Yangjian Liu

Missense mutations in the sodium borate cotransporter SLC4A11 cause late-onset Fuchs corneal dystrophya

S. Amer Riazuddin, Eranga N. Vithana, Li Fong Seet et al. · Human Mutation · 2010 · 133 citations · Full text

Life Sciences, Genetics, Molecular Genetics +17

Functional analyses of variants reveal a significant role for dominant negative and common alleles in oligogenic Bardet–Biedl syndrome

Norann A. Zaghloul, Yangjian Liu, Jantje M. Gerdes et al. · Proceedings of the National Academy of Sciences · 2010 · 119 citations

Life Sciences, Genetics, Molecular Genetics +14

Individuals with mutations in XPNPEP3, which encodes a mitochondrial protein, develop a nephronophthisis-like nephropathy

John F. O’Toole, Yangjian Liu, Erica E. Davis et al. · Journal of Clinical Investigation · 2010 · 118 citations · Full text

Medicine, Genetics, Molecular Genetics +16

Aquaporin 9 is the major pathway for glycerol uptake by mouse erythrocytes, with implications for malarial virulence

Yangjian Liu, Dominique Promeneur, Aleksandra Rojek et al. · Proceedings of the National Academy of Sciences · 2007 · 108 citations · Full text

Life Sciences, Molecular Biology, Physiology +17

Reduced arsenic clearance and increased toxicity in aquaglyceroporin-9-null mice

Jennifer M. Carbrey, Linhua Song, Yao Zhou et al. · Proceedings of the National Academy of Sciences · 2009 · 88 citations · Full text

Veterinary Medicine, Biochemistry, Toxicology +13