Gert‐Jan B. van Ommen

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

Life Sciences, Neurology, Neuroscience +16

Rubinstein-Taybi syndrome caused by mutations in the transcriptional co-activator CBP

Fred Petrif, Rachel H. Giles, Hans G. Dauwerse et al. · Nature · 1995 · 1.2K citations

Life Sciences, Genetics, Molecular Genetics +5

Human Papillomavirus (HPV) Upregulates the Cellular Deubiquitinase UCHL1 to Suppress the Keratinocyte's Innate Immune Response

Rezaul Karim, Bart Tummers, Craig Meyers et al. · PLoS Pathogens · 2013 · 178 citations · Full text

Life Sciences, Immunology, Molecular Biology +17

<i>In vivo</i> comparison of 2′‐<i>O</i>‐methyl phosphorothioate and morpholino antisense oligonucleotides for Duchenne muscular dystrophy exon skipping

Hans Heemskerk, C.L. de Winter, Sjef J. de Kimpe et al. · The Journal of Gene Medicine · 2009 · 171 citations · Full text

Medicine, Molecular Biology, Pharmacology +13

Preclinical PK and PD Studies on 2′-O-Methyl-phosphorothioate RNA Antisense Oligonucleotides in the mdx Mouse Model

Hans Heemskerk, Christa de Winter, Petra van Kuik et al. · Molecular Therapy · 2010 · 137 citations · Full text

Medicine, Pharmacokinetics, Pharmacology +15