Kuang‐Ming Hsiao

1.0k total citations
36 papers, 849 citations indexed

About

Kuang‐Ming Hsiao is a scholar working on Molecular Biology, Cellular and Molecular Neuroscience and Cardiology and Cardiovascular Medicine. According to data from OpenAlex, Kuang‐Ming Hsiao has authored 36 papers receiving a total of 849 indexed citations (citations by other indexed papers that have themselves been cited), including 24 papers in Molecular Biology, 17 papers in Cellular and Molecular Neuroscience and 8 papers in Cardiology and Cardiovascular Medicine. Recurrent topics in Kuang‐Ming Hsiao's work include Genetic Neurodegenerative Diseases (16 papers), Mitochondrial Function and Pathology (9 papers) and Ion channel regulation and function (7 papers). Kuang‐Ming Hsiao is often cited by papers focused on Genetic Neurodegenerative Diseases (16 papers), Mitochondrial Function and Pathology (9 papers) and Ion channel regulation and function (7 papers). Kuang‐Ming Hsiao collaborates with scholars based in Taiwan, United States and Canada. Kuang‐Ming Hsiao's co-authors include Peggy Farnham, Stéphanie McMahon, Huichin Pan, Po-Hsuan Chen, James E. Ferrell, Cheng‐Chung Chou, Lichun Wang, Kuan‐Yu Chen, Shuan‐Yow Li and Li‐Chun Wang and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Genes & Development and PLoS ONE.

In The Last Decade

Kuang‐Ming Hsiao

35 papers receiving 839 citations

Peers

Kuang‐Ming Hsiao
Huichin Pan Taiwan
Rachel Montpetit United States
Kamla Dutt United States
Ken Matsumoto Japan
Holger Bierhoff Germany
Julie Wallis United Kingdom
Graham Brock United States
Catherine R. Begy United States
Johanna P. Laakkonen Finland
R. G. Worton Canada
Huichin Pan Taiwan
Kuang‐Ming Hsiao
Citations per year, relative to Kuang‐Ming Hsiao Kuang‐Ming Hsiao (= 1×) peers Huichin Pan

Countries citing papers authored by Kuang‐Ming Hsiao

Since Specialization
Citations

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

Fields of papers citing papers by Kuang‐Ming Hsiao

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Kuang‐Ming Hsiao. 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 Kuang‐Ming Hsiao. The network helps show where Kuang‐Ming Hsiao may publish in the future.

Co-authorship network of co-authors of Kuang‐Ming Hsiao

This figure shows the co-authorship network connecting the top 25 collaborators of Kuang‐Ming Hsiao. A scholar is included among the top collaborators of Kuang‐Ming Hsiao 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 Kuang‐Ming Hsiao. Kuang‐Ming Hsiao 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, Jiann-Der, Kuang‐Ming Hsiao, Ting‐Chuan Wang, et al.. (2014). Mutual Effect of rs688 and rs5925 in Regulating Low-Density Lipoprotein Receptor Splicing. DNA and Cell Biology. 33(12). 869–875. 8 indexed citations
2.
Lee, Jiann-Der, Kuang‐Ming Hsiao, Tsong‐Hai Lee, et al.. (2014). Genetic Polymorphism of LDLR (rs688) is Associated with Primary Intracerebral Hemorrhage. Current Neurovascular Research. 11(1). 10–15. 12 indexed citations
3.
Chen, Po-Hsuan, Kuang‐Ming Hsiao, & Cheng‐Chung Chou. (2013). Molecular characterization of toxicity mechanism of single-walled carbon nanotubes. Biomaterials. 34(22). 5661–5669. 74 indexed citations
4.
Lee, Jiann-Der, Tsong‐Hai Lee, Yen-Chu Huang, et al.. (2012). Polymorphisms at the LDLR Locus may be Associated with Ischemic Cerebrovascular Disease Independent of Lipid Profile. Current Neurovascular Research. 9(3). 200–206. 11 indexed citations
5.
6.
Hsiao, Kuang‐Ming, Huichin Pan, Chung‐Chin Yao, et al.. (2010). Overcoming the difficulties in laparoscopic management of contracted gallbladders with gallstones: possible role of fundus-down approach. Surgical Endoscopy. 25(1). 284–291. 11 indexed citations
7.
Wang, Lichun, Kuan‐Yu Chen, Huichin Pan, et al.. (2010). Muscleblind participates in RNA toxicity of expanded CAG and CUG repeats in Caenorhabditis elegans. Cellular and Molecular Life Sciences. 68(7). 1255–1267. 52 indexed citations
8.
Huang, Ren-Yu, et al.. (2007). Functional studies of the effect of NO donor on human CLCN1 polymorphism/mutants expressed in Xenopus laevis oocytes. Biochemical and Biophysical Research Communications. 365(4). 724–728. 2 indexed citations
9.
Kuo, Hung‐Chou, et al.. (2006). Novel mutations at carboxyl terminus of CIC-1 channel in myotonia congenita. Acta Neurologica Scandinavica. 113(5). 342–346. 12 indexed citations
10.
Chen, Kuan‐Yu, et al.. (2006). Length-dependent toxicity of untranslated CUG repeats on Caenorhabditis elegans. Biochemical and Biophysical Research Communications. 352(3). 774–779. 20 indexed citations
11.
Wang, Fu‐Der, Wei‐Juin Su, Jen-Fu Shih, et al.. (2006). Screening of Hospital Workers for Pulmonary Tuberculosis in a Medical Center in Taiwan. Infection Control and Hospital Epidemiology. 27(5). 510–511. 5 indexed citations
12.
Jou, Shuo‐Bin, et al.. (2004). Novel CLCN1 mutations in Taiwanese patients with myotonia congenita. Journal of Neurology. 251(6). 666–70. 18 indexed citations
13.
Huang, Chin‐Chang, et al.. (2003). Autosomal Dominant Myotonia Congenita in a Taiwanese Family and Beneficial Response to Mexiletine. 12(3). 130–135. 3 indexed citations
14.
Pan, Huichin, et al.. (2003). Cloning and developmental expression of p73 cDNA in zebrafish. Biochemical and Biophysical Research Communications. 307(2). 395–400. 10 indexed citations
15.
Hsiao, Kuang‐Ming, Hongliang Pan, Chin‐Chang Huang, et al.. (2003). Epidemiological and Genetic Studies of Myotonic Dystrophy Type 1 in Taiwan. Neuroepidemiology. 22(5). 283–289. 21 indexed citations
16.
Pan, Huichin, et al.. (2002). Overexpression but Lack of Mutation and Methylation of p73 in Hepatocellular Carcinoma. Acta Oncologica. 41(6). 550–555. 5 indexed citations
17.
Pan, Huichin, et al.. (2002). Increased (CTG/CAG)n lengths in myotonic dystrophy type 1 and Machado–Joseph disease genes in idiopathic azoospermia patients. Human Reproduction. 17(6). 1578–1583. 24 indexed citations
18.
19.
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
20.
Hsiao, Kuang‐Ming, Stéphanie McMahon, & Peggy Farnham. (1994). Multiple DNA elements are required for the growth regulation of the mouse E2F1 promoter.. Genes & Development. 8(13). 1526–1537. 225 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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