Daniel Daniš
Impact in
- Genetics top 2%
- Genomics and Rare Diseases
- Genomic variations and chromosomal abnormalities
- Genetics and Neurodevelopmental Disorders
- Molecular Biology top 10%
- Biomedical Text Mining and Ontologies
- Bioinformatics and Genomic Networks
- Genomics and Phylogenetic Studies
- RNA modifications and cancer
Papers in
- Genetics 24
- Genomics and Rare Diseases 23
- Genomic variations and chromosomal abnormalities 6
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- Cancer Genomics and Diagnostics 6
- Co-authors
- Peter N. Robinson (16 shared papers)Julius O.B. Jacobsen (10 shared papers)Damian P. Smedley (8 shared papers)Leigh Carmody (6 shared papers)Melissa Anne Haendel (6 shared papers)Michael A. Gargano (5 shared papers)McMurry Julie (5 shared papers)Justin Reese (4 shared papers)
- Journals
- European Journal of Human Genetics (4 papers)The American Journal of Human Genetics (3 papers)Nucleic Acids Research (3 papers)npj Genomic Medicine (2 papers)Human Genetics and Genomics Advances (2 papers)
- Partner nations
- United StatesGermanyUnited Kingdom
In The Last Decade
Daniel Daniš
45 papers receiving 2.1k citations
Daniel Daniš's Hit Papers
Peers
Comparison fields: 5 of 122
- Genetics 973
- Molecular Biology 996
- Cancer Research 170
- Health Informatics 15
- Clinical Biochemistry 41
Countries citing papers authored by Daniel Daniš
This map shows the geographic impact of Daniel Daniš'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 Daniel Daniš with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Daniel Daniš more than expected).
Fields of papers citing papers by Daniel Daniš
This network shows the impact of papers produced by Daniel Daniš. 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 Daniel Daniš. The network helps show where Daniel Daniš may publish in the future.
Co-authors
The 25 scholars most cited alongside Daniel Daniš, 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 47 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 | 2021 | 80 | |
| 5 | 2020 | 72 | |
| 6 | 2022 | 67 | |
| 7 | 2021 | 51 | |
| 8 | 2020 | 44 | |
| 9 | 2022 | 41 | |
| 10 | 2019 | 39 | |
| 11 | 2019 | 38 | |
| 12 | 2020 | 24 | |
| 13 | 2025 | 23 | |
| 14 | 1987 | 20 | |
| 15 | 2022 | 19 | |
| 16 | 2018 | 18 | |
| 17 | 2023 | 16 | |
| 18 | Serum markers of liver fibrogenesis, and liver histology findings in patients with chronic liver diseases. | 2002 | 16 |
| 19 | 2016 | 15 | |
| 20 | 2021 | 14 |
About Daniel Daniš
Daniel Daniš is a scholar working on Genetics, Cancer Research, Molecular Biology, Sensory Systems and Genetics, having authored 47 papers that have together received 2.2k indexed citations. Recurring topics across this work include Genomics and Rare Diseases (23 papers), Biomedical Text Mining and Ontologies (9 papers), RNA modifications and cancer (7 papers), Cancer Genomics and Diagnostics (6 papers), Genomic variations and chromosomal abnormalities (6 papers), RNA Research and Splicing (5 papers), Bioinformatics and Genomic Networks (4 papers) and RNA and protein synthesis mechanisms (4 papers). The work is most often cited by research in Genetics (973 citations), Molecular Biology (996 citations), Cancer Research (170 citations), Health Informatics (15 citations) and Clinical Biochemistry (41 citations). Daniel Daniš has collaborated with scholars based in United States, Germany and United Kingdom. Frequent co-authors include Peter N. Robinson, Julius O.B. Jacobsen, Damian P. Smedley, Leigh Carmody, Melissa Anne Haendel, Michael A. Gargano, McMurry Julie, Justin Reese, Chris Mungall and Valentina Cipriani. Their work appears in journals such as European Journal of Human Genetics, The American Journal of Human Genetics, Nucleic Acids Research, npj Genomic Medicine and Human Genetics and Genomics Advances.
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.