Laure Croisille

1.7k total citations
33 papers, 1.0k citations indexed

About

Laure Croisille is a scholar working on Hematology, Genetics and Genetics. According to data from OpenAlex, Laure Croisille has authored 33 papers receiving a total of 1.0k indexed citations (citations by other indexed papers that have themselves been cited), including 18 papers in Hematology, 11 papers in Genetics and 9 papers in Genetics. Recurrent topics in Laure Croisille's work include Platelet Disorders and Treatments (9 papers), Blood groups and transfusion (8 papers) and Blood disorders and treatments (7 papers). Laure Croisille is often cited by papers focused on Platelet Disorders and Treatments (9 papers), Blood groups and transfusion (8 papers) and Blood disorders and treatments (7 papers). Laure Croisille collaborates with scholars based in France, United States and Italy. Laure Croisille's co-authors include Laure Coulombel, William Vainchenker, A Katz, C Issaad, Najet Debili, J Breton-Gorius, Jean-Baptiste Guichard, Gil Tchernia, Brigitte Izac and Isabelle Auffray and has published in prestigious journals such as Blood, PEDIATRICS and Frontiers in Immunology.

In The Last Decade

Laure Croisille

31 papers receiving 1.0k citations

Peers

Laure Croisille
J Melle France
KS Zuckerman United States
EF Srour United States
A Butturini United States
Sawa Ito United States
SH Bartelmez United States
Juehua Gao United States
J Melle France
Laure Croisille
Citations per year, relative to Laure Croisille Laure Croisille (= 1×) peers J Melle

Countries citing papers authored by Laure Croisille

Since Specialization
Citations

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

Fields of papers citing papers by Laure Croisille

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Laure Croisille. 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 Laure Croisille. The network helps show where Laure Croisille may publish in the future.

Co-authorship network of co-authors of Laure Croisille

This figure shows the co-authorship network connecting the top 25 collaborators of Laure Croisille. A scholar is included among the top collaborators of Laure Croisille 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 Laure Croisille. Laure Croisille 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
2.
Leclerc, Mathieu, Marie Tamagne, Laure Croisille, et al.. (2023). Divergent CD4+ T-cell profiles are associated with anti-HLA alloimmunization status in platelet-transfused AML patients. Frontiers in Immunology. 14. 1165973–1165973. 2 indexed citations
3.
Beaupain, Blandine, Marlène Pasquet, Martin Biosse Duplan, et al.. (2020). Neutropénie en dehors d’un contexte de chimiothérapie : bilan et prise en charge-recommandations du centre de référence. 3(2). 182–195.
4.
Mahévas, Matthieu, Imane Azzaoui, Étienne Crickx, et al.. (2020). Efficacy, safety and immunological profile of combining rituximab with belimumab for adults with persistent or chronic immune thrombocytopenia: results from a prospective phase 2b trial. Haematologica. 106(9). 2449–2457. 39 indexed citations
5.
Chadebech, Philippe, et al.. (2020). New molecular basis associated with CD36‐negative phenotype in the sub‐Saharan African population. Transfusion. 60(11). 2482–2488. 2 indexed citations
6.
Séguier, J., Vincent Barlogis, Laure Croisille, et al.. (2019). Severe Transitory Neonatal Neutropenia Associated with Maternal Autoimmune or Idiopathic Neutropenia. Journal of Clinical Immunology. 39(2). 200–206. 3 indexed citations
7.
Frère, Corinne, Julien Amour, Guillaume Lebreton, et al.. (2018). Perioperative management of a patient with Glanzmann thrombasthenia undergoing a coronary artery bypass graft surgery. Blood Coagulation & Fibrinolysis. 29(3). 327–329. 2 indexed citations
8.
Delbos, Florent, Gérald Bertrand, Laure Croisille, et al.. (2015). Fetal and neonatal alloimmune thrombocytopenia: predictive factors of intracranial hemorrhage. Transfusion. 56(1). 59–66. 34 indexed citations
9.
Kütük, Mehmet Serdar, Laure Croisille, Süreyya Burcu Görkem, et al.. (2014). Fetal intracranial hemorrhage related to maternal autoimmune thrombocytopenic purpura. Child s Nervous System. 30(12). 2147–2150. 8 indexed citations
10.
Guiddir, Tamazoust, Marie‐Louise Frémond, Sophie Candon, et al.. (2014). Anti–TNF-α Therapy May Cause Neonatal Neutropenia. PEDIATRICS. 134(4). e1189–e1193. 43 indexed citations
11.
Grimaldi, David, Florence Canouï‐Poitrine, Laure Croisille, et al.. (2013). Antiplatelet antibodies detected by the MAIPA assay in newly diagnosed immune thrombocytopenia are associated with chronic outcome and higher risk of bleeding. Annals of Hematology. 93(2). 309–315. 23 indexed citations
12.
Gastou, Marc, Thierry Leblanc, Corinne Hurtaud, et al.. (2012). Primary hematopoietic cells from DBA patients with mutations in RPL11 and RPS19 genes exhibit distinct erythroid phenotype in vitro. Cell Death and Disease. 3(7). e356–e356. 58 indexed citations
13.
Pajot, C., D. Pariente, Simon Müller, et al.. (2002). Syndromes inflammatoires fébriles non infectieux de l’enfant : diagnostic, contribution des examens complémentaires. Archives de Pédiatrie. 9(7). 671–678. 2 indexed citations
14.
Croisille, Laure, et al.. (2001). Autoimmune disorders of erythropoiesis. Current Opinion in Hematology. 8(2). 68–73. 7 indexed citations
15.
Chiron, Marielle, Thérèse Cynober, F Miélot, Gil Tchernia, & Laure Croisille. (1999). The GEN.S: a fortuitous finding of a routine screening test for hereditary spherocytosis. PubMed. 41(3). 113–116. 21 indexed citations
16.
Debili, Najet, Laure Coulombel, Laure Croisille, et al.. (1996). Characterization of a bipotent erythro-megakaryocytic progenitor in human bone marrow. Blood. 88(4). 1284–1296. 198 indexed citations
17.
Casadevall, Nicole, Laure Croisille, Isabelle Auffray, Gil Tchernia, & Laure Coulombel. (1994). Age‐related alterations in erythroid and granulopoietic progenitors in Diamond‐Blackfan anaemia. British Journal of Haematology. 87(2). 369–375. 30 indexed citations
18.
Bader‐Meunier, Brigitte, F Miélot, Laure Croisille, et al.. (1994). Refractory anaemia and mitochondrial cytopathy in childhood. British Journal of Haematology. 87(2). 381–385. 38 indexed citations
19.
Tchernia, Gil, et al.. (1993). Diamond Blackfan anaemia: apparent relapse due to B19 parvovirus. European Journal of Pediatrics. 152(3). 209–210. 11 indexed citations
20.
Mohandas, Narla, Alyssa E. Johnson, Janan Wyatt, et al.. (1989). Automated quantitation of cell density distribution and hyperdense cell fraction in RBC disorders. Blood. 74(1). 442–447. 3 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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