Marco Aben

Structural Variants Create New Topological-Associated Domains and Ectopic Retinal Enhancer-Gene Contact in Dominant Retinitis Pigmentosa

Suzanne E. de Bruijn, Alessia Fiorentino, Stephanie Fanucchi et al. · The American Journal of Human Genetics · 2020 · 122 citations · Full text

Medicine, Genetics, Molecular Genetics +16

Normal formation of a vertebrate body plan and loss of tissue maintenance in the absence of ezh2

Bilge San, Naomi D. Chrispijn, Nadine Wittkopp et al. · Scientific Reports · 2016 · 33 citations · Full text

Life Sciences, Developmental Biology, Genetics +16

Whole genome sequencing for USH2A-associated disease reveals several pathogenic deep-intronic variants that are amenable to splice correction

Janine Reurink, Nicole Weisschuh, Alejandro Garanto et al. · Human Genetics and Genomics Advances · 2023 · 28 citations · Full text

Life Sciences, Genetics, Molecular Genetics +17

Loss of the Polycomb group protein Rnf2 results in derepression of tbx-transcription factors and defects in embryonic and cardiac development

Naomi D. Chrispijn, Dei M. Elurbe, Michaela Mickoleit et al. · Scientific Reports · 2019 · 22 citations · Full text

Life Sciences, Genetics, Molecular Genetics +17

Efficient Generation of Knock-In Zebrafish Models for Inherited Disorders Using CRISPR-Cas9 Ribonucleoprotein Complexes

Erik de Vrieze, Suzanne E. de Bruijn, Janine Reurink et al. · International Journal of Molecular Sciences · 2021 · 22 citations · Full text

Life Sciences, Genetics, Molecular Biology +15