Huanan Ren
First Affiliated Hospital of Zhengzhou University(CN)
Publications by Year
Research Areas
Retinal Development and Disorders, Retinal Diseases and Treatments, Connexins and lens biology, melanin and skin pigmentation, RNA regulation and disease
Most-Cited Works
- → Exome Capture Reveals ZNF423 and CEP164 Mutations, Linking Renal Ciliopathies to DNA Damage Response Signaling(2012)391 cited
- → Next generation sequencing-based molecular diagnosis of retinitis pigmentosa: identification of a novel genotype-phenotype correlation and clinical refinements(2013)237 cited
- → Mutations in the unfolded protein response regulator ATF6 cause the cone dysfunction disorder achromatopsia(2015)212 cited
- → Mutations in NMNAT1 cause Leber congenital amaurosis and identify a new disease pathway for retinal degeneration(2012)201 cited
- → Comprehensive molecular diagnosis of 179 Leber congenital amaurosis and juvenile retinitis pigmentosa patients by targeted next generation sequencing(2013)161 cited
- → GPR179 Is Required for Depolarizing Bipolar Cell Function and Is Mutated in Autosomal-Recessive Complete Congenital Stationary Night Blindness(2012)159 cited
- → Next-Generation Sequencing–Based Molecular Diagnosis of a Chinese Patient Cohort With Autosomal Recessive Retinitis Pigmentosa(2013)99 cited
- → A Dominant Mutation in Hexokinase 1 (HK1) Causes Retinitis Pigmentosa(2014)71 cited
- → Comprehensive analysis of patients with Stargardt macular dystrophy reveals new genotype–phenotype correlations and unexpected diagnostic revisions(2014)47 cited
- → Recombinant expression, activity screening and functional characterization identifies three novel endo-1,4-β-glucanases that efficiently hydrolyse cellulosic substrates(2011)43 cited