Ruifang Sui

Publication Activity (10 Years)

Years Active: 2017-2023
Publications (10 Years): 16

Top Topics

Diabetic Retinopathy

Top Venues

Clinical genetics

Graefe's archive for clinical and experimental ophthalmology = Albrecht von Graefes Archiv fur klinische und experimentelle Ophthalmologie

Molecular genetics & genomic medicine

American journal of medical genetics. Part A

This page only lists publications with an associated author ORCID identifier.

Publications

Xing Wei, Tian Zhu, Lei Wang, Ruifang Sui
Leber congenital amaurosis as the initial and essential manifestation in a Chinese patient with autoimmune polyglandular syndrome Type 1. Documenta ophthalmologica. Advances in ophthalmology (2023)
Huajin Li, Xing Wei, Shijing Wu, Tian Zhu, Zixi Sun, Hui Li, Xiaoxu Han, Xuan Zou, Fengxia Yao, Ruifang Sui
Clinical and genetic characterization of a large cohort of Chinese patients with Bietti crystalline retinopathy. Graefe's archive for clinical and experimental ophthalmology = Albrecht von Graefes Archiv fur klinische und experimentelle Ophthalmologie (2023)
Ruifang Sui
Letter to the editor regarding "A novel tandem duplication of PRDM13 in a Chinese family with North Carolina macular dystrophy". Graefe's archive for clinical and experimental ophthalmology = Albrecht von Graefes Archiv fur klinische und experimentelle Ophthalmologie (2023)
Tian Zhu, Hui Li, Xing Wei, Wuyi Li, Zixi Sun, Ruifang Sui
Novel homozygous variant in ARL2BP associated with retinitis pigmentosa, situs inversus, and male infertility in a Chinese patient. Clinical genetics 103 (4) (2022)
Maéva Langouët, Christine Jolicoeur, Awais Javed, Pierre Mattar, Micah D Gearhart, Stephen P Daiger, Mette Bertelsen, Lisbeth Tranebjærg, Nanna D Rendtorff, Karen Grønskov, Catherine Jespersgaard, Rui Chen, Zixi Sun, Hui Li, Najmeh Alirezaie, Jacek Majewski, Vivian J Bardwell, Ruifang Sui, Robert K Koenekoop, Michel Cayouette
Mutations in BCOR , a co-repressor of CRX/OTX2 , are associated with early-onset retinal degeneration. Science advances 8 (36) (2022)
Tian Zhu, Hui Li, Xing Wei, Wuyi Li, Zixi Sun, Ruifang Sui
Novel homozygous variant in ARL2BP associated with retinitis pigmentosa, situs inversus, and male infertility in a Chinese patient. Clinical genetics (2022)
Tian Zhu, Hui Li, Xing Wei, Wuyi Li, Zixi Sun, Ruifang Sui
Novel homozygous variant in ARL2BP associated with retinitis pigmentosa, situs inversus, and male infertility in a Chinese patient. Clinical genetics 103 (4) (2022)
Tian Zhu, Hui Li, Xing Wei, Wuyi Li, Zixi Sun, Ruifang Sui
Novel homozygous variant in ARL2BP associated with retinitis pigmentosa, situs inversus, and male infertility in a Chinese patient. Clinical genetics (2022)
Xing Wei, Hui Li, Shijing Wu, Tian Zhu, Ruifang Sui
Genetic analysis and clinical features of three Chinese patients with Oguchi disease. Documenta ophthalmologica. Advances in ophthalmology (2022)
Tian Zhu, Hui Li, Xing Wei, Wuyi Li, Zixi Sun, Ruifang Sui
Novel homozygous variant in ARL2BP associated with retinitis pigmentosa, situs inversus, and male infertility in a Chinese patient. Clinical genetics 103 (4) (2022)
Shijing Wu, Zhisheng Yuan, Zixi Sun, Fengxia Yao, Ruifang Sui
Leber congenital amaurosis as an initial manifestation in a Chinese patient with thiamine-responsive megaloblastic anemia syndrome. American journal of medical genetics. Part A (2021)
Shijing Wu, Zhisheng Yuan, Zixi Sun, Tian Zhu, Xing Wei, Xuan Zou, Ruifang Sui
A novel tandem duplication of PRDM13 in a Chinese family with North Carolina macular dystrophy. Graefe's archive for clinical and experimental ophthalmology = Albrecht von Graefes Archiv fur klinische und experimentelle Ophthalmologie (2021)
Bin Qu, Shijing Wu, Guanyi Jiao, Xuan Zou, Zhikun Li, Lu Guo, Xuehan Sun, Cheng Huang, Zixi Sun, Ying Zhang, Hui Li, Qi Zhou, Ruifang Sui, Wei Li
Treating Bietti crystalline dystrophy in a high-fat diet-exacerbated murine model using gene therapy. Gene therapy 27 (7-8) (2020)
Xiaoxu Han, Shijing Wu, Min Wang, Hui Li, Yan Huang, Ruifang Sui
Genetic and clinical characterization of mainland Chinese patients with sialidosis type 1. Molecular genetics & genomic medicine 8 (8) (2020)
Shijing Wu, Xuan Zou, Zixi Sun, Tian Zhu, Xing Wei, Ruifang Sui
Unilateral retinocytoma associated with a variant in the RB1 gene. Molecular genetics & genomic medicine 8 (4) (2020)
Qi Zhou, Fengxia Yao, Feng Wang, Hui Li, Rui Chen, Ruifang Sui
A heterozygous mutation in RPGR associated with X-linked retinitis pigmentosa in a patient with Turner syndrome mosaicism (45,X/46,XX). American journal of medical genetics. Part A 176 (1) (2017)