C. Ben Hamida

1.4k total citations
26 papers, 1.1k citations indexed

About

C. Ben Hamida is a scholar working on Molecular Biology, Cellular and Molecular Neuroscience and Surgery. According to data from OpenAlex, C. Ben Hamida has authored 26 papers receiving a total of 1.1k indexed citations (citations by other indexed papers that have themselves been cited), including 11 papers in Molecular Biology, 8 papers in Cellular and Molecular Neuroscience and 5 papers in Surgery. Recurrent topics in C. Ben Hamida's work include Muscle Physiology and Disorders (6 papers), Genetic Neurodegenerative Diseases (6 papers) and Neurological diseases and metabolism (4 papers). C. Ben Hamida is often cited by papers focused on Muscle Physiology and Disorders (6 papers), Genetic Neurodegenerative Diseases (6 papers) and Neurological diseases and metabolism (4 papers). C. Ben Hamida collaborates with scholars based in Tunisia, United States and France. C. Ben Hamida's co-authors include Gillian Butler‐Browne, Jacques Barbet, Stéphanie Decary, Vincent Mouly, Fayçal Hentati, Mongi Ben Hamida, M. Ben Hamida, Hatem Kallel, Hèdi Chelly and Mounir Bouaziz and has published in prestigious journals such as Brain, Neurology and Intensive Care Medicine.

In The Last Decade

C. Ben Hamida

26 papers receiving 1.0k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
C. Ben Hamida Tunisia 12 631 225 223 216 146 26 1.1k
Essam Al Shail Saudi Arabia 12 204 0.3× 417 1.9× 111 0.5× 103 0.5× 73 0.5× 35 907
Bülent Erdoğan Türkiye 17 131 0.2× 59 0.3× 109 0.5× 52 0.2× 428 2.9× 66 1.0k
Mingqiang Shen China 18 486 0.8× 113 0.5× 54 0.2× 74 0.3× 73 0.5× 53 1.1k
Sibylle Schmidt Germany 9 259 0.4× 138 0.6× 27 0.1× 19 0.1× 52 0.4× 14 553
Rong‐Kuo Lyu Taiwan 21 181 0.3× 97 0.4× 238 1.1× 60 0.3× 457 3.1× 73 1.3k
Wen Tang China 13 261 0.4× 148 0.7× 39 0.2× 14 0.1× 104 0.7× 46 795
Tayfun Hakan Türkiye 18 87 0.1× 44 0.2× 140 0.6× 192 0.9× 330 2.3× 60 1.0k
Ying Sheng China 19 493 0.8× 50 0.2× 53 0.2× 25 0.1× 115 0.8× 76 1.0k
Katarzyna Nazimek Poland 20 565 0.9× 81 0.4× 74 0.3× 67 0.3× 59 0.4× 52 992

Countries citing papers authored by C. Ben Hamida

Since Specialization
Citations

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

Fields of papers citing papers by C. Ben Hamida

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of C. Ben Hamida

This figure shows the co-authorship network connecting the top 25 collaborators of C. Ben Hamida. A scholar is included among the top collaborators of C. Ben Hamida 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 C. Ben Hamida. C. Ben Hamida 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.
Bahloul, Mabrouk, Kamilia Chtara, Hatem Kallel, et al.. (2008). Myocardiopathie du péripartum : incidence, physiopathologie, manifestations cliniques, prise en charge thérapeutique et pronostic. Annales Françaises d Anesthésie et de Réanimation. 28(1). 44–60. 10 indexed citations
2.
Bahloul, Mabrouk, Hassen Dammak, Hatem Kallel, et al.. (2007). Les microangiopathies thrombotiques. Incidence, physiopathologie, tableau clinique, prise en charge thérapeutique et pronostic. Journal des Maladies Vasculaires. 32(2). 75–82. 1 indexed citations
3.
Kallel, Hatem, Leila Hergafi, Mabrouk Bahloul, et al.. (2007). Safety and efficacy of colistin compared with imipenem in the treatmentof ventilator-associated pneumonia: a matched case–control study. Intensive Care Medicine. 33(7). 1162–1167. 127 indexed citations
4.
Bahloul, Mabrouk, et al.. (2006). Thrombose post-traumatique de l’artère rénale et déficit en protéine C. Journal des Maladies Vasculaires. 31(5). 277–279. 1 indexed citations
5.
Bahloul, Mabrouk, C. Ben Hamida, Hassen Dammak, et al.. (2006). Les microangiopathies thrombotiques en réanimation. Annales Françaises d Anesthésie et de Réanimation. 25(8). 820–827. 2 indexed citations
6.
Bahloul, Mabrouk, Hassen Dammak, Khaled Trabelsi, et al.. (2006). Stéatose hépatique aiguë gravidique. À propos de 22 cas. Gynécologie Obstétrique & Fertilité. 34(7-8). 597–606. 6 indexed citations
7.
Bahloul, Mabrouk, et al.. (2005). Maladie cœliaque, thrombose veineuse cérébrale et déficit en protéine S, Une association fortuite ?. Journal des Maladies Vasculaires. 30(4). 228–230. 10 indexed citations
8.
Kallel, Hatem, Hatem Ksibi, Hassen Dammak, et al.. (2005). Prevalence of hospital-acquired infection in a Tunisian hospital. Journal of Hospital Infection. 59(4). 343–347. 74 indexed citations
9.
Kéfi, M., Rim Amouri, Adel Driss, et al.. (2003). Phenotype and sarcoglycan expression in Tunisian LGMD 2C patients sharing the same del521-T mutation. Neuromuscular Disorders. 13(10). 779–787. 35 indexed citations
10.
Decary, Stéphanie, C. Ben Hamida, Vincent Mouly, et al.. (2000). Shorter telomeres in dystrophic muscle consistent with extensive regeneration in young children. Neuromuscular Disorders. 10(2). 113–120. 151 indexed citations
11.
Driss, Adel, Rim Amouri, C. Ben Hamida, et al.. (2000). A new locus for autosomal recessive limb-girdle muscular dystrophy in a large consanguineous Tunisian family maps to chromosome 19q13.3. Neuromuscular Disorders. 10(4-5). 240–246. 52 indexed citations
12.
Belal, Samir, C. Ben Hamida, Rim Amouri, et al.. (2000). Linkage to chromosome 13q11-12 of an autosomal recessive cerebellar ataxia in a Tunisian family. Neurology. 54(7). 1408–1414. 52 indexed citations
13.
Hamida, C. Ben, L Cavalier, Samir Belal, et al.. (1997). Homozygosity mapping of giant axonal neuropathy gene to chromosome 16q24.1. Neurogenetics. 1(2). 129–133. 39 indexed citations
14.
Decary, Stéphanie, et al.. (1997). Replicative Potential and Telomere Length in Human Skeletal Muscle: Implications for Satellite Cell-Mediated Gene Therapy. Human Gene Therapy. 8(12). 1429–1438. 244 indexed citations
15.
Wong, Jenny, et al.. (1997). LGMD 2E in Tunisia is caused by a missense mutation Arg91Leu in β-sarcoglycan. Neuromuscular Disorders. 7(6-7). 460–460. 1 indexed citations
16.
Bouaziz, Mounir, et al.. (1996). Cardiac dysfunction (CD) and pulmonary oedema (PE) following severe scorpion envenomation (SSE). Toxicon. 34(2). 157–157. 1 indexed citations
17.
Bejaoui, Khemissa, Koichi Hirabayashi, Fayçal Hentati, et al.. (1995). Linkage of Miyoshi myopathy (distal autosomal recessive muscular dystrophy) locus to chromosome 2p12-14. Neurology. 45(4). 768–772. 112 indexed citations
18.
Soussi‐Yanicostas, Nadia, C. Ben Hamida, Khemissa Bejaoui, et al.. (1992). Evolution of muscle specific proteins in Werdnig-Hoffman's disease. Journal of the Neurological Sciences. 109(1). 111–120. 13 indexed citations
19.
Hamida, Mongi Ben, et al.. (1990). HEREDITARY MOTOR SYSTEM DISEASES (CHRONIC JUVENILE AMYOTROPHIC LATERAL SCLEROSIS). Brain. 113(2). 347–363. 126 indexed citations
20.
Jemni, Mohamed, et al.. (1987). [Renal lithiasis and urothelial tumor].. PubMed. 21(5). 341–5. 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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