Shuan‐Yow Li

1.2k total citations
51 papers, 955 citations indexed

About

Shuan‐Yow Li is a scholar working on Molecular Biology, Sensory Systems and Genetics. According to data from OpenAlex, Shuan‐Yow Li has authored 51 papers receiving a total of 955 indexed citations (citations by other indexed papers that have themselves been cited), including 33 papers in Molecular Biology, 22 papers in Sensory Systems and 11 papers in Genetics. Recurrent topics in Shuan‐Yow Li's work include Hearing, Cochlea, Tinnitus, Genetics (22 papers), Connexins and lens biology (12 papers) and Nicotinic Acetylcholine Receptors Study (10 papers). Shuan‐Yow Li is often cited by papers focused on Hearing, Cochlea, Tinnitus, Genetics (22 papers), Connexins and lens biology (12 papers) and Nicotinic Acetylcholine Receptors Study (10 papers). Shuan‐Yow Li collaborates with scholars based in Taiwan, United States and Poland. Shuan‐Yow Li's co-authors include Jiann‐Jou Yang, Ching‐Chyuan Su, Mao‐Chang Su, Biing-Hui Liu, Ting‐Shuan Wu, Feng‐Yih Yu, Inn‐Chi Lee, Pei‐Ju Liao, Yichun Wang and Shih-Hsin Huang and has published in prestigious journals such as PLoS ONE, Scientific Reports and Biochemical and Biophysical Research Communications.

In The Last Decade

Shuan‐Yow Li

50 papers receiving 938 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Shuan‐Yow Li Taiwan 18 544 316 188 175 94 51 955
Arabandi Ramesh India 16 396 0.7× 457 1.4× 46 0.2× 74 0.4× 164 1.7× 30 775
Ke Xiao China 14 316 0.6× 151 0.5× 30 0.2× 141 0.8× 89 0.9× 36 665
Refugio García‐Villegas Mexico 16 478 0.9× 226 0.7× 73 0.4× 39 0.2× 114 1.2× 33 822
Raphaël Courjaret Qatar 19 527 1.0× 191 0.6× 99 0.5× 54 0.3× 53 0.6× 38 1.0k
Andrea M. Bell United States 7 562 1.0× 943 3.0× 39 0.2× 96 0.5× 46 0.5× 7 1.5k
Preston A. Baecker United States 17 475 0.9× 49 0.2× 110 0.6× 131 0.7× 50 0.5× 22 1.1k
Jianjun Wang China 19 1.3k 2.3× 95 0.3× 120 0.6× 395 2.3× 30 0.3× 96 1.9k
Thomas M. Bennett United States 19 1.1k 2.0× 71 0.2× 268 1.4× 42 0.2× 41 0.4× 47 1.5k

Countries citing papers authored by Shuan‐Yow Li

Since Specialization
Citations

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

Fields of papers citing papers by Shuan‐Yow Li

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Shuan‐Yow Li. 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 Shuan‐Yow Li. The network helps show where Shuan‐Yow Li may publish in the future.

Co-authorship network of co-authors of Shuan‐Yow Li

This figure shows the co-authorship network connecting the top 25 collaborators of Shuan‐Yow Li. A scholar is included among the top collaborators of Shuan‐Yow Li 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 Shuan‐Yow Li. Shuan‐Yow Li 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.
Lee, Inn‐Chi, et al.. (2020). Heteromeric Kv7.2 current changes caused by loss-of-function of KCNQ2 mutations are correlated with long-term neurodevelopmental outcomes. Scientific Reports. 10(1). 13375–13375. 11 indexed citations
2.
Wang, Wen‐Hung, et al.. (2017). Functional analysis of a nonsyndromic hearing loss-associated mutation in the transmembrane II domain of the GJC3 gene. International Journal of Medical Sciences. 14(3). 246–256. 6 indexed citations
3.
Lee, Inn‐Chi, Jiann‐Jou Yang, & Shuan‐Yow Li. (2016). A KCNQ2 E515D mutation associated with benign familial neonatal seizures and continuous spike and waves during slow-wave sleep syndrome in Taiwan. Journal of the Formosan Medical Association. 116(9). 711–719. 15 indexed citations
4.
Wang, Wen‐Hung, Yu‐Fan Liu, Ching‐Chyuan Su, et al.. (2011). A Novel Missense Mutation in the Connexin30 Causes Nonsyndromic Hearing Loss. PLoS ONE. 6(6). e21473–e21473. 16 indexed citations
5.
Chang, Han, et al.. (2010). Polymorphisms of the RET Gene in Hirschsprung Disease, Anorectal Malformation and Intestinal Pseudo-obstruction in Taiwan. Journal of the Formosan Medical Association. 109(1). 32–38. 6 indexed citations
6.
Su, Ching‐Chyuan, et al.. (2010). Mutation R184Q of connexin 26 in hearing loss patients has a dominant-negative effect on connexin 26 and connexin 30. European Journal of Human Genetics. 18(9). 1061–1064. 22 indexed citations
7.
Yang, Jiann‐Jou, et al.. (2009). Expansion of CAG repeats in the spinocerebellar ataxia type 1 (SCA1) gene in idiopathic oligozoospermia patients. Journal of Assisted Reproduction and Genetics. 26(5). 257–261. 5 indexed citations
8.
Yang, Jiann‐Jou, et al.. (2009). A novel mutation in the connexin 29 gene may contribute to nonsyndromic hearing loss. Human Genetics. 127(2). 191–199. 16 indexed citations
9.
Su, Ching‐Chyuan, Jiann‐Jou Yang, Jia‐Ching Shieh, Mao‐Chang Su, & Shuan‐Yow Li. (2006). Identification of Novel Mutations in the <i>KCNQ4</i> Gene of Patients with Nonsyndromic Deafness from Taiwan. Audiology and Neurotology. 12(1). 20–26. 29 indexed citations
10.
Yang, Jiann‐Jou, Pei‐Ju Liao, Ching‐Chyuan Su, & Shuan‐Yow Li. (2005). Expression patterns of connexin 29 (GJE1) in mouse and rat cochlea. Biochemical and Biophysical Research Communications. 338(2). 723–728. 18 indexed citations
11.
Su, Mao‐Chang, Shiann-Yann Lee, Ching‐Ting Tan, et al.. (2005). Taicatoxin inhibits the calcium-dependent slow motility of mammalian outer hair cells. Hearing Research. 203(1-2). 172–179.
12.
Hsieh, Lie‐Jiau, et al.. (2004). Genetic analysis of two subspecies of Reeves' muntjac (Cervidae: Muntiacus reevesi) by karyotyping and satellite DNA analyses. Zoological studies. 43(4). 749–758. 6 indexed citations
13.
Yang, Jiann‐Jou, et al.. (2004). Hearing loss associated with enlarged vestibular aqueduct and Mondini dysplasia is caused by splice-site mutation in the PDS gene. Hearing Research. 199(1-2). 22–30. 49 indexed citations
14.
Liu, Biing-Hui, et al.. (2003). Evaluation of genotoxic risk and oxidative DNA damage in mammalian cells exposed to mycotoxins, patulin and citrinin. Toxicology and Applied Pharmacology. 191(3). 255–263. 160 indexed citations
15.
Su, Mao‐Chang, Ching‐Ting Tan, Ching‐Chyuan Su, et al.. (2003). The effect of L-arginine on slow motility of mammalian outer hair cell. Hearing Research. 178(1-2). 52–58. 2 indexed citations
16.
Wang, Yichun, et al.. (2002). Mutations of Cx26 gene (GJB2) for prelingual deafness in Taiwan. European Journal of Human Genetics. 10(8). 495–498. 57 indexed citations
17.
Hsieh, Mingli, et al.. (2000). Identification of the spinocerebellar ataxia type 7 mutation in Taiwan: application of PCR-based Southern blot. Journal of Neurology. 247(8). 623–629. 14 indexed citations
18.
Li, Chuan, et al.. (1998). ProteinN-Arginine Methylation in Adenosine Dialdehyde-Treated Lymphoblastoid Cells. Archives of Biochemistry and Biophysics. 351(1). 53–59. 25 indexed citations
19.
Li, Shuan‐Yow, et al.. (1993). Molecular and cytogenetic analyses of autism in Taiwan. Human Genetics. 92(5). 441–445. 31 indexed citations
20.
Yeh, Guang‐Perng, et al.. (1987). Cyclopia with Trisomy 13. Australian and New Zealand Journal of Obstetrics and Gynaecology. 27(3). 251–255. 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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