Tudor Groza
TitleCited byYear
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, 2016
3452016
The NEPOMUK project-on the way to the social semantic desktop
S Handschuh, K Möller, T Groza
1742007
SALT-Semantically Annotated $\mbox {\LaTeX} $ for Scientific Publications
T Groza, S Handschuh, K Möller, S Decker
European Semantic Web Conference, 518-532, 2007
1262007
SemVersion: An RDF-based ontology versioning system
M Völkel, T Groza
Proceedings of the IADIS international conference WWW/Internet 2006, 44, 2006
1152006
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
1052015
A review of argumentation for the social semantic web
J Schneider, T Groza, A Passant
Semantic Web 4 (2), 159-218, 2013
1052013
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
872016
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, 2016
792016
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
502008
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
452015
SALT: Weaving the claim web
T Groza, K Möller, S Handschuh, D Trif, S Decker
The Semantic Web, 197-210, 2007
402007
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
352015
A short survey of discourse representation models
T Groza, S Handschuh, T Clark, S Buckingham Shum, A de Waard
342009
The digital revolution in phenotyping
A Oellrich, N Collier, T Groza, D Rebholz-Schuhmann, N Shah, ...
Briefings in bioinformatics 17 (5), 819-830, 2015
302015
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
272016
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, 2018
252018
Phenotyping: targeting genotype's rich cousin for diagnosis
G Baynam, M Walters, P Claes, S Kung, P LeSouef, H Dawkins, ...
Journal of paediatrics and child health 51 (4), 381-386, 2015
242015
The Bone Dysplasia Ontology: integrating genotype and phenotype information in the skeletal dysplasia domain
T Groza, J Hunter, A Zankl
BMC bioinformatics 13 (1), 50, 2012
232012
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
222014
Getting ready for the Human Phenome Project: the 2012 forum of the Human Variome Project
WS Oetting, PN Robinson, MS Greenblatt, RG Cotton, T Beck, JC Carey, ...
Human mutation 34 (4), 661-666, 2013
202013
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Articles 1–20