Area of research
Ophthalmology · Plant Science
Research interest
Research interests include Retinal Diseases and Treatments, Retinal Development and Disorders, Glaucoma and retinal disorders, and Wheat and Barley Genetics and Pathology.
Genome-wide association analyses identify distinct genetic architectures for age-related macular degeneration across ancestries
Progress in the development of modulators targeting Frizzleds
CTNND1 variants cause familial exudative vitreoretinopathy through the Wnt/cadherin axis
Genome‐wide association study reveals structural chromosome variations with phenotypic effects in wheat (<i>Triticum aestivum</i> L.)
Catenin α 1 mutations cause familial exudative vitreoretinopathy by overactivating Norrin/β-catenin signaling
Comparison of different samples for 2019 novel coronavirus detection by nucleic acid amplification tests
Scleral HIF-1α is a prominent regulatory candidate for genetic and environmental interactions in human myopia pathogenesis
An efficient Oligo‐FISH painting system for revealing chromosome rearrangements and polyploidization in Triticeae
A transcriptome-wide association study based on 27 tissues identifies 106 genes potentially relevant for disease pathology in age-related macular degeneration
Genetic factors define CPO and CLO subtypes of nonsyndromicorofacial cleft
Genetic association study of exfoliation syndrome identifies a protective rare variant at LOXL1 and five new susceptibility loci
A Recurrent Missense Mutation in ZP3 Causes Empty Follicle Syndrome and Female Infertility
A large genome-wide association study of age-related macular degeneration highlights contributions of rare and common variants
New loci and coding variants confer risk for age-related macular degeneration in East Asians
Identification of myopia-associated WNT7B polymorphisms provides insights into the mechanism underlying the development of myopia
Identification of a novel MYOC mutation in a Chinese family with primary open-angle glaucoma
Common variants near ABCA1 and in PMM2 are associated with primary open-angle glaucoma
Mistrafficking of prenylated proteins causes retinitis pigmentosa 2
Genetic Variants in PVRL2-TOMM40-APOE Region Are Associated with Human Longevity in a Han Chinese Population
Genome-wide association study identifies ZFHX1B as a susceptibility locus for severe myopia
Identification of a susceptibility locus in <i>STAT4</i> for Behçet's disease in Han Chinese in a genome‐wide association study
Complement factor H genotypes impact risk of age-related macular degeneration by interaction with oxidized phospholipids
ABCB6 Mutations Cause Ocular Coloboma