| Factor VIII gene inversions in severe hemophilia A: results of an international consortium study SE Antonarakis, JP Rossiter, M Young, J Horst, P De Moerloose, ... | 471 | 1995 |
| Influence of the type of factor VIII concentrate on the incidence of factor VIII inhibitors in previously untreated patients with severe hemophilia A CT Goudemand.J, Rothschild. C, Demiguel. V, Vinciguerrat.C, Lambert.T ... Blood 107, 46-51, 2006 | 367 | 2006 |
| Recombinant factor VIII products and inhibitor development in previously untreated boys with severe hemophilia A T Calvez, H Chambost, S Claeyssens-Donadel, R d’Oiron, V Goulet, ... Blood, The Journal of the American Society of Hematology 124 (23), 3398-3408, 2014 | 183 | 2014 |
| ERGIC-53 gene structure and mutation analysis in 19 combined factors V and VIII deficiency families WC Nichols, VH Terry, MA Wheatley, A Yang, A Zivelin, N Ciavarella, ... Blood, The Journal of the American Society of Hematology 93 (7), 2261-2266, 1999 | 104 | 1999 |
| Expanding the Mutation Spectrum Affecting αIIbβ3 Integrin in Glanzmann Thrombasthenia: Screening of the ITGA2B and ITGB3 Genes in a Large International … AT Nurden, X Pillois, M Fiore, MC Alessi, M Bonduel, M Dreyfus, ... Human mutation 36 (5), 548-561, 2015 | 88 | 2015 |
| Analyses of the FranceCoag cohort support differences in immunogenicity among one plasma-derived and two recombinant factor VIII brands in boys with severe hemophilia A T Calvez, H Chambost, R d’Oiron, V Dalibard, V Demiguel, A Doncarli, ... Haematologica 103 (1), 179, 2018 | 62 | 2018 |
| Skewed X-chromosome inactivation in monochorionic diamniotic twin sisters results in severe and mild hemophilia A S Valleix, C Vinciguerra, JM Lavergne, M Leuer, M Delpech, C Negrier Blood, The Journal of the American Society of Hematology 100 (8), 3034-3036, 2002 | 45 | 2002 |
| A case of Glanzmann's thrombasthenia successfully treated with recombinant factor viia during a surgical procedure: observations on the monitoring and the mechanism of action … Y Dargaud, JC Bordet, MC Trzeciak, C Vinciguerra, C Negrier Haematologica 91 (6_Suppl), ECR20-ECR20, 2006 | 44 | 2006 |
| First molecular characterization of an unequal homologous alu-mediated recombination event responsible for hemophilia F Vidal, E Farssac, J Tusell, L Puig, D Gallardo Thrombosis and haemostasis 88 (07), 12-16, 2002 | 40 | 2002 |
| Factor IX gene analysis in 70 unrelated patients with haemophilia B: description of 13 new mutations O Attali, C Vinciguerra, MC Trzeciak, A Durin, G Pernod, V Gay, C Menart, ... Thrombosis and haemostasis 82 (11), 1437-1442, 1999 | 35 | 1999 |
| Two novel mutations in EGF‐like domains of human factor IX dramatically impair intracellular processing and secretion N Enjolras, JL Plantier, MH Rodriguez, M Rea, O Attali, C Vinciguerra, ... Journal of Thrombosis and Haemostasis 2 (7), 1143-1154, 2004 | 32 | 2004 |
| Reccurrent F8 intronic deletion found in mild hemophilia a causes alu exonization Y Jourdy, A Janin, M Fretigny, A Lienhart, C Négrier, D Bozon, ... The American Journal of Human Genetics 102 (2), 199-206, 2018 | 31 | 2018 |
| A nonsense mutation in the GPIIb heavy chain (Ser 870→ stop) impairs platelet GPIIb–IIIa expression C Vinciguerra, A Khelif, M Alemany, F Morle, C Grenier, G Uzan, D Gulino, ... British journal of haematology 95 (2), 399-407, 1996 | 31 | 1996 |
| Illegitimate transcription: its use for studying genetic abnormalities in lymphoblastoid cells from patients with Glanzmann thrombasthenia C Negrier, C Vinciguerra, O Attali, C Grenier, ME Larcher, M Dechavanne British journal of haematology 100 (1), 33-39, 1998 | 30 | 1998 |
| LETTERS TO THE EDITOR: Four cases of hypofibrinogenemia associated with four novel mutations M Hanss, P Ffrench, C Vinciguerra, MA Bertrand, P De Mazancourt Journal of Thrombosis and Haemostasis 3 (10), 2347-2349, 2005 | 29 | 2005 |
| Alloimmunization in Congenital Deficiencies of Platelet Surface Glycoproteins: Focus on Glanzmann's Thrombasthenia and Bernard–Soulier's Syndrome MC Poon, R d'Oiron Seminars in thrombosis and hemostasis 44 (06), 604-614, 2018 | 28 | 2018 |
| Synthesis of GPIbβ with novel transmembrane and cytoplasmic sequences in a Bernard–Soulier patient resulting in GPIb‐defective signaling in CHO cells C Strassel, T David, A Eckly, MJ BAAS, S Moog, C Ravanat, ... Journal of Thrombosis and Haemostasis 4 (1), 217-228, 2006 | 26 | 2006 |
| Description of 10 new mutations in platelet glycoprotein IIb (αIIb) and glycoprotein IIIa (β3) genes C Vinciguerra, JC Bordet, G Beaune, C Grenier, M Dechavanne, ... Platelets 12 (8), 486-495, 2001 | 26 | 2001 |
| Characterisation of 96 mutations in 128 unrelated severe haemophilia A patients from France C Vinciguerra, C Zawadzki, Y Dargaud, G Pernod, C Berger, C Nougier, ... Thrombosis and haemostasis 95 (04), 593-599, 2006 | 25 | 2006 |
| Nonsense mutation in exon-19 of GPIIb associated with thrombasthenic phenotype. Failure of GPIIb (Δ597-1008) to form stable complexes with GPIIIa EG Arias-Salgado, J Tao, C González-Manchón, N Butta, V Vicente, ... Thrombosis and haemostasis 87 (04), 684-691, 2002 | 25 | 2002 |
