Jean‐Pierre Girma

1.4k total citations
32 papers, 870 citations indexed

About

Jean‐Pierre Girma is a scholar working on Hematology, Immunology and Genetics. According to data from OpenAlex, Jean‐Pierre Girma has authored 32 papers receiving a total of 870 indexed citations (citations by other indexed papers that have themselves been cited), including 28 papers in Hematology, 12 papers in Immunology and 8 papers in Genetics. Recurrent topics in Jean‐Pierre Girma's work include Platelet Disorders and Treatments (23 papers), Complement system in diseases (11 papers) and Blood groups and transfusion (10 papers). Jean‐Pierre Girma is often cited by papers focused on Platelet Disorders and Treatments (23 papers), Complement system in diseases (11 papers) and Blood groups and transfusion (10 papers). Jean‐Pierre Girma collaborates with scholars based in France, Netherlands and Japan. Jean‐Pierre Girma's co-authors include Dominique Meyer, Dominique Meyer, Agnès Veyradier, Geneviève Piétu, Rosanne Rabinowitz, William J. Vicic, Harvey J. Weiss, John Rogers, Bernadette Obert and Anne‐Sophie Ribba and has published in prestigious journals such as New England Journal of Medicine, Circulation and Blood.

In The Last Decade

Jean‐Pierre Girma

32 papers receiving 822 citations

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name h Career Trend Papers Cites
Jean‐Pierre Girma France 16 652 326 150 121 117 32 870
Bernadette Obert France 17 896 1.4× 653 2.0× 276 1.8× 124 1.0× 303 2.6× 31 1.2k
Nele Vandeputte Belgium 15 427 0.7× 445 1.4× 193 1.3× 44 0.4× 136 1.2× 23 710
Mark Zogg United States 14 522 0.8× 134 0.4× 127 0.8× 49 0.4× 21 0.2× 22 828
K Takatsuki Japan 13 183 0.3× 269 0.8× 75 0.5× 95 0.8× 95 0.8× 40 756
Jian-Ming Gu United States 14 767 1.2× 104 0.3× 198 1.3× 57 0.5× 21 0.2× 21 978
Robert Yelenosky United States 11 413 0.6× 207 0.6× 106 0.7× 45 0.4× 79 0.7× 12 673
SA Burstein United States 11 398 0.6× 97 0.3× 103 0.7× 31 0.3× 21 0.2× 20 575
Tatsumi Uchida Japan 13 298 0.5× 130 0.4× 158 1.1× 29 0.2× 37 0.3× 59 528
Marie‐Paule Chauveheid France 14 203 0.3× 148 0.5× 112 0.7× 20 0.2× 34 0.3× 33 636
Samantha J. Montague Australia 13 392 0.6× 100 0.3× 66 0.4× 29 0.2× 25 0.2× 26 619

Countries citing papers authored by Jean‐Pierre Girma

Since Specialization
Citations

This map shows the geographic impact of Jean‐Pierre Girma'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 Jean‐Pierre Girma with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Jean‐Pierre Girma more than expected).

Fields of papers citing papers by Jean‐Pierre Girma

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Jean‐Pierre Girma. 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 Jean‐Pierre Girma. The network helps show where Jean‐Pierre Girma may publish in the future.

Co-authorship network of co-authors of Jean‐Pierre Girma

This figure shows the co-authorship network connecting the top 25 collaborators of Jean‐Pierre Girma. A scholar is included among the top collaborators of Jean‐Pierre Girma 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 Jean‐Pierre Girma. Jean‐Pierre Girma is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

20 of 20 papers shown
1.
Loirat, Chantal, Jean‐Pierre Girma, Céline Desconclois, Paul Coppo, & Agnès Veyradier. (2008). Thrombotic thrombocytopenic purpura related to severe ADAMTS13 deficiency in children. Pediatric Nephrology. 24(1). 19–29. 42 indexed citations
2.
Loirat, Chantal, Agnès Veyradier, Jean‐Pierre Girma, Anne‐Sophie Ribba, & Dominique Meyer. (2006). Thrombotic Thrombocytopenic Purpura Associated with von Willebrand Factor-Cleaving Protease (ADAMTS13) Deficiency in Children. Seminars in Thrombosis and Hemostasis. 32(2). 90–97. 30 indexed citations
3.
Mahdian, Reza, Julie Rayes, Jean‐Pierre Girma, et al.. (2006). Comparison of FRETS-VWF73 to full-length VWF as a substrate for ADAMTS13 activity measurement in human plasma samples. Thrombosis and Haemostasis. 95(6). 1049–1051. 11 indexed citations
4.
Veyradier, Agnès, Chantal Loirat, Jean‐Pierre Girma, et al.. (2005). Purpura thrombotique thrombocytopénique par déficit héréditaire en ADAMTS13 (syndrome d’Upshaw-Schulman) : actualités et perspectives. Hématologie. 11(5). 321–334. 3 indexed citations
5.
Veyradier, Agnès & Jean‐Pierre Girma. (2004). Assays of ADAMTS-13 activity. Seminars in Hematology. 41(1). 41–47. 26 indexed citations
6.
Stépanian, Alain, Anne‐Sophie Ribba, Jean‐Maurice Lavergne, et al.. (2003). A new mutation, S1285F, within the A1 loop of von Willebrand factor induces a conformational change in A1 loop with abnormal binding to platelet GPIb and botrocetin causing type 2M von Willebrand disease. British Journal of Haematology. 120(4). 643–651. 15 indexed citations
7.
Veyradier, Agnès, Bernadette Obert, Élie Haddad, et al.. (2003). Severe deficiency of the specific von Willebrand factor-cleaving protease (ADAMTS 13) activity in a subgroup of children with atypical hemolytic uremic syndrome. The Journal of Pediatrics. 142(3). 310–317. 65 indexed citations
8.
Veyradier, Agnès, Anne Marfaing‐Koka, Jean‐Pierre Girma, & Dominique Meyer. (2002). Physiopathologie du purpura thrombotique thrombocytopénique : actualités et perspectives. Hématologie. 8(2). 141–149. 1 indexed citations
9.
Ajzenberg, Nadine, Cécile V. Denis, Agnès Veyradier, et al.. (2002). Complete Defect in vWF-cleaving Protease Activity Associated with Increased Shear-induced Platelet Aggregation in Thrombotic Microangiopathy. Thrombosis and Haemostasis. 87(5). 808–811. 15 indexed citations
10.
Girma, Jean‐Pierre, Agnès Veyradier, & Dominique Meyer. (2002). ADAMTS 13, la protéase spécifique du facteur von Willebrand. médecine/sciences. 18(1). 15–17. 1 indexed citations
11.
Veyradier, Agnès, Jean‐Pierre Girma, & Dominique Meyer. (2001). Protéolyse du facteur Willebrand et purpura thrombotique thrombocytopénique. Hématologie. 7(1). 31–37. 1 indexed citations
12.
13.
Obert, Bernadette, Anne Houllier, Dominique Meyer, & Jean‐Pierre Girma. (1999). Conformational Changes in the A3 Domain of von Willebrand Factor Modulate the Interaction of the A1 Domain With Platelet Glycoprotein Ib. Blood. 93(6). 1959–1968. 43 indexed citations
14.
Ribba, Anne‐Sophie, Jean‐Maurice Lavergne, Jean‐Pierre Girma, & Dominique Meyer. (1995). Bases moléculaires de la maladie de Willebrand. Hématologie. 1(3). 1 indexed citations
15.
Girma, Jean‐Pierre, Anne‐Sophie Ribba, & Dominique Meyer. (1995). Structure-Function Relationship of the A1 Domain of von Willebrand Factor. Thrombosis and Haemostasis. 74(1). 156–160. 11 indexed citations
16.
Meyer, Dominique & Jean‐Pierre Girma. (1993). von Willebrand Factor: Structure and Function. Thrombosis and Haemostasis. 70(1). 99–104. 154 indexed citations
17.
Baruch, Dominique, Bruce R. Bahnak, Jean‐Pierre Girma, & Dominique Meyer. (1989). 6 Von Willebrand factor and platelet function. Baillière s Clinical Haematology. 2(3). 627–672. 16 indexed citations
18.
Lavergne, Jean‐Maurice, Dominique Meyer, Jean‐Pierre Girma, & M J Larrieu. (1982). Precipitating anti‐VIII:C antibodies in two patients with haemophilia A. British Journal of Haematology. 50(1). 135–146. 4 indexed citations
19.
Weiss, Harvey J., Dominique Meyer, Rosanne Rabinowitz, et al.. (1982). Pseudo-von Willebrand's Disease. New England Journal of Medicine. 306(6). 326–333. 172 indexed citations
20.
Girma, Jean‐Pierre, et al.. (1981). Immunoradiometric Assay of Factor VIII: Coagulant Antigen using Four Human Antibodies. Study of 27 Cases of Haemophilia A. British Journal of Haematology. 47(2). 269–282. 31 indexed citations

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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