Search research articles
Contact Us
Filters
Showing results (461-470 of 501) with videos related to
Page
of 51
Sort By:
Progress in Retinal and Eye Research
|
October 18, 2025
Interventions to reduce incidence and progression of myopia in children and adults
Jason C Yam, Xiu Juan Zhang, Ebenezer Zaabaar, et al.
Nature Genetics
|
August 11, 2014
Genome-wide association analysis of Vogt-Koyanagi-Harada syndrome identifies two new susceptibility loci at 1p31.2 and 10q21.3
Shengping Hou, Liping Du, Bo Lei, et al.
Nature Communications
|
September 11, 2023
Contribution of common and rare variants to Asian neovascular age-related macular degeneration subtypes
Qiao Fan, Hengtong Li, Xiaomeng Wang, et al.
Ophthalmic Research
|
June 29, 2026
Correlations between Clinical Activity Score and Serological and Radiological Data in Treatment-naïve Ethnic Han Chinese Thyroid Eye Disease
Kenneth Ka Hei Lai, Fatema Mohamed Ali Abdulla Aljufairi, Jake Uy Sebastian, et al.
Acta Ophthalmologica
|
June 18, 2021
Near work, screen time, outdoor time and myopia in schoolchildren in the Sunflower Myopia AEEC Consortium
Carla Lanca, Jason C Yam, Wen-Jun Jiang, et al.
Investigative Ophthalmology & Visual Science
|
August 30, 2012
Association of genetic variants on 8p21 and 4q12 with age-related macular degeneration in Asian populations
Isao Nakata, Kenji Yamashiro, Yumiko Akagi-Kurashige, et al.
Advanced Science (Weinheim, Baden-Wurttemberg, Germany)
|
March 18, 2026
GHRHR Deficiency Enhances Retinal Ganglion Cell Survival and Visual Functions in Experimental Glaucoma by Inhibiting Ferroptosis
Yan Tong, Ming Ho Yam, Jiaxin Zhang, et al.
The British Journal of Ophthalmology
|
September 4, 2020
Prevalence and predictors of myopic macular degeneration among Asian adults: pooled analysis from the Asian Eye Epidemiology Consortium
Yee Ling Wong, Xiangjia Zhu, Yih Chung Tham, et al.
Human Molecular Genetics
|
August 13, 2013
Genome-wide association study identifies ZFHX1B as a susceptibility locus for severe myopia
Chiea Chuen Khor, Masahiro Miyake, Li Jia Chen, et al.
Nature Genetics
|
September 1, 2014
Common variants near ABCA1 and in PMM2 are associated with primary open-angle glaucoma
Yuhong Chen, Ying Lin, Eranga N Vithana, et al.
Page
of 51
Search research articles
Search
Showing results (461-470 of 501) with videos related to
Sort By:
Page
of 51
Progress in Retinal and Eye Research
|
October 18, 2025
Interventions to reduce incidence and progression of myopia in children and adults
Jason C Yam, Xiu Juan Zhang, Ebenezer Zaabaar, et al.
Nature Genetics
|
August 11, 2014
Genome-wide association analysis of Vogt-Koyanagi-Harada syndrome identifies two new susceptibility loci at 1p31.2 and 10q21.3
Shengping Hou, Liping Du, Bo Lei, et al.
Nature Communications
|
September 11, 2023
Contribution of common and rare variants to Asian neovascular age-related macular degeneration subtypes
Qiao Fan, Hengtong Li, Xiaomeng Wang, et al.
Ophthalmic Research
|
June 29, 2026
Correlations between Clinical Activity Score and Serological and Radiological Data in Treatment-naïve Ethnic Han Chinese Thyroid Eye Disease
Kenneth Ka Hei Lai, Fatema Mohamed Ali Abdulla Aljufairi, Jake Uy Sebastian, et al.
Acta Ophthalmologica
|
June 18, 2021
Near work, screen time, outdoor time and myopia in schoolchildren in the Sunflower Myopia AEEC Consortium
Carla Lanca, Jason C Yam, Wen-Jun Jiang, et al.
Investigative Ophthalmology & Visual Science
|
August 30, 2012
Association of genetic variants on 8p21 and 4q12 with age-related macular degeneration in Asian populations
Isao Nakata, Kenji Yamashiro, Yumiko Akagi-Kurashige, et al.
Advanced Science (Weinheim, Baden-Wurttemberg, Germany)
|
March 18, 2026
GHRHR Deficiency Enhances Retinal Ganglion Cell Survival and Visual Functions in Experimental Glaucoma by Inhibiting Ferroptosis
Yan Tong, Ming Ho Yam, Jiaxin Zhang, et al.
The British Journal of Ophthalmology
|
September 4, 2020
Prevalence and predictors of myopic macular degeneration among Asian adults: pooled analysis from the Asian Eye Epidemiology Consortium
Yee Ling Wong, Xiangjia Zhu, Yih Chung Tham, et al.
Human Molecular Genetics
|
August 13, 2013
Genome-wide association study identifies ZFHX1B as a susceptibility locus for severe myopia
Chiea Chuen Khor, Masahiro Miyake, Li Jia Chen, et al.
Nature Genetics
|
September 1, 2014
Common variants near ABCA1 and in PMM2 are associated with primary open-angle glaucoma
Yuhong Chen, Ying Lin, Eranga N Vithana, et al.
Page
of 51