Wouter Koole

1.7k total citations
17 papers, 1.3k citations indexed

About

Wouter Koole is a scholar working on Molecular Biology, Genetics and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Wouter Koole has authored 17 papers receiving a total of 1.3k indexed citations (citations by other indexed papers that have themselves been cited), including 11 papers in Molecular Biology, 4 papers in Genetics and 3 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Wouter Koole's work include DNA Repair Mechanisms (4 papers), BRCA gene mutations in cancer (4 papers) and CRISPR and Genetic Engineering (4 papers). Wouter Koole is often cited by papers focused on DNA Repair Mechanisms (4 papers), BRCA gene mutations in cancer (4 papers) and CRISPR and Genetic Engineering (4 papers). Wouter Koole collaborates with scholars based in Netherlands, United States and Germany. Wouter Koole's co-authors include Elif Eroğlu, Derk ten Berge, Roel Nusse, Marcel Tijsterman, Christophe Fuerer, Matt Fish, Alex Maas, Ronald K. Siu, Tim Blauwkamp and Dorota Kurek and has published in prestigious journals such as Nucleic Acids Research, Nature Communications and The EMBO Journal.

In The Last Decade

Wouter Koole

16 papers receiving 1.3k citations

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name h Career Trend Papers Cites
Wouter Koole Netherlands 10 1.1k 151 136 132 94 17 1.3k
Shravanti Rampalli India 14 1.3k 1.2× 169 1.1× 154 1.1× 87 0.7× 117 1.2× 20 1.5k
Samer M. I. Hussein Canada 16 1.4k 1.3× 173 1.1× 199 1.5× 173 1.3× 81 0.9× 33 1.8k
Warakorn Kulalert United States 5 1.7k 1.6× 137 0.9× 271 2.0× 213 1.6× 151 1.6× 6 1.8k
Tamar Golan‐Lev Israel 16 1.0k 1.0× 263 1.7× 150 1.1× 106 0.8× 91 1.0× 26 1.2k
Louise Hyslop United Kingdom 11 1.0k 0.9× 132 0.9× 145 1.1× 127 1.0× 65 0.7× 17 1.4k
M. Esther Gallardo Spain 20 986 0.9× 174 1.2× 117 0.9× 114 0.9× 38 0.4× 56 1.6k
Jia-Hui Ng Singapore 10 1.6k 1.4× 211 1.4× 179 1.3× 197 1.5× 88 0.9× 11 1.7k
Andreas Hierholzer Germany 11 711 0.7× 108 0.7× 85 0.6× 95 0.7× 211 2.2× 16 1000
Michaela Patterson United States 18 1.4k 1.3× 231 1.5× 285 2.1× 96 0.7× 80 0.9× 34 1.8k

Countries citing papers authored by Wouter Koole

Since Specialization
Citations

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

Fields of papers citing papers by Wouter Koole

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Wouter Koole. 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 Wouter Koole. The network helps show where Wouter Koole may publish in the future.

Co-authorship network of co-authors of Wouter Koole

This figure shows the co-authorship network connecting the top 25 collaborators of Wouter Koole. A scholar is included among the top collaborators of Wouter Koole 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 Wouter Koole. Wouter Koole is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

17 of 17 papers shown
1.
Bleiker, Eveline M. A., Mary E. Velthuizen, Arjan P. Schouten van der Velden, et al.. (2023). Patients’ experiences with pre-test genetic counseling provided by breast cancer healthcare professionals: Results from a large prospective multicenter study. The Breast. 69. 349–357. 4 indexed citations
2.
Bleiker, Eveline M. A., Cora M. Aalfs, Thijs van Dalen, et al.. (2023). Surgical Oncologists and Nurses in Breast Cancer Care are Ready to Provide Pre-Test Genetic Counseling. Annals of Surgical Oncology. 30(6). 3248–3258. 7 indexed citations
3.
Frederix, G. W. J., Mary E. Velthuizen, Maaike A. van der Aa, et al.. (2022). Mainstream germline genetic testing for patients with epithelial ovarian cancer leads to higher testing rates and a reduction in genetics-related healthcare costs from a healthcare payer perspective. Gynecologic Oncology. 167(1). 115–122. 8 indexed citations
4.
Koole, Wouter, Anne M.L. Jansen, Margreet G.E.M. Ausems, et al.. (2022). EP313/#490 Validation of mutation analysis of ovarian cancer predisposition genes in tumor tissue. A180.2–A181.
5.
Kutzera, Joachim, Wouter Koole, Margreet G.E.M. Ausems, et al.. (2021). Familial Occurrence of Adult Granulosa Cell Tumors: Analysis of Whole-Genome Germline Variants. Cancers. 13(10). 2430–2430. 4 indexed citations
6.
Blom, Maartje, Robbert G. M. Bredius, Marleen E. Jansen, et al.. (2020). Parents’ Perspectives and Societal Acceptance of Implementation of Newborn Screening for SCID in the Netherlands. Journal of Clinical Immunology. 41(1). 99–108. 29 indexed citations
7.
Bruijn, Suzanne E. de, Chang Liu, Cris Lanting, et al.. (2020). A RIPOR2 in-frame deletion is a frequent and highly penetrant cause of adult-onset hearing loss. Journal of Medical Genetics. 58(2). 96–104. 14 indexed citations
8.
Oostrik, Jaap, Andy J. Beynon, Sarina G. Kant, et al.. (2018). De novo and inherited loss-of-function variants of ATP2B2 are associated with rapidly progressive hearing impairment. Human Genetics. 138(1). 61–72. 25 indexed citations
9.
Seyoum, Solomon, et al.. (2017). A Shazam-like Household Water Leakage Detection Method. Procedia Engineering. 186. 452–459. 20 indexed citations
10.
Koole, Wouter, et al.. (2014). A Polymerase Theta-dependent repair pathway suppresses extensive genomic instability at endogenous G4 DNA sites. Nature Communications. 5(1). 3216–3216. 175 indexed citations
11.
Segura‐Bayona, Sandra, et al.. (2014). FANCJ promotes DNA synthesis through G‐quadruplex structures. The EMBO Journal. 33(21). 2521–2533. 115 indexed citations
12.
Koole, Wouter & Marcel Tijsterman. (2014). Mosaic analysis and tumor induction in zebrafish by microsatellite instability-mediated stochastic gene expression. Disease Models & Mechanisms. 7(7). 929–36. 4 indexed citations
13.
Koole, Wouter, Henning Schäfer, Reuven Agami, Gijs van Haaften, & Marcel Tijsterman. (2013). A versatile microsatellite instability reporter system in human cells. Nucleic Acids Research. 41(16). e158–e158. 9 indexed citations
14.
Roerink, Sophie, Wouter Koole, L. Carine Stapel, Ron Romeijn, & Marcel Tijsterman. (2012). A Broad Requirement for TLS Polymerases η and κ, and Interacting Sumoylation and Nuclear Pore Proteins, in Lesion Bypass during C. elegans Embryogenesis. PLoS Genetics. 8(6). e1002800–e1002800. 45 indexed citations
15.
Berge, Derk ten, Dorota Kurek, Tim Blauwkamp, et al.. (2011). Embryonic stem cells require Wnt proteins to prevent differentiation to epiblast stem cells. Nature Cell Biology. 13(9). 1070–1075. 363 indexed citations
16.
Berge, Derk ten, Wouter Koole, Christophe Fuerer, et al.. (2008). Wnt Signaling Mediates Self-Organization and Axis Formation in Embryoid Bodies. Cell stem cell. 3(5). 508–518. 375 indexed citations
17.
Haaften, Gijs van, Ron Romeijn, Joris Pothof, et al.. (2006). Identification of Conserved Pathways of DNA-Damage Response and Radiation Protection by Genome-Wide RNAi. Current Biology. 16(13). 1344–1350. 70 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.

Explore authors with similar magnitude of impact

Breakdown of academic impact, for papers by Shravanti Rampalli Breakdown of academic impact, for papers by Samer M. I. Hussein Breakdown of academic impact, for papers by Warakorn Kulalert Breakdown of academic impact, for papers by Tamar Golan‐Lev Breakdown of academic impact, for papers by Louise Hyslop Breakdown of academic impact, for papers by M. Esther Gallardo Breakdown of academic impact, for papers by Jia-Hui Ng Breakdown of academic impact, for papers by Andreas Hierholzer Breakdown of academic impact, for papers by Michaela Patterson
Rankless by CCL
2026