Tudor Groza
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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
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
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
The NEPOMUK project-on the way to the social semantic desktop
T Groza, S Handschuh, K Moeller
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
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
A review of argumentation for the social semantic web
J Schneider, T Groza, A Passant
Semantic Web 4 (2), 159-218, 2013
SALT-Semantically Annotated $\mbox {\LaTeX} $ for Scientific Publications
T Groza, S Handschuh, K Möller, S Decker
European Semantic Web Conference, 518-532, 2007
SemVersion: An RDF-based ontology versioning system
M Völkel, T Groza
Proceedings of the IADIS international conference WWW/Internet 2006, 44, 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
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
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
The digital revolution in phenotyping
A Oellrich, N Collier, T Groza, D Rebholz-Schuhmann, N Shah, ...
Briefings in bioinformatics 17 (5), 819-830, 2016
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
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
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
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
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
SALT: Weaving the claim web
T Groza, K Möller, S Handschuh, D Trif, S Decker
The Semantic Web, 197-210, 2007
Use of model organism and disease databases to support matchmaking for human disease gene discovery
CJ Mungall, NL Washington, J Nguyen‐Xuan, C Condit, D Smedley, ...
Human mutation 36 (10), 979-984, 2015
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Artiklar 1–20