Hao Wu

2.3k total citations
122 papers, 1.6k citations indexed

About

Hao Wu is a scholar working on Sensory Systems, Epidemiology and Neurology. According to data from OpenAlex, Hao Wu has authored 122 papers receiving a total of 1.6k indexed citations (citations by other indexed papers that have themselves been cited), including 51 papers in Sensory Systems, 39 papers in Epidemiology and 35 papers in Neurology. Recurrent topics in Hao Wu's work include Hearing, Cochlea, Tinnitus, Genetics (51 papers), Meningioma and schwannoma management (39 papers) and Hearing Loss and Rehabilitation (26 papers). Hao Wu is often cited by papers focused on Hearing, Cochlea, Tinnitus, Genetics (51 papers), Meningioma and schwannoma management (39 papers) and Hearing Loss and Rehabilitation (26 papers). Hao Wu collaborates with scholars based in China, France and United States. Hao Wu's co-authors include Tao Yang, Yongchuan Chai, Zhaoyan Wang, Lei Li, Xiuhong Pang, Huan Jia, Xiaoming Wei, Yun Li, Zhiwu Huang and Lingxiang Hu and has published in prestigious journals such as Journal of Neuroscience, PLoS ONE and Scientific Reports.

In The Last Decade

Hao Wu

117 papers receiving 1.6k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Hao Wu China 22 865 549 374 341 314 122 1.6k
Sung Huhn Kim South Korea 23 830 1.0× 483 0.9× 790 2.1× 246 0.7× 365 1.2× 111 1.8k
Rick A. Friedman United States 25 876 1.0× 661 1.2× 431 1.2× 236 0.7× 228 0.7× 53 1.7k
Takeshi Oshima Japan 18 817 0.9× 568 1.0× 334 0.9× 204 0.6× 207 0.7× 77 1.4k
Jinsei Jung South Korea 21 663 0.8× 549 1.0× 361 1.0× 242 0.7× 309 1.0× 121 1.5k
Isabelle Schrauwen United States 25 525 0.6× 690 1.3× 323 0.9× 155 0.5× 450 1.4× 105 1.8k
Akinobu Kakigi Japan 23 1.1k 1.3× 463 0.8× 876 2.3× 291 0.9× 290 0.9× 140 2.0k
Christine T. Dinh United States 18 613 0.7× 147 0.3× 262 0.7× 387 1.1× 202 0.6× 54 1.0k
Hideichi Shinkawa Japan 27 1.2k 1.4× 609 1.1× 757 2.0× 273 0.8× 516 1.6× 105 2.1k
Anders Kinnefors Sweden 18 626 0.7× 162 0.3× 188 0.5× 394 1.2× 211 0.7× 37 979
Sun O Chang South Korea 18 368 0.4× 187 0.3× 347 0.9× 164 0.5× 313 1.0× 46 961

Countries citing papers authored by Hao Wu

Since Specialization
Citations

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

Fields of papers citing papers by Hao Wu

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Hao Wu

This figure shows the co-authorship network connecting the top 25 collaborators of Hao Wu. A scholar is included among the top collaborators of Hao Wu 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 Hao Wu. Hao Wu 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.
Wu, Hao, Shida Zhu, Lina Zhang, Bin Shen, & Lian-Lian Xu. (2024). Association between 5-HTR1A gene C-1019G polymorphism and antidepressant response in patients with major depressive disorder: A meta-analysis. World Journal of Psychiatry. 14(10). 1573–1582. 1 indexed citations
2.
3.
Liu, Hongchao, et al.. (2021). Differences in Calcium Clearance at Inner Hair Cell Active Zones May Underlie the Difference in Susceptibility to Noise-Induced Cochlea Synaptopathy of C57BL/6J and CBA/CaJ Mice. Frontiers in Cell and Developmental Biology. 8. 635201–635201. 8 indexed citations
4.
Chen, Jianqing, Yongchuan Chai, Zhihua Zhang, et al.. (2021). A microscope-assisted endoscopic transcanal transpromontorial approach for vestibular schwannoma resection: a preliminary report. European Archives of Oto-Rhino-Laryngology. 279(1). 75–82. 2 indexed citations
5.
Chen, Penghui, et al.. (2021). Detection and Functional Verification of Noncanonical Splice Site Mutations in Hereditary Deafness. Frontiers in Genetics. 12. 773922–773922. 5 indexed citations
6.
Zhang, Luping, Ru Zhang, Cheng Cheng, et al.. (2020). THOC1 deficiency leads to late-onset nonsyndromic hearing loss through p53-mediated hair cell apoptosis. PLoS Genetics. 16(8). e1008953–e1008953. 20 indexed citations
7.
Chen, Penghui, et al.. (2018). Postnatal Development of Microglia-Like Cells in Mouse Cochlea. Neural Plasticity. 2018. 1–5. 9 indexed citations
8.
Wang, Zhaoyan, Meiping Huang, Yongchuan Chai, et al.. (2018). BoneBridge implantation in patients with single-sided deafness resulting from vestibular schwannoma resection: objective and subjective benefit evaluations. Acta Oto-Laryngologica. 138(10). 877–885. 14 indexed citations
9.
Wang, Xueling, et al.. (2018). A Novel p.G141R Mutation in ILDR1 Leads to Recessive Nonsyndromic Deafness DFNB42 in Two Chinese Han Families. Neural Plasticity. 2018. 1–6. 4 indexed citations
10.
Chai, Yongchuan, et al.. (2018). Strategy for facial nerve management during surgical removal of benign jugular foramen tumors: Outcomes and indications. European Annals of Otorhinolaryngology Head and Neck Diseases. 136(3). S21–S25. 1 indexed citations
11.
He, Lin, et al.. (2017). Targeted next‐generation sequencing and parental genotyping in sporadic Chinese Han deaf patients. Clinical Genetics. 93(4). 899–904. 12 indexed citations
12.
Pang, Xiuhong, et al.. (2016). Mutation in the Hair Cell Specific GenePOU4F3Is a Common Cause for Autosomal Dominant Nonsyndromic Hearing Loss in Chinese Hans. Neural Plasticity. 2016. 1–6. 12 indexed citations
13.
Hu, Lingxiang, et al.. (2016). Diphtheria Toxin-Induced Cell Death Triggers Wnt-Dependent Hair Cell Regeneration in Neonatal Mice. Journal of Neuroscience. 36(36). 9479–9489. 47 indexed citations
14.
Chen, Penghui, et al.. (2016). NLRP3 Is Expressed in the Spiral Ganglion Neurons and Associated with Both Syndromic and Nonsyndromic Sensorineural Deafness. Neural Plasticity. 2016. 1–6. 13 indexed citations
15.
Xiang, Mingliang, et al.. (2015). [Differentiated thyroid cancer in children: a series of 29 cases].. PubMed. 50(7). 573–8. 3 indexed citations
16.
Shi, Jun, et al.. (2015). The Effect of Obstructive Sleep Apnea Syndrome on Growth and Development in Nonobese Children: A Parallel Study of Twins. The Journal of Pediatrics. 166(3). 646–650.e1. 21 indexed citations
17.
18.
Yang, Tao, José Gurrola, Hao Wu, et al.. (2009). Mutations of KCNJ10 Together with Mutations of SLC26A4 Cause Digenic Nonsyndromic Hearing Loss Associated with Enlarged Vestibular Aqueduct Syndrome. The American Journal of Human Genetics. 84(5). 651–657. 124 indexed citations
19.
Shen, Xiaoming, David Zakus, Zhengmin Xu, et al.. (2009). Development of an Effective Public Health Screening Program to Assess Hearing Disabilities among Newborns in Shanghai: A Prospective Cohort Study. World health & population. 11(4). 5–14. 9 indexed citations
20.

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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