Bobei Chen

879 total citations
26 papers, 568 citations indexed

About

Bobei Chen is a scholar working on Molecular Biology, Sensory Systems and Neurology. According to data from OpenAlex, Bobei Chen has authored 26 papers receiving a total of 568 indexed citations (citations by other indexed papers that have themselves been cited), including 11 papers in Molecular Biology, 7 papers in Sensory Systems and 7 papers in Neurology. Recurrent topics in Bobei Chen's work include Hearing, Cochlea, Tinnitus, Genetics (7 papers), Mitochondrial Function and Pathology (7 papers) and Vestibular and auditory disorders (7 papers). Bobei Chen is often cited by papers focused on Hearing, Cochlea, Tinnitus, Genetics (7 papers), Mitochondrial Function and Pathology (7 papers) and Vestibular and auditory disorders (7 papers). Bobei Chen collaborates with scholars based in China, United States and Australia. Bobei Chen's co-authors include Min‐Xin Guan, Jianxin Lü, Li Yang, Yi Zhu, Xiaowen Tang, Ruru Chen, Aifen Yang, Jindan Wang, Jing Zheng and Bohai Feng and has published in prestigious journals such as Journal of Biological Chemistry, PLoS ONE and Science Advances.

In The Last Decade

Bobei Chen

26 papers receiving 554 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Bobei Chen China 15 305 117 84 79 63 26 568
M. Abel Canada 12 92 0.3× 125 1.1× 124 1.5× 105 1.3× 60 1.0× 22 562
Jaimin Patel United States 14 254 0.8× 15 0.1× 62 0.7× 59 0.7× 4 0.1× 33 759
Teizo Ito Japan 12 145 0.5× 48 0.4× 155 1.8× 35 0.4× 9 0.1× 30 487
Jun‐ichi Ohkubo Japan 10 54 0.2× 40 0.3× 76 0.9× 28 0.4× 28 0.4× 57 355
Nancy D. Merner United States 13 267 0.9× 42 0.4× 31 0.4× 44 0.6× 3 0.0× 25 854
Kalpita R. Karan United States 11 202 0.7× 8 0.1× 87 1.0× 19 0.2× 25 0.4× 19 412
Alexandra Taracanova United States 6 96 0.3× 32 0.3× 90 1.1× 25 0.3× 52 0.8× 8 416
Guilherme Cesar Martelossi Cebinelli Brazil 12 196 0.6× 9 0.1× 68 0.8× 176 2.2× 8 0.1× 22 675
Teresa Nutile Italy 14 159 0.5× 91 0.8× 47 0.6× 19 0.2× 3 0.0× 23 505

Countries citing papers authored by Bobei Chen

Since Specialization
Citations

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

Fields of papers citing papers by Bobei Chen

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Bobei Chen

This figure shows the co-authorship network connecting the top 25 collaborators of Bobei Chen. A scholar is included among the top collaborators of Bobei Chen 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 Bobei Chen. Bobei Chen 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.
Li, Yi, Huizhan Liu, Chang-Jun Zhang, et al.. (2022). Mutation of SLC7A14 causes auditory neuropathy and retinitis pigmentosa mediated by lysosomal dysfunction. Science Advances. 8(14). eabk0942–eabk0942. 14 indexed citations
2.
3.
Zhang, Yamei, Ping Wei, Bobei Chen, et al.. (2020). Intranasal fluticasone furoate in pediatric allergic rhinitis: randomized controlled study. Pediatric Research. 89(7). 1832–1839. 13 indexed citations
4.
Zhang, Hui, et al.. (2020). Predictors of the Prevalence of Dyslipidemia and Influencing Factors for Young Health Examination Cohort: A Cross-Sectional Survey. Frontiers in Public Health. 8. 400–400. 18 indexed citations
5.
Yi, Song, et al.. (2020). mTOR/NF-κB signaling pathway protects hippocampal neurons from injury induced by intermittent hypoxia in rats. International Journal of Neuroscience. 131(10). 994–1003. 17 indexed citations
6.
7.
Zhan, Xiang, et al.. (2019). Genetic Polymorphisms and Susceptibility to Sudden Sensorineural Hearing Loss: A Systematic Review. Audiology and Neurotology. 24(1). 8–19. 15 indexed citations
8.
Ni, Guoying, Yi Luan, Shu Chen, et al.. (2019). Human papillomavirus infection among head and neck squamous cell carcinomas in southern China. PLoS ONE. 14(9). e0221045–e0221045. 33 indexed citations
9.
Li, Ziyue, et al.. (2018). Prognostic role of haematological indices in sudden sensorineural hearing loss: Review and meta-analysis. Clinica Chimica Acta. 483. 104–111. 32 indexed citations
10.
Feng, Bohai, et al.. (2017). Efficacy of Sublingual Immunotherapy for House Dust Mite-Induced Allergic Rhinitis: A Meta-Analysis of Randomized Controlled Trials. Allergy Asthma and Immunology Research. 9(3). 220–220. 22 indexed citations
11.
Wang, Meng, Hao Liu, Jing Zheng, et al.. (2016). A Deafness- and Diabetes-associated tRNA Mutation Causes Deficient Pseudouridinylation at Position 55 in tRNAGlu and Mitochondrial Dysfunction. Journal of Biological Chemistry. 291(40). 21029–21041. 67 indexed citations
12.
Wang, Sheng, Jike Lu, Yuan Li, et al.. (2016). Autologous Olfactory Lamina Propria Transplantation for Chronic Spinal Cord Injury: Three-Year Follow-Up Outcomes from a Prospective Double-Blinded Clinical Trial. Cell Transplantation. 25(1). 141–157. 26 indexed citations
13.
Chen, Bobei, Yingying Chen, Xuejun Liu, et al.. (2013). Prevalence of common genetic mutations and clinical characteristics analysis in patients at different ages with nonsyndromic hearing impairment. Hereditas (Beijing). 35(3). 352–358. 2 indexed citations
14.
Peng, Guang-Hua, Bobei Chen, Fang Fang, et al.. (2012). Spectrum and frequency of mitochondrial 12S rRNA variants in the Chinese subjects with nonsynrdomic hearing loss in Zhejiang Prov-ince. Hereditas (Beijing). 34(6). 695–704. 2 indexed citations
15.
Shen, Zhisen, Jing Zheng, Bobei Chen, et al.. (2011). Frequency and spectrum of mitochondrial 12S rRNA variants in 440 Han Chinese hearing impaired pediatric subjects from two otology clinics. Journal of Translational Medicine. 9(1). 4–4. 27 indexed citations
16.
Lü, Jianxin, Yaping Qian, Zhiyuan Li, et al.. (2009). Mitochondrial haplotypes may modulate the phenotypic manifestation of the deafness-associated 12S rRNA 1555A>G mutation. Mitochondrion. 10(1). 69–81. 91 indexed citations
17.
Ding, Yu, Yongyan Li, Li Yang, et al.. (2009). Mitochondrial tRNAGlu A14693G variant may modulate the phenotypic manifestation of deafness-associated 12S rRNA A1555G mutation in a Han Chinese family. Journal of genetics and genomics. 36(4). 241–250. 24 indexed citations
18.
Chen, Bobei, Dongmei Sun, Li Yang, et al.. (2008). Mitochondrial ND5 T12338C, tRNACys T5802C, and tRNAThr G15927A variants may have a modifying role in the phenotypic manifestation of deafness‐associated 12S rRNA A1555G mutation in three Han Chinese pedigrees. American Journal of Medical Genetics Part A. 146A(10). 1248–1258. 47 indexed citations
19.
Wang, Xinjian, Jianxin Lü, Yi Zhu, et al.. (2008). Mitochondrial tRNAThr G15927A mutation may modulate the phenotypic manifestation of ototoxic 12S rRNA A1555G mutation in four Chinese families. Pharmacogenetics and Genomics. 18(12). 1059–1070. 45 indexed citations
20.
Chen, Bobei, et al.. (2003). [The detection and significance of human papilloma virus 11b virus like particles and its serum antibody in juvenile larynx papilloma].. PubMed. 38(6). 417–20. 4 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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