Nico Matentzoglu
Impact in
- Genetics top 5%
- Genomics and Rare Diseases
- Genomic variations and chromosomal abnormalities
- Molecular Biology top 10%
- Biomedical Text Mining and Ontologies
- Bioinformatics and Genomic Networks
- Genomics and Phylogenetic Studies
Papers in
-
- Semantic Web and Ontologies 30
- Natural Language Processing Techniques 6
- Topic Modeling 4
-
- Biomedical Text Mining and Ontologies 44
- Bioinformatics and Genomic Networks 11
- Co-authors
- Bijan Parsia (17 shared papers)Robert Stevens (6 shared papers)Chris Mungall (10 shared papers)Rafael S. Gonçalves (5 shared papers)JAMES M. MALONE (2 shared papers)Birte Glimm (4 shared papers)Ulrike Sattler (6 shared papers)Melissa Anne Haendel (8 shared papers)
- Journals
- Nucleic Acids Research (6 papers)Database (5 papers)Bioinformatics (3 papers)Journal of Web Semantics (3 papers)Journal of Automated Reasoning (2 papers)
- Partner nations
- United KingdomUnited StatesGermany
In The Last Decade
Nico Matentzoglu
61 papers receiving 2.5k citations
Nico Matentzoglu's Hit Papers
Peers
Comparison fields: 5 of 146
- Genetics 728
- Molecular Biology 1.2k
- Artificial Intelligence 542
- Health Informatics 22
- Neurology 140
Countries citing papers authored by Nico Matentzoglu
This map shows the geographic impact of Nico Matentzoglu'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 Nico Matentzoglu with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Nico Matentzoglu more than expected).
Fields of papers citing papers by Nico Matentzoglu
This network shows the impact of papers produced by Nico Matentzoglu. 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 Nico Matentzoglu. The network helps show where Nico Matentzoglu may publish in the future.
Co-authors
The 25 scholars most cited alongside Nico Matentzoglu, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.
All Works
Showing the 20 most-cited of 63 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | The Human Phenotype Ontology in 2021 Hit paper breakdown → | 2020 | 745 |
| 2 | Expansion of the Human Phenotype Ontology (HPO) knowledge base and resources Hit paper breakdown → | 2018 | 484 |
| 3 | The Human Phenotype Ontology in 2024: phenotypes around the world Hit paper breakdown → | 2023 | 190 |
| 4 | 2019 | 179 | |
| 5 | 2021 | 147 | |
| 6 | 2021 | 118 | |
| 7 | 2020 | 65 | |
| 8 | 2018 | 60 | |
| 9 | 2017 | 59 | |
| 10 | 2019 | 57 | |
| 11 | 2024 | 51 | |
| 12 | 2023 | 46 | |
| 13 | 2022 | 43 | |
| 14 | 2013 | 25 | |
| 15 | 2023 | 24 | |
| 16 | OWL Reasoner Evaluation (ORE) Workshop 2013 Results: Short Report. | 2013 | 20 |
| 17 | 2023 | 20 | |
| 18 | 2018 | 13 | |
| 19 | 2021 | 13 | |
| 20 | 2023 | 13 |
About Nico Matentzoglu
Nico Matentzoglu is a scholar working on Artificial Intelligence, Molecular Biology, Genetics, Information Systems and Management Information Systems, having authored 63 papers that have together received 2.6k indexed citations. Recurring topics across this work include Biomedical Text Mining and Ontologies (44 papers), Semantic Web and Ontologies (30 papers), Genomics and Rare Diseases (11 papers), Bioinformatics and Genomic Networks (11 papers), Service-Oriented Architecture and Web Services (7 papers), Natural Language Processing Techniques (6 papers), Topic Modeling (4 papers) and Nutrition, Genetics, and Disease (3 papers). The work is most often cited by research in Genetics (728 citations), Molecular Biology (1.2k citations), Artificial Intelligence (542 citations), Health Informatics (22 citations) and Neurology (140 citations). Nico Matentzoglu has collaborated with scholars based in United Kingdom, United States and Germany. Frequent co-authors include Bijan Parsia, Robert Stevens, Chris Mungall, Rafael S. Gonçalves, JAMES M. MALONE, Birte Glimm, Ulrike Sattler, Melissa Anne Haendel, Peter N. Robinson and Nomi L. Harris. Their work appears in journals such as Nucleic Acids Research, Database, Bioinformatics, Journal of Web Semantics and Journal of Automated Reasoning.
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.