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Fayçal Hentati

Researcher Next ID · RN-015078

Researcher · Neuroscience

National Institute of Neurology Mongi-Ben Hamida

, Tunisia

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Not currently recruitingFunding unknown
Works count
181
Citation count
12,174
H-index
52
i10-index
124

Research interests

Neuroscience
Medicine
Biochemistry, Genetics and Molecular Biology
Genetic Neurodegenerative Diseases
Parkinson's Disease Mechanisms and Treatments
Mitochondrial Function and Pathology
Muscle Physiology and Disorders
Hereditary Neurological Disorders

Publications

  • VPS35 Mutations in Parkinson Disease

    The American Journal of Human Genetics · 2011 · 10.1016/j.ajhg.2011.06.001

  • The gene encoding alsin, a protein with three guanine-nucleotide exchange factor domains, is mutated in a form of recessive amyotrophic lateral sclerosis

    Nature Genetics · 2001 · 10.1038/ng1001-160

  • Dysferlin, a novel skeletal muscle gene, is mutated in Miyoshi myopathy and limb girdle muscular dystrophy

    Nature Genetics · 1998 · 10.1038/1682

  • Ataxia with isolated vitamin E deficiency is caused by mutations in the α–tocopherol transfer protein

    Nature Genetics · 1995 · 10.1038/ng0295-141

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

    Science · 1995 · 10.1126/science.270.5237.819

Current projects

    No projects listed.