Chee‐Seng Ku
Impact in
- Genetics top 5%
- Genomics and Rare Diseases
- Genomic variations and chromosomal abnormalities
- Genetic Associations and Epidemiology
- Genetics and Neurodevelopmental Disorders
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- Cancer Genomics and Diagnostics
Papers in
- Genetics 13
- Genomics and Rare Diseases 10
- Genomic variations and chromosomal abnormalities 9
- Genetic Associations and Epidemiology 3
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- Congenital heart defects research 2
- Genomics and Chromatin Dynamics 2
- Co-authors
- Nasheen Naidoo (9 shared papers)Yudi Pawitan (10 shared papers)D.N. Cooper (8 shared papers)Richie Soong (5 shared papers)Mengchu Wu (4 shared papers)Constantin Polychronakos (2 shared papers)Yik‐Ying Teo (3 shared papers)Xueling Sim (3 shared papers)
- Journals
- Expert Review of Molecular Diagnostics (2 papers)Annals of Neurology (1 paper)Human Mutation (1 paper)Human Genomics (1 paper)Human Genetics (1 paper)
- Partner nations
- SingaporeSwedenUnited Kingdom
In The Last Decade
Chee‐Seng Ku
14 papers receiving 646 citations
Peers
Comparison fields: 5 of 70
- Genetics 371
- Cancer Research 85
- Pathology and Forensic Medicine 64
- Molecular Biology 248
- Genetics 23
Countries citing papers authored by Chee‐Seng Ku
This map shows the geographic impact of Chee‐Seng Ku'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 Chee‐Seng Ku with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Chee‐Seng Ku more than expected).
Fields of papers citing papers by Chee‐Seng Ku
This network shows the impact of papers produced by Chee‐Seng Ku. 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 Chee‐Seng Ku. The network helps show where Chee‐Seng Ku may publish in the future.
Co-authors
The 25 scholars most cited alongside Chee‐Seng Ku, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.
All Works
| # | Work | ||
|---|---|---|---|
| 1 | 2011 | 154 | |
| 2 | 2009 | 122 | |
| 3 | 2011 | 110 | |
| 4 | 2012 | 64 | |
| 5 | 2011 | 58 | |
| 6 | 2012 | 38 | |
| 7 | 2013 | 28 | |
| 8 | 2012 | 28 | |
| 9 | 2010 | 21 | |
| 10 | 2016 | 13 | |
| 11 | 2012 | 12 | |
| 12 | 2011 | 9 | |
| 13 | 2011 | 5 | |
| 14 | 2011 | 1 |
About Chee‐Seng Ku
Chee‐Seng Ku is a scholar working on Genetics, Molecular Biology, Pathology and Forensic Medicine, Pediatrics, Perinatology and Child Health and Cancer Research, having authored 14 papers that have together received 663 indexed citations. Recurring topics across this work include Genomics and Rare Diseases (10 papers), Genomic variations and chromosomal abnormalities (9 papers), Cancer Genomics and Diagnostics (3 papers), Prenatal Screening and Diagnostics (3 papers), Genetic factors in colorectal cancer (3 papers), Genetic Associations and Epidemiology (3 papers), Congenital heart defects research (2 papers) and Genomics and Chromatin Dynamics (2 papers). The work is most often cited by research in Genetics (371 citations), Cancer Research (85 citations), Pathology and Forensic Medicine (64 citations), Molecular Biology (248 citations) and Genetics (23 citations). Chee‐Seng Ku has collaborated with scholars based in Singapore, Sweden and United Kingdom. Frequent co-authors include Nasheen Naidoo, Yudi Pawitan, D.N. Cooper, Richie Soong, Mengchu Wu, Constantin Polychronakos, Yik‐Ying Teo, Xueling Sim, Mark Seielstad and Kee‐Seng Chia. Their work appears in journals such as Expert Review of Molecular Diagnostics, Annals of Neurology, Human Mutation, Human Genomics and Human Genetics.
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.