J. M. Lavergne

Haemophilia A: database of ncleotide substituttions, deletions, insertions and rearrangements of the factor VIII gene

Edward G. D. Tuddenham, D.N. Cooper, Jane Gitschier et al. · Nucleic Acids Research · 1991 · 119 citations · Full text

Repetitive Mutations, Allelic Variant, Genetic Disorder +15

Haemophilia B Due to a De Novo Insertion of a Human-Specific Alu Subfamily Member within the Coding Region of the Factor IX Gene

Dominique Vidaud, Michel Vidaud, Bruce R. Bahnak et al. · European Journal of Human Genetics · 1993 · 115 citations

Autoimmune Disease, Genetics, Pathogenesis +8

Ten candidate ADAMTS13 mutations in six French families with congenital thrombotic thrombocytopenic purpura (Upshaw–Schulman syndrome)

Agnès Veyradier, J. M. Lavergne, Anne‐Sophie Ribba et al. · Journal of Thrombosis and Haemostasis · 2004 · 113 citations · Full text

French Families, Genetic Disorder, Genetics +8

Factor VIII (FVIII) gene mutations in 120 patients with hemophilia A: detection of 26 novel mutations and correlation with FVIII inhibitor development

Yohann Repessé, M. Slaoui, D. Ferrandiz et al. · Journal of Thrombosis and Haemostasis · 2007 · 59 citations · Full text

Fviii Inhibitor Development, Pathogenesis, Hematology +4

Factor VIII genotype and inhibitor development in patients with haemophilia A: highest risk in patients with splice site mutations

J. C. A. Boekhorst, Ghasem Rastegar Lari, Roseline d’Oiron et al. · Haemophilia · 2008 · 43 citations

Genetics, Genetic Epidemiology, Immunology +18