| The human interferon-induced MxA protein inhibits early stages of influenza A virus infection by retaining the incoming viral genome in the cytoplasm H Xiao, MJ Killip, P Staeheli, RE Randall, D Jackson Journal of virology 87 (23), 13053-13058, 2013 | 155 | 2013 |
| Sumoylation of the nucleocapsid protein of severe acute respiratory syndrome coronavirus FQ Li, H Xiao, JP Tam, DX Liu FEBS letters 579 (11), 2387-2396, 2005 | 112 | 2005 |
| Coronavirus spike protein inhibits host cell translation by interaction with eIF3f H Xiao, LH Xu, Y Yamada, DX Liu PLoS one 3 (1), e1494, 2008 | 93 | 2008 |
| Interaction of the coronavirus infectious bronchitis virus membrane protein with β-actin and its implication in virion assembly and budding J Wang, S Fang, H Xiao, B Chen, JP Tam, DX Liu PLoS One 4 (3), e4908, 2009 | 76 | 2009 |
| WDR45 mutation impairs the autophagic degradation of transferrin receptor and promotes ferroptosis PLCW Qiuhong Xiong, Xin Li, Wenjing Li, Guangxin Chen, Han Xiao Front. Mol. Biosci., 2021 | 52 | 2021 |
| A novel α-galactosidase A splicing mutation predisposes to Fabry disease P Li, L Zhang, N Zhao, Q Xiong, YA Zhou, C Wu, H Xiao Frontiers in Genetics 10, 60, 2019 | 18 | 2019 |
| A novel de novo mutation in COL2A1 leading to spondyloepiphyseal dysplasia congenita in a Chinese family Q Xiong, YI Liu, YU Xue, S Liu, J Wang, P Li, C Wu, Y Yang, H Xiao Human Genome Variation 5 (1), 1-3, 2018 | 16 | 2018 |
| Functional evidence for a de novo mutation in WDR45 leading to BPAN in a Chinese girl Q Xiong, W Li, P Li, Z Zhao, C Wu, H Xiao Molecular genetics & genomic medicine 7 (9), e858, 2019 | 13 | 2019 |
| Sumoylation of the nucleocapsid protein of severe acute respiratory syndrome coronavirus by interaction with Ubc9 Q Li, H Xiao, JP Tam, DX Liu The Nidoviruses: Toward Control of SARS and other Nidovirus Diseases, 121-126, 2006 | 12 | 2006 |
| A novel pathogenic splice site variation in STK11 gene results in Peutz–Jeghers syndrome N Zhao, H Wu, P Li, Y Wang, L Dong, H Xiao, C Wu Molecular Genetics & Genomic Medicine 9 (8), e1729, 2021 | 9 | 2021 |
| Whole-exome sequencing analysis of Waardenburg syndrome in a Chinese family JFHX Dezhong Chen, Na Zhao, Jing Wang, Zhuoyu Li, Changxin Wu Nature/HGV 4, 17027, 2017 | 9* | 2017 |
| Feasibility of low-throughput next generation sequencing for germline DNA screening NS Sapari, E Elahi, M Wu, M Loh, HK Ng, X Han, HL Yap, TP Klemm, ... Clinical chemistry 60 (12), 1549-1557, 2014 | 9 | 2014 |
| Two novel hydroxymethylbilane synthase splicing mutations predispose to acute intermittent porphyria Y Zhang, H Xiao, Q Xiong, C Wu, P Li International Journal of Molecular Sciences 22 (20), 11008, 2021 | 6 | 2021 |
| Functional evaluation of a novel GLA causative mutation in Fabry disease P Li, L Zhang, Q Xiong, Z Wang, X Cui, YA Zhou, Y Wang, H Xiao, C Wu Molecular Genetics & Genomic Medicine 7 (9), e864, 2019 | 6 | 2019 |
| Functional Characterization of FH Mutation c.557G>A Underlies Uterine Leiomyomas P Li, Y Wu, H Wu, Q Xiong, N Zhao, G Chen, C Wu, H Xiao International Journal of Molecular Sciences 23 (3), 1452, 2022 | 5 | 2022 |
| Identification of Two Novel Compound Heterozygous EIF2AK3 Mutations Underlying Wolcott–Rallison Syndrome in a Chinese Family N Zhao, Y Yang, P Li, Q Xiong, H Xiao, C Wu Frontiers in pediatrics 9, 679646, 2021 | 5 | 2021 |
| Identification and Functional Evaluation of a Novel TBX4 Mutation Underlies Small Patella Syndrome P Li, W Lan, J Li, Y Zhang, Q Xiong, J Ye, C Wu, H Xiao International Journal of Molecular Sciences 23 (4), 2075, 2022 | 4 | 2022 |
| Identification of a novel compound heterozygous IDUA mutation underlies Mucopolysaccharidoses type I in a Chinese pedigree YA Zhou, P Li, Y Zhang, Q Xiong, C Li, Z Zhao, Y Wang, H Xiao Molecular Genetics & Genomic Medicine 8 (1), e1058, 2020 | 2 | 2020 |
| Identification of a novel COL2A1 variant in a pedigree affected with spondyloepiphyseal dysplasia congenita Y Wang, H Xiao, Z Wang, N Zhao, Y Xue Zhonghua yi xue yi Chuan xue za zhi= Zhonghua Yixue Yichuanxue Zazhi …, 2019 | 1 | 2019 |
| Novel de novo Mutation in the Autophagy Gene WDR45 Causes BPAN in a Chinese Family HXY Xiao, Y Liu, W Li, N Zhao, Q Xiong, P Li, C Wu, Y Yang Journal of Molecular and Genetic Medicine 12 (4), 1-4, 2018 | 1 | 2018 |
James P TamProfessor, Nanyang Technological University確認したメール アドレス: ntu.edu.sg