Dimitris Polychronopoulos
Impact in
- Molecular Biology top 5%
- Gut microbiota and health
- DNA Repair Mechanisms
- Biomedical Text Mining and Ontologies
- Genomics and Chromatin Dynamics
- Cancer Research top 10%
- Cancer Genomics and Diagnostics
Papers in
-
- RNA and protein synthesis mechanisms 10
- Genomics and Phylogenetic Studies 8
- Fractal and DNA sequence analysis 4
- Co-authors
- Richard Charles Jones (1 shared paper)Magdalena Foltman (1 shared paper)Ricky D. Edmondson (1 shared paper)Agnieszka Gambus (1 shared paper)Karim P. M. Labib (1 shared paper)Frederick van Deursen (1 shared paper)Arturo Calzada (1 shared paper)Ge Tan (2 shared papers)
- Journals
- Genetics in Medicine (6 papers)Scientific Reports (4 papers)Brain (3 papers)Nature Communications (3 papers)Nature (1 paper)
- Partner nations
- United KingdomGreeceUnited States
In The Last Decade
Dimitris Polychronopoulos
40 papers receiving 2.7k citations
Dimitris Polychronopoulos's Hit Papers
Peers
Comparison fields: 5 of 134
- Molecular Biology 1.6k
- Cancer Research 266
- Genetics 507
- Oncology 352
- Biotechnology 116
Countries citing papers authored by Dimitris Polychronopoulos
This map shows the geographic impact of Dimitris Polychronopoulos'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 Dimitris Polychronopoulos with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Dimitris Polychronopoulos more than expected).
Fields of papers citing papers by Dimitris Polychronopoulos
This network shows the impact of papers produced by Dimitris Polychronopoulos. 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 Dimitris Polychronopoulos. The network helps show where Dimitris Polychronopoulos may publish in the future.
Co-authors
The 25 scholars most cited alongside Dimitris Polychronopoulos, 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 41 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | Mutational signature in colorectal cancer caused by genotoxic pks+ E. coli Hit paper breakdown → | 2020 | 905 |
| 2 | An overview of the BIOASQ large-scale biomedical semantic indexing and question answering competition Hit paper breakdown → | 2015 | 400 |
| 3 | 100,000 Genomes Pilot on Rare-Disease Diagnosis in Health Care - Preliminary Report. Hit paper breakdown → | 2021 | 290 |
| 4 | 2009 | 210 | |
| 5 | 2021 | 105 | |
| 6 | 2020 | 81 | |
| 7 | 2020 | 78 | |
| 8 | 2017 | 68 | |
| 9 | 2020 | 66 | |
| 10 | 2022 | 55 | |
| 11 | 2023 | 48 | |
| 12 | 2021 | 42 | |
| 13 | 2020 | 38 | |
| 14 | 2020 | 37 | |
| 15 | 2020 | 36 | |
| 16 | 2022 | 29 | |
| 17 | 2022 | 24 | |
| 18 | 2014 | 23 | |
| 19 | 2020 | 23 | |
| 20 | 2017 | 21 |
About Dimitris Polychronopoulos
Dimitris Polychronopoulos is a scholar working on Molecular Biology, Cancer Research, Genetics, Pathology and Forensic Medicine and Cellular and Molecular Neuroscience, having authored 41 papers that have together received 2.7k indexed citations. Recurring topics across this work include RNA and protein synthesis mechanisms (10 papers), Genomics and Phylogenetic Studies (8 papers), Fractal and DNA sequence analysis (4 papers), Genomics and Rare Diseases (3 papers), Genetic factors in colorectal cancer (3 papers), Algorithms and Data Compression (3 papers), Chromosomal and Genetic Variations (3 papers) and Genetic Neurodegenerative Diseases (3 papers). The work is most often cited by research in Molecular Biology (1.6k citations), Cancer Research (266 citations), Genetics (507 citations), Oncology (352 citations) and Biotechnology (116 citations). Dimitris Polychronopoulos has collaborated with scholars based in United Kingdom, Greece and United States. Frequent co-authors include Richard Charles Jones, Magdalena Foltman, Ricky D. Edmondson, Agnieszka Gambus, Karim P. M. Labib, Frederick van Deursen, Arturo Calzada, Ge Tan, Boris Lenhard and Yannis Almirantis. Their work appears in journals such as Genetics in Medicine, Scientific Reports, Brain, Nature Communications and Nature.
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.