M. Ben Hamida

3.2k total citations · 1 hit paper
43 papers, 2.4k citations indexed

About

M. Ben Hamida is a scholar working on Cellular and Molecular Neuroscience, Molecular Biology and Neurology. According to data from OpenAlex, M. Ben Hamida has authored 43 papers receiving a total of 2.4k indexed citations (citations by other indexed papers that have themselves been cited), including 27 papers in Cellular and Molecular Neuroscience, 23 papers in Molecular Biology and 13 papers in Neurology. Recurrent topics in M. Ben Hamida's work include Genetic Neurodegenerative Diseases (19 papers), Hereditary Neurological Disorders (12 papers) and Mitochondrial Function and Pathology (10 papers). M. Ben Hamida is often cited by papers focused on Genetic Neurodegenerative Diseases (19 papers), Hereditary Neurological Disorders (12 papers) and Mitochondrial Function and Pathology (10 papers). M. Ben Hamida collaborates with scholars based in Tunisia, France and United States. M. Ben Hamida's co-authors include Fayçal Hentati, Samir Belal, Christiane Ben Hamida, K. Wessel, Alessandro Filla, B. V. Manyam, S. Massaquoi, T Takayanagi, Paula Coutinho and Norbert Nighoghossian and has published in prestigious journals such as Nature Genetics, Neurology and Annals of Neurology.

In The Last Decade

M. Ben Hamida

42 papers receiving 2.4k citations

Hit Papers

align trajectories

What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if it has ≥500 total citations, achieves ≥1.5× the top-1% citation threshold for papers in the same subfield and year (this is the minimum needed to enter the top 1%, not the average within it), or reaches the top citation threshold in at least one of its specific research topics.

International Cooperative Ataxia Rating Scale for pharmacological assessment of the cerebellar syndrome

1997 1.0k citations P Trouillas, T Takayanagi et al. Journal of the Neurological Sciences profile →

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
M. Ben Hamida Tunisia	22	1.3k	1.2k	681	492	210	43	2.4k
Giovanna Zorzi Italy	30	891 0.7×	898 0.7×	1.1k 1.6×	706 1.4×	71 0.3×	101	2.5k
Hideki Hida Japan	29	811 0.6×	879 0.7×	371 0.5×	498 1.0×	159 0.8×	81	2.2k
Grazia Annesi Italy	27	1.2k 1.0×	1.1k 0.9×	1.2k 1.7×	259 0.5×	203 1.0×	94	2.7k
Jean‐Marc Burgunder Switzerland	33	1.6k 1.2×	1.0k 0.8×	1.6k 2.4×	536 1.1×	322 1.5×	102	3.4k
Marina Romero‐Ramos Denmark	32	1.3k 1.0×	829 0.7×	1.8k 2.7×	1.2k 2.4×	98 0.5×	56	3.0k
Georgia Mandolesi Italy	37	1.1k 0.8×	937 0.8×	680 1.0×	1.2k 2.4×	115 0.5×	81	3.4k
Pau Pástor Spain	36	819 0.6×	952 0.8×	2.2k 3.2×	790 1.6×	146 0.7×	123	3.6k
Isabelle Neveu France	27	739 0.6×	744 0.6×	192 0.3×	211 0.4×	122 0.6×	57	2.5k
Jerònia Lladó Spain	24	849 0.6×	1.1k 0.9×	880 1.3×	442 0.9×	92 0.4×	34	2.7k
R Defendini United States	20	596 0.5×	735 0.6×	369 0.5×	319 0.6×	67 0.3×	31	2.2k

Countries citing papers authored by M. Ben Hamida

Since Specialization

Citations

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

Fields of papers citing papers by M. Ben Hamida

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

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

This figure shows the co-authorship network connecting the top 25 collaborators of M. Ben Hamida. A scholar is included among the top collaborators of M. 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 M. Ben Hamida. M. Ben Hamida 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

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

Gouider‐Khouja, N., Samir Belal, Moncef Feki, et al.. (2001). Effect of vitamin E supplementation in patients with ataxia with vitamin E deficiency. European Journal of Neurology. 8(5). 477–481. 96 indexed citations

Larnaout, A., et al.. (1998). Methylmalonic acidaemia with bilateral globus pallidus involvement: A neuropathological study. Journal of Inherited Metabolic Disease. 21(6). 639–644. 23 indexed citations

Bönnemann, Carsten G., et al.. (1998). LGMD 2E in Tunisia is caused by a homozygous missense mutation in β-sarcoglycan exon 3. Neuromuscular Disorders. 8(3-4). 193–197. 28 indexed citations

Larnaout, A., M. Ben Hamida, & Fayçal Hentati. (1998). A clinicopathological observation of Nyssen-van Bogaert syndrome with second motor neuron degeneration: two distinct clinical entities. Acta Neurologica Scandinavica. 98(6). 452–457. 4 indexed citations

Larnaout, A., Samir Belal, Christiane Ben Hamida, M. Ben Hamida, & Fayçal Hentati. (1998). Atypical ataxia telangiectasia with early childhood lower motor neuron degeneration: a clinicopathological observation in three siblings. Journal of Neurology. 245(4). 231–235. 13 indexed citations

Zouari, M., Moncef Feki, Christiane Ben Hamida, et al.. (1998). Electrophysiological and nerve biopsy: comparative study in Friedreich's ataxia and Friedreich's ataxia phenotype with vitamin E deficiency. Neuromuscular Disorders. 8(6). 416–425. 44 indexed citations

Trouillas, P, T Takayanagi, Mark Hallett, et al.. (1997). International Cooperative Ataxia Rating Scale for pharmacological assessment of the cerebellar syndrome. Journal of the Neurological Sciences. 145(2). 205–211. 1010 indexed citations breakdown →

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

10.

Larnaout, A., Samir Belal, M. Zouari, et al.. (1997). Friedreich's ataxia with isolated vitamin E deficiency: a neuropathological study of a Tunisian patient. Acta Neuropathologica. 93(6). 633–637. 42 indexed citations

11.

Fontaine, Bertrand, Sophie Nicole, Haluk Topaloğlu, et al.. (1996). Recessive Schwartz-Jampel syndrome (SJS): confirmation of linkage to chromosome 1p, evidence of genetic homogeneity and reduction of the SJS locus to a 3-cM interval. Human Genetics. 98(3). 380–385. 20 indexed citations

12.

Hamida, M. Ben, et al.. (1996). Limb-girdle muscular dystrophy 2C: Clinical aspects. Neuromuscular Disorders. 6(6). 493–494. 24 indexed citations

13.

Hamida, Christiane Ben, Nadia Soussi‐Yanicostas, Khemissa Bejaoui, et al.. (1994). Expression of myosin isoforms and of desmin, vimentin and titin in Tunisian Duchenne-like autosomal recessive muscular dystrophy. Journal of the Neurological Sciences. 123(1-2). 114–121. 4 indexed citations

14.

Larnaout, A., et al.. (1994). Clinical and pathological study of three Tunisian siblings with L-2-hydroxyglutaric aciduria. Acta Neuropathologica. 88(4). 367–370. 32 indexed citations

15.

Hamida, M. Ben, et al.. (1993). Prevalence Study of Neurologic Disorders in Kelibia (Tunisia). Neuroepidemiology. 12(5). 285–299. 67 indexed citations

16.

Belal, Samir, Giorgio Sirugo, P.A. Ioannou, et al.. (1992). Study of large inbred Friedreich ataxia families reveals a recombination between D9S15 and the disease locus.. PubMed. 51(6). 1372–6. 11 indexed citations

17.

Dellagi, Koussay, et al.. (1992). Childhood peripheral neuropathy with autoantibodies to myelin glycoprotein Po. Annals of Neurology. 32(5). 700–702. 11 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.

Soussi‐Yanicostas, Nadia, Christiane Ben Hamida, Gillian Butler‐Browne, et al.. (1991). Modification in the expression and localization of contractile and cytoskeletal proteins in Schwartz-Jampel syndrome. Journal of the Neurological Sciences. 104(1). 64–73. 10 indexed citations

20.

Hamida, M. Ben, et al.. (1987). Hypertrophic neuropathy in spinocerebellar degeneration. Acta Neuropathologica. 75(1). 51–61. 2 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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