Xiaodong Jiao
Shanghai Changzheng Hospital(CN)
Publications by Year
Research Areas
Retinal Development and Disorders, Connexins and lens biology, Retinal Diseases and Treatments, Glaucoma and retinal disorders, Genetic factors in colorectal cancer
Most-Cited Works
- → Bietti Crystalline Corneoretinal Dystrophy Is Caused by Mutations in the Novel Gene CYP4V2(2004)284 cited
- → Autosomal Recessive Familial Exudative Vitreoretinopathy Is Associated with Mutations in LRP5(2004)208 cited
- → Mutations in FYCO1 Cause Autosomal-Recessive Congenital Cataracts(2011)151 cited
- The EPHA2 gene is associated with cataracts linked to chromosome 1p.(2008)
- → Detection of Variants in 15 Genes in 87 Unrelated Chinese Patients with Leber Congenital Amaurosis(2011)125 cited
- → Mutations in PIP5K3 Are Associated with François-Neetens Mouchetée Fleck Corneal Dystrophy(2005)124 cited
- → Synergic effect of polymorphisms inERCC65′ flanking region andcomplement factor Hon age-related macular degeneration predisposition(2006)113 cited
- → Mutations in KCNJ13 Cause Autosomal-Dominant Snowflake Vitreoretinal Degeneration(2008)113 cited
- → CDKN2B Polymorphism Is Associated with Primary Open-Angle Glaucoma (POAG) in the Afro-Caribbean Population of Barbados, West Indies(2012)89 cited
- → A genome-wide scan for primary open-angle glaucoma (POAG): the Barbados Family Study of Open-Angle Glaucoma(2003)84 cited