Ewart de Bruijn

7.8k total citations · 2 hit papers
35 papers, 4.3k citations indexed

About

Ewart de Bruijn is a scholar working on Molecular Biology, Cancer Research and Genetics. According to data from OpenAlex, Ewart de Bruijn has authored 35 papers receiving a total of 4.3k indexed citations (citations by other indexed papers that have themselves been cited), including 21 papers in Molecular Biology, 17 papers in Cancer Research and 8 papers in Genetics. Recurrent topics in Ewart de Bruijn's work include Cancer Genomics and Diagnostics (11 papers), Genetic factors in colorectal cancer (7 papers) and CRISPR and Genetic Engineering (7 papers). Ewart de Bruijn is often cited by papers focused on Cancer Genomics and Diagnostics (11 papers), Genetic factors in colorectal cancer (7 papers) and CRISPR and Genetic Engineering (7 papers). Ewart de Bruijn collaborates with scholars based in Netherlands, United Kingdom and United States. Ewart de Bruijn's co-authors include Wigard P. Kloosterman, Ronald H.A. Plasterk, Erno Wienholds, Sakari Kauppinen, Edwin Cuppen, Eugène Berezikov, H. Robert Horvitz, Ezequiel Alvarez-Saavedra, Eric A. Miska and Isaäc J. Nijman and has published in prestigious journals such as Nature, Science and Nucleic Acids Research.

In The Last Decade

Ewart de Bruijn

33 papers receiving 4.3k citations

Hit Papers

align trajectories

What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if it has ≥500 total citations, achieves ≥1.5× the top-1% citation threshold for papers in the same subfield and year (this is the minimum needed to enter the top 1%, not the average within it), or reaches the top citation threshold in at least one of its specific research topics.

MicroRNA Expression in Zebrafish Embryonic Development

2005 1.3k citations Erno Wienholds, Wigard P. Kloosterman et al. Science profile →
A systematic genome-wide analysis of zebrafish protein-coding gene function

2013 445 citations Ewart de Bruijn, Isaäc J. Nijman et al. profile →

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Ewart de Bruijn Netherlands	24	3.2k	2.4k	679	338	299	35	4.3k
Giovanni Stefani United States	15	3.6k 1.1×	2.0k 0.8×	462 0.7×	163 0.5×	116 0.4×	22	4.2k
Frank L. Conlon United States	33	5.4k 1.7×	1.8k 0.7×	690 1.0×	591 1.7×	185 0.6×	87	6.2k
Erno Wienholds Netherlands	19	4.2k 1.3×	2.7k 1.1×	590 0.9×	917 2.7×	389 1.3×	22	5.7k
Bénédicte Mascrez France	20	3.0k 0.9×	983 0.4×	619 0.9×	150 0.4×	294 1.0×	27	3.3k
Qun Pan Canada	32	9.5k 3.0×	3.0k 1.2×	585 0.9×	190 0.6×	493 1.6×	64	10.7k
Stefano Colella France	28	2.3k 0.7×	897 0.4×	1.1k 1.6×	130 0.4×	638 2.1×	50	4.1k
Sarah E. Johnstone United States	12	5.7k 1.8×	1.1k 0.5×	539 0.8×	190 0.6×	316 1.1×	24	6.3k
Björn Menten Belgium	36	2.5k 0.8×	912 0.4×	1.7k 2.5×	143 0.4×	505 1.7×	131	4.3k
Veena Afzal United States	31	4.3k 1.4×	939 0.4×	1.3k 1.9×	214 0.6×	704 2.4×	47	5.7k
Alena Shkumatava France	19	3.2k 1.0×	1.6k 0.7×	416 0.6×	187 0.6×	381 1.3×	29	3.7k

Countries citing papers authored by Ewart de Bruijn

Since Specialization

Citations

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

Fields of papers citing papers by Ewart de Bruijn

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Ewart de Bruijn

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

All Works

Sort: Min cites: Since: Top N: Style:

20 of 20 papers shown

Valle-Inclán, Jose Espejo, Nicolle Besselink, Ewart de Bruijn, et al.. (2022). A multi-platform reference for somatic structural variation detection. Cell Genomics. 2(6). 100139–100139. 17 indexed citations

Tops, Bastiaan B.J., Elisabeth M. P. Steeghs, Veerle M.H. Coupé, et al.. (2021). Micro-costing diagnostics in oncology: from single-gene testing to whole- genome sequencing. Expert Review of Pharmacoeconomics & Outcomes Research. 21(3). 403–413. 23 indexed citations

Roepman, Paul, Ewart de Bruijn, Stef van Lieshout, et al.. (2021). Clinical Validation of Whole Genome Sequencing for Cancer Diagnostics. Journal of Molecular Diagnostics. 23(7). 816–833. 39 indexed citations

Samsom, Kris G., Linda J.W. Bosch, Luuk J. Schipper, et al.. (2020). Study protocol: Whole genome sequencing Implementation in standard Diagnostics for Every cancer patient (WIDE). BMC Medical Genomics. 13(1). 169–169. 24 indexed citations

Monkhorst, Kim, Kris G. Samsom, Luuk J. Schipper, et al.. (2020). 1189O Validation of whole genome sequencing in routine clinical practice. Annals of Oncology. 31. S784–S784. 5 indexed citations

Roepman, Paul, L. Van den Bosch, Kris G. Samsom, et al.. (2019). WGS implementation in standard cancer diagnostics for every cancer patient (WIDE). Annals of Oncology. 30. v575–v575. 3 indexed citations

Roosmalen, Markus J. van, Ivo Renkens, Marleen M. Nieboer, et al.. (2017). Mapping and phasing of structural variation in patient genomes using nanopore sequencing. Nature Communications. 8(1). 1326–1326. 249 indexed citations

Vermunt, Marit W., Sander Tan, Bas Castelijns, et al.. (2016). Epigenomic annotation of gene regulatory alterations during evolution of the primate brain. Nature Neuroscience. 19(3). 494–503. 86 indexed citations

Vermunt, Marit W., Peter Reinink, Jeroen Korving, et al.. (2014). Large-Scale Identification of Coregulated Enhancer Networks in the Adult Human Brain. Cell Reports. 9(2). 767–779. 59 indexed citations

10.

Heesch, Sebastiaan van, Michal Mokrý, Veronika Bošková, et al.. (2013). Systematic biases in DNA copy number originate from isolation procedures. Genome biology. 14(4). R33–R33. 35 indexed citations

11.

Simonis, Marieke, Santosh S. Atanur, Sam Linsen, et al.. (2012). Genetic basis of transcriptome differences between the founder strains of the rat HXB/BXH recombinant inbred panel. Genome biology. 13(4). r31–r31. 22 indexed citations

12.

Vermaat, Joost S.P., Isaäc J. Nijman, Marco J. Koudijs, et al.. (2011). Primary Colorectal Cancers and Their Subsequent Hepatic Metastases Are Genetically Different: Implications for Selection of Patients for Targeted Treatment. Clinical Cancer Research. 18(3). 688–699. 119 indexed citations

13.

Clark, Matthew D., Victor Guryev, Ewart de Bruijn, et al.. (2011). Single Nucleotide Polymorphism (SNP) Panels for Rapid Positional Cloning in Zebrafish. Methods in cell biology. 104. 219–235. 6 indexed citations

14.

Kloosterman, Wigard P., Victor Guryev, Karen Duran, et al.. (2011). Chromothripsis as a mechanism driving complex de novo structural rearrangements in the germline†. Human Molecular Genetics. 20(10). 1916–1924. 225 indexed citations

15.

Harakaľová, Magdaléna, Michal Mokrý, Barbara Hrdličková, et al.. (2011). Multiplexed array-based and in-solution genomic enrichment for flexible and cost-effective targeted next-generation sequencing. Nature Protocols. 6(12). 1870–1886. 51 indexed citations

16.

Mokrý, Michal, Pantelis Hatzis, Ewart de Bruijn, et al.. (2010). Efficient Double Fragmentation ChIP-seq Provides Nucleotide Resolution Protein-DNA Binding Profiles. PLoS ONE. 5(11). e15092–e15092. 34 indexed citations

17.

Nijman, Isaäc J., Michal Mokrý, Ruben van Boxtel, et al.. (2010). Mutation discovery by targeted genomic enrichment of multiplexed barcoded samples. Nature Methods. 7(11). 913–915. 55 indexed citations

18.

Linsen, Sam, Elzo de Wit, Ewart de Bruijn, & Edwin Cuppen. (2010). Small RNA expression and strain specificity in the rat. BMC Genomics. 11(1). 249–249. 69 indexed citations

19.

Feitsma, Harma, Ewart de Bruijn, José van de Belt, Isaäc J. Nijman, & Edwin Cuppen. (2008). Mismatch repair deficiency does not enhance ENU mutagenesis in the zebrafish germ line. Mutagenesis. 23(4). 325–329. 8 indexed citations

20.

Wienholds, Erno, Wigard P. Kloosterman, Eric A. Miska, et al.. (2005). MicroRNA Expression in Zebrafish Embryonic Development. Science. 309(5732). 310–311. 1284 indexed citations breakdown →

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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