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Meeting Abstract (9)
Journal Articles (1)

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Investigative Ophthalmology & Visual Science (10)

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ARVO Annual Meeting Abstract (9)
Genetics (1)

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Eye Anatomy and Disorders (1)
Genetics (1)
Retina (1)

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chinese (other dialects) (1)
chinese people (1)
cohort studies (1)
family (1)
genes (1)
leber's amaurosis (1)
molecular diagnostic techniques (1)
mutation (1)
proband (1)
retinal diseases (1)

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ARVO Annual Meeting Abstract July 2019

Deep learning approach to improve the efficiency and effectiveness of optical coherence tomography (OCT) scans

Lingling Wang; Jianchun Zhao; Xuan Zou; Xuan Chen; Chunhui Jiang; Xing Liu; Hui Xiao; Xiaoli Song; Yao Zhang; Jun Wu; Jie Wang; Dayong Ding; Junfeng Tan; Yuan Tian; Ningjiang Chen

Invest. Ophthalmol. Vis. Sci.. 2019; 60(9):1514. doi:

ARVO Annual Meeting Abstract July 2018

Multimodal imaging of East Asian Patients with Occult Macular Dystrophy (Miyake’s disease): EAOMD Report No. 3

Kwangsic Joo; Lizhu Yang; Kazushige Tsunoda; Mineo Kondo; Yu Fujinami; Gavin Arno; Toshihide Kurihara; Kazuo Tsubota; Takeshi Iwata; Xuan Zou; Hui Li; Yozo Miyake; Kyu Hyung Park; Kaoru Fujinami; Ruifang Sui; Se Joon Woo

Invest. Ophthalmol. Vis. Sci.. 2018; 59(9):1430. doi:

ARVO Annual Meeting Abstract July 2018

Clinical and Genetic Characteristics of East Asian Patients with Occult Macular Dystrophy (Miyake’s disease); EAOMD Report No.1

Kaoru Fujinami; Lizhu Yang; Kwangsic Joo; Kazushige Tsunoda; Yuichi Kawamura; Yu Fujinami; Gavin Arno; Toshihide Kurihara; Kazuo Tsubota; Xuan Zou; Hui Li; Kyu Hyung Park; Takeshi Iwata; Yozo Miyake; Se Joon Woo; Ruifang Sui

Invest. Ophthalmol. Vis. Sci.. 2018; 59(9):1431. doi:

ARVO Annual Meeting Abstract July 2018

Genotype Phenotype Association in East Asian Patients with Occult Macular Dystrophy (Miyake’s disease); EAOMD Report No.4

Yu Fujinami; Lizhu Yang; Kwangsic Joo; Kazushige Tsunoda; Mineo Kondo; Gavin Arno; XIAO LIU; Kazuo Tsubota; Takeshi Iwata; Xuan Zou; Hui Li; Kyu Hyung Park; Yozo Miyake; Se Joon Woo; Ruifang Sui; Kaoru Fujinami

Invest. Ophthalmol. Vis. Sci.. 2018; 59(9):1432. doi:

ARVO Annual Meeting Abstract June 2017

Phenotype and Genotype Characterization of a small cohort of Chinese patients with Occult Macular Dystrophy

Ruifang Sui; Lizhu Yang; Xuan Zou; Huajin Li; Fangtian Dong

Invest. Ophthalmol. Vis. Sci.. 2017; 58(8):581. doi:

ARVO Annual Meeting Abstract September 2016

Phenotypic Variability in RDH12 Retinopathy

Ruifang Sui; Xuan Zou; Zhongqi Ge; Hui Li; Mingchu Xu; Rui Chen; Fangtian Dong

Invest. Ophthalmol. Vis. Sci.. 2016; 57(12):3138. doi:

Genetics June 2015

Comprehensive Molecular Diagnosis of a Large Chinese Leber Congenital Amaurosis Cohort

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Hui Wang; Xia Wang; Xuan Zou; Shan Xu; Hui Li; Zachry Tore Soens; Keqing Wang; Yumei Li; Fangtian Dong; Rui Chen; Ruifang Sui
TAGS: chinese (other dialects), cohort studies, family, genes, molecular diagnostic techniques, mutation, retinal diseases, chinese people, leber's amaurosis, proband
Invest. Ophthalmol. Vis. Sci.. 2015; 56(6):3642-3655. doi: https://doi.org/10.1167/iovs.14-15972

Includes: Supplemental Content

ARVO Annual Meeting Abstract June 2013

Novel de novo mutations in CRX gene associated with Leber congenital amaurosis in Chinese patients

Ruifang Sui; Xuan Zou; Fangtian Dong

Invest. Ophthalmol. Vis. Sci.. 2013; 54(15):1310. doi:

ARVO Annual Meeting Abstract June 2013

RDH12 mutations associated with Leber congenital amaurosis and early-onset severe retinal dystrophy in Chinese patients

Xuan Zou; Fangtian Dong; Ruifang Sui

Invest. Ophthalmol. Vis. Sci.. 2013; 54(15):1311. doi:

ARVO Annual Meeting Abstract March 2012

Transthyretin Ala36pro Mutation In A Chinese Pedigree Of Familial Transthyretin Amyloidosis With Early Ocular Involvement

Ruifang Sui; Fangtian Dong; Xuan Zou

Invest. Ophthalmol. Vis. Sci.. 2012; 53(14):1565. doi:

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Online ISSN: 1552-5783

Investigative Ophthalmology & Visual Science
Journal of Vision
Translational Vision Science & Technology

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Copyright © 2015 Association for Research in Vision and Ophthalmology.

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