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

Alexander Lossos

The Agnes Ginges Center for Human Neurogenetics

Dept. of Neurology

Hadassah University Hospital

POB 12000

Israel

[email]@hadassah.org.il

Name/email consistency: high

 
 
 
 
 
 
 

Affiliations

  • The Agnes Ginges Center for Human Neurogenetics, Dept. of Neurology, Hadassah University Hospital, POB 12000, Israel. 2003 - 2006
  • Department of Neurology, Agnes Ginges Center for Human Neurogenetics, Jerusalem, Israel. 2005

References

  1. Phenotypic variability among adult siblings with Sjögren-Larsson syndrome. Lossos, A., Khoury, M., Rizzo, W.B., Gomori, J.M., Banin, E., Zlotogorski, A., Jaber, S., Abramsky, O., Argov, Z., Rosenmann, H. Arch. Neurol. (2006) [Pubmed]
  2. Hereditary spastic paraplegia with thin corpus callosum: reduction of the SPG11 interval and evidence for further genetic heterogeneity. Lossos, A., Stevanin, G., Meiner, V., Argov, Z., Bouslam, N., Newman, J.P., Gomori, J.M., Klebe, S., Lerer, I., Elleuch, N., Silverstein, S., Durr, A., Abramsky, O., Ben-Nariah, Z., Brice, A. Arch. Neurol. (2006) [Pubmed]
  3. A novel autosomal recessive myopathy with external ophthalmoplegia linked to chromosome 17p13.1-p12. Lossos, A., Baala, L., Soffer, D., Averbuch-Heller, L., Dotan, S., Munnich, A., Lyonnet, S., Gomori, J.M., Genem, A., Neufeld, M., Abramsky, O., Zlotogora, J., Argov, Z. Brain (2005) [Pubmed]
  4. Extended phenotype in the transthyretin Tyr77 familial amyloid polyneuropathy. Lossos, A., Soffer, D., Steiner-Birmanns, B., Hassin-Baer, S., Sadeh, M., Sagi, M., Linetski, E., Abramsky, O., Argov, Z., Rosenmann, H. Eur. Neurol. (2005) [Pubmed]
  5. Early clinical heterogeneity in choreoacanthocytosis. Lossos, A., Dobson-Stone, C., Monaco, A.P., Soffer, D., Rahamim, E., Newman, J.P., Mohiddin, S., Fananapazir, L., Lerer, I., Linetsky, E., Reches, A., Argov, Z., Abramsky, O., Gadoth, N., Sadeh, M., Gomori, J.M., Boher, M., Meiner, V. Arch. Neurol. (2005) [Pubmed]
  6. Late-delayed cerebral involvement in systemic non-Hodgkin lymphoma: a second primary tumor or a tardy recurrence?. Lossos, A., Ashhab, Y., Sverdlin, E., Amir, G., Ben-Yehuda, D., Siegal, T. Cancer (2004) [Pubmed]
  7. Frontotemporal dementia and parkinsonism with the P301S tau gene mutation in a Jewish family. Lossos, A., Reches, A., Gal, A., Newman, J.P., Soffer, D., Gomori, J.M., Boher, M., Ekstein, D., Biran, I., Meiner, Z., Abramsky, O., Rosenmann, H. J. Neurol. (2003) [Pubmed]
 
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