Rui Hua

A Large‐scale, multicenter serum metabolite biomarker identification study for the early detection of hepatocellular carcinoma

Ping Luo, Peiyuan Yin, Rui Hua et al. · Hepatology · 2017 · 369 citations · Full text

Loss-of-function mutations of an inhibitory upstream ORF in the human hairless transcript cause Marie Unna hereditary hypotrichosis

Yaran Wen, Yang Liu, Yiming Xu et al. · Nature Genetics · 2009 · 208 citations

Inhibitory Upstream Orf, Genetic Disorder, Natural Sciences +8

Mutations of the<i>EPHA2</i>receptor tyrosine kinase gene cause autosomal dominant congenital cataract

Tianxiao Zhang, Rui Hua, Wei Xiao et al. · Human Mutation · 2009 · 101 citations · Full text

Human Ccs, Developmental Biology, Ocular Disease +13

Copy-Number Mutations on Chromosome 17q24.2-q24.3 in Congenital Generalized Hypertrichosis Terminalis with or without Gingival Hyperplasia

Miao Sun, Ning Li, Dong Wu et al. · The American Journal of Human Genetics · 2009 · 85 citations · Full text

Gingival Hyperplasia, Cytogenetics, Medicine +9

Distinct Patterns of Constitutive Phosphodiesterase Activity in Mouse Sinoatrial Node and Atrial Myocardium

Rui Hua, Andrew Adamczyk, Courtney Robbins et al. · PLoS ONE · 2012 · 69 citations · Full text