Grid, Djamel

Top Publications

Top Publications Authored or Co-Authored by "Grid, Djamel"

• Homozygous defects in LMNA, encoding lamin A/C nuclear-envelope proteins, cause autosomal recessive axonal neuropathy in human (Charcot-Marie-Tooth disorder type 2) and mouse

  American Journal of Human Genetics, Volume 70, No. 3, Year 2002, Citations 565
• Mutations in SPG11, encoding spatacsin, are a major cause of spastic paraplegia with thin corpus callosum

  Nature Genetics, Volume 39, No. 3, Year 2007, Citations 309
• Molecular and clinical correlations in autosomal dominant cerebellar ataxia with progressive macular dystrophy (SCA7)

  Human Molecular Genetics, Volume 7, No. 2, Year 1998, Citations 275
• CYP7B1 mutations in pure and complex forms of hereditary spastic paraplegia type 5

  Brain, Volume 132, No. 6, Year 2009, Citations 104
• Spine deformities in Charcot-Marie-Tooth 4C caused by SH3TC2 gene mutations

  Neurology, Volume 67, No. 4, Year 2006, Citations 102