Dongyang Kang

1.7k total citations
75 papers, 1.0k citations indexed

About

Dongyang Kang is a scholar working on Sensory Systems, Molecular Biology and Neurology. According to data from OpenAlex, Dongyang Kang has authored 75 papers receiving a total of 1.0k indexed citations (citations by other indexed papers that have themselves been cited), including 42 papers in Sensory Systems, 41 papers in Molecular Biology and 17 papers in Neurology. Recurrent topics in Dongyang Kang's work include Hearing, Cochlea, Tinnitus, Genetics (42 papers), Vestibular and auditory disorders (17 papers) and RNA regulation and disease (12 papers). Dongyang Kang is often cited by papers focused on Hearing, Cochlea, Tinnitus, Genetics (42 papers), Vestibular and auditory disorders (17 papers) and RNA regulation and disease (12 papers). Dongyang Kang collaborates with scholars based in China, United States and Philippines. Dongyang Kang's co-authors include Pu Dai, Yongyi Yuan, Dongyi Han, Huijun Yuan, Shasha Huang, Deliang Huang, Xue Gao, Guojian Wang, Fei Yu and Xin Liu and has published in prestigious journals such as PLoS ONE, Analytical Chemistry and Biochemical and Biophysical Research Communications.

In The Last Decade

Dongyang Kang

72 papers receiving 1.0k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Dongyang Kang China 19 710 582 328 239 105 75 1.0k
Ibis Menéndez United States 11 590 0.8× 487 0.8× 173 0.5× 106 0.4× 131 1.2× 20 776
Laurence Jonard France 15 301 0.4× 379 0.7× 135 0.4× 66 0.3× 90 0.9× 36 742
Diana L. Kolbe United States 5 325 0.5× 248 0.4× 104 0.3× 120 0.5× 86 0.8× 5 484
Atteeq U. Rehman United States 12 315 0.4× 373 0.6× 118 0.4× 71 0.3× 65 0.6× 19 588
Ahmet Karagüzel Türkiye 11 222 0.3× 236 0.4× 104 0.3× 52 0.2× 27 0.3× 24 458
Sedigheh Delmaghani France 10 498 0.7× 479 0.8× 200 0.6× 101 0.4× 128 1.2× 13 764
Xue Gao China 13 301 0.4× 223 0.4× 133 0.4× 100 0.4× 45 0.4× 50 428
Xiaomei Ouyang United States 14 190 0.3× 259 0.4× 95 0.3× 55 0.2× 58 0.6× 32 510
Amal Abu Rayyan Palestinian Territory 12 223 0.3× 356 0.6× 81 0.2× 74 0.3× 45 0.4× 18 632
Mounira Hmani‐Aifa Tunisia 14 256 0.4× 274 0.5× 131 0.4× 67 0.3× 38 0.4× 19 706

Countries citing papers authored by Dongyang Kang

Since Specialization
Citations

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

Fields of papers citing papers by Dongyang Kang

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Dongyang Kang

This figure shows the co-authorship network connecting the top 25 collaborators of Dongyang Kang. A scholar is included among the top collaborators of Dongyang Kang 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 Dongyang Kang. Dongyang Kang 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.
Huang, Shasha, Xue Gao, Yi Jiang, et al.. (2025). Reevaluation of Enlarged Vestibular Aqueduct. JAMA Otolaryngology–Head & Neck Surgery. 151(11). 1046–1046.
2.
Zhang, Lang, Xue Gao, Guojian Wang, et al.. (2024). MPZL2—a common autosomal recessive deafness gene related to moderate sensorineural hearing loss in the Chinese population. BMC Medical Genomics. 17(1). 32–32. 2 indexed citations
3.
Li, Xiaoge, Dejun Zhang, Shasha Huang, et al.. (2023). Exploration of a Novel Noninvasive Prenatal Testing Approach for Monogenic Disorders Based on Fetal Nucleated Red Blood Cells. Clinical Chemistry. 69(12). 1396–1408. 2 indexed citations
4.
Wang, Weiqian, Xue Gao, Shasha Huang, et al.. (2022). Genetic Analysis of the LOXHD1 Gene in Chinese Patients With Non-Syndromic Hearing Loss. Frontiers in Genetics. 13. 825082–825082. 2 indexed citations
5.
6.
Huang, Shasha, et al.. (2022). Quantitative assessment of low-level parental mosaicism of SNVs and CNVs in Waardenburg syndrome. Human Genetics. 142(3). 419–430. 2 indexed citations
7.
8.
Zhao, Weihao, Xue Gao, Song Gao, et al.. (2019). A subunit of V-ATPases, ATP6V1B2, underlies the pathology of intellectual disability. EBioMedicine. 45. 408–421. 25 indexed citations
9.
Su, Yu, Xue Gao, Shasha Huang, et al.. (2018). Clinical and molecular characterization of POU3F4 mutations in multiple DFNX2 Chinese families. BMC Medical Genetics. 19(1). 157–157. 12 indexed citations
10.
Han, Mingyu, Zhifeng Li, Wenlu Wang, et al.. (2017). A quantitative cSMART assay for noninvasive prenatal screening of autosomal recessive nonsyndromic hearing loss caused by GJB2 and SLC26A4 mutations. Genetics in Medicine. 19(12). 1309–1316. 27 indexed citations
11.
Gao, Xue, Yu Su, Yulan Chen, et al.. (2015). Identification of Two Novel Compound Heterozygous PTPRQ Mutations Associated with Autosomal Recessive Hearing Loss in a Chinese Family. PLoS ONE. 10(4). e0124757–e0124757. 11 indexed citations
12.
Huang, Shasha, Dongyang Kang, Mingyu Han, et al.. (2014). Analysis of the heteroplasmy level and transmitted features in hearing-loss pedigrees with mitochondrial 12S rRNA A1555G mutation. BMC Genetics. 15(1). 26–26. 14 indexed citations
13.
Meng, Meng, Xuchao Li, Huijuan Ge, et al.. (2014). Noninvasive prenatal testing for autosomal recessive conditions by maternal plasma sequencing in a case of congenital deafness. Genetics in Medicine. 16(12). 972–976. 38 indexed citations
14.
Lu, Yanping, Xu-ming Bian, Shasha Huang, et al.. (2012). [Prenatal genetic test and clinical guidance for 213 hereditary deaf families].. PubMed. 47(2). 127–31. 3 indexed citations
15.
Dai, Pu, Qi Li, Deliang Huang, et al.. (2008). SLC26A4 c.919-2A>G varies among Chinese ethnic groups as a cause of hearing loss. Genetics in Medicine. 10(8). 586–592. 51 indexed citations
16.
Dai, Pu, Yongyi Yuan, Deliang Huang, et al.. (2008). Molecular Etiology of Hearing Impairment in Inner Mongolia: mutations in SLC26A4 gene and relevant phenotype analysis. Journal of Translational Medicine. 6(1). 74–74. 44 indexed citations
17.
Zhang, Ruining, Xin Liu, Xin Zhang, et al.. (2007). Nonsense mutations in the PAX3 gene cause Waardenburg syndrome type I in two Chinese patients. Chinese Medical Journal. 120(1). 46–49. 12 indexed citations
18.
Dai, Pu, Yongyi Yuan, Dongyang Kang, et al.. (2007). [Sequencing of SLC26A4 exons 7 and 8 and hot spot mutation analysis in 1552 moderate to profound sensorineural hearing loss patients in China].. PubMed. 87(36). 2521–5. 4 indexed citations
19.
Li, Qi, Pu Dai, Deliang Huang, et al.. (2007). [Frequency of SLC26A4 IVS7-2A > G mutation in patients with severe to profound hearing loss from different area and ethnic group in China].. PubMed. 42(12). 893–7. 5 indexed citations
20.
Dai, Pu, Yongyi Yuan, Xin Zhang, et al.. (2006). [Patients suffered from enlarged vestibular aqueduct syndrome in Chifeng deaf and dumb school detected by Pendred's syndrome gene hot spot mutation screening].. PubMed. 41(7). 497–500. 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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