Yin-Hung Lin

755 total citations
15 papers, 392 citations indexed

About

Yin-Hung Lin is a scholar working on Sensory Systems, Neurology and Molecular Biology. According to data from OpenAlex, Yin-Hung Lin has authored 15 papers receiving a total of 392 indexed citations (citations by other indexed papers that have themselves been cited), including 12 papers in Sensory Systems, 9 papers in Neurology and 4 papers in Molecular Biology. Recurrent topics in Yin-Hung Lin's work include Hearing, Cochlea, Tinnitus, Genetics (12 papers), Vestibular and auditory disorders (8 papers) and Hearing Loss and Rehabilitation (4 papers). Yin-Hung Lin is often cited by papers focused on Hearing, Cochlea, Tinnitus, Genetics (12 papers), Vestibular and auditory disorders (8 papers) and Hearing Loss and Rehabilitation (4 papers). Yin-Hung Lin collaborates with scholars based in Taiwan, Mongolia and United States. Yin-Hung Lin's co-authors include Chuan‐Jen Hsu, Chen‐Chi Wu, Pei‐Lung Chen, Yi‐Hsin Lin, Tien‐Chen Liu, Wei‐Shiung Yang, Che‐Ming Wu, Chia‐Cheng Hung, Po‐Nien Tsao and Wei‐Yih Chiu and has published in prestigious journals such as PLoS ONE, Biochemical and Biophysical Research Communications and The Journal of Pediatrics.

In The Last Decade

Yin-Hung Lin

15 papers receiving 385 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Yin-Hung Lin Taiwan	11	292	172	115	104	93	15	392
Manuela Mazzoli Italy	12	295 1.0×	97 0.6×	180 1.6×	165 1.6×	86 0.9×	21	458
Kyu Yup Lee South Korea	8	270 0.9×	135 0.8×	95 0.8×	138 1.3×	56 0.6×	16	362
Diana L. Kolbe United States	5	325 1.1×	248 1.4×	86 0.7×	104 1.0×	120 1.3×	5	484
Liang Zong China	12	337 1.2×	302 1.8×	103 0.9×	108 1.0×	28 0.3×	23	468
Ayako Inoshita Japan	12	151 0.5×	108 0.6×	59 0.5×	42 0.4×	54 0.6×	33	310
Xue Gao China	13	301 1.0×	223 1.3×	45 0.4×	133 1.3×	100 1.1×	50	428
Meghan C. Drummond United States	8	271 0.9×	242 1.4×	61 0.5×	72 0.7×	47 0.5×	10	409
Lingxiang Hu China	10	323 1.1×	169 1.0×	126 1.1×	31 0.3×	49 0.5×	21	512
Kianoush Sheykholeslami United States	11	210 0.7×	100 0.6×	100 0.9×	118 1.1×	37 0.4×	22	354
Christina Sloan-Heggen United States	7	610 2.1×	366 2.1×	175 1.5×	186 1.8×	202 2.2×	10	742

Countries citing papers authored by Yin-Hung Lin

Since Specialization

Citations

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

Fields of papers citing papers by Yin-Hung Lin

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Yin-Hung Lin. 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 Yin-Hung Lin. The network helps show where Yin-Hung Lin may publish in the future.

Co-authorship network of co-authors of Yin-Hung Lin

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

All Works

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15 of 15 papers shown

Chiang, Yu‐Ting, Pei‐Hsuan Lin, Cheng‐Yu Tsai, et al.. (2023). Genetic Factors Contribute to the Phenotypic Variability in GJB2-Related Hearing Impairment. Journal of Molecular Diagnostics. 25(11). 827–837. 5 indexed citations

Yeh, Huei‐Ming, et al.. (2020). Next-generation sequencing and bioinformatics to identify genetic causes of malignant hyperthermia. Journal of the Formosan Medical Association. 120(2). 883–892. 6 indexed citations

Wu, Chen‐Chi, Cheng‐Yu Tsai, Yi‐Hsin Lin, et al.. (2019). Genetic Epidemiology and Clinical Features of Hereditary Hearing Impairment in the Taiwanese Population. Genes. 10(10). 772–772. 32 indexed citations

Lin, Yin-Hung, Tien‐Chen Liu, Yi‐Hsin Lin, et al.. (2019). Prediction Model for Audiological Outcomes in Patients With GJB2 Mutations. Ear and Hearing. 41(1). 143–149. 20 indexed citations

Lin, Yin-Hung, Chen‐Chi Wu, Yi‐Hsin Lin, et al.. (2018). Targeted Next-Generation Sequencing Facilitates Genetic Diagnosis and Provides Novel Pathogenetic Insights into Deafness with Enlarged Vestibular Aqueduct. Journal of Molecular Diagnostics. 21(1). 138–148. 10 indexed citations

Lu, Chun‐Yi, Po‐Nien Tsao, Yingying Ke, et al.. (2018). Concurrent Hearing, Genetic, and Cytomegalovirus Screening in Newborns, Taiwan. The Journal of Pediatrics. 199. 144–150.e1. 29 indexed citations

Lin, Yin-Hung, Cheng‐Yu Tsai, Yi‐Hsin Lin, et al.. (2018). Unique spectra of deafness-associated mutations in Mongolians provide insights into the genetic relationships among Eurasian populations. PLoS ONE. 13(12). e0209797–e0209797. 13 indexed citations

Lin, Pei‐Hsuan, Chuan‐Jen Hsu, Yi‐Hsin Lin, et al.. (2017). Etiologic and Audiologic Characteristics of Patients With Pediatric-Onset Unilateral and Asymmetric Sensorineural Hearing Loss. JAMA Otolaryngology–Head & Neck Surgery. 143(9). 912–912. 34 indexed citations

Wu, Chen‐Chi, Ching‐Hui Tsai, Chia‐Cheng Hung, et al.. (2016). Newborn genetic screening for hearing impairment: a population-based longitudinal study. Genetics in Medicine. 19(1). 6–12. 61 indexed citations

10.

Wu, Ruey‐Meei, Pei‐Lung Chen, Ta‐Fu Chen, et al.. (2016). Clinical heterogeneity of LRRK2 p.I2012T mutation. Parkinsonism & Related Disorders. 33. 36–43. 15 indexed citations

11.

Wu, Chen‐Chi, Yin-Hung Lin, Tien‐Chen Liu, et al.. (2015). Identifying Children With Poor Cochlear Implantation Outcomes Using Massively Parallel Sequencing. Medicine. 94(27). e1073–e1073. 57 indexed citations

12.

Lin, Yin-Hung, et al.. (2014). Identification of a novel GATA3 mutation in a deaf Taiwanese family by massively parallel sequencing. Mutation research. Fundamental and molecular mechanisms of mutagenesis. 771. 1–5. 45 indexed citations

13.

Wu, Chen‐Chi, Yin-Hung Lin, Yingchang Lu, et al.. (2013). Application of Massively Parallel Sequencing to Genetic Diagnosis in Multiplex Families with Idiopathic Sensorineural Hearing Impairment. PLoS ONE. 8(2). e57369–e57369. 35 indexed citations

14.

Lu, Yingchang, Chen‐Chi Wu, Ting‐Hua Yang, et al.. (2013). Differences in the Pathogenicity of the p.H723R Mutation of the Common Deafness-Associated SLC26A4 Gene in Humans and Mice. PLoS ONE. 8(6). e64906–e64906. 23 indexed citations

15.

Hu, Wensi S., et al.. (2007). A proteomic approach to study Salmonella enterica serovar Typhimurium putative transporter YjeH associated with ceftriaxone resistance. Biochemical and Biophysical Research Communications. 361(3). 694–699. 7 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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