Kaitian Chen

478 total citations
36 papers, 353 citations indexed

About

Kaitian Chen is a scholar working on Sensory Systems, Neurology and Molecular Biology. According to data from OpenAlex, Kaitian Chen has authored 36 papers receiving a total of 353 indexed citations (citations by other indexed papers that have themselves been cited), including 23 papers in Sensory Systems, 16 papers in Neurology and 10 papers in Molecular Biology. Recurrent topics in Kaitian Chen's work include Hearing, Cochlea, Tinnitus, Genetics (23 papers), Vestibular and auditory disorders (15 papers) and Cerebral Venous Sinus Thrombosis (7 papers). Kaitian Chen is often cited by papers focused on Hearing, Cochlea, Tinnitus, Genetics (23 papers), Vestibular and auditory disorders (15 papers) and Cerebral Venous Sinus Thrombosis (7 papers). Kaitian Chen collaborates with scholars based in China and United States. Kaitian Chen's co-authors include Hongyan Jiang, Ling Zong, Xuan Wu, Liang Sun, Xuan Wu, Jintao Du, Min Liu, Xianren Wang, Hong-Bo Zhao and Wei Zhou and has published in prestigious journals such as Automatica, Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease and Neuroscience Letters.

In The Last Decade

Kaitian Chen

33 papers receiving 351 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Kaitian Chen China 12 194 136 132 72 62 36 353
Daisuke Yamauchi Japan 9 170 0.9× 203 1.5× 147 1.1× 68 0.9× 30 0.5× 24 457
Allan Kachelmeier United States 10 207 1.1× 166 1.2× 116 0.9× 31 0.4× 44 0.7× 12 363
Min Young Kim South Korea 13 240 1.2× 99 0.7× 182 1.4× 78 1.1× 15 0.2× 31 379
Ayako Inoshita Japan 12 151 0.8× 42 0.3× 108 0.8× 54 0.8× 19 0.3× 33 310
Hong-Joon Park South Korea 16 374 1.9× 143 1.1× 303 2.3× 104 1.4× 25 0.4× 28 553
Kyu Yup Lee South Korea 8 270 1.4× 138 1.0× 135 1.0× 56 0.8× 19 0.3× 16 362
Saima Riazuddin Pakistan 2 168 0.9× 248 1.8× 275 2.1× 18 0.3× 50 0.8× 3 449
Nermin Başerer Türkiye 10 239 1.2× 109 0.8× 175 1.3× 63 0.9× 4 0.1× 18 386
L. Zelante Italy 10 367 1.9× 142 1.0× 316 2.4× 66 0.9× 10 0.2× 13 793
Yoh-ichiro Iwasa Japan 9 200 1.0× 77 0.6× 134 1.0× 61 0.8× 13 0.2× 24 284

Countries citing papers authored by Kaitian Chen

Since Specialization
Citations

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

Fields of papers citing papers by Kaitian Chen

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Kaitian Chen

This figure shows the co-authorship network connecting the top 25 collaborators of Kaitian Chen. A scholar is included among the top collaborators of Kaitian 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 Kaitian Chen. Kaitian 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.
2.
Chen, Kaitian & Hongyan Jiang. (2024). Deficient Gap Junction Coupling in Two Common Hearing Loss-Related Variants of GJB2. Clinical and Experimental Otorhinolaryngology. 17(3). 198–205.
3.
Chen, Kaitian, Changwu Li, Chang‐Zhi Dong, et al.. (2023). A dominant variant in apoptosis-related gene XKR8 is relevant to hereditary auditory neuropathy. Journal of Translational Medicine. 21(1). 279–279.
4.
Mei, Ling, et al.. (2021). Early Functional and Cognitive Declines Measured by Auditory-Evoked Cortical Potentials in Mice With Alzheimer’s Disease. Frontiers in Aging Neuroscience. 13. 710317–710317. 9 indexed citations
5.
Wu, Xuan, et al.. (2019). [Clinical characteristics and etiological analysis of sudden deafness patients with vertigo].. PubMed. 99(28). 2197–2202. 3 indexed citations
6.
Chen, Kaitian, et al.. (2019). [Clinical study of inner ear hemorrhage-associated sudden deafness and vertigo].. PubMed. 54(7). 495–500. 3 indexed citations
7.
Chen, Kaitian, et al.. (2018). Audiological outcomes in sudden sensorineural hearing loss with presumed inner ear hemorrhage. American Journal of Otolaryngology. 40(2). 274–278. 5 indexed citations
8.
Chen, Kaitian, Min Liu, Xuan Wu, Ling Zong, & Hongyan Jiang. (2018). Targeted next generation sequencing reveals OTOF mutations in auditory neuropathy spectrum disorder. International Journal of Pediatric Otorhinolaryngology. 115. 19–23. 13 indexed citations
9.
Chen, Kaitian, Hongyan Jiang, Ling Zong, & Xuan Wu. (2018). Side-related differences in sudden sensorineural hearing loss in children. International Journal of Pediatric Otorhinolaryngology. 114. 5–8. 12 indexed citations
10.
Chen, Kaitian, et al.. (2017). Germinal mosaicism of PAX3 mutation caused Waardenburg syndrome type I. International Journal of Pediatric Otorhinolaryngology. 104. 200–204. 4 indexed citations
11.
Zong, Ling, Kaitian Chen, Xuan Wu, Min Liu, & Hongyan Jiang. (2016). Compound heterozygous MYO7A mutations segregating Usher syndrome type 2 in a Han family. International Journal of Pediatric Otorhinolaryngology. 90. 150–155. 10 indexed citations
12.
Chen, Kaitian, et al.. (2015). Genetic counseling for a three-generation Chinese family with Waardenburg syndrome type II associated with a rare SOX10 mutation. International Journal of Pediatric Otorhinolaryngology. 79(5). 745–748. 8 indexed citations
13.
Chen, Kaitian, Liang Sun, Ling Zong, et al.. (2015). GJB2 and mitochondrial 12S rRNA susceptibility mutations in sudden deafness. European Archives of Oto-Rhino-Laryngology. 273(6). 1393–1398. 6 indexed citations
14.
Liu, Min, et al.. (2015). Novel mutation located in EC7 domain of protocadherin-15 uncovered by targeted massively parallel sequencing in a family segregating non-syndromic deafness DFNB23. International Journal of Pediatric Otorhinolaryngology. 79(7). 983–986. 9 indexed citations
15.
Du, Jintao, Hui Cao, Wei Zhou, et al.. (2014). MicroRNA-200 family members are weakly expressed in the neurosensory epithelia of the developing zebrafish (Danio rerio) inner ear. Genetics and Molecular Research. 13(2). 4187–4201. 4 indexed citations
16.
Wu, Xuan, et al.. (2014). Magnetic resonance imaging-detected inner ear hemorrhage as a potential cause of sudden sensorineural hearing loss. American Journal of Otolaryngology. 35(3). 318–323. 29 indexed citations
17.
Chen, Kaitian, Ling Zong, Min Liu, et al.. (2014). De novo dominant mutation of SOX10 gene in a Chinese family with Waardenburg syndrome type II. International Journal of Pediatric Otorhinolaryngology. 78(6). 926–929. 10 indexed citations
18.
Chen, Kaitian, Ling Zong, Min Liu, et al.. (2014). Developing regional genetic counseling for southern Chinese with nonsyndromic hearing impairment: a unique mutational spectrum. Journal of Translational Medicine. 12(1). 64–64. 24 indexed citations
19.
Chen, Kaitian, et al.. (2012). Low dose macrolide administration for long term is effective for otitis media with effusion in children. Auris Nasus Larynx. 40(1). 46–50. 18 indexed citations
20.
Chen, Kaitian, Wei Zhou, Ling Zong, et al.. (2012). Novel heterozygous mutation c.662_663insG compound with IVS7-2A>G mutation in SLC26A4 gene in a Chinese family with Pendred syndrome. International Journal of Pediatric Otorhinolaryngology. 76(11). 1633–1636. 1 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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