Author

Kamel Ben Othmane

Observed names: K B Othmane, K Ben Othmane, K. Ben Othman, K.Ben Othmane

Institutions: Duke University, Duke Medical Center

Observed institutions: Atrium Health Wake Forest Baptist, University of British Columbia, Inserm, Duke University, Duke Medical Center, National Institute of Neurology Mongi-Ben Hamida, Cyprus Institute of Neurology and Genetics

OpenAlex ID: A5060200210

Mutations in the Dystrophin-Associated Protein γ-Sarcoglycan in Chromosome 13 Muscular Dystrophy

1995 · Satoru Noguchi, Elizabeth M. McNally, et al. · Science · 503

The peripheral myelin protein gene PMP–22 is contained within the Charcot–Marie–Tooth disease type 1A duplication

1992 · V. Timmerman, E. Nelis, et al. · Nature Genetics · 393

Ganglioside-induced differentiation-associated protein-1 is mutant in Charcot-Marie-Tooth disease type 4A/8q21

2001 · Rachel V. Baxter, Kamel Ben Othmane, et al. · Nature Genetics · 374

Linkage of a locus (CMT4A) for autosomal recessive Charcot-Marie-Tooth disease to chromosome 8q

1993 · K.Ben Othmane, F. Hentatl, et al. · Human Molecular Genetics · 180

Linkage of Tunisian autosomal recessive Duchenne–like muscular dystrophy to the pericentromeric region of chromosome 13q

1992 · Kamel Ben Othmane, Mongi Ben Hamida, et al. · Nature Genetics · 175

Localization of a Gene (CMT2A) for Autosomal Dominant Charcot-Marie-Tooth Disease Type 2 to Chromosome 1p and Evidence of Genetic Heterogeneity

1993 · Kamel Ben Othmane, Lefkos T. Middleton, et al. · Genomics · 163

Mild and severe muscular dystrophy caused by a single gamma-sarcoglycan mutation.

1996 · E M McNally, M R Passos-Bueno, et al. · PubMed Central · 156

Identification of a New Locus for Autosomal Recessive Charcot–Marie–Tooth Disease with Focally Folded Myelin on Chromosome 11p15

1999 · Kamel Ben Othmane, Ellen Johnson, et al. · Genomics · 75

Evidence for linkage disequilibrium in chromosome 13-linked Duchenne-like muscular dystrophy (LGMD2C)

1995 · K Ben Othmane, M C Speer, et al. · PubMed Central · 39

Misclassification and linkage of hereditary sensory and autonomic neuropathy type 1 as Charcot-Marie-Tooth disease, type 2B.

1996 · J M Vance, M C Speer, et al. · PubMed Central · 33

Physical and Genetic Mapping of the CMT4A Locus and Exclusion of PMP-2 as the Defect in CMT4A

1995 · K.Ben Othmane, D. Loeb, et al. · Genomics · 27

Report and abstracts of the First International Workshop on Human Chromosome 8 Mapping. Vancouver, British Columbia, May 2-4, 1993.

1993 · S Wood, K Ben Othmane, et al. · PubMed · 14

The gene for hereditary multiple exostoses does not map to the Langer-Giedion region (8q23-q24).

1992 · M Le Merrer, K Ben Othmane, et al. · Journal of Medical Genetics · 10

Fine localization of the CMT4A locus using a PAC contig and haplotype analysis

1998 · Kamel Ben Othmane, Julie M. Rochelle, et al. · Neurogenetics · 9

[Is there a single form of Charcot-Marie-Tooth disease, or are there several variations? A classification difficulty].

1995 · M Ben Hamida, K Ben Othmane, et al. · PubMed · 1

Clinical and genetic aspects of autosomal recessive CMT

1997 · Kamel Ben Othmane, Julie M. Rochelle, et al. · Neuromuscular Disorders

Genetic and physical mapping of the genomic region spanning CMT4A

1994 · Kamel Ben Othmane, Deborah B. Loeb, et al. · The American Journal of Human Genetics

Report of the first international workshop on human chromosome 8 mapping. Final report

1993 · Texas Univ., San Antonio, TX (United States), S Wood, et al.

Works count: 18

Citation count: 2,152

H-index: 12

I10-index: 13