Hamid Azzedine

Publications by Year

Research Areas

Hereditary Neurological Disorders, Neurological diseases and metabolism, Genetic Neurodegenerative Diseases, RNA regulation and disease, Neurogenetic and Muscular Disorders Research

Most-Cited Works

• → Mutations in SPG11, encoding spatacsin, are a major cause of spastic paraplegia with thin corpus callosum(2007)331 cited
• → Mutations in MTMR13, a New Pseudophosphatase Homologue of MTMR2 and Sbf1, in Two Families with an Autosomal Recessive Demyelinating Form of Charcot-Marie-Tooth Disease Associated with Early-Onset Glaucoma(2003)302 cited
• → Mutations in SPG11 are frequent in autosomal recessive spastic paraplegia with thin corpus callosum, cognitive decline and lower motor neuron degeneration(2007)250 cited
• → Dysfunction in endoplasmic reticulum-mitochondria crosstalk underlies SIGMAR1 loss of function mediated motor neuron degeneration(2015)215 cited
• → KIF1A missense mutations in SPG30, an autosomal recessive spastic paraplegia: distinct phenotypes according to the nature of the mutations(2012)153 cited
• → Spine deformities in Charcot-Marie-Tooth 4C caused by SH3TC2 gene mutations(2006)105 cited
• → Spinocerebellar ataxia with sensory neuropathy (SCA25) maps to chromosome 2p(2003)94 cited
• → Autosomal-recessive forms of demyelinating Charcot-Marie-Tooth disease(2006)89 cited
• → Phenotypical Features of a Moroccan Family With Autosomal Recessive Charcot-Marie-Tooth Disease Associated With the S194X Mutation in the GDAP1 Gene(2003)77 cited
• → Mapping of a new form of pure autosomal recessive spastic paraplegia (SPG28)(2005)69 cited