Kœnig, Michel

Top Publications

Top Publications Authored or Co-Authored by "Kœnig, Michel"

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

  Nature Genetics, Volume 9, No. 2, Year 1995, Citations 520
• Senataxin, the ortholog of a yeast RNA helicase, is mutant in ataxia-ocular apraxia 2

  Nature Genetics, Volume 36, No. 3, Year 2004, Citations 473
• The gene encoding gigaxonin, a new member of the cytoskeletal BTB/kelch repeat family, is mutated in giant axonal neuropathy

  Nature Genetics, Volume 26, No. 3, Year 2000, Citations 391
• ADCK3, an Ancestral Kinase, Is Mutated in a Form of Recessive Ataxia Associated with Coenzyme Q10 Deficiency

  American Journal of Human Genetics, Volume 82, No. 3, Year 2008, Citations 301
• Ataxia with oculomotor apraxia type 2: Clinical, biological and genotype/phenotype correlation study of a cohort of 90 patients

  Brain, Volume 132, No. 10, Year 2009, Citations 218