| A global reference for human genetic variation 1000 Genomes Project Consortium Nature 526 (7571), 68-74, 2015 | 16303 | 2015 |
| An integrated map of genetic variation from 1,092 human genomes 1000 Genomes Project Consortium Nature 491 (7422), 56-65, 2012 | 8586 | 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 | 1928 | 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 | 1707 | 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 | 1187 | 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 | 1122 | 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 | 1061 | 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 | 947 | 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 | 785 | 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 | 727 | 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 | 528 | 2014 |
| 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 | 484 | 2020 |
| 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 | 467 | 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 | 427 | 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 | 412 | 2012 |
| Exploring population size changes using SNP frequency spectra X Liu, YX Fu Nature Genetics 47 (5), 555-559, 2015 | 409 | 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 | 309 | 2002 |
| Stairway Plot 2: demographic history inference with folded SNP frequency spectra X Liu, YX Fu Genome Biology 21, 280, 2020 | 297 | 2020 |
| 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 | 272 | 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 | 265 | 2012 |
Chang LiUniversity of South FloridaDirección de correo verificada de usf.edu
