Fethi Mellouli

1.6k total citations
68 papers, 643 citations indexed

About

Fethi Mellouli is a scholar working on Genetics, Immunology and Hematology. According to data from OpenAlex, Fethi Mellouli has authored 68 papers receiving a total of 643 indexed citations (citations by other indexed papers that have themselves been cited), including 30 papers in Genetics, 27 papers in Immunology and 22 papers in Hematology. Recurrent topics in Fethi Mellouli's work include Hemoglobinopathies and Related Disorders (23 papers), Immunodeficiency and Autoimmune Disorders (21 papers) and Iron Metabolism and Disorders (12 papers). Fethi Mellouli is often cited by papers focused on Hemoglobinopathies and Related Disorders (23 papers), Immunodeficiency and Autoimmune Disorders (21 papers) and Iron Metabolism and Disorders (12 papers). Fethi Mellouli collaborates with scholars based in Tunisia, France and United States. Fethi Mellouli's co-authors include Mohamed Béjaoui, Mohamed‐Ridha Barbouche, Imen Ben‐Mustapha, Monia Ouederni, Slama Hmida, Karim Aoun, A. Bouratbine, Koussay Dellagi, Marc Théllier and Salem Abbès and has published in prestigious journals such as SHILAP Revista de lepidopterología, Annals of the New York Academy of Sciences and Journal of Clinical Microbiology.

In The Last Decade

Fethi Mellouli

64 papers receiving 631 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Fethi Mellouli Tunisia 16 240 199 194 124 109 68 643
Kazuhiro Masuoka Japan 21 378 1.6× 588 3.0× 146 0.8× 74 0.6× 45 0.4× 50 1.1k
Beata Wolska‐Kuśnierz Poland 12 315 1.3× 66 0.3× 39 0.2× 101 0.8× 88 0.8× 39 598
Catherine E. Terrell United States 12 524 2.2× 510 2.6× 77 0.4× 256 2.1× 30 0.3× 17 838
Maya Gupta India 15 316 1.3× 153 0.8× 97 0.5× 82 0.7× 97 0.9× 47 537
Oytip Nathalang Thailand 12 97 0.4× 386 1.9× 127 0.7× 46 0.4× 163 1.5× 76 597
Deniz Çağdaş Türkiye 18 569 2.4× 109 0.5× 42 0.2× 121 1.0× 261 2.4× 120 974
P. A. Chervenick United States 17 390 1.6× 359 1.8× 129 0.7× 26 0.2× 116 1.1× 33 923
Maung Maung Oo United States 8 227 0.9× 126 0.6× 76 0.4× 49 0.4× 54 0.5× 11 592
Simona Cardaropoli Italy 21 255 1.1× 70 0.4× 49 0.3× 63 0.5× 82 0.8× 44 1.1k
Xiucai Xu China 17 210 0.9× 121 0.6× 30 0.2× 45 0.4× 57 0.5× 28 755

Countries citing papers authored by Fethi Mellouli

Since Specialization
Citations

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

Fields of papers citing papers by Fethi Mellouli

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Fethi Mellouli

This figure shows the co-authorship network connecting the top 25 collaborators of Fethi Mellouli. A scholar is included among the top collaborators of Fethi Mellouli 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 Fethi Mellouli. Fethi Mellouli 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.
2.
Ouederni, Monia, et al.. (2020). Eryptosis and circulating blood cells microparticules in sickle cell diseases. European Journal of Public Health. 30(Supplement_5). 2 indexed citations
3.
Ouederni, Monia, Ahmed Ben Abdelaziz, Houda Kâabi, et al.. (2019). Predictors of autoimmune hemolytic anemia in beta-thalassemia patients with underlying red blood cells autoantibodies. Blood Cells Molecules and Diseases. 79. 102342–102342. 16 indexed citations
4.
Ouederni, Monia, et al.. (2018). CUTANEOUS MANIFESTATIONS OF PRIMARY IMMUNODEFICIENCY DISEASES IN TUNISIAN CHILDREN. Mediterranean Journal of Hematology and Infectious Diseases. 10(1). e2018065–e2018065. 8 indexed citations
5.
Mekki, Najla, Imen Ben‐Mustapha, Karen Rouault, et al.. (2017). A founder mutation underlies a severe form of phosphoglutamase 3 (PGM3) deficiency in Tunisian patients. Molecular Immunology. 90. 57–63. 21 indexed citations
6.
Ouederni, Monia, et al.. (2017). A 9month-old-boy with atypical hemophagocytic lymphohistiocytosis. Mediterranean Journal of Hematology and Infectious Diseases. 9(1). e2017057–e2017057. 6 indexed citations
7.
Ammar, Slim Ben, et al.. (2016). Genetic link with cholelithiasis among pediatric SCA Tunisian patients: Examples of UGT1A1, SLCO1A2 and SLCO1B1.. PubMed. 21(2). 121–5. 2 indexed citations
8.
Mellouli, Fethi, et al.. (2016). The role of rs1984112_G atCD36gene in increasing reticulocyte level among sickle cell disease patients. Hematology. 22(3). 178–182. 8 indexed citations
9.
Mellouli, Fethi, et al.. (2015). Fetal Hemoglobin in Tunisian Sickle Cell Disease Patient: Relationship with Polymorphic Sequences Cis to the β-Globin Gene. Indian Journal of Hematology and Blood Transfusion. 32(1). 114–119. 4 indexed citations
10.
Ouederni, Monia, Amel Lakhal, Fethi Mellouli, et al.. (2013). Cytogenetic Assessment of Fanconi Anemia in Children With Aplastic Anemia in Tunisia. Journal of Pediatric Hematology/Oncology. 35(7). 547–550. 4 indexed citations
11.
Mellouli, Fethi, Amel Lakhal, Saloua Ladeb, et al.. (2012). Autoimmune Polyglandular Syndrome Type II After Bone Marrow Transplant: Real Transfer or Acceleration of a Programmed Disease?. Experimental and Clinical Transplantation. 10(1). 76–80. 1 indexed citations
12.
Nasr, Moufida Ben, et al.. (2011). Association of Stromal Cell–Derived Factor-1-3′A Polymorphism to Higher Mobilization of Hematopoietic Stem Cells CD34+ in Tunisian Population. Transplantation Proceedings. 43(2). 635–638. 15 indexed citations
13.
Mellouli, Fethi, et al.. (2011). Restriction mapping of βS locus among tunisian sickle‐cell patients. American Journal of Human Biology. 23(6). 815–819. 11 indexed citations
14.
Barbouche, Mohamed‐Ridha, Nermeen Galal, Imen Ben‐Mustapha, et al.. (2011). Primary immunodeficiencies in highly consanguineous North African populations. Annals of the New York Academy of Sciences. 1238(1). 42–52. 43 indexed citations
15.
16.
Mellouli, Fethi, Abderrahman Abdelkefi, Saloua Ladeb, et al.. (2009). Transmission of type 1 diabetes by bone marrow transplantation: A case report. Pediatric Transplantation. 13(1). 119–122. 6 indexed citations
17.
Mellouli, Fethi, Abderrahman Abdelkefi, Saloua Ladeb, et al.. (2008). Possible transfer of vitiligo by allogeneic bone marrow transplantation: A case report. Pediatric Transplantation. 13(8). 1058–1061. 9 indexed citations
18.
Pïcard, Capucine, Fethi Mellouli, Renan Duprez, et al.. (2006). Kaposi’s sarcoma in a child with Wiskott-Aldrich syndrome. European Journal of Pediatrics. 165(7). 453–457. 32 indexed citations
19.
Barbouche, Mohamed‐Ridha, Houda Elloumi‐Zghal, Mohamed Béjaoui, et al.. (2006). Genetic and mutational heterogeneity of autosomal recessive chronic granulomatous disease in Tunisia. Journal of Human Genetics. 51(10). 887–895. 40 indexed citations
20.
Mellouli, Fethi, et al.. (2003). Treatment of a patient with chronic renal failure with rituximab for a follicular lymphoma: safe and successful option of rituximab therapy. European Journal Of Haematology. 71(2). 128–129. 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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