Saïda Ben Arab

837 total citations
19 papers, 555 citations indexed

About

Saïda Ben Arab is a scholar working on Cardiology and Cardiovascular Medicine, Molecular Biology and Otorhinolaryngology. According to data from OpenAlex, Saïda Ben Arab has authored 19 papers receiving a total of 555 indexed citations (citations by other indexed papers that have themselves been cited), including 9 papers in Cardiology and Cardiovascular Medicine, 6 papers in Molecular Biology and 5 papers in Otorhinolaryngology. Recurrent topics in Saïda Ben Arab's work include Ear Surgery and Otitis Media (5 papers), Cardiomyopathy and Myosin Studies (5 papers) and Hearing, Cochlea, Tinnitus, Genetics (4 papers). Saïda Ben Arab is often cited by papers focused on Ear Surgery and Otitis Media (5 papers), Cardiomyopathy and Myosin Studies (5 papers) and Hearing, Cochlea, Tinnitus, Genetics (4 papers). Saïda Ben Arab collaborates with scholars based in Tunisia, France and Austria. Saïda Ben Arab's co-authors include Christine Petit, Parry Guilford, Stéphane Blanchard, Jean Weissenbach, Jacqueline Levilliers, N. Beltaïef, Hammadi Ayadi, Sounira Mehri, Saber Masmoudi and Sinda Zarrouk‐Mahjoub and has published in prestigious journals such as Nature Genetics, SHILAP Revista de lepidopterología and Life Sciences.

In The Last Decade

Saïda Ben Arab

18 papers receiving 543 citations

Peers

Saïda Ben Arab

CCM

OTORH

NEURO

Yosra Bouyacoub Tunisia

Polona Le Quesne Stabej United Kingdom

Michael C. Schneider United States

Carina Frykholm Sweden

Nicolai Kohlschmidt Germany

Maddalena Martella Italy

Marcio Do Cruzeiro France

Morad Khayat Israel

J. Hall United States

Ruen Yao China

Yosra Bouyacoub Tunisia

Saïda Ben Arab

85 ×0.3

222 ×0.9

12 ×0.1

CCM

21 ×0.2

OTORH

40 ×0.5

NEURO

Citations per year, relative to Saïda Ben Arab Saïda Ben Arab (= 1×) peers Yosra Bouyacoub

Countries citing papers authored by Saïda Ben Arab

Since Specialization

Citations

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

Fields of papers citing papers by Saïda Ben Arab

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Saïda Ben Arab. 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 Saïda Ben Arab. The network helps show where Saïda Ben Arab may publish in the future.

Co-authorship network of co-authors of Saïda Ben Arab

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

All Works

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19 of 19 papers shown

Zarrouk‐Mahjoub, Sinda, et al.. (2021). Dilated Cardiomyopathy due to the Novel MT-CYB Missense Mutation m.14757T>C. Journal of Medical Cases. 12(11). 455–459. 1 indexed citations

Zarrouk‐Mahjoub, Sinda, et al.. (2012). Novel m.15434C>A (p.230L>I) Mitochondrial Cytb Gene Missense Mutation Associated with Dilated Cardiomyopathy. SHILAP Revista de lepidopterología. 2012. 1–6. 9 indexed citations

Beltaïef, N., et al.. (2012). HLA class I polymorphisms in Tunisian patients with otosclerosis. Annals of Human Biology. 39(3). 190–194. 2 indexed citations

Zarrouk‐Mahjoub, Sinda, et al.. (2011). Transition m.3308T>C in the ND1 Gene Is Associated with Left Ventricular Hypertrabeculation/Noncompaction. Cardiology. 118(3). 153–158. 10 indexed citations

Arab, Saïda Ben, Ahmed Rebaï, Mouna Mnif, et al.. (2011). No major genes in autoimmune thyroid diseases: complex segregation and epidemiological studies in a large Tunisian pedigree. Journal of Genetics. 90(2). 333–337. 2 indexed citations

Mehri, Sounira, Bruno Baudin, Sinda Zarrouk‐Mahjoub, et al.. (2010). Angiotensin-Converting Enzyme Insertion/Deletion Gene Polymorphism in a Tunisian Healthy and Acute Myocardial Infarction Population. Genetic Testing and Molecular Biomarkers. 14(1). 85–91. 25 indexed citations

Zarrouk‐Mahjoub, Sinda, Sounira Mehri, Amira Zaroui, et al.. (2010). Association of ACE I/D polymorphism in Tunisian patients with dilated cardiomyopathy. Journal of the Renin-Angiotensin-Aldosterone System. 11(3). 187–191. 12 indexed citations

Mehri, Sounira, Nadia Koubaa, S. Hammami, et al.. (2010). Genotypic interactions of renin–angiotensin system genes with diabetes type 2 in a Tunisian population. Life Sciences. 87(1-2). 49–54. 26 indexed citations

Mehri, Sounira, et al.. (2010). Angiotensinogen gene polymorphism in acute myocardial infarction patients. Journal of the Renin-Angiotensin-Aldosterone System. 12(1). 42–47. 19 indexed citations

10.

Hmani‐Aifa, Mounira, Mariem Ben Saïd, Mohamed Ali Mosrati, et al.. (2009). Screening of the DFNB3 Locus: Identification of Three Novel Mutations of MYO15A Associated with Hearing Loss and Further Suggestion for Two Distinctive Genes on This Locus. Genetic Testing and Molecular Biomarkers. 13(1). 147–151. 36 indexed citations

11.

Mehri, Sounira, Nadia Koubaa, Amel Nakbi, et al.. (2009). Relationship between genetic polymorphisms of angiotensin-converting enzyme and methylenetetrahydrofolate reductase as risk factors for type 2 diabetes in Tunisian patients. Clinical Biochemistry. 43(3). 259–266. 33 indexed citations

12.

Mrad, Karima, Emmanuelle Charafe‐Jauffret, Saïda Ben Arab, et al.. (2008). Markers of subtypes in inflammatory breast cancer studied by immunohistochemistry: Prominent expression of P-cadherin. BMC Cancer. 8(1). 28–28. 28 indexed citations

13.

Thys, Melissa, N. Beltaïef, Isabelle Schrauwen, et al.. (2008). A new locus for otosclerosis, OTSC8, maps to the pericentromeric region of chromosome 9. Human Genetics. 123(3). 267–272. 45 indexed citations

14.

Thys, Melissa, N. Beltaïef, Isabelle Schrauwen, et al.. (2007). Clinical and genetic analysis of two Tunisian otosclerosis families. American Journal of Medical Genetics Part A. 143A(14). 1653–1660. 8 indexed citations

15.

Mahjoub, S., et al.. (2007). A Novel Mitochondrial DNA tRNAIle (m.4322dupC) Mutation Associated With Idiopathic Dilated Cardiomyopathy. Diagnostic Molecular Pathology. 16(4). 238–242. 11 indexed citations

16.

Martínez, Consuelo Prado, et al.. (2005). Correlación de la tensión arterial sistólica con variables antropométricas en niñas de 10 a 12 años de dos colonias populares. Dialnet (Universidad de la Rioja). 102–111. 1 indexed citations

17.

Arab, Saïda Ben, et al.. (2004). Consanguinity and endogamy in Northern Tunisia and its impact on non‐syndromic deafness. Genetic Epidemiology. 27(1). 74–79. 62 indexed citations

18.

Arab, Saïda Ben, Mounira Hmani‐Aifa, Françoise Denoyelle, et al.. (2000). Mutations ofGJB2in three geographic isolates from northern Tunisia: evidence for genetic heterogeneity within isolates. Clinical Genetics. 57(6). 439–443. 17 indexed citations

19.

Guilford, Parry, Saïda Ben Arab, Stéphane Blanchard, et al.. (1994). A non–syndromic form of neurosensory, recessive deafness maps to the pericentromeric region of chromosome 13q. Nature Genetics. 6(1). 24–28. 208 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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