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Items: 1 to 50 of 168

1.
2.

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

Zhao M, Cheah FSH, Tan ASC, Lian M, Phang GP, Agarwal A, Chong SS.

Sci Rep. 2019 Nov 11;9(1):16481. doi: 10.1038/s41598-019-52769-3.

3.

Architecture of population-differentiated polymorphisms in the human genome.

Bachtiar M, Jin Y, Wang J, Tan TW, Chong SS, Ban KHK, Lee CGL.

PLoS One. 2019 Oct 17;14(10):e0224089. doi: 10.1371/journal.pone.0224089. eCollection 2019.

4.

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

Bachtiar M, Ooi BNS, Wang J, Jin Y, Tan TW, Chong SS, Lee CGL.

Pharmacogenomics J. 2019 Dec;19(6):516-527. doi: 10.1038/s41397-019-0096-y. Epub 2019 Oct 3.

5.

Comprehensive analysis of transcriptome profiles in hepatocellular carcinoma.

Jin Y, Lee WY, Toh ST, Tennakoon C, Toh HC, Chow PK, Chung AY, Chong SS, Ooi LL, Sung WK, Lee CG.

J Transl Med. 2019 Aug 20;17(1):273. doi: 10.1186/s12967-019-2025-x.

6.

Roles and Regulation of Long Noncoding RNAs in Hepatocellular Carcinoma.

Lim LJ, Wong SYS, Huang F, Lim S, Chong SS, Ooi LL, Kon OL, Lee CG.

Cancer Res. 2019 Oct 15;79(20):5131-5139. doi: 10.1158/0008-5472.CAN-19-0255. Epub 2019 Jul 23. Review.

PMID:
31337653
7.

Circulating microRNAs as Potential Diagnostic and Prognostic Biomarkers in Hepatocellular Carcinoma.

Jin Y, Wong YS, Goh BKP, Chan CY, Cheow PC, Chow PKH, Lim TKH, Goh GBB, Krishnamoorthy TL, Kumar R, Ng TP, Chong SS, Tan HH, Chung AYF, Ooi LLPJ, Chang JPE, Tan CK, Lee CGL.

Sci Rep. 2019 Jul 18;9(1):10464. doi: 10.1038/s41598-019-46872-8.

9.

Association between Bilateral Infarcts Pattern and Detection of Occult Atrial Fibrillation in Embolic Stroke of Undetermined Source (ESUS) Patients with Insertable Cardiac Monitor (ICM).

Yushan B, Tan BYQ, Ngiam NJ, Chan BPL, Luen TH, Sharma VK, Sia CH, Dalakoti M, Chong SS, Kojodjojo P, Yeo LLL.

J Stroke Cerebrovasc Dis. 2019 Sep;28(9):2448-2452. doi: 10.1016/j.jstrokecerebrovasdis.2019.06.025. Epub 2019 Jul 13.

PMID:
31307898
10.

Robust and accurate detection and sizing of repeats within the DMPK gene using a novel TP-PCR test.

Leferink M, Wong DPW, Cai S, Yeo M, Ho J, Lian M, Kamsteeg EJ, Chong SS, Haer-Wigman L, Guan M.

Sci Rep. 2019 Jun 4;9(1):8280. doi: 10.1038/s41598-019-44588-3.

11.

Post-hemithyroidectomy hypothyroidism in non autoimmune thyroiditis patients: Incidence, risk factors and duration of follow up.

Chong SS, Hoh SY, Huang SM.

Asian J Surg. 2019 Nov;42(11):957-962. doi: 10.1016/j.asjsur.2019.01.015. Epub 2019 Apr 12.

12.

Randomized controlled trial comparing bilateral superficial cervical plexus block and local wound infiltration for pain control in thyroid surgery.

Hoh SY, Doon YK, Chong SS, Ng KL.

Asian J Surg. 2019 Dec;42(12):1001-1008. doi: 10.1016/j.asjsur.2019.01.017. Epub 2019 Mar 8.

13.

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

Rajan-Babu IS, Chong SS.

Methods Mol Biol. 2019;1972:199-210. doi: 10.1007/978-1-4939-9213-3_14.

PMID:
30847793
14.

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

Tan VJ, Lian M, Faradz SMH, Winarni TI, Chong SS.

Front Genet. 2018 Nov 27;9:582. doi: 10.3389/fgene.2018.00582. eCollection 2018.

15.

Modifier Ontologies for frequency, certainty, degree, and coverage phenotype modifier.

Endara L, Thessen AE, Cole HA, Walls R, Gkoutos G, Cao Y, Chong SS, Cui H.

Biodivers Data J. 2018 Nov 28;(6):e29232. doi: 10.3897/BDJ.6.e29232. eCollection 2018.

16.

A comparison of aesthetic outcome between tissue adhesive and subcuticular suture in thyroidectomy wound closure in a multiracial country: A randomized controlled trial.

Teoh LY, Chong SS, Hoh SY, Teoh MS, Ng KL.

Asian J Surg. 2019 May;42(5):634-640. doi: 10.1016/j.asjsur.2018.09.014. Epub 2018 Nov 13.

17.

A rapid introduction to neurological biochemistry using Drosophila melanogaster.

Chong SS, Wilkinson AJ, Chawla S.

Invert Neurosci. 2018 Nov 8;18(4):15. doi: 10.1007/s10158-018-0220-8.

PMID:
30406849
18.

Resolving "orphaned" non-specific structures using machine learning and natural language processing methods.

Xu D, Chong SS, Rodenhausen T, Cui H.

Biodivers Data J. 2018 Aug 10;(6):e26659. doi: 10.3897/BDJ.6.e26659. eCollection 2018.

19.

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

Jin Y, Wang J, Bachtiar M, Chong SS, Lee CGL.

Hum Genomics. 2018 Sep 15;12(1):43. doi: 10.1186/s40246-018-0175-1.

20.

Second Primary Malignancies in Patients with Well-differentiated/Dedifferentiated Liposarcoma.

Jung E, Fiore M, Gronchi A, Grignol V, Pollock RE, Chong SS, Chopra S, Hamilton AS, Tseng WW.

Anticancer Res. 2018 Jun;38(6):3535-3542. doi: 10.21873/anticanres.12625.

PMID:
29848707
21.

Temperature sensing using CdSe quantum dot doped poly(methyl methacrylate) microfiber.

Irawati N, Harun SW, Rahman HA, Chong SS, Hamizi NA, Ahmad H.

Appl Opt. 2017 Jun 1;56(16):4675-4679. doi: 10.1364/AO.56.004675.

PMID:
29047599
22.

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

Rajan-Babu IS, Lian M, Cheah FSH, Chen M, Tan ASC, Prasath EB, Loh SF, Chong SS.

Expert Rev Mol Med. 2017 Jul 19;19:e10. doi: 10.1017/erm.2017.10. Review.

23.

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

Zhao M, Cheah FSH, Chen M, Lee CG, Law HY, Chong SS.

PLoS One. 2017 Jul 10;12(7):e0180984. doi: 10.1371/journal.pone.0180984. eCollection 2017.

24.

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

Chandrasekara B, Wijesundera S, Chong SS, Perera HN.

Ceylon Med J. 2017 Jun 30;62(2):92-96.

25.

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.

Lian M, Zhao M, Lee CG, Chong SS.

Clin Chem. 2017 Jun;63(6):1127-1140. doi: 10.1373/clinchem.2017.271528. Epub 2017 Apr 20.

26.

Single-tube tetradecaplex panel of highly polymorphic microsatellite markers < 1 Mb from F8 for simplified preimplantation genetic diagnosis of hemophilia A.

Zhao M, Chen M, Tan ASC, Cheah FSH, Mathew J, Wong PC, Chong SS.

J Thromb Haemost. 2017 Jul;15(7):1473-1483. doi: 10.1111/jth.13685. Epub 2017 Apr 28.

27.

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

Lim GX, Yeo M, Koh YY, Winarni TI, Rajan-Babu IS, Chong SS, Faradz SM, Guan M.

PLoS One. 2017 Mar 9;12(3):e0173279. doi: 10.1371/journal.pone.0173279. eCollection 2017.

28.

Introducing Explorer of Taxon Concepts with a case study on spider measurement matrix building.

Cui H, Xu D, Chong SS, Ramirez M, Rodenhausen T, Macklin JA, Ludäscher B, Morris RA, Soto EM, Koch NM.

BMC Bioinformatics. 2016 Nov 17;17(1):471.

30.

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

Lian M, Law HY, Lee CG, Chong SS.

Expert Rev Mol Diagn. 2016 Nov;16(11):1221-1232. Epub 2016 Oct 8.

PMID:
27665623
31.

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

Rajan-Babu IS, Chong SS.

Genes (Basel). 2016 Oct 14;7(10). pii: E87. Review.

32.

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

Rajan-Babu IS, Lian M, Tran AH, Dang TT, Le HT, Thanh MN, Lee CG, Chong SS.

J Mol Diagn. 2016 Sep;18(5):719-730. doi: 10.1016/j.jmoldx.2016.05.002. Epub 2016 Jul 1.

PMID:
27375073
34.

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

Zhao M, Lee CG, Law HY, Chong SS.

Neurodegener Dis. 2016;16(5-6):348-51. doi: 10.1159/000444714. Epub 2016 May 21.

PMID:
27207688
35.

Social cognitive predictors of academic and life satisfaction: Measurement and structural equivalence across three racial/ethnic groups.

Sheu HB, Mejia A, Rigali-Oiler M, Primé DR, Chong SS.

J Couns Psychol. 2016 Jul;63(4):460-74. doi: 10.1037/cou0000158. Epub 2016 May 12.

PMID:
27177025
36.

Risk Factors of Cognitive Impairment and Brief Cognitive Tests to Predict Cognitive Performance Determined by a Formal Neuropsychological Evaluation of Primary Health Care Patients.

Shaik MA, Chan QL, Xu J, Xu X, Hui RJ, Chong SS, Chen CL, Dong Y.

J Am Med Dir Assoc. 2016 Apr 1;17(4):343-7. doi: 10.1016/j.jamda.2015.12.007. Epub 2016 Jan 16.

PMID:
26785695
38.

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

Chandrasekara CH, Wijesundera WS, Perera HN, Chong SS, Rajan-Babu IS.

PLoS One. 2015 Dec 22;10(12):e0145537. doi: 10.1371/journal.pone.0145537. eCollection 2015.

39.

The reliability and validity of the informant AD8 by comparison with a series of cognitive assessment tools in primary healthcare.

Shaik MA, Xu X, Chan QL, Hui RJ, Chong SS, Chen CL, Dong Y.

Int Psychogeriatr. 2016 Mar;28(3):443-52. doi: 10.1017/S1041610215001702. Epub 2015 Oct 22.

PMID:
26489991
40.

Clinical utility of the informant AD8 as a dementia case finding instrument in primary healthcare.

Chan QL, Xu X, Shaik MA, Chong SS, Hui RJ, Chen CL, Dong Y.

J Alzheimers Dis. 2016;49(1):121-7. doi: 10.3233/JAD-150390.

PMID:
26444776
41.
42.

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.

Bu L, Chen Q, Wang H, Zhang T, Hetmanski JB, Schwender H, Parker M, Chou YH, Yeow V, Chong SS, Zhang B, Jabs EW, Scott AF, Beaty TH.

Birth Defects Res A Clin Mol Teratol. 2015 Oct;103(10):857-62. doi: 10.1002/bdra.23413. Epub 2015 Aug 17.

43.

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

Sun ZJ, Ng KH, Liao P, Zhang Y, Ng JL, Liu ID, Tan PH, Chong SS, Chan YH, Liu J, Davila S, Heng CK, Jordan SC, Soong TW, Yap HK.

Am J Transplant. 2015 Dec;15(12):3229-38. doi: 10.1111/ajt.13378. Epub 2015 Jul 3.

44.

Rapid and reliable preimplantation genetic diagnosis of common hemoglobin Bart's hydrops fetalis syndrome and hemoglobin H disease determinants using an enhanced single-tube decaplex polymerase chain reaction assay.

Chen M, Loh SF, Yu SL, Nair S, Tan HH, Nadarajah S, Wong PC, Ng SC, Prasath EB, Tan AS, Cheah FS, Saw EE, Chong SS.

Am J Hematol. 2015 Sep;90(9):E194-6. doi: 10.1002/ajh.24077. Epub 2015 Aug 14. No abstract available.

45.

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

Rajan-Babu IS, Law HY, Yoon CS, Lee CG, Chong SS.

Expert Rev Mol Med. 2015 May 4;17:e7. doi: 10.1017/erm.2015.5. Review.

46.

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

Lim GX, Loo YL, Mundhofir FE, Cayami FK, Faradz SM, Rajan-Babu IS, Chong SS, Koh YY, Guan M.

J Mol Diagn. 2015 May;17(3):302-14. doi: 10.1016/j.jmoldx.2014.12.005. Epub 2015 Mar 14.

PMID:
25776194
47.

Efficient and highly sensitive screen for myotonic dystrophy type 1 using a one-step triplet-primed PCR and melting curve assay.

Lian M, Rajan-Babu IS, Singh K, Lee CG, Law HY, Chong SS.

J Mol Diagn. 2015 Mar;17(2):128-35. doi: 10.1016/j.jmoldx.2014.10.001.

PMID:
25684273
48.

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

Chen M, Chan JK, Nadarajah S, Tan AS, Chan ML, Mathew J, Saw EE, Lim C, Wong W, Cheah FS, Law HY, Wong PC, Chong SS.

Prenat Diagn. 2015 Jun;35(6):534-43. doi: 10.1002/pd.4568. Epub 2015 Mar 1.

PMID:
25641621
49.

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

Rajan-Babu IS, Teo CR, Lian M, Lee CG, Law HY, Chong SS.

Expert Rev Mol Diagn. 2015 Mar;15(3):431-41. doi: 10.1586/14737159.2015.1001749. Epub 2015 Jan 12.

PMID:
25583300
50.

Disruption of FAT10-MAD2 binding inhibits tumor progression.

Theng SS, Wang W, Mah WC, Chan C, Zhuo J, Gao Y, Qin H, Lim L, Chong SS, Song J, Lee CG.

Proc Natl Acad Sci U S A. 2014 Dec 9;111(49):E5282-91. doi: 10.1073/pnas.1403383111. Epub 2014 Nov 24.

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