Ronald van Eijk

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

Roel A. Ophoff, Gisela M. Terwindt, Monique N. Vergouwe et al. · Cell · 1996 · 2.3K citations · Full text

Channelopathies, Genetic Disorder, Genetics +5

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

Twinkal C. Pansuriya, Ronald van Eijk, Pio D’Adamo et al. · Nature Genetics · 2011 · 546 citations · Full text

Developmental Biology, Somatic Variant, Genetic Disorder +8

BRCA1 genomic deletions are major founder mutations in Dutch breast cancer patients

Anne Petrij-Bosch, Tamara Peelen, Margreethe van Vliet et al. · Nature Genetics · 1997 · 445 citations · Full text

Breast Oncology, Somatic Variant, Medicine +8

E-cadherin transcriptional downregulation by promoter methylation but not mutation is related to epithelial-to-mesenchymal transition in breast cancer cell lines

Marcel Lombaerts, Tom van Wezel, Katja Philippo et al. · British Journal of Cancer · 2006 · 340 citations · Full text

Chromosome 4 localization of a second gene for autosomal dominant polycystic kidney disease

Dorien J.M. Peters, Lia Spruit, Jasper J. Saris et al. · Nature Genetics · 1993 · 272 citations

Mendelian Disorder, Genetic Disorder, Medicine +10