A. Mrabet

984 total citations
59 papers, 716 citations indexed

About

A. Mrabet is a scholar working on Psychiatry and Mental health, Neurology and Physiology. According to data from OpenAlex, A. Mrabet has authored 59 papers receiving a total of 716 indexed citations (citations by other indexed papers that have themselves been cited), including 15 papers in Psychiatry and Mental health, 12 papers in Neurology and 9 papers in Physiology. Recurrent topics in A. Mrabet's work include Epilepsy research and treatment (11 papers), Glycogen Storage Diseases and Myoclonus (5 papers) and Genetics and Neurodevelopmental Disorders (5 papers). A. Mrabet is often cited by papers focused on Epilepsy research and treatment (11 papers), Glycogen Storage Diseases and Myoclonus (5 papers) and Genetics and Neurodevelopmental Disorders (5 papers). A. Mrabet collaborates with scholars based in Tunisia, France and Czechia. A. Mrabet's co-authors include Riadh Gouider, B. Zouari, T. Chkili, M. Ben Hamida, Ahmed Bouhouche, Éric Leguern, Alexis Brice, Marco Di Duca, T. Hammadouche and Nazha Birouk and has published in prestigious journals such as Annals of Neurology, The American Journal of Human Genetics and Epilepsia.

In The Last Decade

A. Mrabet

56 papers receiving 691 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
A. Mrabet Tunisia 12 201 184 179 143 128 59 716
M.V. Padma India 19 249 1.2× 280 1.5× 265 1.5× 196 1.4× 72 0.6× 59 1.1k
Naomi Hino‐Fukuyo Japan 17 160 0.8× 454 2.5× 91 0.5× 107 0.7× 137 1.1× 59 901
Jesús Manuel Eirís Puñal Spain 16 273 1.4× 229 1.2× 64 0.4× 300 2.1× 169 1.3× 91 867
Madhu Nagappa India 15 242 1.2× 149 0.8× 202 1.1× 127 0.9× 53 0.4× 100 895
Roshan Koul Oman 15 269 1.3× 165 0.9× 250 1.4× 265 1.9× 67 0.5× 83 864
Ichiro Kuki Japan 13 192 1.0× 203 1.1× 107 0.6× 106 0.7× 143 1.1× 87 675
Radhika Dhamija United States 16 144 0.7× 222 1.2× 92 0.5× 76 0.5× 193 1.5× 64 721
Galen N. Breningstall United States 19 170 0.8× 540 2.9× 236 1.3× 246 1.7× 93 0.7× 51 1.2k
Maurizio Viri Italy 16 431 2.1× 197 1.1× 150 0.8× 241 1.7× 243 1.9× 34 764
Jeehun Lee South Korea 17 250 1.2× 204 1.1× 101 0.6× 219 1.5× 99 0.8× 80 855

Countries citing papers authored by A. Mrabet

Since Specialization
Citations

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

Fields of papers citing papers by A. Mrabet

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of A. Mrabet

This figure shows the co-authorship network connecting the top 25 collaborators of A. Mrabet. A scholar is included among the top collaborators of A. Mrabet 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 A. Mrabet. A. Mrabet 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.
Ahmed, Imtiaz, et al.. (2020). Delays in management of ST-segment elevation myocardial infarction. Archives of Cardiovascular Diseases Supplements. 12(1). 25–25. 2 indexed citations
2.
Ajili, F., et al.. (2014). Caractéristiques de la maladie de Behçet avec atteinte oculaire en Tunisie : étude monocentrique et revue de la littérature. Pathologie Biologie. 63(2). 85–90. 3 indexed citations
3.
Bibi, Amina, et al.. (2013). No association between an intronic polymorphism in the presenilin-1 gene and Alzheimer disease in a Tunisian population. Journal of Neural Transmission. 120(9). 1355–1358. 5 indexed citations
4.
Béna, Frédérique, A. Mrabet, Michel Guipponi, et al.. (2013). A new locus on chromosome 22q13.31 linked to recessive genetic epilepsy with febrile seizures plus (GEFS+) in a Tunisian consanguineous family. BMC Genetics. 14(1). 93–93. 10 indexed citations
5.
Borhani‐Haghighi, Afshin, Emel Köseoğlu, Melike Mutlu, et al.. (2012). Association of amyotrophic lateral sclerosis and Behcet’s disease: is there a relationship? A multi-national case series. Clinical Rheumatology. 31(4). 733–738. 6 indexed citations
6.
Banasr, Ahmed, et al.. (2011). Posttraumatic epilepsy in Tunisia. Epilepsy & Behavior. 21(4). 417–419.
7.
Benali, Nadia, et al.. (2011). Obsessive–compulsive disorder: a new risk factor for Alzheimer disease?. Neurological Sciences. 32(5). 959–962. 16 indexed citations
8.
Rekik, S., et al.. (2011). Back pain caused by a pseudo-tumorous vertebral collapse: atypical presentation of primary vertebral hydatidosis. BMJ Case Reports. 2011. bcr0220113853–bcr0220113853. 1 indexed citations
9.
Parain, D., et al.. (2010). Epilepsy surgery program in Tunisia: An example of a Tunisian French collaboration. Seizure. 19(2). 74–78. 17 indexed citations
10.
Ollivier, L., Vincent Pommier de Santi, A. Mrabet, et al.. (2009). Infections sexuellement transmissibles et contaminations sexuelles par le virus de l’immunodéficience humaine dans les armées françaises en 2006. Annales de Dermatologie et de Vénéréologie. 136(5). 412–418. 3 indexed citations
11.
Gouider, Riadh, et al.. (2008). Les tuberculomes cérébraux. Revue Neurologique. 159. 795–798. 1 indexed citations
12.
Masmoudi, Saber, et al.. (2008). Association syndrome de Parry-Romberg et dyskinésie paroxystique kinésigénique. Revue Neurologique. 165(5). 489–492. 5 indexed citations
13.
Mrabet, A., et al.. (2007). GEFS+ is not related to the most common mutations of SCN1B, SCN1A and GABRG2 in two Tunisian families. Neurological Sciences. 28(6). 311–314. 4 indexed citations
14.
Masmoudi, Saber, et al.. (2007). Myotonie et hypothyroïdie. Revue Neurologique. 163(8-9). 837–839. 2 indexed citations
15.
Mrabet, A., et al.. (2005). Syndrome de dyke-davidoff-masson : à propos de deux observations. Journal of Neuroradiology. 32(1). 50–53. 10 indexed citations
16.
Mrabet, A., et al.. (2004). Health‐related Quality of Life of People with Epilepsy Compared with a General Reference Population: A Tunisian Study. Epilepsia. 45(7). 838–843. 82 indexed citations
17.
Lalioti, Maria D., Hamish S. Scott, Pierre Genton, et al.. (1998). A PCR Amplification Method Reveals Instability of the Dodecamer Repeat in Progressive Myoclonus Epilepsy (EPM1) and No Correlation between the Size of the Repeat and Age at Onset. The American Journal of Human Genetics. 62(4). 842–847. 52 indexed citations
18.
Baldy-Moulinier, M, Samuel C. Durso, Cinzia Fattore, et al.. (1998). Therapeutic strategies against epilepsy in Mediterranean countries: A report from an international collaborative survey. Seizure. 7(6). 513–520. 14 indexed citations
19.
Labauge, Pierre, Réda Ouazzani, A. Mrabet, et al.. (1997). Allelic heterogeneity of mediterranean myoclonus and the cystatin B gene. Annals of Neurology. 41(5). 686–689. 3 indexed citations
20.
Mrabet, A., et al.. (1991). [Clinical and electrophysiological study of 2 familial cases of Marcus Gunn phenomenon].. PubMed. 147(3). 215–9. 9 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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