Kamel Ben Othmane - Concepedia

Author

Kamel Ben Othmane

Duke Medical Center

Also Known As

K B Othmane, K Ben Othmane, K. Ben Othmane, K.Ben Othmane, Kamel Ben Othmane

Publications

1.7K

Citations

H-Index

Concepts

All Affiliations

Duke Medical Center Duke University Hospital National Institute of Neurology Mongi-Ben Hamida Duke University Cyprus Institute of Neurology and Genetics

About

Kamel Ben Othmane is an author at Duke Medical Center specializing in medicine, genetics, and molecular genetics.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	6	6	808
2	Cell Biology	2	2	377
3	Molecular Biology	2	2	36
4	Public Health	1	1	159
5	Biology	1	1	159

Kamel Ben Othmane

Publications

1.6K

Citations

H-Index

Page 1

	Year	Citations
Mutations in the Dystrophin-Associated Protein γ-Sarcoglycan in Chromosome 13 Muscular Dystrophy S. Noguchi, Elizabeth M. McNally, Kamel Ben Othmane, Science	1995	507
Ganglioside-induced differentiation-associated protein-1 is mutant in Charcot-Marie-Tooth disease type 4A/8q21 Rachel V. Baxter, Kamel Ben Othmane, Julie M. Rochelle, Nature Genetics Disease MechanismPathogenesisExperimental PathologyPathologyDegenerative Disease	2001	367
Linkage of a locus (CMT4A) for autosomal recessive Charcot-Marie-Tooth disease to chromosome 8q Kamel Ben Othmane, F. Hentatl, Felicia Lennon, Human Molecular Genetics	1993	177
Linkage of Tunisian autosomal recessive Duchenne–like muscular dystrophy to the pericentromeric region of chromosome 13q Kamel Ben Othmane, Mongi Ben Hamida, Margaret A. Pericak‐Vance, Nature Genetics Chromosome DynamicsDevelopmental BiologyMendelian DisorderCytogeneticsMedicine	1992	175
Localization of a Gene (CMT2A) for Autosomal Dominant Charcot-Marie-Tooth Disease Type 2 to Chromosome 1p and Evidence of Genetic Heterogeneity Kamel Ben Othmane, Lefkos Middleton, Lorraine Loprest, Genomics BiologyMendelian DisorderGenetic DisorderGeneticsGenetic Epidemiology	1993	159
Mild and severe muscular dystrophy caused by a single gamma-sarcoglycan mutation. Elizabeth M. McNally, Maria-Rita Passos-Bueno, Carsten G. Bönnemann, PubMed	1996	157
Identification of a New Locus for Autosomal Recessive Charcot–Marie–Tooth Disease with Focally Folded Myelin on Chromosome 11p15 Kamel Ben Othmane, Ellen Johnson, Marisa M. Menold, Genomics Mendelian DisorderFocally Folded MyelinChromosome 11P15Genetic DisorderGenetics	1999	71
Physical and Genetic Mapping of the CMT4A Locus and Exclusion of PMP-2 as the Defect in CMT4A Kamel Ben Othmane, Deborah B. Loeb, R. Hayworth-Hodgte, Genomics Genetic DisorderCmt4a LocusGeneticsMolecular BiologyMolecular Genetics	1995	26
The gene for hereditary multiple exostoses does not map to the Langer-Giedion region (8q23-q24). M. Le Merrer, Kamel Ben Othmane, V. Stănescu, Journal of Medical Genetics Langer-giedion RegionMendelian DisorderGenetic DisorderGeneticsPathogenesis	1992	10

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