Xue-bi Cai
Wenzhou, China
Last Updated: 09/26/2026
Save publications for later
Sign Up
Not sure about your diagnosis?
Check Your Symptoms
Found 11 publications
CLEC3B is a novel causative gene for macular-retinal dystrophy.
Journal: Genetics in medicine : official journal of the American College of Medical Genetics
Published: October 17, 2021
Mutational screening of AGRN, SLC39A5, SCO2, P4HA2, BSG, ZNF644, and CPSF1 in a Chinese cohort of 103 patients with nonsyndromic high myopia.
Journal: Molecular vision
Published: July 25, 2020
Expanding the Phenotypic and Genotypic Landscape of Nonsyndromic High Myopia: A Cross-Sectional Study in 731 Chinese Patients.
Journal: Investigative ophthalmology & visual science
Published: September 28, 2019
Whole-exome sequencing identified ARL2 as a novel candidate gene for MRCS (microcornea, rod-cone dystrophy, cataract, and posterior staphyloma) syndrome.
Journal: Clinical genetics
Published: November 19, 2018
miR-183/96 plays a pivotal regulatory role in mouse photoreceptor maturation and maintenance.
Journal: Proceedings of the National Academy of Sciences of the United States of America
Published: June 01, 2017
Mutations in LRP5,FZD4, TSPAN12, NDP, ZNF408, or KIF11 Genes Account for 38.7% of Chinese Patients With Familial Exudative Vitreoretinopathy.
Journal: Investigative ophthalmology & visual science
Published: May 12, 2017
Trio-based exome sequencing arrests de novo mutations in early-onset high myopia.
Journal: Proceedings of the National Academy of Sciences of the United States of America
Published: April 05, 2017
Identification of de novo germline mutations and causal genes for sporadic diseases using trio-based whole-exome/genome sequencing.
Journal: Biological reviews of the Cambridge Philosophical Society
Published: January 16, 2017
Clinical and genetic analyses reveal novel pathogenic ABCA4 mutations in Stargardt disease families.
Clinical and genetic analyses reveal novel pathogenic ABCA4 mutations in Stargardt disease families.
Journal: Scientific reports
Published: May 23, 2016
Novel CHM mutations identified in Chinese families with Choroideremia.
Journal: Scientific reports
Published: May 20, 2016
Showing 1-11 of 11
Last Updated: 09/26/2026