Lysiane Hilbert

869 citations

20 papers · 586 indexed · h-index 14

Co-authors: Claudine Mazurier Dominique Meyer Christine Gaucher Anne‐Sophie Ribba E Fressinaud Jenny Goudemand Édith Fressinaud Claudine Caron
Topics: Platelet Disorders and Treatments (20 papers)Blood groups and transfusion (13 papers)Blood disorders and treatments (8 papers)
Cited by: Hematology Immunology Genetics
Journals: Blood British Journal of Haematology Thrombosis and Haemostasis
Partner nations: France Switzerland Italy

In The Last Decade

Lysiane Hilbert

20 papers receiving 560 citations

Peers

Countries citing papers authored by Lysiane Hilbert

Since Specialization

Citations

This map shows the geographic impact of Lysiane Hilbert's research. It shows the number of citations coming from papers published by authors working in each country. You can also color the map by specialization and compare the number of citations received by Lysiane Hilbert with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Lysiane Hilbert more than expected).

Fields of papers citing papers by Lysiane Hilbert

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Lysiane Hilbert. Nodes represent research fields, and links connect fields that are likely to share authors. Colored nodes show fields that tend to cite the papers produced by Lysiane Hilbert. The network helps show where Lysiane Hilbert may publish in the future.

Co-authorship network of co-authors of Lysiane Hilbert

This figure shows the co-authorship network connecting the top 25 collaborators of Lysiane Hilbert. A scholar is included among the top collaborators of Lysiane Hilbert based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with Lysiane Hilbert. Lysiane Hilbert is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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20 of 20 papers shown

#	Work	Indexed citations
1	Measurement of von Willebrand factor binding to a recombinant fragment of glycoprotein Ibα in an enzyme‐linked immunosorbent assay‐based method: performances in patients with type 2B von Willebrand disease 2006 ·British Journal of Haematology ·Claudine Caron,Lysiane Hilbert,Karen Vanhoorelbeke,Hans Deckmyn,Jenny Goudemand,Claudine Mazurier	11
2	Type 2N von Willebrand disease due to compound heterozygosity for R854Q and a novel R763G mutation at the cleavage site of von Willebrand factor propeptide 2006 ·Thrombosis and Haemostasis ·Paquita Nurden,Claudine Caron,Alan T. Nurden,Jenny Goudemand,Dominique Meyer,Édith Fressinaud,Claudine Mazurier,Lysiane Hilbert,(unknown)	22
3	Type 2N von Willebrand disease. 2005 ·PubMed ·Claudine Mazurier,Lysiane Hilbert	15
4	In vitro study of a triple‐secured von Willebrand factor concentrate 2004 ·Vox Sanguinis ·Claudine Mazurier,(unknown),(unknown),Lysiane Hilbert,(unknown)	21
5	Expression of two type 2N von Willebrand disease mutations identified in exon 18 of von Willebrand factor gene 2004 ·British Journal of Haematology ·Lysiane Hilbert,Sylvie Jorieux,Michaëla Fontenay,(unknown),E Fressinaud,Dominique Meyer,Claudine Mazurier,(unknown)	7
6	A new candidate mutation, G1629R, in a patient with type 2A von Willebrand's disease: basic mechanisms and clinical implications. 2004 ·PubMed ·Lysiane Hilbert,Augusto B. Federici,Luciano Baronciani,(unknown),Claudine Mazurier	3
7	Two novel mutations, Q1053H and C1060R, located in the D3 domain of von Willebrand factor, are responsible for decreased FVIII‐binding capacity 2003 ·British Journal of Haematology ·Lysiane Hilbert,Sylvie Jorieux,Valérie Proulle,Rémi Favier,Jenny Goudemand,(unknown),Dominique Meyer,Édith Fressinaud,Claudine Mazurier,(unknown)	29
8	Identification of a New Type 2M von Willebrand Disease Mutation also at Position 1324 of von Willebrand Factor 2002 ·Thrombosis and Haemostasis ·(unknown),Anne‐Sophie Ribba,(unknown),Claudine Mazurier,Lysiane Hilbert,(unknown)	12
9	Type 2 von Willebrand disease causing defective von Willebrand factor-dependent platelet function 2001 ·Best Practice & Research Clinical Haematology ·Dominique Meyer,E Fressinaud,Lysiane Hilbert,Anne‐Sophie Ribba,Jean‐Maurice Lavergne,Claudine Mazurier	28
10	Type 2N von Willebrand disease: clinical manifestations, pathophysiology, laboratory diagnosis and molecular biology 2001 ·Best Practice & Research Clinical Haematology ·Claudine Mazurier,Jenny Goudemand,Lysiane Hilbert,Claudine Caron,Édith Fressinaud,Dominique Meyer	73
11	A Standard Nomenclature for von Willebrand Factor Gene Mutations and Polymorphisms 2001 ·Thrombosis and Haemostasis ·Jeroen Eikenboom,(unknown),Lysiane Hilbert,Claudine Mazurier,I. R. Peake,J. Evan Sadler,Francesco Rodeghiero,Anne Goodeve	38
12	The arginine-552-cysteine (R1315C) mutation within the A1 loop of von Willebrand factor induces an abnormal folding with a loss of function resulting in type 2A–like phenotype of von Willebrand disease: study of 10 patients and mutated recombinant von Willebrand factor 2001 ·Blood ·Anne‐Sophie Ribba,Lysiane Hilbert,Jean‐Maurice Lavergne,Édith Fressinaud,Catherine Boyer‐Neumann,Catherine Ternisien,I. Juhan‐Vague,Jenny Goudemand,Jean‐Pierre Girma,Claudine Mazurier,Dominique Meyer	27
13	Type 2M vWD Resulting from a Lysine Deletion within a Four Lysine Residue Repeat in the A1 Loop of von Willebrand Factor 2000 ·Thrombosis and Haemostasis ·P. Vincent Jenkins,Christine Gaucher,(unknown),Peter W. Collins,John Pasi,Claudine Mazurier,Lysiane Hilbert	16
14	Identification of new type 2B von Willebrand disease mutations: Arg543Gln, Arg545Pro and Arg578Leu 1998 ·British Journal of Haematology ·Lysiane Hilbert,Christine Gaucher,(unknown),(unknown),Christine Trzeciak,Claudine Mazurier	8
15	Platelet Activation and Aggregation Induced by Recombinant von Willebrand Factors Reproducing Four Type 2B von Willebrand Disease Missense Mutations 1998 ·Thrombosis and Haemostasis ·Lysiane Hilbert,Claudine Mazurier,Christophe de Romeuf	17
16	Gene defects in 150 unrelated French cases with type 2 von Willebrand disease: from the patient to the gene. INSERM Network on Molecular Abnormalities in von Willebrand Disease. 1997 ·PubMed ·Dominique Meyer,E Fressinaud,Céline Gaucher,Lavergne Jm,Lysiane Hilbert,Anne‐Sophie Ribba,Sylvie Jorieux,Claudine Mazurier	81
17	Gene Defects in 150 Unrelated French Cases with Type 2 von Willebrand Disease: from the Patient to the Gene 1997 ·Thrombosis and Haemostasis ·Dominique Meyer,E Fressinaud,Christine Gaucher,J. M. Lavergne,Lysiane Hilbert,Anne‐Sophie Ribba,(unknown),Claudine Mazurier,(unknown)	75
18	Identification of two mutations (Arg611Cys and Arg611His) in the A1 loop of von Willebrand factor (vWF) responsible for type 2 von Willebrand disease with decreased platelet-dependent function of vWF [see comments] 1995 ·Blood ·Lysiane Hilbert,Christine Gaucher,Claudine Mazurier	52
19	Identification of two mutations (Arg611Cys and Arg611His) in the A1 loop of von Willebrand factor (vWF) responsible for type 2 von Willebrand disease with decreased platelet-dependent function of vWF [see comments] 1995 ·Blood ·Lysiane Hilbert,Christine Gaucher,Claudine Mazurier	2
20	Leu 697-->Val mutation in mature von Willebrand factor is responsible for type IIB von Willebrand disease 1994 ·Blood ·Lysiane Hilbert,Christine Gaucher,Christophe de Romeuf,MH Horellou,Tom Vink,Claudine Mazurier	49

About Lysiane Hilbert

Lysiane Hilbert is a scholar working on Hematology, Genetics and Genetics, having authored 20 papers that have together received 586 indexed citations. Recurring topics across this work include Platelet Disorders and Treatments (20 papers), Blood groups and transfusion (13 papers) and Blood disorders and treatments (8 papers). The work is most often cited by research in Hematology (564 citations), Immunology (111 citations) and Genetics (55 citations). Lysiane Hilbert has collaborated with scholars based in France, Switzerland and Italy. Frequent co-authors include Claudine Mazurier, Dominique Meyer, Christine Gaucher, Anne‐Sophie Ribba, E Fressinaud, Jenny Goudemand, Édith Fressinaud, Claudine Caron, Sylvie Jorieux and Christophe de Romeuf. Their work appears in journals such as Blood, British Journal of Haematology and Thrombosis and Haemostasis.

Rankless uses publication and citation data sourced from OpenAlex, an open and comprehensive bibliographic database. While OpenAlex provides broad and valuable coverage of the global research landscape, it—like all bibliographic datasets—has inherent limitations. These include incomplete records, variations in author disambiguation, differences in journal indexing, and delays in data updates. As a result, some metrics and network relationships displayed in Rankless may not fully capture the entirety of a scholar's output or impact.

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