Stephen Van Komen

3.6k citations
25 papers · 2.8k · 1 hit paper · h-index 22

Impact in

    • DNA Repair Mechanisms
    • CRISPR and Genetic Engineering
    • Genomics and Chromatin Dynamics
    • Fungal and yeast genetics research
    • DNA and Nucleic Acid Chemistry
    • Carcinogens and Genotoxicity Assessment

Papers in

    • DNA Repair Mechanisms 22
    • DNA and Nucleic Acid Chemistry 8
    • CRISPR and Genetic Engineering 7
    • Genomics and Chromatin Dynamics 5
    • Cancer therapeutics and mechanisms 3
    • Fungal and yeast genetics research 2
    • Carcinogens and Genotoxicity Assessment 7

Stephen Van Komen

23 papers receiving 2.7k citations

Hit Papers

DNA helicase Srs2 disrupts the Rad51 presynaptic filament 2003 · 506 citations
5060+7+15Years since publication100200300400500

Peers

Stephen Van Komen
Comparison fields: 5 of 63
  • Molecular Biology 2.7k
  • Cancer Research 575
  • Oncology 535
  • Cell Biology 219
  • Aging 23
Replace Patrick Sung with:
Patrick Sung United States
Hengyao Niu United States
Ildikó Unk Hungary
Leonard Wu United Kingdom
Julia Karow United Kingdom
Cecilia Cotta‐Ramusino United States
Rodrigo Bermejo Italy
Kelly M. Trujillo United States
Anneke van Hoffen Netherlands
Matteo Berti United States
Stephen Van Komen relative to Patrick Sung United States Patrick Sung's profile →
Citations per field
00.5×1.5×
Patrick Sung · 1×
Citations per year

Countries citing papers authored by Stephen Van Komen

Since Specialization
Citations

This map shows the geographic impact of Stephen Van Komen'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 Stephen Van Komen with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Stephen Van Komen more than expected).

Fields of papers citing papers by Stephen Van Komen

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Stephen Van Komen. 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 Stephen Van Komen. The network helps show where Stephen Van Komen may publish in the future.

Co-authors

The 25 scholars most cited alongside Stephen Van Komen, 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 Stephen Van Komen Line = papers co-authored together Stephen Van Komen links everyone, so they are left out of the graph.

All Works

20 of 20 papers shown

Showing the 20 most-cited of 25 papers — load more, or switch the sort, to bring in the rest.

#Work
1
DNA helicase Srs2 disrupts the Rad51 presynaptic filament
Hit paper breakdown →
2003506
2 2003341
3 2001188
4 2000188
5 1999166
6 2003160
7 2000157
8 2006147
9 2003147
10 2002119
11 200388
12 200580
13 200461
14 200561
15 200458
16 200256
17 200352
18 200348
19 200444
20 200637

About Stephen Van Komen

Stephen Van Komen is a scholar working on Molecular Biology, Cancer Research, Oncology, Genetics and Reproductive Medicine, having authored 25 papers that have together received 2.8k indexed citations. Recurring topics across this work include DNA Repair Mechanisms (22 papers), DNA and Nucleic Acid Chemistry (8 papers), CRISPR and Genetic Engineering (7 papers), Carcinogens and Genotoxicity Assessment (7 papers), Genomics and Chromatin Dynamics (5 papers), PARP inhibition in cancer therapy (4 papers), Cancer therapeutics and mechanisms (3 papers) and Fungal and yeast genetics research (2 papers). The work is most often cited by research in Molecular Biology (2.7k citations), Cancer Research (575 citations), Oncology (535 citations), Cell Biology (219 citations) and Aging (23 citations). Stephen Van Komen has collaborated with scholars based in United States, Germany and Canada. Frequent co-authors include Patrick Sung, Lumír Krejčí, Stefán Sigurðsson, Michael G. Sehorn, Hannah L. Klein, Galina Petukhova, Kelly M. Trujillo, Jana Villemain, Thomas E. Ellenberger and Ying Li. Their work appears in journals such as Journal of Biological Chemistry, Molecular Cell, Genes & Development, DNA repair and Mutation research. Fundamental and molecular mechanisms of mutagenesis.

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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