Marcia L.E. MacDonald

Mutations in HFE2 cause iron overload in chromosome 1q–linked juvenile hemochromatosis

George Papanikolaou, Mark Samuels, E H Ludwig et al. · Nature Genetics · 2003 · 976 citations · Full text

Juvenile Hemochromatosis, Heme Homeostasis, Iron Metabolism +8

Mutant frizzled-4 disrupts retinal angiogenesis in familial exudative vitreoretinopathy

Johane M. Robitaille, Marcia L.E. MacDonald, Ajamete Kaykas et al. · Nature Genetics · 2002 · 473 citations

Ocular Disease, Vitreous Body, Familial Exudative Vitreoretinopathy +6

Identification of a Novel Gene (HSN2) Causing Hereditary Sensory and Autonomic Neuropathy Type II through the Study of Canadian Genetic Isolates

Ronald G. Lafrenière, Marcia L.E. MacDonald, Marie‐Pierre Dubé et al. · The American Journal of Human Genetics · 2004 · 156 citations · Full text

Mendelian Disorder, Novel Gene, Genetic Disorder +9

Despite Antiatherogenic Metabolic Characteristics, SCD1-Deficient Mice Have Increased Inflammation and Atherosclerosis

Marcia L.E. MacDonald, Miranda Van Eck, Reeni B. Hildebrand et al. · Arteriosclerosis Thrombosis and Vascular Biology · 2008 · 107 citations · Full text

Absence of stearoyl-CoA desaturase-1 ameliorates features of the metabolic syndrome in LDLR-deficient mice

Marcia L.E. MacDonald, Roshni R. Singaraja, Nagat Bissada et al. · Journal of Lipid Research · 2007 · 72 citations · Full text