Kamel Ben Othmane

1.7k citations

10 papers · 1.3k indexed · h-index 9

Impact in

Cellular and Molecular Neuroscience top 2%
- Hereditary Neurological Disorders
- Genetic Neurodegenerative Diseases
Neurology top 5%
- Neurological diseases and metabolism

Papers in

Cellular and Molecular Neuroscience 8
- Hereditary Neurological Disorders 6
- Genetic Neurodegenerative Diseases 2
Cell Biology 4
- Hippo pathway signaling and YAP/TAZ 2

Co-authors: Jeffery M. Vance Fayçal Hentati Mongi Ben Hamida Margaret A. Pericak‐Vance Peter H. Denton Lefkos Middleton Carsten G. Bönnemann Louis M. Kunkel
Journals: Genomics (3 papers)Nature Genetics (2 papers)Journal of Medical Genetics (1 paper)Neurogenetics (1 paper)Human Molecular Genetics (1 paper)
Partner nations: United States Tunisia Cyprus

In The Last Decade

Kamel Ben Othmane

10 papers receiving 1.3k citations

Peers

Countries citing papers authored by Kamel Ben Othmane

Since Specialization

Citations

This map shows the geographic impact of Kamel Ben Othmane'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 Kamel Ben Othmane with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Kamel Ben Othmane more than expected).

Fields of papers citing papers by Kamel Ben Othmane

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network

The 25 scholars most cited alongside Kamel Ben Othmane, 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 Kamel Ben Othmane Line = papers co-authored together Kamel Ben Othmane links everyone, so they are left out of the graph.

All Works

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10 of 10 papers shown

#	Work
1	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
2	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
3	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
4	Mild and severe muscular dystrophy caused by a single gamma-sarcoglycan mutation. PubMed ·Elizabeth M. McNally, Maria-Rita Passos-Bueno, Carsten G. Bönnemann, Mariz Vainzof, Carmen Matilla Vicente, Hart G.W. Lidov, Kamel Ben Othmane, Peter H. Denton, Jeffery M. Vance, Mayana Zatz, Louis M. Kunkel	1996	125
5	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
6	Physical and Genetic Mapping of the CMT4A Locus and Exclusion of PMP-2 as the Defect in CMT4A Genomics ·Kamel Ben Othmane, Deborah B. Loeb, К С Остренко, Fayçal Hentati, Nagesh Rao, Allen D. Roses, M. Ben Hamida, M. A. Pericak‐Vance, Jeffery M. Vance	1995	21
7	Localization of a Gene (CMT2A) for Autosomal Dominant Charcot-Marie-Tooth Disease Type 2 to Chromosome 1p and Evidence of Genetic Heterogeneity Genomics ·Kamel Ben Othmane, Lefkos Middleton, Zhou Fanglong, Charles W. Holtzer, Felicia Lennon, Marvin P. Rozear, M. Chrobak, P. C. Gaskell, Allen D. Roses, Margaret A. Pericak‐Vance, Jeffery M. Vance	1993	120
8	Linkage of a locus (CMT4A) for autosomal recessive Charcot-Marie-Tooth disease to chromosome 8q Human Molecular Genetics ·Kamel Ben Othmane, Ferreira-Santos Ruy, Felicia Lennon, Christiane Ben Hamida, Meet Shah, A.D. Roses, Margaret A Pericak‐Vance, M. Ben Hamida, Jeffery M. Vance	1993	136
9	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
10	The gene for hereditary multiple exostoses does not map to the Langer-Giedion region (8q23-q24). Journal of Medical Genetics ·M. Le Merrer, Kamel Ben Othmane, V. Stănescu, Stanislas Lyonnet, Lionel Van Maldergem, Imran Ali Syed, Arnold Munnich, P Maroteaux	1992	5

About Kamel Ben Othmane

Kamel Ben Othmane is a scholar working on Cellular and Molecular Neuroscience, Cell Biology, Immunology, Genetics and Molecular Biology, having authored 10 papers that have together received 1.3k indexed citations. Recurring topics across this work include Hereditary Neurological Disorders (6 papers), Muscle Physiology and Disorders (3 papers), Hippo pathway signaling and YAP/TAZ (2 papers), Genetic Neurodegenerative Diseases (2 papers), Genomics and Rare Diseases (1 paper), RNA modifications and cancer (1 paper), interferon and immune responses (1 paper) and Neurogenetic and Muscular Disorders Research (1 paper). The work is most often cited by research in Cellular and Molecular Neuroscience (826 citations), Neurology (252 citations), Cell Biology (267 citations), Molecular Biology (852 citations) and Genetics (129 citations). Kamel Ben Othmane has collaborated with scholars based in United States, Tunisia and Cyprus. Frequent co-authors include Jeffery M. Vance, Fayçal Hentati, Mongi Ben Hamida, Margaret A. Pericak‐Vance, Peter H. Denton, Lefkos Middleton, Carsten G. Bönnemann, Louis M. Kunkel, Elizabeth M. McNally and Christiane Ben Hamida. Their work appears in journals such as Genomics, Nature Genetics, Journal of Medical Genetics, Neurogenetics and Human Molecular Genetics.

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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