Linyi Xie

429 total citations
20 papers, 174 citations indexed

About

Linyi Xie is a scholar working on Sensory Systems, Molecular Biology and Neurology. According to data from OpenAlex, Linyi Xie has authored 20 papers receiving a total of 174 indexed citations (citations by other indexed papers that have themselves been cited), including 16 papers in Sensory Systems, 13 papers in Molecular Biology and 9 papers in Neurology. Recurrent topics in Linyi Xie's work include Hearing, Cochlea, Tinnitus, Genetics (16 papers), Vestibular and auditory disorders (9 papers) and Ear Surgery and Otitis Media (3 papers). Linyi Xie is often cited by papers focused on Hearing, Cochlea, Tinnitus, Genetics (16 papers), Vestibular and auditory disorders (9 papers) and Ear Surgery and Otitis Media (3 papers). Linyi Xie collaborates with scholars based in China, Brazil and Israel. Linyi Xie's co-authors include Jing Guan, Lan Lan, Yin Wang, Qiuju Wang, Ju Dong Yang, Dayong Wang, Lan Yu, Kaiwen Wu, Cui Zhao and Dayong Wang and has published in prestigious journals such as Scientific Reports, Hearing Research and Frontiers in Cell and Developmental Biology.

In The Last Decade

Linyi Xie

19 papers receiving 169 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Linyi Xie China	9	128	100	54	36	16	20	174
Xuezhong Liu United States	9	144 1.1×	113 1.1×	64 1.2×	28 0.8×	45 2.8×	14	202
Soumya Korrapati United States	6	141 1.1×	94 0.9×	30 0.6×	40 1.1×	16 1.0×	10	194
Małgorzata Mueller‐Malesińska Poland	6	117 0.9×	111 1.1×	47 0.9×	23 0.6×	29 1.8×	11	173
Birgit Haack Germany	6	126 1.0×	119 1.2×	39 0.7×	21 0.6×	26 1.6×	9	163
Orit Dagan‐Rosenfeld United States	5	68 0.5×	160 1.6×	32 0.6×	22 0.6×	13 0.8×	5	252
Sebastian Gießelmann Germany	3	44 0.3×	82 0.8×	18 0.3×	9 0.3×	12 0.8×	4	117
Khadijeh Jalalvand Iran	8	145 1.1×	101 1.0×	70 1.3×	8 0.2×	37 2.3×	10	169
Radka Kremlíková Pourová Czechia	8	45 0.4×	50 0.5×	27 0.5×	15 0.4×	23 1.4×	18	168
Judith Löffler Austria	7	152 1.2×	179 1.8×	54 1.0×	31 0.9×	15 0.9×	8	275

Countries citing papers authored by Linyi Xie

Since Specialization

Citations

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

Fields of papers citing papers by Linyi Xie

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Linyi Xie

This figure shows the co-authorship network connecting the top 25 collaborators of Linyi Xie. A scholar is included among the top collaborators of Linyi Xie 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 Linyi Xie. Linyi Xie 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

Yang, Chaoyong, Xiaolong Zhang, Lan Lan, et al.. (2025). Identification of genetic mechanisms of non-isolated auditory neuropathy with various phenotypes in Chinese families. Orphanet Journal of Rare Diseases. 20(1). 11–11.

Xie, Linyi, et al.. (2023). [The follow-up study on patients of children with auditory neuropathy].. PubMed. 37(3). 177–180. 1 indexed citations

Xie, Linyi, et al.. (2022). The audiological characteristics of infant auditory neuropathy patients without otoacoustic emission. Laryngoscope Investigative Otolaryngology. 7(6). 2095–2102. 1 indexed citations

Li, Jin, Lan Lan, Linyi Xie, et al.. (2021). Clinical characteristics of patients with unilateral auditory neuropathy. American Journal of Otolaryngology. 42(5). 103143–103143. 5 indexed citations

Wang, Wenjia, Li Jin, Lan Lan, et al.. (2021). Auditory Neuropathy as the Initial Phenotype for Patients With ATP1A3 c.2452 G > A: Genotype–Phenotype Study and CI Management. Frontiers in Cell and Developmental Biology. 9. 749484–749484. 2 indexed citations

Wang, Yin, Yun Gao, Jing Guan, et al.. (2021). Phenotypic Heterogeneity of Post-lingual and/or Milder Hearing Loss for the Patients With the GJB2 c.235delC Homozygous Mutation. Frontiers in Cell and Developmental Biology. 9. 647240–647240. 6 indexed citations

Gao, Yun, Yin Wang, Jing Guan, et al.. (2021). Genetic Susceptibility Study of Chinese Sudden Sensorineural Hearing Loss Patients with Vertigo. Current Medical Science. 41(4). 673–679. 5 indexed citations

Wang, Yin, Dan Bing, Jin Li, et al.. (2020). High Frequency of AIFM1 Variants and Phenotype Progression of Auditory Neuropathy in a Chinese Population. Neural Plasticity. 2020. 1–12. 17 indexed citations

Zhang, Qiujing, Kaiwen Wu, Cui Zhao, et al.. (2020). [Identification of a novel mutation of CEACAM16 gene in a Chinese family with autosomal dominant nonsyndromic hearing loss].. PubMed. 34(9). 777–781. 1 indexed citations

10.

Bing, Dan, Dayong Wang, Lan Lan, et al.. (2019). Serum Bilirubin Level as a Potential Marker for the Hearing Outcome in Severe-Profound Bilateral Sudden Deafness. Otology & Neurotology. 40(6). 728–735. 8 indexed citations

11.

Wang, Hongyang, Jing Guan, Liping Guan, et al.. (2018). Further evidence for “gain-of-function” mechanism of DFNA5 related hearing loss. Scientific Reports. 8(1). 8424–8424. 17 indexed citations

12.

Wang, Yin, Kaiwen Wu, Jing Guan, et al.. (2018). Identification of four TMC1 variations in different Chinese families with hereditary hearing loss. Molecular Genetics & Genomic Medicine. 6(4). 504–513. 18 indexed citations

13.

Du, Wan, Dayong Wang, Bing Han, et al.. (2017). A POU3F4 Mutation Causes Nonsyndromic Hearing Loss in a Chinese X-linked Recessive Family. Chinese Medical Journal. 130(1). 88–92. 12 indexed citations

14.

Wang, Yin, Kaiwen Wu, Lan Yu, et al.. (2017). A novel dominant GJB2 (DFNA3) mutation in a Chinese family. Scientific Reports. 7(1). 34425–34425. 11 indexed citations

15.

Wang, Li, Hongyang Wang, Jing Guan, et al.. (2017). Clinical Auditory Phenotypes Associated with GATA3 Gene Mutations in Familial Hypoparathyroidism-deafness-renal Dysplasia Syndrome. Chinese Medical Journal. 130(6). 703–709. 4 indexed citations

16.

Guan, Jing, Yin Wang, Lan Lan, et al.. (2017). Novel recessive PDZD7 biallelic mutations in two Chinese families with non‐syndromic hearing loss. American Journal of Medical Genetics Part A. 176(1). 99–106. 16 indexed citations

17.

Zhang, Qiujing, Lan Lan, Lan Yu, et al.. (2016). Temperature sensitive auditory neuropathy. Hearing Research. 335. 53–63. 16 indexed citations

18.

Han, Bing, Liang Lan, Liang Zong, et al.. (2016). High frequency ofOTOFmutations in Chinese infants with congenital auditory neuropathy spectrum disorder. Clinical Genetics. 90(3). 238–246. 24 indexed citations

19.

Lan, Lan, Na Li, Yue Qi, et al.. (2015). Identification of a novel mutation of PJVK in the Chinese non-syndromic hearing loss population with low prevalence of the PJVK mutations. Acta Oto-Laryngologica. 135(3). 211–216. 9 indexed citations

20.

Gao, Yun, Dayong Wang, Yin Wang, et al.. (2015). [Cinical and genetic characteristics of familial Meniere's disease: three families report].. PubMed. 50(11). 915–24. 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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