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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:
Author:  Chong, Samuel S
Date Issued:  [2010 TO 2019]

Results 1-20 of 37 (Search time: 0.007 seconds).

Issue DateTitleAuthor(s)
1Jun-2010A genome-wide association study of cleft lip with and without cleft palate identifies risk variants near MAFB and ABCA4Beaty, T.H.; Murray, J.C.; Marazita, M.L.; Munger, R.G.; Ruczinski, I.; Hetmanski, J.B.; Liang, K.Y.; Wu, T.; Murray, T.; Fallin, M.D.; Redett, R.A.; Raymond, G.; Schwender, H.; Jin, S.-C.; Cooper, M.E.; Dunnwald, M.; Mansilla, M.A.; Leslie, E.; Bullard, S.; Lidral, A.C.; Moreno, L.M.; Menezes, R.; Vieira, A.R.; Petrin, A.; Wilcox, A.J.; Lie, R.T.; Jabs, E.W.; Wu-Chou, Y.H.; Chen, P.K.; Wang, H.; Ye, X.; Huang, S.; Yeow, V.; Chong, S.S. ; Jee, S.H.; Shi, B.; Christensen, K.; Melbye, M.; Doheny, K.F.; Pugh, E.W.; Ling, H.; Castilla, E.E.; Czeizel, A.E.; Ma, L.; Field, L.L.; Brody, L.; Pangilinan, F.; Mills, J.L.; Molloy, A.M.; Kirke, P.N.; Scott, J.M.; Arcos-Burgos, M.; Scott, A.F.
22018A 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. 
32018Architecture 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 
42019Architecture 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. 
52012Bmp4 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.
62015Cascade 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.
72019Circulating 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. 
82019Comprehensive 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. 
91-Jul-2019Comprehensive molecular characterization of the transcriptome of HCC patientsLee, CG ; Lee, W; Yu, J; Toh, S ; Tennakoon, C; Toh, H; Chow, P ; Chung, A ; Ooi, LLPJ ; Chong, SS ; Sung, K
101-Sep-2016Defining the Performance Parameters of a Rapid Screening Tool for FMR1 CGG-Repeat Expansions Based on Direct Triplet-Primed PCR and Melt Curve AnalysisRajan-Babu, Indhu-Shree; Lian, Mulias ; Tran, Anh H; Dang, Truong T; Le, Huong T-M; Thanh, Minh N; Lee, Caroline G ; Chong, Samuel S 
111-Nov-2016Defining the performance parameters of a rapid screening tool for myotonic dystrophy type 1 based on triplet-primed PCR and melt curve analysisLian, Mulias ; Law, Hai-Yang ; Lee, Caroline G ; Chong, Samuel S 
121-Jan-2016Enhanced Detection and Sizing of the HTT CAG Repeat Expansion in Huntington Disease Using an Improved Triplet-Primed PCR AssayZhao, Mingjue ; Lee, Caroline G ; Law, Hai-Yang ; Chong, Samuel S 
13Sep-2011Evidence for gene-environment interaction in a genome wide study of nonsyndromic cleft palateBeaty, T.H.; Ruczinski, I.; Murray, J.C.; Marazita, M.L.; Munger, R.G.; Hetmanski, J.B.; Murray, T.; Redett, R.J.; Fallin, M.D.; Liang, K.Y.; Wu, T.; Patel, P.J.; Jin, S.-C.; Zhang, T.X.; Schwender, H.; Wu-Chou, Y.H.; Chen, P.K.; Chong, S.S. ; Cheah, F.; Yeow, V.; Ye, X.; Wang, H.; Huang, S.; Jabs, E.W.; Shi, B.; Wilcox, A.J.; Lie, R.T.; Jee, S.H.; Christensen, K.; Doheny, K.F.; Pugh, E.W.; Ling, H.; Scott, A.F.
142014Evidence 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.
15May-2012Examining markers in 8q24 to explain differences in evidence for association with cleft lip with/without cleft palate between Asians and EuropeansMurray, T.; Taub, M.A.; Ruczinski, I.; Scott, A.F.; Hetmanski, J.B.; Schwender, H.; Patel, P.; Zhang, T.X.; Munger, R.G.; Wilcox, A.J.; Ye, X.; Wang, H.; Wu, T.; Wu-Chou, Y.H.; Shi, B.; Jee, S.H.; Chong, S. ; Yeow, V.; Murray, J.C.; Marazita, M.L.; Beaty, T.H.
1619-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 
171-Oct-2019Identification of lncRNA-mRNA network(s) that modulate prognosis in hepatocellular carcinoma patientsLee, CG; Lim, LJ ; Yu, J; Toh, HC; Chow, PKH ; Chung, AYF ; Ooi, LLPJ ; Chong, SS 
181-Sep-2016Identification of microsatellite markers < 1 Mb from the FMR1 CGG repeat and development of a single-tube tetradecaplex PCR panel of highly polymorphic markers for preimplantation genetic diagnosis of fragile X syndromeChen, Min ; Zhao, Mingjue ; Lee, Caroline G ; Chong, Samuel S 
191-Aug-2016Identification of Novel Microsatellite Markers <1 Mb from the HTT CAG Repeat and Development of a Single-Tube Tridecaplex PCR Panel of Highly Polymorphic Markers for Preimplantation Genetic Diagnosis of Huntington DiseaseZhao, Mingjue ; Chen, Min ; Lee, Caroline G ; Chong, Samuel S 
202019Identification 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.