Ophthalmology
Wei Du
Title: Associate Chief Physician
Interests

Surgical Management of Cataracts: Proficient in performing surgical interventions for a diverse range of cataract conditions.

Advanced Retinal Treatments: Specializes in laser and surgical procedures for complex retinal pathologies, including retinal detachment, macular degeneration, vitreous hemorrhage, and diabetic retinopathy.

Genetic Ophthalmology Research: Engages in research on the pathogenic genes associated with hereditary ophthalmic diseases.

Profile

Email

[email protected]

Phone

+86 18051061796

Profile

Dr. Wei Du is a Deputy Chief Physician in the Ophthalmology Department at the Eighth Affiliated Hospital of Sun Yat-sen University. Recognized as a high-level talent in Shenzhen, he serves as a committee member and director in several ophthalmology branches across Guangdong Province and Shenzhen. Dr. Du leads a national-level scientific research project and has authored or co-authored over ten articles in SCI-indexed and other prestigious journals. He has also contributed to a translated work as a co-translator and participated in the compilation of three other books

Education

2011: Ph.D. in Clinical Medicine, Peking University Health Science Center (Eight-year specialty program)

Publications

1.Retinoblastoma gene expression profiling based on bioinformatics analysis. Jun Mao, Mingzhi Lu, Siduo Lu, Yiqiao Xing, Xuejiao Xu, Ying Chen, Huirong Xu, Wei Zuo, Jingwen Zhou, Wei Du. BMC Med Genomics.?2023 May 13;16(1):101.

2.Wei Du, Fang Chen, Jun Zhu, Zhenggao Xie.The application of modified silicone oil retention sutures in traumatic aphakic eyes with iris loss. Retina. 2022,,Nov 1;42(11):2218-2220.

3.Wei Du, Juan Bu, Jiamei Dong, Yanlei Jia, Jing Li, Chen Liang, Shancheng Si, Lejin Wang. A novel frame-shift mutation in FRMD7 causes X-linked idiopathic congenital nystagmus in a Chinese family. Molecular Vision. 2011; 17: 2765–2768.

4.Jiamei Dong#, Juan Bu#, Wei Du#, Yuan Li, Yanlei Jia, Jianchang Li, Xiaoli Meng, Minghui Yuan, Xiaojuan Peng, Aimin Zhou, Lejin Wang. A new novel mutation in FBN1 causes autosomal dominant Marfan syndrome in a Chinese family. Molecular Vision. 2012; 18: 81–86.