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Publications by Xiaodong Jiao

Mutations in FYCO1 Cause Autosomal-Recessive Congenital Cataracts

American Journal of Human Genetics

English

Mutation in the Intracellular Chloride Channel CLCC1 Associated With Autosomal Recessive Retinitis Pigmentosa

Molecular Biology

Cancer Research

English

The RNA-binding Protein HuR Confers Oxaliplatin Resistance of Colorectal Cancer by Upregulating CDC6

Molecular Cancer Therapeutics

Cancer Research

English

Identification and Population History of CYP4V2 Mutations in Patients With Bietti Crystalline Corneoretinal Dystrophy

European Journal of Human Genetics

English

Evaluation of SNPs on Chromosome 2p With Primary Open Angle Glaucoma in the South Indian Cohort

Investigative Ophthalmology and Visual Science

Molecular Neuroscience

Sensory Systems

English

Detection of Variants in 15 Genes in 87 Unrelated Chinese Patients With Leber Congenital Amaurosis

Multidisciplinary

English

Mutations in KCNJ13 Cause Autosomal-Dominant Snowflake Vitreoretinal Degeneration

American Journal of Human Genetics

English

Bietti Crystalline Corneoretinal Dystrophy Is Caused by Mutations in the Novel Gene CYP4V2

American Journal of Human Genetics

English

High Myopia Is Not Associated With the SNPs in theTGIF, Lumican,TGFB1, andHGFGenes

Investigative Ophthalmology and Visual Science

Molecular Neuroscience

Sensory Systems

English