Ronald van Eijk

7.5k citations

84 papers · 6.2k · 2 hit papers · h-index 36

Impact in

Psychiatry and Mental health top 1%
- Migraine and Headache Studies
Pathology and Forensic Medicine top 2%
- Genetic factors in colorectal cancer

Papers in

Pathology and Forensic Medicine 27
- Genetic factors in colorectal cancer 19
- Lymphoma Diagnosis and Treatment 8
Cancer Research 16
- Cancer Genomics and Diagnostics 13

Co-authors: Rune R. Frants (7 shared papers)Roel A. Ophoff (7 shared papers)Gisela Marie Terwindt (6 shared papers)Michel D. Ferrari (6 shared papers)Tom van Wezel (45 shared papers)Gert‐Jan B. van Ommen (5 shared papers)Monique N. Vergouwe (4 shared papers)Dick Lindhout (3 shared papers)
Journals: BMC Cancer (5 papers)PLoS ONE (4 papers)Nature Genetics (4 papers)Journal of Molecular Diagnostics (4 papers)British Journal of Cancer (3 papers)
Partner nations: Netherlands Belgium United Kingdom

In The Last Decade

Ronald van Eijk

80 papers receiving 5.9k citations

Ronald van Eijk's Hit Papers

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Somatic mosaic IDH1 and IDH2 mutations are associated with enchondroma and spindle cell hemangioma in Ollier disease and Maffucci syndrome 2011 · 423 citations

What are hit papers?

Paper score: A paper's citations measured against the top-1% bar of its own field and year: the square root of citations ÷ bar, so 1 means right at the bar and 2 means four times its citations. The bar blends the citation counts that enter the top 1% of the paper's subfields in its year (weighted 89.5%), of those subfields over all years (0.5%) and of its year across all fields (10%); a subfield and year with fewer than 400 papers takes its year's bar. Papers from 2026 are not scored yet: in an unfinished year, when a paper appeared matters more than how it is cited.

Hit paper: A paper cited at least 1.5× the top-1% bar of its field and year: a paper score of at least √1.5.

2011 Nature Genetics
1996 Cell

Peers

Countries citing papers authored by Ronald van Eijk

Since Specialization

Citations

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

Fields of papers citing papers by Ronald van Eijk

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Ronald van Eijk. 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 Ronald van Eijk. The network helps show where Ronald van Eijk may publish in the future.

Co-authors

The 25 scholars most cited alongside Ronald van Eijk, 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 Ronald van Eijk Line = papers co-authored together Ronald van Eijk 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 84 papers — load more, or switch the sort, to bring in the rest.

#	Work
1	Familial Hemiplegic Migraine and Episodic Ataxia Type-2 Are Caused by Mutations in the Ca2+ Channel Gene CACNL1A4 Cell ·Roel A. Ophoff, Gisela Marie Terwindt, Monique N. Vergouwe, Ronald van Eijk, Peter Josef Oefner, Susan M.G. Hoffman, Jane E. Lamerdin, Harvey W. Mohrenweiser Hit paper breakdown →	1996	1943
2	Somatic mosaic IDH1 and IDH2 mutations are associated with enchondroma and spindle cell hemangioma in Ollier disease and Maffucci syndrome Nature Genetics ·Twinkal C. Pansuriya, Ronald van Eijk, Pio D’Adamo, Maayke A.J.H. van Ruler, Marieke L. Kuijjer, Jan Oosting, Anne‐Marie Cleton-Jansen, Jolieke G. van Oosterwijk Hit paper breakdown →	2011	423
3	BRCA1 genomic deletions are major founder mutations in Dutch breast cancer patients Nature Genetics ·Anne Petrij-Bosch, Tamara Peelen, Margreethe van Vliet, Ronald van Eijk, Renske Olmer, Marion Drüsedau, Frans B.L. Hogervorst, Sandra Hageman	1997	363
4	E-cadherin transcriptional downregulation by promoter methylation but not mutation is related to epithelial-to-mesenchymal transition in breast cancer cell lines British Journal of Cancer ·Marcel Lombaerts, Tom van Wezel, Katja Philippo, Jan Willem F Dierssen, R M E Zimmerman, Jan Oosting, Ronald van Eijk, Paul H.C. Eilers	2006	286
5	Chromosome 4 localization of a second gene for autosomal dominant polycystic kidney disease Nature Genetics ·Dorien J.M. Peters, Lia Spruit, Jasper J. Saris, David Ravine, Lodewijk A. Sandkuijl, Ragnheiður Fossdal, J. Boersma, Ronald van Eijk	1993	219
6	A genome-wide association study of Hodgkin's lymphoma identifies new susceptibility loci at 2p16.1 (REL), 8q24.21 and 10p14 (GATA3) Nature Genetics ·Victor Enciso-Mora, Peter Broderick, Yussanne Ma, Ruth F. Jarrett, Henrik Hjalgrim, Kari Hemminki, Anke van den Berg, Bianca D. Olver	2010	171
7	Rapid KRAS, EGFR, BRAF and PIK3CA Mutation Analysis of Fine Needle Aspirates from Non-Small-Cell Lung Cancer Using Allele-Specific qPCR PLoS ONE ·Ronald van Eijk, Jappe Licht, Melanie Schrumpf, Mehrdad Talebian Yazdi, Dina Ruano, Giusi Irma Forte, Petra M. Nederlof, Maud Veseliç	2011	159
8	Familial hemiplegic migraine locus on 19p13 is involved in the common forms of migraine with and without aura Human Genetics ·Arne May, Roel A. Ophoff, Gisela Marie Terwindt, Ronald van Eijk, Joost Haan, HC Diener, Dick Lindhout, Rune R. Frants	1995	143
9	Genetic Heterogeneity of Familial Hemiplegic Migraine Genomics ·Roel A. Ophoff, Ronald van Eijk, Lodewijk A. Sandkuijl, Gisela Marie Terwindt, C Grubben, Joost Haan, Dick Lindhout, Michel D. Ferrari	1994	125
10	Involvement of the CACNA1A gene containing region on 19p13 in migraine with and without aura Neurology ·Gisela Marie Terwindt, Roel A. Ophoff, Ronald van Eijk, Monique N. Vergouwe, J. Haan, Rune R. Frants, L. A. Sandkuijl, Michel D. Ferrari	2001	113
11	Variable clinical expression of mutations in the P/Q-type calcium channel gene in familial hemiplegic migraine Neurology ·Gisela Marie Terwindt, Roel A. Ophoff, Jean Haan, Monique N. Vergouwe, Ronald van Eijk, Rune R. Frants, Michel D. Ferrari	1998	108
12	Expression of HLA Class I Antigen, Aspirin Use, and Survival After a Diagnosis of Colon Cancer JAMA Internal Medicine ·Marlies S. Reimers, Esther Bastiaannet, Ruth Elizabeth Langley, Ronald van Eijk, Ronald L. P. van Vlierberghe, V.E.P.P. Lemmens, Myrthe P. P. van Herk‐Sukel, Tom van Wezel	2014	92
13	Differential Gene Expression in Ovarian Tumors Reveals Dusp 4 and Serpina 5 As Key Regulators for Benign Behavior of Serous Borderline Tumors Journal of Clinical Oncology ·Nathalie L.G. Sieben, Jan Oosting, Adrienne Margaret Flanagan, Jaime Prat, Guido M.J.M. Roemen, Sandra M. Kolkman-Uljee, Ronald van Eijk, Cees J. Cornelisse	2005	84
14	Whole-Exome Sequencing Studies of Parathyroid Carcinomas Reveal Novel PRUNE2 Mutations, Distinctive Mutational Spectra Related to APOBEC-Catalyzed DNA Mutagenesis and Mutational Enrichment in Kinases Associated With Cell Migration and Invasion The Journal of Clinical Endocrinology & Metabolism ·Willie Yu, John Richard McPherson, Mark Stevenson, Ronald van Eijk, Hong Lee Heng, Paul J. Newey, Anna Gan, Dina Ruano	2014	82
15	High prevalence of MYD88 and CD79B mutations in intravascular large B-cell lymphoma Blood ·Anne M.R. Schrader, Patty M. Jansen, Rein Willemze, Maarten H. Vermeer, Anne‐Marie Cleton-Jansen, Sebastiaan F. Somers, Hendrik Veelken, Ronald van Eijk	2018	78
16	Chromosome 8q23.3 and 11q23.1 Variants Modify Colorectal Cancer Risk in Lynch Syndrome Gastroenterology ·Juul Wijnen, Richard M. Brohet, Ronald van Eijk, Shantie Jagmohan–Changur, Anneke Middeldorp, Carli M.J. Tops, Mario van Puijenbroek, Margreet G.E.M. Ausems	2008	77
17	Statin Use After Diagnosis of Colon Cancer and Patient Survival Gastroenterology ·Philip W. Voorneveld, Marlies S. Reimers, Esther Bastiaannet, Rutger J. Jacobs, Ronald van Eijk, Marjolein M.J. Zanders, Ron M. C. Herings, Myrthe P. P. van Herk‐Sukel	2017	76
18	Genome Haploidisation with Chromosome 7 Retention in Oncocytic Follicular Thyroid Carcinoma PLoS ONE ·Willem Ernst Corver, Dina Ruano, Karin Weijers, Wietske C. E. den Hartog, Merlijn P. van Nieuwenhuizen, Noel F.C.C. de Miranda, Ronald van Eijk, Anneke Middeldorp	2012	73
19	Reliable High-Throughput Genotyping and Loss-of-Heterozygosity Detection in Formalin-Fixed, Paraffin-Embedded Tumors Using Single Nucleotide Polymorphism Arrays Cancer Research ·Esther H. Lips, Jan Willem F Dierssen, Ronald van Eijk, Jan Oosting, Paul H.C. Eilers, Rob A.�E.�M. Tollenaar, Eelco J. de Graaf, Ruben van ‘t Slot	2005	68
20	Assessment of a fully automated high-throughput DNA extraction method from formalin-fixed, paraffin-embedded tissue for KRAS, and BRAF somatic mutation analysis Experimental and Molecular Pathology ·Ronald van Eijk, Hans M. Morreau, Tom van Wezel +1 other	2012	66

About Ronald van Eijk

Ronald van Eijk is a scholar working on Pathology and Forensic Medicine, Cancer Research, Genetics, Dermatology and Oncology, having authored 84 papers that have together received 6.2k indexed citations. Recurring topics across this work include Genetic factors in colorectal cancer (19 papers), Cancer Genomics and Diagnostics (13 papers), Lymphoma Diagnosis and Treatment (8 papers), BRCA gene mutations in cancer (7 papers), Migraine and Headache Studies (6 papers), Cutaneous lymphoproliferative disorders research (5 papers), Genomic variations and chromosomal abnormalities (5 papers) and Thyroid Cancer Diagnosis and Treatment (4 papers). The work is most often cited by research in Psychiatry and Mental health (1.7k citations), Pathology and Forensic Medicine (668 citations), Genetics (949 citations), Cancer Research (424 citations) and Oncology (441 citations). Ronald van Eijk has collaborated with scholars based in Netherlands, Belgium and United Kingdom. Frequent co-authors include Rune R. Frants, Roel A. Ophoff, Gisela Marie Terwindt, Michel D. Ferrari, Tom van Wezel, Gert‐Jan B. van Ommen, Monique N. Vergouwe, Dick Lindhout, Joost Haan and Marten H. Hofker. Their work appears in journals such as BMC Cancer, PLoS ONE, Nature Genetics, Journal of Molecular Diagnostics and British Journal of Cancer.

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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Ronald van Eijk

Ronald van Eijk's Hit Papers

Peers

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Fields of papers citing papers by Ronald van Eijk

All Works

About Ronald van Eijk

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