Neïla Belguith

495 total citations
34 papers, 226 citations indexed

About

Neïla Belguith is a scholar working on Molecular Biology, Genetics and Endocrinology, Diabetes and Metabolism. According to data from OpenAlex, Neïla Belguith has authored 34 papers receiving a total of 226 indexed citations (citations by other indexed papers that have themselves been cited), including 23 papers in Molecular Biology, 18 papers in Genetics and 8 papers in Endocrinology, Diabetes and Metabolism. Recurrent topics in Neïla Belguith's work include RNA modifications and cancer (6 papers), Genetic and Kidney Cyst Diseases (6 papers) and Sexual Differentiation and Disorders (5 papers). Neïla Belguith is often cited by papers focused on RNA modifications and cancer (6 papers), Genetic and Kidney Cyst Diseases (6 papers) and Sexual Differentiation and Disorders (5 papers). Neïla Belguith collaborates with scholars based in Tunisia, France and Belgium. Neïla Belguith's co-authors include Faiza Fakhfakh, Leila Keskes, Hassen Kamoun, Mouna Mnif, M. Hachicha, Emna Mkaouar‐Rebai, Nadia Charfi, Nozha Chakroun, Chahnez Triki and Afifa Sellami and has published in prestigious journals such as Biochemical and Biophysical Research Communications, Gene and Thyroid.

In The Last Decade

Neïla Belguith

33 papers receiving 221 citations

Peers

Neïla Belguith
Federica Buonocore United Kingdom
Masashi Kitagawa Japan
Mahmoud Alzyoud Qatar
P. Ceccarelli Italy
Fabio Sirchia Italy
Julie A. Jurgens United States
Joelle Abou Ghoch Lebanon
Hélène Bry‐Gauillard France
Paula Scaglia Argentina
Stefanie Engert Germany
Federica Buonocore United Kingdom
Neïla Belguith
Citations per year, relative to Neïla Belguith Neïla Belguith (= 1×) peers Federica Buonocore

Countries citing papers authored by Neïla Belguith

Since Specialization
Citations

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

Fields of papers citing papers by Neïla Belguith

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Neïla Belguith

This figure shows the co-authorship network connecting the top 25 collaborators of Neïla Belguith. A scholar is included among the top collaborators of Neïla Belguith 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 Neïla Belguith. Neïla Belguith 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.
Chérif, M., et al.. (2022). Li–Fraumeni syndrome in Tunisian carriers with different and rare tumor phenotype: genotype–phenotype correlation. BMC Medical Genomics. 15(1). 44–44. 4 indexed citations
2.
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
3.
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Abida, Olfa, Nésrine Elloumi, Houda Kanoun, et al.. (2022). Annexin A1 and its receptor gene polymorphisms in systemic lupus erythematosus in the Tunisian population. Clinical Rheumatology. 41(5). 1359–1369. 4 indexed citations
5.
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
6.
Belguith, Neïla, et al.. (2018). First description of a novel mitochondrial mutation in the MT-TI gene associated with multiple mitochondrial DNA deletion and depletion in family with severe dilated mitochondrial cardiomyopathy. Biochemical and Biophysical Research Communications. 497(4). 1049–1054. 8 indexed citations
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Hilbert, Pascale, Asma Ahmed, J. Hachicha, et al.. (2018). Mutational analysis in patients with Autosomal Dominant Polycystic Kidney Disease (ADPKD): Identification of five mutations in the PKD1 gene. Gene. 671. 28–35. 4 indexed citations
9.
Mahfoudh, Nadia, et al.. (2016). Novel cases of Tunisian patients with mutations in the gene encoding 17β-hydroxysteroid dehydrogenase type 3 and a founder effect. The Journal of Steroid Biochemistry and Molecular Biology. 165(Pt A). 86–94. 11 indexed citations
10.
Belguith, Neïla, et al.. (2016). First molecular diagnosis of Donohue syndrome in Africa: novel unusual insertion/deletion mutation in the INSR gene. Molecular Biology Reports. 43(3). 165–173. 3 indexed citations
11.
Sager, Christoph P., Maria Tsachaki, Julia Birk, et al.. (2015). Biochemical analyses and molecular modeling explain the functional loss of 17β-hydroxysteroid dehydrogenase 3 mutant G133R in three Tunisian patients with 46, XY Disorders of Sex Development. The Journal of Steroid Biochemistry and Molecular Biology. 155(Pt A). 147–154. 14 indexed citations
12.
Charfi, Nadia, Nabil Miled, Neïla Belguith, et al.. (2015). Segregation of S292F TPO gene mutation in three large Tunisian families with thyroid dyshormonogenesis: evidence of a founder effect. European Journal of Pediatrics. 174(11). 1491–1501. 3 indexed citations
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Mkaouar‐Rebai, Emna, et al.. (2012). Novel double deletions in the MECP2 gene in Tunisian Rett patient. Gene. 502(2). 163–167. 3 indexed citations
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Abdallah, Fatma Ben, Nozha Chakroun, Afifa Sellami, et al.. (2012). Chromosomal defects in infertile men with poor semen quality. Journal of Assisted Reproduction and Genetics. 29(5). 451–456. 33 indexed citations
17.
Aloulou, Hajer, et al.. (2011). [Bardet - Biedl syndrome in the child. A study of 11 cases].. PubMed. 89(1). 31–6. 3 indexed citations
18.
Feki, Moncef, Nadia Charfi, N. Rekik, et al.. (2010). Descriptive analyses of Turner syndrome: 49 cases in Tunisia. Annales d Endocrinologie. 71(2). 111–116. 10 indexed citations
19.
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
20.
Mkaouar‐Rebai, Emna, Abdelaziz Tlili, Saber Masmoudi, et al.. (2007). Mutational analysis of the mitochondrial tRNALeu(UUR) gene in Tunisian patients with mitochondrial diseases. Biochemical and Biophysical Research Communications. 355(4). 1031–1037. 19 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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