Nicolas Ferrari

Genotypic analysis of thiopurine S-methyltransferase in patients with Crohn's disease and severe myelosuppression during azathioprine therapy

Jean‐Frédéric Colombel, Nicolas Ferrari, Hervé Debuysère et al. · Gastroenterology · 2000 · 614 citations

Inflammation, Autoimmune Disease, Immunology +6

CHARACTERISATION AND USE OF AN INTRAGENIC POLYMORPHIC MARKER FOR DETECTION OF CARRIERS OF HAEMOPHILIA B (FACTOR IX DEFICIENCY)

F. Giannelli, K.H. Andy Choo, Peter R. Winship et al. · The Lancet · 1984 · 128 citations

Factor Ix Deficiency, Haplotype Determination, Medicine +10

Characterization of new mutations in the coding sequence and 5'-untranslated region of the human prostacyclin synthase gene ( CYP8A1)

Dany Chevalier, Christelle Cauffiez, Claudine Bernard et al. · Human Genetics · 2001 · 39 citations

5'-Untranslated Region, New Mutations, Natural Sciences +10

Identification of genetic variants in the human thromboxane synthase gene (CYP5A1)

Dany Chevalier, Jean‐Marc Lo‐Guidice, Elodie Sergent et al. · Mutation Research/Mutation Research Genomics · 2001 · 32 citations

Genetic Variants, Genetic Disorder, Medicine +10

Thiopurine S-methyltransferase genotyping does not predict azathioprine-induced myelosuppression in Crohn's disease

Mimouna Seddik, Frédéric Texier, Nicolas Ferrari et al. · Gastroenterology · 2003 · 10 citations

Inflammation, Autoimmune Disease, Azathioprine-induced Myelosuppression +7