| Familial hemiplegic migraine and episodic ataxia type-2 are caused by mutations in the Ca2+ channel gene CACNL1A4 RA Ophoff, GM Terwindt, MN Vergouwe, R van Eijk, PJ Oefner, ... Cell 87 (3), 543-552, 1996 | 2898 | 1996 |
| Somatic mosaic IDH1 and IDH2 mutations are associated with enchondroma and spindle cell hemangioma in Ollier disease and Maffucci syndrome TC Pansuriya, R van Eijk, P d'Adamo, MAJH van Ruler, ML Kuijjer, ... Nature genetics 43 (12), 1256-1261, 2011 | 567 | 2011 |
| BRCA1 genomic deletions are major founder mutations in Dutch breast cancer patients A Petrij-Bosch, T Peelen, M van Vliet, R Eijk, R Olmer, M Drüsedau, ... Nature genetics 17 (3), 341-345, 1997 | 519 | 1997 |
| E-cadherin transcriptional downregulation by promoter methylation but not mutation is related to epithelial-to-mesenchymal transition in breast cancer cell lines M Lombaerts, T Van Wezel, K Philippo, JWF Dierssen, RME Zimmerman, ... British journal of cancer 94 (5), 661-671, 2006 | 447 | 2006 |
| Chromosome 4 localization of a second gene for autosomal dominant polycystic kidney disease DJM Peters, L Spruit, JJ Saris, D Ravine, LA Sandkuijl, R Fossdal, ... Nature genetics 5 (4), 359-362, 1993 | 353 | 1993 |
| A genome-wide association study of Hodgkin's lymphoma identifies new susceptibility loci at 2p16.1 (REL), 8q24.21 and 10p14 (GATA3) V Enciso-Mora, P Broderick, Y Ma, RF Jarrett, H Hjalgrim, K Hemminki, ... Nature genetics 42 (12), 1126-1130, 2010 | 238 | 2010 |
| Familial hemiplegic migraine locus on 19p13 is involved in the common forms of migraine with and without aura A May, RA Ophoff, GM Terwindt, C Urban, R van Eijk, J Haan, HC Diener, ... Human genetics 96, 604-608, 1995 | 236 | 1995 |
| Rapid KRAS, EGFR, BRAF and PIK3CA Mutation Analysis of Fine Needle Aspirates from Non-Small-Cell Lung Cancer Using Allele-Specific qPCR R van Eijk, J Licht, M Schrumpf, M Talebian Yazdi, D Ruano, GI Forte, ... PloS one 6 (3), e17791, 2011 | 216 | 2011 |
| Genetic heterogeneity of familial hemiplegic migraine RA Ophoff, R van Eijk, LA Sandkuijl, GM Terwindt, CPM Grubben, J Haan, ... Genomics 22 (1), 21-26, 1994 | 189 | 1994 |
| Involvement of the CACNA1A gene containing region on 19p13 in migraine with and without aura GM Terwindt, RA Ophoff, R Van Eijk, MN Vergouwe, J Haan, RR Frants, ... Neurology 56 (8), 1028-1032, 2001 | 181 | 2001 |
| Variable clinical expression of mutations in the P/Q-type calcium channel gene in familial hemiplegic migraine GM Terwindt, RA Ophoff, J Haan, MN Vergouwe, R Van Eijk, RR Frants, ... Neurology 50 (4), 1105-1111, 1998 | 169 | 1998 |
| Expression of HLA class I antigen, aspirin use, and survival after a diagnosis of colon cancer MS Reimers, E Bastiaannet, RE Langley, R van Eijk, RLP van Vlierberghe, ... JAMA internal medicine 174 (5), 732-739, 2014 | 120 | 2014 |
| Differential Gene Expression in Ovarian Tumors Reveals Dusp 4 and Serpina 5 As Key Regulators for Benign Behavior of Serous Borderline Tumors NLG Sieben, J Oosting, AM Flanagan, J Prat, GMJM Roemen, ... Journal of clinical oncology 23 (29), 7257-7264, 2005 | 115 | 2005 |
| Whole-Exome Sequencing Studies of Parathyroid Carcinomas Reveal Novel PRUNE2 Mutations, Distinctive Mutational Spectra Related to APOBEC-Catalyzed … W Yu, JR McPherson, M Stevenson, R van Eijk, HL Heng, P Newey, ... The Journal of Clinical Endocrinology & Metabolism 100 (2), E360-E364, 2015 | 106 | 2015 |
| Reliable high-throughput genotyping and loss-of-heterozygosity detection in formalin-fixed, paraffin-embedded tumors using single nucleotide polymorphism arrays EH Lips, JWF Dierssen, R van Eijk, J Oosting, PHC Eilers, ... Cancer research 65 (22), 10188-10191, 2005 | 103 | 2005 |
| No genomic aberrations in Langerhans cell histiocytosis as assessed by diverse molecular technologies CET da Costa, K Szuhai, R van Eijk, M Hoogeboom, R Sciot, F Mertens, ... Genes, Chromosomes and Cancer 48 (3), 239-249, 2009 | 102 | 2009 |
| Chromosome 8q23. 3 and 11q23. 1 variants modify colorectal cancer risk in Lynch syndrome JT Wijnen, RM Brohet, R Van Eijk, S Jagmohan–Changur, A Middeldorp, ... Gastroenterology 136 (1), 131-137, 2009 | 102 | 2009 |
| Assessment of a fully automated high-throughput DNA extraction method from formalin-fixed, paraffin-embedded tissue for KRAS, and BRAF somatic mutation analysis R van Eijk, L Stevens, H Morreau, T van Wezel Experimental and molecular pathology 94 (1), 121-125, 2013 | 94 | 2013 |
| Integrating chromosomal aberrations and gene expression profiles to dissect rectal tumorigenesis EH Lips, R van Eijk, EJR de Graaf, J Oosting, NFCC de Miranda, ... BMC cancer 8, 1-13, 2008 | 92 | 2008 |
| Genome haploidisation with chromosome 7 retention in oncocytic follicular thyroid carcinoma WE Corver, D Ruano, K Weijers, WCE Den Hartog, ... PloS one 7 (6), e38287, 2012 | 83 | 2012 |
Tom van WezelAssociate professor, Department of Pathology, Leiden University Medical Center, NetherlandsVerified email at lumc.nl
