| A global reference for human genetic variation TG Consortium Nature, 68-74, 2015 | 12737* | 2015 |
| A map of human genome variation from population-scale sequencing 1000 Genomes Project Consortium Nature 467 (7319), 1061, 2010 | 8372 | 2010 |
| An integrated map of genetic variation from 1,092 human genomes 1000 Genomes Project Consortium Nature 491 (7422), 56, 2012 | 7928 | 2012 |
| Finishing the euchromatic sequence of the human genome International Human Genome Sequencing Consortium Nature 431 (7011), 931-945, 2004 | 4862 | 2004 |
| Ensembl 2008 P Flicek, BL Aken, K Beal, B Ballester, M Cáccamo, Y Chen, L Clarke, ... Nucleic acids research 36 (suppl 1), D707-D714, 2008 | 2912* | 2008 |
| Genome sequence of the Brown Norway rat yields insights into mammalian evolution University of Utah Weiss Robert B. 14 Dunn Diane M. 14, ... Nature 428 (6982), 493-521, 2004 | 2457 | 2004 |
| An integrated map of structural variation in 2,504 human genomes PH Sudmant, T Rausch, EJ Gardner, RE Handsaker, A Abyzov, ... Nature 526 (7571), 75-81, 2015 | 2090 | 2015 |
| The Ensembl genome database project T Hubbard, D Barker, E Birney, G Cameron, Y Chen, L Clark, T Cox, J Cuff, ... Nucleic acids research 30 (1), 38-41, 2002 | 1879 | 2002 |
| Ensembl 2007 TJP Hubbard, BL Aken, K Beal, B Ballester, M Cáccamo, Y Chen, ... Nucleic acids research 35 (suppl_1), D610-D617, 2007 | 1560 | 2007 |
| Evolutionary and biomedical insights from the rhesus macaque genome RA Gibbs, J Rogers, MG Katze, R Bumgarner, GM Weinstock, ER Mardis, ... science 316 (5822), 222-234, 2007 | 1423 | 2007 |
| A systematic survey of loss-of-function variants in human protein-coding genes DG MacArthur, S Balasubramanian, A Frankish, N Huang, J Morris, ... Science 335 (6070), 823-828, 2012 | 1273 | 2012 |
| The Genome Sequence of Caenorhabditis briggsae: A Platform for Comparative Genomics LD Stein, Z Bao, D Blasiar, T Blumenthal, MR Brent, N Chen, A Chinwalla, ... PLoS biology 1 (2), e45, 2003 | 1089 | 2003 |
| The Ensembl gene annotation system BL Aken, S Ayling, D Barrell, L Clarke, V Curwen, S Fairley, ... Database 2016, 2016 | 991 | 2016 |
| Ensembl 2009 TJP Hubbard, BL Aken, S Ayling, B Ballester, K Beal, E Bragin, S Brent, ... Nucleic acids research 37 (suppl_1), D690-D697, 2009 | 948 | 2009 |
| Lineage-specific genome architecture links enhancers and non-coding disease variants to target gene promoters BM Javierre, OS Burren, SP Wilder, R Kreuzhuber, SM Hill, S Sewitz, ... Cell 167 (5), 1369-1384. e19, 2016 | 858 | 2016 |
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| Multi-platform discovery of haplotype-resolved structural variation in human genomes MJP Chaisson, AD Sanders, X Zhao, A Malhotra, D Porubsky, T Rausch, ... Nature communications 10 (1), 1784, 2019 | 616 | 2019 |
| Ensembl 2005 T Hubbard, D Andrews, M Cáccamo, G Cameron, Y Chen, M Clamp, ... Nucleic acids research 33 (suppl_1), D447-D453, 2005 | 578 | 2005 |
Paul FlicekUniversity of Cambridge, Wellcome Sanger Institute, European Bioinformatics InstituteVerified email at cam.ac.uk
