Chi‐Ren Tsai

1.6k total citations
54 papers, 1.2k citations indexed

About

Chi‐Ren Tsai is a scholar working on Molecular Biology, Clinical Biochemistry and Pulmonary and Respiratory Medicine. According to data from OpenAlex, Chi‐Ren Tsai has authored 54 papers receiving a total of 1.2k indexed citations (citations by other indexed papers that have themselves been cited), including 26 papers in Molecular Biology, 16 papers in Clinical Biochemistry and 9 papers in Pulmonary and Respiratory Medicine. Recurrent topics in Chi‐Ren Tsai's work include Metabolism and Genetic Disorders (16 papers), Mitochondrial Function and Pathology (10 papers) and Genomics and Rare Diseases (5 papers). Chi‐Ren Tsai is often cited by papers focused on Metabolism and Genetic Disorders (16 papers), Mitochondrial Function and Pathology (10 papers) and Genomics and Rare Diseases (5 papers). Chi‐Ren Tsai collaborates with scholars based in Taiwan, United States and United Kingdom. Chi‐Ren Tsai's co-authors include Ching‐Shiang Chi, Hsiu-Fen Lee, Huei‐Jane Lee, Chin‐Chan Lee, Chiao‐Yin Sun, Heng-Jung Hsu, Mai-Szu Wu, I‐Wen Wu, Liang‐Jen Wang and Chia‐Chi Chou and has published in prestigious journals such as Journal of Clinical Oncology, PLoS ONE and Clinical Infectious Diseases.

In The Last Decade

Chi‐Ren Tsai

53 papers receiving 1.2k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Chi‐Ren Tsai Taiwan 22 431 279 196 172 137 54 1.2k
Shigehiko Kamoshita Japan 22 837 1.9× 188 0.7× 176 0.9× 262 1.5× 146 1.1× 103 2.1k
Christian J. Hendriksz United Kingdom 34 644 1.5× 426 1.5× 152 0.8× 1.0k 6.0× 102 0.7× 135 3.7k
Ina Knerr Germany 29 808 1.9× 626 2.2× 127 0.6× 178 1.0× 123 0.9× 110 2.5k
Peter J. Stahl United States 23 402 0.9× 159 0.6× 78 0.4× 40 0.2× 37 0.3× 60 1.4k
Zhejun Cai China 27 771 1.8× 45 0.2× 323 1.6× 217 1.3× 54 0.4× 52 1.9k
Pranesh Chakraborty Canada 27 802 1.9× 511 1.8× 198 1.0× 197 1.1× 59 0.4× 100 2.0k
Martina Huemer Austria 26 855 2.0× 1.3k 4.5× 85 0.4× 241 1.4× 78 0.6× 74 2.4k
Arnold H. Slyper United States 18 401 0.9× 127 0.5× 48 0.2× 105 0.6× 89 0.6× 42 1.3k
Daniel L. Metzger Canada 29 649 1.5× 29 0.1× 135 0.7× 171 1.0× 196 1.4× 82 2.5k
Masahiko Kawai Japan 21 436 1.0× 108 0.4× 274 1.4× 81 0.5× 104 0.8× 136 1.7k

Countries citing papers authored by Chi‐Ren Tsai

Since Specialization
Citations

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

Fields of papers citing papers by Chi‐Ren Tsai

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Chi‐Ren Tsai. 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 Chi‐Ren Tsai. The network helps show where Chi‐Ren Tsai may publish in the future.

Co-authorship network of co-authors of Chi‐Ren Tsai

This figure shows the co-authorship network connecting the top 25 collaborators of Chi‐Ren Tsai. A scholar is included among the top collaborators of Chi‐Ren Tsai 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 Chi‐Ren Tsai. Chi‐Ren Tsai 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.
Chi, Ching‐Shiang, et al.. (2025). Genotype–phenotype variations in PURA syndrome: Asian and non-Asian perspectives from a systematic review. Orphanet Journal of Rare Diseases. 20(1). 376–376.
2.
Chi, Ching‐Shiang, Chi‐Ren Tsai, & Hsiu-Fen Lee. (2024). Resolving unsolved whole-genome sequencing data in paediatric neurological disorders: a cohort study. Archives of Disease in Childhood. 109(9). 730–735. 2 indexed citations
3.
Chi, Ching‐Shiang, Chi‐Ren Tsai, & Hsiu-Fen Lee. (2023). Biallelic SHQ1 variants in early infantile hypotonia and paroxysmal dystonia as the leading manifestation. Human Genetics. 142(8). 1029–1041. 5 indexed citations
4.
Lee, Hsiu-Fen, Ching‐Shiang Chi, & Chi‐Ren Tsai. (2020). Electroclinical variability of pyridoxine-dependent epilepsy caused by ALDH7A1 gene mutations in four Taiwanese children. Brain and Development. 42(5). 393–401. 4 indexed citations
5.
Tsai, Chi‐Ren, et al.. (2018). Antisense oligonucleotides modulate dopa decarboxylase function in aromatic l-amino acid decarboxylase deficiency. Human Mutation. 39(12). 2072–2082. 5 indexed citations
6.
Lee, Hsiu-Fen, et al.. (2015). Late infantile metachromatic leukodystrophy: Clinical manifestations of five Taiwanese patients and Genetic features in Asia. Orphanet Journal of Rare Diseases. 10(1). 144–144. 21 indexed citations
7.
Tseng, Jeng‐Sen, Chih‐Liang Wang, Ming‐Shyan Huang, et al.. (2014). Impact of EGFR Mutation Detection Methods on the Efficacy of Erlotinib in Patients with Advanced EGFR-Wild Type Lung Adenocarcinoma. PLoS ONE. 9(9). e107160–e107160. 11 indexed citations
8.
Wang, Liang‐Jen, Mai-Szu Wu, Heng-Jung Hsu, et al.. (2012). The Relationship between Psychological Factors, Inflammation, and Nutrition in Patients with Chronic Renal Failure Undergoing Hemodialysis. The International Journal of Psychiatry in Medicine. 44(2). 105–118. 33 indexed citations
9.
Chi, Ching‐Shiang, Hsiu-Fen Lee, & Chi‐Ren Tsai. (2012). Tyrosine Hydroxylase Deficiency in Taiwanese Infants. Pediatric Neurology. 46(2). 77–82. 21 indexed citations
10.
Chi, Ching‐Shiang, et al.. (2011). Lactate peak on brain MRS in children with syndromic mitochondrial diseases. Journal of the Chinese Medical Association. 74(7). 305–309. 24 indexed citations
11.
Lee, Hsiu-Fen, et al.. (2011). Epileptic Seizures in Infants and Children With Mitochondrial Diseases. Pediatric Neurology. 45(3). 169–174. 16 indexed citations
12.
Chi, Ching‐Shiang, Hsiu-Fen Lee, Chi‐Ren Tsai, Huei‐Jane Lee, & Lianghui Chen. (2010). Clinical Manifestations in Children With Mitochondrial Diseases. Pediatric Neurology. 43(3). 183–189. 14 indexed citations
13.
Wang, Jiaan‐Der, et al.. (2010). Clinical Features and Therapeutic Response in Taiwanese Children With Wilson's Disease: 12 Years of Experience in a Single Center. Pediatrics & Neonatology. 51(2). 124–129. 12 indexed citations
14.
Li, Jieyuan, Chia‐Chi Hsu, & Chi‐Ren Tsai. (2009). Spinocerebellar variant of adrenoleukodystrophy with a novel ABCD1 gene mutation. Journal of the Neurological Sciences. 290(1-2). 163–165. 13 indexed citations
15.
Lee, Hsiu-Fen, Chi‐Ren Tsai, Ching‐Shiang Chi, Huei‐Jane Lee, & Clayton Chi‐Chang Chen. (2009). Leigh Syndrome: Clinical and Neuroimaging Follow-Up. Pediatric Neurology. 40(2). 88–93. 61 indexed citations
16.
Chen, Po‐Yen, et al.. (2008). Do Serological Tests Provide Adequate Rapid Diagnosis of <i>Mycoplasma pneumoniae</i> Infection?. Japanese Journal of Infectious Diseases. 61(5). 397–399. 9 indexed citations
17.
Shu, San‐Ging, et al.. (2006). Seventeen Alpha-hydroxylase Deficiency. Journal of the Formosan Medical Association. 105(2). 177–181. 22 indexed citations
18.
Kuan, Yu‐Hsiang, Ruey‐Hseng Lin, Hui‐Yi Lin, et al.. (2006). Activation of phosphoinositide 3-kinase and Src family kinase is required for respiratory burst in rat neutrophils stimulated with artocarpol A. Biochemical Pharmacology. 71(12). 1735–1746. 8 indexed citations
19.
Chang, Tung‐Ming, Ching‐Shiang Chi, Chi‐Ren Tsai, Hsiu-Fen Lee, & Mu‐Chun Li. (2004). Paralytic ileus in MELAS with phenotypic features of MNGIE. Pediatric Neurology. 31(5). 374–377. 24 indexed citations
20.
Chi, Ching‐Shiang, et al.. (2000). New mutations of the HPRT gene in Lesch-Nyhan syndrome. Pediatric Neurology. 23(4). 332–335. 23 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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