Herty Liany
Herty Liany
Geverifieerd e-mailadres voor u.nus.edu
Titel
Geciteerd door
Geciteerd door
Jaar
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
2112013
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), 1-11, 2015
1262015
Discovery of six new susceptibility loci and analysis of pleiotropic effects in leprosy
H Liu, A Irwanto, G Yu, Y Yu, Y Sun, C Wang, Z Wang, Y Okada, H Low, ...
Nature genetics 47 (3), 267-271, 2015
1002015
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
612013
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
412014
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
372014
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
282014
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
272014
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
252016
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
222017
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
202015
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
182013
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), 1-9, 2015
172015
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
142018
Analysis of POFUT1 gene mutation in a Chinese family with Dowling-Degos disease
M Chen, Y Li, H Liu, Y Yu, G Yu, C Wang, F Bao, H Liany, Z Wang, Z Shi, ...
PloS one 9 (8), e104496, 2014
122014
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
92016
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
92013
Predicting synthetic lethal interactions using heterogeneous data sources
H Liany, A Jeyasekharan, V Rajan
Bioinformatics 36 (7), 2209-2216, 2020
82020
Integrative analysis identifies key molecular signatures underlying neurodevelopmental deficits in fragile X syndrome
KH Utami, NH Skotte, AR Colašo, NABM Yusof, B Sim, XY Yeo, HG Bae, ...
Biological Psychiatry 88 (6), 500-511, 2020
62020
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
32019
Het systeem kan de bewerking nu niet uitvoeren. Probeer het later opnieuw.
Artikelen 1–20