Hammadi Ayadi

4.3k total citations
137 papers, 2.6k citations indexed

About

Hammadi Ayadi is a scholar working on Molecular Biology, Genetics and Sensory Systems. According to data from OpenAlex, Hammadi Ayadi has authored 137 papers receiving a total of 2.6k indexed citations (citations by other indexed papers that have themselves been cited), including 55 papers in Molecular Biology, 37 papers in Genetics and 33 papers in Sensory Systems. Recurrent topics in Hammadi Ayadi's work include Hearing, Cochlea, Tinnitus, Genetics (33 papers), Diabetes and associated disorders (21 papers) and Thyroid Disorders and Treatments (16 papers). Hammadi Ayadi is often cited by papers focused on Hearing, Cochlea, Tinnitus, Genetics (33 papers), Diabetes and associated disorders (21 papers) and Thyroid Disorders and Treatments (16 papers). Hammadi Ayadi collaborates with scholars based in Tunisia, France and United States. Hammadi Ayadi's co-authors include Saber Masmoudi, Christine Petit, Mohamed Drira, Ahmed Rebaï, Dominique Weil, Gallia G. Levy, Stéphane Blanchard, Fabienne Lévi-Acobas, Mounira Hmani‐Aifa and M. Abid and has published in prestigious journals such as Journal of Biological Chemistry, Nature Genetics and SHILAP Revista de lepidopterología.

In The Last Decade

Hammadi Ayadi

134 papers receiving 2.6k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Hammadi Ayadi Tunisia 29 1.3k 792 673 382 349 137 2.6k
Atsushi Watanabe Japan 29 1.1k 0.9× 243 0.3× 438 0.7× 369 1.0× 320 0.9× 137 3.0k
Mordechai Shohat Israel 26 1.7k 1.3× 512 0.6× 540 0.8× 64 0.2× 237 0.7× 83 2.9k
Henricus P. M. Kunst Netherlands 32 987 0.8× 999 1.3× 253 0.4× 611 1.6× 569 1.6× 131 3.2k
Andreas Janecke Austria 37 2.2k 1.7× 309 0.4× 1.3k 1.9× 60 0.2× 271 0.8× 132 4.4k
Nejat Mahdieh Iran 17 860 0.7× 438 0.6× 394 0.6× 86 0.2× 228 0.7× 95 1.6k
Marco Seri Italy 38 2.3k 1.8× 133 0.2× 1.4k 2.0× 329 0.9× 205 0.6× 193 5.3k
Célia Bádenas Spain 33 2.2k 1.8× 234 0.3× 1.4k 2.2× 53 0.1× 107 0.3× 139 3.9k
Annick Raas‐Rothschild Israel 34 1.7k 1.3× 290 0.4× 898 1.3× 39 0.1× 106 0.3× 108 3.8k
L.‐C. Tsui Canada 26 1.3k 1.1× 154 0.2× 547 0.8× 78 0.2× 103 0.3× 50 2.5k
Tetsuji Yamashita Japan 28 681 0.5× 383 0.5× 82 0.1× 57 0.1× 123 0.4× 79 2.5k

Countries citing papers authored by Hammadi Ayadi

Since Specialization
Citations

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

Fields of papers citing papers by Hammadi Ayadi

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Hammadi Ayadi

This figure shows the co-authorship network connecting the top 25 collaborators of Hammadi Ayadi. A scholar is included among the top collaborators of Hammadi Ayadi 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 Hammadi Ayadi. Hammadi Ayadi 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.
Mnif, Mouna, Sandra A. Rebuffat, Ahmed Rebaï, et al.. (2012). IL-1β a potential factor for discriminating between thyroid carcinoma and atrophic thyroiditis. European Cytokine Network. 23(3). 101–106. 12 indexed citations
2.
Ayadi, Imen, et al.. (2012). DNA Repair Gene Polymorphisms at XRCC1 (Arg194Trp, Arg280His, and Arg399Gln) in a Healthy Tunisian Population: Interethnic Variation and Functional Prediction. Genetic Testing and Molecular Biomarkers. 16(10). 1218–1225. 2 indexed citations
3.
4.
Mnif, Fatma, et al.. (2011). Association of Genetic Variations in TCF7L2 , SLC30A8 , HHEX , LOC387761 , and EXT2 with Type 2 Diabetes Mellitus in Tunisia. Genetic Testing and Molecular Biomarkers. 15(6). 399–405. 28 indexed citations
5.
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
6.
Molina, Laurence, Nicolas Salvetat, Sabine Pérès, et al.. (2011). Analysis of the variability of human normal urine by 2D-GE reveals a “public” and a “private” proteome. Journal of Proteomics. 75(1). 70–80. 16 indexed citations
7.
Bahloul, Ali, et al.. (2011). Retracted: Genotyping of Tunisian azoospermic men with Sertoli cell-only and maturation arrest. Andrologia. 50(4). e1088–e1088. 4 indexed citations
8.
Schrauwen, Isabelle, Erik Fransén, Megan Ealy, et al.. (2010). Genetic variants in RELN are associated with otosclerosis in a non‐European population from Tunisia. Annals of Human Genetics. 74(5). 399–405. 17 indexed citations
9.
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
10.
Sfar, Imen, Hassen Hadj Kacem, R. Bardi, et al.. (2010). (AT) Repeat in the 3′ Untranslated Region of the CTLA-4 Gene and Susceptibility to Acute Allograft Rejection in Tunisian Renal Transplantation. Transplantation Proceedings. 42(10). 4314–4317. 7 indexed citations
11.
Bahloul, Ali, et al.. (2009). Genetic association between AZF region polymorphism and Klinefelter syndrome. Reproductive BioMedicine Online. 19(4). 547–551. 18 indexed citations
12.
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
13.
Yoshimi, Noriko, B. Hammami, Mouna Mnif, et al.. (2009). Two missense mutations in SLC26A4 gene: a molecular and functional study. Clinical Genetics. 78(1). 74–80. 11 indexed citations
14.
Rekik, N., et al.. (2008). Association of calpain-10 polymorphisms with type 2 diabetes in the Tunisian population. Diabetes & Metabolism. 34(3). 273–278. 17 indexed citations
15.
Kacem, Hassen Hadj, et al.. (2006). Evidence for linkage and association between autoimmune thyroid diseases and the 18q12–q21 region in a large Tunisian family. International Journal of Immunogenetics. 33(1). 25–32. 5 indexed citations
16.
Bahloul, Ali, et al.. (2006). SCREENING OF Y CHROMOSOME MICRODELETIONS IN TUNISIAN INFERTILE MEN. Archives of Andrology. 52(3). 169–174. 9 indexed citations
17.
Rebaï, Ahmed, et al.. (2001). Lack of linkage and association between autoimmune thyroid diseases and the CTLA-4 gene in a large tunisian family. Human Immunology. 62(11). 1245–1250. 11 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.
Fakhfakh, Faiza, et al.. (1999). Analysis of Immunoglobulin VH and TCR Cβ Polymorphisms in a Large Family with Thyroid Autoimmune Disorder. PubMed. 16(4). 185–191. 12 indexed citations
20.
Ayadi, Hammadi, Patrice N. Marche, & Pierre‐André Cazenave. (1991). Evolution of the rabbit immunoglobulin ? chain genes. Immunogenetics. 34(3). 201–7. 5 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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