Tudor Groza

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Siegfried HandschuhChair of Data Science and Natural Language Processing, University of St.GallenDirección de correo verificada de unisg.ch
Peter RobinsonProfessor of Computational Biology, The Jackson Laboratory for Genomic MedicineDirección de correo verificada de jax.org
Jane HunterThe University of QueenslandDirección de correo verificada de itee.uq.edu.au
Andreas ZanklUniversity of SydneyDirección de correo verificada de sydney.edu.au
Melissa HaendelUniversity of Colorado Anschutz Medical CampusDirección de correo verificada de tislab.org
Christopher J MungallLawrence Berkeley National LaboratoryDirección de correo verificada de lbl.gov
Stefan DeckerFraunhofer FIT, RWTH Aachen UniversityDirección de correo verificada de informatik.rwth-aachen.de
Sebastian KöhlerExpert AI engineer, Ada Health; Member of Monarch InitiativeDirección de correo verificada de ada.com
Damian SmedleyQueen Mary University of LondonDirección de correo verificada de qmul.ac.uk
Gareth BaynamClinical Professor, Faculty of Medicine and Health Sciences, University of WesternDirección de correo verificada de health.wa.gov.au
Anika Cawthorn (formerly Oellrich)University College LondonDirección de correo verificada de ucl.ac.uk
Nigel CollierProfessor of Natural Language Processing, University of CambridgeDirección de correo verificada de cam.ac.uk
Julie A McMurryUniversity of Colorado, AnschutzDirección de correo verificada de cuanschutz.edu
Nicole L WashingtonHelixDirección de correo verificada de helix.com
Helen ParkinsonEuropean Bioinformatics Institute - Head of Knowledge Management Section, Team LeaderDirección de correo verificada de ebi.ac.uk
Nicole VasilevskyCritical Path InstituteDirección de correo verificada de tislab.org

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Tudor Groza

European Bioinformatics Institute

Dirección de correo verificada de ebi.ac.uk - Página principal

Deep phenotyping Phenotype ontologies Text mining Phenotype-genotype integration Phenotype-driven disorder prediction


Título Ordenar por citas Ordenar por año Ordenar por título	Citado por Citado por	Año
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	774	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	629	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	295	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	250	2016
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	249	2020
The NHGRI-EBI GWAS Catalog: knowledgebase and deposition resource E Sollis, A Mosaku, A Abid, A Buniello, M Cerezo, L Gil, T Groza, O Güneş, ... Nucleic acids research 51 (D1), D977-D985, 2023	238	2023
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	215	2015
The NEPOMUK project-on the way to the social semantic desktop T Groza, S Handschuh, K Moeller	186	2007
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	181	2020
SALT-semantically annotated for scientific publications T Groza, S Handschuh, K Möller, S Decker European Semantic Web Conference, 518-532, 2007	160	2007
A review of argumentation for the social semantic web J Schneider, T Groza, A Passant Semantic Web 4 (2), 159-218, 2013	144	2013
SemVersion: An RDF-based ontology versioning system M Völkel, T Groza Proceedings of the IADIS international conference WWW/Internet 2006, 44, 2006	133	2006
36th international symposium on intensive care and emergency medicine: Brussels, Belgium. 15-18 March 2016 RM Bateman, MD Sharpe, JE Jagger, CG Ellis, J Solé-Violán, ... Critical care 20, 13-182, 2016	122	2016
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	107	2018
GA4GH: International policies and standards for data sharing across genomic research and healthcare HL Rehm, AJH Page, L Smith, JB Adams, G Alterovitz, LJ Babb, ... Cell genomics 1 (2), 2021	106	2021
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	80	2017
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, bav005, 2015	79	2015
The International Mouse Phenotyping Consortium: comprehensive knockout phenotyping underpinning the study of human disease T Groza, FL Gomez, HH Mashhadi, V Muñoz-Fuentes, O Gunes, R Wilson, ... Nucleic acids research 51 (D1), D1038-D1045, 2023	76	2023
The digital revolution in phenotyping A Oellrich, N Collier, T Groza, D Rebholz-Schuhmann, N Shah, ... Briefings in bioinformatics 17 (5), 819-830, 2016	69	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	68	2014

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