Grants:
As Principle Investigator
2 years: An Innovative Single Cell Multiplex Assay for Reliable and Accurate Preimplantation Genetic Diagnosis of Spinal Muscular Atrophy
Funding Agency: KTP-NUCMI
As Co-Principle Investigator
2 years: Simultaneous Molecular Testing for FRAXA/FMR1 and FRAXE/FMR2 Trinucleotide Repeat Hyperexpansions in X-Linked Intellectual Disability Using a Robust Duplex Triplet-Primed PCR AssayFunding Agency: KTP-NUCMI
1. Zhao M, Chen M, Tan ASC, Cheah FSH, Mathew J, Wong PC, Chong SS (2017). Single-tube tetradecaplex panel of highly polymorphic microsatellite markers < 1 Mb from F8 for simplified preimplantation genetic diagnosis of hemophilia A. Journal of Thrombosis and Haemostasis : JTH, 15(7):1473-1483. doi: 10.1111/jth.13685
2. Rajan-Babu IS, Lian M, Cheah FSH, Chen M, Tan ASC, Prasath EB, … Chong SS (2017). FMR1 CGG repeat expansion mutation detection and linked haplotype analysis for reliable and accurate preimplantation genetic diagnosis of fragile X syndrome. Expert Reviews in Molecular Medicine, 19:e10. doi: 10.1017/erm.2017.10
3. Chen M, Tan AS, Cheah FS, Saw EE, Chong SS (2015). 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. Electrophoresis, 36(23):2914-24. doi: 10.1002/elps.201500146
4. Chen M, Loh SF, Yu SL, Nair S, Tan HH, Cheah FS, … Chong SS (2015). 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. American Journal of Hematology, 90(9):E194-6. doi: 10.1002/ajh.24077
5. Chen M, Chan JK, Nadarajah S, Tan AS, Chan ML, Cheah FS, … Chong SS (2015). Single-tube nonaplex microsatellite PCR panel for preimplantation genetic diagnosis of Hb Bart's hydrops fetalis syndrome. Prenatal Diagnosis, 35(6):534-43. doi: 10.1002/pd.4568
