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Marco Tartaglia

Reparto di Genetica Molecolare

Laboratorio di Biologia Cellulare

Istituto Superiore di Sanità

Viale Regina Elena

Italy

[email]@iss.it

Name/email consistency: high

 
 
 
 
 
 
 

Affiliations

  • Reparto di Genetica Molecolare, Laboratorio di Biologia Cellulare, Istituto Superiore di Sanità, Viale Regina Elena, Italy. 1999 - 2007
  • Dipartimento di Biologia Cellulare e Neuroscienze, Istituto Superiore di Sanità, Italy. 2004 - 2006

References

  1. Gain-of-function SOS1 mutations cause a distinctive form of Noonan syndrome. Tartaglia, M., Pennacchio, L.A., Zhao, C., Yadav, K.K., Fodale, V., Sarkozy, A., Pandit, B., Oishi, K., Martinelli, S., Schackwitz, W., Ustaszewska, A., Martin, J., Bristow, J., Carta, C., Lepri, F., Neri, C., Vasta, I., Gibson, K., Curry, C.J., Siguero, J.P., Digilio, M.C., Zampino, G., Dallapiccola, B., Bar-Sagi, D., Gelb, B.D. Nat. Genet. (2007) [Pubmed]
  2. Diversity and functional consequences of germline and somatic PTPN11 mutations in human disease. Tartaglia, M., Martinelli, S., Stella, L., Bocchinfuso, G., Flex, E., Cordeddu, V., Zampino, G., Burgt, I., Palleschi, A., Petrucci, T.C., Sorcini, M., Schoch, C., Foa, R., Emanuel, P.D., Gelb, B.D. Am. J. Hum. Genet. (2006) [Pubmed]
  3. Somatic PTPN11 mutations in childhood acute myeloid leukaemia. Tartaglia, M., Martinelli, S., Iavarone, I., Cazzaniga, G., Spinelli, M., Giarin, E., Petrangeli, V., Carta, C., Masetti, R., Aricò, M., Locatelli, F., Basso, G., Sorcini, M., Pession, A., Biondi, A. Br. J. Haematol. (2005) [Pubmed]
  4. Germ-line and somatic PTPN11 mutations in human disease. Tartaglia, M., Gelb, B.D. Eur. J. Med. Genet (2005) [Pubmed]
  5. Noonan syndrome and related disorders: genetics and pathogenesis. Tartaglia, M., Gelb, B.D. Annu. Rev. Genomics. Hum. Genet (2005) [Pubmed]
  6. SHP-2 and myeloid malignancies. Tartaglia, M., Niemeyer, C.M., Shannon, K.M., Loh, M.L. Curr. Opin. Hematol. (2004) [Pubmed]
  7. Genetic evidence for lineage-related and differentiation stage-related contribution of somatic PTPN11 mutations to leukemogenesis in childhood acute leukemia. Tartaglia, M., Martinelli, S., Cazzaniga, G., Cordeddu, V., Iavarone, I., Spinelli, M., Palmi, C., Carta, C., Pession, A., Aricò, M., Masera, G., Basso, G., Sorcini, M., Gelb, B.D., Biondi, A. Blood (2004) [Pubmed]
  8. Paternal germline origin and sex-ratio distortion in transmission of PTPN11 mutations in Noonan syndrome. Tartaglia, M., Cordeddu, V., Chang, H., Shaw, A., Kalidas, K., Crosby, A., Patton, M.A., Sorcini, M., van der Burgt, I., Jeffery, S., Gelb, B.D. Am. J. Hum. Genet. (2004) [Pubmed]
  9. Fibroblast growth factor receptor mutational screening in newborns affected by metopic synostosis. Tartaglia, M., Bordoni, V., Velardi, F., Basile, R.T., Saulle, E., Tenconi, R., Di Rocco, C., Battaglia, P.A. Childs. Nerv. Syst (1999) [Pubmed]
 
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