Mariem Ben Saïd

652 total citations
26 papers, 369 citations indexed

About

Mariem Ben Saïd is a scholar working on Sensory Systems, Molecular Biology and Genetics. According to data from OpenAlex, Mariem Ben Saïd has authored 26 papers receiving a total of 369 indexed citations (citations by other indexed papers that have themselves been cited), including 14 papers in Sensory Systems, 12 papers in Molecular Biology and 10 papers in Genetics. Recurrent topics in Mariem Ben Saïd's work include Hearing, Cochlea, Tinnitus, Genetics (14 papers), Genetics and Neurodevelopmental Disorders (6 papers) and Ear Surgery and Otitis Media (5 papers). Mariem Ben Saïd is often cited by papers focused on Hearing, Cochlea, Tinnitus, Genetics (14 papers), Genetics and Neurodevelopmental Disorders (6 papers) and Ear Surgery and Otitis Media (5 papers). Mariem Ben Saïd collaborates with scholars based in Tunisia, United States and United Arab Emirates. Mariem Ben Saïd's co-authors include Saber Masmoudi, Abdelmonem Ghorbel, Mounira Hmani‐Aifa, Hammadi Ayadi, Nabil Driss, Imen Chakchouk, Abdelaziz Tlili, Z. Benzina, Rahul Mittal and M’hamed Grati and has published in prestigious journals such as SHILAP Revista de lepidopterología, PLoS ONE and Scientific Reports.

In The Last Decade

Mariem Ben Saïd

24 papers receiving 363 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Mariem Ben Saïd Tunisia	11	214	174	101	95	46	26	369
Nabil Driss Tunisia	8	142 0.7×	123 0.7×	70 0.7×	51 0.5×	73 1.6×	25	298
I Huber Netherlands	5	276 1.3×	245 1.4×	89 0.9×	104 1.1×	57 1.2×	7	439
Ανδρέας Παμπάνος Greece	12	186 0.9×	233 1.3×	76 0.8×	140 1.5×	44 1.0×	28	459
Kathy Ushakov Israel	11	213 1.0×	235 1.4×	54 0.5×	24 0.3×	39 0.8×	12	466
Xuezhong Liu United States	11	350 1.6×	461 2.6×	87 0.9×	77 0.8×	45 1.0×	14	659
Chufeng He China	14	172 0.8×	286 1.6×	59 0.6×	73 0.8×	37 0.8×	52	447
Xiuhong Pang China	13	203 0.9×	185 1.1×	71 0.7×	38 0.4×	54 1.2×	25	323
Yoh-ichiro Iwasa Japan	9	200 0.9×	134 0.8×	77 0.8×	28 0.3×	61 1.3×	24	284
TB Friedman United States	9	260 1.2×	238 1.4×	110 1.1×	49 0.5×	47 1.0×	9	407
Zippora Brownstein Israel	14	327 1.5×	363 2.1×	125 1.2×	45 0.5×	139 3.0×	25	620

Countries citing papers authored by Mariem Ben Saïd

Since Specialization

Citations

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

Fields of papers citing papers by Mariem Ben Saïd

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Mariem Ben Saïd

This figure shows the co-authorship network connecting the top 25 collaborators of Mariem Ben Saïd. A scholar is included among the top collaborators of Mariem Ben Saïd 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 Mariem Ben Saïd. Mariem Ben Saïd 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

Bouzid, Amal, Amal Souissi, Fakher Frikha, et al.. (2025). Whole exome sequencing identifies ABHD14A and MRNIP as novel candidate genes for developmental language disorder. Scientific Reports. 15(1). 367–367.

Saïd, Mariem Ben, Saber Masmoudi, Angela Brieger, et al.. (2024). Functional analysis of MMR gene VUS from potential Lynch syndrome patients. PLoS ONE. 19(6). e0304141–e0304141. 1 indexed citations

Saïd, Mariem Ben, Amal Souissi, Faiza Fakhfakh, et al.. (2023). Customized targeted massively parallel sequencing enables the identification of novel pathogenic variants in Tunisian patients with developmental and epileptic encephalopathy. Epilepsia Open. 9(5). 1697–1709. 3 indexed citations

Ayed, Ikhlas Ben, Amal Souissi, Mariem Ben Saïd, et al.. (2023). A new case with the recurrent PURA p.(Phe233del) pathogenic variant: Expansion of the phenotype and review of the literature. International Journal of Developmental Neuroscience. 83(4). 383–395. 3 indexed citations

Triki, Chahnez, et al.. (2023). First report of Tunisian patients with CDKL5‐related encephalopathy. Epilepsia Open. 9(3). 906–917. 1 indexed citations

Sassi, Samia Ben, et al.. (2022). A Tunisian patient with CLCN2 ‐related leukoencephalopathy. SHILAP Revista de lepidopterología. 10(12). e6737–e6737. 1 indexed citations

Souissi, Amal, Mariem Ben Saïd, Ikhlas Ben Ayed, et al.. (2021). Novel pathogenic mutations and further evidence for clinical relevance of genes and variants causing hearing impairment in Tunisian population. Journal of Advanced Research. 31. 13–24. 18 indexed citations

Souissi, Amal, et al.. (2021). Expanding the Clinical and Molecular Spectrum of HARS2-Perrault Syndrome: Identification of a Novel Homozygous Missense Variant in the HARS2 gene. Genetic Testing and Molecular Biomarkers. 25(8). 528–539. 3 indexed citations

Ayed, Ikhlas Ben, Amal Bouzid, Amal Souissi, et al.. (2021). Further insights into the spectrum phenotype of TRAPPC9 and CDK5RAP2 genes, segregating independently in a large Tunisian family with intellectual disability and microcephaly. European Journal of Medical Genetics. 64(12). 104373–104373. 4 indexed citations

10.

Souissi, Amal, Baha Eddine Abdelmalek, Imen Chakchouk, et al.. (2021). Molecular insights into MYO3A kinase domain variants explain variability in both severity and progression of DFNB30 hearing impairment. Journal of Biomolecular Structure and Dynamics. 40(21). 10940–10951.

11.

Chakchouk, Imen, Mariem Ben Saïd, Ibtihel Smeti, et al.. (2015). NADf Chip, a Two-Color Microarray for Simultaneous Screening of Multigene Mutations Associated with Hearing Impairment in North African Mediterranean Countries. Journal of Molecular Diagnostics. 17(2). 155–161. 18 indexed citations

12.

Grati, M’hamed, Imen Chakchouk, Qi Ma, et al.. (2015). A missense mutation in DCDC2 causes human recessive deafness DFNB66, likely by interfering with sensory hair cell and supporting cell cilia length regulation. Human Molecular Genetics. 24(9). 2482–2491. 75 indexed citations

13.

Saïd, Mariem Ben, Salma Ben‐Salem, W. Bouassida, et al.. (2013). Posterior microphthalmia and nanophthalmia in Tunisia caused by a founder c.1059_1066insC mutation of the PRSS56 gene. Gene. 528(2). 288–294. 17 indexed citations

14.

Mosrati, Mohamed Ali, Isabelle Schrauwen, Mariem Ben Saïd, et al.. (2012). Genome-wide analysis reveals a novel autosomal-recessive hearing loss locus DFNB80 on chromosome 2p16.1-p21. Journal of Human Genetics. 58(2). 98–101. 3 indexed citations

15.

Saïd, Mariem Ben, Z. Benzina, Felipe Moreno, et al.. (2012). Segregation of a new mutation in SLC26A4 and p.E47X mutation in GJB2 within a consanguineous Tunisian family affected with Pendred syndrome. International Journal of Pediatric Otorhinolaryngology. 76(6). 832–836. 13 indexed citations

16.

Saïd, Mariem Ben, Mounira Hmani‐Aifa, B. Hammami, et al.. (2011). DFNB66 and DFNB67 loci are non allelic and rarely contribute to autosomal recessive nonsyndromic hearing loss. European Journal of Medical Genetics. 54(6). e565–e569. 8 indexed citations

17.

Saïd, Mariem Ben, Malek Mnejja, Ilhem Charfeddine, et al.. (2011). A novel missense mutation in the ESRRB gene causes DFNB35 hearing loss in a Tunisian family. European Journal of Medical Genetics. 54(6). e535–e541. 19 indexed citations

18.

Saïd, Mariem Ben, Mounira Hmani‐Aifa, Shahid Mahmood Baig, et al.. (2010). High Frequency of the p.R34X Mutation in the TMC1 Gene Associated with Nonsyndromic Hearing Loss Is Due to Founder Effects. Genetic Testing and Molecular Biomarkers. 14(3). 307–311. 37 indexed citations

19.

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

20.

Tlili, Abdelaziz, Mounira Hmani‐Aifa, Mariem Ben Saïd, et al.. (2008). <i>TMC1</i> but Not <i>TMC2</i> Is Responsible for Autosomal Recessive Nonsyndromic Hearing Impairment in Tunisian Families. Audiology and Neurotology. 13(4). 213–218. 52 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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