Samuel S. Chong

Associate Professor

National University of Singapore (NUS)

Singapore

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Samuel S. Chong is an Associate Professor at the National University of Singapore. His research focuses on preimplantation genetic testing, molecular genetics, and the development of innovative diagnostic tools in the context of genetic disorders. Recent publications include work on methods for detecting pathogenic variants and assessing genetic responses in diseases such as Spinocerebellar Ataxia and Rheumatoid Arthritis.

Articles (12)

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2025

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2024

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2022

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2022

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2022

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2022

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2021

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2021

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2021

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2021

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2021

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2021

Collaborators (2)

Vivienne Tan

Lecturer

National University of Singapore

SINGAPORE

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Caroline Lee

Associate Professor

National University of Singapore (NUS)

SINGAPORE

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Samuel S. Chong

Research Interests

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Articles (12)

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

Preimplantation Genetic Testing of Spinocerebellar Ataxia Type 3/Machado–Joseph Disease—Robust Tools for Direct and Indirect Detection of the ATXN3 (CAG)n Repeat Expansion

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

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

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

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

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

Clinicopathological‐associated regulatory network of deregulated circrnas in hepatocellular carcinoma

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

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

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

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

Collaborators (2)

Vivienne Tan

Caroline Lee

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