Christophe Marçais

Niemann-Pick C1 Disease: Correlations between NPC1 Mutations, Levels of NPC1 Protein, and Phenotypes Emphasize the Functional Significance of the Putative Sterol-Sensing Domain and of the Cysteine-Rich Luminal Loop

Gilles Millat, Christophe Marçais, Catherine Tomasetto et al. · The American Journal of Human Genetics · 2001 · 212 citations · Full text

Npc1 Mutations, Signal Transduction, Npc1 Protein +7

Niemann-Pick C1 Disease: The I1061T Substitution Is a Frequent Mutant Allele in Patients of Western European Descent and Correlates with a Classic Juvenile Phenotype

Gilles Millat, Christophe Marçais, Mohammad A. Rafi et al. · The American Journal of Human Genetics · 1999 · 204 citations · Full text

Mendelian Disorder, Genetic Disorder, Genetics +12

Apoa5 Q139X truncation predisposes to late-onset hyperchylomicronemia due to lipoprotein lipase impairment

Christophe Marçais · Journal of Clinical Investigation · 2005 · 168 citations · Full text

Metabolic Disorder, Genetics, Haplotype Analysis +18

Genetic heterogeneity of hepatocellular carcinoma.

Hilal Ünsal, Christophe Marçais, Michael C. Kew et al. · Proceedings of the National Academy of Sciences · 1994 · 160 citations · Full text

P53 Mutations, Hepatology, Hbv Sequences +15

Retinoblastoma and p <i>53</i> tumor suppressor genes in human hepatoma cell lines

Alain Puisieux, Katherine Galvin, Frédéric Troalen et al. · The FASEB Journal · 1993 · 126 citations