Mark Verheul

2.4k citations

29 papers · 1.7k · h-index 19

Impact in

Cancer Research top 5%
- MicroRNA in disease regulation
- Cancer Genomics and Diagnostics
- Cancer-related molecular mechanisms research
Behavioral Neuroscience top 5%

Papers in

Molecular Biology 14
- Single-cell and spatial transcriptomics 3
- CRISPR and Genetic Engineering 3
- Circular RNAs in diseases 2
- Receptor Mechanisms and Signaling 2
Cancer Research 13
- Cancer Genomics and Diagnostics 10
- MicroRNA in disease regulation 3

Co-authors: Edwin Cuppen (15 shared papers)Victor Guryev (7 shared papers)José van de Belt (4 shared papers)Ronald H.A. Plasterk (3 shared papers)Ruben van Boxtel (15 shared papers)Bart M. G. Smits (4 shared papers)Berend Olivier (3 shared papers)Judith R. Homberg (3 shared papers)
Journals: BMC Genomics (3 papers)Cell stem cell (1 paper)Blood (1 paper)Carcinogenesis (1 paper)The Pharmacogenomics Journal (1 paper)
Partner nations: Netherlands Germany United States

In The Last Decade

Mark Verheul

27 papers receiving 1.6k citations

Peers

Countries citing papers authored by Mark Verheul

Since Specialization

Citations

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

Fields of papers citing papers by Mark Verheul

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authors

The 25 scholars most cited alongside Mark Verheul, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.

Border = papers with Mark Verheul Line = papers co-authored together Mark Verheul links everyone, so they are left out of the graph.

All Works

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20 of 20 papers shown

Showing the 20 most-cited of 29 papers — load more, or switch the sort, to bring in the rest.

#	Work
1	Many novel mammalian microRNA candidates identified by extensive cloning and RAKE analysis Genome Research ·Eugène Berezikov, Geert van Tetering, Mark Verheul, José van de Belt, Linda van Laake, Joost B. Vos, Robert E. Verloop, Marc van de Wetering, Victor Guryev, Shuji Takada, Anton Jan van Zonneveld, Hiroyuki Mano, Ronald H.A. Plasterk, Edwin Cuppen	2006	232
2	Characterization of the serotonin transporter knockout rat: A selective change in the functioning of the serotonergic system Neuroscience ·Judith R. Homberg, Berend Olivier, Bart M. G. Smits, Joram D. Mul, Josine Mudde, Mark Verheul, O.F.M. Nieuwenhuizen, A.R. Cools, Eric Ronken, T.I.F.H. Cremers, Anton N. M. Schoffelmeer, Bart Ellenbroek, Edwin Cuppen	2007	202
3	Distribution and functional impact of DNA copy number variation in the rat Nature Genetics ·Victor Guryev, Kathrin Saar, Tatjana Adamović, Mark Verheul, Sebastiaan van Heesch, Stuart A. Cook, Michal Pravenec, Timothy J. Aitman, Howard J. Jacob, James D. Shull, Norbert Hübner, Edwin Cuppen	2008	169
4	Somatic Mutations Reveal Lineage Relationships and Age-Related Mutagenesis in Human Hematopoiesis Cell Reports ·Fernando G. Osorio, Axel Rosendahl Huber, Rurika Oka, Mark Verheul, Sachin Patel, Karlijn Hasaart, Lisanne de la Fonteijne, Ignacio Varela, Fernando D. Camargo, Ruben van Boxtel	2018	157
5	Cloning and expression of new microRNAs from zebrafish Nucleic Acids Research ·Wigard P. Kloosterman, Florian Steiner, Eugène Berezikov, Ewart de Bruijn, José van de Belt, Mark Verheul, Edwin Cuppen, Ronald H.A. Plasterk	2006	151
6	Generation of gene knockouts and mutant models in the laboratory rat by ENU-driven target-selected mutagenesis Pharmacogenetics and Genomics ·Bart M. G. Smits, Josine Mudde, José van de Belt, Mark Verheul, Berend Olivier, Judith R. Homberg, Victor Guryev, Alexander R. Cools, Bart Ellenbroek, Ronald H.A. Plasterk, Edwin Cuppen	2006	151
7	MutationalPatterns: the one stop shop for the analysis of mutational processes BMC Genomics ·Freek Manders, Arianne M. Brandsma, Jurrian K. de Kanter, Mark Verheul, Rurika Oka, Markus J. van Roosmalen, Bastiaan van der Roest, Arne van Hoeck, Edwin Cuppen, Ruben van Boxtel	2022	92
8	Adaptations in pre- and postsynaptic 5-HT1A receptor function and cocaine supersensitivity in serotonin transporter knockout rats Psychopharmacology ·Judith R. Homberg, Sietse F. de Boer, Halfdan S. Raasø, Berend Olivier, Mark Verheul, Eric Ronken, Alexander R. Cools, Bart Ellenbroek, Anton N. M. Schoffelmeer, Louk J. M. J. Vanderschuren, Taco J. De Vries, Edwin Cuppen	2008	86
9	Haplotype Block Structure Is Conserved across Mammals PLoS Genetics ·Victor Guryev, Bart M. G. Smits, José van de Belt, Mark Verheul, Norbert Hübner, Edwin Cuppen	2006	60
10	Improved detection of colibactin-induced mutations by genotoxic E. coli in organoids and colorectal cancer Cancer Cell ·Axel Rosendahl Huber, Cayetano Pleguezuelos‐Manzano, Jens Puschhof, Joske Ubels, Charelle Boot, Aurelia Saftien, Mark Verheul, Laurianne Trabut, Niels M. Groenen, Markus van Roosmalen, Kyanna S. Ouyang, Henry M. Wood, Philip Quirke, Gerrit A. Meijer, Edwin Cuppen, Hans Clevers, Ruben van Boxtel	2024	51
11	SMN1 gene duplications are associated with sporadic ALS Neurology ·Hylke M. Blauw, C. Barnes, Paul W.J. van Vught, Wouter van Rheenen, Mark Verheul, Edwin Cuppen, Jan H. Veldink, Leonard H. van den Berg	2012	47
12	A genome-wide SNP panel for mapping and association studies in the rat BMC Genomics ·Isaäc J. Nijman, Sylvia Kuipers, Mark Verheul, Victor Guryev, Edwin Cuppen	2008	47
13	A Functional Screen Identifies Specific MicroRNAs Capable of Inhibiting Human Melanoma Cell Viability PLoS ONE ·Jos B. Poell, Rick J. van Haastert, Thijs de Gunst, Iman J. Schultz, Willemijn M. Gommans, Mark Verheul, Francesco Cerisoli, Paula I. van Noort, Grégoire Prévost, Roel Q.J. Schaapveld, Edwin Cuppen	2012	46
14	Improved generation of rat gene knockouts by target-selected mutagenesis in mismatch repair-deficient animals BMC Genomics ·Ruben van Boxtel, Pim W. Toonen, Mark Verheul, Henk S. van Roekel, Isaäc J. Nijman, Victor Guryev, Edwin Cuppen	2008	26
15	Antiviral treatment causes a unique mutational signature in cancers of transplantation recipients Cell stem cell ·Jurrian K. de Kanter, Flavia Peci, Eline Bertrums, Axel Rosendahl Huber, Anaïs van Leeuwen, Markus J. van Roosmalen, Freek Manders, Mark Verheul, Rurika Oka, Arianne M. Brandsma, Marc Bierings, Mirjam E. Belderbos, Ruben van Boxtel	2021	25
16	Mutation accumulation and developmental lineages in normal and Down syndrome human fetal haematopoiesis Scientific Reports ·Karlijn Hasaart, Freek Manders, Marie‐Louise van der Hoorn, Mark Verheul, Tomasz Poplonski, Ewart Kuijk, Susana M. Chuva de Sousa Lopes, Ruben van Boxtel	2020	22
17	Elevated Mutational Age in Blood of Children Treated for Cancer Contributes to Therapy-Related Myeloid Neoplasms Cancer Discovery ·Eline J.M. Bertrums, Axel Rosendahl Huber, Jurrian K. de Kanter, Arianne M. Brandsma, Anaïs J.C.N. van Leeuwen, Mark Verheul, Marry M. van den Heuvel‐Eibrink, Rurika Oka, Markus J. van Roosmalen, Hester A. de Groot‐Kruseman, C. Michel Zwaan, Bianca F. Goemans, Ruben van Boxtel	2022	18
18	Mutation Signatures of Pediatric Acute Myeloid Leukemia and Normal Blood Progenitors Associated with Differential Patient Outcomes Blood Cancer Discovery ·Arianne M. Brandsma, Eline J.M. Bertrums, Markus J. van Roosmalen, Damon A. Hofman, Rurika Oka, Mark Verheul, Freek Manders, Joske Ubels, Mirjam E. Belderbos, Ruben van Boxtel	2021	18
19	Systematic generation of in vivo G protein-coupled receptor mutants in the rat The Pharmacogenomics Journal ·Ruben van Boxtel, Bas Vroling, Pim W. Toonen, Isaäc J. Nijman, H van Roekel, Mark Verheul, Coos Baakman, Victor Guryev, Gert Vriend, Edwin Cuppen	2010	18
20	Lack of DNA mismatch repair protein MSH6 in the rat results in hereditary non-polyposis colorectal cancer-like tumorigenesis Carcinogenesis ·Ruben van Boxtel, Pim W. Toonen, Henk S. van Roekel, Mark Verheul, Bart M. G. Smits, Jeroen Korving, Alain de Bruin, Edwin Cuppen	2008	17

About Mark Verheul

Mark Verheul is a scholar working on Molecular Biology, Cancer Research, Hematology, Genetics and Cellular and Molecular Neuroscience, having authored 29 papers that have together received 1.7k indexed citations. Recurring topics across this work include Cancer Genomics and Diagnostics (10 papers), Acute Myeloid Leukemia Research (4 papers), Single-cell and spatial transcriptomics (3 papers), MicroRNA in disease regulation (3 papers), CRISPR and Genetic Engineering (3 papers), Circular RNAs in diseases (2 papers), Receptor Mechanisms and Signaling (2 papers) and Genomic variations and chromosomal abnormalities (2 papers). The work is most often cited by research in Cancer Research (520 citations), Behavioral Neuroscience (83 citations), Biological Psychiatry (53 citations), Cellular and Molecular Neuroscience (272 citations) and Molecular Biology (844 citations). Mark Verheul has collaborated with scholars based in Netherlands, Germany and United States. Frequent co-authors include Edwin Cuppen, Victor Guryev, José van de Belt, Ronald H.A. Plasterk, Ruben van Boxtel, Bart M. G. Smits, Berend Olivier, Judith R. Homberg, Bart Ellenbroek and Eugène Berezikov. Their work appears in journals such as BMC Genomics, Cell stem cell, Blood, Carcinogenesis and The Pharmacogenomics Journal.

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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