Publications
Chang, C. H.*, Chew, E. G. Y.*, Lian, M. M., Tandiono, M., Li, Z., Chung, S. J., Tan, L. C. S., Au, W.-L., Prakash, K. M., Ahmad-Annuar, A., Tan, A. H., Mok, V., Chan, A. Y. Y., Lin, J.-J., Jeon, B. S., Khor, C. C., Lim, S.-Y., Tan, E.-K., & Foo, J. N. (2025). Rare SV2C coding variants in Parkinson's disease risk. Journal of Parkinson's Disease, 1877718X241300298.https://doi.org/10.1177/1877718X241300298
Chew, E. G. Y., Liu, Z., Li, Z., Chung, S. J., Lian, M. M., Tandiono, M., Ng, E. Y., Tan, L. C. S., Chng, W. L., Tan, T. J., Peh, E. K. L., Ho, Y. S., Chen, X. Y., Lim, E. Y. T., Chang, C. H. , Leong, J. J., Heng, Y. J., Peh, T. X., Chan, L.-L., … Foo, J. N. (2024). Exome sequencing in Asian populations identifies low-frequency and rare coding variation influencing Parkinson's disease risk. Nature Aging.https://doi.org/10.1038/s43587-024-00760-7
Chang, C. H., Lim, K. L., & Foo, J. N. (2024). Synaptic Vesicle Glycoprotein 2C: a role in Parkinson's disease. Frontiers in Cellular Neuroscience, 18.https://doi.org/10.3389/fncel.2024.1437144
Ali, G., Awan, N. B., Sadia, Khawaja, A. W., Foo, J. N., Khor, C. C., Chang, C.-H. , Chew, E. G., Kiani, F. R., & Jelani, M. (2020). Identification of a recurrent nonsense mutation in HR gene responsible for atrichia with papular lesions in two Kashmiri families. The Journal of Gene Medicine, 22(5), e3167.https://doi.org/10.1002/jgm.3167
Conference Posters
“Functional Characterisation of SV2C and its variants as a Parkinson's Disease-associated Gene.” Neuroscience 2023, Society for Neuroscience, Washington D.C., United States.