Chufeng He

768 citations

52 papers · 447 · h-index 14

Impact in

Sensory Systems top 2%
- Hearing, Cochlea, Tinnitus, Genetics
Cell Biology top 10%
- melanin and skin pigmentation

Papers in

Molecular Biology 33
- RNA regulation and disease 19
- Connexins and lens biology 8
- Developmental Biology and Gene Regulation 5
Sensory Systems 20
- Hearing, Cochlea, Tinnitus, Genetics 19

Co-authors: Yong Feng (42 shared papers)Lingyun Mei (40 shared papers)Hongsheng Chen (23 shared papers)Lu Jiang (16 shared papers)Yalan Liu (26 shared papers)Xinzhang Cai (17 shared papers)Kun Xia (4 shared papers)Jia‐Da Li (11 shared papers)
Journals: PLoS ONE (6 papers)Biochemical and Biophysical Research Communications (4 papers)Gene (3 papers)Nutrients (3 papers)International Journal of Pediatric Otorhinolaryngology (3 papers)
Partner nations: China United States Hong Kong

In The Last Decade

Chufeng He

50 papers receiving 445 citations

Peers

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-authors

The 25 scholars most cited alongside Chufeng He, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.

Border = papers with Chufeng He Line = papers co-authored together Chufeng He links everyone, so they are left out of the graph.

All Works

Sort: Min cites: Since: Top N: Style:

20 of 20 papers shown

Showing the 20 most-cited of 52 papers — load more, or switch the sort, to bring in the rest.

#	Work
1	Novel mutations of PAX3, MITF, and SOX10 genes in Chinese patients with type I or type II Waardenburg syndrome Biochemical and Biophysical Research Communications ·Hongsheng Chen, Lu Jiang, Zhiguo Xie, Lingyun Mei, Chufeng He, Zhengmao Hu, Kun Xia, Yong Feng	2010	57
2	Functional analysis of Waardenburg syndrome-associated PAX3 and SOX10 mutations: report of a dominant-negative SOX10 mutation in Waardenburg syndrome type II Human Genetics ·Hua Zhang, Hongsheng Chen, Hunjin Luo, Jing An, Lin Sun, Lingyun Mei, Chufeng He, Lu Jiang, Wen G. Jiang, Kun Xia, Jia‐Da Li, Yong Feng	2011	34
3	Genetic insights, disease mechanisms, and biological therapeutics for Waardenburg syndrome Gene Therapy ·Silin Huang, Jian Song, Chufeng He, Xinzhang Cai, Kai Yuan, Lingyun Mei, Yong Feng	2021	30
4	Functional analysis of MITF gene mutations associated with Waardenburg syndrome type 2 FEBS Letters ·Hua Zhang, Hunjin Luo, Hongsheng Chen, Lingyun Mei, Chufeng He, Lu Jiang, Jia‐Da Li, Yong Feng	2012	22
5	A New Genetic Diagnostic for Enlarged Vestibular Aqueduct Based on Next-Generation Sequencing PLoS ONE ·Yalan Liu, Lili Wang, Yong Feng, Chufeng He, Deyuan Liu, Xinzhang Cai, Lu Jiang, Hongsheng Chen, Chang Liu, Hong Wu, Lingyun Mei	2016	21
6	Proband Whole-Exome Sequencing Identified Genes Responsible for Autosomal Recessive Non-Syndromic Hearing Loss in 33 Chinese Nuclear Families Frontiers in Genetics ·Shushan Sang, Jie Ling, Xuezhong Liu, Lingyun Mei, Xinzhang Cai, Taoxi Li, Wu Li, Meng Li, Jie Wen, Xianlin Liu, Jing Liu, Yalan Liu, Hongsheng Chen, Chufeng He, Yong Feng	2019	20
7	Novel mutations in the SOX10 gene in the first two Chinese cases of type IV Waardenburg syndrome Biochemical and Biophysical Research Communications ·Lu Jiang, Hongsheng Chen, Wen G. Jiang, Zhengmao Hu, Lingyun Mei, Jingjie Xue, Chufeng He, Yalan Liu, Kun Xia, Yong Feng	2011	18
8	Functional analysis of a nonstop mutation in MITF gene identified in a patient with Waardenburg syndrome type 2 Journal of Human Genetics ·Jie Sun, Ziqi Hao, Hunjin Luo, Chufeng He, Lingyun Mei, Yalan Liu, Xueping Wang, Zhijie Niu, Hongsheng Chen, Jia‐Da Li, Yong Feng	2017	18
9	LEF-1 Regulates Tyrosinase Gene Transcription In Vitro PLoS ONE ·Xueping Wang, Yalan Liu, Hongsheng Chen, Lingyun Mei, Chufeng He, Lu Jiang, Zhijie Niu, Jie Sun, Hunjin Luo, Jia‐Da Li, Yong Feng	2015	17
10	Identification and functional analysis of a novel mutation in the SOX10 gene associated with Waardenburg syndrome type IV Gene ·Hong-Han Wang, Hongsheng Chen, Jia‐Da Li, Hua Zhang, Lingyun Mei, Chufeng He, Xingwei Wang, Meichao Men, Lu Jiang, Xinbin Liao, Hong Wu, Yong Feng	2014	17
11	A novel frameshift mutation of SMPX causes a rare form of X-linked nonsyndromic hearing loss in a Chinese family PLoS ONE ·Zhijie Niu, Yong Feng, Lingyun Mei, Jie Sun, Xueping Wang, Juncheng Wang, Zhengmao Hu, Yunpeng Dong, Hongsheng Chen, Chufeng He, Yalan Liu, Xinzhang Cai, Xuezhong Liu, Lu Jiang	2017	15
12	A rapid improved multiplex ligation detection reaction method for the identification of gene mutations in hereditary hearing loss PLoS ONE ·Yalan Liu, Chang Hu, Chang Liu, Deyuan Liu, Lingyun Mei, Chufeng He, Lu Jiang, Hong Wu, Hongsheng Chen, Yong Feng	2019	13
13	A novel ABHD12 nonsense variant in Usher syndrome type 3 family with genotype-phenotype spectrum review Gene ·Taoxi Li, Yong Feng, Yalan Liu, Chufeng He, Jing Liu, Hongsheng Chen, Yuyuan Deng, Meng Li, Wu Li, Jian Song, Zhijie Niu, Shushan Sang, Jie Wen, Meichao Men, Xiao‐Ya Chen, Jia‐Da Li, Xuezhong Liu, Jie Ling	2019	13
14	Type 2 cytokines promote angiogenesis in ischemic muscle via endothelial IL-4Rα signaling Cell Reports ·Huixian Li, Chufeng He, Ruiwen Zhu, Francis M. Chen, Lin Wang, Fung Ping Leung, Xiao Yu Tian, Gary Tse, Wing Tak Wong	2023	13
15	Application of a New Genetic Deafness Microarray for Detecting Mutations in the Deaf in China PLoS ONE ·Hong Wu, Yong Feng, Lu Jiang, Qian Pan, Yalan Liu, Chang Liu, Chufeng He, Hongsheng Chen, Xueming Liu, Chang Hu, Yiqiao Hu, Lingyun Mei	2016	12
16	A novel mutation in the SMPX gene associated with X-linked nonsyndromic sensorineural hearing loss in a Chinese family Journal of Human Genetics ·Yuyuan Deng, Zhijie Niu, Liang‐Liang Fan, Jie Ling, Hongsheng Chen, Xinzhang Cai, Lingyun Mei, Chufeng He, Xuewei Zhang, Jie Wen, Meng Li, Wu Li, Taoxi Li, Shushan Sang, Yalan Liu, Yong Feng	2018	10
17	Wnt signaling pathway involvement in genotypic and phenotypic variations in Waardenburg syndrome type 2 with MITF mutations Journal of Human Genetics ·Xueping Wang, Yalan Liu, Lingyun Mei, Chufeng He, Zhijie Niu, Jie Sun, Yulin Zhao, Yong Feng, Hua Zhang	2018	9
18	Otological manifestations in branchiootorenal spectrum disorder: A systematic review and meta‐analysis Clinical Genetics ·Anhai Chen, Jian Song, Frederic Acke, Lingyun Mei, Xinzhang Cai, Yong Feng, Chufeng He	2021	8
19	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 ·Zhijie Niu, Yong Feng, Zhengmao Hu, Jia‐Da Li, Jie Sun, Hongsheng Chen, Chufeng He, Xueping Wang, Lu Jiang, Yalan Liu, Xinzhang Cai, Lili Wang, Yuxiang Cai, Xuezhong Liu, Lingyun Mei	2017	8
20	A comprehensive genotype–phenotype evaluation of eight Chinese probands with Waardenburg syndrome BMC Medical Genomics ·Sijun Li, Mengyao Qin, Shuang Mao, Lingyun Mei, Xinzhang Cai, Yong Feng, Chufeng He, Jian Song	2022	8

About Chufeng He

Chufeng He is a scholar working on Molecular Biology, Sensory Systems, Cell Biology, Cancer Research and Surgery, having authored 52 papers that have together received 447 indexed citations. Recurring topics across this work include RNA regulation and disease (19 papers), Hearing, Cochlea, Tinnitus, Genetics (19 papers), melanin and skin pigmentation (14 papers), Connexins and lens biology (8 papers), Cancer-related molecular mechanisms research (7 papers), Biochemical Analysis and Sensing Techniques (5 papers), Developmental Biology and Gene Regulation (5 papers) and Vestibular and auditory disorders (4 papers). The work is most often cited by research in Sensory Systems (172 citations), Cell Biology (141 citations), Otorhinolaryngology (37 citations), Neurology (59 citations) and Molecular Biology (286 citations). Chufeng He has collaborated with scholars based in China, United States and Hong Kong. Frequent co-authors include Yong Feng, Lingyun Mei, Hongsheng Chen, Lu Jiang, Yalan Liu, Xinzhang Cai, Kun Xia, Jia‐Da Li, Zhengmao Hu and Jian Song. Their work appears in journals such as PLoS ONE, Biochemical and Biophysical Research Communications, Gene, Nutrients and International Journal of Pediatric Otorhinolaryngology.

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.

Explore authors with similar magnitude of impact

Chufeng He

Impact in

Papers in i

In The Last Decade

Chufeng He

Peers

Countries citing papers authored by Chufeng He

Fields of papers citing papers by Chufeng He

All Works

About Chufeng He

Explore authors with similar magnitude of impact

Papers in