Xue Gao

850 total citations
50 papers, 428 citations indexed

About

Xue Gao is a scholar working on Sensory Systems, Molecular Biology and Neurology. According to data from OpenAlex, Xue Gao has authored 50 papers receiving a total of 428 indexed citations (citations by other indexed papers that have themselves been cited), including 30 papers in Sensory Systems, 27 papers in Molecular Biology and 14 papers in Neurology. Recurrent topics in Xue Gao's work include Hearing, Cochlea, Tinnitus, Genetics (30 papers), Vestibular and auditory disorders (14 papers) and RNA regulation and disease (9 papers). Xue Gao is often cited by papers focused on Hearing, Cochlea, Tinnitus, Genetics (30 papers), Vestibular and auditory disorders (14 papers) and RNA regulation and disease (9 papers). Xue Gao collaborates with scholars based in China, United States and Japan. Xue Gao's co-authors include Pu Dai, Yongyi Yuan, Shasha Huang, Guojian Wang, Dongyang Kang, Yu Su, Mingyu Han, Feng Xin, Xi Lin and Fei Yu and has published in prestigious journals such as PLoS ONE, Journal of Affective Disorders and Advanced Science.

In The Last Decade

Xue Gao

47 papers receiving 421 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Xue Gao China	13	301	223	133	100	45	50	428
Parna Chattaraj United States	10	266 0.9×	230 1.0×	253 1.9×	105 1.1×	41 0.9×	14	469
Hong-Joon Park South Korea	16	374 1.2×	303 1.4×	143 1.1×	104 1.0×	85 1.9×	28	553
Mariem Ben Saïd Tunisia	11	214 0.7×	174 0.8×	101 0.8×	46 0.5×	42 0.9×	26	369
Diana L. Kolbe United States	5	325 1.1×	248 1.1×	104 0.8×	120 1.2×	86 1.9×	5	484
Yin-Hung Lin Taiwan	11	292 1.0×	172 0.8×	104 0.8×	93 0.9×	115 2.6×	15	392
Yoh-ichiro Iwasa Japan	9	200 0.7×	134 0.6×	77 0.6×	61 0.6×	53 1.2×	24	284
Ahmet Karagüzel Türkiye	11	222 0.7×	236 1.1×	104 0.8×	52 0.5×	27 0.6×	24	458
TB Friedman United States	9	260 0.9×	238 1.1×	110 0.8×	47 0.5×	46 1.0×	9	407
Nabil Driss Tunisia	8	142 0.5×	123 0.6×	70 0.5×	73 0.7×	21 0.5×	25	298
Aki Oshima Japan	8	187 0.6×	149 0.7×	91 0.7×	42 0.4×	37 0.8×	12	306

Countries citing papers authored by Xue Gao

Since Specialization

Citations

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

Fields of papers citing papers by Xue Gao

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Xue Gao

This figure shows the co-authorship network connecting the top 25 collaborators of Xue Gao. A scholar is included among the top collaborators of Xue Gao 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 Xue Gao. Xue Gao is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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20 of 20 papers shown

Huang, Shasha, Xue Gao, Yi Jiang, et al.. (2025). Reevaluation of Enlarged Vestibular Aqueduct. JAMA Otolaryngology–Head & Neck Surgery. 151(11). 1046–1046.

Wei, Guanghua, Xue Gao, Lu Zheng, et al.. (2025). Single Administration of AAV‐m Atp6v1b2 Gene Therapy Rescues Hearing and Vestibular Disorders Caused by Atp6v1b2 ‐Induced Lysosomal Dysfunction in Hair Cells. Advanced Science. 12(29). e2408878–e2408878. 2 indexed citations

Wang, Shipeng, et al.. (2025). Resilience analysis and recovery strategy for interdependent automated container port networks under cascading failures. Reliability Engineering & System Safety. 265. 111495–111495. 1 indexed citations

Zhang, Han, Jia Li, Zhide Hu, et al.. (2025). Design, synthesis and biological activity of novel sulfonatocalix[4]arene-based organophosphorus toxicant scavengers. Bioorganic Chemistry. 165. 109067–109067.

Gao, Xue, et al.. (2024). Unveiling the link between glymphatic function and cortical microstructures in post-traumatic stress disorder. Journal of Affective Disorders. 365. 341–350. 5 indexed citations

Wang, Shipeng, Haiyan Wang, Xue Gao, et al.. (2024). Correlation analysis of failure risk factors in automated container port logistics systems from a resilience perspective. Journal of Sea Research. 202. 102552–102552. 1 indexed citations

Yang, Kun, Weiqian Wang, Mingyu Han, et al.. (2022). A newborn male with Myhre syndrome, hearing loss, and complete syndactyly of fingers 3–4. Molecular Genetics & Genomic Medicine. 11(3). e2103–e2103. 4 indexed citations

Wu, Jie, Yu Su, Yang Wang, et al.. (2022). Molecular diagnose of a large hearing loss population from China by targeted genome sequencing. Journal of Human Genetics. 67(11). 643–649. 15 indexed citations

Huang, Shasha, Xue Gao, Mingyu Han, et al.. (2022). Analysis of the genotype–phenotype correlation of MYO15A variants in Chinese non-syndromic hearing loss patients. BMC Medical Genomics. 15(1). 71–71. 2 indexed citations

10.

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

11.

Gao, Xue, Pu Dai, & Yongyi Yuan. (2021). Genetic architecture and phenotypic landscape of deafness and onychodystrophy syndromes. Human Genetics. 141(3-4). 821–838. 4 indexed citations

12.

Huang, Shasha, Xue Gao, Yu‐Feng Wang, et al.. (2020). Prelingual Sensorineural Hearing Loss Caused by a Novel GJB2 Dominant Mutation in a Chinese Family. BioMed Research International. 2020(1). 6370386–6370386. 2 indexed citations

13.

Yuan, Yongyi, Qi Li, Yu Su, et al.. (2019). Comprehensive genetic testing of Chinese SNHL patients and variants interpretation using ACMG guidelines and ethnically matched normal controls. European Journal of Human Genetics. 28(2). 231–243. 30 indexed citations

14.

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

15.

Yuan, Yongyi, Xue Gao, Bangqing Huang, et al.. (2016). Phenotypic Heterogeneity in a DFNA20/26 family segregating a novel ACTG1 mutation. BMC Genetics. 17(1). 33–33. 17 indexed citations

16.

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

17.

Gao, Xue, Guojian Wang, Yongyi Yuan, et al.. (2014). Novel Compound Heterozygous Mutations in MYO7A Associated with Usher Syndrome 1 in a Chinese Family. PLoS ONE. 9(7). e103415–e103415. 7 indexed citations

18.

Su, Yu, Wenxue Tang, Xue Gao, et al.. (2014). A Novel Mutation in the TECTA Gene in a Chinese Family with Autosomal Dominant Nonsyndromic Hearing Loss. PLoS ONE. 9(2). e89240–e89240. 6 indexed citations

19.

Xin, Feng, Yongyi Yuan, Xiaoming Deng, et al.. (2013). Genetic mutations in nonsyndromic deafness patients of Chinese minority and han ethnicities in Yunnan, China. Journal of Translational Medicine. 11(1). 312–312. 42 indexed citations

20.

Gao, Xue, Guojian Wang, Yongyi Yuan, et al.. (2013). Novel compound heterozygous mutations in the MYO15A gene in autosomal recessive hearing loss identified by whole-exome sequencing. Journal of Translational Medicine. 11(1). 284–284. 24 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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