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KU CHEE SENG

rp08754

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

Publications

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Department:  CANCER SCIENCE INSTITUTE OF SINGAPORE

Results 1-20 of 20 (Search time: 0.005 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. 
13Aug-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.
14Apr-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. 
15Jan-2012Exome sequencing: Dual role as a discovery and diagnostic toolKu, C.-S. ; Cooper, D.N.; Polychronakos, C.; Naidoo, N. ; Wu, M. ; Soong, R. 
16Apr-2012Exome sequencing: A transient technology for molecular diagnostics?Ku, C.-S. ; Cooper, D.N.
17Sep-2011Exome diagnostics: Already a reality?Polychronakos, C.; Seng, K.C. 
182007Comment 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.
19Feb-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.
20Jul-2012100 Breast cancer genome sequencing: Heterogeneity-based diagnostic and therapeutic perspectivesKu, C.-S.