1. ScholarBank@NUS

KU CHEE SENG

rp08754

Collaboration Map View Statistics Email Alert RSS Feed

Profile

Full Name
KU CHEE SENG
Variants
Seng, K.C.
Ku, C.-S.
Ku, C.S.
 
Main Affiliation
 
Faculty
 
Email
cmekcs@nus.edu.sg
 

Publications

Results 1-20 of 28 (Search time: 0.008 seconds).

Issue DateTitleAuthor(s)
1Jul-2012100 Breast cancer genome sequencing: Heterogeneity-based diagnostic and therapeutic perspectivesKu, C.-S. 
2Feb-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.
3Jul-2011A population-based study of copy number variants and regions of homozygosity in healthy Swedish individualsTeo, S.-M. ; Ku, C.-S. ; Naidoo, N. ; Hall, P.; Chia, K.-S. ; Salim, A. ; Pawitan, Y.
42007Comment 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.
5Aug-2011Copy number polymorphisms in new HapMap III and Singapore populationsKu, C.-S. ; Teo, S.-M. ; Naidoo, N. ; Sim, X. ; Teo, Y.-Y. ; Pawitan, Y.; Seielstad, M.; Chia, K.-S. ; Salim, A. 
6Sep-2011Exome diagnostics: Already a reality?Polychronakos, C.; Seng, K.C. 
7Apr-2012Exome sequencing: A transient technology for molecular diagnostics?Ku, C.-S. ; Cooper, D.N.
8Jan-2012Exome sequencing: Dual role as a discovery and diagnostic toolKu, C.-S. ; Cooper, D.N.; Polychronakos, C.; Naidoo, N. ; Wu, M. ; Soong, R. 
9Apr-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. 
10Aug-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.
112010Genomic copy number variations in three southeast Asian populationsKu, C.-S. ; Sim, X. ; Ong, R.T.H.; Teo, Y.-Y. ; Chia, K.-S. ; Salim, A. ; Pawitan, Y. ; Seielstad, M. ; Lee, E.J.D. 
122009How many genetic variants remain to be discovered?Pawitan, Y.; Seng, K.C. ; Magnusson, P.K.E.
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. 
142010Molecular epidemiology and its current clinical use in cancer managementHartman, M. ; Loy, E.Y. ; Ku, C.S. ; Chia, K.S. 
15Jan-2011Regions of homozygosity and their impact on complex diseases and traitsKu, C.S. ; Naidoo, N. ; Teo, S.M. ; Pawitan, Y.
16Feb-2012Regions of homozygosity in three Southeast Asian populationsTeo, S.-M. ; Ku, C.-S. ; Salim, A. ; Naidoo, N. ; Chia, K.-S. ; Pawitan, Y.
17Apr-2011Revisiting Mendelian disorders through exome sequencingKu, C.-S. ; Naidoo, N. ; Pawitan, Y.
182009Singapore Genome Variation Project: A haplotype map of three Southeast Asian populationsTeo, Y.-Y. ; Sim, X. ; Ong, R.T.H.; Ku, C.-S. ; Chia, K.-S. ; Small, K.S.; Tan, A.K.S.; Chen, J.; Tantoso, E.; Seielstad, M.; Lee, E.J.D. 
192009Singapore Genome Variation Project: A haplotype map of three Southeast Asian populationsTeo, Y.-Y. ; Sim, X. ; Ong, R.T.H.; Ku, C.-S. ; Chia, K.-S. ; Small, K.S.; Tan, A.K.S.; Chen, J.; Tantoso, E.; Seielstad, M. ; Lee, E.J.D. 
20Apr-2012Solid cancer: Evaluating potential efficacy of epigenetic drugsKu, C.-S.