Ruru Y. Guo
Tianjin Key Laboratory Of Retinal Functions And Diseases, Tianjin Branch Of National Clinical Research Center For Ocular Disease
Tianjin, China
Tianjin, China
Last Updated: 09/26/2026
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Found 26 publications
Associations Between Serum Uric Acid Levels and Glaucoma: Results From the LifeLines Cohort and UK Biobank.
Journal: Investigative ophthalmology & visual science
Published: June 29, 2026
Serum Klotho Levels and Major Age-Related Ocular Disorders: A Cross-Sectional and Genetic Association Study.
Journal: Translational vision science & technology
Published: May 01, 2026
Characteristics and regional reference standards of peak expiratory flow in children and adolescents in high-altitude regions of Xizang, China: a cross-sectional study
Journal: Zhonghua jie he he hu xi za zhi = Zhonghua jiehe he huxi zazhi = Chinese journal of tuberculosis and respiratory diseases
Published: March 30, 2026
Compound heterozygous mutations in the USH2A gene causing non-syndromic retinitis pigmentosa.
Journal: Ophthalmic genetics
Published: March 10, 2026
Sex- and Age-related differences and determinants of ganglion cell complex and retinal nerve fiber layer thickness: A SS-OCT based study.
Journal: Photodiagnosis and photodynamic therapy
Published: January 22, 2026
Association Between Chronic Kidney Disease and Glaucoma: Results From the Lifelines Cohort Study and UK Biobank.
Journal: Investigative ophthalmology & visual science
Published: December 03, 2025
Mucilage-enhanced dew absorption facilitates DNA repair in seed embryo of the desert ephemeral Alyssum linifolium.
Journal: Plant physiology and biochemistry : PPB
Published: June 30, 2025
Spatial Distribution and Chronic Ecological risk Assessment of Typical Phthalate Esters in the Surface Waters of China.
Journal: Bulletin of environmental contamination and toxicology
Published: September 03, 2024
Association between primary angle closure glaucoma and uric acid levels in serum and aqueous humor.
Journal: Heliyon
Published: January 02, 2024
Novel and recurrent FBN1 mutations causing Marfan syndrome in two Chinese families.
Journal: Frontiers in medicine
Published: November 01, 2022
Novel clinical presentation and PAX6 mutation in families with congenital aniridia.
Journal: Frontiers in medicine
Published: September 12, 2022
Last Updated: 09/26/2026