Emna Gouider

475 total citations
53 papers, 301 citations indexed

About

Emna Gouider is a scholar working on Hematology, Genetics and Molecular Biology. According to data from OpenAlex, Emna Gouider has authored 53 papers receiving a total of 301 indexed citations (citations by other indexed papers that have themselves been cited), including 41 papers in Hematology, 13 papers in Genetics and 10 papers in Molecular Biology. Recurrent topics in Emna Gouider's work include Hemophilia Treatment and Research (20 papers), Platelet Disorders and Treatments (12 papers) and Blood Coagulation and Thrombosis Mechanisms (12 papers). Emna Gouider is often cited by papers focused on Hemophilia Treatment and Research (20 papers), Platelet Disorders and Treatments (12 papers) and Blood Coagulation and Thrombosis Mechanisms (12 papers). Emna Gouider collaborates with scholars based in Tunisia, Switzerland and United States. Emna Gouider's co-authors include Balkis Meddeb, Ramzi Jeddi, Pierre Fenaux, Olfa Bahri, Sara C. Meyer, H. Abid, Bernhard Lämmle, Johanna A. Kremer Hovinga, Sylvia von Mackensen and Nissaf Ben Alaya and has published in prestigious journals such as SHILAP Revista de lepidopterología, Journal of Medical Virology and Thrombosis Research.

In The Last Decade

Emna Gouider

46 papers receiving 285 citations

Peers

Emna Gouider
CW McMillan United States
Houry Leblebjian United States
PM Ness United States
V.A.J.M. Kunst Netherlands
S Avery Australia
Emna Gouider
Citations per year, relative to Emna Gouider Emna Gouider (= 1×) peers Zefarina Zulkafli

Countries citing papers authored by Emna Gouider

Since Specialization
Citations

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

Fields of papers citing papers by Emna Gouider

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Emna Gouider

This figure shows the co-authorship network connecting the top 25 collaborators of Emna Gouider. A scholar is included among the top collaborators of Emna Gouider 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 Emna Gouider. Emna Gouider 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.
Abdelkarim, Mohamed, et al.. (2025). Ex vivo evaluation of Allium sativum extract on acute myeloid leukemia cells and leukemia stem cell populations. Medical Oncology. 42(12). 536–536.
2.
John, M. Joseph, Jeffrey S. Stonebraker, Glenn F. Pierce, et al.. (2024). Global prophylaxis trends in hemophilia: a macroeconomic analysis and its association with world development indicators. Expert Review of Hematology. 17(12). 947–956.
3.
Gouider, Emna, et al.. (2024). Flow cytometry for meningeal infiltration in B acute lymphoblastic leukemia in a low middle income country. Cytometry Part B Clinical Cytometry. 106(5). 405–411.
4.
Gouider, Emna, et al.. (2024). Clot waveform analysis in hemophilia carriers. Blood Coagulation & Fibrinolysis. 36(1). 8–13.
5.
Ekiaby, Magdy El, et al.. (2023). Challenges associated with access to plasma‐derived medicinal products in low middle‐income and low‐income countries. Vox Sanguinis. 119(2). 166–170. 3 indexed citations
6.
Iorio, Alfonso, Magdy El Ekiaby, Emna Gouider, et al.. (2023). PB0837 Analysis of the Change in Diagnosis of von Willebrand Disease by Region and Economic Status. Research and Practice in Thrombosis and Haemostasis. 7. 101562–101562. 1 indexed citations
7.
Gouider, Emna, et al.. (2023). Clot waveform analysis in acute promyelocytic leukemia. Blood Coagulation & Fibrinolysis. 35(1). 27–31. 2 indexed citations
8.
Gouider, Emna, et al.. (2022). Clinical phenotype and F7 gene genotype in 40 Tunisian patients with congenital factor VII deficiency. Blood Coagulation & Fibrinolysis. 33(5). 280–284. 1 indexed citations
9.
Gouider, Emna, et al.. (2020). Haemodialysis Tunisian patient with acquired factor V inhibitor associated to arteriovenous shunt thrombosis. Annales de biologie clinique. 78(2). 206–209. 6 indexed citations
10.
Gouider, Emna, et al.. (2014). Seroprevalency of transfusion-transmitted infections in first-time volunteer and replacement donors in Tunisia. Transfusion Clinique et Biologique. 21(6). 303–308. 15 indexed citations
11.
Chelbi, Anis, et al.. (2014). Diagnostic de lignée dans les leucémies aiguës : confrontation entre cytologie et immunophénotypage. Pathologie Biologie. 62(6). 345–347. 3 indexed citations
12.
Salah, N. Ben, et al.. (2013). Connaissances médicales en matière de sécurité immunologique en transfusion érythrocytaire en Tunisie : évaluation d’un CD-ROM d’auto-enseignement. Transfusion Clinique et Biologique. 20(4). 448–453. 5 indexed citations
13.
Meddeb, Balkis, et al.. (2011). Factor VIII haplotypes frequencies in Tunisian hemophiliacs A. Diagnostic Pathology. 6(1). 54–54. 6 indexed citations
14.
Wigren, Edvard, et al.. (2011). Analysis of newly detected mutations in the MCFD2 gene giving rise to combined deficiency of coagulation factors V and VIII. Haemophilia. 17(5). e923–7. 11 indexed citations
15.
Jeddi, Ramzi, et al.. (2008). Secondary chronic myelomonocytic leukemia with monosomy 7 after successful treatment of acute promyelocytic leukemia. Pathologie Biologie. 56(3). 162–163. 4 indexed citations
16.
Meyer, Sara C., Ramzi Jeddi, Balkis Meddeb, et al.. (2008). A first case of congenital TTP on the African continent due to a new homozygous mutation in the catalytic domain of ADAMTS13. Annals of Hematology. 87(8). 663–666. 22 indexed citations
18.
Gouider, Emna, et al.. (2007). [Hemoglobin C disease: report of 16 Tunisian cases].. PubMed. 85(3). 209–11. 2 indexed citations
19.
Triki, Hinda, et al.. (2005). Infections par des virus transmissibles par le sang chez des hémophiles en Tunisie. Transfusion Clinique et Biologique. 12(4). 301–305. 20 indexed citations
20.
Guermazi, Sami, et al.. (2001). Syndromes de défibrination atypiques et leucémies aiguës à translocation t(9,22) ; à propos de deux observations. Pathologie Biologie. 49(3). 232–236. 2 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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