perisylvian syndromes. Gordon, N. Dev. Med. Child. Neurol (2002) [Pubmed]
  24. Pantothenate kinase-associated neurodegeneration (Hallervorden-Spatz syndrome). Gordon, N. Eur. J. Paediatr. Neurol. (2002) [Pubmed]
  25. Infantile neuroaxonal dystrophy (Seitelberger's disease). Gordon, N. Dev. Med. Child. Neurol (2002) [Pubmed]
  26. Sudden unexpected death in epilepsy. Gordon, N. Dev. Med. Child. Neurol (2001) [Pubmed]
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