Zixi Sun - Concepedia

Author

Zixi Sun

Chinese Academy of Medical Sciences & Peking Union Medical College ORCID

Also Known As

Z H Sun, Z.H. Sun, ZIXI SUN, Zixi Sun

Publications

571

Citations

H-Index

Concepts

All Affiliations

Chinese Academy of Medical Sciences & Peking Union Medical College Peking Union Medical College Hospital Baylor College of Medicine Baylor Genetics Moorfields Eye Hospital

About

Zixi Sun is an author at Chinese Academy of Medical Sciences & Peking Union Medical College specializing in medicine, ophthalmology, and genetics.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	6	6	165
2	Health Sciences	1	1	26
3	Public Health	1	1	12
4	Cell Biology	1	1	77
5	Metabolism	1	1	26

Zixi Sun

Publications

481

Citations

H-Index

Page 1

	Year	Citations
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
<i>CEP78</i> is mutated in a distinct type of Usher syndrome Qing Fu, Mingchu Xu, Chen Xue, Journal of Medical Genetics	2016	50
Mutations in<i>POMGNT1</i>cause non-syndromic retinitis pigmentosa Mingchu Xu, Takeyuki Yamada, Zixi Sun, Human Molecular Genetics	2016	47
Prevalence and risk factors for pterygium: a cross-sectional study in Han and Manchu ethnic populations in Hebei, China Zhouxian Pan, Jiantao Cui, Guangliang Shan, BMJ Open	2019	41
Mutations in crystallin genes result in congenital cataract associated with other ocular abnormalities. Zixi Sun, Qi Zhou, Huajin Li, PubMed	2017	29
PHENOTYPIC VARIABILITY OF RECESSIVE RDH12-ASSOCIATED RETINAL DYSTROPHY Xuan Zou, Qing Fu, Fang Sha, Retina	2018	26
Treating Bietti crystalline dystrophy in a high-fat diet-exacerbated murine model using gene therapy Bin Qu, Shijing Wu, Guanyi Jiao, Gene Therapy Metabolic SyndromeUrologyBody CompositionGrowth HormoneMetabolic Bone Disease	2020	26
IFT81 as a Candidate Gene for Nonsyndromic Retinal Degeneration. Rachayata Dharmat, Wei Liu, Zhongqi Ge, PubMed	2017	22
Whole-exome sequencing revealed HKDC1 as a candidate gene associated with autosomal-recessive retinitis pigmentosa Lin Zhang, Zixi Sun, Peiquan Zhao, Human Molecular Genetics Ocular DiseaseGeneticsPathologyHkdc1 Ko RetinaMolecular Genetics	2018	22
Novel variants in PNPLA6 causing syndromic retinal dystrophy Shijing Wu, Zixi Sun, Tian Zhu, Experimental Eye Research Ocular DiseaseRetinaOphthalmologyNovel VariantsGenetics	2020	17

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