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 · 130 citations · Full text

Missense Mutations, Ocular Disease, Developmental Biology +15

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

Genetics, Renal Pathology, Pathology +18

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 · 116 citations

Genetics, Genetic Epidemiology, Immunology +21

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 · 107 citations · Full text

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

Inflammation, Electrolyte Disorder, Reduced Arsenic Clearance +15