Biblio

Author Title Type [ Year(Asc)]
Filters: Author is Lim, Weng Khong  [Clear All Filters]
2024
Moynihan D, Monaco S, Ting TWah, Narasimhalu K, Hsieh J, Kam S, Lim JYing, Lim WKhong, Davila S, Bylstra Y, et al. Cluster analysis and visualisation of electronic health records data to identify undiagnosed patients with rare genetic diseases. Sci Rep. 2024;14(1):5056.
2023
Fan Q, Li H, Wang X, Tham Y-C, Teo KYi Chong, Yasuda M, Lim WKhong, Kwan YPing, Teo JXian, Chen C-J, et al. Contribution of common and rare variants to Asian neovascular age-related macular degeneration subtypes. Nat Commun. 2023;14(1):5574.
Kuderna LFK, Gao H, Janiak MC, Kuhlwilm M, Orkin JD, Bataillon T, Manu S, Valenzuela A, Bergman J, Rousselle M, et al. A global catalog of whole-genome diversity from 233 primate species. Science. 2023;380(6648):906-913.
Kuderna LFK, Ulirsch JC, Rashid S, Ameen M, Sundaram L, Hickey G, Cox AJ, Gao H, Kumar A, Aguet F, et al. Identification of constrained sequence elements across 239 primate genomes. Nature. 2023.
Gao H, Hamp T, Ede J, Schraiber JG, McRae J, Singer-Berk M, Yang Y, Dietrich ASD, Fiziev PP, Kuderna LFK, et al. The landscape of tolerated genetic variation in humans and primates. Science. 2023;380(6648):eabn8153.
Lim S-Y, Closas AMarl FDy, Tan AHuey, Lim JLun, Tan YJayne, Vijayanathan Y, Tay YWen, Khalid RBinti Abdu, Ng WKeong, Kanesalingam R, et al. New insights from a multi-ethnic Asian progressive supranuclear palsy cohort. Parkinsonism Relat Disord. 2023;108:105296.
Wong E, Bertin N, Hebrard M, Tirado-Magallanes R, Bellis C, Lim WKhong, Chua CYong, Tong PMei Lin, Chua R, Mak K, et al. The Singapore National Precision Medicine Strategy. Nat Genet. 2023.
2022
Chan SHoai, Bylstra Y, Teo JXian, Kuan JLing, Bertin N, Gonzalez-Porta M, Hebrard M, Tirado-Magallanes R, Tan JHui Juan, Jeyakani J, et al. Analysis of clinically relevant variants from ancestrally diverse Asian genomes. Nat Commun. 2022;13(1):6694.
2019
Ooi WFong, Nargund AM, Lim KJunliang, Zhang S, Xing M, Mandoli A, Lim JQuan, Ho SWei Ting, Guo Y, Yao X, et al. Integrated paired-end enhancer profiling and whole-genome sequencing reveals recurrent and enhancer hijacking in primary gastric adenocarcinoma. Gut. 2019.
2018
Toh MRen, Chiang JBang, Chong STing, Chan SHoai, Ishak NDiana Bint, Courtney E, Lee WHao, Al SMuhammad F, Allen JCarson, Lim KHon, et al. Germline Pathogenic Variants in Homologous Recombination and DNA Repair Genes in an Asian Cohort of Young-Onset Colorectal Cancer. JNCI Cancer Spectr. 2018;2(4):pky054.
2016
Ho SSW, Zhang WYL, Tan NYi Jie, Khatoo M, Suter MA, Tripathi S, Cheung FSG, Lim WKhong, Tan PHoon, Ngeow J, et al. The DNA Structure-Specific Endonuclease MUS81 Mediates DNA Sensor STING-Dependent Host Rejection of Prostate Cancer Cells. Immunity. 2016.
2015
Tan J, Ong CKiat, Lim WKhong, Ng CChuan Youn, Thike AAye, Ng LMoy, Rajasegaran V, Myint SSwe, Nagarajan S, Thangaraju S, et al. Genomic landscapes of breast fibroepithelial tumors. Nat Genet. 2015.
Kongpetch S, Jusakul A, Ong CKiat, Lim WKhong, Rozen SG, Tan P, Teh BTean. Pathogenesis of cholangiocarcinoma: From genetics to signalling pathways. Best Pract Res Clin Gastroenterol. 2015;29(2):233-244.
2014
Chong TWen, Goh FYiqian, Sim MYi, Huang HHong, Thike DAye Aye, Lim WKhong, Teh BTean, Tan PHoon. CD1d expression in renal cell carcinoma is associated with higher relapse rates, poorer cancer-specific and overall survival. J Clin Pathol. 2014.
Lim WKhong, Ong CKiat, Tan J, Thike AAye, Ng CChuan Youn, Rajasegaran V, Myint SSwe, Nagarajan S, Nasir NDiyana Md, McPherson JR, et al. Exome sequencing identifies highly recurrent MED12 somatic mutations in breast fibroadenoma. Nat Genet. 2014.