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Exome sequencing in Asian populations identifies low-frequency and rare coding variation influencing Parkinson's disease risk.
Chew EG, Liu Z, Li Z, Chung SJ, Lian MM, Tandiono M, Heng YJ, Ng EY, Tan LC, Chng WL, Tan TJ, Peh EK, Ho YS, Chen XY, Lim EY, Chang CH, Leong JJ, Peh TX, Chan LL, Chao Y, Au WL, Prakash KM, Lim JL, Tay YW, Mok V, Chan AY, Lin JJ, Jeon BS, Song K, Tham CC, Pang CP, Ahn J, Park KH, Wiggs JL, Aung T, Tan AH, Ahmad Annuar A, Makarious MB, Blauwendraat C, Nalls MA, Robak LA, Alcalay RN, Gan-Or Z, Reynolds R, Lim SY, Xia Y, Khor CC, Tan EK, Wang Z, Foo JN. Chew EG, et al. Among authors: tham cc. Nat Aging. 2024 Nov 21. doi: 10.1038/s43587-024-00760-7. Online ahead of print. Nat Aging. 2024. PMID: 39572736
Association of polymorphisms in the HTRA1 gene with myopia.
Chen SY, Xu YM, Tam POS, Pang CP, Tham CC, Yam JC, Chen LJ. Chen SY, et al. Among authors: tham cc. Br J Ophthalmol. 2024 Oct 15:bjo-2024-325935. doi: 10.1136/bjo-2024-325935. Online ahead of print. Br J Ophthalmol. 2024. PMID: 39406463
Associations of genetic variants for refractive error and axial length in adults with ocular endophenotypes in children: a cross-sectional and longitudinal study.
Zaabaar E, Shing E, Zhang XJ, Wang Y, Kam KW, Zhang Y, Yip WWK, Young AL, Tam POS, Tham CC, Pang CP, Yam JC, Chen LJ. Zaabaar E, et al. Among authors: tham cc. Br J Ophthalmol. 2024 Sep 26:bjo-2024-325606. doi: 10.1136/bjo-2024-325606. Online ahead of print. Br J Ophthalmol. 2024. PMID: 39326895
537 results