Chung‐Hsing Wang

1.2k total citations
56 papers, 837 citations indexed

About

Chung‐Hsing Wang is a scholar working on Genetics, Molecular Biology and Surgery. According to data from OpenAlex, Chung‐Hsing Wang has authored 56 papers receiving a total of 837 indexed citations (citations by other indexed papers that have themselves been cited), including 20 papers in Genetics, 19 papers in Molecular Biology and 8 papers in Surgery. Recurrent topics in Chung‐Hsing Wang's work include Genomic variations and chromosomal abnormalities (6 papers), Lysosomal Storage Disorders Research (5 papers) and DNA Repair Mechanisms (4 papers). Chung‐Hsing Wang is often cited by papers focused on Genomic variations and chromosomal abnormalities (6 papers), Lysosomal Storage Disorders Research (5 papers) and DNA Repair Mechanisms (4 papers). Chung‐Hsing Wang collaborates with scholars based in Taiwan, United States and Japan. Chung‐Hsing Wang's co-authors include Fuu‐Jen Tsai, Wei‐De Lin, I‐Ching Chou, Yen-Ling Song, Winton Cheng, Chang‐Hai Tsai, DA-TIAN BAU, Che-Chen Lin, Cheng‐Chieh Lin and Hung‐Rong Yen and has published in prestigious journals such as Journal of Clinical Oncology, PLoS ONE and The Journal of Clinical Endocrinology & Metabolism.

In The Last Decade

Chung‐Hsing Wang

54 papers receiving 809 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 16 341 156 142 98 89 56 837
Judit Bene Hungary 17 381 1.1× 179 1.1× 61 0.4× 65 0.7× 165 1.9× 77 1.0k
Tatsuo Yamamoto Japan 22 363 1.1× 226 1.4× 378 2.7× 264 2.7× 90 1.0× 80 1.5k
David Laperrière Canada 11 462 1.4× 283 1.8× 162 1.1× 34 0.3× 94 1.1× 13 1.2k
Ferenc Somogyvári Hungary 17 252 0.7× 73 0.5× 101 0.7× 24 0.2× 82 0.9× 60 909
Christopher F. MacManus United States 14 380 1.1× 105 0.7× 304 2.1× 30 0.3× 78 0.9× 16 1.1k
Qiang Du China 19 377 1.1× 109 0.7× 152 1.1× 42 0.4× 68 0.8× 36 889
Satomi Hashimoto Japan 12 217 0.6× 70 0.4× 84 0.6× 45 0.5× 63 0.7× 25 545
Katie M. Dixon Australia 17 202 0.6× 101 0.6× 284 2.0× 24 0.2× 79 0.9× 37 1.2k
Anindita Biswas United States 13 557 1.6× 128 0.8× 84 0.6× 68 0.7× 78 0.9× 22 1.1k
Brady Gaynor United States 10 112 0.3× 112 0.7× 74 0.5× 23 0.2× 83 0.9× 16 578

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.
Wang, Chung‐Hsing, Yu‐Nan Huang, Wen‐Ling Liao, et al.. (2024). GBA1 as a risk gene for osteoporosis in the specific populations and its role in the development of Gaucher disease. Orphanet Journal of Rare Diseases. 19(1). 144–144. 4 indexed citations
2.
Chou, Yen‐Yin, Pao‐Lin Kuo, Hui‐Pin Hsiao, et al.. (2024). Syndromic ciliopathy: a taiwanese single-center study. BMC Medical Genomics. 17(1). 106–106. 1 indexed citations
3.
Huang, Yu‐Nan, Wen‐Ling Liao, Jing‐Yang Huang, et al.. (2024). Long‐term safety and efficacy of glucagon‐like peptide‐1 receptor agonists in individuals with obesity and without type 2 diabetes: A global retrospective cohort study. Diabetes Obesity and Metabolism. 26(11). 5222–5232. 13 indexed citations
4.
Liao, Wen‐Ling, et al.. (2023). Combining polygenic risk scores and human leukocyte antigen variants for personalized risk assessment of type 1 diabetes in the Taiwanese population. Diabetes Obesity and Metabolism. 25(10). 2928–2936. 5 indexed citations
5.
Lin, Yi‐Chun, et al.. (2023). Trends in age at menarche from 1943 through 1989 in Taiwan: A retrospective population-based analysis. Pediatrics & Neonatology. 65(1). 64–70. 3 indexed citations
6.
Lin, Wei‐De, Fuu‐Jen Tsai, & Chung‐Hsing Wang. (2023). Identification of a novel deletion mutation in PHKA2 in a taiwanese patient with type IXa glycogen storage disease. Pediatrics & Neonatology. 64(4). 465–467. 2 indexed citations
7.
Lin, Ro‐Ting, et al.. (2022). Genome-wide causal mediation analysis identifies genetic loci associated with uterine fibroids mediated by age at menarche. Human Reproduction. 37(9). 2197–2212. 6 indexed citations
8.
Chen, Chao‐Chun, Chien‐Chung Kuo, Pei‐Chen Hsu, et al.. (2022). Significant Contribution of Interleukin-18 Genotypes to Childhood Acute Lymphocytic Leukemia Risk in Taiwanese. Anticancer Research. 42(11). 5283–5290. 4 indexed citations
9.
Cheng, Chi‐Fung, Wen‐Miin Liang, Chung‐Hsing Wang, et al.. (2022). Your height affects your health: genetic determinants and health-related outcomes in Taiwan. BMC Medicine. 20(1). 250–250. 16 indexed citations
10.
Lee, Ni‐Chung, Yin‐Hsiu Chien, Chung‐Hsing Wang, et al.. (2022). Safety and efficacy of eliglustat combined to enzyme replacement therapy for lymphadenopathy in patients with Gaucher disease type 3. Molecular Genetics and Metabolism Reports. 31. 100867–100867. 7 indexed citations
11.
Hsu, Pei‐Chen, Chao‐Chun Chen, Ya–Chen Yang, et al.. (2022). Contribution of Cyclin-dependent Kinase Inhibitor 1B Genotypes to Childhood Leukemia Risk. In Vivo. 36(4). 1637–1642. 6 indexed citations
12.
Huang, Yen‐Hua, Chung‐Hsing Wang, Yin‐Hsiu Chien, et al.. (2021). RNA-seq of peripheral blood mononuclear cells of congenital generalized lipodystrophy type 2 patients. Scientific Data. 8(1). 265–265. 4 indexed citations
13.
Wu, Tien‐Yuan, Chung‐Hsing Wang, Ni Tien, et al.. (2020). A Population-Based Cohort Study on the Association of Hyperthyroidism With the Risk of Hyperlipidemia and the Effects of Anti-thyroid Drugs on Hepatic Gene Expression. Frontiers in Medicine. 7. 228–228. 6 indexed citations
14.
Chuang, Po‐Jen & Chung‐Hsing Wang. (2017). An Efficient Group-based Data Backup and Recovery Scheme in Cloud Computing Systems.. Journal of information science and engineering. 33. 183–198.
15.
Wen, Su‐Ying, et al.. (2016). Nrf2 Activation as a Protective Feedback to Limit Cell Death in High Glucose‐Exposed Cardiomyocytes. Journal of Cellular Biochemistry. 118(7). 1659–1669. 18 indexed citations
16.
Lin, Wei‐De, et al.. (2015). Identification and Characterization of Mutations in the CLCN7 Gene in a Taiwanese Patient with Infantile Malignant Osteopetrosis. Pediatrics & Neonatology. 57(2). 155–157. 3 indexed citations
17.
Chou, I‐Ching, et al.. (2014). Successful control with carbamazepine of family with paroxysmal kinesigenic dyskinesia of PRRT2 mutation. Biomedicine. 4(2). 15–15. 10 indexed citations
18.
Chang, Yu‐Tzu, I‐Ching Chou, Chung‐Hsing Wang, et al.. (2012). Chromosome 10q Deletion del (10)(q26.1q26.3) is Associated with Cataract. Pediatrics & Neonatology. 54(2). 132–136. 11 indexed citations
19.
Wang, Chung‐Hsing, Wei‐De Lin, DA-TIAN BAU, I‐Ching Chou, & Fuu‐Jen Tsai. (2011). Genetic and clinical profiles of spondylocostal dysostosis patients in Taiwan. American Journal of Medical Genetics Part A. 155(12). 3132–3135. 3 indexed citations
20.
Lee, Cheng-Chun, et al.. (2002). A Novel Nonsense Mutation of the Sedlin Gene in a Family with Spondyloepiphyseal Dysplasia Tarda. Human Heredity. 54(1). 54–56. 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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