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Author

Pei-Zeng Yang

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Open access Sep 2026

A Rare De Novo Missense Mutation in IFT122 Confers a Genetic Susceptibility Factor of Idiopathic Pediatric Uveitis Via Trio‐based Whole‐Exome Sequencing

ABSTRACT Idiopathic pediatric uveitis (IPU) is a leading cause of irreversible vision loss in children; however, the genetic and molecular mechanisms underlying this condition remain unclear. Herein, trio‐based whole‐exome sequencing was performed in 28 affected families and targeted sequencing was performed in 1953 sp...

Qian Zhou, Jia-Xing Huang, Yi-Lin Wang et al. · 0 citations
Open access Sep 2026

Association and Age Heterogeneity of Systemic Metabolomic Signatures With Age-Related Cataract: A Mendelian Randomization and Heterogeneity Analysis

Purpose To evaluate systemic metabolomic signatures associated with age-related cataract and prioritize signals with age-stable or age-heterogeneous patterns. Methods We performed two-sample Mendelian randomization (MR) analyses of 249 Nightingale Health metabolomic traits against age-related cataract in FinnGen 12. Hi...

Zhangluxi Liu, A. Lu, Siyuan He et al. · 0 citations

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