S. Chong

发表

Architecture of polymorphisms in the human genome reveals functionally important and positively selected variants in immune response and drug transporter genes

Jingbo Wang, Yu Jin, M. Bachtiar, 2018, Human Genomics.

Mining Potential Functionally Significant Polymorphisms at the ATP-Binding- Cassette Transporter Genes

S. Chong, Z. Wang, J. Wang, 2009 .

Contribution of DNA sequence and CAG size to mutation frequencies of intermediate alleles for Huntington disease: evidence from single sperm analyses.

G. van den Engh, D. Sillence, M. Hayden, 1997, Human molecular genetics.

Genomic evidence for recent positive selection at the human MDR1 gene locus.

Kun Tang, K. Tang, S. Chong, 2004, Human molecular genetics.

Evidence for gene‐environment interaction in a genome wide study of nonsyndromic cleft palate

Holger Schwender, Ingo Ruczinski, Jacqueline B Hetmanski, 2011, Genetic epidemiology.

Signatures of recent positive selection at the ATP-binding cassette drug transporter superfamily gene loci.

Jingbo Wang, S. Chong, Caroline G L Lee, 2007, Human molecular genetics.

Disruption of FAT10–MAD2 binding inhibits tumor progression

C. Chan, S. Chong, Yun Gao, 2014, Proceedings of the National Academy of Sciences.

Spinocerebellar ataxia type 2 with focal epilepsy--an unusual association.

S. Chong, N. Tan, Y. Zhou, 2004, Annals of the Academy of Medicine, Singapore.

The FGF and FGFR Gene Family and Risk of Cleft Lip with or Without Cleft Palate

Holger Schwender, Ingo Ruczinski, Alan F. Scott, 2013, The Cleft palate-craniofacial journal : official publication of the American Cleft Palate-Craniofacial Association.

REViewer: haplotype-resolved visualization of read alignments in and around tandem repeats

Phillip A. Richmond, M. Eberle, H. Rehm, 2021, Genome Medicine.

Genomic organization of the murine Miller-Dieker/lissencephaly region: conservation of linkage with the human region.

D. Ledbetter, W. Pavan, A. Wynshaw-Boris, 1997, Genome research.

14-3-3 epsilon has no homology to LIS1 and lies telomeric to it on chromosome 17p13.3 outside the Miller-Dieker syndrome chromosome region.

D. Ledbetter, A. Tanigami, S. Chong, 1996, Genome research.

Simplified Preimplantation Genetic Diagnosis of Common Determinants of Hemoglobin Bart ’ s Hydrops Fetalis Syndrome Using a Multiplex-Microsatellite PCR Assay

Prasath, S. Loh, M. Choolani, 2012 .

Simplified PGD of common determinants of haemoglobin Bart's hydrops fetalis syndrome using multiplex-microsatellite PCR.

S. Loh, M. Choolani, S. Chong, 2010, Reproductive biomedicine online.

Molecular Correlates and Recent Advancements in the Diagnosis and Screening of FMR1-Related Disorders

S. Chong, Indhu-Shree Rajan-Babu, 2016, Genes.

Towards precision medicine: interrogating the human genome to identify drug pathways associated with potentially functional, population-differentiated polymorphisms

T. Tan, Jingbo Wang, Yu Jin, 2019, The Pharmacogenomics Journal.

Network of clinically-relevant lncRNAs-mRNAs associated with prognosis of hepatocellular carcinoma patients

P. Chow, C. Chan, P. Cheow, 2020, Scientific Reports.

Robust amplification and ethidium-visible detection of the fragile X syndrome CGG repeat using Pfu polymerase.

E. Eichler, D. Nelson, S. Chong, 1994, American journal of medical genetics.

X- linked markers in DMD associated with oral clefts

R. T. Lie, T. Beaty, Hong Wang, 2013 .

X-linked markers in the Duchenne muscular dystrophy gene associated with oral clefts.

R. T. Lie, T. Beaty, I. Ruczinski, 2013, European journal of oral sciences.

A genome-wide association study of cleft lip with and without cleft palate identifies risk variants near MAFB and ABCA4

Holger Schwender, Ingo Ruczinski, Jacqueline B Hetmanski, 2010, Nature Genetics.

Genome wide study of maternal and parent‐of‐origin effects on the etiology of orofacial clefts

R. T. Lie, T. Beaty, I. Ruczinski, 2012, American journal of medical genetics. Part A.

A genome-wide association study of cleft lip with and without cleft palate identifies risk variants near MAFB and ABCA 4

Hong Wang, Holger Schwender, Ingo Ruczinski, 2010 .

Evidence for gene-environment interaction in a genome wide study of isolated, non-syndromic cleft palate

Holger Schwender, Ingo Ruczinski, Alan F. Scott, 2011 .

Examining Markers in 8q24 to Explain Differences in Evidence for Association With Cleft Lip With/Without Cleft Palate Between Asians and Europeans

Holger Schwender, Ingo Ruczinski, Tao Wu, 2012, Genetic epidemiology.

Analysis of candidate genes on chromosome 2 in oral cleft case-parent trios from three populations

T. Beaty, E. Jabs, A. F. Scott, 2006, Human Genetics.

Single-tube multiplex-PCR screen for common deletional determinants of α-thalassemia

D. Higgs, C. Boehm, G. Cutting, 2000 .

Cystic fibrosis transmembrane conductance regulator (CFTR) gene mutations in Asians with chronic pulmonary disease: a pilot study.

Daniel Y. T. Goh, L. Shek, S. Chong, 2006, Journal of cystic fibrosis : official journal of the European Cystic Fibrosis Society.

Possible Gene-Gene Interaction of KIR2DL4 With its Cognate Ligand HLA-G in Modulating Risk for Preeclampsia

Y. Chan, Y. Chong, S. Chong, 2009, Reproductive Sciences.

Simultaneous genotyping of seven single-nucleotide polymorphisms in the MDR1 gene by single-tube multiplex minisequencing.

K. Tang, S. Chong, Caroline G L Lee, 2003, Clinical chemistry.

The FRAXA and FRAXE allele repeat size of boys from the Avon

S. Chong, 2020 .

Molecular cloning of the cDNA encoding a human renal sodium phosphate transport protein and its assignment to chromosome 6p21.3-p23.

H. Zoghbi, K. Kristjánsson, S. Chong, 1993, Genomics.

Rapid carrier screening for beta-thalassemia by single-step allele-specific PCR and detection.

S. Chong, H. Law, A. S. Tan, 2007, Clinical biochemistry.

Preimplantation single-cell analysis of multiple genetic loci by whole-genome amplification.

K. Kristjánsson, S. Chong, M. Hughes, 1994, Proceedings of the National Academy of Sciences of the United States of America.

Zebrafish twist1 is expressed in craniofacial, vertebral, and renal precursors

E. Jabs, S. Chong, F. Cheah, 2007, Development Genes and Evolution.

Cascade Screening for Fragile X Syndrome/CGG Repeat Expansions in Children Attending Special Education in Sri Lanka

S. Chong, W. Wijesundera, Indhu-Shree Rajan-Babu, 2015, PloS one.

Fragile X CGG repeat variation in Tamil Nadu, South India: a comparison of radioactive and methylation-specific polymerase chain reaction in CGG repeat sizing.

S. Chong, B. Thelma, N. Indhumathi, 2012, Genetic testing and molecular biomarkers.

Identification 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 Atrophy

A. Agarwal, S. Chong, A. S. Tan, 2019, Front. Genet..

FMR1 gene CGG repeat distribution among the three individual cohorts with intellectual disability, autism, and primary ovarian insufficiency from Tamil Nadu, Southern India

S. Chong, C. Srisailapathy, Jeffrey Justin Margret, 2021, Advanced genetics.

Prevalence of Fragile X Syndrome among children receiving special education and carrier states in first degree relatives.

S. Chong, S. Wijesundera, H. Perera, 2017, The Ceylon medical journal.

Validation of a commercially available test that enables the quantification of the numbers of CGG trinucleotide repeat expansion in FMR1 gene

Y. Y. Koh, S. Chong, T. Winarni, 2017, PloS one.

Preimplantation single cell analyses of dystrophin gene deletions using whole genome amplification

K. Kristjánsson, I. V. D. Veyver, S. Chong, 1994, Nature Genetics.

Novel CFTR gene mutation in a patient with CBAVD.

Daniel Y. T. Goh, S. Chong, D. Goh, 2007, Journal of cystic fibrosis : official journal of the European Cystic Fibrosis Society.

A rapid and reliable 7-deletion multiplex polymerase chain reaction assay for alpha-thalassemia.

P. Low, S. Chong, A. S. Tan, 2001, Blood.

Determining the cause of patchwork HBA1 and HBA2 genes: recurrent gene conversion or crossing over fixation events.

S. Chong, H. Najmabadi, M. Steinberg, 2006, Haematologica.

Determining the cause of patchwork HBA 1 and HBA 2 genes : recurrent gene

S. Chong, H. Najmabadi, M. Steinberg, 2006 .

Triplet-Repeat Primed PCR and Capillary Electrophoresis for Characterizing the Fragile X Mental Retardation 1 CGG Repeat Hyperexpansions.

S. Chong, Indhu-Shree Rajan-Babu, 2019, Methods in molecular biology.

Defining the Performance Parameters of a Rapid Screening Tool for FMR1 CGG-Repeat Expansions Based on Direct Triplet-Primed PCR and Melt Curve Analysis.

S. Chong, A. Tran, Caroline G. Lee, 2016, The Journal of molecular diagnostics : JMD.

De fi ning the Performance Parameters of a Rapid Screening Tool for FMR 1 CGG-Repeat Expansions

S. Chong, Caroline G. Lee, Indhu-Shree Rajan-Babu, 2016 .

Genetic Interactions Between TRPC6 and NPHS1 Variants Affect Posttransplant Risk of Recurrent Focal Segmental Glomerulosclerosis

C. Heng, T. Soong, S. Chong, 2015, American journal of transplantation : official journal of the American Society of Transplantation and the American Society of Transplant Surgeons.

Multiplex minisequencing screen for common Southeast Asian and Indian beta-thalassemia mutations.

S. Chong, S. Kham, Wen Wang, 2003, Clinical chemistry.

Roles and Regulation of Long non-coding RNAs in Hepatocellular Carcinoma.

S. Chong, O. Kon, Caroline G. Lee, 2019, Cancer research.

Extracellular matrix‐dependent regulation of angiogenin expression in human placenta

S. Chong, A. Roy, A. Loganath, 2005, Journal of cellular biochemistry.

Single-Tube Multiplex-PCR Screen for Anti-3.7 and Anti-4.2 α-Globin Gene Triplications

W. Erber, S. Chong, D. Chui, 2003 .

Accurate DNA-based diagnostic and carrier testing for X-linked adrenoleukodystrophy.

H. Moser, C. Boehm, G. Cutting, 1999, Molecular genetics and metabolism.

Simplified multiplex-PCR diagnosis of common southeast asian deletional determinants of alpha-thalassemia.

D. Higgs, C. Boehm, G. Cutting, 2000, Clinical chemistry.

Single-tube multiplex-PCR screen for common deletional determinants of alpha-thalassemia.

D. Higgs, C. Boehm, G. Cutting, 2000, Blood.

Hemoglobin H disease classification by isoelectric focusing: molecular verification of 110 cases from Thailand.

S. Chong, P. Sutcharitchan, A. S. Tan, 2005, Clinical chemistry.

A Patient with β-Thalassemia Intermedia Secondary to Homozygosity for a Polyadenylation Signal Mutation (AATAAA > AATAGA) (HBB: C.*112A > G) on the β-Globin Gene

S. Chong, K. Tan, V. Sampath, 2016, Hemoglobin.

Novel evidence of association with nonsyndromic cleft lip with or without cleft palate was shown for single nucleotide polymorphisms in FOXF2 gene in an Asian population.

T. Beaty, Hong Wang, E. Jabs, 2015, Birth defects research. Part A, Clinical and molecular teratology.

Fetal polymorphisms at the ABCB1-transporter gene locus are associated with susceptibility to non-syndromic oral cleft malformations

T. Beaty, I. Ruczinski, S. Chong, 2013, European Journal of Human Genetics.

BMP4 Was Associated with NSCL/P in an Asian Population

T. Beaty, I. Ruczinski, E. Jabs, 2012, PloS one.

ROR2 gene is associated with risk of non-syndromic cleft palate in an Asian population.

T. Beaty, I. Ruczinski, E. Jabs, 2012, Chinese medical journal.

Strong linkage disequilibrium at the nucleotide analogue transporter ABCC5 gene locus

K. Tang, S. Chong, E. Lee, 2005, Pharmacogenetics and genomics.

Microsatellite markers within --SEA breakpoints for prenatal diagnosis of HbBarts hydrops fetalis.

Y. Chan, E. Koay, M. Rauff, 2007, Clinical chemistry.

A functional polymorphism within the MRP1 gene locus identified through its genomic signature of positive selection.

K. Tang, S. Chong, E. Lee, 2005, Human molecular genetics.

Differential parental transmission of markers in RUNX2 among cleft case‐parent trios from four populations

T. Beaty, I. Ruczinski, E. Jabs, 2008, Genetic epidemiology.

A revision of the lissencephaly and Miller-Dieker syndrome critical regions in chromosome 17p13.3.

D. Ledbetter, A. Tanigami, W. Dobyns, 1997, Human molecular genetics.

Nucleotide sequence analyses of the MRP1 gene in four populations suggest negative selection on its coding region

S. Chong, Zihua Wang, H. Ambrose, 2006, BMC Genomics.

Functional coding haplotypes and machine-learning feature elimination identifies predictors of Methotrexate Response in Rheumatoid Arthritis patients

L. Tucker-Kellogg, C. Khor, S. Chong, 2022, EBioMedicine.

Single-step scalable-throughput molecular screening for Huntington disease.

C. Lee, S. Chong, Wen Wang, 2008, Clinical chemistry.

Interleukin-13 genetic polymorphisms in Singapore Chinese children correlate with long-term outcome of minimal-change disease.

Chew-Kiat Heng, C. Heng, S. Chong, 2005, Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association.

Successful preimplantation genetic diagnosis of Hb Bart's hydrops fetalis in Singapore after fresh and frozen embryo replacement cycles.

S. Chong, A. S. Tan, Wen Wang, 2009, Annals of the Academy of Medicine, Singapore.

First successful preimplantation genetic diagnosis in Singapore--avoidance of beta-thalassaemia major.

S. Chong, A. S. Tan, Wen Wang, 2009, Annals of the Academy of Medicine, Singapore.

Expression and fate of CAT reporter gene microinjected into fertilized medaka (Oryzias latipes) eggs in the form of plasmid DNA, recombinant phage particles and its DNA

S. Chong, J. Vielkind, 1989, Theoretical and Applied Genetics.

Evaluation of a fish gene transfer system : expression, fate, and germline transmission of CAT recombinant plasmid and phage sequences microinjected into newly fertilized eggs of the Japanese medaka, Oryzias latipes (Temminck & Schlegel)

S. Chong, 1988 .

Association between genes on chromosome 4p16 and non-syndromic oral clefts in four populations

T. Beaty, E. Jabs, A. F. Scott, 2010, European Journal of Human Genetics.

Preimplantation genetic diagnosis of chromosome translocations by analysis of polymorphic short tandem repeats.

S. Loh, M. Choolani, S. Chong, 2012, Singapore medical journal.

An update on ABCB1 pharmacogenetics: insights from a 3D model into the location and evolutionary conservation of residues corresponding to SNPs associated with drug pharmacokinetics

M. Bachtiar, S. Chong, J. Wang, 2011, The Pharmacogenomics Journal.

Preimplantation prevention of X-linked disease: reliable and rapid sex determination of single human cells by restriction analysis of simultaneously amplified ZFX and ZFY sequences.

K. Kristjánsson, S. Chong, A. Handyside, 1993, Human molecular genetics.

Genomic, cDNA, and embryonic expression analysis of zebrafish transforming growth factor beta 3 (tgfβ3)

E. Jabs, S. Chong, F. Cheah, 2005, Developmental dynamics : an official publication of the American Association of Anatomists.

Analysis of MDR1 haplotypes in Parkinson's disease in a white population

Y. Teo, K. Tang, S. Chong, 2004, Neuroscience Letters.

Distinct haplotype profiles and strong linkage disequilibrium at the MDR1 multidrug transporter gene locus in three ethnic Asian populations.

Kun Tang, K. Tang, S. Chong, 2002, Pharmacogenetics.

tgfβ3 regulation of chondrogenesis and osteogenesis in zebrafish is mediated through formation and survival of a subpopulation of the cranial neural crest

E. Jabs, S. Chong, Christoph Winkler, 2010, Mechanisms of Development.

Effect of MDR1 haplotype on risk of Parkinson disease.

Y. Teo, K. Tang, J. Woo, 2005, Archives of neurology.

Characterization of Single Nucleotide Polymorphisms in 13 Members of the ABC Drug Transporter Genes in Three Different Populations

S. Chong, Zihua Wang, Caroline G. L. Lee, 2007 .

MDR1, the blood–brain barrier transporter, is associated with Parkinson’s disease in ethnic Chinese

Y. Cheung, K. Tang, S. Chong, 2004, Journal of Medical Genetics.

Cranio-lenticulo-sutural dysplasia is caused by a SEC23A mutation leading to abnormal endoplasmic-reticulum-to-Golgi trafficking

J. Christopher Fromme, R. Schekman, L. Orci, 2006, Nature Genetics.

Single-tube multiplex-PCR screen for anti-3.7 and anti-4.2 alpha-globin gene triplications.

W. Erber, S. Chong, D. Chui, 2003, Clinical chemistry.

Single-tube methylation-specific duplex-PCR assay for rapid and accurate diagnosis of Fragile X Mental Retardation 1–related disorders

S. Chong, H. Law, Indhu-Shree Rajan-Babu, 2015, Expert review of molecular diagnostics.

Screening for CGG repeat expansion in the FMR1 gene by melting curve analysis of combined 5' and 3' direct triplet-primed PCRs.

C. Lee, S. Chong, H. Law, 2012, Clinical chemistry.

Association between IRF6 and nonsyndromic cleft lip with or without cleft palate in four populations

Jacqueline B Hetmanski, Alan F Scott, Terri H Beaty, 2007, Genetics in Medicine.

Molecular analysis of human platelet antigen system 1 antigen on single cells can be applied to preimplantation genetic diagnosis for prevention of alloimmune thrombocytopenia.

K. Kristjánsson, I. V. D. Veyver, S. Chong, 1994, American journal of obstetrics and gynecology.

Interstitial deletion of 4p15.32p16.3 in a boy with minor anomalies, hearing loss, borderline intelligence, and oligodontia.

S. Chong, C. Kozma, J. Meck, 1999, American journal of medical genetics.

Identification 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 syndrome

S. Chong, M. Zhao, C. G. Lee, 2016, Genetics in Medicine.

Simplified strategy for rapid first-line screening of fragile X syndrome: closed-tube triplet-primed PCR and amplicon melt peak analysis

S. Chong, H. Law, C. Yoon, 2015, Expert Reviews in Molecular Medicine.

The Promoter Region of the MDR1 Gene Is Largely Invariant, but Different Single Nucleotide Polymorphism Haplotypes Affect MDR1 Promoter Activity Differently in Different Cell Lines

Jingbo Wang, S. Chong, S. Ngoi, 2006, Molecular Pharmacology.

The Promoter Region of the MDR 1 Gene Is Largely Invariant , but Different Single Nucleotide Polymorphism Haplotypes Affect MDR 1 Promoter Activity Differently in Different Cell Lines

Jingbo Wang, S. Chong, S. Ngoi, 2006 .

Genomic, cDNA and embryonic expression analysis of zebrafish IRF6, the gene mutated in the human oral clefting disorders Van der Woude and popliteal pterygium syndromes.

E. Jabs, S. Chong, Jin Ben, 2005, Gene expression patterns : GEP.

Dinucleotide repeats negatively modulate the promoter activity of Cyr61 and is unstable in hepatocellular carcinoma patients

C. Lee, S. Chong, L. Ooi, 2005, Oncogene.

Architecture of population-differentiated polymorphisms in the human genome

T. Tan, Jingbo Wang, Yu Jin, 2019, PloS one.

Evidence that TGFA influences risk to cleft lip with/without cleft palate through unconventional genetic mechanisms

T. Beaty, E. Jabs, A. F. Scott, 2009, Human Genetics.

Clinicopathological-Associated Regulatory Network of Deregulated circRNAs in Hepatocellular Carcinoma

C. Chan, P. Cheow, S. Lee, 2021, Cancers.

Comprehensive analysis of transcriptome profiles in hepatocellular carcinoma

W. Sung, P. Chow, Chandana Tennakoon, 2019, Journal of Translational Medicine.

Maternal transmission effects of the PAX genes among cleft case–parent trios from four populations

T. Beaty, E. Jabs, A. F. Scott, 2009, European Journal of Human Genetics.

Excess maternal transmission of markers in TCOF1 among cleft palate case‐parent trios from three populations

T. Beaty, E. Jabs, A. F. Scott, 2008, American journal of medical genetics. Part A.

Gametic and somatic tissue–specific heterogeneity of the expanded SCA1 CAG repeat in spinocerebellar ataxia type 1

H. Zoghbi, H. Orr, S. Subramony, 1995, Nature Genetics.

Robust fragile X (CGG)n genotype classification using a methylation specific triple PCR assay

C. Boehm, G. Cutting, S. Chong, 2004, Journal of Medical Genetics.

Joint 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 Consortium

T. Beaty, E. Jabs, A. F. Scott, 2014, PloS one.

Rapid Molecular Screen of Spinocerebellar Ataxia Types 1, 2, and 3 by Triplet-Primed PCR and Melting Curve Analysis.

S. Chong, H. Law, Y. Soong, 2021, The Journal of molecular diagnostics : JMD.

Clinical report: a case of Williams Syndrome and Klinefelter Syndrome.

S. Chong, J. Lum, D. Goh, 2006, Annals of the Academy of Medicine, Singapore.

FAT10 Plays a Role in the Regulation of Chromosomal Stability*

Siew Hong Leong, K. Jeang, C. Lee, 2006, Journal of Biological Chemistry.

Paternal contribution of HLA-G*0106 significantly increases risk for pre-eclampsia in multigravid pregnancies.

Y. Chan, Y. Chong, S. Chong, 2008, Molecular human reproduction.

Evidence of Gene−Environment Interaction for Two Genes on Chromosome 4 and Environmental Tobacco Smoke in Controlling the Risk of Nonsyndromic Cleft Palate

T. Beaty, I. Ruczinski, M. Taub, 2014, PloS one.

Robust Performance of Potentially Functional SNPs in Machine Learning Models for the Prediction of Atorvastatin-Induced Myalgia

Jianjun Liu, J. Tan, Yu Jin, 2021, Frontiers in Pharmacology.

Improved high sensitivity screen for Huntington disease using a one-step triplet-primed PCR and melting curve assay

S. Chong, H. Law, M. Zhao, 2017, PloS one.

Robust Preimplantation Genetic Testing Strategy for Myotonic Dystrophy Type 1 by Bidirectional Triplet-Primed Polymerase Chain Reaction Combined With Multi-microsatellite Haplotyping Following Whole-Genome Amplification

S. Chong, M. Lian, C. G. Lee, 2019, Front. Genet..

Single-Tube Dodecaplex PCR Panel of Polymorphic Microsatellite Markers Closely Linked to the DMPK CTG Repeat for Preimplantation Genetic Diagnosis of Myotonic Dystrophy Type 1.

S. Chong, M. Lian, M. Zhao, 2017, Clinical chemistry.

Defining the performance parameters of a rapid screening tool for myotonic dystrophy type 1 based on triplet-primed PCR and melt curve analysis

S. Chong, H. Law, M. Lian, 2016, Expert review of molecular diagnostics.

Cloning, genetic mapping, and expression analysis of a mouse renal sodium-dependent phosphate cotransporter.

K. Kristjánsson, C. Kozak, S. Chong, 1995, The American journal of physiology.

Single-cell analysis of the RhD blood type for use in preimplantation diagnosis in the prevention of severe hemolytic disease of the newborn.

N. Fisk, S. Chong, A. Handyside, 1995, American journal of obstetrics and gynecology.

Methylation-specific triplet-primed PCR and melting curve analysis as a rapid screening tool for identifying actionable FMR1 genotypes.

C. Lee, S. Chong, H. Law, 2013, Clinical chemistry.

Molecular strategies for pre-implantation genetic diagnosis of single gene and chromosomal disorders.

S. Chong, A. S. Tan, B. Jiang, 2012, Best practice & research. Clinical obstetrics & gynaecology.

Detection and discrimination between deletional and non-deletional Prader-Willi and Angelman syndromes by methylation-specific PCR and quantitative melting curve analysis.

S. Chong, H. Law, Wen Wang, 2009, The Journal of molecular diagnostics : JMD.

Validation of a Commercially Available Screening Tool for the Rapid Identification of CGG Trinucleotide Repeat Expansions in FMR1.

Y. Y. Koh, S. Chong, F. Mundhofir, 2015, The Journal of molecular diagnostics : JMD.

Circulating microRNAs as Potential Diagnostic and Prognostic Biomarkers in Hepatocellular Carcinoma

P. Chow, C. Chan, P. Cheow, 2019, Scientific Reports.

Network of clinically-relevant lncRNAs-mRNAs associated with prognosis of hepatocellular carcinoma patients

P. Chow, C. Chan, P. Cheow, 2020, Scientific Reports.

Highly deregulated lncRNA LOC is associated with overall worse prognosis in Hepatocellular Carcinoma patients

Lay Hiang Ling, C. Chan, P. Cheow, 2021, Journal of Cancer.

Simplified molecular diagnosis of fragile X syndrome by fluorescent methylation-specific PCR and GeneScan analysis.

S. Chong, J. Lum, S. Tay, 2006, Clinical chemistry.

The role of single nucleotide polymorphisms (SNPs) in understanding complex disorders and pharmacogenomics.

S. Chong, C. G. Lee, S. Kao, 2000, Annals of the Academy of Medicine, Singapore.

Single‐Cell DNA and FISH Analysis for Application to Preimplantation Genetic Diagnosis

S. Weremowicz, S. Chong, M. Hughes, 2010, Current protocols in human genetics.

High-Throughput Methylation-Specific Triplet-Primed PCR and Melting Curve Analysis for Selective and Reliable Identification of Actionable FMR1 Genotypes

S. Chong, H. Law, Indhu-Shree Rajan-Babu, 2022, The Journal of Molecular Diagnostics.

A Single Common Assay for Robust and Rapid Fragile X Mental Retardation Syndrome Screening From Dried Blood Spots

S. Chong, S. Faradz, T. Winarni, 2018, Front. Genet..

FMR1 CGG repeat expansion mutation detection and linked haplotype analysis for reliable and accurate preimplantation genetic diagnosis of fragile X syndrome

S. Loh, S. Chong, A. S. Tan, 2017, Expert Reviews in Molecular Medicine.

FMR 1 CGG repeat expansion mutation detection and linked haplotype analysis for reliable and accurate preimplantation genetic diagnosis of fragile X syndrome

S. Loh, S. Chong, A. S. Tan, 2017 .

Diagnostic Pitfall in PCR-Based α-Thalassemia Genotyping Resulting from a (G→C) Polymorphism at Nucleotide 71 3′ to the α2-Globin Gene Termination Codon

S. Chong, D. Chui, L. Chan, 2006 .

Diagnostic pitfall in PCR-based alpha-thalassemia genotyping resulting from a (G->C) polymorphism at nucleotide 71 3' to the alpha2-globin gene termination codon.

S. Chong, D. Chui, L. Chan, 2006, Clinical chemistry.

Point mutations and an intragenic deletion in LIS1, the lissencephaly causative gene in isolated lissencephaly sequence and Miller-Dieker syndrome.

D. Ledbetter, W. Dobyns, S. Chong, 1997, Human molecular genetics.

Comprehensive analysis of transcriptome profiles in hepatocellular carcinoma

W. Sung, P. Chow, Chandana Tennakoon, 2019, Journal of Translational Medicine.

Repeat expansion and methylation-sensitive triplet-primed polymerase chain reaction for fragile X mental retardation 1 gene screening in institutionalised intellectually disabled individuals.

S. Chong, T. Winarni, M. Guan, 2020, Singapore medical journal.

Circulating microRNAs as Potential Diagnostic and Prognostic Biomarkers in Hepatocellular Carcinoma

P. Chow, C. Chan, P. Cheow, 2019, Scientific Reports.

Machine Learning using Genetic and Clinical Data Identifies a Signature that Robustly Predicts Methotrexate Response in Rheumatoid Arthritis.

L. Tucker-Kellogg, C. Khor, S. Chong, 2022, Rheumatology.

Identification 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 Disease.

C. Lee, S. Chong, Min Chen, 2016, Clinical chemistry.

Phylogenetic and evolutionary relationships and developmental expression patterns of the zebrafish twist gene family

B. Venkatesh, E. Jabs, S. Chong, 2009, Development Genes and Evolution.

Single‐Cell DNA and FISH Analysis for Application to Preimplantation Genetic Diagnosis

S. Chong, M. Hughes, P. Miron, 2002, Current protocols in human genetics.

Single-step scalable-throughput molecular screening for Huntington disease.

C. Lee, S. Chong, Wen Wang, 2008, Clinical chemistry.

Robust Preimplantation Genetic Testing of Huntington Disease by Combined Triplet-Primed PCR Analysis of the HTT CAG Repeat and Multi-Microsatellite Haplotyping

A. Agarwal, S. Chong, M. Lian, 2019, Scientific Reports.

Enhanced Detection and Sizing of the HTT CAG Repeat Expansion in Huntington Disease Using an Improved Triplet-Primed PCR Assay

S. Chong, H. Law, C. G. Lee, 2016, Neurodegenerative Diseases.

"Reconstituted" alpha-thalassemia genomic samples as positive controls for the molecular diagnostic laboratory.

S. Chong, Wen Wang, Arnold S C Tan, 2002, Clinical chemistry.