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Wenmin Sun

Showing results (71-80 of 95) with videos related to

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Nature Communications|June 13, 2024
Altered chromatin topologies caused by balanced chromosomal translocation lead to central iris hypoplasiaWenmin Sun, Dan Xiong, Jiamin Ouyang, et al.
Genes|April 28, 2023
<i>FDXR</i>-Associated Oculopathy: Congenital Amaurosis and Early-Onset Severe Retinal Dystrophy as Common Presenting Features in a Chinese PopulationShutong Yi, Yuxi Zheng, Zhen Yi, et al.
Frontiers in Cell and Developmental Biology|December 20, 2021
Novel <i>BMP4</i> Truncations Resulted in Opposite Ocular Anomalies: Pathologic Myopia Rather Than MicrophthalmiaYi Jiang, Jiamin Ouyang, Xueqing Li, et al.
American Journal of Ophthalmology|March 29, 2023
Pathogenic Variants in CEP290 or IQCB1 Cause Earlier-Onset Retinopathy in Senior-Loken Syndrome Compared to Those in INVS, NPHP3, or NPHP4Junwen Wang, Shiqiang Li, Yi Jiang, et al.
Progress in Retinal and Eye Research|May 31, 2025
Genetic architecture of congenital cataracts: correlation of pathogenic variants with morphology and clinical outcomesDongwei Guo, Yi Jiang, Yuxi Zheng, et al.
Investigative Ophthalmology & Visual Science|January 30, 2025
ABCA4 Deep Intronic Variants Contributed to Nearly Half of Unsolved Stargardt Cases With a Milder PhenotypeYingwei Wang, Pangfeng Wang, Zhen Yi, et al.
The British Journal of Ophthalmology|September 30, 2022
Genetic and clinical landscape of <i>ARR3</i>-associated MYP26: the most common cause of Mendelian early-onset high myopia with a unique inheritanceYingwei Wang, Xueshan Xiao, Xueqing Li, et al.
The British Journal of Ophthalmology|October 14, 2021
Clinical and genetic features of retinoschisis in 120 families with <i>RS1</i> mutationsSainan Xiao, Wenmin Sun, Xueshan Xiao, et al.
Investigative Ophthalmology & Visual Science|August 22, 2022
Clinical and Genetic Analysis of RDH12-Associated Retinopathy in 27 Chinese Families: A Hypomorphic Allele Leads to Cone-Rod DystrophyJunwen Wang, Yingwei Wang, Shiqiang Li, et al.
International Journal of Molecular Sciences|April 13, 2023
New Insight into the Genotype-Phenotype Correlation of <i>PRPH2</i>-Related Diseases Based on a Large Chinese Cohort and Literature ReviewYingwei Wang, Junwen Wang, Yi Jiang, et al.
Pageof 10

Showing results (71-80 of 95) with videos related to

Sort By:
Pageof 10
Nature Communications|June 13, 2024
Altered chromatin topologies caused by balanced chromosomal translocation lead to central iris hypoplasiaWenmin Sun, Dan Xiong, Jiamin Ouyang, et al.
Genes|April 28, 2023
<i>FDXR</i>-Associated Oculopathy: Congenital Amaurosis and Early-Onset Severe Retinal Dystrophy as Common Presenting Features in a Chinese PopulationShutong Yi, Yuxi Zheng, Zhen Yi, et al.
Frontiers in Cell and Developmental Biology|December 20, 2021
Novel <i>BMP4</i> Truncations Resulted in Opposite Ocular Anomalies: Pathologic Myopia Rather Than MicrophthalmiaYi Jiang, Jiamin Ouyang, Xueqing Li, et al.
American Journal of Ophthalmology|March 29, 2023
Pathogenic Variants in CEP290 or IQCB1 Cause Earlier-Onset Retinopathy in Senior-Loken Syndrome Compared to Those in INVS, NPHP3, or NPHP4Junwen Wang, Shiqiang Li, Yi Jiang, et al.
Progress in Retinal and Eye Research|May 31, 2025
Genetic architecture of congenital cataracts: correlation of pathogenic variants with morphology and clinical outcomesDongwei Guo, Yi Jiang, Yuxi Zheng, et al.
Investigative Ophthalmology & Visual Science|January 30, 2025
ABCA4 Deep Intronic Variants Contributed to Nearly Half of Unsolved Stargardt Cases With a Milder PhenotypeYingwei Wang, Pangfeng Wang, Zhen Yi, et al.
The British Journal of Ophthalmology|September 30, 2022
Genetic and clinical landscape of <i>ARR3</i>-associated MYP26: the most common cause of Mendelian early-onset high myopia with a unique inheritanceYingwei Wang, Xueshan Xiao, Xueqing Li, et al.
The British Journal of Ophthalmology|October 14, 2021
Clinical and genetic features of retinoschisis in 120 families with <i>RS1</i> mutationsSainan Xiao, Wenmin Sun, Xueshan Xiao, et al.
Investigative Ophthalmology & Visual Science|August 22, 2022
Clinical and Genetic Analysis of RDH12-Associated Retinopathy in 27 Chinese Families: A Hypomorphic Allele Leads to Cone-Rod DystrophyJunwen Wang, Yingwei Wang, Shiqiang Li, et al.
International Journal of Molecular Sciences|April 13, 2023
New Insight into the Genotype-Phenotype Correlation of <i>PRPH2</i>-Related Diseases Based on a Large Chinese Cohort and Literature ReviewYingwei Wang, Junwen Wang, Yi Jiang, et al.
Pageof 10