Imed Feki

1.6k total citations
35 papers, 503 citations indexed

About

Imed Feki is a scholar working on Cellular and Molecular Neuroscience, Neurology and Neurology. According to data from OpenAlex, Imed Feki has authored 35 papers receiving a total of 503 indexed citations (citations by other indexed papers that have themselves been cited), including 9 papers in Cellular and Molecular Neuroscience, 7 papers in Neurology and 5 papers in Neurology. Recurrent topics in Imed Feki's work include Hereditary Neurological Disorders (7 papers), Neurological diseases and metabolism (5 papers) and Genetic Neurodegenerative Diseases (5 papers). Imed Feki is often cited by papers focused on Hereditary Neurological Disorders (7 papers), Neurological diseases and metabolism (5 papers) and Genetic Neurodegenerative Diseases (5 papers). Imed Feki collaborates with scholars based in Tunisia, France and Saudi Arabia. Imed Feki's co-authors include Alexis Brice, Chokri Mhiri, Giovanni Stévanin, Alexandra Dürr, Amir Boukhris, Paola S. Denora, Nizar Elleuch, Jean‐Pascal Lefaucheur, Cyril Goizet and Jérémy Truchetto and has published in prestigious journals such as The American Journal of Human Genetics, Movement Disorders and Journal of Mathematical Analysis and Applications.

In The Last Decade

Imed Feki

32 papers receiving 495 citations

Peers

Imed Feki

CMN

NEURO

GENET

Camila Zaverucha-do-Valle Brazil

Holger Hengel Germany

Katrien Smets Belgium

Nazanin Ghazanfari Australia

Ágnes Patzkó United States

Samantha L. Sison United States

Elisabeth Dirren Switzerland

Andrew J. Schwab United States

Katia Cikurel United Kingdom

Nicholas Blair Australia

Camila Zaverucha-do-Valle Brazil

Imed Feki

250 ×0.8

CMN

136 ×0.7

NEURO

46 ×0.3

NEURO

99 ×0.9

GENET

13 ×0.2

Citations per year, relative to Imed Feki Imed Feki (= 1×) peers Camila Zaverucha-do-Valle

Countries citing papers authored by Imed Feki

Since Specialization

Citations

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

Fields of papers citing papers by Imed Feki

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Imed Feki

This figure shows the co-authorship network connecting the top 25 collaborators of Imed Feki. A scholar is included among the top collaborators of Imed Feki 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 Imed Feki. Imed Feki 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

Feki, Imed, Xianyi Zeng, Adel Ghith, et al.. (2016). Selecting Multiple Evaluator’s Perception-Oriented Relevant Physical Features of Consumer Goods by Using Fuzzy Data Sensitivity and OWA Operators. International Journal of Computational Intelligence Systems. 9(2). 213–213. 1 indexed citations

Feki, Imed, et al.. (2014). On Lp–L1 estimates of logarithmic-type in Hardy–Sobolev spaces of the disk and the annulus. Journal of Mathematical Analysis and Applications. 419(2). 1248–1260.

Alroughani, Raed, Hany Aref, Saeed Bohlega, et al.. (2014). Natalizumab treatment for multiple sclerosis: Middle East and North Africa regional recommendations for patient selection and monitoring. BMC Neurology. 14(1). 27–27. 4 indexed citations

Alroughani, Raed, Hany Aref, Saeed Bohlega, et al.. (2014). Natalizumab treatment for multiple sclerosis: Middle East and North Africa regional recommendations for patient selection and monitoring. Multiple Sclerosis and Related Disorders. 3(6). 753–754. 1 indexed citations

Boukhris, Amir, et al.. (2013). Deletion analysis of SMN and NAIP genes in Tunisian patients with spinal muscular atrophy. Annals of Indian Academy of Neurology. 16(1). 57–57. 2 indexed citations

Boukhris, Amir, Imed Feki, Nizar Elleuch, et al.. (2010). A new locus (SPG46) maps to 9p21.2-q21.12 in a Tunisian family with a complicated autosomal recessive hereditary spastic paraplegia with mental impairment and thin corpus callosum. Neurogenetics. 11(4). 441–448. 30 indexed citations

Marzouk, S., et al.. (2010). Thromboses artérielles multiples au cours de la maladie de Behçet. La Revue de Médecine Interne. 31(6). e1–e4. 2 indexed citations

Stévanin, Giovanni, Imed Feki, Paola S. Denora, et al.. (2009). Tunisian hereditary spastic paraplegias: clinical variability supported by genetic heterogeneity. Clinical Genetics. 75(6). 527–536. 41 indexed citations

Feki, Imed, et al.. (2009). Les anomalies cardiaques au cours de la dystrophie myotonique de Steinert. La Revue de Médecine Interne. 30(7). 573–577. 1 indexed citations

10.

Feki, Imed, et al.. (2009). Optimal logarithmic estimates in Hardy–Sobolev spaces H k , ∞ . Comptes Rendus Mathématique. 347(17-18). 1001–1006. 3 indexed citations

11.

Hanein, Sylvain, Elodie Martin, Amir Boukhris, et al.. (2008). Identification of the SPG15 Gene, Encoding Spastizin, as a Frequent Cause of Complicated Autosomal-Recessive Spastic Paraplegia, Including Kjellin Syndrome. The American Journal of Human Genetics. 82(4). 992–1002. 148 indexed citations

12.

Boukhris, Amir, Giovanni Stévanin, Imed Feki, et al.. (2008). Hereditary Spastic Paraplegia With Mental Impairment and Thin Corpus Callosum in Tunisia. Archives of Neurology. 65(3). 393–402. 38 indexed citations

13.

Zouch, Wassim, et al.. (2007). Combining WMN and FOCUSS recursive approach to estimating the current density distribution in the brain. Conference proceedings. 1. 598–601. 6 indexed citations

14.

Boukhris, Amir, et al.. (2007). Spastic paraplegia 15: Linkage and clinical description of three Tunisian families. Movement Disorders. 23(3). 429–433. 14 indexed citations

15.

Feki, Imed, et al.. (2007). Paraplégie spastique familiale avec amyotrophie sévère des mains (syndrome de Silver?). Revue Neurologique. 163(4). 476–479. 2 indexed citations

16.

Feki, Imed, et al.. (2007). Apport des échanges plasmatiques dans le traitement de la myasthénie : étude de 11 cas. La Revue de Médecine Interne. 29(2). 87–93. 1 indexed citations

17.

Feki, Imed, et al.. (2005). Chronic inflammatory joint disease revealing borderline leprosy. Joint Bone Spine. 73(3). 314–317. 11 indexed citations

18.

Feki, Imed, Chakib Marrakchi, M. Ben Hmida, et al.. (2004). Epidemic West Nile Virus Encephalitis in Tunisia. Neuroepidemiology. 24(1-2). 1–7. 22 indexed citations

19.

Feki, Imed & Jean‐Pascal Lefaucheur. (2001). Correlation between nerve conduction studies and clinical scores in diabetic neuropathy. Muscle & Nerve. 24(4). 555–558. 27 indexed citations

20.

Fontaine, Bertrand, Claire-Sophie Davoine, Alexandra Dürr, et al.. (2000). A New Locus for Autosomal Dominant Pure Spastic Paraplegia, on Chromosome 2q24-q34. The American Journal of Human Genetics. 66(2). 702–707. 65 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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