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Xiao Liu (刘晓)
Xiao Liu (刘晓)
Associate Professor, Shenzhen International Graduate School, Tsinghua University
在 sz.tsinghua.edu.cn 的电子邮件经过验证 - 首页
标题
引用次数
引用次数
年份
A global reference for human genetic variation
1000 Genomes Project Consortium
Nature 526 (7571), 68, 2015
14764*2015
An integrated map of genetic variation from 1,092 human genomes
1000 Genomes Project Consortium
Nature 491 (7422), 56, 2012
82642012
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
18462015
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
17322010
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
13772010
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
9762012
An abundance of rare functional variants in 202 drug target genes sequenced in 14,002 people
MR Nelson, D Wegmann, MG Ehm, D Kessner, P St. Jean, C Verzilli, ...
Science 337 (6090), 100-104, 2012
8012012
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
7282012
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
5612013
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), 158-163, 2015
4972015
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
3762010
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
3652012
Punctuated bursts in human male demography inferred from 1,244 worldwide Y-chromosome sequences
GD Poznik, Y Xue, FL Mendez, TF Willems, A Massaia, MA Wilson Sayres, ...
Nature genetics 48 (6), 593-599, 2016
3552016
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), 12992, 2016
2942016
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
2072011
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
2062014
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
2022016
Efficient and unique cobarcoding of second-generation sequencing reads from long DNA molecules enabling cost-effective and accurate sequencing, haplotyping, and de novo assembly
O Wang, R Chin, X Cheng, MKY Wu, Q Mao, J Tang, Y Sun, E Anderson, ...
Genome research 29 (5), 798-808, 2019
1912019
Novel loci and pathways significantly associated with longevity
YI Zeng, C Nie, J Min, X Liu, M Li, H Chen, H Xu, M Wang, T Ni, Y Li, ...
Scientific reports 6 (1), 21243, 2016
1822016
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
1802013
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