Eveline J. Kamping

2.8k total citations · 1 hit paper
23 papers, 1.2k citations indexed

About

Eveline J. Kamping is a scholar working on Pathology and Forensic Medicine, Molecular Biology and Cancer Research. According to data from OpenAlex, Eveline J. Kamping has authored 23 papers receiving a total of 1.2k indexed citations (citations by other indexed papers that have themselves been cited), including 12 papers in Pathology and Forensic Medicine, 7 papers in Molecular Biology and 7 papers in Cancer Research. Recurrent topics in Eveline J. Kamping's work include Genetic factors in colorectal cancer (9 papers), Cancer Genomics and Diagnostics (6 papers) and Colorectal Cancer Treatments and Studies (3 papers). Eveline J. Kamping is often cited by papers focused on Genetic factors in colorectal cancer (9 papers), Cancer Genomics and Diagnostics (6 papers) and Colorectal Cancer Treatments and Studies (3 papers). Eveline J. Kamping collaborates with scholars based in Netherlands, United Kingdom and Germany. Eveline J. Kamping's co-authors include Roland P. Kuiper, Ad Geurts van Kessel, Estelle Verburgh, Saskia Langemeijer, Ruth Knops, Marion Massop, M Berends, Peter Vandenberghe, Théo de Witte and Joop H. Jansen and has published in prestigious journals such as Nature Genetics, The Journal of Clinical Endocrinology & Metabolism and Genome Research.

In The Last Decade

Eveline J. Kamping

23 papers receiving 1.2k citations

Hit 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 Saskia Langemeijer, Roland P. Kuiper et al. Nature Genetics profile →

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Eveline J. Kamping Netherlands	14	610	378	252	229	191	23	1.2k
Jane E. Churpek United States	18	360 0.6×	621 1.6×	282 1.1×	241 1.1×	161 0.8×	45	1.1k
TuDung T. Nguyen United States	15	771 1.3×	389 1.0×	139 0.6×	275 1.2×	264 1.4×	27	1.4k
Henrik Lilljebjörn Sweden	22	588 1.0×	673 1.8×	226 0.9×	264 1.2×	338 1.8×	51	1.6k
Zhenya Tang United States	20	375 0.6×	456 1.2×	332 1.3×	177 0.8×	335 1.8×	111	1.2k
Roberta La Starza Italy	24	796 1.3×	976 2.6×	370 1.5×	124 0.5×	170 0.9×	91	1.8k
Michael Neat United Kingdom	18	493 0.8×	557 1.5×	166 0.7×	89 0.4×	259 1.4×	38	1.1k
Tilmann Bochtler Germany	25	1.1k 1.9×	576 1.5×	429 1.7×	160 0.7×	561 2.9×	71	1.7k
Mara Rosenberg United States	11	523 0.9×	270 0.7×	99 0.4×	193 0.8×	250 1.3×	22	1.4k
James Dalton United States	8	550 0.9×	497 1.3×	188 0.7×	111 0.5×	210 1.1×	14	1.3k
Y Hayashi Japan	26	926 1.5×	1.2k 3.1×	292 1.2×	237 1.0×	321 1.7×	47	2.3k

Countries citing papers authored by Eveline J. Kamping

Since Specialization

Citations

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

Fields of papers citing papers by Eveline J. Kamping

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Eveline J. Kamping. 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 Eveline J. Kamping. The network helps show where Eveline J. Kamping may publish in the future.

Co-authorship network of co-authors of Eveline J. Kamping

This figure shows the co-authorship network connecting the top 25 collaborators of Eveline J. Kamping. A scholar is included among the top collaborators of Eveline J. Kamping 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 Eveline J. Kamping. Eveline J. Kamping 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

Neveling, Kornelia, Michael D. Gallagher, Joyce Lee, et al.. (2025). Optical genome mapping enables accurate testing of large repeat expansions. Genome Research. 35(4). 810–823. 2 indexed citations

Pennings, Maartje, Michael Kwint, Jeroen van Reeuwijk, et al.. (2024). Uncovering recessive alleles in rare Mendelian disorders by genome sequencing of 174 individuals with monoallelic pathogenic variants. European Journal of Human Genetics. 33(1). 56–64. 1 indexed citations

Geerlings, Maartje J., Eveline J. Kamping, Daniel von Rhein, et al.. (2022). Clinical Validity of Tumor-Informed Circulating Tumor DNA Analysis in Patients Undergoing Surgery of Colorectal Metastases. Diseases of the Colon & Rectum. 66(6). 796–804. 2 indexed citations

Kroeze, Leonie I., Richarda M. de Voer, Eveline J. Kamping, et al.. (2020). Evaluation of a Hybrid Capture–Based Pan-Cancer Panel for Analysis of Treatment Stratifying Oncogenic Aberrations and Processes. Journal of Molecular Diagnostics. 22(6). 757–769. 43 indexed citations

Pouwer, Anne-Floor W., L.C.G. van den Einden, M. van der Linden, et al.. (2020). Clonal Relationship Between Lichen Sclerosus, Differentiated Vulvar Intra-epithelial Neoplasia and Non HPV-related Vulvar Squamous Cell Carcinoma. Cancer Genomics & Proteomics. 17(2). 151–160. 12 indexed citations

Simons, Michiel, Femke Simmer, Johan Bulten, et al.. (2019). Two types of primary mucinous ovarian tumors can be distinguished based on their origin. Modern Pathology. 33(4). 722–733. 26 indexed citations

Broek, Roel W. Ten, Astrid Eijkelenboom, C.J.M. van der Vleuten, et al.. (2019). Comprehensive molecular and clinicopathological analysis of vascular malformations: A study of 319 cases. Genes Chromosomes and Cancer. 58(8). 541–550. 50 indexed citations

Zhang, Junxiao, Xiaoyan Wang, Richarda M. de Voer, et al.. (2017). A molecular inversion probe-based next-generation sequencing panel to detect germline mutations in Chinese early-onset colorectal cancer patients. Oncotarget. 8(15). 24533–24547. 10 indexed citations

Eijkelenboom, Astrid, Eveline J. Kamping, Kornelia Neveling, et al.. (2016). Reliable Next-Generation Sequencing of Formalin-Fixed, Paraffin-Embedded Tissue Using Single Molecule Tags. Journal of Molecular Diagnostics. 18(6). 851–863. 82 indexed citations

10.

Stevens‐Kroef, Marian, Konnie M. Hebeda, Eugène T.P. Verwiel, et al.. (2015). Microarray-based genomic profiling and in situ hybridization on fibrotic bone marrow biopsies for the identification of numerical chromosomal abnormalities in myelodysplastic syndrome. Molecular Cytogenetics. 8(1). 33–33. 4 indexed citations

11.

Vlenterie, Myrella, Melissa H.S. Hillebrandt-Roeffen, Uta Flucke, et al.. (2015). Next generation sequencing in synovial sarcoma reveals novel gene mutations. Oncotarget. 6(33). 34680–34690. 43 indexed citations

12.

Jongmans, Marjolijn C.J., Eugène T.P. Verwiel, Yvonne F. Heijdra, et al.. (2012). Revertant Somatic Mosaicism by Mitotic Recombination in Dyskeratosis Congenita. The American Journal of Human Genetics. 90(3). 426–433. 74 indexed citations

13.

Mekenkamp, Leonie J., Jolien Tol, Jeroen R. Dijkstra, et al.. (2012). Beyond KRAS mutation status: influence of KRAScopy number status and microRNAs on clinical outcome to cetuximab in metastatic colorectal cancer patients. BMC Cancer. 12(1). 292–292. 55 indexed citations

14.

Venkatachalam, Ramprasath, Eugène T.P. Verwiel, Eveline J. Kamping, et al.. (2010). Identification of candidate predisposing copy number variants in familial and early‐onset colorectal cancer patients. International Journal of Cancer. 129(7). 1635–1642. 61 indexed citations

15.

Venkatachalam, Ramprasath, Marjolijn J. L. Ligtenberg, Nicoline Hoogerbrugge, et al.. (2010). Germline epimutation of the tumor suppressor gene PTPRJ in early onset familial colorectal cancer. Cancer Genetics and Cytogenetics. 203(1). 59–59. 1 indexed citations

16.

Langemeijer, Saskia, Roland P. Kuiper, M Berends, et al.. (2009). Acquired mutations in TET2 are common in myelodysplastic syndromes. Nature Genetics. 41(7). 838–842. 548 indexed citations breakdown →

17.

Kuiper, Roland P., Lilian Vreede, Ramprasath Venkatachalam, et al.. (2009). The tumor suppressor gene FBXW7 is disrupted by a constitutional t(3;4)(q21;q31) in a patient with renal cell cancer. Cancer Genetics and Cytogenetics. 195(2). 105–111. 22 indexed citations

18.

Schraders, Margit, Simon V. van Reijmersdal, Eveline J. Kamping, et al.. (2009). High-resolution genomic profiling of pediatric lymphoblastic lymphomas reveals subtle differences with pediatric acute lymphoblastic leukemias in the B-lineage. Cancer Genetics and Cytogenetics. 191(1). 27–33. 23 indexed citations

19.

Letteboer, Tom G.W., Eveline J. Kamping, Repke J. Snijder, et al.. (2004). Hereditary hemorrhagic telangiectasia: ENG and ALK-1 mutations in Dutch patients. Human Genetics. 116(1-2). 8–16. 80 indexed citations

20.

Mannonen, Laura, et al.. (2003). IFN-γ induced persistent Chlamydia pneumoniae infection in HL and Mono Mac 6 cells: characterization by real-time quantitative PCR and culture. Microbial Pathogenesis. 36(1). 41–50. 23 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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