Karim Ouahchi

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

Yi Yang, Afif Hentati, Han‐Xiang Deng et al. · Nature Genetics · 2001 · 731 citations

Neurodegenerative Diseases, Amyotrophic Lateral Sclerosis, Genetics +5

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

Karim Ouahchi, Makoto Arita, Herbert J. Kayden et al. · Nature Genetics · 1995 · 563 citations

Genetic Disorder, Genetics, Inherited Metabolic Disease +4

Ataxia with Isolated Vitamin E Deficiency: Heterogeneity of Mutations and Phenotypic Variability in a Large Number of Families

L Cavalier, Karim Ouahchi, Herbert J. Kayden et al. · The American Journal of Human Genetics · 1998 · 305 citations · Full text

Sequence Alterations within CYP7B1 Implicate Defective Cholesterol Homeostasis in Motor-Neuron Degeneration

Maria K. Tsaousidou, Karim Ouahchi, Thomas T. Warner et al. · The American Journal of Human Genetics · 2008 · 182 citations · Full text

Neurodegenerative Diseases, Molecular Neuroscience, Oxysterol +10

Linkage of a commoner form of recessive amyotrophic lateral sclerosis to chromosome 15q15-q22 markers

Afif Hentati, Karim Ouahchi, Margaret A. Pericak‐Vance et al. · Neurogenetics · 1998 · 169 citations

Amyotrophic Lateral Sclerosis, Mendelian Disorder, Genetic Disorder +6