Mongi Ben Hamida

4.1k total citations
27 papers, 2.4k citations indexed

About

Mongi Ben Hamida is a scholar working on Molecular Biology, Cellular and Molecular Neuroscience and Neurology. According to data from OpenAlex, Mongi Ben Hamida has authored 27 papers receiving a total of 2.4k indexed citations (citations by other indexed papers that have themselves been cited), including 14 papers in Molecular Biology, 10 papers in Cellular and Molecular Neuroscience and 9 papers in Neurology. Recurrent topics in Mongi Ben Hamida's work include Neurological diseases and metabolism (9 papers), Neurogenetic and Muscular Disorders Research (7 papers) and Hereditary Neurological Disorders (7 papers). Mongi Ben Hamida is often cited by papers focused on Neurological diseases and metabolism (9 papers), Neurogenetic and Muscular Disorders Research (7 papers) and Hereditary Neurological Disorders (7 papers). Mongi Ben Hamida collaborates with scholars based in Tunisia, United States and France. Mongi Ben Hamida's co-authors include Fayçal Hentati, Jeffery M. Vance, Kamel Ben Othmane, Herbert J. Kayden, Christiane Ben Hamida, Karim Ouahchi, Michel Fardeau, Keizo Inoue, Ronald J. Sokol and Makoto Arita and has published in prestigious journals such as Science, Nature Genetics and Brain.

In The Last Decade

Mongi Ben Hamida

27 papers receiving 2.3k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Mongi Ben Hamida Tunisia 18 1.3k 1.0k 637 442 434 27 2.4k
Barbara Castellotti Italy 25 987 0.7× 757 0.7× 670 1.1× 341 0.8× 252 0.6× 65 1.8k
A E Harding United Kingdom 31 1.7k 1.3× 1.3k 1.3× 791 1.2× 234 0.5× 468 1.1× 61 3.1k
W.‐Y. Hung United States 14 621 0.5× 362 0.4× 562 0.9× 388 0.9× 305 0.7× 29 1.3k
Ali Benomar Morocco 21 1.5k 1.1× 1.7k 1.7× 709 1.1× 158 0.4× 346 0.8× 69 2.3k
Rim Amouri Tunisia 24 702 0.5× 667 0.7× 541 0.8× 69 0.2× 345 0.8× 58 1.5k
Hitoshi Warita Japan 32 1.0k 0.8× 523 0.5× 1.1k 1.8× 646 1.5× 394 0.9× 113 2.4k
Faisal Fecto United States 13 669 0.5× 287 0.3× 984 1.5× 532 1.2× 314 0.7× 19 1.6k
Alessandra Tessa Italy 29 1.6k 1.2× 1.0k 1.0× 251 0.4× 280 0.6× 496 1.1× 139 2.5k
Ornella Cuomo Italy 27 1.1k 0.8× 573 0.6× 184 0.3× 82 0.2× 309 0.7× 68 1.9k
Lyndsey Braun United States 14 1.3k 1.0× 440 0.4× 1.1k 1.7× 1.0k 2.3× 591 1.4× 20 2.7k

Countries citing papers authored by Mongi Ben Hamida

Since Specialization
Citations

This map shows the geographic impact of Mongi 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 Mongi 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 Mongi Ben Hamida more than expected).

Fields of papers citing papers by Mongi Ben Hamida

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Mongi Ben Hamida

This figure shows the co-authorship network connecting the top 25 collaborators of Mongi Ben Hamida. A scholar is included among the top collaborators of Mongi 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 Mongi Ben Hamida. Mongi 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.
Gouider‐Khouja, N., A. Larnaout, Rim Amouri, et al.. (2003). Autosomal recessive parkinsonism linked to parkin gene in a Tunisian family. Clinical, genetic and pathological study. Parkinsonism & Related Disorders. 9(5). 247–251. 69 indexed citations
2.
Othmane, Kamel Ben, Julie M. Rochelle, Jason Stajich, et al.. (2001). Ganglioside-induced differentiation-associated protein-1 is mutant in Charcot-Marie-Tooth disease type 4A/8q21. Nature Genetics. 30(1). 21–22. 271 indexed citations
3.
Cavalier, L, Rim Amouri, Samir Belal, et al.. (2000). Giant axonal neuropathy locus refinement to a < 590 kb critical interval. European Journal of Human Genetics. 8(7). 527–534. 18 indexed citations
4.
Copp, Richard P., Thomas Wısnıewskı, Fayçal Hentati, et al.. (1999). Localization of α-tocopherol transfer protein in the brains of patients with ataxia with vitamin E deficiency and other oxidative stress related neurodegenerative disorders. Brain Research. 822(1-2). 80–87. 97 indexed citations
5.
Othmane, Kamel Ben, Marisa M. Menold, Felicia L. Graham, et al.. (1999). Identification of a New Locus for Autosomal Recessive Charcot–Marie–Tooth Disease with Focally Folded Myelin on Chromosome 11p15. Genomics. 62(3). 344–349. 60 indexed citations
6.
Hentati, Afif, Karim Ouahchi, Margaret A. Pericak‐Vance, et al.. (1998). Linkage of a commoner form of recessive amyotrophic lateral sclerosis to chromosome 15q15-q22 markers. Neurogenetics. 2(1). 55–60. 126 indexed citations
7.
Liu, Jing, Chenyan Wu, Khemissa Bejaoui, et al.. (1998). Generation of a 3-Mb PAC Contig Spanning the Miyoshi Myopathy/Limb-Girdle Muscular Dystrophy (MM/LGMD2B) Locus on Chromosome 2p13. Genomics. 49(1). 23–29. 13 indexed citations
8.
Othmane, Kamel Ben, Julie M. Rochelle, Mongi Ben Hamida, et al.. (1998). Fine localization of the CMT4A locus using a PAC contig and haplotype analysis. Neurogenetics. 2(1). 18–23. 8 indexed citations
9.
Hosler, Betsy A., Peter C. Sapp, Ralph Berger, et al.. (1998). Refined mapping and characterization of the recessive familial amyotrophic lateral sclerosis locus ( ALS2 ) on chromosome 2q33. Neurogenetics. 2(1). 34–42. 21 indexed citations
10.
Nicole, Sophie, Christiane Ben Hamida, Peter Beighton, et al.. (1995). Localization of the Schwartz–Jampel syndrome (SJS) locus to chromosome 1p34–p36.1 by homozygosity mapping. Human Molecular Genetics. 4(9). 1633–1636. 36 indexed citations
11.
Noguchi, S., Elizabeth M. McNally, Kamel Ben Othmane, et al.. (1995). Mutations in the Dystrophin-Associated Protein γ-Sarcoglycan in Chromosome 13 Muscular Dystrophy. Science. 270(5237). 819–822. 414 indexed citations
12.
Hentati, Afif, Margaret A. Pericak‐Vance, Felicia Lennon, et al.. (1994). Linkage of a locus for autosomal dominant familial spastic paraplegia to chromosome 2p markers. Human Molecular Genetics. 3(10). 1867–1871. 71 indexed citations
13.
Hentati, Afif, Khemissa Bejaoui, Margaret A. Pericak‐Vance, et al.. (1994). Linkage of recessive familial amyotrophic lateral sclerosis to chromosome 2q33–q35. Nature Genetics. 7(3). 425–428. 164 indexed citations
14.
Hamida, Christiane Ben, Nadia Soussi‐Yanicostas, Gillian Butler‐Browne, et al.. (1994). Biochemical and immunocytochemical analysis in chronic proximal spinal muscular atrophy. Muscle & Nerve. 17(4). 400–410. 7 indexed citations
15.
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
16.
Othmane, Kamel Ben, Mongi Ben Hamida, Margaret A. Pericak‐Vance, et al.. (1992). Linkage of Tunisian autosomal recessive Duchenne–like muscular dystrophy to the pericentromeric region of chromosome 13q. Nature Genetics. 2(4). 315–317. 144 indexed citations
17.
Hamida, Christiane Ben, et al.. (1992). Age-dependent axonal loss in nerve biopsy of patients with xeroderma pigmentosum. Neuromuscular Disorders. 2(5-6). 361–369. 7 indexed citations
18.
Hamida, Mongi Ben, et al.. (1990). HEREDITARY MOTOR SYSTEM DISEASES (CHRONIC JUVENILE AMYOTROPHIC LATERAL SCLEROSIS). Brain. 113(2). 347–363. 126 indexed citations
19.
Belhadj, Omrane, et al.. (1987). Pyrimidine pathways enzymes in human tumors of brain and associated tissues: Potentialities for the therapeutic use of N-(Phosphonacetyl-l-aspartate and 1-β-d-arabinofuranosylcytosine. European Journal of Cancer and Clinical Oncology. 23(10). 1485–1490. 16 indexed citations
20.
Hamida, Mongi Ben, et al.. (1981). Les atrophies péronières en Tunisie. Journal of the Neurological Sciences. 50(3). 335–356. 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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