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Wenmin Sun

Showing results (81-90 of 95) with videos related to

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Investigative Ophthalmology & Visual Science|December 11, 2025
Ubap1l Knockout Mice Model Recapitulates Retinal Degeneration Phenotype Observed in Patients and Exhibits Irregular Photoreceptor MorphologyYingwei Wang, Shuhan Zhang, Yuxi Zheng, et al.
Investigative Ophthalmology & Visual Science|April 25, 2023
Unique Haplotypes in OPN1LW as a Common Cause of High Myopia With or Without Protanopia: A Potential Window Into Myopic MechanismYingwei Wang, Wenmin Sun, Xueshan Xiao, et al.
Investigative Ophthalmology & Visual Science|January 8, 2024
Clinical and Genetic Landscape of Ectopia Lentis Based on a Cohort of Patients From 156 FamiliesDongwei Guo, Shiqiang Li, Xueshan Xiao, et al.
Molecular Vision|April 9, 2026
Insight into genes responsible for cornea plana, megalocornea, keratoconus and brittle cornea syndromeDi Zhu, Yuxi Zheng, Yi Jiang, et al.
Zoological Research|January 6, 2026
<i>ARR3</i> variant-induced cone mosaicism alters cone subtype composition and disrupts phototransductionJiamin Ouyang, Zhen Yi, Yi Jiang, et al.
Brain : a Journal of Neurology|October 18, 2024
Clinical and genetic landscape of optic atrophy in 826 families: insights from 50 nuclear genesYuxi Zheng, Panfeng Wang, Shiqiang Li, et al.
Investigative Ophthalmology & Visual Science|March 14, 2023
The Genetic Confirmation and Clinical Characterization of LOXL3-Associated MYP28: A Common Type of Recessive Extreme High MyopiaYi Jiang, Lin Zhou, Yingwei Wang, et al.
The British Journal of Ophthalmology|May 15, 2024
Clinical features of patients with mutations in genes for nanophthalmosXueqing Li, Hui Xiao, Yihua Su, et al.
Human Genetics|September 21, 2022
Truncation mutations in MYRF underlie primary angle closure glaucomaJiamin Ouyang, Wenmin Sun, Huangxuan Shen, et al.
Plos One|June 19, 2013
Exome sequencing of 47 chinese families with cone-rod dystrophy: mutations in 25 known causative genesLi Huang, Qingyan Zhang, Shiqiang Li, et al.
Pageof 10

Showing results (81-90 of 95) with videos related to

Sort By:
Pageof 10
Investigative Ophthalmology & Visual Science|December 11, 2025
Ubap1l Knockout Mice Model Recapitulates Retinal Degeneration Phenotype Observed in Patients and Exhibits Irregular Photoreceptor MorphologyYingwei Wang, Shuhan Zhang, Yuxi Zheng, et al.
Investigative Ophthalmology & Visual Science|April 25, 2023
Unique Haplotypes in OPN1LW as a Common Cause of High Myopia With or Without Protanopia: A Potential Window Into Myopic MechanismYingwei Wang, Wenmin Sun, Xueshan Xiao, et al.
Investigative Ophthalmology & Visual Science|January 8, 2024
Clinical and Genetic Landscape of Ectopia Lentis Based on a Cohort of Patients From 156 FamiliesDongwei Guo, Shiqiang Li, Xueshan Xiao, et al.
Molecular Vision|April 9, 2026
Insight into genes responsible for cornea plana, megalocornea, keratoconus and brittle cornea syndromeDi Zhu, Yuxi Zheng, Yi Jiang, et al.
Zoological Research|January 6, 2026
<i>ARR3</i> variant-induced cone mosaicism alters cone subtype composition and disrupts phototransductionJiamin Ouyang, Zhen Yi, Yi Jiang, et al.
Brain : a Journal of Neurology|October 18, 2024
Clinical and genetic landscape of optic atrophy in 826 families: insights from 50 nuclear genesYuxi Zheng, Panfeng Wang, Shiqiang Li, et al.
Investigative Ophthalmology & Visual Science|March 14, 2023
The Genetic Confirmation and Clinical Characterization of LOXL3-Associated MYP28: A Common Type of Recessive Extreme High MyopiaYi Jiang, Lin Zhou, Yingwei Wang, et al.
The British Journal of Ophthalmology|May 15, 2024
Clinical features of patients with mutations in genes for nanophthalmosXueqing Li, Hui Xiao, Yihua Su, et al.
Human Genetics|September 21, 2022
Truncation mutations in MYRF underlie primary angle closure glaucomaJiamin Ouyang, Wenmin Sun, Huangxuan Shen, et al.
Plos One|June 19, 2013
Exome sequencing of 47 chinese families with cone-rod dystrophy: mutations in 25 known causative genesLi Huang, Qingyan Zhang, Shiqiang Li, et al.
Pageof 10