Florence Quélin

Thrombin generation in patients with factor XI deficiency and clinical bleeding risk

Lucia Rugeri, Florence Quélin, B. Chatard et al. · Haemophilia · 2010 · 78 citations

Medicine, Hematology, Hematology Physiology +16

Molecular basis of severe factor XI deficiency in seven families from the west of France. Seven novel mutations, including an ancient Q88X mutation

Florence Quélin, Marc Trossaërt, Marianne Sigaud et al. · Journal of Thrombosis and Haemostasis · 2004 · 61 citations · Full text

Life Sciences, Genetics, Molecular Genetics +8

Fibrinogen angers with a new deletion (γ GVYYQ 346‐350) causes hypofibrinogenemia with hepatic storage

Nina Dib, Florence Quélin, Catherine Ternisien et al. · Journal of Thrombosis and Haemostasis · 2007 · 35 citations · Full text

Life Sciences, Genetics, Molecular Genetics +9

Identification of five novel mutations in the factor XI gene (F11) of patients with factor XI deficiency

Florence Quélin, Florence Mathonnet, Catherine Potentini-Esnault et al. · Blood Coagulation & Fibrinolysis · 2005 · 21 citations

Life Sciences, Genetics, Molecular Genetics +16

The natural occurrence of human fibrinogen variants disrupting inter-chain disulfide bonds (A Cys36Gly, A Cys36Arg and A Cys45Tyr) confirms the role of N-terminal A  disulfide bonds in protein assembly and secretion

Michel Hanss, Catherine Pouymayou, M. T. Blouch et al. · Haematologica · 2011 · 12 citations · Full text

Life Sciences, Biochemistry, Molecular Biology +13