Xiaoming Liu
Xiaoming Liu
Associate Professor, College of Public Health, University of South Florida
Verified email at - Homepage
Cited by
Cited by
A global reference for human genetic variation
1000 Genomes Project Consortium
Nature 526 (7571), 68-74, 2015
An integrated map of genetic variation from 1,092 human genomes
1000 Genomes Project Consortium
Nature 491 (7422), 56-65, 2012
Evolution and functional impact of rare coding variation from deep sequencing of human exomes
JA Tennessen, AW Bigham, TD O’Connor, W Fu, EE Kenny, S Gravel, ...
science 337 (6090), 64-69, 2012
Sequencing of 53,831 diverse genomes from the NHLBI TOPMed Program
D Taliun, DN Harris, MD Kessler, J Carlson, ZA Szpiech, R Torres, ...
Nature 590 (7845), 290-299, 2021
Comparison and integration of deleteriousness prediction methods for nonsynonymous SNVs in whole exome sequencing studies
C Dong, P Wei, X Jian, R Gibbs, E Boerwinkle, K Wang, X Liu
Human Molecular Genetics 24 (8), 2125-2137, 2015
Analysis of 6,515 exomes reveals the recent origin of most human protein-coding variants
W Fu, TD O’Connor, G Jun, HM Kang, G Abecasis, SM Leal, S Gabriel, ...
Nature 493 (7431), 216-220, 2013
dbNSFP v3.0: A One-Stop Database of Functional Predictions and Annotations for Human Nonsynonymous and Splice-Site SNVs
X Liu, C Wu, C Li, E Boerwinkle
Human Mutation 37 (3), 235-241, 2016
dbNSFP: a lightweight database of human nonsynonymous SNPs and their functional predictions
X Liu, X Jian, E Boerwinkle
Human mutation 32 (8), 894-899, 2011
Exome sequencing identifies rare LDLR and APOA5 alleles conferring risk for myocardial infarction
R Do, NO Stitziel, HH Won, AB Jørgensen, S Duga, PA Merlini, A Kiezun, ...
Nature 518 (7537), 102-106, 2015
dbNSFP v2. 0: A Database of Human Non‐synonymous SNVs and Their Functional Predictions and Annotations
X Liu, X Jian, E Boerwinkle
Human mutation 34 (9), E2393-E2402, 2013
In silico prediction of splice-altering single nucleotide variants in the human genome
X Jian, E Boerwinkle, X Liu
Nucleic acids research 42 (22), 13534-13544, 2014
Integrating sequence and array data to create an improved 1000 Genomes Project haplotype reference panel
O Delaneau, J Marchini, 1000 Genomes Project Consortium
Nature Communications 5, 2014
Integrative annotation of variants from 1092 humans: application to cancer genomics
E Khurana, Y Fu, V Colonna, XJ Mu, HM Kang, T Lappalainen, A Sboner, ...
Science 342 (6154), 1235587, 2013
TGFB2 mutations cause familial thoracic aortic aneurysms and dissections associated with mild systemic features of Marfan syndrome
C Boileau, DC Guo, N Hanna, ES Regalado, D Detaint, L Gong, M Varret, ...
Nature genetics 44 (8), 916-921, 2012
dbNSFP v4: a comprehensive database of transcript-specific functional predictions and annotations for human nonsynonymous and splice-site SNVs
X Liu, C Li, C Mou, Y Dong, Y Tu
Genome Medicine 12, 103, 2020
Exploring population size changes using SNP frequency spectra
X Liu, YX Fu
Nature Genetics 47 (5), 555-559, 2015
Genome-wide scan for familial nasopharyngeal carcinoma reveals evidence of linkage to chromosome 4
BJ Feng, W Huang, YY Shugart, MK Lee, F Zhang, JC Xia, HY Wang, ...
Nature genetics 31 (4), 395-399, 2002
Deep resequencing reveals excess rare recent variants consistent with explosive population growth
A Coventry, LM Bull-Otterson, X Liu, AG Clark, TJ Maxwell, J Crosby, ...
Nature communications 1 (1), 131, 2010
Exome sequencing of extreme phenotypes identifies DCTN4 as a modifier of chronic Pseudomonas aeruginosa infection in cystic fibrosis
MJ Emond, T Louie, J Emerson, W Zhao, RA Mathias, MR Knowles, ...
Nature genetics 44 (8), 886-889, 2012
Whole-exome sequencing identifies rare and low-frequency coding variants associated with LDL cholesterol
LA Lange, Y Hu, H Zhang, C Xue, EM Schmidt, ZZ Tang, C Bizon, ...
The American Journal of Human Genetics 94 (2), 233-245, 2014
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