Monia Ouederni

717 total citations
29 papers, 204 citations indexed

About

Monia Ouederni is a scholar working on Genetics, Hematology and Infectious Diseases. According to data from OpenAlex, Monia Ouederni has authored 29 papers receiving a total of 204 indexed citations (citations by other indexed papers that have themselves been cited), including 11 papers in Genetics, 8 papers in Hematology and 6 papers in Infectious Diseases. Recurrent topics in Monia Ouederni's work include Hemoglobinopathies and Related Disorders (11 papers), Erythrocyte Function and Pathophysiology (5 papers) and Immunodeficiency and Autoimmune Disorders (5 papers). Monia Ouederni is often cited by papers focused on Hemoglobinopathies and Related Disorders (11 papers), Erythrocyte Function and Pathophysiology (5 papers) and Immunodeficiency and Autoimmune Disorders (5 papers). Monia Ouederni collaborates with scholars based in Tunisia, France and Bahrain. Monia Ouederni's co-authors include Mohamed Béjaoui, Fethi Mellouli, Laurent Abel, Danielle Canioni, Monia Khémiri, Barbara Lisowska‐Grospierre, Yves Lévy, Marianne Debré, Capucine Pïcard and Julie Bruneau and has published in prestigious journals such as SHILAP Revista de lepidopterología, Blood and Frontiers in Immunology.

In The Last Decade

Monia Ouederni

26 papers receiving 202 citations

Peers

Monia Ouederni

IMMUN

GENET

HEMAT

GENET

EPIDE

Robert Greiner United States

Krisztián Kállay Hungary

Beth A. Martin United States

Kristen Cole United States

Bella Shadur Australia

Daniel Suez United States

Agnieszka Tomaszewska Poland

Achille Aouba France

Jessica Serafinelli Italy

Valentina Strohmeier Germany

Robert Greiner United States

Monia Ouederni

92 ×1.1

IMMUN

47 ×0.8

GENET

65 ×1.0

HEMAT

31 ×0.8

GENET

25 ×0.7

EPIDE

Citations per year, relative to Monia Ouederni Monia Ouederni (= 1×) peers Robert Greiner

Countries citing papers authored by Monia Ouederni

Since Specialization

Citations

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

Fields of papers citing papers by Monia Ouederni

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Monia Ouederni

This figure shows the co-authorship network connecting the top 25 collaborators of Monia Ouederni. A scholar is included among the top collaborators of Monia Ouederni 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 Monia Ouederni. Monia Ouederni 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

Lorusso, Alessio, Najla Mekki, Iolanda Mangone, et al.. (2025). SARS-CoV-2 excretion and genetic evolution in nasopharyngeal and stool samples from primary immunodeficiency and immunocompetent pediatric patients. Virology Journal. 22(1). 9–9.

Taı̈eb, Alain, et al.. (2025). Sideroblastic anemia in children: challenges in diagnosis and management in three cases. Annals of Hematology. 104(4). 2537–2543. 1 indexed citations

Drechsel, Oliver, Sindy Böttcher, Najla Mekki, et al.. (2024). Reversion of neurovirulent mutations, recombination and high intra‐host diversity in vaccine‐derived poliovirus excreted by patients with primary immune deficiency. Journal of Medical Virology. 96(9). e29918–e29918. 2 indexed citations

Mekki, Najla, Imen Ben‐Mustapha, Jamel Ammar, et al.. (2023). Diagnostic challenge in a series of eleven patients with hyper IgE syndromes. Frontiers in Immunology. 13. 1057679–1057679. 8 indexed citations

Curini, Valentina, Maurilia Marcacci, Salma Abid, et al.. (2022). Full Genome Characterization of Respiratory Syncytial Virus Causing a Fatal Infection in an Immunocompromised Patient in Tunisia. Pathogens. 11(7). 758–758.

Mellouli, Fethi, et al.. (2022). Long-Term Observational Study of Chronic Granulomatous Disease About 41 Patients From Tunisia and Comparison to Other Long-Term Follow-Up Studies. Clinical Pediatrics. 61(9). 629–644.

Bouguerra, Ghada, et al.. (2021). Biochemical, Cellular, and Proteomic Characterization of Hereditary Spherocytosis Among Tunisians. Cellular Physiology and Biochemistry. 55(1). 117–129. 1 indexed citations

Messaoud, Olfa, Sahar Elouej, Fethi Mellouli, et al.. (2021). FANCA Gene Mutations in North African Fanconi Anemia Patients. Frontiers in Genetics. 12. 610050–610050. 2 indexed citations

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

10.

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

11.

Ouederni, Monia, et al.. (2019). Consanguineous unions and endogamy in families of beta-thalassaemia patients from two Mediterranean populations: Tunisia and Italy. Annals of Human Biology. 46(7-8). 610–615. 3 indexed citations

12.

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

13.

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

14.

Ouederni, Monia, et al.. (2016). Myocardial and liver iron overload, assessed using T2* magnetic resonance imaging with an excel spreadsheet for post processing in Tunisian thalassemia major patients. Annals of Hematology. 96(1). 133–139. 15 indexed citations

15.

Ouederni, Monia, et al.. (2015). Acute lactic acidosis as a complication of thiamine-free parenteral nutrition in two neutropenic children. Nutrition Clinique et Métabolisme. 29(3). 159–162. 1 indexed citations

16.

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

17.

Youssef, Yosra Ben, Ahlem Amouri, Hatem Elghezal, et al.. (2012). Création et rapport du registre tunisien de l’anémie de Fanconi (TFAR). Archives de Pédiatrie. 19(5). 467–475. 5 indexed citations

18.

Ouederni, Monia, et al.. (2012). Oral HPV infection and MHC class II deficiency (A study of two cases with atypical outcome). Clinical and Molecular Allergy. 10(1). 6–6. 14 indexed citations

19.

Khémiri, Monia, et al.. (2008). Bronchogenic cyst: An uncommon cause of congenital lobar emphysema. Respiratory Medicine. 102(11). 1663–1666. 16 indexed citations

20.

Ouederni, Monia, et al.. (2008). Successful treatment of influenza A virus by oseltamivir in bone marrow transplant recipients. Pediatric Transplantation. 14(2). 178–181. 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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