Tudor Groza

9.2k citations
123 papers · 5.6k · 7 hit papers · h-index 28

Impact in

  • Genetics top 1%
    • Genomics and Rare Diseases
    • Genetic Associations and Epidemiology
    • Genomic variations and chromosomal abnormalities

Papers in

    • Semantic Web and Ontologies 39
    • Topic Modeling 21
    • Natural Language Processing Techniques 10
    • Genomics and Rare Diseases 37

Tudor Groza

118 papers receiving 5.4k citations

Tudor Groza's Hit Papers

The Human Phenotype Ontology in 2024: phenotypes around the world 2023 · 190 citations
1900+3+6Years since publication250500750

Peers

Tudor Groza
Comparison fields: 5 of 182
  • Genetics 2.0k
  • Health Informatics 54
  • Molecular Biology 2.4k
  • Artificial Intelligence 982
  • Information Systems and Management 196
Replace Vasilevsky Nicole with:
Vasilevsky Nicole United States
Georgios V. Gkoutos United Kingdom
Sebastian Köhler Germany
Patricia L. Whetzel United States
Matthew Brush United States
Julius O.B. Jacobsen United Kingdom
Neil R. Smalheiser United States
Simon M. Lin United States
Amelia Ireland United Kingdom
Faraz Faghri United States
Tudor Groza relative to Vasilevsky Nicole United States Vasilevsky Nicole's profile →
Citations per field
00.5×1.5×2.1×
Vasilevsky Nicole · 1×
Citations per year

Countries citing papers authored by Tudor Groza

Since Specialization
Citations

This map shows the geographic impact of Tudor Groza's research. It shows the number of citations coming from papers published by authors working in each country. You can also color the map by specialization and compare the number of citations received by Tudor Groza with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Tudor Groza more than expected).

Fields of papers citing papers by Tudor Groza

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Tudor Groza. Nodes represent research fields, and links connect fields that are likely to share authors. Colored nodes show fields that tend to cite the papers produced by Tudor Groza. The network helps show where Tudor Groza may publish in the future.

Co-authors

The 25 scholars most cited alongside Tudor Groza, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.

Border = papers with Tudor Groza Line = papers co-authored together Tudor Groza links everyone, so they are left out of the graph.

All Works

20 of 20 papers shown

Showing the 20 most-cited of 123 papers — load more, or switch the sort, to bring in the rest.

#Work
1
The NHGRI-EBI GWAS Catalog: knowledgebase and deposition resource
Hit paper breakdown →
2022912
2
The Human Phenotype Ontology in 2017
Hit paper breakdown →
2016580
3
Expansion of the Human Phenotype Ontology (HPO) knowledge base and resources
Hit paper breakdown →
2018484
4
How many rare diseases are there?
Hit paper breakdown →
2019338
5 2016333
6
The International Mouse Phenotyping Consortium: comprehensive knockout phenotyping underpinning the study of human disease
Hit paper breakdown →
2022241
7
GA4GH: International policies and standards for data sharing across genomic research and healthcare
Hit paper breakdown →
2021198
8 2016193
9
The Human Phenotype Ontology in 2024: phenotypes around the world
Hit paper breakdown →
2023190
10 2015181
11 2019179
12
Bioinformatics and Biomedicine (BIBM), 2013 IEEE International Conference on
201394
13 201889
14 200788
15 201378
16 202267
17 200765
18
SemVersion: RDF-based ontology versioning system
200659
19 201652
20 201752

About Tudor Groza

Tudor Groza is a scholar working on Artificial Intelligence, Genetics, Molecular Biology, Information Systems and Management and Information Systems, having authored 123 papers that have together received 5.6k indexed citations. Recurring topics across this work include Biomedical Text Mining and Ontologies (57 papers), Semantic Web and Ontologies (39 papers), Genomics and Rare Diseases (37 papers), Topic Modeling (21 papers), Bioinformatics and Genomic Networks (12 papers), Natural Language Processing Techniques (10 papers), Cancer Genomics and Diagnostics (8 papers) and Service-Oriented Architecture and Web Services (8 papers). The work is most often cited by research in Genetics (2.0k citations), Health Informatics (54 citations), Molecular Biology (2.4k citations), Artificial Intelligence (982 citations) and Information Systems and Management (196 citations). Tudor Groza has collaborated with scholars based in Australia, United States and United Kingdom. Frequent co-authors include Siegfried Handschuh, Jane Hunter, Anika Oellrich, Nigel Collier, Peter N. Robinson, Melissa Anne Haendel, Sebastian Köhler, Chris Mungall, Stefan Decker and Andreas Zankl. Their work appears in journals such as Nucleic Acids Research, PLoS ONE, The American Journal of Human Genetics, Journal of Biomedical Informatics and Journal of Biomedical Semantics.

Rankless uses publication and citation data sourced from OpenAlex, an open and comprehensive bibliographic database. While OpenAlex provides broad and valuable coverage of the global research landscape, it—like all bibliographic datasets—has inherent limitations. These include incomplete records, variations in author disambiguation, differences in journal indexing, and delays in data updates. As a result, some metrics and network relationships displayed in Rankless may not fully capture the entirety of a scholar's output or impact.

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