Chee Seng Ku

754 total citations
6 papers, 472 citations indexed

About

Chee Seng Ku is a scholar working on Genetics, Cancer Research and Molecular Biology. According to data from OpenAlex, Chee Seng Ku has authored 6 papers receiving a total of 472 indexed citations (citations by other indexed papers that have themselves been cited), including 6 papers in Genetics, 3 papers in Cancer Research and 1 paper in Molecular Biology. Recurrent topics in Chee Seng Ku's work include Genomic variations and chromosomal abnormalities (4 papers), Genomics and Rare Diseases (3 papers) and Cancer Genomics and Diagnostics (3 papers). Chee Seng Ku is often cited by papers focused on Genomic variations and chromosomal abnormalities (4 papers), Genomics and Rare Diseases (3 papers) and Cancer Genomics and Diagnostics (3 papers). Chee Seng Ku collaborates with scholars based in Sweden, Singapore and Greece. Chee Seng Ku's co-authors include Yudi Pawitan, Kee Seng Chia, En Yun Loy, Shu Mei Teo, Agus Salim, Nasheen Naidoo, Mikael Hartman, D.N. Cooper, Dimosthenis Ziogas and Margaret Tzaphlidou and has published in prestigious journals such as Bioinformatics, The Lancet Oncology and Human Genetics.

In The Last Decade

Chee Seng Ku

6 papers receiving 465 citations

Peers

Chee Seng Ku

GENET

MB

CR

PS

EPIDE

Rajini Haraksingh United States

Adrian Tan Singapore

Laura A. Crinnion United Kingdom

S. Krithika India

H. Shuen Lo United States

Eddie Cano-Gamez United Kingdom

Yi‐Liang Wei China

Pauline A. Fujita United States

Yuanxin Ye China

Rajini Haraksingh United States

Chee Seng Ku

217 ×0.7

GENET

245 ×1.2

MB

96 ×0.9

CR

59 ×1.3

PS

11 ×0.5

EPIDE

Citations per year, relative to Chee Seng Ku Chee Seng Ku (= 1×) peers Rajini Haraksingh

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

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6 of 6 papers shown

1.

Ku, Chee Seng, et al.. (2012). Research and clinical applications of cancer genome sequencing. Current Opinion in Obstetrics & Gynecology. 25(1). 3–10. 8 indexed citations

2.

Teo, Shu Mei, Yudi Pawitan, Chee Seng Ku, Kee Seng Chia, & Agus Salim. (2012). Statistical challenges associated with detecting copy number variations with next-generation sequencing. Bioinformatics. 28(21). 2711–2718. 155 indexed citations

3.

Ku, Chee Seng, En Yun Loy, Agus Salim, Yudi Pawitan, & Kee Seng Chia. (2010). The discovery of human genetic variations and their use as disease markers: past, present and future. Journal of Human Genetics. 55(7). 403–415. 69 indexed citations

4.

Hartman, Mikael, En Yun Loy, Chee Seng Ku, & Kee Seng Chia. (2010). Molecular epidemiology and its current clinical use in cancer management. The Lancet Oncology. 11(4). 383–390. 33 indexed citations

5.

Ku, Chee Seng, Nasheen Naidoo, Shu Mei Teo, & Yudi Pawitan. (2010). Regions of homozygosity and their impact on complex diseases and traits. Human Genetics. 129(1). 1–15. 76 indexed citations

6.

Ku, Chee Seng, En Yun Loy, Yudi Pawitan, & Kee Seng Chia. (2010). The pursuit of genome-wide association studies: where are we now?. Journal of Human Genetics. 55(4). 195–206. 131 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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