Xiaoguang Yu
Wenzhou, 325027, China
Last Updated: 09/26/2026
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Found 11 publications
Association of Human Leukocyte Antigen Polymorphisms With Moderate-to-Severe Dry Eye With and Without Sjögren's Syndrome.
Journal: Investigative ophthalmology & visual science
Published: July 22, 2025
Clinical and Molecular Landscape of GLRA2 in X-Linked Early-Onset High Myopia.
Journal: Investigative ophthalmology & visual science
Published: April 14, 2025
The MAGIC Cohort Study: Genetic Associations of Anisometropia in Chinese Population.
Journal: Genomics, proteomics & bioinformatics
Published: March 31, 2025
Analysis of gene mutation spectrum for early-onset high myopia based on whole-exome sequencing.
Journal: The British journal of ophthalmology
Published: March 17, 2025
Whole-exome sequencing reveals sex difference in the genetic architecture of high myopia.
Journal: Journal of medical genetics
Published: October 26, 2024
Associations between RetNet gene polymorphisms and the efficacy of orthokeratology for myopia control: a retrospective clinical study.
Journal: Eye and vision (London, England)
Published: September 04, 2024
Trio-based whole-exome sequencing of 200 Chinese patients with keratoconus.
Journal: Experimental eye research
Published: August 12, 2024
Whole-genome sequencing identifies novel loci for keratoconus and facilitates risk stratification in a Han Chinese population.
Journal: Eye and vision (London, England)
Published: May 22, 2024
Screening Mutations of the Monogenic Syndromic High Myopia by Whole Exome Sequencing From MAGIC Project.
Journal: Investigative ophthalmology & visual science
Published: February 05, 2024
Whole-Exome Sequencing Among School-Aged Children With High Myopia.
Journal: JAMA network open
Published: December 01, 2023
Sequencing of 19,219 exomes identifies a low-frequency variant in FKBP5 promoter predisposing to high myopia in a Han Chinese population.
Journal: Cell reports
Published: August 23, 2022
Showing 1-11 of 11
Last Updated: 09/26/2026