Qinjun Wei

680 total citations
43 papers, 501 citations indexed

About

Qinjun Wei is a scholar working on Molecular Biology, Sensory Systems and Neurology. According to data from OpenAlex, Qinjun Wei has authored 43 papers receiving a total of 501 indexed citations (citations by other indexed papers that have themselves been cited), including 26 papers in Molecular Biology, 21 papers in Sensory Systems and 12 papers in Neurology. Recurrent topics in Qinjun Wei's work include Hearing, Cochlea, Tinnitus, Genetics (20 papers), Vestibular and auditory disorders (10 papers) and Cancer-related molecular mechanisms research (7 papers). Qinjun Wei is often cited by papers focused on Hearing, Cochlea, Tinnitus, Genetics (20 papers), Vestibular and auditory disorders (10 papers) and Cancer-related molecular mechanisms research (7 papers). Qinjun Wei collaborates with scholars based in China, Germany and Netherlands. Qinjun Wei's co-authors include Xin Cao, Yajie Lu, Guangqian Xing, Jun Yao, Zhibin Chen, Xingkuan Bu, Huiqin Tian, Aidong Zhou, Cui Zhang and Xiaofei Shen and has published in prestigious journals such as Scientific Reports, Biochemical and Biophysical Research Communications and Experimental Cell Research.

In The Last Decade

Qinjun Wei

42 papers receiving 499 citations

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name h Career Trend Papers Cites
Qinjun Wei China 14 301 216 84 74 61 43 501
Xin Cao China 16 415 1.4× 244 1.1× 104 1.2× 81 1.1× 79 1.3× 57 719
Dragana Vuckovic United Kingdom 14 170 0.6× 201 0.9× 65 0.8× 43 0.6× 9 0.1× 28 486
Tae-Jun Kwon South Korea 10 192 0.6× 149 0.7× 32 0.4× 18 0.2× 16 0.3× 25 319
Sung‐Kyun Moon South Korea 10 148 0.5× 184 0.9× 102 1.2× 47 0.6× 8 0.1× 19 476
Yuki Miyasaka Japan 12 185 0.6× 101 0.5× 31 0.4× 13 0.2× 52 0.9× 35 408
R. A. Fisher United Kingdom 10 232 0.8× 89 0.4× 37 0.4× 25 0.3× 64 1.0× 20 423
Wendy Hutchison Australia 13 540 1.8× 55 0.3× 27 0.3× 39 0.5× 45 0.7× 20 785
Julie A. Alosi United States 9 170 0.6× 197 0.9× 38 0.5× 58 0.8× 9 0.1× 12 406
Angelien Heister Netherlands 10 227 0.8× 84 0.4× 61 0.7× 11 0.1× 21 0.3× 10 437
Xiaorei Sai Japan 10 268 0.9× 42 0.2× 9 0.1× 15 0.2× 151 2.5× 13 434

Countries citing papers authored by Qinjun Wei

Since Specialization
Citations

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

Fields of papers citing papers by Qinjun Wei

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Qinjun Wei

This figure shows the co-authorship network connecting the top 25 collaborators of Qinjun Wei. A scholar is included among the top collaborators of Qinjun Wei 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 Qinjun Wei. Qinjun Wei is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

20 of 20 papers shown
1.
Zhang, Cheng, Qian Yang, Yajie Lu, et al.. (2025). <i>Osbpl2</i> deficiency inhibits Rho/ROCK2/p-ERM signaling and impairs actin cytoskeletal regulation in auditory cells. Journal of Biomedical Research. 39(6). 574–574. 1 indexed citations
2.
Yang, Qian, Yajie Lu, Zhibin Chen, et al.. (2025). OSBPL2 deficiency impaired cochlear blood-labyrinth barrier via activation of NF-κB signaling pathway. Hearing Research. 467. 109432–109432.
3.
Zhang, Cheng, Yajie Lu, Jun Yao, et al.. (2022). Mutations in OSBPL2 cause hearing loss associated with primary cilia defects via sonic hedgehog signaling. JCI Insight. 7(4). 12 indexed citations
4.
Wei, Qinjun, et al.. (2021). Oxysterol-binding protein-like 2 contributes to the developmental progression of preadipocytes by binding to β-catenin. Cell Death Discovery. 7(1). 109–109. 2 indexed citations
5.
Liao, Shijie, et al.. (2021). Application of ultrasound in the closed reduction and percutaneous pinning in supracondylar humeral fractures. Journal of Orthopaedic Surgery and Research. 16(1). 588–588. 3 indexed citations
6.
Wei, Qinjun, Jun Yao, Yajie Lu, et al.. (2020). OSBPL2 Is Required for the Binding of COPB1 to ATGL and the Regulation of Lipid Droplet Lipolysis. iScience. 23(7). 101252–101252. 25 indexed citations
7.
Yao, Jun, et al.. (2019). Comparative transcriptome analysis of auditory OC-1 cells and zebrafish inner ear tissues in the absence of human OSBPL2 orthologues. Biochemical and Biophysical Research Communications. 521(1). 42–49. 7 indexed citations
8.
Zhang, Cui, Min Zhang, Jun Yao, et al.. (2019). OSBPL2 deficiency upregulate SQLE expression increasing intracellular cholesterol and cholesteryl ester by AMPK/SP1 and SREBF2 signalling pathway. Experimental Cell Research. 383(2). 111512–111512. 26 indexed citations
9.
Lu, Yajie, et al.. (2017). Genetic analysis of CLDN14 in the Chinese population affected with non-syndromic hearing loss. International Journal of Pediatric Otorhinolaryngology. 105. 6–11. 6 indexed citations
10.
Liu, Chunyu, Jun Yao, Qinjun Wei, Guangqian Xing, & Xin Cao. (2016). Spatial and temporal expression patterns of Osbpl2a and Osbpl2b during zebrafish embryonic development. International Journal of Pediatric Otorhinolaryngology. 84. 174–179. 5 indexed citations
11.
Shen, Xiaofei, Qinjun Wei, Jun Yao, et al.. (2015). IVS8+1 DelG, a Novel Splice Site Mutation Causing DFNA5 Deafness in a Chinese Family. Chinese Medical Journal. 128(18). 2510–2515. 21 indexed citations
12.
Xing, Guangqian, Jun Yao, Bin Wu, et al.. (2014). Identification of OSBPL2 as a novel candidate gene for progressive nonsyndromic hearing loss by whole-exome sequencing. Genetics in Medicine. 17(3). 210–218. 52 indexed citations
13.
Wei, Qinjun, Hongmei Zhu, Zhibin Chen, et al.. (2014). Targeted genomic capture and massively parallel sequencing to identify novel variants causing Chinese hereditary hearing loss. Journal of Translational Medicine. 12(1). 311–311. 35 indexed citations
14.
Shen, Xiaofei, Jun Yao, Qinjun Wei, et al.. (2014). Identification of I411K, a novel missense EYA4 mutation causing autosomal dominant non-syndromic hearing loss. International Journal of Molecular Medicine. 34(6). 1467–1472. 18 indexed citations
15.
Wei, Qinjun, Shuai Wang, Jun Yao, et al.. (2013). Genetic mutations of GJB2 and mitochondrial 12S rRNA in nonsyndromic hearing loss in Jiangsu Province of China. Journal of Translational Medicine. 11(1). 163–163. 20 indexed citations
16.
Wei, Qinjun, Wei He, Yajie Lu, Jun Yao, & Xin Cao. (2012). Effect of the tumor suppressor gene ING4 on the proliferation of MCF-7 human breast cancer cells. Oncology Letters. 4(3). 438–442. 18 indexed citations
17.
Chen, Jie, Qinjun Wei, Jun Yao, et al.. (2012). Identification of two heterozygous deafness mutations inSLC26A4 (PDS)in a Chinese family with two siblings. International Journal of Audiology. 52(2). 134–138. 4 indexed citations
18.
Zhang, Wei, et al.. (2011). Screening of High-yield Hyaluronic Acid-producing Strain by Low Energy Ion Implantation. Food Science. 32(7). 269. 1 indexed citations
19.
Xing, Guangqian, Zhibin Chen, Qinjun Wei, et al.. (2006). Mitochondrial 12S rRNA A827G mutation is involved in the genetic susceptibility to aminoglycoside ototoxicity. Biochemical and Biophysical Research Communications. 346(4). 1131–1135. 31 indexed citations
20.
Xing, Guangqian, Zhibin Chen, Qinjun Wei, et al.. (2006). Maternally inherited non-syndromic hearing loss associated with mitochondrial 12S rRNA A827G mutation in a Chinese family. Biochemical and Biophysical Research Communications. 344(4). 1253–1257. 35 indexed citations

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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