Linhua Zhang

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

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

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

ABCA1 mRNA and Protein Distribution Patterns Predict Multiple Different Roles and Levels of Regulation

Cheryl L. Wellington, E Walker, Agripina Suarez et al. · Laboratory Investigation · 2002 · 298 citations · Full text

Transcriptional Regulation, Functional Genomics, Molecular Regulation +10

Aberrant allele frequencies of the SNPs located in microRNA target sites are potentially associated with human cancers

Zhenbao Yu, Zhen Li, Normand Jolicoeur et al. · Nucleic Acids Research · 2007 · 268 citations · Full text