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 · 806 citations

Pharmacy, Nephrology, Physiology +13

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 · 258 citations · Full text

Life Sciences, Genetics, Molecular Biology +17

Homozygous SLC2A9 Mutations Cause Severe Renal Hypouricemia

Dganit Dinour, Nicola K. Gray, Susan Campbell et al. · Journal of the American Society of Nephrology · 2009 · 241 citations

Medicine, Genetics, Molecular Genetics +17

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 · 190 citations

Medicine, Genetics, Ophthalmology +17

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

Life Sciences, Genetics, Molecular Biology +7