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

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Joanna C. Jen

Department of Neurology

UCLA School of Medicine

Los Angeles

CA 90095-1769

USA

[email]@ucla.edu

Name/email consistency: high

 
 
 
 
 
 
 

Affiliations

  • Department of Neurology, UCLA School of Medicine, Los Angeles, CA 90095-1769, USA. 1999 - 2009
  • UCLA Neurology, Los Angeles, California, USA. 2009
  • UCLA Neurology, 90095-1769, USA. 2004
  • University of California at Los Angeles, Department of Neurology, 710 Westwood Plaza, Box 951769, USA. 2000

References

  1. Familial episodic ataxia: a model for migrainous vertigo. Jen, J.C., Baloh, R.W. Ann. N. Y. Acad. Sci. (2009) [Pubmed]
  2. Bilateral vestibulopathy: clinical, diagnostic, and genetic considerations. Jen, J.C. Semin. Neurol (2009) [Pubmed]
  3. Recent advances in the genetics of recurrent vertigo and vestibulopathy. Jen, J.C. Curr. Opin. Neurol. (2008) [Pubmed]
  4. Effects of failure of development of crossing brainstem pathways on ocular motor control. Jen, J.C. Prog. Brain Res. (2008) [Pubmed]
  5. Hereditary episodic ataxias. Jen, J.C. Ann. N. Y. Acad. Sci. (2008) [Pubmed]
  6. Prolonged hemiplegic episodes in children due to mutations in ATP1A2. Jen, J.C., Klein, A., Boltshauser, E., Cartwright, M.S., Roach, E.S., Mamsa, H., Baloh, R.W. J. Neurol. Neurosurg. Psychiatr. (2007) [Pubmed]
  7. Primary episodic ataxias: diagnosis, pathogenesis and treatment. Jen, J.C., Graves, T.D., Hess, E.J., Hanna, M.G., Griggs, R.C., Baloh, R.W. Brain (2007) [Pubmed]
  8. Genetic heterogeneity of autosomal dominant nonprogressive congenital ataxia. Jen, J.C., Lee, H., Cha, Y.H., Nelson, S.F., Baloh, R.W. Neurology (2006) [Pubmed]
  9. Clinical spectrum of episodic ataxia type 2. Jen, J., Kim, G.W., Baloh, R.W. Neurology (2004) [Pubmed]
  10. Mutations in a human ROBO gene disrupt hindbrain axon pathway crossing and morphogenesis. Jen, J.C., Chan, W.M., Bosley, T.M., Wan, J., Carr, J.R., Rüb, U., Shattuck, D., Salamon, G., Kudo, L.C., Ou, J., Lin, D.D., Salih, M.A., Kansu, T., Al Dhalaan, H., Al Zayed, Z., MacDonald, D.B., Stigsby, B., Plaitakis, A., Dretakis, E.K., Gottlob, I., Pieh, C., Traboulsi, E.I., Wang, Q., Wang, L., Andrews, C., Yamada, K., Demer, J.L., Karim, S., Alger, J.R., Geschwind, D.H., Deller, T., Sicotte, N.L., Nelson, S.F., Baloh, R.W., Engle, E.C. Science (2004) [Pubmed]
  11. No mutations in CACNA1A and ATP1A2 in probands with common types of migraine. Jen, J.C., Kim, G.W., Dudding, K.A., Baloh, R.W. Arch. Neurol. (2004) [Pubmed]
  12. Suggestive linkage to chromosome 6q in families with bilateral vestibulopathy. Jen, J.C., Wang, H., Lee, H., Sabatti, C., Trent, R., Hannigan, I., Brantberg, K., Halmagyi, G.M., Nelson, S.F., Baloh, R.W. Neurology (2004) [Pubmed]
  13. Familial horizontal gaze palsy with progressive scoliosis maps to chromosome 11q23-25. Jen, J., Coulin, C.J., Bosley, T.M., Salih, M.A., Sabatti, C., Nelson, S.F., Baloh, R.W. Neurology (2002) [Pubmed]
  14. Loss-of-function EA2 mutations are associated with impaired neuromuscular transmission. Jen, J., Wan, J., Graves, M., Yu, H., Mock, A.F., Coulin, C.J., Kim, G., Yue, Q., Papazian, D.M., Baloh, R.W. Neurology (2001) [Pubmed]
  15. Familial Episodic Ataxias and Related Ion Channel Disorders. Jen, J. Curr. Treat. Options. Neurol (2000) [Pubmed]
  16. Calcium channelopathies in the central nervous system. Jen, J. Curr. Opin. Neurobiol. (1999) [Pubmed]
  17. A novel nonsense mutation in CACNA1A causes episodic ataxia and hemiplegia. Jen, J., Yue, Q., Nelson, S.F., Yu, H., Litt, M., Nutt, J., Baloh, R.W. Neurology (1999) [Pubmed]
 
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