C
Christiane Dross
Publications - 4
Citations - 1781
Christiane Dross is an academic researcher. The author has contributed to research in topics: Familial Mediterranean fever & MEFV. The author has an hindex of 3, co-authored 4 publications receiving 1686 citations.
Papers
More filters
Journal ArticleDOI
A candidate gene for familial Mediterranean fever
Alain Bernot,Christian Clepet,Corinne Dasilva,Catherine Devaud,Jean-Louis Petit,Christophe Caloustian,Corinne Cruaud,Delphine Samson,Françoise Pulcini,Jean Weissenbach,Roland Heilig,Cécile Notanicola,Cécile Domingo,Michael Rozenbaum,Eldad Ben-Chetrit,Rezzan Topaloglu,Marie Dewalle,Christiane Dross,Philippe Hadjari,Madeleine Dupont,Jacques Demaille,Isabelle Touitou,Nizar Smaoui,Brigitte Nedelec,Jean-Philippe Mery,Habiba Chaabouni,Marc Delpech,Gilles Grateau +27 more
TL;DR: A minimal co-segregating region of 60 kb containing the FMF gene (MEFV) is defined and one of these transcripts encodes a new protein (marenostrin) related to the ret-finger protein and to butyrophilin.
Journal ArticleDOI
Non-Founder Mutations in the MEFV Gene Establish This Gene as the Cause of Familial Mediterranean Fever (FMF)
Alain Bernot,Corinne Da Silva,Jean-Louis Petit,Corinne Cruaud,Christophe Caloustian,Valérie Castet,Mehdi Ahmed-Arab,Christiane Dross,Madeleine Dupont,Daniel Cattan,Nizar Smaoui,Catherine Dodé,Christophe Pêcheux,Brigitte Nedelec,Jean Medaxian,Michel Rozenbaum,Itshak Rosner,Marc Delpech,Gilles Grateau,Jacques Demaille,Jean Weissenbach,Isabelle Touitou +21 more
TL;DR: The marenostrin/pyrin-encoding gene is definitively established as the MEFV locus, and mutations found in 120 apparently non-founder FMF chromosomes are confirmed.
Journal ArticleDOI
Phenotype-genotype correlation in Jewish patients suffering from familial Mediterranean fever (FMF).
Marie Dewalle,Cécile Domingo,Michel Rozenbaum,Eldad Ben-Chetrit,Daniel Cattan,Alain Bernot,Christiane Dross,Madeleine Dupont,Cécile Notarnicola,Micha Levy,Itzhak Rosner,Jacques Demaille,Isabelle Touitou +12 more
TL;DR: It was shown that homozygosity for this mutation was significantly associated with a more severe form of the disease and the present result strongly suggests the potential prognostic value of the presence of this mutation.