| The human phenotype ontology in 2017 S Köhler, NA Vasilevsky, M Engelstad, E Foster, J McMurry, S Aymé, ... Nucleic acids research 45 (D1), D865-D876, 2017 | 490 | 2017 |
| Expansion of the Human Phenotype Ontology (HPO) knowledge base and resources S Köhler, L Carmody, N Vasilevsky, JOB Jacobsen, D Danis, JP Gourdine, ... Nucleic acids research 47 (D1), D1018-D1027, 2019 | 473 | 2019 |
| The human phenotype ontology in 2017 S Kohler, NA Vasilevsky, M Engelstad, E Foster, J McMurry, S Ayme, ... | 223 | 2017 |
| The Monarch Initiative: an integrative data and analytic platform connecting phenotypes to genotypes across species CJ Mungall, JA McMurry, S Köhler, JP Balhoff, C Borromeo, M Brush, ... Nucleic acids research 45 (D1), D712-D722, 2017 | 217 | 2017 |
| A whole-genome analysis framework for effective identification of pathogenic regulatory variants in Mendelian disease D Smedley, M Schubach, JOB Jacobsen, S Köhler, T Zemojtel, ... The American Journal of Human Genetics 99 (3), 595-606, 2016 | 190 | 2016 |
| The human phenotype ontology: semantic unification of common and rare disease T Groza, S Köhler, D Moldenhauer, N Vasilevsky, G Baynam, T Zemojtel, ... The American Journal of Human Genetics 97 (1), 111-124, 2015 | 183 | 2015 |
| The NEPOMUK project-on the way to the social semantic desktop T Groza, S Handschuh, K Moeller | 182 | 2007 |
| SALT-Semantically Annotated $\mbox {\LaTeX} $ for Scientific Publications T Groza, S Handschuh, K Möller, S Decker European Semantic Web Conference, 518-532, 2007 | 141 | 2007 |
| A review of argumentation for the social semantic web J Schneider, T Groza, A Passant Semantic Web 4 (2), 159-218, 2013 | 139 | 2013 |
| SemVersion: An RDF-based ontology versioning system M Völkel, T Groza Proceedings of the IADIS international conference WWW/Internet 2006, 44, 2006 | 124 | 2006 |
| The Monarch Initiative in 2019: an integrative data and analytic platform connecting phenotypes to genotypes across species KA Shefchek, NL Harris, M Gargano, N Matentzoglu, D Unni, M Brush, ... Nucleic acids research 48 (D1), D704-D715, 2020 | 100 | 2020 |
| How many rare diseases are there? M Haendel, N Vasilevsky, D Unni, C Bologa, N Harris, H Rehm, ... Nature Reviews Drug Discovery 19 (2), 77-78, 2020 | 89 | 2020 |
| CogStack-experiences of deploying integrated information retrieval and extraction services in a large National Health Service Foundation Trust hospital R Jackson, I Kartoglu, C Stringer, G Gorrell, A Roberts, X Song, H Wu, ... BMC medical informatics and decision making 18 (1), 1-13, 2018 | 70 | 2018 |
| Automatic concept recognition using the human phenotype ontology reference and test suite corpora T Groza, S Köhler, S Doelken, N Collier, A Oellrich, D Smedley, FM Couto, ... Database 2015, 2015 | 70 | 2015 |
| The digital revolution in phenotyping A Oellrich, N Collier, T Groza, D Rebholz-Schuhmann, N Shah, ... Briefings in bioinformatics 17 (5), 819-830, 2016 | 61 | 2016 |
| Matchmaker exchange NLM Sobreira, H Arachchi, OJ Buske, JX Chong, B Hutton, J Foreman, ... Current protocols in human genetics 95 (1), 9.31. 1-9.31. 15, 2017 | 59 | 2017 |
| Expressing argumentative discussions in social media sites C Lange, U Bojars, T Groza, JG Breslin, S Handschuh Social Data on the Web (SDoW), Workshop at the 7th International Semantic …, 2008 | 59 | 2008 |
| Navigating the phenotype frontier: the monarch initiative JA McMurry, S Köhler, NL Washington, JP Balhoff, C Borromeo, M Brush, ... Genetics 203 (4), 1491-1495, 2016 | 52 | 2016 |
| Identifying scientific artefacts in biomedical literature: The evidence based medicine use case H Hassanzadeh, T Groza, J Hunter Journal of biomedical informatics 49, 159-170, 2014 | 50 | 2014 |
| 36th International Symposium on Intensive Care and Emergency Medicine RM Bateman, MD Sharpe, JE Jagger, CG Ellis, J Solé-Violán, ... Critical Care 20 (2), 13-182, 2016 | 48 | 2016 |
Peter RobinsonProfessor of Computational Biology, The Jackson Laboratory for Genomic MedicineVerified email at jax.org
