Roland P. Kuiper

10.8k total citations · 3 hit papers
123 papers, 5.4k citations indexed

About

Roland P. Kuiper is a scholar working on Molecular Biology, Public Health, Environmental and Occupational Health and Pathology and Forensic Medicine. According to data from OpenAlex, Roland P. Kuiper has authored 123 papers receiving a total of 5.4k indexed citations (citations by other indexed papers that have themselves been cited), including 63 papers in Molecular Biology, 41 papers in Public Health, Environmental and Occupational Health and 29 papers in Pathology and Forensic Medicine. Recurrent topics in Roland P. Kuiper's work include Acute Lymphoblastic Leukemia research (39 papers), Cancer Genomics and Diagnostics (26 papers) and Genetic factors in colorectal cancer (21 papers). Roland P. Kuiper is often cited by papers focused on Acute Lymphoblastic Leukemia research (39 papers), Cancer Genomics and Diagnostics (26 papers) and Genetic factors in colorectal cancer (21 papers). Roland P. Kuiper collaborates with scholars based in Netherlands, Germany and United States. Roland P. Kuiper's co-authors include Ad Geurts van Kessel, Marjolijn J. L. Ligtenberg, Nicoline Hoogerbrugge, Peter M. Hoogerbrugge, Frank N. van Leeuwen, Saskia Langemeijer, Ruth Knops, Marion Massop, Bert A. van der Reijden and Peter Vandenberghe and has published in prestigious journals such as Science, Nucleic Acids Research and Nature Communications.

In The Last Decade

Roland P. Kuiper

118 papers receiving 5.3k citations

Hit Papers

3 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.

Acquired mutations in TET2 are common in myelodysplastic syndromes

2009 548 citations Roland P. Kuiper, Ad Geurts van Kessel et al. profile →
Heritable somatic methylation and inactivation of MSH2 in families with Lynch syndrome due to deletion of the 3′ exons of TACSTD1

2008 546 citations Roland P. Kuiper, Ad Geurts van Kessel et al. profile →
Somatic mutations of the histone methyltransferase gene EZH2 in myelodysplastic syndromes

2010 541 citations Roland P. Kuiper et al. profile →

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Roland P. Kuiper Netherlands	35	2.6k	1.5k	1.2k	1.1k	1.1k	123	5.4k
Masashi Sanada Japan	33	2.2k 0.9×	1.3k 0.8×	369 0.3×	920 0.8×	633 0.6×	118	4.1k
Christa Fonatsch Germany	49	2.9k 1.1×	4.0k 2.6×	1.4k 1.2×	479 0.4×	1.2k 1.0×	197	7.7k
Jan Trka Czechia	34	1.5k 0.6×	2.1k 1.4×	2.0k 1.6×	465 0.4×	452 0.4×	149	3.7k
Naomi Galili United States	37	4.0k 1.6×	3.6k 2.3×	932 0.8×	781 0.7×	1.2k 1.0×	121	8.1k
Juan C. Cigudosa Spain	43	3.4k 1.3×	1.3k 0.9×	271 0.2×	1.2k 1.1×	1.5k 1.4×	149	6.0k
Norihiko Kawamata Japan	38	2.2k 0.9×	745 0.5×	381 0.3×	588 0.5×	1.4k 1.2×	96	4.0k
Patrick A. Zweidler‐McKay United States	35	1.8k 0.7×	839 0.5×	487 0.4×	690 0.6×	1.1k 1.0×	128	3.7k
Gerald Wulf Germany	32	2.9k 1.1×	751 0.5×	486 0.4×	849 0.7×	1.9k 1.7×	152	5.3k
Jochen Harbott Germany	51	2.4k 0.9×	4.4k 2.9×	4.2k 3.5×	430 0.4×	1.0k 0.9×	166	7.3k
Gudrun Göhring Germany	37	2.7k 1.0×	3.1k 2.0×	559 0.5×	770 0.7×	498 0.4×	183	5.1k

Countries citing papers authored by Roland P. Kuiper

Since Specialization

Citations

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

Fields of papers citing papers by Roland P. Kuiper

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Roland P. Kuiper. 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 Roland P. Kuiper. The network helps show where Roland P. Kuiper may publish in the future.

Co-authorship network of co-authors of Roland P. Kuiper

This figure shows the co-authorship network connecting the top 25 collaborators of Roland P. Kuiper. A scholar is included among the top collaborators of Roland P. Kuiper 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 Roland P. Kuiper. Roland P. Kuiper 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

Krijger, Ronald R. de, Lennart Kester, Saskia Hopman, et al.. (2025). Novel Findings in Pediatric and Adolescent Patients With Cancer and a Germline SMARCA4 Variant. Pediatric Blood & Cancer. 72(9). e31872–e31872.

Gorris, Mark A.J., Gerty Schreibelt, Sjors Middelkamp, et al.. (2025). Unraveling mutagenic processes influencing the tumor mutational patterns of individuals with constitutional mismatch repair deficiency. Nature Communications. 16(1). 4459–4459. 2 indexed citations

Hirsch, Steffen, Lennart Kester, Mariëtte E.G. Kranendonk, et al.. (2024). Molecular analysis of cancer genomes in children with Lynch syndrome: Exploring causal associations. International Journal of Cancer. 154(8). 1455–1463. 4 indexed citations

Antić, Željko, Stefan H. Lelieveld, Marley Yeong, et al.. (2024). Mutational mechanisms in multiply relapsed pediatric acute lymphoblastic leukemia. Leukemia. 38(11). 2366–2375. 3 indexed citations

Nakano, Yoshiko, Roland P. Kuiper, Kim E. Nichols, et al.. (2024). Update on Recommendations for Cancer Screening and Surveillance in Children with Genomic Instability Disorders. Clinical Cancer Research. 30(22). 5009–5020. 8 indexed citations

Maese, Luke, Marcin W. Włodarski, Alison A. Bertuch, et al.. (2024). Update on Recommendations for Surveillance for Children with Predisposition to Hematopoietic Malignancy. Clinical Cancer Research. 30(19). 4286–4295. 3 indexed citations

Bladergroen, Reno S., Lennart Kester, Marijn A. Vermeulen, et al.. (2024). T-cell lymphoblastic lymphoma compared with T-cell acute lymphoblastic leukemia: similar subtypes and different fusions. PubMed. 1(3). 100029–100029. 2 indexed citations

Padilla, Laura, Birgit Burkhardt, Andishe Attarbaschi, et al.. (2023). ¹⁸F‐FDG‐PET/CT imaging in diagnostic workup of pediatric precursor B‐cell lymphoblastic lymphoma. Pediatric Blood & Cancer. 70(11). e30642–e30642. 2 indexed citations

Hopman, Saskia, Machteld I. Bosscha, Charlotte J. Dommering, et al.. (2023). Assessment of Cancer Predisposition Syndromes in a National Cohort of Children With a Neoplasm. JAMA Network Open. 6(2). e2254157–e2254157. 19 indexed citations

10.

Smits, Willem K., Carlo Vermeulen, Shunsuke Kimura, et al.. (2023). Elevated enhancer-oncogene contacts and higher oncogene expression levels by recurrent CTCF inactivating mutations in acute T cell leukemia. Cell Reports. 42(4). 112373–112373. 5 indexed citations

11.

Krijger, Ronald R. de, Marjolijn C.J. Jongmans, Roland P. Kuiper, et al.. (2021). Clinical and Molecular Characteristics and Outcome of Cystic Partially Differentiated Nephroblastoma and Cystic Nephroma: A Narrative Review of the Literature. Cancers. 13(5). 997–997. 11 indexed citations

12.

Butler, Miriam, Dorette S. van Ingen Schenau, Jiangyan Yu, et al.. (2021). BTK inhibition sensitizes acute lymphoblastic leukemia to asparaginase by suppressing the amino acid response pathway. Blood. 138(23). 2383–2395. 17 indexed citations

13.

Gorris, Mark A.J., Marjolijn C.J. Jongmans, Roland P. Kuiper, et al.. (2021). Challenges of Neoantigen Targeting in Lynch Syndrome and Constitutional Mismatch Repair Deficiency Syndrome. Cancers. 13(10). 2345–2345. 5 indexed citations

14.

Yu, Jiangyan, Željko Antić, Simon V. van Reijmersdal, et al.. (2017). Accurate detection of low-level mosaic mutations in pediatric acute lymphoblastic leukemia using single molecule tagging and deep-sequencing. Leukemia & lymphoma. 59(7). 1690–1699. 5 indexed citations

15.

Wang, Chenliang, Junxiao Zhang, Roland P. Kuiper, et al.. (2015). Perivascular Epithelioid Cell Tumor of Gastrointestinal Tract. Medicine. 94(3). e393–e393. 11 indexed citations

16.

Moorman, Anthony V., Julie Irving, Amir Enshaei, et al.. (2015). Composite Index for Risk Prediction in Relapsed Childhood Acute Lymphoblastic Leukaemia. Haematologica. 100. 195–196. 3 indexed citations

17.

Veer, Arian van der, Esmé Waanders, Rob Pieters, et al.. (2013). Independent prognostic value of BCR-ABL1-like signature and IKZF1 deletion, but not high CRLF2 expression, in children with B-cell precursor ALL. Blood. 122(15). 2622–2629. 187 indexed citations

18.

Waanders, Esmé, Blanca Scheijen, Laurens T. van der Meer, et al.. (2012). The Origin and Nature of Tightly Clustered BTG1 Deletions in Precursor B-Cell Acute Lymphoblastic Leukemia Support a Model of Multiclonal Evolution. PLoS Genetics. 8(2). e1002533–e1002533. 59 indexed citations

19.

Szczepański, Tomasz, Vincent H. J. van der Velden, Esmé Waanders, et al.. (2011). Late Recurrence of Childhood T-Cell Acute Lymphoblastic Leukemia Frequently Represents a Second Leukemia Rather Than a Relapse: First Evidence for Genetic Predisposition. Journal of Clinical Oncology. 29(12). 1643–1649. 51 indexed citations

20.

Martens, Gerard J.M., et al.. (1996). The neuroendocrine chaperone 7B2 assists transport of prohormone convertase PC2 through the secretory pathway. The Journal of Physiology. 2 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.

Explore authors with similar magnitude of impact