Mouna Mnif

968 total citations
84 papers, 680 citations indexed

About

Mouna Mnif is a scholar working on Endocrinology, Diabetes and Metabolism, Molecular Biology and Genetics. According to data from OpenAlex, Mouna Mnif has authored 84 papers receiving a total of 680 indexed citations (citations by other indexed papers that have themselves been cited), including 43 papers in Endocrinology, Diabetes and Metabolism, 29 papers in Molecular Biology and 16 papers in Genetics. Recurrent topics in Mouna Mnif's work include Thyroid Disorders and Treatments (16 papers), Mitochondrial Function and Pathology (11 papers) and Diabetes and associated disorders (10 papers). Mouna Mnif is often cited by papers focused on Thyroid Disorders and Treatments (16 papers), Mitochondrial Function and Pathology (11 papers) and Diabetes and associated disorders (10 papers). Mouna Mnif collaborates with scholars based in Tunisia, France and Poland. Mouna Mnif's co-authors include Nadia Charfi, M. Abid, Hammadi Ayadi, Mohamed Abid, Ahmed Rebaï, Faiza Fakhfakh, N. Rekik, Emna Mkaouar‐Rebai, Mahdi Kamoun and Fatma Mnif and has published in prestigious journals such as SHILAP Revista de lepidopterología, Biochemical and Biophysical Research Communications and Gene.

In The Last Decade

Mouna Mnif

75 papers receiving 665 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Mouna Mnif Tunisia 16 315 277 176 95 80 84 680
Dinane Samara‐Boustani France 16 356 1.1× 443 1.6× 213 1.2× 165 1.7× 64 0.8× 31 799
A Kashiwagi United States 14 226 0.7× 271 1.0× 140 0.8× 95 1.0× 22 0.3× 27 749
Anja Lisbeth Frederiksen Denmark 14 233 0.7× 199 0.7× 87 0.5× 81 0.9× 99 1.2× 46 552
Sara Roos Sweden 11 299 0.9× 54 0.2× 112 0.6× 80 0.8× 52 0.7× 16 968
Radha Ramachandran United Kingdom 15 363 1.2× 120 0.4× 69 0.4× 174 1.8× 51 0.6× 37 886
Silke Rosinger Germany 13 111 0.4× 233 0.8× 240 1.4× 175 1.8× 129 1.6× 19 621
Cheol Woo Ko South Korea 13 244 0.8× 149 0.5× 166 0.9× 136 1.4× 11 0.1× 50 680
Jürgen Herwig Germany 9 157 0.5× 192 0.7× 379 2.2× 100 1.1× 102 1.3× 12 705
Yardena Tenenbaum‐Rakover Israel 20 609 1.9× 537 1.9× 395 2.2× 135 1.4× 38 0.5× 52 1.3k
Christopher Cahill United States 8 194 0.6× 193 0.7× 53 0.3× 135 1.4× 35 0.4× 8 484

Countries citing papers authored by Mouna Mnif

Since Specialization
Citations

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

Fields of papers citing papers by Mouna Mnif

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Mouna Mnif

This figure shows the co-authorship network connecting the top 25 collaborators of Mouna Mnif. A scholar is included among the top collaborators of Mouna Mnif 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 Mouna Mnif. Mouna Mnif 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.
Mnif, Mouna, et al.. (2024). Prevalence, sociodemographic factors and psychological distress related to compulsive buying online. European Psychiatry. 67(S1). S406–S407. 1 indexed citations
2.
Charfi, Nadia, et al.. (2023). Diagnosis and management of pituitary apoplexy: a Tunisian data. Chinese Neurosurgical Journal. 9(1). 17–17. 3 indexed citations
3.
Mnif, Mouna, et al.. (2023). EEG power spectrum analysis for Tunisian schizophrenic patients. European Psychiatry. 66(S1). S1075–S1075. 1 indexed citations
4.
Féki, I., et al.. (2023). Diabetes Distress and Illness Perceptions in Tunisian Type 2 Diabetes Patients. Diabetes Metabolic Syndrome and Obesity. Volume 16. 3547–3556. 2 indexed citations
5.
Keskes, Leila, et al.. (2022). Molecular mechanisms underlying the defects of two novel mutations in the HSD17B3 gene found in the Tunisian population. The Journal of Steroid Biochemistry and Molecular Biology. 227. 106235–106235. 2 indexed citations
6.
Stoupa, Athanasia, Dulanjalee Kariyawasam, Gabor Szinnai, et al.. (2021). High Diagnostic Yield of Targeted Next-Generation Sequencing in a Cohort of Patients With Congenital Hypothyroidism Due to Dyshormonogenesis. Frontiers in Endocrinology. 11. 545339–545339. 17 indexed citations
7.
Keskes, Leila, et al.. (2020). The first concurrent detection of mitochondrial DNA m.3243A>G mutation, deletion, and depletion in a family with mitochondrial diabetes. Molecular Genetics & Genomic Medicine. 8(7). e1292–e1292. 6 indexed citations
8.
Mnif, Fatma, et al.. (2019). Successful Treatment of Insulin Allergy with Desensitization Therapy: A Case Report and Literature Review. Iranian Journal of Allergy Asthma and Immunology. 18(5). 572–583. 5 indexed citations
9.
Boukedi, Hanen, Slim Tounsi, Hassen Kamoun, et al.. (2017). Association study of apoptosis gene polymorphisms in mitochondrial diabetes: A potential role in the pathogenicity of MD. Gene. 639. 18–26. 4 indexed citations
10.
Charfi, Nadia, Abdelaziz Tlili, Leila Keskes, et al.. (2016). Whole mitochondrial genome screening of a family with maternally inherited diabetes and deafness (MIDD) associated with retinopathy: A putative haplotype associated to MIDD and a novel MT-CO2 m.8241T>G mutation. Journal of Diabetes and its Complications. 31(1). 253–259. 13 indexed citations
11.
Charfi, Nadia, et al.. (2013). Hyperthyroidism: A rare cause of pulmonary embolism: Report of two cases. Indian Journal of Endocrinology and Metabolism. 17(6). 1104–1107. 6 indexed citations
12.
Mkaouar‐Rebai, Emna, et al.. (2013). A mitochondrial implication in a Tunisian patient with Friedreich's ataxia-like. Pathologie Biologie. 62(1). 41–48. 1 indexed citations
13.
Mnif, Mouna, Sandra A. Rebuffat, Ahmed Rebaï, et al.. (2012). IL-1β a potential factor for discriminating between thyroid carcinoma and atrophic thyroiditis. European Cytokine Network. 23(3). 101–106. 12 indexed citations
14.
Yoshimi, Noriko, B. Hammami, Mouna Mnif, et al.. (2009). Two missense mutations in SLC26A4 gene: a molecular and functional study. Clinical Genetics. 78(1). 74–80. 11 indexed citations
15.
Kamoun, Mahdi, Mouna Mnif, N. Rekik, et al.. (2009). Ganglioneuroma of adrenal gland in a patient with Turner syndrome. Annals of Diagnostic Pathology. 14(2). 133–136. 12 indexed citations
16.
Rekik, N., et al.. (2009). Hyperparathyroidism-jaw tumor syndrome: A case report. Annales d Endocrinologie. 71(2). 121–126. 16 indexed citations
17.
Kallel, Rim, Mouna Mnif, B. Hammami, et al.. (2009). Cancer papillaire sur goitre dyshormonogénétique. Annales d Endocrinologie. 70(6). 485–488. 5 indexed citations
18.
19.
Rebaï, Ahmed, et al.. (2004). Analysis of MHC genes in a Tunisian isolate with autoimmune thyroid diseases: implication of TNF −308 gene polymorphism. Journal of Autoimmunity. 23(1). 75–80. 28 indexed citations
20.
Mnif, Mouna, et al.. (2001). Hypothyroïdie après radiothérapie externe. À propos de 15 cas. Cancer/Radiothérapie. 5(3). 279–282. 1 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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