1. ScholarBank@NUS

Siong-Chuan, Samuel Chong

rp00511

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Full Name
Siong-Chuan, Samuel Chong
Variants
Chong S.S.
Chong, S.
Chong, S.S.
Chong, S.S.C.
 
Main Affiliation
 
Faculty
 
Email
paecs@nus.edu.sg
 

Publications

Refined By:
Policy:  Open
Date Issued:  [2010 TO 2019]

Results 1-20 of 20 (Search time: 0.011 seconds).

Issue DateTitleAuthor(s)
12018A single common assay for robust and rapid fragile X mental retardation syndrome screening from dried blood spotsTan, V.J.; Lian, M. ; Faradz, S.M.H.; Winarni, T.I..; Chong, S.S. 
22018Architecture of polymorphisms in the human genome reveals functionally important and positively selected variants in immune response and drug transporter genesJin, Y ; Wang, J ; Bachtiar, M ; Chong, S.S ; Lee, C.G.L 
32019Architecture of population-differentiated polymorphisms in the human genomeBachtiar, M. ; Jin, Y.; Wang, J. ; Tan, T.W. ; Chong, S.S. ; Ban, K.H.K. ; Lee, C.G.L. 
42012Bmp4 was associated with nscl/p in an asian populationChen Q.; Wang H.; Hetmanski J.B.; Zhang T.; Ruczinski I.; Schwender H.; Liang K.Y.; Fallin M.D.; Redett R.J.; Raymond G.V.; Chou Y.-H.; ChenPhilip K.-T.; Yeow V.; Chong S.S. ; Cheah F.S.H. ; Jabs E.W.; Scott A.F.; Beaty T.H.
52015Cascade screening for fragile X syndrome/CGG repeat expansions in children attending special education in Sri LankaChandrasekara C.H.W.M.R.B.; Wijesundera W.S.S.; Perera H.N.; Chong S.S. ; Rajan-Babu I.-S.
62019Circulating microRNAs as Potential Diagnostic and Prognostic Biomarkers in Hepatocellular CarcinomaJin, Y.; Wong, Y.S.; Goh, B.K.P.; Chan, C.Y.; Cheow, P.C.; Chow, P.K.H. ; Lim, T.K.H.; Goh, G.B.B.; Krishnamoorthy, T.L.; Kumar, R. ; Ng, T.P. ; Chong, S.S. ; Tan, H.H.; Chung, A.Y.F.; Ooi, L.L.P.J. ; Chang, J.P.E.; Tan, C.K.; Lee, C.G.L. 
72019Comprehensive analysis of transcriptome profiles in hepatocellular carcinomaJin, Y. ; Lee, W.Y.; Toh, S.T. ; Tennakoon, C.; Toh, H.C.; Chow, P.K.-H. ; Chung, A.Y.-F. ; Chong, S.S. ; Ooi, L.L.-P.-J. ; Sung, W.-K. ; Lee, C.G.-L. 
82014Evidence of gene-environment interaction for two genes on chromosome 4 and environmental tobacco smoke in controlling the risk of nonsyndromic cleft palateWu T.; Schwender H.; Ruczinski I.; Murray J.C.; Marazita M.L.; Munger R.G.; Hetmanski J.B.; Parker M.M.; Wang P.; Murray T.; Taub M.; Li S.; Redett R.J.; Fallin M.D.; Liang K.Y.; Wu-Chou Y.H.; Chong S.S. ; Yeow V.; Ye X.; Wang H.; Huang S.; Jabs E.W.; Shi B.; Wilcox A.J.; Jee S.H.; Scott A.F.; Beaty T.H.
919-Jul-2017FMR1 CGG repeat expansion mutation detection and linked haplotype analysis for reliable and accurate preimplantation genetic diagnosis of fragile X syndromeRajan-Babu, Indhu-Shree; Lian, Mulias; Cheah, Felicia SH; Chen, Min; Tan, Arnold SC; Prasath, Ethiraj B; Loh, Seong Feei ; Chong, Samuel S 
102019Identification of Novel Microsatellite Markers Flanking the SMN1 and SMN2 Duplicated Region and Inclusion Into a Single-Tube Tridecaplex Panel for Haplotype-Based Preimplantation Genetic Testing of Spinal Muscular AtrophyZhao, M. ; Lian, M.; Cheah, F.S.H.; Tan, A.S.C. ; Agarwal, A.; Chong, S.S. 
112017Improved high sensitivity screen for huntington disease using a one-step triplet-primed PCR and melting curve assayZhao M. ; Cheah F.S.H.; Chen M. ; Lee C.G. ; Law H.-Y. ; Chong S.S. 
122014Joint testing of genotypic and gene-environment interaction identified novel association for BMP4 with non-syndromic CL/P in an asian population using data from an International Cleft ConsortiumChen Q.; Wang H.; Schwender H.; Zhang T.; Hetmanski J.B.; Chou Y.-H.W.; Ye X.; Yeow V.; Chong S.S. ; Zhang B.; Jabs E.W.; Parker M.M.; Scott A.F.; Beaty T.H.
132016Molecular correlates and recent advancements in the diagnosis and screening of FMR1-related disordersRajan-Babu, I.-S; Chong, S.S 
142014Potentially functional SNPs (pfSNPs) as novel genomic predictors of 5-FU response in metastatic colorectal cancer patientsWang J. ; Wang X. ; Zhao M.; Choo S.P.; Ong S.J.; Ong S.Y.K.; Chong S.S. ; Teo Y.Y. ; Lee C.G.L. 
152019Robust Preimplantation Genetic Testing of Huntington Disease by Combined Triplet-Primed PCR Analysis of the HTT CAG Repeat and Multi-Microsatellite HaplotypingZhao, M. ; Cheah, F.S.H.; Tan, A.S.C. ; Lian, M.; Phang, G.P.; Agarwal, A.; Chong, S.S. 
162019Robust preimplantation genetic testing strategy for myotonic dystrophy type 1 by bidirectional triplet-primed polymerase chain reaction combined with multi-microsatellite haplotyping following whole-genome amplificationLian, M.; Lee, C.G. ; Chong, S.S. 
171-Oct-2019Robust strategy for preimplantation genetic testing of myotonic dystrophy type 1 by bidirectional triplet-primed PCR combined with multi-microsatellite haplotyping following whole genome amplificationLian, M; Lee, CG ; Chong, SS 
182012ROR2 gene is associated with risk of non-syndromic cleft palate in an Asian populationWang H.; Hetmanski J.B.; Ruczinski I.; Liang K.Y.; Daniele Fallin M.; Redett R.J.; Raymond G.V.; Wu Chou Y.-H.; Chen P.K.-T.; Yeow V.; Chong S.S. ; Cheah F.S.H. ; Jabs E.W.; Scott A.F.; Beaty T.H.
191-Dec-2019Towards precision medicine: interrogating the human genome to identify drug pathways associated with potentially functional, population-differentiated polymorphismsBachtiar, Maulana ; Ooi, Brandon Nick Sern ; Wang, Jingbo ; Jin, Yu; Tan, Tin Wee ; Chong, Samuel S ; Lee, Caroline GL 
202017Validation of a commercially available test that enables the quantification of the numbers of CGG trinucleotide repeat expansion in FMR1 geneLim G.X.Y.; Yeo M.; Koh Y.Y.; Winarni T.I.; Rajan-Babu I.-S.; Chong S.S. ; Faradz S.M.H.; Guan M.