Chung-Hsing Wang

801 total citations
24 papers, 590 citations indexed

About

Chung-Hsing Wang is a scholar working on Molecular Biology, Genetics and Pathology and Forensic Medicine. According to data from OpenAlex, Chung-Hsing Wang has authored 24 papers receiving a total of 590 indexed citations (citations by other indexed papers that have themselves been cited), including 17 papers in Molecular Biology, 6 papers in Genetics and 5 papers in Pathology and Forensic Medicine. Recurrent topics in Chung-Hsing Wang's work include DNA Repair Mechanisms (5 papers), Genetic factors in colorectal cancer (4 papers) and Connective tissue disorders research (4 papers). Chung-Hsing Wang is often cited by papers focused on DNA Repair Mechanisms (5 papers), Genetic factors in colorectal cancer (4 papers) and Connective tissue disorders research (4 papers). Chung-Hsing Wang collaborates with scholars based in Taiwan, United States and Canada. Chung-Hsing Wang's co-authors include Fuu‐Jen Tsai, Wei-De Lin, Tung-Yuan Lai, Hsin-Yueh Liang, Wei‐Wen Kuo, Da‐Tian Bau, Chang-Fang Chiu, Chia-Wen Tsai, Yushin Tsai and Dau‐Ming Niu and has published in prestigious journals such as PLoS ONE, Scientific Reports and Diabetologia.

In The Last Decade

Chung-Hsing Wang

24 papers receiving 577 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Chung-Hsing Wang Taiwan 14 291 154 93 66 63 24 590
T. Shirotani Japan 8 316 1.1× 162 1.1× 72 0.8× 98 1.5× 20 0.3× 11 623
Fabienne Nigon France 17 328 1.1× 79 0.5× 106 1.1× 84 1.3× 18 0.3× 25 1.1k
Yi Ma China 13 326 1.1× 121 0.8× 93 1.0× 41 0.6× 21 0.3× 24 942
Olga Bushueva Russia 19 300 1.0× 155 1.0× 74 0.8× 86 1.3× 18 0.3× 76 716
Matthew J. Wither United States 18 342 1.2× 315 2.0× 95 1.0× 62 0.9× 36 0.6× 24 919
Danielle Duffy United States 17 326 1.1× 94 0.6× 130 1.4× 48 0.7× 20 0.3× 42 1.2k
Hermann Joseph Gröne Germany 8 323 1.1× 88 0.6× 78 0.8× 54 0.8× 61 1.0× 8 863
Takenobu Kamada Japan 9 457 1.6× 174 1.1× 158 1.7× 137 2.1× 39 0.6× 20 995
Elizabeth Kensicki United States 10 479 1.6× 154 1.0× 205 2.2× 35 0.5× 28 0.4× 10 918
Ariel Brautbar United States 16 278 1.0× 104 0.7× 94 1.0× 267 4.0× 15 0.2× 39 1.0k

Countries citing papers authored by Chung-Hsing Wang

Since Specialization
Citations

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

Fields of papers citing papers by Chung-Hsing Wang

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Chung-Hsing Wang. 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 Chung-Hsing Wang. The network helps show where Chung-Hsing Wang may publish in the future.

Co-authorship network of co-authors of Chung-Hsing Wang

This figure shows the co-authorship network connecting the top 25 collaborators of Chung-Hsing Wang. A scholar is included among the top collaborators of Chung-Hsing Wang 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 Chung-Hsing Wang. Chung-Hsing Wang 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.
Lin, Wei-De, Fuu‐Jen Tsai, & Chung-Hsing Wang. (2019). Mild osteochondrodysplasia with acanthosis nigricans in a short-statured Taiwanese family due to the p.Lys650Gln mutation in FGFR3. Pediatrics & Neonatology. 60(6). 686–688. 1 indexed citations
2.
Lin, Wei-De, Mei‐Chyn Chao, Shao‐Yin Chu, et al.. (2018). Congenital generalized lipodystrophy in Taiwan. Journal of the Formosan Medical Association. 118(1). 142–147. 10 indexed citations
3.
Lin, Ying-Ju, Chung-Hsing Wang, Chih‐Hsin Tang, et al.. (2017). Association of human height-related genetic variants with familial short stature in Han Chinese in Taiwan. Scientific Reports. 7(1). 6372–6372. 22 indexed citations
4.
Lin, Yi‐Chun, et al.. (2017). Improved final predicted height with the injection of leuprolide in children with earlier puberty: A retrospective cohort study. PLoS ONE. 12(10). e0185080–e0185080. 11 indexed citations
5.
6.
Wang, Chung-Hsing, et al.. (2017). Identification of one novel homozygous mutation in the NPR2 gene in a patient from Taiwan with acromesomelic dysplasia Maroteaux type. Pediatrics & Neonatology. 59(3). 322–323. 2 indexed citations
7.
Lin, Hsiang‐Yu, Chih‐Kuang Chuang, Chung-Hsing Wang, et al.. (2016). Long-term galsulfase enzyme replacement therapy in Taiwanese mucopolysaccharidosis VI patients: A case series. Molecular Genetics and Metabolism Reports. 7. 63–69. 26 indexed citations
8.
Liao, Hsuan-Chieh, Chuan-Chi Chiang, Dau‐Ming Niu, et al.. (2014). Detecting multiple lysosomal storage diseases by tandem mass spectrometry — A national newborn screening program in Taiwan. Clinica Chimica Acta. 431. 80–86. 91 indexed citations
9.
Lin, Wei-De, Wuh‐Liang Hwu, Chung-Hsing Wang, & Fuu‐Jen Tsai. (2014). Mutant EXT1 in Taiwanese Patients with Multiple Hereditary Exostoses. Biomedicine. 4(2). 11–11. 3 indexed citations
10.
Lin, Shuan-Pei, Chia‐Chi Hsu, Dau‐Ming Niu, et al.. (2014). Two Frequent Mutations Associated with the Classic Form of Propionic Acidemia in Taiwan. Biochemical Genetics. 52(9-10). 415–429. 13 indexed citations
11.
Wang, Chung-Hsing, Fuu‐Jen Tsai, Kao-Pin Hwang, et al.. (2014). Enterovirus infection is associated with an increased risk of childhood type 1 diabetes in Taiwan: a nationwide population-based cohort study. Diabetologia. 58(1). 79–86. 31 indexed citations
12.
Lai, Tung-Yuan, et al.. (2013). Antioxidant effects of diallyl trisulfide on high glucose-induced apoptosis are mediated by the PI3K/Akt-dependent activation of Nrf2 in cardiomyocytes. International Journal of Cardiology. 168(2). 1286–1297. 131 indexed citations
13.
Wang, Chung-Hsing, Kang‐Hsi Wu, Yung‐Li Yang, et al.. (2012). Association between Ataxia Telangiectasia Mutated Gene Polymorphisms and Childhood Leukemia in Taiwan. The Chinese Journal of Physiology. 54(6). 413–8. 10 indexed citations
14.
Lin, Wei-De, Shuan-Pei Lin, Chung-Hsing Wang, et al.. (2011). RUNX2 mutations in Taiwanese patients with cleidocranial dysplasia. Genetics and Molecular Biology. 34(2). 201–204. 13 indexed citations
15.
Wu, Kang‐Hsi, Chung-Hsing Wang, Yung‐Li Yang, et al.. (2010). Significant association of XRCC4 single nucleotide polymorphisms with childhood leukemia in Taiwan.. PubMed. 30(2). 529–33. 21 indexed citations
16.
Lin, Wei-De, Shuan-Pei Lin, Chung-Hsing Wang, et al.. (2008). Genetic analysis of mucopolysaccharidosis type VI in Taiwanese patients. Clinica Chimica Acta. 394(1-2). 89–93. 23 indexed citations
17.
Lin, Wei-De, Chung-Hsing Wang, Chien‐Chen Lai, et al.. (2008). Molecular analysis of Taiwanese patients with 3-Hydroxy-3-methylglutaryl CoA lyase deficiency. Clinica Chimica Acta. 401(1-2). 33–36. 4 indexed citations
18.
Bau, Da‐Tian, Hsien-Chang Tseng, Chung-Hsing Wang, et al.. (2008). Oral cancer and genetic polymorphism of DNA double strand break gene Ku70 in Taiwan. Oral Oncology. 44(11). 1047–1051. 59 indexed citations
19.
Wang, Chung-Hsing, Kang‐Hsi Wu, Fuu‐Jen Tsai, Ching-Tien Peng, & Chang‐Hai Tsai. (2006). Comparison of Oral and Subcutaneous Iron Chelation Therapies in the Prevention of Major Endocrinopathies in β-Thalassemia Major Patients. Hemoglobin. 30(2). 257–262. 14 indexed citations
20.
Lin, Wei-De, Chung-Hsing Wang, Cheng‐Chung Lee, et al.. (2006). Genetic mutation profile of isovaleric acidemia patients in Taiwan. Molecular Genetics and Metabolism. 90(2). 134–139. 28 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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