Betsie Boucher

Mutations in the ABC 1 gene in familial HDL deficiency with defective cholesterol efflux

Michel Marcil, Angela Brooks‐Wilson, Susanne M. Clee et al. · The Lancet · 1999 · 357 citations

Abc 1, Mendelian Disorder, Familial Hdl Deficiency +12

Age and residual cholesterol efflux affect HDL cholesterol levels and coronary artery disease in ABCA1 heterozygotes

Susanne M. Clee, John J.P. Kastelein, Marjel van Dam et al. · Journal of Clinical Investigation · 2000 · 318 citations · Full text

Cellular Cholesterol Transport and Efflux in Fibroblasts Are Abnormal in Subjects With Familial HDL Deficiency

Michel Marcil, Lu Yu, Larbi Krimbou et al. · Arteriosclerosis Thrombosis and Vascular Biology · 1999 · 89 citations

Decreased cellular cholesterol efflux is a common cause of familial hypoalphalipoproteinemia: role of the ABCA1 gene mutations

Stephanie Mott, Lu Yu, Michel Marcil et al. · Atherosclerosis · 2000 · 80 citations

Lipid Disorder, Cellular Cholesterol Efflux, Familial Hypoalphalipoproteinemia +11

Fenofibrate raises plasma homocysteine levels in the fasted and fed states

Rachel Bissonnette, Eileen P. Treacy, Rima Rozen et al. · Atherosclerosis · 2001 · 63 citations

Biochemistry, Fed States, Medicine +4