Hongbin Lv

418 total citations
28 papers, 288 citations indexed

About

Hongbin Lv is a scholar working on Molecular Biology, Ophthalmology and Sensory Systems. According to data from OpenAlex, Hongbin Lv has authored 28 papers receiving a total of 288 indexed citations (citations by other indexed papers that have themselves been cited), including 20 papers in Molecular Biology, 11 papers in Ophthalmology and 4 papers in Sensory Systems. Recurrent topics in Hongbin Lv's work include Retinal Diseases and Treatments (11 papers), Retinal Development and Disorders (11 papers) and Hearing, Cochlea, Tinnitus, Genetics (4 papers). Hongbin Lv is often cited by papers focused on Retinal Diseases and Treatments (11 papers), Retinal Development and Disorders (11 papers) and Hearing, Cochlea, Tinnitus, Genetics (4 papers). Hongbin Lv collaborates with scholars based in China, United States and Macao. Hongbin Lv's co-authors include Jingliang Cheng, Junjiang Fu, Jiewen Fu, Lisha Yang, Chunli Wei, Shangyi Fu, Rui Chen, Qi Zhou, Md. Asaduzzaman Khan and Liyuan Jiang and has published in prestigious journals such as Scientific Reports, Journal of Colloid and Interface Science and Frontiers in Immunology.

In The Last Decade

Hongbin Lv

26 papers receiving 284 citations

Peers

Countries citing papers authored by Hongbin Lv

Since Specialization

Citations

This map shows the geographic impact of Hongbin Lv's research. It shows the number of citations coming from papers published by authors working in each country. You can also color the map by specialization and compare the number of citations received by Hongbin Lv with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Hongbin Lv more than expected).

Fields of papers citing papers by Hongbin Lv

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Hongbin Lv. Nodes represent research fields, and links connect fields that are likely to share authors. Colored nodes show fields that tend to cite the papers produced by Hongbin Lv. The network helps show where Hongbin Lv may publish in the future.

Co-authorship network of co-authors of Hongbin Lv

This figure shows the co-authorship network connecting the top 25 collaborators of Hongbin Lv. A scholar is included among the top collaborators of Hongbin Lv based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with Hongbin Lv. Hongbin Lv is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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20 of 20 papers shown

#	Work	Indexed citations
1	Exploring the correlations between six serological inflammatory markers and different stages of type 2 diabetic retinopathy 2025 ·Scientific Reports ·(unknown), (unknown), Bin Fan, Xiaohu Chen, Hongbin Lv, Yan Dai	6
2	Nanozyme cascade reaction system for diabetic retinopathy therapy via glycometabolism and microenvironment regulation 2025 ·Journal of Colloid and Interface Science ·Min Tian, (unknown), Yang Xiao, (unknown), Yue Yang, Yuting Liu, Xi Zheng, Yang Liu, Guang Li, Hongbin Lv, Zheng Li	0
3	Targeting oxidative stress in diabetic retinopathy: mechanisms, pathology, and novel treatment approaches 2025 ·Frontiers in Immunology ·Wei He, Patrick Y. Tang, Hongbin Lv	7
4	Sirt3 Protects Retinal Pigment Epithelial Cells From High Glucose-Induced Injury by Promoting Mitophagy Through the AMPK/mTOR/ULK1 Pathway 2024 ·Translational Vision Science & Technology ·Wei Yang, (unknown), Hongbin Lv, Zhiru Zhang, (unknown), (unknown), (unknown), Xueqin Zhang, Jie Chen, Yue He	10
5	Comprehensive exploration of hub genes involved in oxidative stress in rhegmatogenous retinal detachment based on bioinformatics analysis 2024 ·Experimental Eye Research ·(unknown), (unknown), Xiaohong Xiang, (unknown), Yang Cao, Jun Zeng, Hongbin Lv	1
6	YTHDC1 aggravates high glucose-induced retinal vascular endothelial cell injury via m6A modification of CDK6 2024 ·Biology Direct ·(unknown), Min Tian, Yang Cao, Min Tang, Xiaohong Xiang, Lu Guo, Hongbin Lv	6
7	Lychee seed polyphenol ameliorates DR via inhibiting inflammasome/apoptosis and angiogenesis in hRECs and db/db mice 2023 ·Biomedicine & Pharmacotherapy ·Xiaohong Xiang, (unknown), Xiaofang Wang, Qin Xu, Chong‐Lin Yu, Changlong He, Tao Long, (unknown), Chen Xue, Xiaogang Zhou, Jianming Wu, Dalian Qin, Anguo Wu, Yong Tang, Hongbin Lv	9
8	Tert-butylhydroquinone protects the retina from oxidative stress in STZ-induced diabetic rats via the PI3K/Akt/eNOS pathway 2022 ·European Journal of Pharmacology ·(unknown), Juan Wang, Fang Wei, Qing Gu, Min Tian, Hongbin Lv	9
9	Identification of a De Novo Heterozygous Missense ACTB Variant in Baraitser–Winter Cerebrofrontofacial Syndrome 2022 ·Frontiers in Genetics ·(unknown), Junting Huang, Longqian Liu, Hongbin Lv, Danian Chen, Wei Fan	0
10	Extracellular vesicles derived from human umbilical cord mesenchymal stem cells relieves diabetic retinopathy through a microRNA-30c-5p-dependent mechanism 2022 ·Diabetes Research and Clinical Practice ·Yue He, Zhiru Zhang, Tianyu Yao, (unknown), Jinhua Gan, Hongbin Lv, Jie Chen	21
11	Novel compound heterozygous missense variants (c.G955A and c.A1822C) of CACNA2D4 likely causing autosomal recessive retinitis pigmentosa in a Chinese patient 2021 ·3 Biotech ·Jingliang Cheng, Qi Zhou, Jiewen Fu, Chunli Wei, Lianmei Zhang, (unknown), Hongbin Lv, Songyot Anuchapreeda, Junjiang Fu	3
12	Targeted Next-Generation Sequencing Identified Novel Compound Heterozygous Variants in the CDH23 Gene Causing Usher Syndrome Type ID in a Chinese Patient 2020 ·Frontiers in Genetics ·Lianmei Zhang, Jingliang Cheng, Qi Zhou, Md. Asaduzzaman Khan, Jiewen Fu, (unknown), Suan Sun, Hongbin Lv, Junjiang Fu	13
13	Novel compound heterozygous EYS variants may be associated with arRP in a large Chinese pedigree 2020 ·Bioscience Reports ·Chunli Wei, Ting Xiao, Jingliang Cheng, Jiewen Fu, Qi Zhou, Lisha Yang, Hongbin Lv, Junjiang Fu	4
14	A case of Usher syndrome type IIA caused by a rare USH2A homozygous frameshift variant with maternal uniparental disomy (UPD) in a Chinese family 2020 ·Journal of Cellular and Molecular Medicine ·Jiewen Fu, Shiyi Shen, Jingliang Cheng, Hongbin Lv, Junjiang Fu	11
15	A novel splicing mutation in the PRPH2 gene causes autosomal dominant retinitis pigmentosa in a Chinese pedigree 2019 ·Journal of Cellular and Molecular Medicine ·Jingliang Cheng, Jiewen Fu, Qi Zhou, Xiaohong Xiang, Chunli Wei, Lisha Yang, Shangyi Fu, Md. Asaduzzaman Khan, Hongbin Lv, (unknown), (unknown)	18
16	A novel, homozygous nonsense variant of the CDHR1 gene in a Chinese family causes autosomal recessive retinal dystrophy by NGS‐based genetic diagnosis 2018 ·Journal of Cellular and Molecular Medicine ·Jiewen Fu, Lu Ma, Jingliang Cheng, Lisha Yang, Chunli Wei, Shangyi Fu, Hongbin Lv, Rui Chen, Junjiang Fu	18
17	A novel homozygous variant of GPR98 causes usher syndrome type IIC in a consanguineous Chinese family by next generation sequencing 2018 ·BMC Medical Genetics ·Chunli Wei, Lisha Yang, Jingliang Cheng, Saber İmani, Shangyi Fu, Hongbin Lv, Yumei Li, Rui Chen, Elaine Lai‐Han Leung, Junjiang Fu	14
18	Diagnostic value of a combination of next-generation sequencing, chorioretinal imaging and metabolic analysis: lessons from a consanguineous Chinese family with gyrate atrophy of the choroid and retina stemming from a novel OAT variant 2018 ·British Journal of Ophthalmology ·Junting Huang, Jiewen Fu, Shangyi Fu, Lisha Yang, (unknown), (unknown), Jingliang Cheng, Yumei Li, Hongbin Lv, Rui Chen, Longqian Liu, Junjiang Fu	11
19	Establishment and rapid detection of a heterozygous missense mutation in the CACNA1F gene by ARMS technique with double-base mismatched primers 2015 ·Genetics and Molecular Research ·(unknown), Li Zhu, (unknown), (unknown), Qi Zhou, Md. Asaduzzaman Khan, (unknown), Jingliang Cheng, Hongbin Lv, Junjiang Fu	1
20	[Researching a novel NPC-related candidate suppressor gene BRD7 by two-dimensional gel electrophoresis and MALDI-TOF-MS]. 2003 ·PubMed ·Cong Peng, Songping Liang, Chen Tan, Hongbin Lv, (unknown), Min Zhou, (unknown), Xiaolin Li, Guiyuan Li	6

Rankless uses publication and citation data sourced from OpenAlex, an open and comprehensive bibliographic database. While OpenAlex provides broad and valuable coverage of the global research landscape, it—like all bibliographic datasets—has inherent limitations. These include incomplete records, variations in author disambiguation, differences in journal indexing, and delays in data updates. As a result, some metrics and network relationships displayed in Rankless may not fully capture the entirety of a scholar's output or impact.

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