Nicolle Besselink

2.1k citations

28 papers · 1.2k indexed · h-index 17

Co-authors: Edwin Cuppen Marco J. Koudijs Roel Janssen Sander Boymans Arne van Hoeck Ewart Kuijk Marlous Hoogstraat Corine M. Beaufort
Topics: Cancer Genomics and Diagnostics (19 papers)Epigenetics and DNA Methylation (5 papers)Acute Lymphoblastic Leukemia research (4 papers)
Cited by: Cancer Research Oncology Reproductive Medicine
Journals: Science Nature Communications Blood
Partner nations: Netherlands Germany United States

In The Last Decade

Nicolle Besselink

28 papers receiving 1.2k citations

Peers

Countries citing papers authored by Nicolle Besselink

Since Specialization

Citations

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

Fields of papers citing papers by Nicolle Besselink

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Nicolle Besselink

This figure shows the co-authorship network connecting the top 25 collaborators of Nicolle Besselink. A scholar is included among the top collaborators of Nicolle Besselink 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 Nicolle Besselink. Nicolle Besselink 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	Nanopore-based consensus sequencing enables accurate multimodal tumor cell-free DNA profiling 2025 ·Genome Research ·Li‐Ting Chen,Myrthe Jager,(unknown),(unknown),Tom van den Ende,Willem Vanderlinden,(unknown),Marc Pagès-Gallego,Ymke van der Pol,Nicolle Besselink,Norbert Moldován,Nizar Hami,Wigard P. Kloosterman,Hanneke W. M. van Laarhoven,Florent Moulière,Ronald P. Zweemer,Jan Lipfert,Sarah Derks,Alessio Marcozzi,Jeroen de Ridder	3
2	Direct detection of 8-oxo-dG using nanopore sequencing 2025 ·Nature Communications ·Marc Pagès-Gallego,(unknown),Nicolle Besselink,Roy Straver,(unknown),Carlo Vermeulen,Alessio Marcozzi,Markus J. van Roosmalen,Ruben van Boxtel,Boudewijn Burgering,Tobias B. Dansen,Jeroen de Ridder	2
3	NGS-based Aspergillus detection in plasma and lung lavage of children with invasive pulmonary aspergillosis 2025 ·npj Genomic Medicine ·(unknown),(unknown),Li‐Ting Chen,Myrthe Jager,Nicolle Besselink,Carlo Vermeulen,Ferry Hagen,Tjomme van der Bruggen,Caroline A. Lindemans,Tom F.W. Wolfs,Louis Bont,Jeroen de Ridder	2
4	The genome-wide mutational consequences of DNA hypomethylation 2023 ·Scientific Reports ·Nicolle Besselink,(unknown),Carlo Vermeulen,Sander Boymans,Jeroen de Ridder,Arne van Hoeck,Edwin Cuppen,Ewart Kuijk	44
5	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
6	Recurrent exon-deleting activating mutations in AHR act as drivers of urinary tract cancer 2022 ·Scientific Reports ·(unknown),(unknown),Eric Kalkhoven,(unknown),Nicolle Besselink,Charles Shale,Bishoy M. Faltas,Peter Priestley,Ewart Kuijk,Edwin Cuppen	3
7	Precancerous liver diseases do not cause increased mutagenesis in liver stem cells 2021 ·Communications Biology ·Luan Nguyen,Myrthe Jager,Ruby Lieshout,Petra E. de Ruiter,Mauro D. Locati,Nicolle Besselink,Bastiaan van der Roest,Roel Janssen,Sander Boymans,Jeroen de Jonge,Jan N.M. IJzermans,Michail Doukas,Monique M.A. Verstegen,Ruben van Boxtel,Luc J. W. van der Laan,Edwin Cuppen,Ewart Kuijk	9
8	GRIDSS2: comprehensive characterisation of somatic structural variation using single breakend variants and structural variant phasing 2021 ·Genome biology ·Daniel Cameron,Jonathan Baber,Charles Shale,Jose Espejo Valle-Inclán,Nicolle Besselink,Arne van Hoeck,Roel Janssen,Edwin Cuppen,Peter Priestley,Anthony T. Papenfuss	74
9	The mutational impact of culturing human pluripotent and adult stem cells 2020 ·Nature Communications ·Ewart Kuijk,Myrthe Jager,Bastiaan van der Roest,Mauro D. Locati,Arne van Hoeck,Jerome Korzelius,Roel Janssen,Nicolle Besselink,Sander Boymans,Ruben van Boxtel,Edwin Cuppen	86
10	5-Fluorouracil treatment induces characteristic T>G mutations in human cancer 2019 ·Nature Communications ·(unknown),Bastiaan van der Roest,Nicolle Besselink,Roel Janssen,Sander Boymans,John W.M. Martens,Marie‐Laure Yaspo,Peter Priestley,Ewart Kuijk,Edwin Cuppen,Arne van Hoeck	138
11	Prioritization of genes driving congenital phenotypes of patients with de novo genomic structural variants 2019 ·Genome Medicine ·Sjors Middelkamp,(unknown),Jacques C. Giltay,Jerome Korzelius,Nicolle Besselink,Sander Boymans,Roel Janssen,(unknown),Ellen van Binsbergen,Markus J. van Roosmalen,Ron Hochstenbach,Daniela Giachino,Michael E. Talkowski,Wigard P. Kloosterman,Edwin Cuppen	17
12	Deficiency of nucleotide excision repair is associated with mutational signature observed in cancer 2019 ·Genome Research ·Myrthe Jager,Francis Blokzijl,Ewart Kuijk,Johanna Bertl,(unknown),Roel Janssen,Nicolle Besselink,Sander Boymans,Joep de Ligt,Jakob Skou Pedersen,Jan H.J. Hoeijmakers,Joris Pothof,Ruben van Boxtel,Edwin Cuppen	57
13	Fibroblast growth factor receptor signaling in pediatric B-cell precursor acute lymphoblastic leukemia 2019 ·Scientific Reports ·Isabel S. Jerchel,(unknown),Ingrid M. Ariës,Judith M. Boer,Nicolle Besselink,Marco J. Koudijs,Rob Pieters,Monique L. den Boer	5
14	Measuring mutation accumulation in single human adult stem cells by whole-genome sequencing of organoid cultures 2017 ·Nature Protocols ·Myrthe Jager,Francis Blokzijl,Valentina Sasselli,Sander Boymans,Roel Janssen,Nicolle Besselink,Hans Clevers,Ruben van Boxtel,Edwin Cuppen	46
15	JAK2 aberrations in childhood B-cell precursor acute lymphoblastic leukemia 2017 ·Oncotarget ·Elisabeth M. P. Steeghs,Isabel S. Jerchel,(unknown),(unknown),Judith M. Boer,Aurélie Boeree,Cesca van de Ven,Marco J. Koudijs,Nicolle Besselink,Hester A. de Groot‐Kruseman,C. Michel Zwaan,Martin A. Horstmann,Rob Pieters,Monique L. den Boer	37
16	Effective Therapeutic Intervention and Comprehensive Genetic Analysis of mTOR Signaling in PEComa : A Case Report 2015 ·Nature Biotechnology ·Fleur Weeber,Marco J. Koudijs,Marlous Hoogstraat,Nicolle Besselink,Stef van Lieshout,Isaäc J. Nijman,Edwin Cuppen,G.J.A. Offerhaus,Emile E. Voest	1
17	Effective Therapeutic Intervention and Comprehensive Genetic Analysis of mTOR Signaling in PEComa: A Case Report. 2015 ·PubMed ·Fleur Weeber,Marco J. Koudijs,Marlous Hoogstraat,Nicolle Besselink,Stef van Lieshout,Isaäc J. Nijman,Edwin Cuppen,G.J.A. Offerhaus,Emile E. Voest	3
18	Comparison of Next-Generation Sequencing and Mutation-Specific Platforms in Clinical Practice 2015 ·American Journal of Clinical Pathology ·John W. J. Hinrichs,(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),Marco J. Koudijs,Nicolle Besselink,Stefan M. Willems,Roel A. de Weger	38
19	Next generation sequencing of triple negative breast cancer to find predictors for chemotherapy response 2015 ·Breast Cancer Research ·Esther H. Lips,Magali Michaut,Marlous Hoogstraat,Lennart Mulder,Nicolle Besselink,Marco J. Koudijs,Edwin Cuppen,Emile E. Voest,René Bernards,Petra M. Nederlof,Jelle Wesseling,Sjoerd Rodenhuis,Lodewyk F.A. Wessels	53
20	Simultaneous Detection of Clinically Relevant Mutations and Amplifications for Routine Cancer Pathology 2014 ·Journal of Molecular Diagnostics ·Marlous Hoogstraat,John W. J. Hinrichs,Nicolle Besselink,(unknown),(unknown),Ton Peeters,Isaäc J. Nijman,Roel A. de Weger,Emile E. Voest,Stefan M. Willems,Edwin Cuppen,Marco J. Koudijs	27

About Nicolle Besselink

Nicolle Besselink is a scholar working on Cancer Research, Genetics and Hematology, having authored 28 papers that have together received 1.2k indexed citations. Recurring topics across this work include Cancer Genomics and Diagnostics (19 papers), Epigenetics and DNA Methylation (5 papers) and Acute Lymphoblastic Leukemia research (4 papers). The work is most often cited by research in Cancer Research (440 citations), Oncology (350 citations) and Reproductive Medicine (94 citations). Nicolle Besselink has collaborated with scholars based in Netherlands, Germany and United States. Frequent co-authors include Edwin Cuppen, Marco J. Koudijs, Roel Janssen, Sander Boymans, Arne van Hoeck, Ewart Kuijk, Marlous Hoogstraat, Corine M. Beaufort, Marcel Smid and Jozien Helleman. Their work appears in journals such as Science, Nature Communications 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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