Erwin Boutsma

780 citations
5 papers · 643 · h-index 5

Impact in

    • 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
    • Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities

Papers in

    • Epigenetics and DNA Methylation 4
    • Genomics and Chromatin Dynamics 1
    • Cancer-related gene regulation 1
    • RNA modifications and cancer 1
    • Genetics and Neurodevelopmental Disorders 2
    • Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities 1

Erwin Boutsma

5 papers receiving 638 citations

Peers

Erwin Boutsma
Comparison fields: 5 of 48
  • Molecular Biology 592
  • Genetics 135
  • Cancer Research 38
  • Aging 4
  • Cell Biology 29
Replace Mónica Román-Trufero with:
Mónica Román-Trufero United Kingdom
M. Lutz Germany
Judith Luciani France
Tamie Endoh Japan
Avril Smith Germany
Mathieu Tardat France
David-Emlyn Parfitt United Kingdom
David Dickerson United States
Andrew Fedoriw United States
Maxim Nekrasov Australia
Erwin Boutsma relative to Mónica Román-Trufero United Kingdom Mónica Román-Trufero's profile →
Citations per field
00.5×1.6×
Mónica Román-Trufero · 1×
Citations per year

Countries citing papers authored by Erwin Boutsma

Since Specialization
Citations

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

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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.

Border = papers with Erwin Boutsma Line = papers co-authored together Erwin Boutsma links everyone, so they are left out of the graph.

All Works

5 of 5 papers shown
#Work
1 2008271
2 2005258
3 200892
4 200411
5 200811

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.

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