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

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Lorraine N. Clark

Taub Institute for Research on Alzheimer's Disease and the Aging Brain

College of Physicians and Surgeons

Columbia University

New York

USA

[email]@columbia.edu

Name/email consistency: high

 
 
 
 
 
 
 

Affiliations

  • Taub Institute for Research on Alzheimer's Disease and the Aging Brain, College of Physicians and Surgeons, Columbia University, New York, USA. 2004 - 2011
  • Department of Pathology, Columbia University, New York, New York 10032, USA. 2003 - 2007
  • Institute for Cancer Genetics, Columbia University College of Physicians and Surgeons, New York, USA. 2002

References

  1. Genome-Wide association study identifies candidate genes for Parkinson's disease in an Ashkenazi Jewish population. Liu, X., Cheng, R., Verbitsky, M., Kisselev, S., Browne, A., Mejia-Sanatana, H., Louis, E.D., Cote, L.J., Andrews, H., Waters, C., Ford, B., Frucht, S., Fahn, S., Marder, K., Clark, L.N., Lee, J.H. BMC Med. Genet. (2011) [Pubmed]
  2. Replication of the LINGO1 gene association with essential tremor in a North American population. Clark, L.N., Park, N., Kisselev, S., Rios, E., Lee, J.H., Louis, E.D. Eur. J. Hum. Genet. (2010) [Pubmed]
  3. Mutations in the Parkinson's disease genes, Leucine Rich Repeat Kinase 2 (LRRK2) and Glucocerebrosidase (GBA), are not associated with essential tremor. Clark, L.N., Kisselev, S., Park, N., Ross, B., Verbitsky, M., Rios, E., Alcalay, R.N., Lee, J.H., Louis, E.D. Parkinsonism Relat. Disord. (2010) [Pubmed]
  4. Mutations in the glucocerebrosidase gene are associated with early-onset Parkinson disease. Clark, L.N., Ross, B.M., Wang, Y., Mejia-Santana, H., Harris, J., Louis, E.D., Cote, L.J., Andrews, H., Fahn, S., Waters, C., Ford, B., Frucht, S., Ottman, R., Marder, K. Neurology (2007) [Pubmed]
  5. Construction and validation of a Parkinson's disease mutation genotyping array for the Parkin gene. Clark, L.N., Haamer, E., Mejia-Santana, H., Harris, J., Lesage, S., Durr, A., Bs, S.J., Hedrich, K., Louis, E.D., Cote, L.J., Andrews, H., Fahn, S., Waters, C., Ford, B., Frucht, S., Scott, W., Klein, C., Brice, A., Roomere, H., Ottman, R., Marder, K. Mov. Disord. (2007) [Pubmed]
  6. Case-control study of the parkin gene in early-onset Parkinson disease. Clark, L.N., Afridi, S., Karlins, E., Wang, Y., Mejia-Santana, H., Harris, J., Louis, E.D., Cote, L.J., Andrews, H., Fahn, S., Waters, C., Ford, B., Frucht, S., Ottman, R., Marder, K. Arch. Neurol. (2006) [Pubmed]
  7. Frequency of LRRK2 mutations in early- and late-onset Parkinson disease. Clark, L.N., Wang, Y., Karlins, E., Saito, L., Mejia-Santana, H., Harris, J., Louis, E.D., Cote, L.J., Andrews, H., Fahn, S., Waters, C., Ford, B., Frucht, S., Ottman, R., Marder, K. Neurology (2006) [Pubmed]
  8. Pilot association study of the beta-glucocerebrosidase N370S allele and Parkinson's disease in subjects of Jewish ethnicity. Clark, L.N., Nicolai, A., Afridi, S., Harris, J., Mejia-Santana, H., Strug, L., Cote, L.J., Louis, E.D., Andrews, H., Waters, C., Ford, B., Frucht, S., Fahn, S., Mayeux, R., Ottman, R., Marder, K. Mov. Disord. (2005) [Pubmed]
  9. Analysis of an early-onset Parkinson's disease cohort for DJ-1 mutations. Clark, L.N., Afridi, S., Mejia-Santana, H., Harris, J., Louis, E.D., Cote, L.J., Andrews, H., Singleton, A., Wavrant De-Vrieze, F., Hardy, J., Mayeux, R., Fahn, S., Waters, C., Ford, B., Frucht, S., Ottman, R., Marder, K. Mov. Disord. (2004) [Pubmed]
  10. The Saitohin 'Q7R' polymorphism and tau haplotype in multi-ethnic Alzheimer disease and Parkinson's disease cohorts. Clark, L.N., Levy, G., Tang, M.X., Mejia-Santana, H., Ciappa, A., Tycko, B., Cote, L.J., Louis, E.D., Mayeux, R., Marder, K. Neurosci. Lett. (2003) [Pubmed]
  11. The Tnfrh1 (Tnfrsf23) gene is weakly imprinted in several organs and expressed at the trophoblast-decidua interface. Clark, L., Wei, M., Cattoretti, G., Mendelsohn, C., Tycko, B. BMC Genet. (2002) [Pubmed]
 
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