Christine Vinciguerra

Author

Also Known As

C Vinciguerra, C. VINCIGUERRA, C. Vinciguerra, CHRISTINE VINCIGUERRA, Christine Vinciguerra, Christine Vinciguerrat, François Vialard, Vinciguerra, Christine

Publications

1.6K

Citations

H-Index

Concepts

All Affiliations

Inserm Hospices Civils de Lyon Université Claude Bernard Lyon 1 Hôpital Edouard Herriot Centre National de la Recherche Scientifique

About

Christine Vinciguerra is an author at Inserm specializing in medicine, genetics, and hematology.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	11	11	269
2	Cell Biology	3	3	62
3	Engineering	1	1	13
4	Health Sciences	1	1	14
5	Public Health	1	1	19

Christine Vinciguerra

Publications

1.4K

Citations

H-Index

Page 1

	Year	Citations
Factor VIII gene inversions in severe hemophilia A: results of an international consortium study JP Rossiter, Michele Young, J. Horst, Blood	1995	358
Influence of the type of factor VIII concentrate on the incidence of factor VIII inhibitors in previously untreated patients with severe hemophilia A Jenny Goudemand, Chantal Rothschild, Virginie Demiguel, Blood	2005	293
Recombinant factor VIII products and inhibitor development in previously untreated boys with severe hemophilia A Thierry Calvez, Hérvè Chambost, Ségolène Claeyssens‐Donadel, Blood	2014	148
ERGIC-53 gene structure and mutation analysis in 19 combined factors V and VIII deficiency families. William C. Nichols, Valeri H. Terry, Matthew Wheatley, PubMed	1999	92
Expanding the Mutation Spectrum Affecting αIIbβ3 Integrin in Glanzmann Thrombasthenia: Screening of the<i>ITGA2B</i>and<i>ITGB3</i>Genes in a Large International Cohort Alan T. Nurden, Xavier Pillois, Mathieu Fiore, Human Mutation Inherited Bleeding DisorderGeneticsMolecular BiologyPathologyPlatelet Pathobiology	2015	87
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 Thierry Calvez, Hérvè Chambost, Roseline d’Oiron, Haematologica	2017	59
Skewed X-chromosome inactivation in monochorionic diamniotic twin sisters results in severe and mild hemophilia A Sophie Valleix, Christine Vinciguerra, Jean‐Maurice Lavergne, Blood	2002	34
Two novel mutations in EGF‐like domains of human factor IX dramatically impair intracellular processing and secretion Nathalie Enjolras, J‐L. Plantier, M-H. E. Rodriguez, Journal of Thrombosis and Haemostasis Signal TransductionDevelopmental BiologyEgf‐like DomainsSignaling PathwayNovel Mutations	2004	28
Reccurrent F8 Intronic Deletion Found in Mild Hemophilia A Causes Alu Exonization Yohann Jourdy, Alexandre Janin, Mathilde Frétigny, The American Journal of Human Genetics GeneticsPathogenesisHematologyPathologyHeme Signaling	2018	28
A nonsense mutation in the GPIIb heavy chain (Ser 870 → stop) impairs platelet GPIIb–IIIa expression Christine Vinciguerra, Abderrahim Khélif, Mónica Alemany, British Journal of Haematology	1996	25

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