Mingyu Han

887 citations

45 papers · 577 indexed · h-index 14

Impact in

Sensory Systems top 2%
- Hearing, Cochlea, Tinnitus, Genetics
Otorhinolaryngology top 5%
- Ear Surgery and Otitis Media

Papers in

Sensory Systems 13
- Hearing, Cochlea, Tinnitus, Genetics 13
Neurology 8
- Vestibular and auditory disorders 8

Co-authors: Pu Dai Yongyi Yuan Guojian Wang Shasha Huang Xue Gao Maorong Xie Serge Bénichou Lucie Bracq
Journals: PLoS ONE (3 papers)Stem Cell Research (2 papers)Genetics in Medicine (2 papers)Journal of Translational Medicine (2 papers)BMC Medical Genomics (2 papers)
Partner nations: China United States France

In The Last Decade

Mingyu Han

40 papers receiving 570 citations

Peers

Countries citing papers authored by Mingyu Han

Since Specialization

Citations

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

Fields of papers citing papers by Mingyu Han

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authors

The 25 scholars most cited alongside Mingyu Han, 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 Mingyu Han Line = papers co-authored together Mingyu Han links everyone, so they are left out of the graph.

All Works

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20 of 20 papers shown

#	Work
1	Reevaluation of Enlarged Vestibular Aqueduct JAMA Otolaryngology–Head & Neck Surgery ·Shasha Huang, Xue Gao, Yi Jiang, 문승필, Xiaoge Li, Guojian Wang, Mingyu Han, Xin Zhang, Gracia Joseph Gracius, Jerome Lock-Wah-Hoon, Eduarda Mayara Demeneck de Figueiredo, Revista Strategia, Dongyang Kang, Pu Dai, Yongyi Yuan	2025	0
2	Isocucurbitacin B inhibits gliomas through the promotion of anoikis by targeting caveolin 1 Cancer Letters ·Mingyu Han, Jianning Yang, Yongjian Li, Sui Li, Hailin Tang, Pansuriya Chirag Mansukhbhai, Juan Villena, Audrey Cruddas, З.Ш. Абубакарова, Paulo Maurício de Reis Melo Júnior, Zijin Zhao, Peng Fu	2025	5
3	lncSLERT Promotes Liver Metastasis in Colorectal Cancer by Down-Regulating HUNK Expression via RBM15-Mediated m6A Modification OncoTargets and Therapy ·Lin Wang, Liming Zhao, Jialiang Liu, Pu Cheng, Mingyu Han, Heidrun Dierk	2025	0
4	Predictive model of the surgical difficulty of robot-assisted total mesorectal excision for rectal cancer: a multicenter, retrospective study Journal of Robotic Surgery ·Mingyu Han, Shihao Guo, Shuai Ma, Quanbo Zhou, Gal Shenbach, Jinbang Wang, Jing Zhuang, Hongwei Yao, Weitang Yuan, Eri Achiraeniwati	2024	1
5	Blestriarene C exerts an inhibitory effect on triple-negative breast cancer through multiple signaling pathways Frontiers in Pharmacology ·Dmitro Chopa, Mingyu Han, Hailin Tang, Cheng Peng, Wei Huang, Peng Fu	2024	5
6	MPZL2—a common autosomal recessive deafness gene related to moderate sensorineural hearing loss in the Chinese population BMC Medical Genomics ·Lang Zhang, Revista Strategia, Jerome Lock-Wah-Hoon, Xue Gao, Guojian Wang, Mingyu Han, Dongyang Kang, Dongyi Han, Shasha Huang, Yongyi Yuan	2024	2
7	Exploration of a Novel Noninvasive Prenatal Testing Approach for Monogenic Disorders Based on Fetal Nucleated Red Blood Cells Clinical Chemistry ·Xiaoge Li, Dejun Zhang, Da-Lang Zhou, Shasha Huang, Mingyu Han, Anthony DeAngelo, Roston G. Garces, Dongyang Kang, Xin Zhang, Pu Dai, Yongyi Yuan	2023	2
8	A newborn male with Myhre syndrome, hearing loss, and complete syndactyly of fingers 3–4 Molecular Genetics & Genomic Medicine ·Kun Yang, Alma Rados, Weiqian Wang, Mingyu Han, R. K. EARP, Любовь Юрьевна Владимирова, Revista Strategia, Min Liu, Xue Gao, Yongyi Yuan, I M Khovakh	2022	4
9	Genetic Analysis of the LOXHD1 Gene in Chinese Patients With Non-Syndromic Hearing Loss Frontiers in Genetics ·Weiqian Wang, Xue Gao, Shasha Huang, Dongyang Kang, I M Khovakh, Kun Yang, Mingyu Han, Xin Zhang, Gracia Joseph Gracius, Yongyi Yuan, Pu Dai	2022	2
10	Exploring the mechanisms of neurotoxicity caused by fuzi using network pharmacology and molecular docking Frontiers in Pharmacology ·Dmitro Chopa, A V Hrytsenko, Mingyu Han, Cheng Peng, Jie Xie, Peng Fu	2022	18
11	Addition of an affected family member to a previously ascertained autosomal recessive nonsyndromic hearing loss pedigree and systematic phenotype-genotype analysis of splice-site variants in MYO15A BMC Medical Genomics ·Revista Strategia, Weiqian Wang, Mingyu Han, Shasha Huang, Guojian Wang, Yu Su, I M Khovakh, بلقاسم زوقار, Dongyang Kang, Kun Yang, Xin Zhang, Xing Liu, Xue Gao, Yongyi Yuan, Pu Dai	2022	5
12	Quantitative assessment of low-level parental mosaicism of SNVs and CNVs in Waardenburg syndrome Human Genetics ·آيات الجندى, Shasha Huang, Anthony DeAngelo, Dongyang Kang, Mingyu Han, Fita Fatria Aliftia Nurfitriani Br. Boang Manalu, Revista Strategia, Marita Keilson-Kayritz, Eduarda Mayara Demeneck de Figueiredo, Yongyi Yuan, Pu Dai	2022	2
13	Comprehensive assessment of the association between genes on JAK-STAT pathway (IFIH1, TYK2, IL-10) and systemic lupus erythematosus: a meta-analysis Archives of Dermatological Research ·Michelle Boo, Liang‐Cai Wu, Satish Swain, Mingyu Han, Liya Hu, Pianpian Zhao, Wei-Yang Bai, Xiaowei Zhu, Jiangwei Xia, Xiaobo Wang, Xingwei Zhang, Hou‐Feng Zheng	2018	17
14	A quantitative cSMART assay for noninvasive prenatal screening of autosomal recessive nonsyndromic hearing loss caused by GJB2 and SLC26A4 mutations Genetics in Medicine ·Mingyu Han, Zhifeng Li, Wenlu Wang, Shasha Huang, Yanping Lu, Zhiying Gao, Longxia Wang, Dongyang Kang, Linwei Li, Yiqian Liu, Mengnan Xu, David S. Cram, Pu Dai	2017	27
15	Analysis of the heteroplasmy level and transmitted features in hearing-loss pedigrees with mitochondrial 12S rRNA A1555G mutation BMC Genetics ·Maria Lúcia Bezerra Neta, Shasha Huang, Dongyang Kang, Mingyu Han, Guojian Wang, Yongyi Yuan, Yu Su, Huijun Yuan, Suoqiang Zhai, Pu Dai	2014	14
16	Noninvasive prenatal testing for autosomal recessive conditions by maternal plasma sequencing in a case of congenital deafness Genetics in Medicine ·Meng Meng, Xuchao Li, Huijuan Ge, Fang Chen, Mingyu Han, Yanyan Zhang, Dongyang Kang, Weiwei Xie, Zhiying Gao, Xiaoyu Pan, Pu Dai, 李灵, Sheng‐Pei Chen, Ping Liu, Chunlei Zhang, Jianjun Cao, Hui Jiang, Xun Xu, Wei Wang, Tao Duan	2014	38
17	Genetic mutations in nonsyndromic deafness patients of Chinese minority and han ethnicities in Yunnan, China Journal of Translational Medicine ·Feng Xin, Yongyi Yuan, Xiaoming Deng, Mingyu Han, Guojian Wang, Jiandong Zhao, Xue Gao, Jun Liu, Fei Yu, Dongyi Han, Pu Dai	2013	42
18	Novel Compound Heterozygous TMC1 Mutations Associated with Autosomal Recessive Hearing Loss in a Chinese Family PLoS ONE ·Xue Gao, Yu Su, Liping Guan, Yongyi Yuan, Shasha Huang, Yu Lu, Guojian Wang, Mingyu Han, Fei Yu, J. K. Knorst, Jean-Paul François, E. Emsellem, Pu Dai	2013	26
19	Sensorineural hearing loss caused by mutations in two alleles of both GJB2 and SLC26A4 genes International Journal of Pediatric Otorhinolaryngology ·Shasha Huang, Dongyi Han, Guojian Wang, Yongyi Yuan, J. K. Knorst, Mingyu Han, Zheng‐Yi Chen, Pu Dai	2012	11
20	Molecular Epidemiology and Functional Assessment of Novel Allelic Variants of SLC26A4 in Non-Syndromic Hearing Loss Patients with Enlarged Vestibular Aqueduct in China PLoS ONE ·Yongyi Yuan, Weiwei Guo, Jie Tang, Guozheng Zhang, Guojian Wang, Mingyu Han, Xun Zhang, Shiming Yang, David Z. Z. He, Pu Dai	2012	63

About Mingyu Han

Mingyu Han is a scholar working on Sensory Systems, Neurology, Virology, Cancer Research and Pharmacology, having authored 45 papers that have together received 577 indexed citations. Recurring topics across this work include Hearing, Cochlea, Tinnitus, Genetics (13 papers), Vestibular and auditory disorders (8 papers), RNA regulation and disease (5 papers), Prenatal Screening and Diagnostics (5 papers), Cancer-related molecular mechanisms research (4 papers), Genomic variations and chromosomal abnormalities (4 papers), interferon and immune responses (3 papers) and Gut microbiota and health (3 papers). The work is most often cited by research in Sensory Systems (204 citations), Otorhinolaryngology (75 citations), Neurology (118 citations), Biological Psychiatry (13 citations) and Infectious Diseases (72 citations). Mingyu Han has collaborated with scholars based in China, United States and France. Frequent co-authors include Pu Dai, Yongyi Yuan, Guojian Wang, Shasha Huang, Xue Gao, Maorong Xie, Serge Bénichou, Lucie Bracq, Jérôme Bouchet and Dongyang Kang. Their work appears in journals such as PLoS ONE, Stem Cell Research, Genetics in Medicine, Journal of Translational Medicine and BMC Medical Genomics.

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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