Mongi Ben Hamida

4.1k citations

27 papers · 2.6k · h-index 19

Impact in

Cellular and Molecular Neuroscience top 2%
- Genetic Neurodegenerative Diseases
- Hereditary Neurological Disorders
Neurology top 2%
- Amyotrophic Lateral Sclerosis Research
- Neurological diseases and metabolism

Papers in

Molecular Biology 14
- Muscle Physiology and Disorders 6
- Coenzyme Q10 studies and effects 3
Cellular and Molecular Neuroscience 10
- Hereditary Neurological Disorders 7

Co-authors: Fayçal Hentati (18 shared papers)Kamel Ben Othmane (5 shared papers)Jeffery M. Vance (5 shared papers)Herbert J. Kayden (2 shared papers)Christiane Ben Hamida (9 shared papers)Karim Ouahchi (2 shared papers)Michel Fardeau (2 shared papers)Ronald J. Sokol (1 shared paper)
Journals: Nature Genetics (4 papers)Journal of the Neurological Sciences (3 papers)Neurogenetics (3 papers)Human Molecular Genetics (2 papers)Genomics (2 papers)
Partner nations: Tunisia United States France

In The Last Decade

Mongi Ben Hamida

27 papers receiving 2.4k citations

Peers

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-authors

The 25 scholars most cited alongside Mongi 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 Mongi Ben Hamida Line = papers co-authored together Mongi 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 27 papers — load more, or switch the sort, to bring in the rest.

#	Work
1	Ataxia with isolated vitamin E deficiency is caused by mutations in the α–tocopherol transfer protein Nature Genetics ·Karim Ouahchi, Makoto Arita, Herbert J. Kayden, Fayçal Hentati, Mongi Ben Hamida, Ronald J. Sokol, Hiroyuki Arai, Keizo Inoue, Jean‐Louis Mandel, (unknown)	1995	470
2	Mutations in the Dystrophin-Associated Protein γ-Sarcoglycan in Chromosome 13 Muscular Dystrophy Science ·S. Noguchi, Elizabeth M. McNally, Kamel Ben Othmane, Yasuko Hagiwara, Yuji Mizuno, Mikiharu Yoshida, Hideko Yamamoto, Carsten G. Bönnemann, Emanuela Gussoni, Peter H. Denton, Theodoros Kyriakides, Lefkos Middleton, Fayçal Hentati, Mongi Ben Hamida, Ikuya Nonaka, Jeffery M. Vance, Louis M. Kunkel, Eijiro Ozawa	1995	434
3	Ganglioside-induced differentiation-associated protein-1 is mutant in Charcot-Marie-Tooth disease type 4A/8q21 Nature Genetics ·Rachel V. Baxter, Kamel Ben Othmane, Julie M. Rochelle, Jason Stajich, Christine Hulette, Susan Dew-Knight, Fayçal Hentati, Mongi Ben Hamida, Sophie Bel-Vialar, Judy E. Stenger, John R. Gilbert, Margaret A. Pericak‐Vance, Jeffery M. Vance	2001	294
4	Linkage of recessive familial amyotrophic lateral sclerosis to chromosome 2q33–q35 Nature Genetics ·Afif Hentati, Khemissa Bejaoui, Margaret A. Pericak‐Vance, Fayçal Hentati, Marcy C. Speer, Wu-Yen Hung, Denise A. Figlewicz, Jonathan L. Haines, Jackie B. Rimmler, Christiane Ben Hamida, Mongi Ben Hamida, Robert H. Brown, Teepu Siddique	1994	174
5	Linkage of Tunisian autosomal recessive Duchenne–like muscular dystrophy to the pericentromeric region of chromosome 13q Nature Genetics ·Kamel Ben Othmane, Mongi Ben Hamida, Margaret A. Pericak‐Vance, Christiane Ben Hamida, Samir Blel, Susan C. Carter, A. Bowcock, Konstantin Petruhkin, T. Conrad Gilliam, Allen D. Roses, Fayçal Hentati, Jeffery M. Vance	1992	149
6	Severe childhood muscular dystrophy affecting both sexes and frequent in tunisia Muscle & Nerve ·Mongi Ben Hamida, Michel Fardeau, (unknown)	1983	143
7	HEREDITARY MOTOR SYSTEM DISEASES (CHRONIC JUVENILE AMYOTROPHIC LATERAL SCLEROSIS) Brain ·Mongi Ben Hamida, F. Hentati, C. Ben Hamida	1990	139
8	Linkage of a commoner form of recessive amyotrophic lateral sclerosis to chromosome 15q15-q22 markers Neurogenetics ·Afif Hentati, Karim Ouahchi, Margaret A. Pericak‐Vance, Deepak Nijhawan, Arsalan Ahmad, (unknown), Jackie B. Rimmler, W.‐Y. Hung, Beate Schlotter, Akhtar Ahmed, Mongi Ben Hamida, Fay x E al Hentati, Teepu Siddique	1998	135
9	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 ·Richard P. Copp, Thomas Wısnıewskı, Fayçal Hentati, A. Larnaout, Mongi Ben Hamida, Herbert J. Kayden	1999	110
10	Linkage of a locus for autosomal dominant familial spastic paraplegia to chromosome 2p markers Human Molecular Genetics ·Afif Hentati, Margaret A. Pericak‐Vance, Felicia Lennon, Brad Wasserman, Fayçal Hentati, T.R. Juneja, Misha Angrist, W.‐Y. Hung, Rose-Mary Boustany, Saeed Bohlega, Zafar Iqbal, Carl H. Huether, Mongi Ben Hamida, Teepu Siddique	1994	79
11	Multiple cranial nerve deficits associated with the Arnold‐Chiari malformation Neurology ·Robert L. Sieben, Mongi Ben Hamida, Kenneth I. Shulman	1971	76
12	Autosomal recessive parkinsonism linked to parkin gene in a Tunisian family. Clinical, genetic and pathological study Parkinsonism & Related Disorders ·N. Gouider‐Khouja, A. Larnaout, Rim Amouri, Sana Sfar, Samir Belal, Christiane Ben Hamida, Mongi Ben Hamida, Nobutaka Hattori, Yoshikuni Mizuno, Fayçal Hentati	2003	72
13	Identification of a New Locus for Autosomal Recessive Charcot–Marie–Tooth Disease with Focally Folded Myelin on Chromosome 11p15 Genomics ·Kamel Ben Othmane, Ellen Johnson, Marisa M. Menold, Felicia L. Graham, Mongi Ben Hamida, Osamu Hasegawa, Allison D. Rogala, Akio Ohnishi, Margaret A. Pericak‐Vance, Fayçal Hentati, Jeffery M. Vance	1999	61
14	Localization of the Schwartz–Jampel syndrome (SJS) locus to chromosome 1p34–p36.1 by homozygosity mapping Human Molecular Genetics ·Sophie Nicole, Christiane Ben Hamida, Peter Beighton, Selim Bakouri, Samir Belal, Norma B. Romero, Denis Viljoen, G Ponsot, Azza Sammoud, Jean Weissenbach, Michel Fardeau, Mongi Ben Hamida, Bertrand Fontaine, Fayçal Hentati	1995	47
15	Giant axonal neuropathy with inherited multisystem degeneration in a Tunisian kindred Neurology ·Mongi Ben Hamida, Fayçal Hentati, Christiane Ben Hamida	1990	40
16	Morphometric study of the sensory nerve in classical (or Charcot disease) and juvenile amyotrophic lateral sclerosis Journal of the Neurological Sciences ·Mongi Ben Hamida, Fethi Letaief, Fayçal Hentati, Christiane Ben Hamida	1987	23
17	Refined mapping and characterization of the recessive familial amyotrophic lateral sclerosis locus ( ALS2 ) on chromosome 2q33 Neurogenetics ·Betsy A. Hosler, Peter C. Sapp, Ralph Berger, Gilmore O’Neill, Khemissa Bejaoui, Mongi Ben Hamida, Fayçal Hentati, Wendy Chin, Diane McKenna‐Yasek, Jonathan L. Haines, David Patterson, H. Robert Horvitz, R. H. Brown, Caitlin Day	1998	22
18	Phenylketonuria: An Underlying Etiology of Autistic Syndrome. A Case Report Journal of Child Neurology ·Najoua Miladi, A. Larnaout, N. Kaabachi, M. Béchir Helayem, Mongi Ben Hamida	1992	21
19	Giant axonal neuropathy locus refinement to a < 590 kb critical interval European Journal of Human Genetics ·L Cavalier, Christiane BenHamida, Rim Amouri, Samir Belal, Pascale Bomont, Nadège Lagarde, Lætitia Gressin, David F. Callen, Ercan Demir, Haluk Topaloğlu, P. Landrieu, Catherine Ioos, Mongi Ben Hamida, Michel Kœnig, Fayçal Hentati	2000	19
20	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 ·Saïda Madani, Jean Baillon, J. Friés, Omrane Belhadj, (unknown), Mongi Ben Hamida, Guy Hervé	1987	18

About Mongi Ben Hamida

Mongi Ben Hamida is a scholar working on Molecular Biology, Cellular and Molecular Neuroscience, Neurology, Genetics and Cell Biology, having authored 27 papers that have together received 2.6k indexed citations. Recurring topics across this work include Neurological diseases and metabolism (8 papers), Hereditary Neurological Disorders (7 papers), Neurogenetic and Muscular Disorders Research (7 papers), Muscle Physiology and Disorders (6 papers), Amyotrophic Lateral Sclerosis Research (4 papers), Skin and Cellular Biology Research (3 papers), Coenzyme Q10 studies and effects (3 papers) and Vitamin C and Antioxidants Research (2 papers). The work is most often cited by research in Cellular and Molecular Neuroscience (1.1k citations), Neurology (437 citations), Biochemistry (293 citations), Neurology (669 citations) and Genetics (449 citations). Mongi Ben Hamida has collaborated with scholars based in Tunisia, United States and France. Frequent co-authors include Fayçal Hentati, Kamel Ben Othmane, Jeffery M. Vance, Herbert J. Kayden, Christiane Ben Hamida, Karim Ouahchi, Michel Fardeau, Ronald J. Sokol, Makoto Arita and Keizo Inoue. Their work appears in journals such as Nature Genetics, Journal of the Neurological Sciences, Neurogenetics, Human Molecular Genetics and Genomics.

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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