Chufeng He

768 total citations
52 papers, 447 citations indexed

About

Chufeng He is a scholar working on Molecular Biology, Sensory Systems and Cell Biology. According to data from OpenAlex, Chufeng He has authored 52 papers receiving a total of 447 indexed citations (citations by other indexed papers that have themselves been cited), including 33 papers in Molecular Biology, 20 papers in Sensory Systems and 15 papers in Cell Biology. Recurrent topics in Chufeng He's work include Hearing, Cochlea, Tinnitus, Genetics (19 papers), RNA regulation and disease (19 papers) and melanin and skin pigmentation (14 papers). Chufeng He is often cited by papers focused on Hearing, Cochlea, Tinnitus, Genetics (19 papers), RNA regulation and disease (19 papers) and melanin and skin pigmentation (14 papers). Chufeng He collaborates with scholars based in China, United States and Hong Kong. Chufeng He's co-authors include Yong Feng, Lingyun Mei, Hongsheng Chen, Lu Jiang, Yalan Liu, Xinzhang Cai, Jia‐Da Li, Kun Xia, Zhengmao Hu and Jian Song and has published in prestigious journals such as PLoS ONE, Journal of Agricultural and Food Chemistry and Biochemical and Biophysical Research Communications.

In The Last Decade

Chufeng He

50 papers receiving 445 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Chufeng He China 14 286 172 141 73 59 52 447
Stuart Townsend United Kingdom 7 287 1.0× 109 0.6× 79 0.6× 50 0.7× 35 0.6× 8 411
Leenamaija Pakarinen Finland 7 334 1.2× 299 1.7× 67 0.5× 43 0.6× 72 1.2× 9 463
Saima Riazuddin Pakistan 2 275 1.0× 168 1.0× 42 0.3× 34 0.5× 248 4.2× 3 449
Mariem Ben Saïd Tunisia 11 174 0.6× 214 1.2× 17 0.1× 95 1.3× 101 1.7× 26 369
Yecheng Jin China 11 186 0.7× 146 0.8× 37 0.3× 28 0.4× 44 0.7× 21 332
Majida Charif Morocco 17 417 1.5× 167 1.0× 37 0.3× 114 1.6× 105 1.8× 51 617
Marcio Do Cruzeiro France 8 184 0.6× 89 0.5× 20 0.1× 29 0.4× 27 0.5× 12 353
Tobias Eisenberger Germany 11 437 1.5× 75 0.4× 66 0.5× 165 2.3× 28 0.5× 14 531
Emma Bedoukian United States 13 238 0.8× 61 0.4× 30 0.2× 119 1.6× 25 0.4× 31 375
Aki Oshima Japan 8 149 0.5× 187 1.1× 17 0.1× 19 0.3× 91 1.5× 12 306

Countries citing papers authored by Chufeng He

Since Specialization
Citations

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

Fields of papers citing papers by Chufeng He

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Chufeng He

This figure shows the co-authorship network connecting the top 25 collaborators of Chufeng He. A scholar is included among the top collaborators of Chufeng He 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 Chufeng He. Chufeng He 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.
He, Chufeng, et al.. (2024). PAX3 mutation suppress otic progenitors proliferation and induce apoptosis by inhibiting WNT1/β-catenin signaling pathway in WS1 patient iPSC-derived inner ear organoids. Biochemical and Biophysical Research Communications. 698. 149510–149510. 3 indexed citations
2.
3.
Ling, Jie, Xin Peng, Xianlin Liu, et al.. (2023). 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. Clinical and Experimental Otorhinolaryngology. 16(4). 342–358. 2 indexed citations
4.
Qin, Mengyao, Lingyun Mei, Xinzhang Cai, et al.. (2022). A comprehensive genotype–phenotype evaluation of eight Chinese probands with Waardenburg syndrome. BMC Medical Genomics. 15(1). 230–230. 8 indexed citations
5.
Song, Jian, Frederic Acke, Lingyun Mei, et al.. (2021). Otological manifestations in branchiootorenal spectrum disorder: A systematic review and meta‐analysis. Clinical Genetics. 100(1). 3–13. 8 indexed citations
6.
Huang, Silin, Jian Song, Chufeng He, et al.. (2021). Genetic insights, disease mechanisms, and biological therapeutics for Waardenburg syndrome. Gene Therapy. 29(9). 479–497. 30 indexed citations
7.
Liu, Yalan, Chang Liu, Deyuan Liu, et al.. (2019). A rapid improved multiplex ligation detection reaction method for the identification of gene mutations in hereditary hearing loss. PLoS ONE. 14(4). e0215212–e0215212. 13 indexed citations
8.
Feng, Yong, Yalan Liu, Chufeng He, et al.. (2019). A novel ABHD12 nonsense variant in Usher syndrome type 3 family with genotype-phenotype spectrum review. Gene. 704. 113–120. 13 indexed citations
9.
Song, Jian, Xueming Liu, Jia‐Da Li, et al.. (2018). [Mechanism for synergistic effect of IRF4 and MITF on tyrosinase promoter].. PubMed. 43(5). 461–468. 1 indexed citations
10.
Wen, Jie, Yalan Liu, Jie Ling, et al.. (2018). Reproductive guidance through prenatal diagnosis and genetic counseling for recessive hereditary hearing loss in high-risk families. International Journal of Pediatric Otorhinolaryngology. 115. 114–119. 2 indexed citations
11.
Liu, Yalan, Lingyun Mei, Chufeng He, et al.. (2017). Functional analysis of a SOX10 gene mutation associated with Waardenburg syndrome II. Biochemical and Biophysical Research Communications. 493(1). 258–262. 3 indexed citations
12.
Feng, Yong, Zhengmao Hu, Jia‐Da Li, et al.. (2017). Exome sequencing identifies a novel missense mutation of WFS1 as the cause of non-syndromic low-frequency hearing loss in a Chinese family. International Journal of Pediatric Otorhinolaryngology. 100. 1–7. 8 indexed citations
13.
Li, Jia‐Da, Fen Tang, Jie Sun, et al.. (2017). Identification and functional analysis of a novel mutation in the PAX3 gene associated with Waardenburg syndrome type I. Gene. 642. 362–366. 5 indexed citations
14.
Feng, Yong, Haibo Li, Hong Wu, et al.. (2016). Digenic mutations involving both the BSND and GJB2 genes detected in Bartter syndrome type IV. International Journal of Pediatric Otorhinolaryngology. 92. 17–20. 5 indexed citations
15.
Chen, Hongsheng, Jia‐Da Li, Hua Zhang, et al.. (2014). Identification and functional analysis of a novel mutation in the SOX10 gene associated with Waardenburg syndrome type IV. Gene. 538(1). 36–41. 17 indexed citations
16.
Zhang, Hua, Hongsheng Chen, Lingyun Mei, et al.. (2012). Functional analysis of MITF gene mutations associated with Waardenburg syndrome type 2. FEBS Letters. 586(23). 4126–4131. 22 indexed citations
17.
Zhang, Hua, Hongsheng Chen, Jing An, et al.. (2011). Functional analysis of Waardenburg syndrome-associated PAX3 and SOX10 mutations: report of a dominant-negative SOX10 mutation in Waardenburg syndrome type II. Human Genetics. 131(3). 491–503. 34 indexed citations
18.
Jiang, Lu, Honghan Wang, Yalan Liu, et al.. (2011). Unique penetrance of hearing loss in a five-generation Chinese family with the mitochondrial 12S rRNA 1555A > G mutation. Acta Oto-Laryngologica. 131(9). 970–975. 3 indexed citations
19.
Jiang, Lu, Yalan Liu, Yong Feng, et al.. (2011). Gene localization in a Chinese family with autosomal dominant non-syndromic deafness. Acta Oto-Laryngologica. 131(10). 1061–1068. 2 indexed citations
20.
Chen, Hongsheng, Lu Jiang, Zhiguo Xie, et al.. (2010). Novel mutations of PAX3, MITF, and SOX10 genes in Chinese patients with type I or type II Waardenburg syndrome. Biochemical and Biophysical Research Communications. 397(1). 70–74. 57 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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