Tso‐Ren Wang

449 total citations
37 papers, 313 citations indexed

About

Tso‐Ren Wang is a scholar working on Genetics, Molecular Biology and Clinical Biochemistry. According to data from OpenAlex, Tso‐Ren Wang has authored 37 papers receiving a total of 313 indexed citations (citations by other indexed papers that have themselves been cited), including 16 papers in Genetics, 12 papers in Molecular Biology and 9 papers in Clinical Biochemistry. Recurrent topics in Tso‐Ren Wang's work include Metabolism and Genetic Disorders (9 papers), Genomic variations and chromosomal abnormalities (5 papers) and Lysosomal Storage Disorders Research (5 papers). Tso‐Ren Wang is often cited by papers focused on Metabolism and Genetic Disorders (9 papers), Genomic variations and chromosomal abnormalities (5 papers) and Lysosomal Storage Disorders Research (5 papers). Tso‐Ren Wang collaborates with scholars based in Taiwan. Tso‐Ren Wang's co-authors include Wuh‐Liang Hwu, Jia‐Woei Hou, Pen‐Jung Wang, Guey‐Jen Lee‐Chen, Mei‐Hwei Chang, Chuan‐Liang Kao, Hey‐Chi Hsu, Chin‐Yun Lee, Kuo‐Inn Tsou Yau and Yu‐Zen Shen and has published in prestigious journals such as Human Molecular Genetics, SLEEP and Journal of Medical Genetics.

In The Last Decade

Tso‐Ren Wang

36 papers receiving 300 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Tso‐Ren Wang Taiwan 12 96 92 62 55 52 37 313
Luis González Gutiérrez-Solana Spain 12 155 1.6× 54 0.6× 87 1.4× 194 3.5× 38 0.7× 59 458
M. Tardieu France 11 217 2.3× 26 0.3× 110 1.8× 118 2.1× 48 0.9× 36 424
Anke Schumann Germany 11 179 1.9× 64 0.7× 149 2.4× 75 1.4× 37 0.7× 32 379
Charlotte Thiels Germany 11 225 2.3× 46 0.5× 40 0.6× 66 1.2× 20 0.4× 25 399
Léna Damaj France 11 186 1.9× 109 1.2× 108 1.7× 71 1.3× 80 1.5× 19 479
Juan Francisco Cabello Chile 11 86 0.9× 30 0.3× 107 1.7× 126 2.3× 35 0.7× 32 287
Thatjana Gardeitchik Netherlands 13 233 2.4× 162 1.8× 105 1.7× 78 1.4× 27 0.5× 19 419
Danijela Petković Ramadža Croatia 9 134 1.4× 49 0.5× 118 1.9× 103 1.9× 24 0.5× 26 280
Sabine Grønborg Denmark 11 207 2.2× 69 0.8× 74 1.2× 64 1.2× 42 0.8× 25 330
Merçè Pineda Spain 13 302 3.1× 78 0.8× 300 4.8× 43 0.8× 85 1.6× 19 562

Countries citing papers authored by Tso‐Ren Wang

Since Specialization
Citations

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

Fields of papers citing papers by Tso‐Ren Wang

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Tso‐Ren Wang

This figure shows the co-authorship network connecting the top 25 collaborators of Tso‐Ren Wang. A scholar is included among the top collaborators of Tso‐Ren 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 Tso‐Ren Wang. Tso‐Ren 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.
Chien, Yin‐Hsiu, Shu-Chuan Chiang, Ai-Chu Huang, et al.. (2005). Phenylalanine hydroxylase deficiency: intelligence of patients after early dietary treatment.. PubMed. 45(6). 320–3. 4 indexed citations
2.
Chiang, Shu‐Chuan, Yu‐May Lee, Tso‐Ren Wang, & Wuh‐Liang Hwu. (1999). Allele distribution at the FMR1 locus in the general Chinese population. Clinical Genetics. 55(5). 353–356. 11 indexed citations
3.
Lu, Frank Leigh, Pen‐Jung Wang, Wuh‐Liang Hwu, Kuo‐Inn Tsou Yau, & Tso‐Ren Wang. (1999). Neonatal type of nonketotic hyperglycinemia. Pediatric Neurology. 20(4). 295–300. 27 indexed citations
4.
Ko, Tsang‐Ming, Wuh‐Liang Hwu, Yuwan Lin, et al.. (1999). Molecular genetic study of Pompe disease in Chinese patients in Taiwan. Human Mutation. 13(5). 380–380. 2 indexed citations
5.
Tsai, Fuu‐Jen, Wuh‐Liang Hwu, Shuan-Pei Lin, et al.. (1998). Two common mutations 934C to G and 937C to G of fibroblast growth factor receptor 2 (FGFR2) gene in Chinese patients with apert syndrome. Human Mutation. 11(S1). S18–S19. 1 indexed citations
6.
Wang, Pen‐Jung, Wuh‐Liang Hwu, Wang‐Tso Lee, Tso‐Ren Wang, & Yu‐Zen Shen. (1997). Duplication of proteolipid protein gene: A possible major cause of Pelizaeus-Merzbacher disease. Pediatric Neurology. 17(2). 125–128. 20 indexed citations
7.
Lin, Jiuann‐Huey, Mei‐Hwei Chang, Ru‐Jeng Teng, Kuo‐Inn Tsou Yau, & Tso‐Ren Wang. (1997). Congenital short bowel syndrome with left acheiria: report of one case.. PubMed. 38(5). 393–5. 2 indexed citations
8.
Hwu, Wuh‐Liang, et al.. (1996). Arylsulfatase A pseudodeficiency in Chinese. Human Genetics. 97(2). 148–149. 4 indexed citations
9.
Lu, Chun‐Yi, Jia‐Woei Hou, Pen‐Jung Wang, Hsiu‐Hui Chiu, & Tso‐Ren Wang. (1996). Homocystinuria presenting as fatal common carotid artery occlusion. Pediatric Neurology. 15(2). 159–162. 14 indexed citations
10.
Hwu, Wuh‐Liang, et al.. (1995). Glucose-6-phosphatase gene G327A mutation is common in Chinese patients with glycogen storage disease type la. Human Molecular Genetics. 4(6). 1095–1096. 23 indexed citations
11.
Wang, Tso‐Ren, et al.. (1995). Galloway‐Mowat syndrome in Taiwan. American Journal of Medical Genetics. 58(3). 245–248. 14 indexed citations
12.
Hou, Jia‐Woei & Tso‐Ren Wang. (1995). Molecular cytogenetic studies of duplication 9q32→q34.3 inserted into 9q13. Clinical Genetics. 48(3). 148–150. 12 indexed citations
13.
Hou, Jia‐Woei & Tso‐Ren Wang. (1995). Transient tyrosinemia presenting as lactic acidosis in a term baby: report of one case.. PubMed. 36(3). 217–20. 1 indexed citations
14.
Wang‐Wuu, Sheng, et al.. (1994). Cytogenetic study of mentally retarded children in Taipei. Journal of Biomedical Science. 1(2). 100–104. 8 indexed citations
15.
Wang, Tso‐Ren, Wuh‐Liang Hwu, Jia Hou, Shih‐Jie Chou, & Christina Liu. (1993). Fragile-X mental retardation--a combination of cytogenetic and molecular approaches, with greater emphasis on DNA analysis.. PubMed. 34(2). 105–12. 1 indexed citations
16.
Chuang, Lee‐Ming, et al.. (1991). Esterase D and retinoblastoma gene loci are tightly linked to Wilson's disease in Chinese pedigrees from Taiwan. Human Genetics. 87(4). 465–8. 12 indexed citations
17.
Wuu, Kuang-Dong, Shuan‐Yow Li, Jia‐Yuh Chen, et al.. (1991). Chromosomal and biochemical screening on mentally retarded school children in Taiwan. The Japanese Journal of Human Genetics. 36(3). 267–274. 13 indexed citations
18.
Teng, Ru‐Jeng, Pen‐Jung Wang, Tso‐Ren Wang, & Yu‐Zen Shen. (1989). Apert syndrome associated with septo-optic dysplasia. Pediatric Neurology. 5(6). 384–388. 9 indexed citations
19.
Wang, Tso‐Ren, Shio‐Jean Lin, John M. Opitz, & James F. Reynolds. (1987). Further evidence for genetic heterogeneity of whistling face or Freeman‐Sheldon syndrome in a Chinese family. American Journal of Medical Genetics. 28(2). 471–475. 12 indexed citations
20.
Chang, Mei‐Hwei, Hey‐Chi Hsu, Chin‐Yun Lee, Tso‐Ren Wang, & Chuan‐Liang Kao. (1987). Neonatal Hepatitis. Journal of Pediatric Gastroenterology and Nutrition. 6(2). 203–207. 33 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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