Xiaoming Liu

Cited by

	All	Since 2016
Citations	24147	17853
h-index	40	36
i10-index	66	57

3800

1900

950

2850

2012201320142015201620172018201920202021215 1055 1968 2473 3012 3328 3334 3690 3744 737

Co-authors

Xueqiu JianGlenn Biggs Institute for Alzheimer’s & Neurodegenerative Diseases, UT Health San AntonioVerified email at uthscsa.edu
Chang LiUniversity of South FloridaVerified email at usf.edu
Kai WangChildren's Hospital of PhiladelphiaVerified email at email.chop.edu
Peng WeiAssociate Professor, The University of Texas MD Anderson Cancer CenterVerified email at mdanderson.org
Andrew JohnsonNIHVerified email at nhlbi.nih.gov
Fuli YuBaylor College of MedicineVerified email at bcm.edu
L Adrienne CupplesProfessor of BiostatisticsVerified email at bu.edu
Joshua C. BisUniversity of Washington, Cardiovascular Health Research UnitVerified email at uw.edu
Jennifer BrodyUniversity of WashingtonVerified email at uw.edu
Chunlei WuAssociate Professor, The Scripps Research InstituteVerified email at scripps.edu
Jin YuThe Feinstein Institute for Medical ResearchVerified email at northwell.edu
Degui ZhiAssociate Professor, University of Texas Health Science Center at HoustonVerified email at uth.tmc.edu
Shizhong HanJohns HopkinsVerified email at uiowa.edu
Chengsong ZhuUniversity of Texas Southwestern Medical CenterVerified email at utsouthwestern.edu
Taylor MaxwellAssociate Professor, Computational Biology Institute, The George Washington UniversityVerified email at gwu.edu
Huiqi QuChildren's Hospital of PhiladelphiaVerified email at email.chop.edu
Zewei Luo

Xiaoming Liu

Associate Professor, College of Public Health, University of South Florida

Verified email at usf.edu - Homepage

population genetics bioinformatics human genomics


Title Sort by citations Sort by year Sort by title	Cited by Cited by	Year
A global reference for human genetic variation 1000 Genomes Project Consortium Nature 526 (7571), 68-74, 2015	7435*	2015
An integrated map of genetic variation from 1,092 human genomes 1000 Genomes Project Consortium Nature 491 (7422), 56-65, 2012	6817	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	1569	2012
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	897	2013
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	640	2011
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	602	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	578	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	561	2016
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	545	2015
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	357	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	287	2012
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	276	2014
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	273	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), 1-6, 2010	241	2010
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	239	2014
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	207	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	199	2014
Exploring population size changes using SNP frequency spectra X Liu, YX Fu Nature Genetics 47 (5), 555-559, 2015	189	2015
Recurrent gain-of-function mutation in PRKG1 causes thoracic aortic aneurysms and acute aortic dissections D Guo, E Regalado, DE Casteel, RL Santos-Cortez, L Gong, JJ Kim, ... The American Journal of Human Genetics 93 (2), 398-404, 2013	142	2013
Whole-genome sequence-based analysis of high-density lipoprotein cholesterol AC Morrison, A Voorman, AD Johnson, X Liu, J Yu, A Li, D Muzny, F Yu, ... Nature genetics 45 (8), 899, 2013	138	2013

The system can't perform the operation now. Try again later.

Articles 1–20

Citations per year

Duplicate citations

Merged citations

Add co-authorsCo-authors

Upload PDF

Follow this author

Cited by

Co-authors