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Christine Vinciguerra

Observed names: C Vinciguerra, C. VINCIGUERRA, C. Vinciguerra, Christine VINCIGUERRA, Christine Vinciguera, Christine Vinciguerra. Coordinateur Claude Négrier, Christine Vinciguerrat, Vinciguerra, Christine
Observed institutions: Lyon 1 Université, University of Geneva, Cincinnati Children's Hospital Medical Center, Hôpital Necker-Enfants Malades, University of Bonn, Inserm, Institut Pasteur, Saint Joseph University, Université de Lyon, Assistance Publique – Hôpitaux de Paris, Yokohama City University Hospital, Hospices Civils de Lyon, Hôpital Edouard Herriot, Hôpital Purpan, Hôtel-Dieu de France, Hôpital de la Timone, Bicêtre Hospital, Hémostase & Thrombose
ORCID: 0000-0002-1676-9872
Observed ORCID: 0000-0002-1676-9872
OpenAlex ID: A5059337487
Factor VIII gene inversions in severe hemophilia A: results of an international consortium study
1995 · SE Antonarakis, JP Rossiter, et al. · Blood · 357
Influence of the type of factor VIII concentrate on the incidence of factor VIII inhibitors in previously untreated patients with severe hemophilia A
2005 · Jenny Goudemand, Chantal Rothschild, et al. · Blood · 300
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Recombinant factor VIII products and inhibitor development in previously untreated boys with severe hemophilia A
2014 · Thierry Calvez, Hervé Chambost, et al. · Blood · 151
Expanding the Mutation Spectrum Affecting αIIbβ3 Integrin in Glanzmann Thrombasthenia: Screening of theITGA2BandITGB3Genes in a Large International Cohort
2015 · Alan T. Nurden, Xavier Pillois, et al. · Human Mutation · 98
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ERGIC-53 gene structure and mutation analysis in 19 combined factors V and VIII deficiency families.
1999 · W C Nichols, V H Terry, et al. · PubMed · 89
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
2017 · Thierry Calvez, Hervé Chambost, et al. · Haematologica · 65
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PFMG2025–integrating genomic medicine into the national healthcare system in France
2025 · Caroline Abadie, Aldja Abderrahmane, et al. · The Lancet Regional Health - Europe · 61
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Skewed X-chromosome inactivation in monochorionic diamniotic twin sisters results in severe and mild hemophilia A
2002 · Sophie Valleix, Christine Vinciguerra, et al. · Blood · 36
Reccurrent F8 Intronic Deletion Found in Mild Hemophilia A Causes Alu Exonization
2018 · Yohann Jourdy, Alexandre Janin, et al. · The American Journal of Human Genetics · 33
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Two novel mutations in EGF‐like domains of human factor IX dramatically impair intracellular processing and secretion
2004 · N. Enjolras, J‐L. Plantier, et al. · Journal of Thrombosis and Haemostasis · 30
LETTERS TO THE EDITOR: Four cases of hypofibrinogenemia associated with four novel mutations
2005 · M. HANSS, P. FFRENCH, et al. · Journal of Thrombosis and Haemostasis · 23
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Synthesis of GPIbβ with novel transmembrane and cytoplasmic sequences in a Bernard–Soulier patient resulting in GPIb‐defective signaling in CHO cells
2005 · C. STRASSEL, T. DAVID, et al. · Journal of Thrombosis and Haemostasis · 22
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Characterisation of 96 mutations in 128 unrelated severe haemophilia A patients from France
2006 · Christine Vinciguerra, Christophe Zawadzki, et al. · Thrombosis and Haemostasis · 19
Biliary lithiasis in early pregnancy and abnormal development of facial and distal limb bones (Binder syndrome): A possible role for vitamin K deficiency
2005 · Jessica Jaillet, Elisabeth Robert-Gnansia, et al. · Birth Defects Research Part A Clinical and Molecular Teratology · 19
Description of 10 new mutations in platelet glycoprotein IIb (αIIb) and glycoprotein IIIa (β3) genes
2001 · C. Vinciguerra, J. C. Bordet, et al. · Platelets · 19
A nonsense mutation in the GPIIb heavy chain (Ser 870 → stop) impairs platelet GPIIb–IIIa expression
1996 · C. VINCIGUERRA, A. KHELIF, et al. · British Journal of Haematology · 19
Molecular Study of Glanzmann Thrombasthenia in 3 Patients Issued from 2 Different Families
1995 · C Vinciguerra, M C Trzeciak, et al. · Thrombosis and Haemostasis · 19
Identification of new F8 deep intronic variations in patients with haemophilia A
2020 · Amy Dericquebourg, Yohann Jourdy, et al. · Haemophilia · 17
Splicing analysis of 26 F8 nucleotide variations using a minigene assay
2019 · Yohann Jourdy, Mathilde Fretigny, et al. · Haemophilia · 16
Characterization of five associations of F8 missense mutations containing FVIII B domain mutations
2016 · Y. Jourdy, C. Nougier, et al. · Haemophilia · 16
First report of molecular diagnosis of Tunisian hemophiliacs A: Identification of 8 novel causative mutations
2012 · Hejer Elmahmoudi, Houssein Khodjet-el-khil, et al. · Diagnostic Pathology · 16
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Severe hemophilia A caused by an unbalanced chromosomal rearrangement identified using nanopore sequencing
2019 · Nicolas Chatron, Caroline Schluth‐Bolard, et al. · Journal of Thrombosis and Haemostasis · 15
Study of six patients with complete F9 deletion characterized by cytogenetic microarray: role of the SOX3 gene in intellectual disability
2016 · Y. Jourdy, N. Chatron, et al. · Journal of Thrombosis and Haemostasis · 15
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Molecular cytogenetic characterization of five F8 complex rearrangements: utility for haemophilia A genetic counselling
2017 · Y. Jourdy, N. Chatron, et al. · Haemophilia · 13
Rapid diagnosis of the French gypsy mutation in Glanzmann thrombasthenia using high-resolution melting analysis
2010 · Mathieu Fiore, Christine Vinciguerra, et al. · Thrombosis and Haemostasis · 13
Works count: 75
Citation count: 1,658
H-index: 17
I10-index: 29
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