Xiao Liu (刘晓)
Xiao Liu (刘晓)
Associate Professor, Graduate School at Shenzhen, Tsinghua University
Verified email at sz.tsinghua.edu.cn - Homepage
Cited by
Cited by
A global reference for human genetic variation
1000 Genomes Project Consortium
Nature 526 (7571), 68, 2015
An integrated map of genetic variation from 1,092 human genomes
1000 Genomes Project Consortium
Nature 491 (7422), 56, 2012
Sequencing of 50 human exomes reveals adaptation to high altitude
X Yi, Y Liang, E Huerta-Sanchez, X Jin, ZXP Cuo, JE Pool, X Xu, H Jiang, ...
science 329 (5987), 75-78, 2010
The sequence and de novo assembly of the giant panda genome
R Li, W Fan, G Tian, H Zhu, L He, J Cai, Q Huang, Q Cai, B Li, Y Bai, ...
Nature 463 (7279), 311-317, 2010
Molecular analysis of gastric cancer identifies subtypes associated with distinct clinical outcomes
R Cristescu, J Lee, M Nebozhyn, KM Kim, JC Ting, SS Wong, J Liu, ...
Nature medicine 21 (5), 449-456, 2015
An abundance of rare functional variants in 202 drug target genes sequenced in 14,002 people
MR Nelson, D Wegmann, MG Ehm, D Kessner, PS Jean, C Verzilli, ...
Science 337 (6090), 100-104, 2012
Genome-wide survey of recurrent HBV integration in hepatocellular carcinoma
WK Sung, H Zheng, S Li, R Chen, X Liu, Y Li, NP Lee, WH Lee, ...
Nature genetics 44 (7), 765-769, 2012
Single-cell exome sequencing reveals single-nucleotide mutation characteristics of a kidney tumor
X Xu, Y Hou, X Yin, L Bao, A Tang, L Song, F Li, S Tsang, K Wu, H Wu, ...
Cell 148 (5), 886-895, 2012
Whole-genome sequencing identifies recurrent mutations in hepatocellular carcinoma
Z Kan, H Zheng, X Liu, S Li, TD Barber, Z Gong, H Gao, K Hao, ...
Genome research 23 (9), 1422-1433, 2013
Resequencing of 200 human exomes identifies an excess of low-frequency non-synonymous coding variants
Y Li, N Vinckenbosch, G Tian, E Huerta-Sanchez, T Jiang, H Jiang, ...
Nature genetics 42 (11), 969-972, 2010
Frequent mutations of genes encoding ubiquitin-mediated proteolysis pathway components in clear cell renal cell carcinoma
G Guo, Y Gui, S Gao, A Tang, X Hu, Y Huang, W Jia, Z Li, M He, L Sun, ...
Nature genetics 44 (1), 17-19, 2012
Genome-wide profiling of HPV integration in cervical cancer identifies clustered genomic hot spots and a potential microhomology-mediated integration mechanism
Z Hu, D Zhu, W Wang, W Li, W Jia, X Zeng, W Ding, L Yu, X Wang, ...
Nature genetics 47 (2), 158, 2015
Punctuated bursts in human male demography inferred from 1,244 worldwide Y-chromosome sequences
GD Poznik, Y Xue, FL Mendez, TF Willems, A Massaia, MAW Sayres, ...
Nature genetics 48 (6), 593-599, 2016
BIPES, a cost-effective high-throughput method for assessing microbial diversity
HW Zhou, DF Li, NFY Tam, XT Jiang, H Zhang, HF Sheng, J Qin, X Liu, ...
The ISME journal 5 (4), 741-749, 2011
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
Association between variants of PRDM1 and NDP52 and Crohn's disease, based on exome sequencing and functional studies
D Ellinghaus, H Zhang, S Zeissig, S Lipinski, A Till, T Jiang, B Stade, ...
Gastroenterology 145 (2), 339-347, 2013
Comprehensive comparison of three commercial human whole-exome capture platforms
Y Xu, H Jiang, C Tyler-Smith, Y Xue, T Jiang, J Wang, M Wu, X Liu, G Tian, ...
Genome biology 12 (9), 1-12, 2011
Genomic and oncogenic preference of HBV integration in hepatocellular carcinoma
LH Zhao, X Liu, HX Yan, WY Li, X Zeng, Y Yang, J Zhao, SP Liu, ...
Nature communications 7 (1), 1-10, 2016
Exome sequencing-driven discovery of coding polymorphisms associated with common metabolic phenotypes
A Albrechtsen, N Grarup, Y Li, T SparsÝ, G Tian, H Cao, T Jiang, SY Kim, ...
Diabetologia 56 (2), 298-310, 2013
Deep sequencing of the MHC region in the Chinese population contributes to studies of complex disease
F Zhou, H Cao, X Zuo, T Zhang, X Zhang, X Liu, R Xu, G Chen, Y Zhang, ...
Nature genetics 48 (7), 740-746, 2016
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