Full Name
KU CHEE SENG
(not current staff)
Variants
Seng, K.C.
Ku, C.-S.
Ku, C.S.
 
 
 
Email
ephkcs@nus.edu.sg
 
 

Publications

Results 1-20 of 21 (Search time: 0.006 seconds).

Issue DateTitleAuthor(s)
1Oct-2012Trametinib plus dabrafenib: Targeting RAS-MAPK pathway for BRAF V600-mutant melanomaKu, C.-S. 
2May-2008The success of the genome-wide association approach: A brief story of a long struggleSeng, K.C. ; Seng, C.K. 
32010The pursuit of genome-wide association studies: Where are we nowKu, C.S. ; Loy, E.Y. ; Chia, K.S. ; Pawitan, Y. 
42010The pursuit of genome-wide association studies: Where are we nowKu, C.S. ; Loy, E.Y. ; Chia, K.S. ; Pawitan, Y.
5Jul-2010The discovery of human genetic variations and their use as disease markers: Past, present and futureKu, C.S. ; Loy, E.Y.; Salim, A. ; Pawitan, Y.; Chia, K.S. 
6May-2012The 'sequence everything' approach and personalized clinical decision challengesKu, C.-S. ; Cooper, D.N.; Roukos, D.H.
7Mar-2012Technological advances in DNA sequence enrichment and sequencing for germline genetic diagnosisKu, C.-S. ; Wu, M. ; Cooper, D.N.; Naidoo, N. ; Pawitan, Y.; Pang, B.; Iacopetta, B.; Soong, R. 
8Nov-2011Studying the epigenome using next generation sequencingKu, C.S. ; Naidoo, N. ; Wu, M. ; Soong, R. 
9Apr-2012Solid cancer: Evaluating potential efficacy of epigenetic drugsKu, C.-S. 
10Apr-2011Revisiting Mendelian disorders through exome sequencingKu, C.-S. ; Naidoo, N. ; Pawitan, Y.
11Jan-2011Regions of homozygosity and their impact on complex diseases and traitsKu, C.S. ; Naidoo, N. ; Teo, S.M. ; Pawitan, Y.
122010Molecular epidemiology and its current clinical use in cancer managementHartman, M. ; Loy, E.Y. ; Ku, C.S. ; Chia, K.S. 
132011Human genetics and genomics a decade after the release of the draft sequence of the human genomeNaidoo, N. ; Pawitan, Y.; Soong, R. ; Cooper, D.N.; Ku, C.-S. 
14Aug-2012Gene discovery in familial cancer syndromes by exome sequencing: Prospects for the elucidation of familial colorectal cancer type XKu, C.-S. ; Cooper, D.N.; Wu, M. ; Roukos, D.H.; Pawitan, Y.; Soong, R. ; Iacopetta, B.
15Apr-2012Exome versus transcriptome sequencing in identifying coding region variantsKu, C.-S. ; Wu, M. ; Cooper, D.N.; Naidoo, N. ; Pawitan, Y.; Pang, B.; Iacopetta, B.; Soong, R. 
16Jan-2012Exome sequencing: Dual role as a discovery and diagnostic toolKu, C.-S. ; Cooper, D.N.; Polychronakos, C.; Naidoo, N. ; Wu, M. ; Soong, R. 
17Apr-2012Exome sequencing: A transient technology for molecular diagnostics?Ku, C.-S. ; Cooper, D.N.
18Sep-2011Exome diagnostics: Already a reality?Polychronakos, C.; Seng, K.C. 
192007Comment on: Chang et al. (2007) association study of the genetic polymorphisms of the transcription factor 7-like 2 (TCF7l2) gene and type 2 diabetes in the Chinese population: Diabetes 56:2631-2637 [3]Ku, C.-S. ; Khaw, M.; Kee, S.C.
20Feb-2013A new paradigm emerges from the study of de novo mutations in the context of neurodevelopmental diseaseKu, C.S. ; Polychronakos, C.; Tan, E.K. ; Naidoo, N. ; Pawitan, Y.; Roukos, D.H.; Mort, M.; Cooper, D.N.