Lu Yu

Mutations in ABC1 in Tangier disease and familial high-density lipoprotein deficiency

Angela Brooks‐Wilson, Michel Marcil, Susanne M. Clee et al. · Nature Genetics · 1999 · 1.7K citations

Mendelian Disorder, Disease Mechanism, Genetic Disorder +13

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

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

Abnormal Causal Connectivity by Structural Deficits in First-Episode, Drug-Naive Schizophrenia at Rest

Weihua Guo, Feng Liu, Jin Liu et al. · Schizophrenia Bulletin · 2014 · 82 citations · Full text

Neuropsychology, Neuropsychiatry, Social Sciences +20

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