Niels de Wind

5.9k total citations · 2 hit papers
89 papers, 4.6k citations indexed

About

Niels de Wind is a scholar working on Molecular Biology, Cancer Research and Pathology and Forensic Medicine. According to data from OpenAlex, Niels de Wind has authored 89 papers receiving a total of 4.6k indexed citations (citations by other indexed papers that have themselves been cited), including 59 papers in Molecular Biology, 47 papers in Cancer Research and 41 papers in Pathology and Forensic Medicine. Recurrent topics in Niels de Wind's work include DNA Repair Mechanisms (48 papers), Genetic factors in colorectal cancer (41 papers) and Cancer Genomics and Diagnostics (28 papers). Niels de Wind is often cited by papers focused on DNA Repair Mechanisms (48 papers), Genetic factors in colorectal cancer (41 papers) and Cancer Genomics and Diagnostics (28 papers). Niels de Wind collaborates with scholars based in Netherlands, United States and Denmark. Niels de Wind's co-authors include Hein te Riele, Marleen Dekker, Miroslav Radman, Anton Berns, Jacob G. Jansen, A. L. J. Gielkens, H.H.K. Winterwerp, Titia K. Sixma, Meindert H. Lamers and Anton Berns and has published in prestigious journals such as Nature, Cell and Proceedings of the National Academy of Sciences.

In The Last Decade

Niels de Wind

88 papers receiving 4.5k citations

Hit Papers

Inactivation of the mouse Msh2 gene results in mismatch r... 1995 2026 2005 2015 1995 2000 200 400 600

Peers

Niels de Wind
Mila Janković United States
Patricia J. Gearhart United States
F. Nina Papavasiliou United States
Steven R. Tronick United States
Beverly E. Griffin United Kingdom
Timothy F. Kowalik United States
Michael Lagunoff United States
Zhen Lin United States
Niels de Wind
Citations per year, relative to Niels de Wind Niels de Wind (= 1×) peers Lori Frappier

Countries citing papers authored by Niels de Wind

Since Specialization
Citations

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

Fields of papers citing papers by Niels de Wind

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Niels de Wind. 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 Niels de Wind. The network helps show where Niels de Wind may publish in the future.

Co-authorship network of co-authors of Niels de Wind

This figure shows the co-authorship network connecting the top 25 collaborators of Niels de Wind. A scholar is included among the top collaborators of Niels de Wind based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with Niels de Wind. Niels de Wind is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

20 of 20 papers shown
1.
Tsaalbi‐Shtylik, Anastasia, Rurika Oka, Freek Manders, et al.. (2024). DNA mismatch repair controls the mutagenicity of Polymerase ζ-dependent translesion synthesis at methylated guanines. DNA repair. 142. 103755–103755. 2 indexed citations
2.
Li, Zhiquan, Yuan Li, Lin Wang, et al.. (2023). Rev1 deficiency induces a metabolic shift in MEFs that can be manipulated by the NAD+ precursor nicotinamide riboside. Heliyon. 9(6). e17392–e17392. 1 indexed citations
3.
Lam, A., Carli M.J. Tops, Liselotte P. van Hest, et al.. (2023). Discordant Staining Patterns and Microsatellite Results in Tumors of MSH6 Pathogenic Variant Carriers. Modern Pathology. 36(9). 100240–100240. 9 indexed citations
4.
Song, Peng, Shaojun Liu, Dekang Liu, et al.. (2022). CNOT6: A Novel Regulator of DNA Mismatch Repair. Cells. 11(3). 521–521. 7 indexed citations
5.
Drost, Mark, Scott D. Kathe, Fabienne M.G.R. Calléja, et al.. (2020). Two integrated and highly predictive functional analysis-based procedures for the classification of MSH6 variants in Lynch syndrome. Genetics in Medicine. 22(5). 847–856. 16 indexed citations
6.
Jansen, Jacob G., et al.. (2020). DNA mismatch repair-dependent DNA damage responses and cancer. DNA repair. 93. 102923–102923. 52 indexed citations
7.
Gool, Inge C. van, Emily Rayner, Elisabeth M. Osse, et al.. (2018). Adjuvant Treatment for POLE Proofreading Domain–Mutant Cancers: Sensitivity to Radiotherapy, Chemotherapy, and Nucleoside Analogues. Clinical Cancer Research. 24(13). 3197–3203. 58 indexed citations
8.
Jansen, Jacob G., Anastasia Tsaalbi‐Shtylik, & Niels de Wind. (2015). Roles of mutagenic translesion synthesis in mammalian genome stability, health and disease. DNA repair. 29. 56–64. 35 indexed citations
9.
Temviriyanukul, Piya, Matty Meijers, J.J.W.A. Boei, et al.. (2012). Different Sets of Translesion Synthesis DNA Polymerases Protect From Genome Instability Induced by Distinct Food-Derived Genotoxins. Toxicological Sciences. 127(1). 130–138. 17 indexed citations
10.
Liberti, Sascha Emilie, Anne Lützen, Mark Drost, et al.. (2012). Functional characterization ofMLH1missense variants identified in lynch syndrome patients. Human Mutation. 33(12). 1647–1655. 15 indexed citations
11.
Dekker, Marleen, Marieke Aarts, Robert G. Dekker, et al.. (2011). Transient suppression of MLH1 allows effective single-nucleotide substitution by single-stranded DNA oligonucleotides. Mutation research. Fundamental and molecular mechanisms of mutagenesis. 715(1-2). 52–60. 11 indexed citations
12.
Yang, In‐Young, Keiji Hashimoto, Niels de Wind, Ian A. Blair, & Masaaki Moriya. (2008). Two Distinct Translesion Synthesis Pathways across a Lipid Peroxidation-derived DNA Adduct in Mammalian Cells. Journal of Biological Chemistry. 284(1). 191–198. 24 indexed citations
13.
Jansen, Jacob G., Maria Fousteri, & Niels de Wind. (2007). Send in the Clamps: Control of DNA Translesion Synthesis in Eukaryotes. Molecular Cell. 28(4). 522–529. 44 indexed citations
14.
Niessen, Renée C., Anne Lützen, Rolf H. Sijmons, et al.. (2007). Functional analysis helps to clarify the clinical importance of unclassified variants in DNA mismatch repair genes. Human Mutation. 28(11). 1047–1054. 42 indexed citations
15.
Borgdorff, Viola, et al.. (2006). DNA mismatch repair mediates protection from mutagenesis induced by short-wave ultraviolet light. DNA repair. 5(11). 1364–1372. 18 indexed citations
16.
Jansen, Jacob G., Petra Langerak, Anastasia Tsaalbi‐Shtylik, et al.. (2006). Strand-biased defect in C/G transversions in hypermutating immunoglobulin genes in Rev1-deficient mice. The Journal of Experimental Medicine. 203(2). 319–323. 171 indexed citations
17.
Oosten, Marijke van, Claude Backendorf, Heggert Rebel, et al.. (2004). Mismatch repair protein Msh2 contributes to UVB-induced cell cycle arrest in epidermal and cultured mouse keratinocytes. DNA repair. 4(1). 81–89. 24 indexed citations
18.
Wind, Niels de & John B. Hays. (2001). Mismatch repair: praying for genome stability. Current Biology. 11(14). R545–R548. 8 indexed citations
19.
Wagenaar, F., J. M. A. Pol, Ben Peeters, et al.. (1995). The US3-encoded protein kinase from pseudorabies virus affects egress of virions from the nucleus. Journal of General Virology. 76(7). 1851–1859. 100 indexed citations

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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