Yunqi He
Chengdu, China
Last Updated: 09/26/2026
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Found 15 publications
Unveiling Endothelial Cell Expression Profiles in FEVR: Identification of Key Genes Associated With Pathological Neovascularisation in a FZD4M105V Mouse Model.
Journal: Clinical & experimental ophthalmology
Published: April 19, 2025
Mendelian Randomization Analysis Identifies Causal Effects of Multi-Site Chronic Pain on Obstructive Sleep Apnea.
Journal: Nature and science of sleep
Published: July 31, 2024
Identification of Novel FZD4 Mutations in Familial Exudative Vitreoretinopathy and Investigating the Pathogenic Mechanisms of FZD4 Mutations.
Journal: Investigative ophthalmology & visual science
Published: April 01, 2024
Frameshift variants in the C-terminal of CTNNB1 cause familial exudative vitreoretinopathy by AXIN1-mediated ubiquitin-proteasome degradation condensation.
Journal: International journal of biological macromolecules
Published: September 01, 2023
Characterization of a novel heterozygous frameshift variant in NDP gene that causes familial exudative vitreoretinopathy in female patients.
Journal: Molecular genetics and genomics : MGG
Published: March 14, 2023
A comprehensive functional analysis on the pathogenesis of novel TSPAN12 and NDP variants in familial exudative vitreoretinopathy.
Journal: Clinical genetics
Published: August 19, 2022
Defective EMC1 drives abnormal retinal angiogenesis via Wnt/β-catenin signaling and may be associated with the pathogenesis of familial exudative vitreoretinopathy.
Journal: Genes & diseases
Published: April 27, 2022
Identification of Two Novel Variants in the LRP5 Gene that Cause Familial Exudative Vitreoretinopathy.
Journal: Genetic testing and molecular biomarkers
Published: March 04, 2022
Whole-Exome Sequencing Reveals Novel NDP Variants in X-Linked Familial Exudative Vitreoretinopathy.
Journal: European journal of ophthalmology
Published: January 17, 2022
CTNND1 variants cause familial exudative vitreoretinopathy through the Wnt/cadherin axis.
Journal: JCI insight
Published: January 12, 2022
A novel frameshift variant in the TSPAN12 gene causes autosomal dominant FEVR.
Journal: Molecular genetics & genomic medicine
Published: December 18, 2021
Novel truncating variants in CTNNB1 cause familial exudative vitreoretinopathy.
Journal: Journal of medical genetics
Published: October 07, 2021
Last Updated: 09/26/2026