Ikhlas Ben Ayed

533 total citations
12 papers, 40 citations indexed

About

Ikhlas Ben Ayed is a scholar working on Molecular Biology, Genetics and Sensory Systems. According to data from OpenAlex, Ikhlas Ben Ayed has authored 12 papers receiving a total of 40 indexed citations (citations by other indexed papers that have themselves been cited), including 8 papers in Molecular Biology, 6 papers in Genetics and 3 papers in Sensory Systems. Recurrent topics in Ikhlas Ben Ayed's work include Genetics and Neurodevelopmental Disorders (4 papers), Hearing, Cochlea, Tinnitus, Genetics (3 papers) and Genomics and Rare Diseases (2 papers). Ikhlas Ben Ayed is often cited by papers focused on Genetics and Neurodevelopmental Disorders (4 papers), Hearing, Cochlea, Tinnitus, Genetics (3 papers) and Genomics and Rare Diseases (2 papers). Ikhlas Ben Ayed collaborates with scholars based in Tunisia, United Arab Emirates and United Kingdom. Ikhlas Ben Ayed's co-authors include Saber Masmoudi, Amal Souissi, Amal Bouzid, Abdelaziz Tlili, Mariem Ben Saïd, Hassen Kamoun, Chahnez Triki, Mohamed Ali Mosrati, Abdullah Ahmed Gibriel and Baha Eddine Abdelmalek and has published in prestigious journals such as PLoS ONE, Frontiers in Neurology and Journal of Advanced Research.

In The Last Decade

Ikhlas Ben Ayed

10 papers receiving 39 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Ikhlas Ben Ayed Tunisia	4	22	13	11	5	4	12	40
Benjamin Moore United States	4	34 1.5×	23 1.8×	2 0.2×	3 0.6×	3 0.8×	6	55
Ulvi Gerst Talas United Kingdom	2	15 0.7×	9 0.7×	2 0.2×	9 1.8×	7 1.8×	4	39
Anna Lehman Canada	4	32 1.5×	30 2.3×	3 0.3×	2 0.4×	5 1.3×	8	66
My Linh Thibodeau Canada	4	33 1.5×	4 0.3×	11 1.0×	1 0.2×	5 1.3×	5	43
Jin Fang Chai China	5	32 1.5×	27 2.1×		4 0.8×	5 1.3×	13	72
Anna Krasnenko Russia	6	31 1.4×	10 0.8×		6 1.2×	4 1.0×	11	63
Aidan Thomas Canada	5	19 0.9×	17 1.3×		5 1.0×	5 1.3×	7	56
Tanja Klein‐Rodewald Germany	4	33 1.5×	9 0.7×	2 0.2×	5 1.0×	2 0.5×	5	54
Anand Saggar United Kingdom	4	6 0.3×	10 0.8×	6 0.5×	3 0.6×	1 0.3×	7	31
John T. McGuire United States	4	23 1.0×	5 0.4×	2 0.2×	2 0.4×		4	51

Countries citing papers authored by Ikhlas Ben Ayed

Since Specialization

Citations

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

Fields of papers citing papers by Ikhlas Ben Ayed

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Ikhlas Ben Ayed

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

All Works

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12 of 12 papers shown

Ayed, Ikhlas Ben, et al.. (2025). Genetic profiling of inherited colorectal cancer syndromes in Tunisian patients. PLoS ONE. 20(6). e0326343–e0326343.

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, Yoshiko Murakami, Amal Souissi, et al.. (2023). Case report: Functional analysis of the p.Arg507Trp variant of the PIGT gene supporting the moderate epilepsy phenotype of mutations in the C-terminal region. Frontiers in Neurology. 14. 1092887–1092887. 2 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

Abida, Olfa, Nésrine Elloumi, E. Bahloul, et al.. (2022). Evaluation of X chromosome inactivation in endemic Tunisian pemphigus foliaceus. Molecular Genetics & Genomic Medicine. 10(12). e2080–e2080. 1 indexed citations

Bouzid, Amal, Adel Tekari, Neha Singh, et al.. (2022). Genetic Association of rs1021188 and DNA Methylation Signatures of TNFSF11 in the Risk of Conductive Hearing Loss. Frontiers in Medicine. 9. 870244–870244. 3 indexed citations

Saïd, Mariem Ben, Ikhlas Ben Ayed, Amal Souissi, et al.. (2022). Custom Next‐Generation Sequencing Identifies Novel Mutations Expanding the Molecular and clinical spectrum of isolated Hearing Impairment or along with defects of the retina, the thyroid, and the kidneys. Molecular Genetics & Genomic Medicine. 10(2). e1868–e1868. 2 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

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.

Ayed, Ikhlas Ben, Amal Bouzid, Amal Souissi, et al.. (2021). 8q21.11 microdeletion syndrome: Delineation of HEY1 as a candidate gene in neurodevelopmental and cardiac defects. Molecular Genetics & Genomic Medicine. 9(11). e1811–e1811. 3 indexed citations

11.

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.

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

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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