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

Marguerite Neerman-Arbez

Department of Genetic Medicine and Development

University Medical School

University of Geneva




Name/email consistency: high



  • Department of Genetic Medicine and Development, University Medical School, University of Geneva, Geneva, Switzerland. 1999 - 2007
  • Centre Médical Universitaire, Geneva, Switzerland. 2001


  1. Mutations in the fibrinogen gene cluster accounting for congenital afibrinogenemia: an update and report of 10 novel mutations. Neerman-Arbez, M., de Moerloose, P. Hum. Mutat. (2007) [Pubmed]
  2. Molecular basis of fibrinogen deficiency. Neerman-Arbez, M. Pathophysiol. Haemost. Thromb. (2006) [Pubmed]
  3. Expression and analysis of a split premature termination codon in FGG responsible for congenital afibrinogenemia: escape from RNA surveillance mechanisms in transfected cells. Neerman-Arbez, M., Germanos-Haddad, M., Tzanidakis, K., Vu, D., Deutsch, S., David, A., Morris, M.A., de Moerloose, P. Blood (2004) [Pubmed]
  4. Prenatal diagnosis for congenital afibrinogenemia caused by a novel nonsense mutation in the FGB gene in a Palestinian family. Neerman-Arbez, M., Vu, D., Abu-Libdeh, B., Bouchardy, I., Morris, M.A. Blood (2003) [Pubmed]
  5. Molecular analysis of the fibrinogen gene cluster in 16 patients with congenital afibrinogenemia: novel truncating mutations in the FGA and FGG genes. Neerman-Arbez, M., de Moerloose, P., Honsberger, A., Parlier, G., Arnuti, B., Biron, C., Borg, J.Y., Eber, S., Meili, E., Peter-Salonen, K., Ripoll, L., Vervel, C., d'Oiron, R., Staeger, P., Antonarakis, S.E., Morris, M.A. Hum. Genet. (2001) [Pubmed]
  6. Fibrinogen gene mutations accounting for congenital afibrinogenemia. Neerman-Arbez, M. Ann. N. Y. Acad. Sci. (2001) [Pubmed]
  7. The molecular basis of inherited afibrinogenaemia. Neerman-Arbez, M. Thromb. Haemost. (2001) [Pubmed]
  8. Mutations in the fibrinogen aalpha gene account for the majority of cases of congenital afibrinogenemia. Neerman-Arbez, M., de Moerloose, P., Bridel, C., Honsberger, A., Schönbörner, A., Rossier, C., Peerlinck, K., Claeyssens, S., Di Michele, D., d'Oiron, R., Dreyfus, M., Laubriat-Bianchin, M., Dieval, J., Antonarakis, S.E., Morris, M.A. Blood (2000) [Pubmed]
  9. The 11 kb FGA deletion responsible for congenital afibrinogenaemia is mediated by a short direct repeat in the fibrinogen gene cluster. Neerman-Arbez, M., Antonarakis, S.E., Honsberger, A., Morris, M.A. Eur. J. Hum. Genet. (1999) [Pubmed]
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