Ronald van Eijk

7.6k citations

81 papers · 5.2k · 1 hit paper · h-index 34

Impact in

Psychiatry and Mental health top 0.5%
- Migraine and Headache Studies
Pathology and Forensic Medicine top 0.5%
- Genetic factors in colorectal cancer
- Trigeminal Neuralgia and Treatments

Papers in

Pathology and Forensic Medicine 22
- Genetic factors in colorectal cancer 15
- Lymphoma Diagnosis and Treatment 6
Cancer Research 22
- Cancer Genomics and Diagnostics 17

Co-authors: Michel D. Ferrari (6 shared papers)Roel A. Ophoff (6 shared papers)Rune R. Frants (6 shared papers)Gisela M. Terwindt (6 shared papers)Tom van Wezel (46 shared papers)Monique N. Vergouwe (4 shared papers)Joost Haan (3 shared papers)Dick Lindhout (3 shared papers)
Journals: BMC Cancer (5 papers)Journal of Molecular Diagnostics (4 papers)PLoS ONE (4 papers)Genes Chromosomes and Cancer (3 papers)Gastroenterology (3 papers)
Partner nations: Netherlands United States Belgium

In The Last Decade

Ronald van Eijk

77 papers receiving 5.0k citations

Ronald van Eijk's Hit Papers

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Familial Hemiplegic Migraine and Episodic Ataxia Type-2 Are Caused by Mutations in the Ca2+ Channel Gene CACNL1A4 1996 · 1.9k citations

Peers

Countries citing papers authored by Ronald van Eijk

Since Specialization

Citations

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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 81 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 M. Terwindt, Monique N. Vergouwe, Ronald van Eijk, Peter J. Oefner, Susan M.G. Hoffman, Jane E. Lamerdin, Harvey W. Mohrenweiser, Dennis E. Bulman, Maurizio Ferrari, Joost Haan, Dick Lindhout, Gert‐Jan B. van Ommen, Marten H. Hofker, Michel D. Ferrari, Rune R. Frants Hit paper breakdown →	1996	1887
2	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, S. Hageman, Petronella J.W. Arts, Marjolijn J. L. Ligtenberg, Hanne Meijers-Heijboer, Jan G.M. Klijn, Hans F. A. Vasen, Cees J. Cornelisse, Laura J. van’t Veer, Egbert Bakker, Gert‐Jan B. van Ommen, Peter Devilee	1997	331
3	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, Bob van de Water, Cees J. Cornelisse, A-M Cleton-Jansen	2006	285
4	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, Søren Nørby, Constantinos Deltas, Alkis Pierides, J.E. Briessenden, RuneR. Frants, G.J.B. van Ommen, M.H. Breuning	1993	215
5	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, Klaus F. Rabe, Jouke T. Annema, Vincent T.H.B.M. Smit, Hans Morreau, Tom van Wezel	2011	154
6	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 M. Terwindt, Christine Urban, Ronald van Eijk, Joost Haan, H.-C. Diener, Dick Lindhout, Rune R. Frants, Lodewijk A. Sandkuijl, Michel D. Ferrari	1995	141
7	Genetic Heterogeneity of Familial Hemiplegic Migraine Genomics ·Roel A. Ophoff, Ronald van Eijk, Lodewijk A. Sandkuijl, Gisela M. Terwindt, C Grubben, Joost Haan, Dick Lindhout, Michel D. Ferrari, Rune R. Frants	1994	122
8	Involvement of the CACNA1A gene containing region on 19p13 in migraine with and without aura Neurology ·Gisela M. Terwindt, Roel A. Ophoff, Ronald van Eijk, Monique N. Vergouwe, J. Haan, Rune R. Frants, L. Sandkuijl, Michel D. Ferrari	2001	111
9	Variable clinical expression of mutations in the P/Q-type calcium channel gene in familial hemiplegic migraine Neurology ·Gisela M. Terwindt, Roel A. Ophoff, J. Haan, Monique N. Vergouwe, Ronald van Eijk, Rune R. Frants, Michel D. Ferrari	1998	108
10	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 E. Langley, Ronald van Eijk, Ronald L. P. van Vlierberghe, V.E.P.P. Lemmens, Myrthe P. P. van Herk‐Sukel, Tom van Wezel, Riccardo Fodde, Peter J.K. Kuppen, Hans Morreau, Cornelis J.�H. van de Velde, Gerrit‐Jan Liefers	2014	85
11	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 M. Flanagan, Jaime Prat, Guido M.J.M. Roemen, Sandra Kolkman-Uljee, Ronald van Eijk, Cees J. Cornelisse, Gert Jan Fleuren, Manon van Engeland	2005	79
12	Whole-Exome Sequencing Studies of Parathyroid Carcinomas Reveal NovelPRUNE2Mutations, 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 R. McPherson, Mark Stevenson, Ronald van Eijk, Hong Lee Heng, Paul Newey, Anna Gan, Dina Ruano, Dachuan Huang, Song Ling Poon, Choon Kiat Ong, Tom van Wezel, Branca Cavaco, Steve Rozen, Patrick Tan, Bin Tean Teh, Rajesh V. Thakker, Hans Morreau	2014	77
13	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, Liudmila L. Kodach, Tom van Wezel, Peter J.K. Kuppen, Hans Morreau, Cornelis J.�H. van de Velde, James C.H. Hardwick, Gerrit‐Jan Liefers	2017	71
14	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, Cisca Wijmenga, Hans Morreau, Tom van Wezel	2005	70
15	Genome Haploidisation with Chromosome 7 Retention in Oncocytic Follicular Thyroid Carcinoma PLoS ONE ·Willem E. 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, Ekaterina S. Jordanova, Jan Oosting, Ellen Kapiteijn, Guido C. Hovens, (unknown), Tom van Wezel, Hans Morreau	2012	64
16	No genomic aberrations in Langerhans cell histiocytosis as assessed by diverse molecular technologies Genes Chromosomes and Cancer ·Cristiana E.T. da Costa, Károly Szuhai, Ronald van Eijk, Manja Hoogeboom, (unknown), Fredrik Mertens, Helga Björgvinsdóttir, Maria Dêbiec‐Rychter, Ronald R. de Krijger, Pancras C.W. Hogendoorn, R. Maarten Egeler, Nicola Annels	2008	62
17	Two dephosphorylation pathways of inositol 1,4,5-trisphosphate in homogenates of the cellular slime mould Dictyostelium discoideum Biochemical Journal ·Michiel M. Van Lookeren Campagne, Christophé Erneux, Ronald van Eijk, Peter J.M. Van Haastert	1988	59
18	Cell Cycle/Apoptosis Molecule Expression Correlates with Imatinib Response in Patients with Advanced Gastrointestinal Stromal Tumors Clinical Cancer Research ·Salvatore Romeo, Maria Dêbiec‐Rychter, M. van Glabbeke, Heidi Van Paassen, Paola Comite, Ronald van Eijk, Jan Oosting, Jaap Verweij, Philippe Terrier, Ulrike Schneider, Raf Sciot, Jean‐Yves Blay, Pancras C.W. Hogendoorn	2009	59
19	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, Lisa Stevens, Hans Morreau, Tom van Wezel	2012	58
20	High-resolution copy number analysis of paraffin-embedded archival tissue using SNP BeadArrays Genome Research ·Jan Oosting, Esther H. Lips, Ronald van Eijk, Paul H.C. Eilers, Károly Szuhai, Cisca Wijmenga, Hans Morreau, Tom van Wezel	2007	56

About Ronald van Eijk

Ronald van Eijk is a scholar working on Pathology and Forensic Medicine, Cancer Research, Molecular Biology, Oncology and Genetics, having authored 81 papers that have together received 5.2k indexed citations. Recurring topics across this work include Cancer Genomics and Diagnostics (17 papers), Genetic factors in colorectal cancer (15 papers), Genomic variations and chromosomal abnormalities (7 papers), Molecular Biology Techniques and Applications (6 papers), Lymphoma Diagnosis and Treatment (6 papers), BRCA gene mutations in cancer (5 papers), Migraine and Headache Studies (4 papers) and Colorectal Cancer Treatments and Studies (4 papers). The work is most often cited by research in Psychiatry and Mental health (1.4k citations), Pathology and Forensic Medicine (1.1k citations), Neurology (461 citations), Endocrine and Autonomic Systems (310 citations) and Cancer Research (626 citations). Ronald van Eijk has collaborated with scholars based in Netherlands, United States and Belgium. Frequent co-authors include Michel D. Ferrari, Roel A. Ophoff, Rune R. Frants, Gisela M. Terwindt, Tom van Wezel, Monique N. Vergouwe, Joost Haan, Dick Lindhout, Marten H. Hofker and Dennis E. Bulman. Their work appears in journals such as BMC Cancer, Journal of Molecular Diagnostics, PLoS ONE, Genes Chromosomes and Cancer and Gastroenterology.

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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