M. Ben Hamida

3.2k citations

43 papers · 2.4k · 1 hit paper · h-index 22

Impact in

Cellular and Molecular Neuroscience top 1%
- Genetic Neurodegenerative Diseases
- Hereditary Neurological Disorders
Neurology top 2%
- Neurological disorders and treatments
- Parkinson's Disease Mechanisms and Treatments
- Vestibular and auditory disorders
- Neurological diseases and metabolism

Papers in

Cellular and Molecular Neuroscience 27
- Genetic Neurodegenerative Diseases 19
- Hereditary Neurological Disorders 12
Molecular Biology 23
- Mitochondrial Function and Pathology 10
- Muscle Physiology and Disorders 10

Co-authors: Fayçal Hentati (27 shared papers)Samir Belal (16 shared papers)Christiane Ben Hamida (14 shared papers)B. V. Manyam (1 shared paper)T Takayanagi (1 shared paper)Lawrence J. Schut (1 shared paper)Robert D. Currier (1 shared paper)Hans‐Christoph Diener (1 shared paper)
Journals: Neurology (7 papers)Neuromuscular Disorders (7 papers)Journal of the Neurological Sciences (4 papers)Acta Neuropathologica (3 papers)Journal of Inherited Metabolic Disease (2 papers)
Partner nations: Tunisia France United States

In The Last Decade

M. Ben Hamida

42 papers receiving 2.4k citations

Hit Papers

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International Cooperative Ataxia Rating Scale for pharmacological assessment of the cerebellar syndrome 1997 · 1.0k citations

Peers

Countries citing papers authored by M. Ben Hamida

Since Specialization

Citations

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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-authors

The 25 scholars most cited alongside M. Ben Hamida, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.

Border = papers with M. Ben Hamida Line = papers co-authored together M. Ben Hamida links everyone, so they are left out of the graph.

All Works

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20 of 20 papers shown

Showing the 20 most-cited of 43 papers — load more, or switch the sort, to bring in the rest.

#	Work
1	International Cooperative Ataxia Rating Scale for pharmacological assessment of the cerebellar syndrome Journal of the Neurological Sciences ·P Trouillas, T Takayanagi, Mark Hallett, Robert D. Currier, S. H. Subramony, K. Wessel, Alan Bryer, Hans‐Christoph Diener, S. Massaquoi, Christopher M. Gómez, Paula Coutinho, M. Ben Hamida, G Campanella, Alessandro Filla, Lawrence J. Schut, D. Timann, J Honnorat, Norbert Nighoghossian, B. V. Manyam Hit paper breakdown →	1997	1010
2	Localization of Friedreich ataxia phenotype with selective vitamin E deficiency to chromosome 8q by homozygosity mapping Nature Genetics ·Christiane Ben Hamida, Nathalie Doerflinger, Samir Belal, Catherine Y. Linder, Laurence Reutenauer, Colette Dib, Gàbor Gyapay, Alain Vignal, Denis Le Paslier, Daniel Cohen, Massimo Pandolfo, Vahe Mokini, Giuseppe Novelli, F. Hentati, M. Ben Hamida, Jean‐Louis Mandel, Michel Kœnig	1993	163
3	Linkage of a locus (CMT4A) for autosomal recessive Charcot-Marie-Tooth disease to chromosome 8q Human Molecular Genetics ·Kamel Ben Othmane, F. Hentatl, Felicia Lennon, Christiane Ben Hamida, Samir Blel, A.D. Roses, Margaret A Pericak‐Vance, M. Ben Hamida, Jeffery M. Vance	1993	136
4	Linkage of Miyoshi myopathy (distal autosomal recessive muscular dystrophy) locus to chromosome 2p12-14 Neurology ·Khemissa Bejaoui, Koichi Hirabayashi, Fayçal Hentati, J. L. Haines, C. Ben Hamida, Samir Belal, Robert G. Miller, D. McKenna‐Yasek, J. Weissenbach, Lewis P. Rowland, Robert C. Griggs, T. L. Munsat, M. Ben Hamida, Kiichi Arahata, Robert Brown	1995	112
5	Effect of vitamin E supplementation in patients with ataxia with vitamin E deficiency European Journal of Neurology ·S. Gabsi, N. Gouider‐Khouja, Samir Belal, Moncef Feki, M. Kéfi, Ilhem Turki, M. Ben Hamida, Herbert J. Kayden, R Mebazaa, F. Hentati	2001	96
6	Friedreich's ataxia phenotype not linked to chromosome 9 and associated with selective autosomal recessive vitamin E deficiency in two inbred Tunisian families Neurology ·M. Ben Hamida, Samir Belal, Giorgio Sirugo, Christiane Ben Hamida, Kyproula Panayides, P. Ionannou, J. Beckmann, Jean‐Louis Mandel, F. Hentati, M. Koenig, Lefkos Middleton	1993	96
7	Prevalence Study of Neurologic Disorders in Kelibia (Tunisia) Neuroepidemiology ·Neila Attia Romdhane, M. Ben Hamida, Ali Mrabet, A. Larnaout, Samar Samoud, A. Ben Hamda, M. Ben Hamda, S. Oueslati	1993	67
8	A new locus for autosomal recessive limb-girdle muscular dystrophy in a large consanguineous Tunisian family maps to chromosome 19q13.3 Neuromuscular Disorders ·Adel Driss, Rim Amouri, C. Ben Hamida, Sihem Souilem, N. Gouider‐Khouja, M. Ben Hamida, Fayçal Hentati	2000	52
9	Linkage to chromosome 13q11-12 of an autosomal recessive cerebellar ataxia in a Tunisian family Neurology ·Najiba Fekih Mrissa, Samir Belal, C. Ben Hamida, Rim Amouri, Ilhem Turki, Ridha Mrissa, M. Ben Hamida, F. Hentati	2000	52
10	Novel mutations in spastin gene and absence of correlation with age at onset of symptoms Neurology ·Afif Hentati, Han‐Xiang Deng, Hong Zhai, W. Chen, Yi Yang, Wu-Yen Hung, Anser C. Azim, Saeed Bohlega, Rup Tandan, Carolyn L. Warner, Nigel G. Laing, Franca Cambi, Hiroshi Mitsumoto, Raymond P. Roos, Rose-Mary Boustany, M. Ben Hamida, Fayçal Hentati, Teepu Siddique	2000	51
11	Prevalence of Epilepsy in Kelibia, Tunisia Epilepsia ·N Attia-Romdhane, A. Mrabet, M. Ben Hamida	1993	47
12	Electrophysiological and nerve biopsy: comparative study in Friedreich's ataxia and Friedreich's ataxia phenotype with vitamin E deficiency Neuromuscular Disorders ·M. Zouari, Moncef Feki, Christiane Ben Hamida, A. Larnaout, Ilhem Turki, Samir Belal, Abderraouf Mebazaa, M. Ben Hamida, Fayçal Hentati	1998	44
13	Friedreich's ataxia with isolated vitamin E deficiency: a neuropathological study of a Tunisian patient Acta Neuropathologica ·A. Larnaout, Samir Belal, M. Zouari, Moncef Feki, Christiane Ben Hamida, Hans H. Goebel, M. Ben Hamida, Fayçal Hentati	1997	42
14	Clinical and genetic analysis of a Tunisian family with autosomal dominant cerebellar ataxia type 1linked to the SCA2 locus Neurology ·Samir Belal, Géraldine Cancel‐Tassin, Giovanni Stévanin, Fayçal Hentati, C. Khati, Christiane Ben Hamida, G Auburger, Yves Agid, M. Ben Hamida, Alexis Brice	1994	42
15	Homozygosity mapping of giant axonal neuropathy gene to chromosome 16q24.1 Neurogenetics ·C. Ben Hamida, L Cavalier, Samir Belal, H. Sanhaji, Nathalie Nadal, C. Barhoumi, Najiba Fekih Mrissa, Naïma Marzouki, Jean‐Louis Mandel, M. Ben Hamida, M. Kœnig, Fayçal Hentati	1997	39
16	Linkage of a new locus for autosomal recessive axonal form of Charcot–Marie–Tooth disease to chromosome 8q21.3 Neuromuscular Disorders ·C. Barhoumi, Rim Amouri, Christiane Ben Hamida, M. Ben Hamida, Samia Machghoul, M Gueddiche, Fayçal Hentati	2001	36
17	Phenotype and sarcoglycan expression in Tunisian LGMD 2C patients sharing the same del521-T mutation Neuromuscular Disorders ·M. Kéfi, Rim Amouri, Adel Driss, C. Ben Hamida, M. Ben Hamida, Louis M. Kunkel, Fayçal Hentati	2003	35
18	Clinical and pathological study of three Tunisian siblings with L-2-hydroxyglutaric aciduria Acta Neuropathologica ·A. Larnaout, Fayçal Hentati, Samir Belal, C. H. Ben Hamida, M. Ben Hamida, Naziha Kaabachi	1994	32
19	LGMD 2E in Tunisia is caused by a homozygous missense mutation in β-sarcoglycan exon 3 Neuromuscular Disorders ·Carsten G. Bönnemann, Jenny Wong, Ch. Ben Hamida, M. Ben Hamida, Fayçal Hentati, Louis M. Kunkel	1998	28
20	Limb-girdle muscular dystrophy 2C: Clinical aspects Neuromuscular Disorders ·M. Ben Hamida, Ch. Ben Hamida, M. Zouari, Samir Belal, Fayçal Hentati	1996	24

About M. Ben Hamida

M. Ben Hamida is a scholar working on Cellular and Molecular Neuroscience, Molecular Biology, Neurology, Neurology and Cell Biology, having authored 43 papers that have together received 2.4k indexed citations. Recurring topics across this work include Genetic Neurodegenerative Diseases (19 papers), Hereditary Neurological Disorders (12 papers), Mitochondrial Function and Pathology (10 papers), Muscle Physiology and Disorders (10 papers), Neurological diseases and metabolism (7 papers), Metabolism and Genetic Disorders (5 papers), Botulinum Toxin and Related Neurological Disorders (4 papers) and Amyotrophic Lateral Sclerosis Research (4 papers). The work is most often cited by research in Cellular and Molecular Neuroscience (1.3k citations), Neurology (492 citations), Neurology (681 citations), Biochemistry (144 citations) and Molecular Biology (1.2k citations). M. Ben Hamida has collaborated with scholars based in Tunisia, France and United States. Frequent co-authors include Fayçal Hentati, Samir Belal, Christiane Ben Hamida, B. V. Manyam, T Takayanagi, Lawrence J. Schut, Robert D. Currier, Hans‐Christoph Diener, S. H. Subramony and Alessandro Filla. Their work appears in journals such as Neurology, Neuromuscular Disorders, Journal of the Neurological Sciences, Acta Neuropathologica and Journal of Inherited Metabolic Disease.

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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