Association between telomere length and risk of cancer and non-neoplastic diseases: a mendelian randomization study PC Haycock, S Burgess, A Nounu, J Zheng, GN Okoli, J Bowden, ... Jama oncology 3 (5), 636-651, 2017 | 530 | 2017 |
Seventy-five genetic loci influencing the human red blood cell. P van der Harst, W Zhang, LI Mateo, A Rendon, N Verweij, J Sehmi, ... Nature, 2012 | 391 | 2012 |
Meta-analysis of genome-wide association studies identifies ten loci influencing allergic sensitization K Bønnelykke, MC Matheson, TH Pers, R Granell, DP Strachan, AC Alves, ... Nature genetics 45 (8), 902-906, 2013 | 302 | 2013 |
Genome-wide association analysis identifies 11 risk variants associated with the asthma with hay fever phenotype MAR Ferreira, MC Matheson, CS Tang, R Granell, W Ang, J Hui, AK Kiefer, ... Journal of Allergy and Clinical Immunology 133 (6), 1564-1571, 2014 | 263 | 2014 |
Genome-wide association study identifies NRG1 as a susceptibility locus for Hirschsprung's disease MM Garcia-Barcelo, CS Tang, ES Ngan, VC Lui, Y Chen, M So, TY Leon, ... Proceedings of the National Academy of Sciences 106 (8), 2694-2699, 2009 | 211 | 2009 |
Genome-wide association study identifies a susceptibility locus for biliary atresia on 10q24. 2 MM Garcia-Barceló, MY Yeung, XP Miao, CSM Tang, G Chen, MT So, ... Human molecular genetics 19 (14), 2917-2925, 2010 | 166 | 2010 |
Exome chip meta-analysis identifies novel loci and East Asian–specific coding variants that contribute to lipid levels and coronary artery disease X Lu, GM Peloso, DJ Liu, Y Wu, H Zhang, W Zhou, J Li, CS Tang, ... Nature genetics 49 (12), 1722-1730, 2017 | 144 | 2017 |
Exome-wide association analysis reveals novel coding sequence variants associated with lipid traits in Chinese CS Tang, H Zhang, CYY Cheung, M Xu, JCY Ho, W Zhou, SS Cherny, ... Nature communications 6 (1), 10206, 2015 | 100 | 2015 |
A polygenic risk score improves risk stratification of coronary artery disease: a large-scale prospective Chinese cohort study X Lu, Z Liu, Q Cui, F Liu, J Li, X Niu, C Shen, D Hu, K Huang, J Chen, ... European heart journal 43 (18), 1702-1711, 2022 | 99 | 2022 |
A gene-based test of association using canonical correlation analysis CS Tang, MAR Ferreira Bioinformatics 28 (6), 845-850, 2012 | 98 | 2012 |
Whole-exome sequencing identifies MST1R as a genetic susceptibility gene in nasopharyngeal carcinoma W Dai, H Zheng, AKL Cheung, CS Tang, JMY Ko, BWY Wong, ... Proceedings of the National Academy of Sciences 113 (12), 3317-3322, 2016 | 96 | 2016 |
Common genetic variants regulating ADD3 gene expression alter biliary atresia risk G Cheng, CSM Tang, EHM Wong, WWC Cheng, MT So, X Miao, R Zhang, ... Journal of hepatology 59 (6), 1285-1291, 2013 | 95 | 2013 |
Two-stage genome-wide association study identifies variants in CAMSAP1L1 as susceptibility loci for epilepsy in Chinese Y Guo, LW Baum, PC Sham, V Wong, PW Ng, CHT Lui, NC Sin, TH Tsoi, ... Human Molecular Genetics 21 (5), 1184-1189, 2012 | 90 | 2012 |
Whole exome sequencing coupled with unbiased functional analysis reveals new Hirschsprung disease genes H Gui, D Schriemer, WW Cheng, RK Chauhan, G Antiňolo, C Berrios, ... Genome biology 18, 1-13, 2017 | 88 | 2017 |
Identification of genes associated with Hirschsprung disease, based on whole-genome sequence analysis, and potential effects on enteric nervous system development CS Tang, P Li, FPL Lai, AX Fu, ST Lau, MT So, KNC Lui, Z Li, X Zhuang, ... Gastroenterology 155 (6), 1908-1922. e5, 2018 | 73 | 2018 |
Mutations in the NRG1 gene are associated with Hirschsprung disease CSM Tang, ESW Ngan, WK Tang, MT So, G Cheng, XP Miao, TYY Leon, ... Human genetics 131, 67-76, 2012 | 70 | 2012 |
HLA‐B* 38: 02: 01 predicts carbimazole/methimazole‐induced agranulocytosis CL Cheung, CW Sing, CSM Tang, VKF Cheng, M Pirmohamed, CH Choi, ... Clinical Pharmacology & Therapeutics 99 (5), 555-561, 2016 | 69 | 2016 |
Genome-Wide Copy Number Analysis Uncovers a New HSCR Gene: NRG3 CSM Tang, G Cheng, MT So, BHK Yip, XP Miao, EHM Wong, ESW Ngan, ... PLoS Genetics 8 (5), e1002687, 2012 | 67 | 2012 |
A Genome-Wide Linkage and Association Scan Reveals Novel Loci for Hypertension and Blood Pressure Traits Y Guo, B Tomlinson, T Chu, YJ Fang, H Gui, CS Tang, BH Yip, SS Cherny, ... PloS one 7 (2), e31489, 2012 | 49 | 2012 |
Identification of a wide spectrum of ciliary gene mutations in nonsyndromic biliary atresia patients implicates ciliary dysfunction as a novel disease mechanism WY Lam, CSM Tang, MT So, H Yue, JS Hsu, PHY Chung, JM Nicholls, ... EBioMedicine 71, 2021 | 45 | 2021 |