Xinhua Shu

SLC2A9 is a newly identified urate transporter influencing serum urate concentration, urate excretion and gout

Véronique Vitart, Igor Rudan, Caroline Hayward et al. · Nature Genetics · 2008 · 790 citations

Urological Research, Renal Function, Serum Urate Concentration +8

Interaction between chromatin proteins MECP2 and ATRX is disrupted by mutations that cause inherited mental retardation

Xinsheng Nan, Jianghui Hou, Alan Maclean et al. · Proceedings of the National Academy of Sciences · 2007 · 254 citations · Full text

Epigenetic Change, Genetics, Mecp2-atrx Interaction +20

Homozygous SLC2A9 Mutations Cause Severe Renal Hypouricemia

Dganit Dinour, Nicola K. Gray, Susan Campbell et al. · Journal of the American Society of Nephrology · 2009 · 232 citations

Genetics, Renal Pathology, Genetic Epidemiology +16

Mutation in a short-chain collagen gene, CTRP5 , results in extracellular deposit formation in late-onset retinal degeneration: a genetic model for age-related macular degeneration

Caroline Hayward, Xinhua Shu, Artur V. Cideciyan et al. · Human Molecular Genetics · 2003 · 189 citations

RPGR-ORF15, Which Is Mutated in Retinitis Pigmentosa, Associates with SMC1, SMC3, and Microtubule Transport Proteins

Hemant Khanna, Toby W. Hurd, Concepción Lillo et al. · Journal of Biological Chemistry · 2005 · 170 citations · Full text

Photoreceptor Cell, Signal Transduction, Retina +14