Works matching AU Chong, Samuel S.

Results: 72

A Strategy Potentially Suitable for Combined Preimplantation Genetic Testing of Aneuploidy and Monogenic Disease That Permits Direct Detection of Pathogenic Variants Including Repeat Expansions and Gene Deletions †.

Published in:

International Journal of Molecular Sciences, 2025, v. 26, n. 10, p. 4532, doi. 10.3390/ijms26104532

By:

Tan, Vivienne J.;
Liang, Ying;
Tan, Arnold S.;
Wong, Simin;
Asherah, Nur;
Chua, Pengyian;
Lee, Caroline G.;
Choolani, Mahesh A.;
Dang, Truong;
Chong, Samuel S.

Publication type:

Article

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

Published in:

Genetic Epidemiology, 2011, v. 35, n. 6, p. 469, doi. 10.1002/gepi.20595

By:

Beaty, Terri H.;
Ruczinski, Ingo;
Murray, Jeffrey C.;
Marazita, Mary L.;
Munger, Ronald G.;
Hetmanski, Jacqueline B.;
Murray, Tanda;
Redett, Richard J.;
Fallin, M. Daniele;
Liang, Kung Yee;
Wu, Tao;
Patel, Poorav J.;
Jin, Sheng-Chih;
Zhang, Tian Xiao;
Schwender, Holger;
Wu-Chou, Yah Huei;
Chen, Philip K.;
Chong, Samuel S.;
Cheah, Felicia;
Yeow, Vincent

Publication type:

Article

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

Published in:

Genetic Epidemiology, 2008, v. 32, n. 6, p. 505, doi. 10.1002/gepi.20323

By:

Sull, Jae Woong;
Liang, Kung-Yee;
Hetmanski, Jacqueline B.;
Fallin, Margaret Daniele;
Ingersoll, Roxann G.;
Park, Jiwan;
Wu-Chou, Yah-Huei;
Chen, Philip K.;
Chong, Samuel S.;
Cheah, Felicia;
Yeow, Vincent;
Park, Beyoung Yun;
Jee, Sun Ha;
Jabs, Ethylin Wang;
Redett, Richard;
Jung, Euiju;
Ruczinski, Ingo;
Scott, Alan F.;
Beaty, Terri H.

Publication type:

Article

pfSNP: An integrated potentially functional SNP resource that facilitates hypotheses generation through knowledge syntheses.

Published in:

Human Mutation, 2011, v. 32, n. 1, p. 19, doi. 10.1002/humu.21331

By:

Wang, Jingbo;
Ronaghi, Mostafa;
Chong, Samuel S.;
Lee, Caroline G.L.

Publication type:

Article

Triplet‐Primed PCR Assays for Accurate Screening of FMR1 CGG Repeat Expansion and Genotype Verification.

Published in:

Current Protocols, 2022, v. 2, n. 5, p. 1, doi. 10.1002/cpz1.427

By:

Rajan‐Babu, Indhu‐Shree;
Lian, Mulias;
Chong, Samuel S.

Publication type:

Article

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

Published in:

Genes, 2016, v. 7, n. 10, p. 87, doi. 10.3390/genes7100087

By:

Rajan-Babu, Indhu-Shree;
Chong, Samuel S.

Publication type:

Article

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

Published in:

European Journal of Human Genetics, 2010, v. 18, n. 6, p. 726, doi. 10.1038/ejhg.2009.228

By:

Ingersoll, Roxann G.;
Hetmanski, Jacqueline;
Ji-Wan Park;
Fallin, M. Daniele;
McIntosh, Iain;
Yah-Huei Wu-Chou;
Chen, Philip K.;
Yeow, Vincent;
Chong, Samuel S.;
Cheah, Felicia;
Jae Woong Sull;
Sun Ha Jee;
Hong Wang;
Tao Wu;
Murray, Tanda;
Shangzhi Huang;
Xiaoqian Ye;
Jabs, Ethylin Wang;
Redett, Richard;
Raymond, Gerald

Publication type:

Article

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

Published in:

European Journal of Human Genetics, 2009, v. 17, n. 6, p. 831, doi. 10.1038/ejhg.2008.250

By:

Jae Woong Sull;
Kung-Yee Liang;
Hetmanski, Jacqueline B.;
Fallin, Margaret Daniele;
Ingersoll, Roxanne G.;
Jiwan Park;
Yah-Huei Wu-Chou;
Chen, Philip K.;
Chong, Samuel S.;
Cheah, Felicia;
Yeow, Vincent;
Beyoung Yun Park;
Sun Ha Jee;
Jabs, Ethylin W.;
Redett, Richard;
Scott, Alan F.;
Beaty, Terri H.

Publication type:

Article

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

Published in:

2006

By:

Boyadjiev, Simeon A.;
Fromme, J. Christopher;
Ben, Jin;
Chong, Samuel S.;
Nauta, Christopher;
Hur, David J.;
Zhang, George;
Hamamoto, Susan;
Schekman, Randy;
Ravazzola, Mariella;
Orci, Lelio;
Eyaid, Wafaa

Publication type:

Letter

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

Published in:

BMC Genomics, 2006, v. 7, p. 1, doi. 10.1186/1471-2164-7-111

By:

Wang, Zihua;
Sew, Pui-Hoon;
Ambrose, Helen;
Ryan, Stephen;
Chong, Samuel S;
Lee, Edmund JD;
Lee, Caroline GL

Publication type:

Article

Potentially Functional SNPs (pfSNPs) as Novel Genomic Predictors of 5-FU Response in Metastatic Colorectal Cancer Patients.

Published in:

PLoS ONE, 2014, v. 9, n. 11, p. 1, doi. 10.1371/journal.pone.0111694

By:

Wang, Jingbo;
Wang, Xu;
Zhao, Mingjue;
Choo, Su Pin;
Ong, Sin Jen;
Ong, Simon Y. K.;
Chong, Samuel S.;
Teo, Yik Ying;
Lee, Caroline G. L.

Publication type:

Article

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.

Published in:

PLoS ONE, 2014, v. 9, n. 10, p. 1, doi. 10.1371/journal.pone.0109038

By:

Chen, Qianqian;
Wang, Hong;
Schwender, Holger;
Zhang, Tianxiao;
Hetmanski, Jacqueline B.;
Chou, Yah-Huei Wu;
Ye, Xiaoqian;
Yeow, Vincent;
Chong, Samuel S.;
Zhang, Bo;
Jabs, Ethylin Wang;
Parker, Margaret M.;
Scott, Alan F.;
Beaty, Terri H.

Publication type:

Article

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

Published in:

PLoS ONE, 2014, v. 9, n. 2, p. 1, doi. 10.1371/journal.pone.0088088

By:

Wu, Tao;
Schwender, Holger;
Ruczinski, Ingo;
Murray, Jeffrey C.;
Marazita, Mary L.;
Munger, Ronald G.;
Hetmanski, Jacqueline B.;
Parker, Margaret M.;
Wang, Ping;
Murray, Tanda;
Taub, Margaret;
Li, Shuai;
Redett, Richard J.;
Fallin, M. Daniele;
Liang, Kung Yee;
Wu-Chou, Yah Huei;
Chong, Samuel S.;
Yeow, Vincent;
Ye, Xiaoqian;
Wang, Hong

Publication type:

Article

BMP4 Was Associated with NSCL/P in an Asian Population.

Published in:

PLoS ONE, 2012, v. 7, n. 4, p. 1, doi. 10.1371/journal.pone.0035347

By:

Chen, Qianqian;
Wang, Hong;
Hetmanski, Jacqueline B.;
Zhang, Tianxiao;
Ruczinski, Ingo;
Schwender, Holger;
Liang, Kung Yee;
Fallin, M. Daniele;
Redett, Richard J.;
Raymond, Gerald V.;
Chou, Yah- Huei Wu;
Chen, Philip Kuo-Ting;
Yeow, Vincent;
Chong, Samuel S.;
Cheah, Felicia S. H.;
Jabs, Ethylin Wang;
Scott, Alan F.;
Beaty, Terri H.

Publication type:

Article

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

Published in:

Cleft Palate Craniofacial Journal, 2013, v. 50, n. 1, p. 96, doi. 10.1597/11-132

By:

Hong Wang;
Tianxiao Zhang;
Tao Wu;
Hetmanski, Jacqueline B.;
Ruczinski, Ingo;
Schwender, Holger;
Kung Vee Liang;
Murray, Tanda;
Fallin, M. Daniele;
Redett, Richard J.;
Raymond, Gerald V.;
Sheng-Chih Jin;
Wu Chou, Yah-Huei;
Chen, Philip Kuo-Ting;
Yeow, Vincent;
Chong, Samuel S.;
Cheah, Felicia S. H.;
Sun Ha Jee;
Jabs, Ethylin W.;
Scott, Alan F.

Publication type:

Article

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

Published in:

American Journal of Medical Genetics. Part A, 2012, v. 158A, n. 4, p. 784, doi. 10.1002/ajmg.a.35257

By:

Shi, Min;
Murray, Jeffrey C.;
Marazita, Mary L.;
Munger, Ronald G.;
Ruczinski, Ingo;
Hetmanski, Jacqueline B.;
Wu, Tao;
Murray, Tanda;
Redett, Richard J.;
Wilcox, Allen J.;
Lie, Rolv T.;
Jabs, Ethylin Wang;
Wu-Chou, Yah Huei;
Chen, Philip K.;
Wang, Hong;
Ye, Xiaoqian;
Yeow, Vincent;
Chong, Samuel S.;
Shi, Bing;
Christensen, Kaare

Publication type:

Article

Robust preimplantation genetic testing of the common F8 Inv22 pathogenic variant of severe hemophilia A using a highly polymorphic multi-marker panel encompassing the paracentric inversion.

Published in:

Thrombosis Journal, 2023, v. 21, n. 1, p. 1, doi. 10.1186/s12959-023-00552-w

By:

Nguyen, Minh Tam;
Nguyen, Thanh Tung;
Nguyen, Duy Bac;
Nguyen, Thi Mai;
Nguyen, Kim Ngan;
Ngo, Van Nhat Minh;
Nguyen, Van Dieu;
Tran, Ngoc Anh;
Lian, Mulias;
Tan, Arnold S. C.;
Chong, Samuel S.;
Dang, Tien Truong

Publication type:

Article

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

Published in:

Human Genetics, 2009, v. 126, n. 3, p. 385, doi. 10.1007/s00439-009-0680-3

By:

Jae Woong Sull;
Kung-Yee Liang;
Hetmanski, Jacqueline B.;
Tao Wu;
Fallin, Margaret Daniele;
Ingersoll, Roxann G.;
Ji Wan Park;
Yah-Huei Wu-Chou;
Chen, Philip K.;
Chong, Samuel S.;
Cheah, Felicia;
Yeow, Vincent;
Beyoung Yun Park;
Sun Ha Jee;
Jabs, Ethylin Wang;
Redett, Richard;
Scott, Alan F.;
Beaty, Terri H.

Publication type:

Article

Point Mutations and an Intragenic Deletion in LIS1, the Lissencephaly Causative Gene in Isolated Lissencephaly Sequence and Miller-Dieker Syndrome.

Published in:

Human Molecular Genetics, 1997, v. 6, n. 2, p. 157, doi. 10.1093/hmg/6.2.157

By:

Lo Nigro, Cristiana;
Chong, Samuel S.;
Smith, Ann C. M.;
Dobyns, William B.;
Carrozzo, Romeo;
Ledbetter, David H.

Publication type:

Article

A Revision of the Lissencephaly and Miller-Dieker Syndrome Critical Regions in Chromosome 17p13.3.

Published in:

Human Molecular Genetics, 1997, v. 6, n. 2, p. 147, doi. 10.1093/hmg/6.2.147

By:

Chong, Samuel S.;
Pack, Svetlana D.;
Roschke, Anna V.;
Tanigami, Akira;
Carrozzo, Romeo;
Smith, Ann C. M.;
Dobyns, William B.;
Ledbetter, David H.

Publication type:

Article

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.

Published in:

Human Molecular Genetics, 1993, v. 2, n. 8, p. 1187

By:

Chong, Samuel S.;
Kristjansson, Kristlelfur;
Cota, Juan;
Handyslde, Alan H.;
Hughes, Mark R.

Publication type:

Article

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

Published in:

Molecular Human Reproduction, 2008, v. 14, n. 5, p. 317, doi. 10.1093/molehr/gan013

By:

Tan, Chia Yee;
Ho, Julia F.V.;
Chong, Yap Seng;
Loganath, Annamalai;
Chan, Yiong Huak;
Ravichandran, Jeganathan;
Lee, Caroline G.;
Chong, Samuel S.

Publication type:

Article

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

Published in:

PLoS ONE, 2017, v. 12, n. 7, p. 1, doi. 10.1371/journal.pone.0180984

By:

Zhao, Mingjue;
Cheah, Felicia S. H.;
Chen, Min;
Lee, Caroline G.;
Law, Hai-Yang;
Chong, Samuel S.

Publication type:

Article

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

Published in:

PLoS ONE, 2017, v. 12, n. 3, p. 1, doi. 10.1371/journal.pone.0173279

By:

Lim, Grace X. Y.;
Yeo, Minli;
Koh, Yvonne Y.;
Winarni, Tri Indah;
Rajan-Babu, Indhu-Shree;
Chong, Samuel S.;
Faradz, Sultana M. H.;
Guan, Ming

Publication type:

Article

Identification of novel microsatellite markers <1 Mb from the HBB gene and development of a single-tube pentadecaplex PCR panel of highly polymorphic markers for preimplantation genetic diagnosis of beta-thalassemia.

Published in:

Electrophoresis, 2015, v. 36, n. 23, p. 2914, doi. 10.1002/elps.201500146

By:

Chen, Min;
Tan, Arnold S. C.;
Cheah, Felicia S. H.;
Saw, Eugene E. L.;
Chong, Samuel S.

Publication type:

Article

Clinical application of targeted long read sequencing in prenatal beta‐thalassemia testing and genetic counseling.

Published in:

2024

By:

Chin, Hui‐Lin;
Benton, Miles C.;
Yang, Lin;
Poon, Kok Siong;
Tan, Karen M. L.;
Jamuar, Saumya S.;
Foo, Roger;
Law, Hai Yang;
Goh, Denise Li‐Meng;
Chong, Samuel S.;
de Sessions, Paola Florez

Publication type:

Case Study

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

Published in:

Scientific Reports, 2020, v. 10, n. 1, p. 1, doi. 10.1038/s41598-020-67742-8

By:

Lim, Lee Jin;
Jin, Yu;
Yang, Henry;
Chung, Alexander Y. F.;
Goh, Brian K. P.;
Chow, Pierce K. H.;
Chan, Chung Yip;
Blanks, William K.;
Cheow, Peng Chung;
Lee, Ser Yee;
Lim, Tony K. H.;
Chong, Samuel S.;
Ooi, London L. P. J.;
Lee, Caroline G.

Publication type:

Article

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

Published in:

Human Molecular Genetics, 2007, v. 16, n. 11, p. 1367, doi. 10.1093/hmg/ddm087

By:

Wang, Zihua;
Wang, Jingbo;
Tantoso, Erwin;
Wang, Baoshuang;
Tai, Amy Y.P.;
Ooi, London L.P.J.;
Chong, Samuel S.;
Lee, Caroline G.L.

Publication type:

Article

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

Published in:

Human Molecular Genetics, 2005, v. 14, n. 14, p. 2075, doi. 10.1093/hmg/ddi212

By:

Wang, Zihua;
Wang, Baoshuang;
Tang, Kun;
Lee, Edmund J.D.;
Chong, Samuel S.;
Lee, Caroline G.L.

Publication type:

Article

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

Published in:

Human Molecular Genetics, 2004, v. 13, n. 8, p. 783, doi. 10.1093/hmg/ddh099

By:

Tang, Kun;
Wong, Li Peng;
Lee, Edmund J.D.;
Chong, Samuel S.;
Lee, Caroline G.L.

Publication type:

Article

Machine Learning Identifies a Signature of Nine Exosomal RNAs That Predicts Hepatocellular Carcinoma.

Published in:

Cancers, 2023, v. 15, n. 14, p. 3749, doi. 10.3390/cancers15143749

By:

Yap, Josephine Yu Yan;
Goh, Laura Shih Hui;
Lim, Ashley Jun Wei;
Chong, Samuel S.;
Lim, Lee Jin;
Lee, Caroline G.

Publication type:

Article

Clinicopathological-Associated Regulatory Network of Deregulated circRNAs in Hepatocellular Carcinoma.

Published in:

Cancers, 2021, v. 13, n. 11, p. 2772, doi. 10.3390/cancers13112772

By:

Han, Jian;
Thurnherr, Thomas;
Chung, Alexander Y. F.;
Goh, Brian K. P.;
Chow, Pierce K. H.;
Chan, Chung Yip;
Cheow, Peng Chung;
Lee, Ser Yee;
Lim, Tony K. H.;
Chong, Samuel S.;
Ooi, London L. P. J.;
Lee, Caroline G.

Publication type:

Article

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

Published in:

European Journal of Human Genetics, 2013, v. 21, n. 12, p. 1436, doi. 10.1038/ejhg.2013.25

By:

Omoumi, Ardeshir;
Wang, Zihua;
Yeow, Vincent;
Wu-Chou, Yah-Huei;
Chen, Philip K;
Ruczinski, Ingo;
Cheng, Joanne;
Cheah, Felicia S H;
Lee, Caroline G;
Beaty, Terri H;
Chong, Samuel S

Publication type:

Article

Single-tube nonaplex microsatellite PCR panel for preimplantation genetic diagnosis of Hb Bart's hydrops fetalis syndrome.

Published in:

Prenatal Diagnosis, 2015, v. 35, n. 6, p. 534, doi. 10.1002/pd.4568

By:

Chen, Min;
Chan, Jerry K. Y.;
Nadarajah, Sadhana;
Tan, Arnold S. C.;
Chan, Melinda L. H.;
Mathew, Joyce;
Saw, Eugene E. L.;
Lim, Cheryl;
Wong, Wendy;
Cheah, Felicia S. H.;
Law, Hai‐Yang;
Wong, Peng‐Cheang;
Chong, Samuel S.

Publication type:

Article

Noninvasive prenatal exclusion of haemoglobin Bart's using foetal DNA from maternal plasma.

Published in:

Prenatal Diagnosis, 2010, v. 30, n. 1, p. 65, doi. 10.1002/pd.2413

By:

Ho, Sherry S. Y.;
Chong, Samuel S. C.;
Koay, Evelyn S. C.;
Ponnusamy, Sukumar;
Chiu, Lily;
Chan, Yiong Huak;
Rauff, Mary;
Baig, Sonia;
Chan, Jerry;
Su, Lin Lin;
Biswas, Arijit;
Hahn, Sinuhe;
Choolani, Mahesh

Publication type:

Article

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

Published in:

Nephrology Dialysis Transplantation, 2005, v. 20, n. 4, p. 728, doi. 10.1093/ndt/gfh648

By:

Chang-Li Wei;
Wai Cheung;
Chew-Kiat Heng;
Novi Arty;
Samuel S. Chong;
Bee-Wah Lee;
Ken-Lee Puah;
Hui-Kim Yap

Publication type:

Article

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

Published in:

Frontiers in Pharmacology, 2021, v. 11, p. N.PAG, doi. 10.3389/fphar.2021.605764

By:

Ooi, Brandon N. S.;
Raechell;
Ying, Ariel F.;
Koh, Yong Zher;
Jin, Yu;
Yee, Sherman W. L.;
Lee, Justin H. S.;
Chong, Samuel S.;
Tan, Jack W. C.;
Liu, Jianjun;
Lee, Caroline G.;
Drum, Chester L.

Publication type:

Article

FMR1 CGG Repeat Patterns and Flanking Haplotypes in Three Asian Populations and Their Relationship With Repeat Instability.

Published in:

Annals of Human Genetics, 2006, v. 70, n. 6, p. 784, doi. 10.1111/j.1469-1809.2006.00265.x

By:

Zhou, Youyou;
Tang, Kun;
Law, Hai-Yang;
Ng, Ivy S. L.;
Lee, Caroline G. L.;
Chong, Samuel S.

Publication type:

Article

Third-Generation Single-Molecule Sequencing for Preimplantation Genetic Testing of Aneuploidy and Segmental Imbalances.

Published in:

Clinical Chemistry, 2023, v. 69, n. 8, p. 881, doi. 10.1093/clinchem/hvad062

By:

Tan, Vivienne J.;
Timing Liu;
Zainul Arifin;
Pak, Beatrice;
Tan, Arnold S. C.;
Simin Wong;
Chiea-Chuen Khor;
Yang, Henry;
Lee, Caroline G.;
Zhongwei Huang;
Choolani, Mahesh A.;
Chong, Samuel S.

Publication type:

Article

Single-Tube Screen for Rapid Detection of Repeat Expansions in Seven Common Spinocerebellar Ataxias.

Published in:

Clinical Chemistry, 2022, v. 68, n. 6, p. 794, doi. 10.1093/clinchem/hvac011

By:

Mulias Lian;
Chanin Limwongse;
Chui-Sheun Yoon;
Lee, Caroline G.;
Hai-Yang Law;
Chong, Samuel S.

Publication type:

Article

A Novel Indel in the Alpha Globin 2 (HBA2) Gene Resulting in False Positive -α3.7 on Multiplex gap-PCR Assay.

Published in:

Clinical Chemistry, 2021, v. 67, n. 9, p. 1284, doi. 10.1093/clinchem/hvab113

By:

Kok-Siong Poon;
Lin Lin Su;
Chong, Samuel S.;
Karen Mei-Ling Tan

Publication type:

Article

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.

Published in:

Clinical Chemistry, 2017, v. 63, n. 6, p. 1127, doi. 10.1373/clinchem.2017.271528

By:

Lian, Mulias;
Mingjue Zhao;
Lee, Caroline G.;
Chong, Samuel S.

Publication type:

Article

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.

Published in:

Clinical Chemistry, 2016, v. 62, n. 8, p. 1096, doi. 10.1373/clinchem.2016.255711

By:

Mingjue Zhao;
Min Chen;
Lee, Caroline G.;
Chong, Samuel S.

Publication type:

Article

Methylation-Specific Triplet-Primed PCR and Melting Curve Analysis as a Rapid Screening Tool for Identifying Actionable FMR1 Genotypes.

Published in:

Clinical Chemistry, 2013, v. 59, n. 11, p. 1668, doi. 10.1373/clinchem.2013.206771

By:

Teo, Clara R. L.;
Rajan-Babu, Indhu-Shree;
Hai-Yang Law;
Lee, Caroline G.;
Chong, Samuel S.

Publication type:

Article

Screening for CGG Repeat Expansion in the FMR1 Gene by Melting Curve Analysis of Combined 5' and 3' Direct Triplet-Primed PCRs.

Published in:

Clinical Chemistry, 2012, v. 58, n. 3, p. 568, doi. 10.1373/clinchem.2011.174615

By:

Teo, Clara R. L.;
Hai-Yang Law;
Lee, Caroline G.;
Chong, Samuel S.

Publication type:

Article

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

Published in:

Advanced Genetics, 2021, v. 2, n. 2, p. 1, doi. 10.1002/ggn2.10048

By:

Nagarathinam, Indhumathi;
Chong, Samuel S.;
B. K., Thelma;
Justin Margret, Jeffrey;
Venkataraman, Viswanathan;
Natarajan Padmavathy, Karthikeyen;
Srisailapathy, C. R. Srikumari

Publication type:

Article

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

Published in:

Reproductive BioMedicine Online (Reproductive Healthcare Limited), 2010, v. 21, n. 5, p. 642, doi. 10.1016/j.rbmo.2010.06.021

By:

Wen Wang;
Yap, Christine H. A.;
Seong Feei Loh;
Tan, Arnold S. C.;
Mui Nee Lim;
Prasath, Ethiraj B.;
Chan, Melinda L. H.;
Wei Chin Tan;
Jiang, Boran;
Gare Hoon Yeo;
Mathew, Joyce;
Ho, Angela;
Ho, Sherry S. Y.;
Peng Cheang Wong;
Choolani, Mahesh A.;
Chong, Samuel S.

Publication type:

Article

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

Published in:

Oncogene, 2005, v. 24, n. 24, p. 3999, doi. 10.1038/sj.onc.1208550

By:

Baoshuang Wang;
Jianwei Ren;
Ooi, London L P J;
Chong, Samuel S;
Lee, Caroline G L

Publication type:

Article

Evidence of differential selection for the −α3.7 and −α4.2 single-α-globin gene deletions within the same population.

Published in:

European Journal of Haematology, 2013, v. 90, n. 3, p. 210, doi. 10.1111/ejh.12058

By:

Yap, Zhi Min;
Sun, Kar Mun;
Teo, Clara R.L.;
Tan, Arnold S.C.;
Chong, Samuel S.

Publication type:

Article

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

Published in:

PLoS ONE, 2015, v. 10, n. 12, p. 1, doi. 10.1371/journal.pone.0145537

By:

Chandrasekara, C. H. W. M. R. Bhagya;
Wijesundera, W. S. Sulochana;
Perera, Hemamali N.;
Chong, Samuel S.;
Rajan-Babu, Indhu-Shree

Publication type:

Article