Daniel Daniš
Impact in
- Genetics top 10%
- Genomics and Rare Diseases
- Genomic variations and chromosomal abnormalities
- Genetics and Neurodevelopmental Disorders
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- Cancer Genomics and Diagnostics
Papers in
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- Biomedical Text Mining and Ontologies 6
- RNA Research and Splicing 3
- RNA modifications and cancer 3
- Genetics 11
- Genomics and Rare Diseases 10
- Genomic variations and chromosomal abnormalities 2
- Co-authors
- Peter N. Robinson (17 shared papers)Julius O.B. Jacobsen (9 shared papers)Damian Smedley (7 shared papers)Leigh Carmody (6 shared papers)Julie A. McMurry (4 shared papers)Michael Gargano (5 shared papers)Melissa Haendel (5 shared papers)Justin Reese (4 shared papers)
- Journals
- The American Journal of Human Genetics (2 papers)Bioinformatics (1 paper)Genome Medicine (1 paper)npj Genomic Medicine (1 paper)Hormone Research in Paediatrics (1 paper)
- Partner nations
- United StatesGermanyUnited Kingdom
In The Last Decade
Daniel Daniš
28 papers receiving 395 citations
Peers
Comparison fields: 5 of 67
- Genetics 195
- Cancer Research 43
- Molecular Biology 169
- Clinical Biochemistry 12
- Geophysics 20
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 30 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 2020 | 56 | |
| 2 | 2020 | 35 | |
| 3 | 2019 | 34 | |
| 4 | 2021 | 34 | |
| 5 | 2022 | 30 | |
| 6 | 2020 | 21 | |
| 7 | 1987 | 20 | |
| 8 | 2022 | 18 | |
| 9 | 2018 | 17 | |
| 10 | Serum markers of liver fibrogenesis, and liver histology findings in patients with chronic liver diseases. | 2002 | 15 |
| 11 | 2016 | 14 | |
| 12 | 2017 | 13 | |
| 13 | 2020 | 12 | |
| 14 | 2018 | 10 | |
| 15 | 2019 | 9 | |
| 16 | [The 2007 World Health Organisation classification of tumours of the central nervous system, comparison with 2000 classification]. | 2008 | 9 |
| 17 | 2024 | 8 | |
| 18 | 2022 | 8 | |
| 19 | 2019 | 8 | |
| 20 | 2020 | 8 |
About Daniel Daniš
Daniel Daniš is a scholar working on Molecular Biology, Genetics, Cancer Research, Surgery and Sensory Systems, having authored 30 papers that have together received 402 indexed citations. Recurring topics across this work include Genomics and Rare Diseases (10 papers), Biomedical Text Mining and Ontologies (6 papers), Cancer Genomics and Diagnostics (5 papers), RNA Research and Splicing (3 papers), RNA modifications and cancer (3 papers), Hyperglycemia and glycemic control in critically ill and hospitalized patients (2 papers), Hearing, Cochlea, Tinnitus, Genetics (2 papers) and Genomic variations and chromosomal abnormalities (2 papers). The work is most often cited by research in Genetics (195 citations), Cancer Research (43 citations), Molecular Biology (169 citations), Clinical Biochemistry (12 citations) and Geophysics (20 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 Smedley, Leigh Carmody, Julie A. McMurry, Michael Gargano, Melissa Haendel, Justin Reese, Chris Mungall and Daniela Gašperíková. Their work appears in journals such as The American Journal of Human Genetics, Bioinformatics, Genome Medicine, npj Genomic Medicine and Hormone Research in Paediatrics.
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.