Gert‐Jan B. van Ommen
Publications by Year
Research Areas
Muscle Physiology and Disorders, Genetic Neurodegenerative Diseases, Genetic Associations and Epidemiology, Mitochondrial Function and Pathology, Chromosomal and Genetic Variations
Most-Cited Works
- → Familial Hemiplegic Migraine and Episodic Ataxia Type-2 Are Caused by Mutations in the Ca2+ Channel Gene CACNL1A4(1996)2,331 cited
- → Rubinstein-Taybi syndrome caused by mutations in the transcriptional co-activator CBP(1995)1,217 cited
- → Human Papillomavirus (HPV) Upregulates the Cellular Deubiquitinase UCHL1 to Suppress the Keratinocyte's Innate Immune Response(2013)177 cited
- → In vivo comparison of 2′‐O‐methyl phosphorothioate and morpholino antisense oligonucleotides for Duchenne muscular dystrophy exon skipping(2009)169 cited
- → Preclinical PK and PD Studies on 2′-O-Methyl-phosphorothioate RNA Antisense Oligonucleotides in the mdx Mouse Model(2010)137 cited
- → A high-quality human reference panel reveals the complexity and distribution of genomic structural variants(2016)117 cited
- → On attitudes and appreciation 6 months after predictive DNA testing for huntington disease in the Dutch program(1993)110 cited
- → A 10-megabase physical map of human Xp21, including the Duchenne muscular dystrophy gene(1988)103 cited
- → Construction of a 1.2-Mb Contig Surrounding, and Molecular Analysis of, the Human CREB-Binding Protein (CBP/CREBBP) Gene on Chromosome 16p13.3(1997)84 cited
- → Antisense-induced exon skipping for duplications in Duchenne muscular dystrophy(2007)67 cited