Tso‐Ren Wang
Impact in
- Clinical Biochemistry top 10%
- Metabolism and Genetic Disorders
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- Genetics and Neurodevelopmental Disorders
- Genomic variations and chromosomal abnormalities
Papers in
- Genetics 16
- Genetics and Neurodevelopmental Disorders 5
- Genomic variations and chromosomal abnormalities 5
- Connective tissue disorders research 4
-
- Fibroblast Growth Factor Research 3
- Co-authors
- Wuh‐Liang Hwu (17 shared papers)Jia‐Woei Hou (10 shared papers)Pen‐Jung Wang (6 shared papers)Guey‐Jen Lee‐Chen (1 shared paper)Mei‐Hwei Chang (5 shared papers)Chin‐Yun Lee (2 shared papers)Chuan‐Liang Kao (2 shared papers)Hey‐Chi Hsu (1 shared paper)
- Journals
- Human Mutation (4 papers)Pediatric Neurology (4 papers)Clinical Genetics (2 papers)Human Genetics (2 papers)Journal of Pediatric Gastroenterology and Nutrition (2 papers)
- Partner nations
- Taiwan
In The Last Decade
Tso‐Ren Wang
36 papers receiving 300 citations
Peers
Comparison fields: 5 of 53
- Clinical Biochemistry 62
- Genetics 92
- Rheumatology 47
- Pediatrics, Perinatology and Child Health 52
- Biochemistry 18
Countries citing papers authored by Tso‐Ren Wang
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
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-authors
The 25 scholars most cited alongside Tso‐Ren Wang, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.
All Works
Showing the 20 most-cited of 37 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 1987 | 33 | |
| 2 | 1999 | 27 | |
| 3 | 1997 | 26 | |
| 4 | 1995 | 23 | |
| 5 | 1997 | 20 | |
| 6 | 1996 | 19 | |
| 7 | 1995 | 14 | |
| 8 | 1996 | 14 | |
| 9 | 1991 | 13 | |
| 10 | 1991 | 12 | |
| 11 | 1987 | 12 | |
| 12 | 1995 | 12 | |
| 13 | 1999 | 11 | |
| 14 | Cranial MR spectroscopy of tetrahydrobiopterin deficiency. | 2002 | 10 |
| 15 | 1989 | 9 | |
| 16 | 1994 | 8 | |
| 17 | Carnitine transport defect presenting with hyperammonemia: report of one case. | 2000 | 8 |
| 18 | 1996 | 4 | |
| 19 | Phenylalanine hydroxylase deficiency: intelligence of patients after early dietary treatment. | 2005 | 4 |
| 20 | A 20-year follow-up of a male patient with type Ia glycogen storage disease. | 2003 | 4 |
About Tso‐Ren Wang
Tso‐Ren Wang is a scholar working on Genetics, Molecular Biology, Clinical Biochemistry, Physiology and Rheumatology, having authored 37 papers that have together received 313 indexed citations. Recurring topics across this work include Metabolism and Genetic Disorders (9 papers), Lysosomal Storage Disorders Research (5 papers), Genetics and Neurodevelopmental Disorders (5 papers), Genomic variations and chromosomal abnormalities (5 papers), Connective tissue disorders research (4 papers), Folate and B Vitamins Research (4 papers), Neonatal Health and Biochemistry (3 papers) and Fibroblast Growth Factor Research (3 papers). The work is most often cited by research in Clinical Biochemistry (62 citations), Genetics (92 citations), Rheumatology (47 citations), Pediatrics, Perinatology and Child Health (52 citations) and Biochemistry (18 citations). Tso‐Ren Wang has collaborated with scholars based in Taiwan. Frequent co-authors include Wuh‐Liang Hwu, Jia‐Woei Hou, Pen‐Jung Wang, Guey‐Jen Lee‐Chen, Mei‐Hwei Chang, Chin‐Yun Lee, Chuan‐Liang Kao, Hey‐Chi Hsu, Yu‐Zen Shen and Kuo‐Inn Tsou Yau. Their work appears in journals such as Human Mutation, Pediatric Neurology, Clinical Genetics, Human Genetics and Journal of Pediatric Gastroenterology and Nutrition.
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.