Tsang‐Ming Ko
Impact in
- Genetics top 2%
- Neurogenetic and Muscular Disorders Research
- Hemoglobinopathies and Related Disorders
- Forensic and Genetic Research
- Genomic variations and chromosomal abnormalities
- Sensory Systems top 5%
- Hearing, Cochlea, Tinnitus, Genetics
Papers in
- Genetics 34
- Genomic variations and chromosomal abnormalities 19
- Hemoglobinopathies and Related Disorders 13
- Forensic and Genetic Research 8
- Neurogenetic and Muscular Disorders Research 5
-
- Prenatal Screening and Diagnostics 24
- Fetal and Pediatric Neurological Disorders 5
- Co-authors
- Hsiao‐Lin Hwa (23 shared papers)Li‐Hui Tseng (20 shared papers)Fon‐Jou Hsieh (12 shared papers)Chien‐Hao Huang (7 shared papers)Chih‐Ping Chen (29 shared papers)Wayseen Wang (28 shared papers)Tzu‐Yao Lee (5 shared papers)Wuh‐Liang Hwu (4 shared papers)
- Journals
- Prenatal Diagnosis (12 papers)Human Genetics (3 papers)International Journal of Legal Medicine (3 papers)Taiwanese Journal of Obstetrics and Gynecology (26 papers)Human Mutation (2 papers)
- Partner nations
- TaiwanUnited StatesChina
In The Last Decade
Tsang‐Ming Ko
81 papers receiving 1.3k citations
Peers
Comparison fields: 5 of 93
- Genetics 351
- Sensory Systems 94
- Pediatrics, Perinatology and Child Health 314
- Genetics 384
- Hepatology 66
Countries citing papers authored by Tsang‐Ming Ko
This map shows the geographic impact of Tsang‐Ming Ko'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 Tsang‐Ming Ko with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Tsang‐Ming Ko more than expected).
Fields of papers citing papers by Tsang‐Ming Ko
This network shows the impact of papers produced by Tsang‐Ming Ko. 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 Tsang‐Ming Ko. The network helps show where Tsang‐Ming Ko may publish in the future.
Co-authors
The 25 scholars most cited alongside Tsang‐Ming Ko, 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 85 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 2017 | 121 | |
| 2 | 2001 | 103 | |
| 3 | 2003 | 101 | |
| 4 | 1984 | 90 | |
| 5 | 1991 | 60 | |
| 6 | 1999 | 53 | |
| 7 | 2007 | 51 | |
| 8 | 1992 | 44 | |
| 9 | 1999 | 38 | |
| 10 | 1994 | 34 | |
| 11 | 2007 | 33 | |
| 12 | 2016 | 30 | |
| 13 | 2018 | 25 | |
| 14 | 1998 | 22 | |
| 15 | 1995 | 21 | |
| 16 | 1993 | 20 | |
| 17 | 2013 | 19 | |
| 18 | 2020 | 18 | |
| 19 | 1994 | 17 | |
| 20 | 1993 | 16 |
About Tsang‐Ming Ko
Tsang‐Ming Ko is a scholar working on Genetics, Pediatrics, Perinatology and Child Health, Molecular Biology, Genetics and Epidemiology, having authored 85 papers that have together received 1.4k indexed citations. Recurring topics across this work include Prenatal Screening and Diagnostics (24 papers), Genomic variations and chromosomal abnormalities (19 papers), Hemoglobinopathies and Related Disorders (13 papers), Forensic and Genetic Research (8 papers), Fetal and Pediatric Neurological Disorders (5 papers), Neurogenetic and Muscular Disorders Research (5 papers), Molecular Biology Techniques and Applications (5 papers) and Parvovirus B19 Infection Studies (4 papers). The work is most often cited by research in Genetics (351 citations), Sensory Systems (94 citations), Pediatrics, Perinatology and Child Health (314 citations), Genetics (384 citations) and Hepatology (66 citations). Tsang‐Ming Ko has collaborated with scholars based in Taiwan, United States and China. Frequent co-authors include Hsiao‐Lin Hwa, Li‐Hui Tseng, Fon‐Jou Hsieh, Chien‐Hao Huang, Chih‐Ping Chen, Wayseen Wang, Tzu‐Yao Lee, Wuh‐Liang Hwu, Schu‐Rern Chern and Yuh‐Jyh Jong. Their work appears in journals such as Prenatal Diagnosis, Human Genetics, International Journal of Legal Medicine, Taiwanese Journal of Obstetrics and Gynecology and Human Mutation.
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.