Corine Gartioux

A complete genomic screen for multiple sclerosis underscores a role for the major histocompatability complex

J. L. Haines, Monica Ter‐Minassian, A. Bazyk et al. · Nature Genetics · 1996 · 653 citations

Complete Genomic Screen, Neurological Disorder, Medicine +11

Early onset collagen VI myopathies: Genetic and clinical correlations

Laura Briñas, Pascale Richard, Susana Quijano‐Roy et al. · Annals of Neurology · 2010 · 132 citations · Full text

Vacuoliting Megalencephalic Leukoencephalopathy with Subcortical Cysts, Mapped to Chromosome 22qtel

Meral Topçu, Corine Gartioux, Florence Ribiérre et al. · The American Journal of Human Genetics · 2000 · 94 citations · Full text

Neurobiology Of Disease, Neurological Disorder, Neuroanatomy +7

A single homozygous point mutation in a 3′untranslated region motif of selenoprotein N mRNA causes SEPN1‐related myopathy

Valérie Allamand, Pascale Richard, Alain Lescure et al. · EMBO Reports · 2006 · 94 citations · Full text

Transcriptional Regulation, Genetic Disorder, Natural Sciences +7

Dominant and recessive COL6A1 mutations in Ullrich scleroatonic muscular dystrophy

Betti Giusti, Laura Lucarini, Valentina Pietroni et al. · Annals of Neurology · 2005 · 78 citations