Saoussen Trabelsi

1.6k total citations
16 papers, 137 citations indexed

About

Saoussen Trabelsi is a scholar working on Molecular Biology, Genetics and Cancer Research. According to data from OpenAlex, Saoussen Trabelsi has authored 16 papers receiving a total of 137 indexed citations (citations by other indexed papers that have themselves been cited), including 7 papers in Molecular Biology, 5 papers in Genetics and 4 papers in Cancer Research. Recurrent topics in Saoussen Trabelsi's work include Glioma Diagnosis and Treatment (5 papers), MicroRNA in disease regulation (3 papers) and Epigenetics and DNA Methylation (2 papers). Saoussen Trabelsi is often cited by papers focused on Glioma Diagnosis and Treatment (5 papers), MicroRNA in disease regulation (3 papers) and Epigenetics and DNA Methylation (2 papers). Saoussen Trabelsi collaborates with scholars based in Tunisia, United Kingdom and France. Saoussen Trabelsi's co-authors include Saad Hasan Mohammed Ali, Moncef Mokni, Kalthoum Tlili, Mohamed Tahar Yacoubi, Dorra H’mida-Ben Brahim, Sihem Hmissa, M Chaâbouni, Paul Coucke, Yves Morel and Maher Kharrat and has published in prestigious journals such as Annals of Oncology, Neuro-Oncology and Molecular Neurobiology.

In The Last Decade

Saoussen Trabelsi

15 papers receiving 136 citations

Peers

Saoussen Trabelsi

GENET

PRM

Emine İkbal Atlı Türkiye

Yuanchen Ma China

Takeyuki Nakamura Japan

Alia Shamikh Sweden

Mitchell W. Dillon United States

Amandine Septier France

Melitta Kitzwoegerer Austria

Stefano Petrocchi Italy

Celeste Owen Canada

Heather A. Ely United States

Emine İkbal Atlı Türkiye

Saoussen Trabelsi

119 ×1.5

51 ×1.3

GENET

33 ×1.0

46 ×1.7

GENET

12 ×0.5

PRM

Citations per year, relative to Saoussen Trabelsi Saoussen Trabelsi (= 1×) peers Emine İkbal Atlı

Countries citing papers authored by Saoussen Trabelsi

Since Specialization

Citations

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

Fields of papers citing papers by Saoussen Trabelsi

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Saoussen Trabelsi

This figure shows the co-authorship network connecting the top 25 collaborators of Saoussen Trabelsi. A scholar is included among the top collaborators of Saoussen Trabelsi 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 Saoussen Trabelsi. Saoussen Trabelsi is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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16 of 16 papers shown

Trabelsi, Saoussen, et al.. (2024). Equivocating and Deliberating on the Probability of COVID-19 Infection Serving as a Risk Factor for Lung Cancer and Common Molecular Pathways Serving as a Link. Pathogens. 13(12). 1070–1070. 3 indexed citations

Rischin, Danny, Brett Hughes, Nicole Basset‐Séguin, et al.. (2021). 1066P Extended-dose cemiplimab in patients with advanced cutaneous squamous cell carcinoma (CSCC): Primary analysis of phase II results. Annals of Oncology. 32. S886–S887. 1 indexed citations

Trabelsi, Saoussen, et al.. (2016). Assessment of MYCN amplification status in Tunisian neuroblastoma: CISH and MLPA combining approach.. PubMed. 93(8-9). 527–31. 2 indexed citations

Trabelsi, Saoussen, I. Chabchoub, Anna Burford, et al.. (2016). Molecular Diagnostic and Prognostic Subtyping of Gliomas in Tunisian Population. Molecular Neurobiology. 54(4). 2381–2394. 13 indexed citations

Coster, Peter De, et al.. (2016). Characterization of a novel mutation in PAX9 gene in a family with non-syndromic dental agenesis. Archives of Oral Biology. 71. 110–116. 16 indexed citations

Trabelsi, Saoussen, Sergey Popov, Anna Burford, et al.. (2015). Meningeal Hemangiopericytomas and Meningomas: a Comparative Immunohistochemical and Genetic Study. Asian Pacific Journal of Cancer Prevention. 16(16). 6871–6876. 16 indexed citations

Trabelsi, Saoussen, et al.. (2015). MGMT methylation assessment in glioblastoma: MS-MLPA versus human methylation 450K beadchip array and immunohistochemistry. Clinical & Translational Oncology. 18(4). 391–397. 13 indexed citations

Trabelsi, Saoussen, Sergey Popov, Anna Burford, et al.. (2015). Adult recurrent pilocytic astrocytoma: Clinical, histopathological and molecular study. Neurochirurgie. 61(6). 392–397. 8 indexed citations

Bouali, Nouha, Soumaya Mougou, Jérôme Bouligand, et al.. (2015). Analysis of FMR1 gene premutation and X chromosome cytogenetic abnormalities in 100 Tunisian patients presenting premature ovarian failure. Annales d Endocrinologie. 76(6). 671–678. 9 indexed citations

10.

Mackay, Alan, Maria Vinci, Anna Burford, et al.. (2015). HG-11 * INTEGRATIVE MOLECULAR META-ANALYSIS OF 700 PEDIATRIC HIGH GRADE GLIOMA AND DIPG DEFINES WIDESPREAD INTER- AND INTRA-TUMORAL HETEROGENEITY. Neuro-Oncology. 17(suppl 3). iii12–iii13.

11.

Brahim, Dorra H’mida-Ben, et al.. (2014). Modulation at Age of Onset in Tunisian Huntington Disease Patients: Implication of New Modifier Genes. PubMed. 2014(1). 210418–210418. 5 indexed citations

12.

Trabelsi, Saoussen, Dorra H’mida-Ben Brahim, Imed Harrabi, et al.. (2014). Glioma Epidemiology in the Central Tunisian Population: 1993-2012. Asian Pacific Journal of Cancer Prevention. 15(20). 8753–8757. 19 indexed citations

13.

Trabelsi, Saoussen, Soumaya Mougou, Moez Gribaa, et al.. (2014). Partial KCNQ1OT1 hypomethylation: A disguised familial Beckwith–Wiedemann syndrome as a sporadic adrenocortical tumor. PubMed. 4. 1–3. 5 indexed citations

14.

Trabelsi, Saoussen, et al.. (2012). Thromboses artérielles néonatales non causées par un cathétérisme artériel : à propos de 4 observations. Archives de Pédiatrie. 19(4). 413–418. 2 indexed citations

15.

Trabelsi, Saoussen, et al.. (2011). Hallucinations auditives induites par le voriconazole : illustration par le monitorage plasmatique. Journal de Mycologie Médicale. 21(3). 214–216. 1 indexed citations

16.

Kharrat, Maher, Saoussen Trabelsi, M Chaâbouni, et al.. (2010). Only two mutations detected in 15 Tunisian patients with 11β‐hydroxylase deficiency: the p.Q356X and the novel p.G379V. Clinical Genetics. 78(4). 398–401. 24 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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