Chee‐Seng Ku

1.2k total citations
14 papers, 661 citations indexed

About

Chee‐Seng Ku is a scholar working on Genetics, Molecular Biology and Pathology and Forensic Medicine. According to data from OpenAlex, Chee‐Seng Ku has authored 14 papers receiving a total of 661 indexed citations (citations by other indexed papers that have themselves been cited), including 13 papers in Genetics, 5 papers in Molecular Biology and 3 papers in Pathology and Forensic Medicine. Recurrent topics in Chee‐Seng Ku's work include Genomics and Rare Diseases (10 papers), Genomic variations and chromosomal abnormalities (9 papers) and Genetic Associations and Epidemiology (3 papers). Chee‐Seng Ku is often cited by papers focused on Genomics and Rare Diseases (10 papers), Genomic variations and chromosomal abnormalities (9 papers) and Genetic Associations and Epidemiology (3 papers). Chee‐Seng Ku collaborates with scholars based in Singapore, Sweden and United Kingdom. Chee‐Seng Ku's co-authors include Nasheen Naidoo, Yudi Pawitan, D.N. Cooper, Richie Soong, Mengchu Wu, Constantin Polychronakos, Edmund J.D. Lee, Mark Seielstad, Kee‐Seng Chia and Xueling Sim and has published in prestigious journals such as Annals of Neurology, Genome Research and Molecular Psychiatry.

In The Last Decade

Chee‐Seng Ku

14 papers receiving 643 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Chee‐Seng Ku Singapore 11 402 295 105 74 41 14 661
Bartolomeo Augello Italy 18 199 0.5× 439 1.5× 62 0.6× 83 1.1× 80 2.0× 33 882
Raili Ermel Estonia 6 357 0.9× 416 1.4× 73 0.7× 25 0.3× 19 0.5× 7 668
Wanda E. Filipiak United States 8 234 0.6× 407 1.4× 34 0.3× 71 1.0× 39 1.0× 11 906
Ruben van’t Slot Netherlands 12 316 0.8× 225 0.8× 48 0.5× 37 0.5× 38 0.9× 16 691
Jenny Lord United Kingdom 16 409 1.0× 410 1.4× 67 0.6× 50 0.7× 30 0.7× 33 813
Nusrat Rabbee United States 9 241 0.6× 207 0.7× 36 0.3× 41 0.6× 58 1.4× 17 648
Kit San Yeung Hong Kong 13 245 0.6× 252 0.9× 30 0.3× 49 0.7× 32 0.8× 29 529
Eric Bareke Canada 14 167 0.4× 403 1.4× 129 1.2× 41 0.6× 57 1.4× 42 639
Yuan Wei China 14 169 0.4× 229 0.8× 31 0.3× 56 0.8× 55 1.3× 37 585

Countries citing papers authored by Chee‐Seng Ku

Since Specialization
Citations

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

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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-authorship network of co-authors of Chee‐Seng Ku

This figure shows the co-authorship network connecting the top 25 collaborators of Chee‐Seng Ku. A scholar is included among the top collaborators of Chee‐Seng Ku 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 Chee‐Seng Ku. Chee‐Seng Ku is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

14 of 14 papers shown
1.
Ku, Chee‐Seng, D.N. Cooper, & George P. Patrinos. (2016). The Rise and Rise of Exome Sequencing. Public Health Genomics. 19(6). 315–324. 13 indexed citations
2.
Ku, Chee‐Seng, Eng King Tan, & D.N. Cooper. (2013). From the periphery to centre stage: de novo single nucleotide variants play a key role in human genetic disease. Journal of Medical Genetics. 50(4). 203–211. 27 indexed citations
3.
Ku, Chee‐Seng, Constantin Polychronakos, Eng‐King Tan, et al.. (2012). A new paradigm emerges from the study of de novo mutations in the context of neurodevelopmental disease. Molecular Psychiatry. 18(2). 141–153. 65 indexed citations
4.
Ku, Chee‐Seng, D.N. Cooper, Mengchu Wu, et al.. (2012). Gene discovery in familial cancer syndromes by exome sequencing: prospects for the elucidation of familial colorectal cancer type X. Modern Pathology. 25(8). 1055–1068. 28 indexed citations
5.
Ku, Chee‐Seng, Mengchu Wu, D.N. Cooper, et al.. (2012). Technological advances in DNA sequence enrichment and sequencing for germline genetic diagnosis. Expert Review of Molecular Diagnostics. 12(2). 159–173. 12 indexed citations
6.
Ku, Chee‐Seng, Mengchu Wu, D.N. Cooper, et al.. (2012). Exome versus transcriptome sequencing in identifying coding region variants. Expert Review of Molecular Diagnostics. 12(3). 241–251. 38 indexed citations
7.
Ku, Chee‐Seng, Nasheen Naidoo, & Yudi Pawitan. (2011). Revisiting Mendelian disorders through exome sequencing. Human Genetics. 129(4). 351–370. 154 indexed citations
8.
Ku, Chee‐Seng, Shu Mei Teo, Nasheen Naidoo, et al.. (2011). Copy number polymorphisms in new HapMap III and Singapore populations. Journal of Human Genetics. 56(8). 552–560. 1 indexed citations
9.
Naidoo, Nasheen, Yudi Pawitan, Richie Soong, D.N. Cooper, & Chee‐Seng Ku. (2011). Human genetics and genomics a decade after the release of the draft sequence of the human genome. Human Genomics. 5(6). 577–577. 59 indexed citations
10.
Ku, Chee‐Seng, D.N. Cooper, Constantin Polychronakos, et al.. (2011). Exome sequencing: Dual role as a discovery and diagnostic tool. Annals of Neurology. 71(1). 5–14. 109 indexed citations
11.
Teo, Shu Mei, Chee‐Seng Ku, Agus Salim, et al.. (2011). Regions of homozygosity in three Southeast Asian populations. Journal of Human Genetics. 57(2). 101–108. 5 indexed citations
12.
Teo, Shu Mei, Chee‐Seng Ku, Nasheen Naidoo, et al.. (2011). A population-based study of copy number variants and regions of homozygosity in healthy Swedish individuals. Journal of Human Genetics. 56(7). 524–533. 9 indexed citations
13.
Ku, Chee‐Seng, Yudi Pawitan, Xueling Sim, et al.. (2010). Genomic copy number variations in three Southeast Asian populations. Human Mutation. 31(7). 851–857. 21 indexed citations
14.
Teo, Yik‐Ying, Xueling Sim, Rick Twee‐Hee Ong, et al.. (2009). Singapore Genome Variation Project: A haplotype map of three Southeast Asian populations. Genome Research. 19(11). 2154–2162. 120 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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