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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

Refined By:
Date Issued:  [2010 TO 2019]

Results 1-20 of 23 (Search time: 0.013 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.
4Aug-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. 
5Sep-2011Exome diagnostics: Already a reality?Polychronakos, C.; Seng, K.C. 
6Apr-2012Exome sequencing: A transient technology for molecular diagnostics?Ku, C.-S. ; Cooper, D.N.
7Jan-2012Exome sequencing: Dual role as a discovery and diagnostic toolKu, C.-S. ; Cooper, D.N.; Polychronakos, C.; Naidoo, N. ; Wu, M. ; Soong, R. 
8Apr-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. 
9Aug-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.
102010Genomic 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. 
112011Human 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. 
122010Molecular epidemiology and its current clinical use in cancer managementHartman, M. ; Loy, E.Y. ; Ku, C.S. ; Chia, K.S. 
13Jan-2011Regions of homozygosity and their impact on complex diseases and traitsKu, C.S. ; Naidoo, N. ; Teo, S.M. ; Pawitan, Y.
14Feb-2012Regions of homozygosity in three Southeast Asian populationsTeo, S.-M. ; Ku, C.-S. ; Salim, A. ; Naidoo, N. ; Chia, K.-S. ; Pawitan, Y.
15Apr-2011Revisiting Mendelian disorders through exome sequencingKu, C.-S. ; Naidoo, N. ; Pawitan, Y.
16Apr-2012Solid cancer: Evaluating potential efficacy of epigenetic drugsKu, C.-S. 
17Nov-2011Studying the epigenome using next generation sequencingKu, C.S. ; Naidoo, N. ; Wu, M. ; Soong, R. 
18Mar-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. 
19May-2012The 'sequence everything' approach and personalized clinical decision challengesKu, C.-S. ; Cooper, D.N.; Roukos, D.H.
20Jul-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.