Hsiang‐Yu Lin

5.8k total citations
167 papers, 3.1k citations indexed

About

Hsiang‐Yu Lin is a scholar working on Physiology, Epidemiology and Genetics. According to data from OpenAlex, Hsiang‐Yu Lin has authored 167 papers receiving a total of 3.1k indexed citations (citations by other indexed papers that have themselves been cited), including 63 papers in Physiology, 51 papers in Epidemiology and 48 papers in Genetics. Recurrent topics in Hsiang‐Yu Lin's work include Lysosomal Storage Disorders Research (60 papers), Trypanosoma species research and implications (36 papers) and Glycogen Storage Diseases and Myoclonus (26 papers). Hsiang‐Yu Lin is often cited by papers focused on Lysosomal Storage Disorders Research (60 papers), Trypanosoma species research and implications (36 papers) and Glycogen Storage Diseases and Myoclonus (26 papers). Hsiang‐Yu Lin collaborates with scholars based in Taiwan, United States and United Kingdom. Hsiang‐Yu Lin's co-authors include Chih‐Kuang Chuang, Dau‐Ming Niu, Shuan‐Pei Lin, Ming‐Ren Chen, Ching‐Shih Chen, Chang‐Shi Chen, Jing‐Ru Weng, Bai‐Horng Su, Wuh‐Liang Hwu and Jui‐Hsing Chang and has published in prestigious journals such as SHILAP Revista de lepidopterología, Scientific Reports and International Journal of Molecular Sciences.

In The Last Decade

Hsiang‐Yu Lin

161 papers receiving 3.0k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Hsiang‐Yu Lin Taiwan 30 1.4k 993 711 509 506 167 3.1k
Úrsula da Silveira Matte Brazil 28 1.1k 0.8× 574 0.6× 1.0k 1.4× 269 0.5× 244 0.5× 204 2.8k
Shuan‐Pei Lin Taiwan 26 683 0.5× 415 0.4× 593 0.8× 609 1.2× 284 0.6× 163 2.1k
María L. Couce Spain 30 916 0.7× 377 0.4× 1.2k 1.7× 529 1.0× 651 1.3× 242 3.6k
Hiroyuki Ida Japan 29 2.0k 1.4× 733 0.7× 982 1.4× 206 0.4× 293 0.6× 189 3.5k
Pietro Strisciuglio Italy 30 532 0.4× 411 0.4× 1.1k 1.5× 356 0.7× 442 0.9× 131 2.9k
Rita Barone Italy 33 876 0.6× 378 0.4× 1.6k 2.3× 415 0.8× 268 0.5× 184 4.4k
Daniela Concolino Italy 24 661 0.5× 328 0.3× 630 0.9× 407 0.8× 260 0.5× 130 1.9k
Katherine A. Kelly United States 32 758 0.5× 337 0.3× 1.1k 1.5× 213 0.4× 133 0.3× 98 3.6k
Meinrad Peterlik Austria 40 391 0.3× 357 0.4× 1.2k 1.7× 698 1.4× 205 0.4× 148 4.4k
Deborah Elstein Israel 34 4.3k 3.0× 1.6k 1.7× 1.5k 2.2× 143 0.3× 333 0.7× 201 5.4k

Countries citing papers authored by Hsiang‐Yu Lin

Since Specialization
Citations

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

Fields of papers citing papers by Hsiang‐Yu Lin

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Hsiang‐Yu 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 Hsiang‐Yu Lin. The network helps show where Hsiang‐Yu Lin may publish in the future.

Co-authorship network of co-authors of Hsiang‐Yu Lin

This figure shows the co-authorship network connecting the top 25 collaborators of Hsiang‐Yu Lin. A scholar is included among the top collaborators of Hsiang‐Yu 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 Hsiang‐Yu Lin. Hsiang‐Yu Lin 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, Chung‐Lin, et al.. (2025). Understanding Genetic Screening: Harnessing Health Information to Prevent Disease Risks. International Journal of Medical Sciences. 22(4). 903–919. 4 indexed citations
2.
Lee, Chung‐Lin, et al.. (2024). Whole Exome Sequencing Facilitates Early Diagnosis of Lesch–Nyhan Syndrome: A Case Series. Diagnostics. 14(24). 2809–2809. 1 indexed citations
3.
Lin, Hsiang‐Yu, et al.. (2024). Mature neurons from iPSCs unveil neurodegeneration-related pathways in mucopolysaccharidosis type II: GSK-3β inhibition for therapeutic potential. Cell Death and Disease. 15(4). 302–302. 1 indexed citations
4.
Su, Chin‐Hui, et al.. (2023). Endoscopic and Image Analysis of the Airway in Patients with Mucopolysaccharidosis Type IVA. Journal of Personalized Medicine. 13(3). 494–494. 2 indexed citations
5.
Chang, Yu‐Chia, et al.. (2022). Epidemiological evolution of early-onset neonatal sepsis over 12 years: A single center, population-based study in central Taiwan. Journal of Neonatal-Perinatal Medicine. 15(3). 575–582. 3 indexed citations
6.
Lee, Chung‐Lin, et al.. (2022). Long-Term Cardiovascular Findings in Williams Syndrome: A Single Medical Center Experience in Taiwan. Journal of Personalized Medicine. 12(5). 817–817. 1 indexed citations
7.
Lin, Hsiang‐Yu, Chih‐Kuang Chuang, Chung‐Lin Lee, et al.. (2020). Cardiac Evaluation Using Two-Dimensional Speckle-Tracking Echocardiography and Conventional Echocardiography in Taiwanese Patients with Mucopolysaccharidoses. Diagnostics. 10(2). 62–62. 10 indexed citations
8.
Lin, Hsiang‐Yu, Chih‐Kuang Chuang, Chung‐Lin Lee, et al.. (2018). Mucopolysaccharidosis III in Taiwan: Natural history, clinical and molecular characteristics of 28 patients diagnosed during a 21‐year period. American Journal of Medical Genetics Part A. 176(9). 1799–1809. 23 indexed citations
9.
Huang, Wei-Hsin, et al.. (2016). Study of seven single-nucleotide polymorphisms identified in East Asians for association with obesity in a Taiwanese population. BMJ Open. 6(8). e011713–e011713. 11 indexed citations
10.
Lin, Hsiang‐Yu, Chih‐Kuang Chuang, Chung‐Lieh Hung, et al.. (2016). Cardiac structure and function and effects of enzyme replacement therapy in patients with mucopolysaccharidoses I, II, IVA and VI. Molecular Genetics and Metabolism. 117(4). 431–437. 34 indexed citations
11.
Lin, Hsiang‐Yu, et al.. (2014). Cardiovascular abnormalities in Taiwanese patients with mucopolysaccharidosis. Molecular Genetics and Metabolism. 111(4). 493–498. 26 indexed citations
12.
Lin, Hsiang‐Yu, et al.. (2013). Prevention of necrotizing enterocolitis in preterm very low birth weight infants: Is it feasible?. Journal of the Formosan Medical Association. 113(8). 490–497. 33 indexed citations
13.
Lin, Hsiang‐Yu, Shou‐Chuan Shih, Chih‐Kuang Chuang, et al.. (2013). Assessment of bone mineral density by dual energy x-ray absorptiometry in patients with mucopolysaccharidoses. Orphanet Journal of Rare Diseases. 8(1). 71–71. 32 indexed citations
14.
Lin, Hsiang‐Yu, Ming‐Ren Chen, Chih‐Kuang Chuang, et al.. (2010). Enzyme replacement therapy for mucopolysaccharidosis VI—experience in Taiwan. Journal of Inherited Metabolic Disease. 33(S3). 421–427. 23 indexed citations
15.
Lin, Hsiang‐Yu, Chih‐Kuang Chuang, Dau‐Ming Niu, et al.. (2009). Incidence of the mucopolysaccharidoses in Taiwan, 1984–2004. American Journal of Medical Genetics Part A. 149A(5). 960–964. 150 indexed citations
16.
Lin, Hsiang‐Yu, Shuan‐Pei Lin, Chih‐Kuang Chuang, Ming‐Ren Chen, & Chia-Ying Chang. (2008). Intravenous Pamidronate Therapy in Taiwanese Patients with Osteogenesis Imperfecta. Pediatrics & Neonatology. 49(5). 161–165. 9 indexed citations
17.
Chang, Chia-Ying, Shuan‐Pei Lin, Hsiang‐Yu Lin, et al.. (2008). X-linked Myotubular Myopathy with a Novel MTM1 Mutation in a Taiwanese Child. Journal of the Formosan Medical Association. 107(12). 965–970. 2 indexed citations
18.
Lin, Hsiang‐Yu, Chang‐Shi Chen, Jing‐Ru Weng, & Ching‐Shih Chen. (2006). Targeting histone deacetylase in cancer therapy. Medicinal Research Reviews. 26(4). 397–413. 213 indexed citations
19.
Tsai, Fuu‐Jen, Chang‐Hai Tsai, Ching‐Tien Peng, et al.. (1999). Molecular Diagnosis of Apert Syndrome in Chinese Patients. 40(1). 31–33. 4 indexed citations
20.
Zielenski, Julian, D. Markiewicz, Hsiang‐Yu Lin, et al.. (1995). Skipping of exon 12 as a consequence of a point mutation (1898 + 5G → T) in the cystic fibrosis transmembrane conductance regulator gene found in a consanguineous Chinese family. Clinical Genetics. 47(3). 125–132. 30 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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