| HLA-B*13:01 and the Dapsone Hypersensitivity Syndrome FR Zhang, H Liu, A Irwanto, XA Fu, Y Li, GQ Yu, YX Yu, MF Chen, HQ Low, ... New England Journal of Medicine 369 (17), 1620-1628, 2013 | 342 | 2013 |
| Genome-wide meta-analysis identifies multiple novel associations and ethnic heterogeneity of psoriasis susceptibility X Yin, HQ Low, L Wang, Y Li, E Ellinghaus, J Han, X Estivill, L Sun, X Zuo, ... Nature communications 6 (1), 6916, 2015 | 206 | 2015 |
| Discovery of six new susceptibility loci and analysis of pleiotropic effects in leprosy H Liu, A Irwanto, X Fu, G Yu, Y Yu, Y Sun, C Wang, Z Wang, Y Okada, ... Nature genetics 47 (3), 267-271, 2015 | 131 | 2015 |
| A rare lysosomal enzyme gene SMPD1 variant (p. R591C) associates with Parkinson's disease JN Foo, H Liany, JX Bei, XQ Yu, J Liu, WL Au, KM Prakash, LC Tan, ... Neurobiology of aging 34 (12), 2890. e13-2890. e15, 2013 | 94 | 2013 |
| Impaired Development of Neural‐Crest Cell‐Derived Organs and Intellectual Disability Caused by MED13L Haploinsufficiency KH Utami, CL Winata, AM Hillmer, I Aksoy, HT Long, H Liany, EGY Chew, ... Human mutation 35 (11), 1311-1320, 2014 | 65 | 2014 |
| Genome-wide analysis of protein-coding variants in leprosy H Liu, Z Wang, Y Li, G Yu, X Fu, C Wang, W Liu, Y Yu, F Bao, A Irwanto, ... Journal of Investigative Dermatology 137 (12), 2544-2551, 2017 | 46 | 2017 |
| Genome-wide linkage, exome sequencing and functional analyses identify ABCB6 as the pathogenic gene of dyschromatosis universalis hereditaria H Liu, Y Li, KKH Hung, N Wang, C Wang, X Chen, D Sheng, X Fu, K See, ... PLoS One 9 (2), e87250, 2014 | 45 | 2014 |
| Predicting synthetic lethal interactions using heterogeneous data sources H Liany, A Jeyasekharan, V Rajan Bioinformatics 36 (7), 2209-2216, 2020 | 42 | 2020 |
| Exome sequencing and rare variant analysis reveals multiple filaggrin mutations in Bangladeshi families with atopic eczema and additional risk genes M Pigors, JEA Common, XFCC Wong, S Malik, CA Scott, N Tabarra, ... Journal of Investigative Dermatology 138 (12), 2674-2677, 2018 | 38 | 2018 |
| Integrative analysis identifies key molecular signatures underlying neurodevelopmental deficits in fragile X syndrome KH Utami, NH Skotte, AR Colaço, NABM Yusof, B Sim, XY Yeo, HG Bae, ... Biological Psychiatry 88 (6), 500-511, 2020 | 37 | 2020 |
| Targeted next-generation sequencing to diagnose disorders of HDL cholesterol SN Sadananda, JN Foo, MT Toh, L Cermakova, L Trigueros-Motos, ... Journal of Lipid Research 56 (10), 1993-2001, 2015 | 37 | 2015 |
| A Synonymous Variant in IL10RA Affects RNA Splicing in Paediatric Patients with Refractory Inflammatory Bowel Disease SH Oh, J Baek, H Liany, JN Foo, KM Kim, SCO Yang, J Liu, K Song Journal of Crohn's and Colitis 10 (11), 1366-1371, 2016 | 34 | 2016 |
| Discovery of a novel genetic susceptibility locus on X chromosome for systemic lupus erythematosus Z Zhu, Z Liang, H Liany, C Yang, L Wen, Z Lin, Y Sheng, Y Lin, L Ye, ... Arthritis research & therapy 17, 1-9, 2015 | 32 | 2015 |
| Analysis of non-synonymous-coding variants of Parkinson's disease-related pathogenic and susceptibility genes in East Asian populations JN Foo, LC Tan, H Liany, TH Koh, ID Irwan, YY Ng, A Ahmad-Annuar, ... Human molecular genetics 23 (14), 3891-3897, 2014 | 32 | 2014 |
| An association study of TOLL and CARD with leprosy susceptibility in Chinese population H Liu, F Bao, A Irwanto, X Fu, N Lu, G Yu, Y Yu, Y Sun, H Low, Y Li, ... Human molecular genetics 22 (21), 4430-4437, 2013 | 32 | 2013 |
| DNAJ mutations are rare in Chinese Parkinson's disease patients and controls JN Foo, H Liany, LC Tan, WL Au, KM Prakash, J Liu, EK Tan Neurobiology of aging 35 (4), 935. e1-935. e2, 2014 | 30 | 2014 |
| Analysis of POFUT1 Gene Mutation in a Chinese Family with Dowling-Degos Disease M Chen, Y Li, H Liu, X Fu, Y Yu, G Yu, C Wang, F Bao, H Liany, Z Wang, ... PLoS One 9 (8), e104496, 2014 | 13 | 2014 |
| Linking a genome‐wide association study signal to a LRRK2 coding variant in Parkinson's disease JN Foo, SJ Chung, LC Tan, H Liany, HS Ryu, M Hong, TH Koh, ID Irwan, ... Movement Disorders 31 (4), 484-487, 2016 | 11 | 2016 |
| The association between rare large duplication of 16p11. 2 and schizophrenia in the Singaporean Chinese population. X Zheng, JX Bei, H Xu, J Lee, SA Chong, K Sim, H Liany, TE Shyong, ... Schizophrenia research 146 (1-3), 368-369, 2013 | 10 | 2013 |
| Evaluation of novel Parkinson's disease candidate genes in the Chinese population EGY Chew, H Liany, LCS Tan, WL Au, KM Prakash, AA Annuar, ... Neurobiology of aging 74, 235. e1-235. e4, 2019 | 8 | 2019 |
