Lingyun Mei

900 total citations
61 papers, 531 citations indexed

About

Lingyun Mei is a scholar working on Molecular Biology, Sensory Systems and Cell Biology. According to data from OpenAlex, Lingyun Mei has authored 61 papers receiving a total of 531 indexed citations (citations by other indexed papers that have themselves been cited), including 34 papers in Molecular Biology, 32 papers in Sensory Systems and 17 papers in Cell Biology. Recurrent topics in Lingyun Mei's work include Hearing, Cochlea, Tinnitus, Genetics (30 papers), RNA regulation and disease (21 papers) and melanin and skin pigmentation (15 papers). Lingyun Mei is often cited by papers focused on Hearing, Cochlea, Tinnitus, Genetics (30 papers), RNA regulation and disease (21 papers) and melanin and skin pigmentation (15 papers). Lingyun Mei collaborates with scholars based in China, United States and Saudi Arabia. Lingyun Mei's co-authors include Yong Feng, Chufeng He, Hongsheng Chen, Lu Jiang, Yalan Liu, Xinzhang Cai, Kun Xia, Jia‐Da Li, Zhengmao Hu and Jian Song and has published in prestigious journals such as PLoS ONE, Biochemical and Biophysical Research Communications and FEBS Letters.

In The Last Decade

Lingyun Mei

59 papers receiving 530 citations

Peers

Countries citing papers authored by Lingyun Mei

Since Specialization

Citations

This map shows the geographic impact of Lingyun Mei'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 Lingyun Mei with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Lingyun Mei more than expected).

Fields of papers citing papers by Lingyun Mei

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Lingyun Mei. 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 Lingyun Mei. The network helps show where Lingyun Mei may publish in the future.

Co-authorship network of co-authors of Lingyun Mei

This figure shows the co-authorship network connecting the top 25 collaborators of Lingyun Mei. A scholar is included among the top collaborators of Lingyun Mei 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 Lingyun Mei. Lingyun Mei 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	Ferroptosis contributes to lead-induced cochlear spiral ganglion neurons injury 2024 ·Toxicology ·(unknown), Lingyun Mei, Lu Wang, (unknown), Kelei Gao, (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), Xuewen Wu	2
2	PAX3 mutation suppress otic progenitors proliferation and induce apoptosis by inhibiting WNT1/β-catenin signaling pathway in WS1 patient iPSC-derived inner ear organoids 2024 ·Biochemical and Biophysical Research Communications ·(unknown), Chufeng He, Lingyun Mei, Xuewen Wu, Yong Feng, Jian Song	3
3	ABCC1 deficiency potentiated noise-induced hearing loss in mice by impairing cochlear antioxidant capacity 2024 ·Redox Biology ·Jing Liu, (unknown), Yong Feng, Xianlin Liu, (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), Jie Ling, Lingyun Mei	10
4	Susceptibility of immature spiral ganglion neurons to aminoglycoside-induced ototoxicity is mediated by the TRPV1 channel in mice 2023 ·Hearing Research ·(unknown), Jing Liu, Xuewen Wu, (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), Yuan Zeng, Lingyun Mei, Kelei Gao	1
5	A Novel <i>EYA1</i> Mutation Causing Alternative RNA Splicing in a Chinese Family With Branchio-Oto Syndrome: Implications for Molecular Diagnosis and Clinical Application 2023 ·Clinical and Experimental Otorhinolaryngology ·(unknown), Jie Ling, Xin Peng, Xianlin Liu, (unknown), (unknown), Mengyao Qin, (unknown), (unknown), Jian Song, (unknown), Lu Ma, (unknown), Lingyun Mei, Chufeng He, Yong Feng	2
6	Short-term effects of intravenous batroxobin in treatment of sudden sensorineural hearing loss: a propensity score-matched study 2023 ·Frontiers in Neurology ·(unknown), (unknown), Lingyun Mei, (unknown), Xinzhang Cai, (unknown), Hong Wu, Xin Wang, Xuewen Wu	6
7	A comprehensive genotype–phenotype evaluation of eight Chinese probands with Waardenburg syndrome 2022 ·BMC Medical Genomics ·(unknown), Mengyao Qin, (unknown), Lingyun Mei, Xinzhang Cai, Yong Feng, Chufeng He, Jian Song	8
8	Otological manifestations in branchiootorenal spectrum disorder: A systematic review and meta‐analysis 2021 ·Clinical Genetics ·(unknown), Jian Song, Frederic Acke, Lingyun Mei, Xinzhang Cai, Yong Feng, Chufeng He	8
9	New Genotypes and Phenotypes in Patients with 3 Subtypes of Waardenburg Syndrome Identified by Diagnostic Next-Generation Sequencing 2019 ·Neural Plasticity ·(unknown), Lingyun Mei, Hongsheng Chen, Xinzhang Cai, Yalan Liu, (unknown), Xue Zhong Liu, Denise Yan, Jie Ling, Yong Feng	18
10	Effect of systemic lupus erythematosus and rheumatoid arthritis on sudden sensorineural hearing loss 2019 ·The Laryngoscope ·Shaobing Xie, Hongting Ning, (unknown), (unknown), Jiang Qian, Yanni Zhang, Lingyun Mei, Yong Feng, Xuewen Wu	9
11	A rapid improved multiplex ligation detection reaction method for the identification of gene mutations in hereditary hearing loss 2019 ·PLoS ONE ·Yalan Liu, (unknown), Chang Liu, Deyuan Liu, Lingyun Mei, Chufeng He, Lu Jiang, Hong Wu, Hongsheng Chen, Yong Feng	13
12	[Mechanism for synergistic effect of IRF4 and MITF on tyrosinase promoter]. 2018 ·PubMed ·Jian Song, Xueming Liu, Jia‐Da Li, (unknown), Zhen Peng, Hongsheng Chen, Lingyun Mei, Chufeng He, Yong Feng	1
13	Reproductive guidance through prenatal diagnosis and genetic counseling for recessive hereditary hearing loss in high-risk families 2018 ·International Journal of Pediatric Otorhinolaryngology ·(unknown), (unknown), Jie Wen, Yalan Liu, Jie Ling, Hongsheng Chen, Xinzhang Cai, Lingyun Mei, (unknown), Meng Li, (unknown), (unknown), Chufeng He, Yong Feng	2
14	Functional analysis of a SOX10 gene mutation associated with Waardenburg syndrome II 2017 ·Biochemical and Biophysical Research Communications ·(unknown), (unknown), Yalan Liu, Lingyun Mei, Chufeng He, (unknown), Jie Sun, Yulin Zhao, Yong Feng	3
15	Exome sequencing identifies a novel missense mutation of WFS1 as the cause of non-syndromic low-frequency hearing loss in a Chinese family 2017 ·International Journal of Pediatric Otorhinolaryngology ·(unknown), Yong Feng, Zhengmao Hu, Jia‐Da Li, Jie Sun, Hongsheng Chen, Chufeng He, (unknown), Lu Jiang, Yalan Liu, Xinzhang Cai, Lili Wang, Yuxiang Cai, Xuezhong Liu, Lingyun Mei	8
16	Identification and functional analysis of a novel mutation in the PAX3 gene associated with Waardenburg syndrome type I 2017 ·Gene ·(unknown), Jia‐Da Li, Fen Tang, Jie Sun, (unknown), Lu Jiang, Lingyun Mei, Hongsheng Chen, Yalan Liu, Xinzhang Cai, Yong Feng, Chufeng He	5
17	A novel deletion mutation in RS1 gene caused X-linked juvenile retinoschisis in a Chinese family 2014 ·Eye ·Yuzhou Huang, Lingyun Mei, Baoheng Gui, Wan‐Fu Su, Desheng Liang, Lingqian Wu, Qian Pan	5
18	Functional analysis of MITF gene mutations associated with Waardenburg syndrome type 2 2012 ·FEBS Letters ·Hua Zhang, (unknown), Hongsheng Chen, Lingyun Mei, Chufeng He, Lu Jiang, Jia‐Da Li, Yong Feng	22
19	Functional analysis of Waardenburg syndrome-associated PAX3 and SOX10 mutations: report of a dominant-negative SOX10 mutation in Waardenburg syndrome type II 2011 ·Human Genetics ·Hua Zhang, Hongsheng Chen, (unknown), Jing An, Lin Sun, Lingyun Mei, Chufeng He, Lu Jiang, Wen G. Jiang, Kun Xia, Jia‐Da Li, Yong Feng	34
20	Novel mutations of PAX3, MITF, and SOX10 genes in Chinese patients with type I or type II Waardenburg syndrome 2010 ·Biochemical and Biophysical Research Communications ·Hongsheng Chen, Lu Jiang, Zhiguo Xie, Lingyun Mei, Chufeng He, Zhengmao Hu, Kun Xia, Yong Feng	57

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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