Edwin Cuppen
Impact in
- Cancer Research top 0.1%
- Cancer Genomics and Diagnostics
- MicroRNA in disease regulation
- Cancer-related molecular mechanisms research
- Aging top 0.5%
Papers in
-
- CRISPR and Genetic Engineering 27
- Genomics and Chromatin Dynamics 17
- DNA Repair Mechanisms 14
-
- Cancer Genomics and Diagnostics 70
- MicroRNA in disease regulation 17
- Co-authors
- Ronald H.A. Plasterk (22 shared papers)Eugène Berezikov (18 shared papers)Isaäc J. Nijman (33 shared papers)Hans Clevers (22 shared papers)Ruben van Boxtel (28 shared papers)Victor Guryev (37 shared papers)Albert J. Vilella (1 shared paper)Pjotr Prins (1 shared paper)
- Journals
- PLoS ONE (14 papers)Nature Communications (13 papers)Annals of Oncology (11 papers)Genome Research (11 papers)BMC Genomics (10 papers)
- Partner nations
- NetherlandsUnited StatesGermany
In The Last Decade
Edwin Cuppen
273 papers receiving 20.0k citations
Edwin Cuppen's Hit Papers
Peers
Comparison fields: 5 of 187
- Cancer Research 5.0k
- Aging 374
- Molecular Biology 10.9k
- Oncology 3.6k
- Genetics 3.3k
Countries citing papers authored by Edwin Cuppen
This map shows the geographic impact of Edwin Cuppen'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 Edwin Cuppen with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Edwin Cuppen more than expected).
Fields of papers citing papers by Edwin Cuppen
This network shows the impact of papers produced by Edwin Cuppen. 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 Edwin Cuppen. The network helps show where Edwin Cuppen may publish in the future.
Co-authors
The 25 scholars most cited alongside Edwin Cuppen, 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 280 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | Sambamba: fast processing of NGS alignment formats Hit paper breakdown → | 2015 | 1309 |
| 2 | Functional Repair of CFTR by CRISPR/Cas9 in Intestinal Stem Cell Organoids of Cystic Fibrosis Patients Hit paper breakdown → | 2013 | 1050 |
| 3 | Sequential cancer mutations in cultured human intestinal stem cells Hit paper breakdown → | 2015 | 801 |
| 4 | Mammalian Mirtron Genes Hit paper breakdown → | 2007 | 588 |
| 5 | Identification of Multipotent Luminal Progenitor Cells in Human Prostate Organoid Cultures Hit paper breakdown → | 2014 | 543 |
| 6 | 2013 | 446 | |
| 7 | 2006 | 394 | |
| 8 | 2003 | 366 | |
| 9 | 2006 | 364 | |
| 10 | 2018 | 359 | |
| 11 | 2015 | 358 | |
| 12 | 2003 | 341 | |
| 13 | 2017 | 320 | |
| 14 | Pan-cancer landscape of homologous recombination deficiency Hit paper breakdown → | 2020 | 301 |
| 15 | 2014 | 289 | |
| 16 | 2017 | 254 | |
| 17 | 2006 | 229 | |
| 18 | 2011 | 227 | |
| 19 | 2020 | 210 | |
| 20 | 2019 | 207 |
About Edwin Cuppen
Edwin Cuppen is a scholar working on Molecular Biology, Cancer Research, Genetics, Oncology and Pulmonary and Respiratory Medicine, having authored 280 papers that have together received 20.3k indexed citations. Recurring topics across this work include Cancer Genomics and Diagnostics (70 papers), CRISPR and Genetic Engineering (27 papers), Genetic factors in colorectal cancer (21 papers), Genomics and Rare Diseases (18 papers), Genomics and Chromatin Dynamics (17 papers), MicroRNA in disease regulation (17 papers), Genomic variations and chromosomal abnormalities (15 papers) and DNA Repair Mechanisms (14 papers). The work is most often cited by research in Cancer Research (5.0k citations), Aging (374 citations), Molecular Biology (10.9k citations), Oncology (3.6k citations) and Genetics (3.3k citations). Edwin Cuppen has collaborated with scholars based in Netherlands, United States and Germany. Frequent co-authors include Ronald H.A. Plasterk, Eugène Berezikov, Isaäc J. Nijman, Hans Clevers, Ruben van Boxtel, Victor Guryev, Albert J. Vilella, Pjotr Prins, Artem Tarasov and Arne van Hoeck. Their work appears in journals such as PLoS ONE, Nature Communications, Annals of Oncology, Genome Research and BMC Genomics.
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.