Mongi Ben Hamida

4.1k citations

27 papers · 2.4k indexed · h-index 18

Impact in

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

Papers in

Neurology 9
- Neurological diseases and metabolism 9
- Amyotrophic Lateral Sclerosis Research 4
- Parkinson's Disease Mechanisms and Treatments 3
Genetics 7
- Neurogenetic and Muscular Disorders Research 7

Co-authors: Fayçal Hentati Jeffery M. Vance Kamel Ben Othmane Herbert J. Kayden Christiane Ben Hamida Karim Ouahchi Michel Fardeau Keizo Inoue
Journals: Nature Genetics (4 papers)Neurogenetics (3 papers)Journal of the Neurological Sciences (3 papers)Human Molecular Genetics (2 papers)Neurology (2 papers)
Partner nations: Tunisia United States France

In The Last Decade

Mongi Ben Hamida

27 papers receiving 2.3k 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-authorship network

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

#	Work
1	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	69
2	Ganglioside-induced differentiation-associated protein-1 is mutant in Charcot-Marie-Tooth disease type 4A/8q21 Nature Genetics ·健剛横正, Kamel Ben Othmane, Julie M. Rochelle, Jason Stajich, Christine Hulette, Imani Jaoko, Fayçal Hentati, Mongi Ben Hamida, Sophie Bel-Vialar, Atle Svandal, John R. Gilbert, Margaret A. Pericak‐Vance, Jeffery M. Vance	2001	271
3	Giant axonal neuropathy locus refinement to a < 590 kb critical interval European Journal of Human Genetics ·L Cavalier, Bai Zuojin, Rim Amouri, Samir Belal, Pascale Bomont, Shahvaysi Farhad, Laëtitia Gressin, David F. Callen, Ercan Demir, Haluk Topaloğlu, P. Landrieu, A Sebastianelli, Mongi Ben Hamida, Michel Kœnig, Fayçal Hentati	2000	18
4	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	97
5	Identification of a New Locus for Autosomal Recessive Charcot–Marie–Tooth Disease with Focally Folded Myelin on Chromosome 11p15 Genomics ·Kamel Ben Othmane, Andrés Fernández-Companioni, Marisa M. Menold, Felicia L. Graham, Mongi Ben Hamida, Osamu Hasegawa, 徐增瑞 Xu Zengrui, Akio Ohnishi, Margaret A. Pericak‐Vance, Fayçal Hentati, Jeffery M. Vance	1999	60
6	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, Yang Yuan, Jedsada Chavalitkul, W.‐Y. Hung, Beate Schlotter, Mojgan Hemmatian, Mongi Ben Hamida, C Rakshitha, Teepu Siddique	1998	126
7	Generation of a 3-Mb PAC Contig Spanning the Miyoshi Myopathy/Limb-Girdle Muscular Dystrophy (MM/LGMD2B) Locus on Chromosome 2p13 Genomics ·Jing Liu, Chenyan Wu, 苏鸣, Khemissa Bejaoui, Betsy A. Hosler, Jeffrey C. Gingrich, Mongi Ben Hamida, Fayçal Hentati, Erwin Schurr, Peter J. de Jong, Miss Thresia Zacharia	1998	13
8	Fine localization of the CMT4A locus using a PAC contig and haplotype analysis Neurogenetics ·Kamel Ben Othmane, Julie M. Rochelle, Mongi Ben Hamida, Brandon D. Slotterbeck, Nagesh Rao, Fayçal Hentati, Margaret A. Pericak‐Vance, Jeffery M. Vance	1998	8
9	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, Sherry Lansing, Diane McKenna‐Yasek, Jonathan L. Haines, David Patterson, H. Robert Horvitz, R. H. Brown, C. Akshay	1998	21
10	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, Libanio Pinheiro, Samir Belal, Norma B. Romero, Denis Viljoen, G Ponsot, Azza Sammoud, Jean Weissenbach, Michel Fardeau, Mongi Ben Hamida, Bertrand Fontaine, Fayçal Hentati	1995	36
11	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	414
12	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, Mirna G. García‐Castillo, Fayçal Hentati, T.R. Juneja, Misha Angrist, W.‐Y. Hung, Rose-Mary Boustany, Saeed Bohlega, Zafar Iqbal, Miaomiao Li, Mongi Ben Hamida, Teepu Siddique	1994	71
13	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, Jedsada Chavalitkul, Christiane Ben Hamida, Mongi Ben Hamida, Robert H. Brown, Teepu Siddique	1994	164
14	Biochemical and immunocytochemical analysis in chronic proximal spinal muscular atrophy Muscle & Nerve ·Christiane Ben Hamida, Nadia Soussi‐Yanicostas, Gillian Butler‐Browne, Khemissa Bejaoui, Fayçal Hentati, Mongi Ben Hamida	1994	7
15	Duchenne muscular dystrophy in Tunisia: A clinical and morphological study of 77 cases Journal of the Neurological Sciences ·Mongi Ben Hamida, 芳治清田, Ilhem Turki, Hauwau Abdulrahman Aliyu	1992	8
16	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, Meet Shah, Chia-Hui Lee, A. Bowcock, Irina Sergeevna Fadyakina, T. Conrad Gilliam, Allen D. Roses, Fayçal Hentati, Jeffery M. Vance	1992	144
17	Age-dependent axonal loss in nerve biopsy of patients with xeroderma pigmentosum Neuromuscular Disorders ·麻里子大江, Christiane Ben Hamida, Tibor Ferenc, Mohamed Ridha Kamoun, Vaitheeshwaran Y Hari Varma, Mongi Ben Hamida	1992	7
18	HEREDITARY MOTOR SYSTEM DISEASES (CHRONIC JUVENILE AMYOTROPHIC LATERAL SCLEROSIS) Brain ·Mongi Ben Hamida, 麻里子大江, C. Ben Hamida	1990	126
19	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 ·Suttisa Duchanee, Yee-Huang Ku, Julia Hodecker, Omrane Belhadj, Ali Bettaı̈eb, Mongi Ben Hamida, R. Graf · Stolzalpe	1987	16
20	Les atrophies péronières en Tunisie Journal of the Neurological Sciences ·Mongi Ben Hamida, Júlio Mário Maia, Christiane Ben Hamida, Priyadi Prihaswan	1981	5

About Mongi Ben Hamida

Mongi Ben Hamida is a scholar working on Neurology, Genetics, Cellular and Molecular Neuroscience, Neurology and Cell Biology, having authored 27 papers that have together received 2.4k indexed citations. Recurring topics across this work include Neurological diseases and metabolism (9 papers), Neurogenetic and Muscular Disorders Research (7 papers), Hereditary Neurological Disorders (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 Parkinson's Disease Mechanisms and Treatments (3 papers). The work is most often cited by research in Cellular and Molecular Neuroscience (1.0k citations), Neurology (434 citations), Biochemistry (272 citations), Neurology (637 citations) and Genetics (442 citations). Mongi Ben Hamida has collaborated with scholars based in Tunisia, United States and France. Frequent 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. Their work appears in journals such as Nature Genetics, Neurogenetics, Journal of the Neurological Sciences, Human Molecular Genetics and Neurology.

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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