Ruifang Sui - Concepedia

Author

Ruifang Sui

Peking Union Medical College Hospital ORCID

Also Known As

R F Sui, R Sui, R. Sui, Rui-Fang Sui, Rui-fang SUI, Rui-fang Sui, Ruichen Sui, Ruifang Sui, Ruihao Sui, Ruixiu Sui

187

Publications

3.2K

Citations

H-Index

Concepts

All Affiliations

Peking Union Medical College Hospital Chinese Academy of Medical Sciences & Peking Union Medical College Baylor College of Medicine Baylor Genetics McGill University Health Centre

About

Ruifang Sui is an author at Peking Union Medical College Hospital specializing in medicine, genetics, and ophthalmology.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	19	22	1.9K
2	Public Health	3	3	73
3	Health Sciences	2	2	103
4	Natural Sciences	2	2	111
5	Engineering	1	1	17

Ruifang Sui

Publications

2.8K

Citations

H-Index

Page 1

	Year	Citations
Refractive error study in children: results from Shunyi District, China Jialiang Zhao, Xiangjun Pan, Ruifang Sui, American Journal of Ophthalmology Population ChildrenOphthalmologyMedicinePediatricsRefractive Error Study	2000	586
Next generation sequencing-based molecular diagnosis of retinitis pigmentosa: identification of a novel genotype-phenotype correlation and clinical refinements Feng Wang, Hui Wang, Han-Fang Tuan, Human Genetics Molecular Diagnostic TechniquesRetinitis PigmentosaGeneticsMedicineNext-generation Sequencing	2013	235
Visual acuity and quality of life outcomes in patients with cataract in Shunyi County, China Jialiang Zhao, Ruifang Sui, Lijan Jia, American Journal of Ophthalmology Life OutcomesOphthalmologyMedicineShunyi CountyRehabilitation	1998	152
Prevalence of blindness and cataract surgery in Shunyi County, China Jialiang Zhao, Lijan Jia, Ruifang Sui, American Journal of Ophthalmology Ophthalmic SurgeryOcular DiseaseOphthalmologyMedicineShunyi County	1998	109
Comprehensive Molecular Diagnosis of a Large Chinese Leber Congenital Amaurosis Cohort Hui Wang, Xia Wang, Xuan Zou, Investigative Ophthalmology & Visual Science	2015	107
Next-Generation Sequencing–Based Molecular Diagnosis of a Chinese Patient Cohort With Autosomal Recessive Retinitis Pigmentosa Qing Fu, Feng Wang, Hui Wang, Investigative Ophthalmology & Visual Science	2013	99
Oral 9-cis retinoid for childhood blindness due to Leber congenital amaurosis caused by RPE65 or LRAT mutations: an open-label phase 1b trial Robert K. Koenekoop, Ruifang Sui, Juliana Maria Ferraz Sallum, The Lancet Ocular DiseaseRetinaOphthalmologyOral 9-CisGenetics	2014	99
Mutations in human IFT140 cause non-syndromic retinal degeneration Mingchu Xu, Lizhu Yang, Feng Wang, Human Genetics Ocular DiseaseRetinaOphthalmologyGenetic DisorderGenetics	2015	82
Mutations in the Spliceosome Component CWC27 Cause Retinal Degeneration with or without Additional Developmental Anomalies Mingchu Xu, Ya‐Jing Xie, Hana Abouzeid, The American Journal of Human Genetics Ocular DiseaseDevelopmental BiologyRetinaOphthalmologyAdditional Developmental Anomalies	2017	77
Bacteria‐Targeting Photodynamic Nanoassemblies for Efficient Treatment of Multidrug‐Resistant Biofilm Infected Keratitis Yiwen Zhu, Shijing Wu, Yujie Sun, Advanced Functional Materials Corneal PerforationAntimicrobial ChemotherapyBacterial PathogensDrug ResistanceNanomedicine	2021	77

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