| An integrated map of genetic variation from 1,092 human genomes 1000 Genomes Project Consortium Nature 491 (7422), 56, 2012 | 8228 | 2012 |
| The ensembl variant effect predictor W McLaren, L Gil, SE Hunt, HS Riat, GRS Ritchie, A Thormann, P Flicek, ... Genome biology 17, 1-14, 2016 | 6063 | 2016 |
| Ensembl 2012 P Flicek, MR Amode, D Barrell, K Beal, S Brent, D Carvalho-Silva, ... Nucleic acids research 40 (D1), D84-D90, 2012 | 1168 | 2012 |
| Ensembl 2013 P Flicek, I Ahmed, MR Amode, D Barrell, K Beal, S Brent, ... Nucleic acids research 41 (D1), D48-D55, 2012 | 1160 | 2012 |
| Ensembl 2011 P Flicek, MR Amode, D Barrell, K Beal, S Brent, Y Chen, P Clapham, ... Nucleic acids research 39 (suppl_1), D800-D806, 2010 | 886 | 2010 |
| The African genome variation project shapes medical genetics in Africa D Gurdasani, T Carstensen, F Tekola-Ayele, L Pagani, I Tachmazidou, ... Nature 517 (7534), 327-332, 2015 | 615 | 2015 |
| Modernizing reference genome assemblies DM Church, VA Schneider, T Graves, K Auger, F Cunningham, N Bouk, ... PLoS biology 9 (7), e1001091, 2011 | 583 | 2011 |
| Functional annotation of noncoding sequence variants GRS Ritchie, I Dunham, E Zeggini, P Flicek Nature methods 11 (3), 294-296, 2014 | 581 | 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 | 423 | 2013 |
| 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 | 349 | 2016 |
| Signalling signalhood and the emergence of communication TC Scott-Phillips, S Kirby, GRS Ritchie Cognition 113 (2), 226-233, 2009 | 228 | 2009 |
| The Ensembl REST API: Ensembl data for any language A Yates, K Beal, S Keenan, W McLaren, M Pignatelli, GRS Ritchie, ... Bioinformatics 31 (1), 143-145, 2015 | 199 | 2015 |
| Computational approaches to identify functional genetic variants in cancer genomes Nature methods 10 (8), 723-729, 2013 | 188 | 2013 |
| GARFIELD classifies disease-relevant genomic features through integration of functional annotations with association signals V Iotchkova, GRS Ritchie, M Geihs, S Morganella, JL Min, K Walter, ... Nature genetics 51 (2), 343-353, 2019 | 165 | 2019 |
| Uganda genome resource enables insights into population history and genomic discovery in Africa D Gurdasani, T Carstensen, S Fatumo, G Chen, CS Franklin, ... Cell 179 (4), 984-1002. e36, 2019 | 164 | 2019 |
| A fast, effective local search for scheduling independent jobs in heterogeneous computing environments G Ritchie, J Levine Proceedings of the 22nd workshop of the UK Planning and Scheduling Special …, 2003 | 158 | 2003 |
| Whole-genome sequencing coupled to imputation discovers genetic signals for anthropometric traits I Tachmazidou, D Süveges, JL Min, GRS Ritchie, J Steinberg, K Walter, ... The American Journal of Human Genetics 100 (6), 865-884, 2017 | 157 | 2017 |
| A hybrid ant algorithm for scheduling independent jobs in heterogeneous computing environments G Ritchie, J Levine | 142 | 2004 |
| Comparison of GENCODE and RefSeq gene annotation and the impact of reference geneset on variant effect prediction A Frankish, B Uszczynska, GRS Ritchie, JM Gonzalez, D Pervouchine, ... BMC genomics 16, 1-11, 2015 | 114 | 2015 |
| Integrative epigenomics, transcriptomics and proteomics of patient chondrocytes reveal genes and pathways involved in osteoarthritis J Steinberg, GRS Ritchie, TI Roumeliotis, RL Jayasuriya, MJ Clark, ... Scientific reports 7 (1), 1-11, 2017 | 107 | 2017 |
