Biblio
Analysis of clinically relevant variants from ancestrally diverse Asian genomes. Nat Commun. 2022;13(1):6694.
Author Correction: Analysis and visualisation of electronic health records data to identify undiagnosed patients with rare genetic diseases. Sci Rep. 2024;14(1):10084.
CD1d expression in renal cell carcinoma is associated with higher relapse rates, poorer cancer-specific and overall survival. J Clin Pathol. 2014.
. Cluster analysis and visualisation of electronic health records data to identify undiagnosed patients with rare genetic diseases. Sci Rep. 2024;14(1):5056.
Contribution of common and rare variants to Asian neovascular age-related macular degeneration subtypes. Nat Commun. 2023;14(1):5574.
The DNA Structure-Specific Endonuclease MUS81 Mediates DNA Sensor STING-Dependent Host Rejection of Prostate Cancer Cells. Immunity. 2016.
Exome sequencing identifies highly recurrent MED12 somatic mutations in breast fibroadenoma. Nat Genet. 2014.
Genomic landscapes of breast fibroepithelial tumors. Nat Genet. 2015.
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.
A global catalog of whole-genome diversity from 233 primate species. Science. 2023;380(6648):906-913.
The landscape of tolerated genetic variation in humans and primates. Science. 2023;380(6648):eabn8153.
New insights from a multi-ethnic Asian progressive supranuclear palsy cohort. Parkinsonism Relat Disord. 2023;108:105296.
Pathogenesis of cholangiocarcinoma: From genetics to signalling pathways. Best Pract Res Clin Gastroenterol. 2015;29(2):233-244.
. The Singapore National Precision Medicine Strategy. Nat Genet. 2023.