| Initial whole-genome sequencing and analysis of the host genetic contribution to COVID-19 severity and susceptibility F Wang, S Huang, R Gao, Y Zhou, C Lai, Z Li, W Xian, X Qian, Z Li, ... Cell discovery 6 (1), 83, 2020 | 214 | 2020 |
| Genomic analyses from non-invasive prenatal testing reveal genetic associations, patterns of viral infections, and Chinese population history S Liu, S Huang, F Chen, L Zhao, Y Yuan, SS Francis, L Fang, Z Li, L Lin, ... Cell 175 (2), 347-359. e14, 2018 | 210 | 2018 |
| Rapid detection of structural variation in a human genome using nanochannel-based genome mapping technology H Cao, AR Hastie, D Cao, ET Lam, Y Sun, H Huang, X Liu, L Lin, ... GigaScience 3 (1), 2047-217X-3-34, 2014 | 209 | 2014 |
| Novel variation and de novo mutation rates in population-wide de novo assembled Danish trios S Besenbacher, S Liu, JMG Izarzugaza, J Grove, K Belling, J Bork-Jensen, ... Nature communications 6 (1), 5969, 2015 | 186 | 2015 |
| An atlas of DNA methylomes in porcine adipose and muscle tissues M Li, H Wu, Z Luo, Y Xia, J Guan, T Wang, Y Gu, L Chen, K Zhang, J Ma, ... Nature communications 3 (1), 850, 2012 | 178 | 2012 |
| Sequencing and de novo assembly of 150 genomes from Denmark as a population reference L Maretty, JM Jensen, B Petersen, JA Sibbesen, S Liu, P Villesen, L Skov, ... Nature 548 (7665), 87-91, 2017 | 161 | 2017 |
| Structural variation in two human genomes mapped at single-nucleotide resolution by whole genome de novo assembly Y Li, H Zheng, R Luo, H Wu, H Zhu, R Li, H Cao, B Wu, S Huang, H Shao, ... Nature biotechnology 29 (8), 723-730, 2011 | 144 | 2011 |
| De novo assembly of a haplotype-resolved human genome H Cao, H Wu, R Luo, S Huang, Y Sun, X Tong, Y Xie, B Liu, H Yang, ... Nature biotechnology 33 (6), 617-622, 2015 | 84 | 2015 |
| Bisulfite sequencing reveals that Aspergillus flavus holds a hollow in DNA methylation SY Liu, JQ Lin, HL Wu, CC Wang, SJ Huang, YF Luo, JH Sun, JX Zhou, ... PloS one 7 (1), e30349, 2012 | 70 | 2012 |
| Systematic assessment of reduced representation bisulfite sequencing to human blood samples: A promising method for large-sample-scale epigenomic studies L Wang, J Sun, H Wu, S Liu, J Wang, B Wu, S Huang, N Li, J Wang, ... Journal of biotechnology 157 (1), 1-6, 2012 | 58 | 2012 |
| Identifying occult maternal malignancies from 1.93 million pregnant women undergoing noninvasive prenatal screening tests X Ji, J Li, Y Huang, PL Sung, Y Yuan, Q Liu, Y Chen, J Ju, Y Zhou, ... Genetics in Medicine 21 (10), 2293-2302, 2019 | 44 | 2019 |
| Discovery, genotyping and characterization of structural variation and novel sequence at single nucleotide resolution from de novo genome assemblies on a … S Liu, S Huang, J Rao, W Ye, Genome Denmark Consortium, A Krogh, ... Gigascience 4 (1), s13742-015-0103-4, 2015 | 24 | 2015 |
| Stochastic anomaly of methylome but persistent SRY hypermethylation in disorder of sex development in canine somatic cell nuclear transfer YH Jeong, H Lu, CH Park, M Li, H Luo, JJ Kim, S Liu, KH Ko, S Huang, ... Scientific reports 6 (1), 31088, 2016 | 22 | 2016 |
| Assembly and analysis of 100 full MHC haplotypes from the Danish population JM Jensen, P Villesen, RM Friborg, T Mailund, S Besenbacher, ... Genome research 27 (9), 1597-1607, 2017 | 20 | 2017 |
| The Born in Guangzhou Cohort Study enables generational genetic discoveries S Huang, S Liu, M Huang, JR He, C Wang, T Wang, X Feng, Y Kuang, ... Nature 626 (7999), 565-573, 2024 | 5 | 2024 |
| Method of reconstructing haplotype of diploid and system thereof S Huang, P Sun, H Wu, J Wang, J Wang, H Yang US Patent App. 14/369,604, 2015 | 5 | 2015 |
| CMDB: the comprehensive population genome variation database of China Z Li, X Jiang, M Fang, Y Bai, S Liu, S Huang, X Jin Nucleic acids research 51 (D1), D890-D895, 2023 | 4 | 2023 |
| Genome-wide association and Mendelian randomisation analysis among 30,699 Chinese pregnant women identifies novel genetic and molecular risk factors for gestational diabetes … J Zhen, Y Gu, P Wang, W Wang, S Bian, S Huang, H Liang, M Huang, ... Diabetologia 67 (4), 703-713, 2024 | | 2024 |
| Base mutation detection method and apparatus based on sequencing data, and storage medium S Liu, S Huang, X Jin US Patent App. 17/522,920, 2022 | | 2022 |
| 基于组装的人类基因组群体结构性变异研究 黄树嘉 华南理工大学, 2015 | | 2015 |
Siyang LiuSchool of Public Health (Shenzhen), Sun-Yat-Sen UniversityVerified email at mail.sysu.edu.cn
