Erwin Boutsma
Impact in
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- Epigenetics and DNA Methylation
- Genomics and Chromatin Dynamics
- Ubiquitin and proteasome pathways
- Pluripotent Stem Cells Research
- Cancer-related gene regulation
- RNA modifications and cancer
- CRISPR and Genetic Engineering
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- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities
Papers in
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- Epigenetics and DNA Methylation 4
- Genomics and Chromatin Dynamics 1
- Cancer-related gene regulation 1
- RNA modifications and cancer 1
- Genetics 2
- Genetics and Neurodevelopmental Disorders 2
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities 1
- Co-authors
- Maarten van Lohuizen (5 shared papers)Petra van der Stoop (3 shared papers)Els Verhoeven (2 shared papers)Anders H. Lund (2 shared papers)Inmaculada Hernández‐Muñoz (2 shared papers)Dmitri A. Nusinow (1 shared paper)Barbara Panning (1 shared paper)York Marahrens (1 shared paper)
- Journals
- PLoS ONE (2 papers)Cold Spring Harbor Symposia on Quantitative Biology (1 paper)Proceedings of the National Academy of Sciences (1 paper)Nature Genetics (1 paper)
- Partner nations
- NetherlandsUnited StatesSwitzerland
In The Last Decade
Erwin Boutsma
5 papers receiving 638 citations
Peers
Comparison fields: 5 of 48
- Molecular Biology 592
- Genetics 135
- Cancer Research 38
- Aging 4
- Cell Biology 29
Countries citing papers authored by Erwin Boutsma
This map shows the geographic impact of Erwin Boutsma'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 Erwin Boutsma with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Erwin Boutsma more than expected).
Fields of papers citing papers by Erwin Boutsma
This network shows the impact of papers produced by Erwin Boutsma. 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 Erwin Boutsma. The network helps show where Erwin Boutsma may publish in the future.
Co-authors
The 25 scholars most cited alongside Erwin Boutsma, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.
All Works
| # | Work | ||
|---|---|---|---|
| 1 | 2008 | 271 | |
| 2 | 2005 | 258 | |
| 3 | 2008 | 92 | |
| 4 | 2004 | 11 | |
| 5 | 2008 | 11 |
About Erwin Boutsma
Erwin Boutsma is a scholar working on Molecular Biology, Genetics, Computer Networks and Communications, Infectious Diseases and Organic Chemistry, having authored 5 papers that have together received 643 indexed citations. Recurring topics across this work include Epigenetics and DNA Methylation (4 papers), Genetics and Neurodevelopmental Disorders (2 papers), Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (1 paper), Genomics and Chromatin Dynamics (1 paper), Cancer-related gene regulation (1 paper), Opportunistic and Delay-Tolerant Networks (1 paper), RNA modifications and cancer (1 paper) and Caching and Content Delivery (1 paper). The work is most often cited by research in Molecular Biology (592 citations), Genetics (135 citations), Cancer Research (38 citations), Aging (4 citations) and Cell Biology (29 citations). Erwin Boutsma has collaborated with scholars based in Netherlands, United States and Switzerland. Frequent co-authors include Maarten van Lohuizen, Petra van der Stoop, Els Verhoeven, Anders H. Lund, Inmaculada Hernández‐Muñoz, Dmitri A. Nusinow, Barbara Panning, York Marahrens, Haruhiko Koseki and Urszula Brykczynska. Their work appears in journals such as PLoS ONE, Cold Spring Harbor Symposia on Quantitative Biology, Proceedings of the National Academy of Sciences and Nature Genetics.
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.