Ivo Renkens

3.5k total citations
21 papers, 1.3k citations indexed

About

Ivo Renkens is a scholar working on Molecular Biology, Cancer Research and Genetics. According to data from OpenAlex, Ivo Renkens has authored 21 papers receiving a total of 1.3k indexed citations (citations by other indexed papers that have themselves been cited), including 15 papers in Molecular Biology, 9 papers in Cancer Research and 7 papers in Genetics. Recurrent topics in Ivo Renkens's work include Cancer Genomics and Diagnostics (9 papers), Genomic variations and chromosomal abnormalities (5 papers) and Genomics and Phylogenetic Studies (5 papers). Ivo Renkens is often cited by papers focused on Cancer Genomics and Diagnostics (9 papers), Genomic variations and chromosomal abnormalities (5 papers) and Genomics and Phylogenetic Studies (5 papers). Ivo Renkens collaborates with scholars based in Netherlands, United States and Germany. Ivo Renkens's co-authors include Wigard P. Kloosterman, Markus J. van Roosmalen, Edwin Cuppen, Jeroen de Ridder, Isaäc J. Nijman, Victor Guryev, Jose Espejo Valle-Inclán, Ewart de Bruijn, Karen Duran and Emile E. Voest and has published in prestigious journals such as Nature Communications, Nature Genetics and Blood.

In The Last Decade

Ivo Renkens

21 papers receiving 1.3k citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Ivo Renkens Netherlands	15	894	524	306	251	105	21	1.3k
Markus J. van Roosmalen Netherlands	17	650 0.7×	352 0.7×	344 1.1×	151 0.6×	180 1.7×	26	1.1k
Anita Göndör Sweden	15	1.9k 2.1×	421 0.8×	338 1.1×	308 1.2×	162 1.5×	27	2.1k
Kerry J. Schimenti United States	18	1.1k 1.3×	344 0.7×	184 0.6×	216 0.9×	88 0.8×	24	1.4k
Christina Ernst United Kingdom	14	1.1k 1.2×	190 0.4×	214 0.7×	304 1.2×	66 0.6×	21	1.4k
Mark T. Ross United Kingdom	17	699 0.8×	403 0.8×	220 0.7×	197 0.8×	120 1.1×	35	1.2k
Rahul Karnik United States	14	1.6k 1.8×	294 0.6×	259 0.8×	83 0.3×	115 1.1×	25	1.8k
Mitchell L. Leibowitz United States	8	1.0k 1.1×	425 0.8×	226 0.7×	252 1.0×	130 1.2×	9	1.3k
Igor Chernukhin United Kingdom	23	1.4k 1.5×	358 0.7×	165 0.5×	168 0.7×	393 3.7×	44	1.8k
Ondřej Gojiš United Kingdom	11	1.2k 1.3×	296 0.6×	298 1.0×	112 0.4×	279 2.7×	18	1.6k
Dione K. Bailey United States	9	2.3k 2.6×	733 1.4×	727 2.4×	284 1.1×	125 1.2×	10	2.8k

Countries citing papers authored by Ivo Renkens

Since Specialization

Citations

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

Fields of papers citing papers by Ivo Renkens

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Ivo Renkens

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

All Works

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20 of 20 papers shown

Elferink, Martin, Laura Campello Blasco, Ivo Renkens, et al.. (2025). Long-read sequencing identifies copy-specific markers of SMN gene conversion in spinal muscular atrophy. Genome Medicine. 17(1). 26–26. 1 indexed citations

Renkens, Ivo, Robert Duran, Gijs van Haaften, et al.. (2023). CRISPR‐Cas9 enrichment, a new strategy in microbial metagenomics to investigate complex genomic regions: The case of an environmental integron. Molecular Ecology Resources. 23(6). 1288–1298. 2 indexed citations

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

Mulet‐Lazaro, Roger, Claudia Erpelinck-Verschueren, Eric M. Bindels, et al.. (2021). Allele-specific expression of GATA2 due to epigenetic dysregulation in CEBPA double-mutant AML. Blood. 138(2). 160–177. 13 indexed citations

Marcozzi, Alessio, Myrthe Jager, Martin Elferink, et al.. (2021). Accurate detection of circulating tumor DNA using nanopore consensus sequencing. npj Genomic Medicine. 6(1). 106–106. 31 indexed citations

Valle-Inclán, Jose Espejo, Lisanne F. van Dessel, Markus J. van Roosmalen, et al.. (2021). Optimizing Nanopore sequencing-based detection of structural variants enables individualized circulating tumor DNA-based disease monitoring in cancer patients. Genome Medicine. 13(1). 86–86. 21 indexed citations

Blank, Sam de, Ivo Renkens, Liset Westera, et al.. (2020). Partner independent fusion gene detection by multiplexed CRISPR-Cas9 enrichment and long read nanopore sequencing. Nature Communications. 11(1). 2861–2861. 47 indexed citations

Vermeulen, Carlo, Amin Allahyar, Britta A. M. Bouwman, et al.. (2020). Multi-contact 4C: long-molecule sequencing of complex proximity ligation products to uncover local cooperative and competitive chromatin topologies. Nature Protocols. 15(2). 364–397. 30 indexed citations

Allahyar, Amin, Carlo Vermeulen, Britta A. M. Bouwman, et al.. (2018). Enhancer hubs and loop collisions identified from single-allele topologies. Nature Genetics. 50(8). 1151–1160. 162 indexed citations

10.

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

11.

Francioli, Laurent C., Paz Polak, Amnon Koren, et al.. (2015). Genome-wide patterns and properties of de novo mutations in humans. Nature Genetics. 47(7). 822–826. 238 indexed citations

12.

Pagter, Mirjam S. de, Markus J. van Roosmalen, Annette F. Baas, et al.. (2015). Chromothripsis in Healthy Individuals Affects Multiple Protein-Coding Genes and Can Result in Severe Congenital Abnormalities in Offspring. The American Journal of Human Genetics. 96(4). 651–656. 80 indexed citations

13.

Hoogstraat, Marlous, Mirjam S. de Pagter, Geert A. Cirkel, et al.. (2013). Genomic and transcriptomic plasticity in treatment-naïve ovarian cancer. Genome Research. 24(2). 200–211. 63 indexed citations

14.

VOSSEN, C.Y., Bobby P. C. Koeleman, Sandra J. Hasstedt, et al.. (2013). Genetic variants associated with protein C levels. Journal of Thrombosis and Haemostasis. 11(4). 715–723. 2 indexed citations

15.

Hochstenbach, Ron, Martin Poot, Isaäc J. Nijman, et al.. (2012). Discovery of variants unmasked by hemizygous deletions. European Journal of Human Genetics. 20(7). 748–753. 14 indexed citations

16.

Hochstenbach, Ron, Mariëlle van Gijn, Pieter-Jaap Krijtenburg, et al.. (2012). Gain of FAM123B and ARHGEF9 in an Obese Man with Intellectual Disability, Congenital Heart Defects and Multiple Supernumerary Ring Chromosomes. Molecular Syndromology. 3(6). 274–283. 7 indexed citations

17.

Harakaľová, Magdaléna, Marie-José van den Boogaard, Richard J. Sinke, et al.. (2012). X-exome sequencing identifies a HDAC8 variant in a large pedigree with X-linked intellectual disability, truncal obesity, gynaecomastia, hypogonadism and unusual face. Journal of Medical Genetics. 49(8). 539–543. 50 indexed citations

18.

Kloosterman, Wigard P., Marlous Hoogstraat, Masoumeh Tavakoli‐Yaraki, et al.. (2011). Chromothripsis is a common mechanism driving genomic rearrangements in primary and metastatic colorectal cancer. Genome biology. 12(10). R103–R103. 161 indexed citations

19.

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

20.

Harakaľová, Magdaléna, Isaäc J. Nijman, Jelena Medic, et al.. (2011). Genomic DNA Pooling Strategy for Next-Generation Sequencing-Based Rare Variant Discovery in Abdominal Aortic Aneurysm Regions of Interest—Challenges and Limitations. Journal of Cardiovascular Translational Research. 4(3). 271–280. 18 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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