Mounir Kefi

424 total citations
7 papers, 221 citations indexed

About

Mounir Kefi is a scholar working on Molecular Biology, Neurology and Cellular and Molecular Neuroscience. According to data from OpenAlex, Mounir Kefi has authored 7 papers receiving a total of 221 indexed citations (citations by other indexed papers that have themselves been cited), including 4 papers in Molecular Biology, 4 papers in Neurology and 3 papers in Cellular and Molecular Neuroscience. Recurrent topics in Mounir Kefi's work include Parkinson's Disease Mechanisms and Treatments (3 papers), Neurological diseases and metabolism (2 papers) and Mitochondrial Function and Pathology (2 papers). Mounir Kefi is often cited by papers focused on Parkinson's Disease Mechanisms and Treatments (3 papers), Neurological diseases and metabolism (2 papers) and Mitochondrial Function and Pathology (2 papers). Mounir Kefi collaborates with scholars based in Tunisia, United States and United Kingdom. Mounir Kefi's co-authors include Fayçal Hentati, Rim Amouri, M. Zouari, Matthew J. Farrer, Mary Hulihan, Lefkos Middleton, Samia Ben Yahmed, Rachel A. Gibson, Samia Ben Sassi and Jennifer M. Kachergus and has published in prestigious journals such as The Lancet Neurology, Movement Disorders and Human Mutation.

In The Last Decade

Mounir Kefi

7 papers receiving 212 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Mounir Kefi Tunisia	6	159	82	70	64	51	7	221
A. B. Singleton United States	7	149 0.9×	104 1.3×	113 1.6×	64 1.0×	87 1.7×	8	269
Daniela Corongiu Italy	8	113 0.7×	61 0.7×	96 1.4×	47 0.7×	39 0.8×	12	239
G. Volpe Italy	7	302 1.9×	183 2.2×	87 1.2×	107 1.7×	59 1.2×	9	373
Alice Prigent France	7	109 0.7×	76 0.9×	57 0.8×	30 0.5×	51 1.0×	9	201
Janet Brooks United States	7	104 0.7×	55 0.7×	52 0.7×	37 0.6×	32 0.6×	13	196
Bjørg Warø Norway	5	194 1.2×	65 0.8×	66 0.9×	47 0.7×	58 1.1×	5	246
Emna Hentati Tunisia	5	105 0.7×	49 0.6×	42 0.6×	42 0.7×	41 0.8×	6	152
Uladzislau Rudakou Canada	9	122 0.8×	51 0.6×	55 0.8×	41 0.6×	66 1.3×	9	208
Sachiko Noda Japan	7	142 0.9×	86 1.0×	142 2.0×	41 0.6×	71 1.4×	14	332
Petra Leitner Germany	6	359 2.3×	145 1.8×	161 2.3×	115 1.8×	106 2.1×	7	459

Countries citing papers authored by Mounir Kefi

Since Specialization

Citations

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

Fields of papers citing papers by Mounir Kefi

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Mounir Kefi

This figure shows the co-authorship network connecting the top 25 collaborators of Mounir Kefi. A scholar is included among the top collaborators of Mounir Kefi 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 Mounir Kefi. Mounir Kefi is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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7 of 7 papers shown

1.

Sassi, Samia Ben, et al.. (2010). Cerebral Venous Thrombosis Presenting With Cerebellar Ataxia and Cortical Blindness. Journal of Stroke and Cerebrovascular Diseases. 19(6). 507–509. 8 indexed citations

2.

Jasińska‐Myga, Barbara, Jennifer M. Kachergus, Carles Vilariño‐Güell, et al.. (2010). Comprehensive sequencing of the LRRK2 gene in patients with familial Parkinson's disease from North Africa. Movement Disorders. 25(13). 2052–2058. 14 indexed citations

3.

Kefi, Mounir, et al.. (2010). A Novel Heteroplasmic tRNASer(UCN) mtDNA Point Mutation Associated With Progressive Ophthalmoplegia and Dysphagia. Diagnostic Molecular Pathology. 19(1). 28–32. 4 indexed citations

4.

Amouri, Rim, et al.. (2009). Allelic ROBO3 Heterogeneity in Tunisian Patients with Horizontal Gaze Palsy with Progressive Scoliosis. Journal of Molecular Neuroscience. 39(3). 337–341. 25 indexed citations

5.

Bouhlal, Yosr, M. Zouari, Mounir Kefi, et al.. (2008). Autosomal Recessive Ataxia Caused by Three Distinct Gene Defects in a Single Consanguineous Family. Journal of Neurogenetics. 22(2). 139–148. 17 indexed citations

6.

Hulihan, Mary, Jennifer M. Kachergus, Liling Warren, et al.. (2008). LRRK2 Gly2019Ser penetrance in Arab–Berber patients from Tunisia: a case-control genetic study. The Lancet Neurology. 7(7). 591–594. 120 indexed citations

7.

Vilariño‐Güell, Carles, Alexandra I. Soto, Sarah Lincoln, et al.. (2008). ATP13A2variability in Parkinson disease. Human Mutation. 30(3). 406–410. 33 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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