Dongyang Kang

1.7k citations

75 papers · 1.0k · h-index 19

Impact in

Sensory Systems top 0.5%
- Hearing, Cochlea, Tinnitus, Genetics
Otorhinolaryngology top 2%
- Ear Surgery and Otitis Media

Papers in

Sensory Systems 42
- Hearing, Cochlea, Tinnitus, Genetics 42
Molecular Biology 41
- RNA regulation and disease 12
- Connexins and lens biology 12
- Mitochondrial Function and Pathology 10
- RNA and protein synthesis mechanisms 8

Co-authors: Pu Dai (64 shared papers)Yongyi Yuan (47 shared papers)Dongyi Han (26 shared papers)Huijun Yuan (21 shared papers)Shasha Huang (39 shared papers)Deliang Huang (11 shared papers)Xue Gao (25 shared papers)Guojian Wang (16 shared papers)
Journals: PLoS ONE (5 papers)Genetics in Medicine (4 papers)International Journal of Pediatric Otorhinolaryngology (4 papers)Journal of Translational Medicine (4 papers)BMC Medical Genomics (4 papers)
Partner nations: China United States Philippines

In The Last Decade

Dongyang Kang

72 papers receiving 1.0k citations

Peers

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-authors

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

All Works

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20 of 20 papers shown

Showing the 20 most-cited of 75 papers — load more, or switch the sort, to bring in the rest.

#	Work
1	Comprehensive molecular etiology analysis of nonsyndromic hearing impairment from typical areas in China Journal of Translational Medicine ·Yongyi Yuan, Yiwen You, Deliang Huang, Jinghong Cui, Yong Wang, Qiang Wang, Fei Yu, Dongyang Kang, Huijun Yuan, Dongyi Han, Pu Dai	2009	130
2	Cosegregation of the G7444A mutation in the mitochondrial COI/tRNA^Ser(UCN) genes with the 12S rRNA A1555G mutation in a Chinese family with aminoglycoside‐induced and nonsyndromic hearing loss American Journal of Medical Genetics Part A ·Huijun Yuan, Yaping Qian, Yanjun Xu, Juyang Cao, Linna Bai, Weidong Shen, Fei Ji, Xin Zhang, Dongyang Kang, Jun Qin Mo, John H. Greinwald, Dongyi Han, Suoqiang Zhai, Wie‐Yen Young, Min‐Xin Guan	2005	72
3	The prevalence of the 235delC GJB2 mutation in a Chinese deaf population Genetics in Medicine ·Pu Dai, Fei Yu, Bing Han, Yongyi Yuan, Qi Li, Guojian Wang, Xin Liu, Jia He, Deliang Huang, Dongyang Kang, Xin Zhang, Huijun Yuan, Eric Schmitt, Dongyi Han, Lee‐Jun C. Wong	2007	65
4	SLC26A4 c.919-2A>G varies among Chinese ethnic groups as a cause of hearing loss Genetics in Medicine ·Pu Dai, Qi Li, Deliang Huang, Yongyi Yuan, Dongyang Kang, David T. Miller, Hong Shao, Qingwen Zhu, Jia He, Fei Yu, Xin Liu, Bing Han, Huijun Yuan, Orah S. Platt, Dongyi Han, Bai-Lin Wu	2008	51
5	Molecular Etiology of Hearing Impairment in Inner Mongolia: mutations in SLC26A4 gene and relevant phenotype analysis Journal of Translational Medicine ·Pu Dai, Yongyi Yuan, Deliang Huang, Xiuhui Zhu, Fei Yu, Dongyang Kang, Huijun Yuan, Bai-Lin Wu, Dongyi Han, Lee‐Jun C. Wong	2008	44
6	Extremely low penetrance of deafness associated with the mitochondrial 12S rRNA mutation in 16 Chinese families: Implication for early detection and prevention of deafness Biochemical and Biophysical Research Communications ·Pu Dai, Xin Liu, Dongyi Han, Yaping Qian, Deliang Huang, Huijun Yuan, Weiming Li, Fei Yu, Ruining Zhang, Hongyan Lin, Yong He, Youjun Yu, Quanzhu Sun, Huaiyi Qin, Ronghua Li, Xin Zhang, Dongyang Kang, Juyang Cao, Wie‐Yen Young, Min‐Xin Guan	2005	43
7	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, Fanglu Chi, Sheng‐Pei Chen, Ping Liu, Chunlei Zhang, Jianjun Cao, Hui Jiang, Xun Xu, Wei Wang, Tao Duan	2014	38
8	Extremely discrepant mutation spectrum of SLC26A4 between Chinese patients with isolated Mondini deformity and enlarged vestibular aqueduct Journal of Translational Medicine ·Shasha Huang, Dongyi Han, Yongyi Yuan, Guojian Wang, Dongyang Kang, Xin Zhang, Xiaofei Yan, Xiaoxiao Meng, Min Dong, Pu Dai	2011	37
9	Coexistence of mitochondrial 12S rRNA C1494T and CO1/tRNASer(UCN) G7444A mutations in two Han Chinese pedigrees with aminoglycoside-induced and non-syndromic hearing loss Biochemical and Biophysical Research Communications ·Huijun Yuan, Jing Chen, Xin Liu, Jing Cheng, Xinjian Wang, Li Yang, Shuzhi Yang, Juyang Cao, Dongyang Kang, Pu Dai, Suoqiang Zhai, Dongyi Han, Wie‐Yen Young, Min‐Xin Guan	2007	35
10	Genetic and Phenotypic Heterogeneity in Chinese Patients with Waardenburg Syndrome Type II PLoS ONE ·Shuzhi Yang, Shuzhi Yang, Pu Dai, Xin Liu, Dongyang Kang, Xin Zhang, Yang Wei–yan, Chengyong Zhou, Shiming Yang, Huijun Yuan	2013	31
11	Comprehensive genetic testing of Chinese SNHL patients and variants interpretation using ACMG guidelines and ethnically matched normal controls European Journal of Human Genetics ·Yongyi Yuan, Qi Li, Yu Su, Qiongfen Lin, Xue Gao, Hankui Liu, Shasha Huang, Dongyang Kang, N. Wendell Todd, Douglas E. Mattox, Jianguo Zhang, Xi Lin, Pu Dai	2019	30
12	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
13	Mutation Spectrum of Common Deafness-Causing Genes in Patients with Non-Syndromic Deafness in the Xiamen Area, China PLoS ONE ·Yi Jiang, Shasha Huang, Tao Deng, Lihua Wu, Juan Chen, Dongyang Kang, Xiufeng Xu, Ruiyu Li, Dongyi Han, Pu Dai	2015	27
14	A subunit of V-ATPases, ATP6V1B2, underlies the pathology of intellectual disability EBioMedicine ·Weihao Zhao, Xue Gao, Shiwei Qiu, Bo Gao, Song Gao, Xin Zhang, Dongyang Kang, Weiju Han, Pu Dai, Yongyi Yuan	2019	25
15	Novel compound heterozygous mutations in the MYO15A gene in autosomal recessive hearing loss identified by whole-exome sequencing Journal of Translational Medicine ·Xue Gao, Qingyan Zhu, Yueshuai Song, Guojian Wang, Yongyi Yuan, Feng Xin, Shasha Huang, Dongyang Kang, Mingyu Han, Liping Guan, Jianguo Zhang, Pu Dai	2013	24
16	Identification of a novel mutation in POU3F4 for prenatal diagnosis in a Chinese family with X-linked nonsyndromic hearing loss Journal of genetics and genomics ·Jianzhong Li, Jing Cheng, Yanping Lu, Yu Lu, Aiting Chen, Yi Sun, Dongyang Kang, Xin Zhang, Pu Dai, Dongyi Han, Huijun Yuan	2010	20
17	KCNJ10 May Not Be a Contributor to Nonsyndromic Enlargement of Vestibular Aqueduct (NSEVA) in Chinese Subjects PLoS ONE ·Jiandong Zhao, Yongyi Yuan, Shasha Huang, Bangqing Huang, Jing Cheng, Dongyang Kang, Guojian Wang, Dongyi Han, Pu Dai	2014	20
18	Mutations at position 7445 in the precursor of mitochondrial tRNASer(UCN) gene in three maternal Chinese pedigrees with sensorineural hearing loss Mitochondrion ·Jing Chen, Huijun Yuan, Jianxin Lü, Xin Liu, Guojian Wang, Yi Zhu, Jing Cheng, Xinjian Wang, Bing Han, Li Yang, Shuzhi Yang, Aifeng Yang, Qing Sun, Dongyang Kang, Xin Zhang, Pu Dai, Suoqiang Zhai, Dongyi Han, Wie‐Yen Young, Min‐Xin Guan	2008	19
19	Analysis of genotype–phenotype relationships in 90 Chinese probands with Waardenburg syndrome Human Genetics ·Guojian Wang, Xiaohong Li, Xue Gao, Yu Su, Mingyu Han, Bo Gao, Chang Guo, Dongyang Kang, Shasha Huang, Yongyi Yuan, Pu Dai	2021	19
20	Noninvasive and Accurate Detection of Hereditary Hearing Loss Mutations with Buccal Swab Based on Droplet Digital PCR Analytical Chemistry ·Fang Wang, Lingxiang Zhu, Baoxia Liu, Xiurui Zhu, Nan Wang, Tao Deng, Dongyang Kang, Junmin Pan, Wenjun Yang, Huafang Gao, Yong Guo	2018	17

About Dongyang Kang

Dongyang Kang is a scholar working on Sensory Systems, Molecular Biology, Neurology, Otorhinolaryngology and Immunology, having authored 75 papers that have together received 1.0k indexed citations. Recurring topics across this work include Hearing, Cochlea, Tinnitus, Genetics (42 papers), Vestibular and auditory disorders (17 papers), RNA regulation and disease (12 papers), Connexins and lens biology (12 papers), Mitochondrial Function and Pathology (10 papers), Ear Surgery and Otitis Media (9 papers), RNA and protein synthesis mechanisms (8 papers) and Prenatal Screening and Diagnostics (4 papers). The work is most often cited by research in Sensory Systems (710 citations), Otorhinolaryngology (239 citations), Neurology (328 citations), Endocrine and Autonomic Systems (73 citations) and Molecular Biology (582 citations). Dongyang Kang has collaborated with scholars based in China, United States and Philippines. Frequent co-authors include Pu Dai, Yongyi Yuan, Dongyi Han, Huijun Yuan, Shasha Huang, Deliang Huang, Xue Gao, Guojian Wang, Fei Yu and Xin Liu. Their work appears in journals such as PLoS ONE, Genetics in Medicine, International Journal of Pediatric Otorhinolaryngology, 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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