Ilhem Turki

912 total citations
46 papers, 425 citations indexed

About

Ilhem Turki is a scholar working on Molecular Biology, Neurology and Epidemiology. According to data from OpenAlex, Ilhem Turki has authored 46 papers receiving a total of 425 indexed citations (citations by other indexed papers that have themselves been cited), including 16 papers in Molecular Biology, 14 papers in Neurology and 9 papers in Epidemiology. Recurrent topics in Ilhem Turki's work include DNA Repair Mechanisms (6 papers), Botulinum Toxin and Related Neurological Disorders (5 papers) and Genetic Neurodegenerative Diseases (5 papers). Ilhem Turki is often cited by papers focused on DNA Repair Mechanisms (6 papers), Botulinum Toxin and Related Neurological Disorders (5 papers) and Genetic Neurodegenerative Diseases (5 papers). Ilhem Turki collaborates with scholars based in Tunisia, France and United States. Ilhem Turki's co-authors include Samir Belal, M. Ben Hamida, N. Gouider‐Khouja, F. Hentati, Rim Amouri, Moncef Feki, Ichraf Kraoua, Fayçal Hentati, M. Kéfi and Herbert J. Kayden and has published in prestigious journals such as Neurology, International Journal of Biological Macromolecules and BioMed Research International.

In The Last Decade

Ilhem Turki

35 papers receiving 414 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Ilhem Turki Tunisia 9 255 234 118 100 46 46 425
S. Di Donato Italy 12 331 1.3× 283 1.2× 149 1.3× 54 0.5× 29 0.6× 17 487
M. Kéfi Tunisia 10 211 0.8× 143 0.6× 92 0.8× 20 0.2× 28 0.6× 14 326
Celeste Panteghini Italy 13 133 0.5× 79 0.3× 118 1.0× 106 1.1× 42 0.9× 25 329
Michela Ripolone Italy 13 349 1.4× 121 0.5× 72 0.6× 15 0.1× 63 1.4× 40 526
Fai Tsang Singapore 10 149 0.6× 87 0.4× 180 1.5× 61 0.6× 17 0.4× 13 414
Chiara Reale Italy 11 121 0.5× 113 0.5× 157 1.3× 87 0.9× 29 0.6× 19 320
Zhi-hua Yang China 8 179 0.7× 60 0.3× 99 0.8× 45 0.5× 63 1.4× 15 324
Gamze Güven Türkiye 11 124 0.5× 56 0.2× 125 1.1× 172 1.7× 45 1.0× 27 362
Mailis Liiv Estonia 7 390 1.5× 57 0.2× 71 0.6× 34 0.3× 46 1.0× 9 559
Amar Mubaidin Jordan 7 125 0.5× 88 0.4× 150 1.3× 116 1.2× 14 0.3× 10 297

Countries citing papers authored by Ilhem Turki

Since Specialization
Citations

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

Fields of papers citing papers by Ilhem Turki

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Ilhem Turki

This figure shows the co-authorship network connecting the top 25 collaborators of Ilhem Turki. A scholar is included among the top collaborators of Ilhem Turki 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 Ilhem Turki. Ilhem Turki 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.
Turki, Ilhem, et al.. (2024). Diabète de Type 1 et Syndrome Métabolique : Exploration d'une Relation Complexe. La Tunisie Médicale. 102(12). 1031–1034.
2.
Turki, Ilhem, Saad Hasan Mohammed Ali, Christian G. Bouwkamp, et al.. (2024). Genetic investigation of the ubiquitin-protein ligase E3A gene as putative target in Angelman syndrome. World Journal of Clinical Cases. 12(3). 503–516. 1 indexed citations
3.
Kraoua, Ichraf, et al.. (2024). Immunity in the Progeroid Model of Cockayne Syndrome: Biomarkers of Pathological Aging. Cells. 13(5). 402–402. 5 indexed citations
4.
Kraoua, Ichraf, Nadège Calmels, Cathy Obringer, et al.. (2022). Heterogeneous clinical features in Cockayne syndrome patients and siblings carrying the same CSA mutations. Orphanet Journal of Rare Diseases. 17(1). 121–121. 7 indexed citations
5.
Kraoua, Ichraf, Dimitri Schlemmer, Catherine Caillaud, et al.. (2022). Plasma GM2 ganglioside potential biomarker for diagnosis, prognosis and disease monitoring of GM2-Gangliosidosis. Molecular Genetics and Metabolism. 138(2). 106983–106983. 5 indexed citations
6.
Benrhouma, Hanène, et al.. (2021). Autoimmune Encephalitis in Tunisia: Report of a Pediatric Cohort. Journal of Immunology Research. 2021. 1–7. 7 indexed citations
7.
Achour, N. Ben, et al.. (2017). Childhood opsoclonus–myoclonus syndrome: A case series from Tunisia. Brain and Development. 39(9). 751–755. 6 indexed citations
8.
Mrabet, Saloua, N. Ben Achour, Ichraf Kraoua, et al.. (2015). Anti-Ma2-encephalitis in a 2 year-old child: A newly diagnosed case and literature review. European Journal of Paediatric Neurology. 19(6). 737–742. 15 indexed citations
9.
Kraoua, Ichraf, et al.. (2015). Status dystonicus in childhood.. PubMed. 93(12). 756–9. 19 indexed citations
10.
Mrabet, Saloua, et al.. (2015). Mixed movements disorders as an initial feature of pediatric lupus. Brain and Development. 37(9). 904–906. 5 indexed citations
11.
Benrhouma, Hanène, Sonia Nagi, Ichraf Kraoua, et al.. (2015). Tableau encéphalitique révélant une maladie de Wilson chez un garçon de 12 ans. Archives de Pédiatrie. 22(8). 892–894.
12.
Kraoua, Ichraf, et al.. (2014). Lesch Nyhan syndrome: A novel complex mutation in a Tunisian child. Brain and Development. 36(10). 921–923. 2 indexed citations
13.
Benrhouma, Hanène, et al.. (2012). Aspects cliniques et thérapeutiques des dystonies en Tunisie : étude prospective sur cinq ans. Revue Neurologique. 169(1). 47–52. 2 indexed citations
14.
Kraoua, Ichraf, et al.. (2008). Tuberculose cérébromédiastinale chez un enfant atteint de syndrome de Say-Barber-Miller probable : un lien de causalité ?. Revue Neurologique. 165(12). 1111–1116. 1 indexed citations
15.
Turki, Ilhem, et al.. (2005). L’hydatidose ptérygoïdienne. Revue de Stomatologie et de Chirurgie Maxillo-faciale. 106(1). 27–29. 9 indexed citations
16.
Amouri, Rim, Ilhem Turki, Karim Ouahchi, et al.. (2003). Phenotypic Features and Genetic Findings in Sacsin-Related Autosomal Recessive Ataxia in Tunisia. Archives of Neurology. 60(7). 982–982. 75 indexed citations
17.
Gouider‐Khouja, N., Samir Belal, Moncef Feki, et al.. (2001). Effect of vitamin E supplementation in patients with ataxia with vitamin E deficiency. European Journal of Neurology. 8(5). 477–481. 96 indexed citations
18.
Zouari, M., Moncef Feki, Christiane Ben Hamida, et al.. (1998). Electrophysiological and nerve biopsy: comparative study in Friedreich's ataxia and Friedreich's ataxia phenotype with vitamin E deficiency. Neuromuscular Disorders. 8(6). 416–425. 44 indexed citations
19.
Hamida, Mongi Ben, et al.. (1992). Duchenne muscular dystrophy in Tunisia: A clinical and morphological study of 77 cases. Journal of the Neurological Sciences. 107(1). 60–64. 8 indexed citations
20.
Turki, Ilhem, Hans Kresse, J Scotto, & Marc Tardieu. (1989). Sanfilippo Disease, Type C: Three Cases in the Same Family. Neuropediatrics. 20(2). 90–92. 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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