Ivo Renkens

3.5k citations

21 papers · 1.3k indexed · h-index 15

Co-authors: Wigard P. Kloosterman Markus J. van Roosmalen Edwin Cuppen Jeroen de Ridder Isaäc J. Nijman Victor Guryev Jose Espejo Valle-Inclán Ewart de Bruijn
Topics: Cancer Genomics and Diagnostics (9 papers)Genomic variations and chromosomal abnormalities (5 papers)Genomics and Phylogenetic Studies (5 papers)
Cited by: Cancer Research Genetics Molecular Biology
Journals: Nature Communications Nature Genetics Blood
Partner nations: Netherlands United States Germany

In The Last Decade

Ivo Renkens

21 papers receiving 1.3k citations

Peers

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

#	Work	Indexed citations
1	Long-read sequencing identifies copy-specific markers of SMN gene conversion in spinal muscular atrophy 2025 ·Genome Medicine ·(unknown),Martin Elferink,(unknown),(unknown),Laura Campello Blasco,(unknown),(unknown),Ivo Renkens,(unknown),(unknown),Carlo Vermeulen,Roy Straver,Hanneke W. M. van Deutekom,Jan H. Veldink,Fay‐Lynn Asselman,Eduardo F. Tizzano,Renske I. Wadman,W. Ludo van der Pol,(unknown),Ewout J. N. Groen	1
2	CRISPR‐Cas9 enrichment, a new strategy in microbial metagenomics to investigate complex genomic regions: The case of an environmental integron 2023 ·Molecular Ecology Resources ·(unknown),(unknown),(unknown),Ivo Renkens,Robert Duran,Gijs van Haaften,Glen R. Monroe,Béatrice Lauga,Christine Cagnon	2
3	A multi-platform reference for somatic structural variation detection 2022 ·Cell Genomics ·Jose Espejo Valle-Inclán,Nicolle Besselink,Ewart de Bruijn,Daniel Cameron,Jana Ebler,Joachim Kutzera,Stef van Lieshout,Tobias Marschall,Marcel Nelen,Peter Priestley,Ivo Renkens,Margaretha G.M. Roemer,Markus J. van Roosmalen,Aaron M. Wenger,Bauke Ylstra,Remond J.A. Fijneman,Wigard P. Kloosterman,Edwin Cuppen	17
4	Allele-specific expression of GATA2 due to epigenetic dysregulation in CEBPA double-mutant AML 2021 ·Blood ·Roger Mulet‐Lazaro,(unknown),Claudia Erpelinck-Verschueren,Eric M. Bindels,Mathijs A. Sanders,Carlo Vermeulen,Ivo Renkens,Peter J.M. Valk,Ari Melnick,Jeroen de Ridder,Michael Rehli,Claudia Gebhard,Ruud Delwel,Bas J. Wouters	13
5	Accurate detection of circulating tumor DNA using nanopore consensus sequencing 2021 ·npj Genomic Medicine ·Alessio Marcozzi,Myrthe Jager,Martin Elferink,Roy Straver,(unknown),(unknown),Li‐Ting Chen,Ivo Renkens,Joyce van Kuik,Chris H.J. Terhaard,Remco de Bree,Lot A. Devriese,Stefan M. Willems,Wigard P. Kloosterman,Jeroen de Ridder	31
6	Optimizing Nanopore sequencing-based detection of structural variants enables individualized circulating tumor DNA-based disease monitoring in cancer patients 2021 ·Genome Medicine ·Jose Espejo Valle-Inclán,(unknown),(unknown),Lisanne F. van Dessel,Markus J. van Roosmalen,Jean Helmijr,Ivo Renkens,Roel Janssen,Sam de Blank,Chris J. de Witte,John W.M. Martens,Maurice P.H.M. Jansen,Martijn P. Lolkema,Wigard P. Kloosterman	21
7	Partner independent fusion gene detection by multiplexed CRISPR-Cas9 enrichment and long read nanopore sequencing 2020 ·Nature Communications ·(unknown),Sam de Blank,Ivo Renkens,Liset Westera,(unknown),Jose Espejo Valle-Inclán,Rocío Chamorro González,Anton G. Henssen,Markus J. van Roosmalen,Ronald W. Stam,Emile E. Voest,Wigard P. Kloosterman,Gijs van Haaften,Glen R. Monroe	47
8	Multi-contact 4C: long-molecule sequencing of complex proximity ligation products to uncover local cooperative and competitive chromatin topologies 2020 ·Nature Protocols ·Carlo Vermeulen,Amin Allahyar,Britta A. M. Bouwman,Peter H.L. Krijger,Marjon J.A.M. Verstegen,Geert Geeven,Christian Valdes‐Quezada,Ivo Renkens,Roy Straver,Wigard P. Kloosterman,Jeroen de Ridder,Wouter de Laat	30
9	Enhancer hubs and loop collisions identified from single-allele topologies 2018 ·Nature Genetics ·Amin Allahyar,Carlo Vermeulen,Britta A. M. Bouwman,Peter H.L. Krijger,Marjon J.A.M. Verstegen,Geert Geeven,Melissa van Kranenburg,Mark Pieterse,Roy Straver,Judith H.I. Haarhuis,Kees Jalink,Hans Teunissen,Ivo Renkens,Wigard P. Kloosterman,Benjamin D. Rowland,Elzo de Wit,Jeroen de Ridder,Wouter de Laat	162
10	Mapping and phasing of structural variation in patient genomes using nanopore sequencing 2017 ·Nature Communications ·(unknown),Markus J. van Roosmalen,Ivo Renkens,Marleen M. Nieboer,Sjors Middelkamp,Joep de Ligt,Giulia Pregno,Daniela Giachino,Giorgia Mandrile,Jose Espejo Valle-Inclán,Jerome Korzelius,Ewart de Bruijn,Edwin Cuppen,Michael E. Talkowski,Tobias Marschall,Jeroen de Ridder,Wigard P. Kloosterman	249
11	Genome-wide patterns and properties of de novo mutations in humans 2015 ·Nature Genetics ·Laurent C. Francioli,Paz Polak,Amnon Koren,Androniki Menelaou,Sung Chun,Ivo Renkens,Cornelia M. van Duijn,Morris A. Swertz,Cisca Wijmenga,Gert‐Jan B. van Ommen,P. Eline Slagboom,Dorret I. Boomsma,Kai Ye,Victor Guryev,Peter F. Arndt,Wigard P. Kloosterman,(unknown),Shamil Sunyaev	238
12	Chromothripsis in Healthy Individuals Affects Multiple Protein-Coding Genes and Can Result in Severe Congenital Abnormalities in Offspring 2015 ·The American Journal of Human Genetics ·Mirjam S. de Pagter,Markus J. van Roosmalen,Annette F. Baas,Ivo Renkens,Karen Duran,Ellen van Binsbergen,Masoumeh Tavakoli‐Yaraki,Ron Hochstenbach,Lars T. van der Veken,Edwin Cuppen,Wigard P. Kloosterman	80
13	Genomic and transcriptomic plasticity in treatment-naïve ovarian cancer 2013 ·Genome Research ·Marlous Hoogstraat,Mirjam S. de Pagter,Geert A. Cirkel,Markus J. van Roosmalen,Timothy T. Harkins,Karen Duran,(unknown),Ivo Renkens,Petronella O. Witteveen,Clarence Lee,Isaäc J. Nijman,(unknown),Ruben van ‘t Slot,Trudy N. Jonges,Martijn P. Lolkema,Marco J. Koudijs,Ronald P. Zweemer,Emile E. Voest,Edwin Cuppen,Wigard P. Kloosterman	63
14	Genetic variants associated with protein C levels 2013 ·Journal of Thrombosis and Haemostasis ·C.Y. VOSSEN,Bobby P. C. Koeleman,Sandra J. Hasstedt,Isaäc J. Nijman,Ivo Renkens,Peter Callas,Frits R. Rosendaal,Edwin G. Bovill	2
15	Gain of <b><i>FAM123B</i></b> and <b><i>ARHGEF9 </i></b>in an Obese Man with Intellectual Disability, Congenital Heart Defects and Multiple Supernumerary Ring Chromosomes 2012 ·Molecular Syndromology ·Ron Hochstenbach,Mariëlle van Gijn,Pieter-Jaap Krijtenburg,(unknown),Ruben van ‘t Slot,Ivo Renkens,Marc J. Eleveld,Jasper J. van der Smagt,Martin Poot	7
16	Discovery of variants unmasked by hemizygous deletions 2012 ·European Journal of Human Genetics ·Ron Hochstenbach,Martin Poot,Isaäc J. Nijman,Ivo Renkens,Karen Duran,Ruben van’t Slot,Ellen van Binsbergen,Bert van der Zwaag,Maartje J. Vogel,Pauline Terhal,Hans Kristian Ploos van Amstel,Wigard P. Kloosterman,Edwin Cuppen	14
17	X-exome sequencing identifies a HDAC8 variant in a large pedigree with X-linked intellectual disability, truncal obesity, gynaecomastia, hypogonadism and unusual face 2012 ·Journal of Medical Genetics ·Magdaléna Harakaľová,Marie-José van den Boogaard,Richard J. Sinke,Stef van Lieshout,(unknown),Karen Duran,Ivo Renkens,Pauline Terhal,Carolien G. F. de Kovel,Isaäc J. Nijman,Mieke M. van Haelst,Nine Knoers,Gijs van Haaften,Wigard P. Kloosterman,Raoul C. M. Hennekam,Edwin Cuppen,Hans Kristian Ploos van Amstel	50
18	Chromothripsis is a common mechanism driving genomic rearrangements in primary and metastatic colorectal cancer 2011 ·Genome biology ·Wigard P. Kloosterman,Marlous Hoogstraat,(unknown),Masoumeh Tavakoli‐Yaraki,Ivo Renkens,Joost S.P. Vermaat,Markus J. van Roosmalen,Stef van Lieshout,Isaäc J. Nijman,Wijnand Roessingh,Ruben van ‘t Slot,José van de Belt,Victor Guryev,Marco J. Koudijs,Emile E. Voest,Edwin Cuppen	161
19	Multiplexed array-based and in-solution genomic enrichment for flexible and cost-effective targeted next-generation sequencing 2011 ·Nature Protocols ·Magdaléna Harakaľová,Michal Mokrý,Barbara Hrdličková,Ivo Renkens,Karen Duran,(unknown),Nico Lansu,(unknown),Ewart de Bruijn,Isaäc J. Nijman,Wigard P. Kloosterman,Edwin Cuppen	51
20	Genomic DNA Pooling Strategy for Next-Generation Sequencing-Based Rare Variant Discovery in Abdominal Aortic Aneurysm Regions of Interest—Challenges and Limitations 2011 ·Journal of Cardiovascular Translational Research ·Magdaléna Harakaľová,Isaäc J. Nijman,Jelena Medic,Michal Mokrý,Ivo Renkens,Jan D. Blankensteijn,Wigard P. Kloosterman,Annette F. Baas,Edwin Cuppen	18

About Ivo Renkens

Ivo Renkens is a scholar working on Cancer Research, Internal Medicine and Genetics, having authored 21 papers that have together received 1.3k indexed citations. Recurring topics across this work include Cancer Genomics and Diagnostics (9 papers), Genomic variations and chromosomal abnormalities (5 papers) and Genomics and Phylogenetic Studies (5 papers). The work is most often cited by research in Cancer Research (306 citations), Genetics (524 citations) and Molecular Biology (894 citations). Ivo Renkens has collaborated with scholars based in Netherlands, United States and Germany. Frequent 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 Masoumeh Tavakoli‐Yaraki. Their work appears in journals such as Nature Communications, Nature Genetics and Blood.

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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