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

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Patrick F. Chinnery

Mitochondrial Research Group and Institute of Human Genetics

Newcastle University

The Medical School

Framlington Place

UK

[email]@ncl.ac.uk

Name/email consistency: high

 
 
 
 
 
 
 

Affiliations

  • Mitochondrial Research Group and Institute of Human Genetics, Newcastle University, The Medical School, Framlington Place, UK. 2007 - 2010
  • Institutes for Ageing and Health and Human Genetics, Newcastle University, Newcastle upon Tyne NE2 4HH, UK. 2010
  • Mitochondrial Research Group, Newcastle University, Newcastle upon Tyne, UK. 2005 - 2007
  • Department of Neurology, the University of Newcastle upon Tyne, UK. 2001 - 2007
  • Department of Neurology, The University of Newcastle upon Tyne, The Medical School, Framlington Place, United Kingdom. 1999 - 2006
  • Newcastle upon Tyne, United Kingdom. 2004
  • Neurology, The Medical School, Framlington Place, NE2 4HH, UK. 2003

References

  1. Defining neurogenetic phenotypes (or how to compare needles in haystacks). Chinnery, P.F. Brain (2010) [Pubmed]
  2. Mitochondrial DNA haplogroups and risk of transient ischaemic attack and ischaemic stroke: a genetic association study. Chinnery, P.F., Elliott, H.R., Syed, A., Rothwell, P.M. Lancet. Neurol (2010) [Pubmed]
  3. 155th ENMC workshop: polymerase gamma and disorders of mitochondrial DNA synthesis, 21-23 September 2007, Naarden, The Netherlands. Chinnery, P.F., Zeviani, M. Neuromuscul. Disord. (2008) [Pubmed]
  4. Mitochondrial DNA haplogroups and type 2 diabetes: a study of 897 cases and 1010 controls. Chinnery, P.F., Mowbray, C., Patel, S.K., Elson, J.L., Sampson, M., Hitman, G.A., McCarthy, M.I., Hattersley, A.T., Walker, M. J. Med. Genet. (2007) [Pubmed]
  5. Clinical features and natural history of neuroferritinopathy caused by the FTL1 460InsA mutation. Chinnery, P.F., Crompton, D.E., Birchall, D., Jackson, M.J., Coulthard, A., Lombès, A., Quinn, N., Wills, A., Fletcher, N., Mottershead, J.P., Cooper, P., Kellett, M., Bates, D., Burn, J. Brain (2007) [Pubmed]
  6. Mutations in SUCLA2: a tandem ride back to the Krebs cycle. Chinnery, P.F. Brain (2007) [Pubmed]
  7. Treatment for mitochondrial disorders. Chinnery, P., Majamaa, K., Turnbull, D., Thorburn, D. Cochrane. Database. Syst. Rev (2006) [Pubmed]
  8. Role of the mitochondrial DNA 16184-16193 poly-C tract in type 2 diabetes. Chinnery, P.F., Elliott, H.R., Patel, S., Lambert, C., Keers, S.M., Durham, S.E., McCarthy, M.I., Hitman, G.A., Hattersley, A.T., Walker, M. Lancet (2005) [Pubmed]
  9. Genetics in reverse. Chinnery, P.F., Cartlidge, N.E., Tennant, S., Birchall, D., Stenhouse, S.A. Lancet (2004) [Pubmed]
  10. New approaches to the treatment of mitochondrial disorders. Chinnery, P.F. Reprod. Biomed. Online (2004) [Pubmed]
  11. Limbic encephalitis: Not a picture to forget. Chinnery, P.F., Cottrell, D.A., Birchall, D., Griffiths, T.D. Neurology (2004) [Pubmed]
  12. Risk of developing a mitochondrial DNA deletion disorder. Chinnery, P.F., DiMauro, S., Shanske, S., Schon, E.A., Zeviani, M., Mariotti, C., Carrara, F., Lombes, A., Laforet, P., Ogier, H., Jaksch, M., Lochmüller, H., Horvath, R., Deschauer, M., Thorburn, D.R., Bindoff, L.A., Poulton, J., Taylor, R.W., Matthews, J.N., Turnbull, D.M. Lancet (2004) [Pubmed]
  13. Infantile hereditary spastic paraparesis due to codominant mutations in the spastin gene. Chinnery, P.F., Keers, S.M., Holden, M.J., Ramesh, V., Dalton, A. Neurology (2004) [Pubmed]
  14. Searching for nuclear-mitochondrial genes. Chinnery, P.F. Trends Genet. (2003) [Pubmed]
  15. Neuroferritinopathy in a French family with late onset dominant dystonia. Chinnery, P.F., Curtis, A.R., Fey, C., Coulthard, A., Crompton, D., Curtis, A., Lombés, A., Burn, J. J. Med. Genet. (2003) [Pubmed]
  16. Clinical progression of mitochondrial myopathy is associated with the random accumulation of cytochrome c oxidase negative skeletal muscle fibres. Chinnery, P.F., Howel, D., Turnbull, D.M., Johnson, M.A. J. Neurol. Sci. (2003) [Pubmed]
  17. Mitochondria. Chinnery, P.F., Schon, E.A. J. Neurol. Neurosurg. Psychiatr. (2003) [Pubmed]
  18. 116th ENMC international workshop: the treatment of mitochondrial disorders, 14th-16th March 2003, Naarden, The Netherlands. Chinnery, P.F., Bindoff, L.A. Neuromuscul. Disord. (2003) [Pubmed]
  19. Late-onset axial jerky dystonia due to the DYT1 deletion. Chinnery, P.F., Reading, P.J., McCarthy, E.L., Curtis, A., Burn, D.J. Mov. Disord. (2002) [Pubmed]
  20. Modulating heteroplasmy. Chinnery, P.F. Trends Genet. (2002) [Pubmed]
  21. Normokalemic periodic paralysis revisited: does it exist?. Chinnery, P.F., Walls, T.J., Hanna, M.G., Bates, D., Fawcett, P.R. Ann. Neurol. (2002) [Pubmed]
  22. Accumulation of mitochondrial DNA mutations in ageing, cancer, and mitochondrial disease: is there a common mechanism?. Chinnery, P.F., Samuels, D.C., Elson, J., Turnbull, D.M. Lancet (2002) [Pubmed]
  23. Inheritance of mitochondrial disorders. Chinnery, P.F. Mitochondrion (2002) [Pubmed]
  24. Leber hereditary optic neuropathy: Does heteroplasmy influence the inheritance and expression of the G11778A mitochondrial DNA mutation?. Chinnery, P.F., Andrews, R.M., Turnbull, D.M., Howell, N.N. Am. J. Med. Genet. (2001) [Pubmed]
  25. No correlation between muscle A3243G mutation load and mitochondrial function in vivo. Chinnery, P.F., Taylor, D.J., Manners, D., Styles, P., Lodi, R. Neurology (2001) [Pubmed]
  26. The spectrum of hearing loss due to mitochondrial DNA defects. Chinnery, P.F., Elliott, C., Green, G.R., Rees, A., Coulthard, A., Turnbull, D.M., Griffiths, T.D. Brain (2000) [Pubmed]
  27. Relaxed replication of mtDNA: A model with implications for the expression of disease. Chinnery, P.F., Samuels, D.C. Am. J. Hum. Genet. (1999) [Pubmed]
  28. Nonrandom tissue distribution of mutant mtDNA. Chinnery, P.F., Zwijnenburg, P.J., Walker, M., Howell, N., Taylor, R.W., Lightowlers, R.N., Bindoff, L., Turnbull, D.M. Am. J. Med. Genet. (1999) [Pubmed]
 
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