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Developmental Dynamics : an Official Publication of the American Association of Anatomists|March 11, 2022
The zebrafish cohesin protein Sgo1 is required for cardiac function and eye developmentSarah M Kamel, Sanne Broekman, Federico Tessadori, et al.
Cells|June 28, 2023
Generation and Characterization of a Zebrafish Model for ADGRV1-Associated Retinal Dysfunction Using CRISPR/Cas9 Genome Editing TechnologyMerel Stemerdink, Sanne Broekman, Theo Peters, et al.
Zebrafish|October 4, 2018
Poor Splice-Site Recognition in a Humanized Zebrafish Knockin Model for the Recurrent Deep-Intronic c.7595-2144A>G Mutation in USH2ARalph Slijkerman, Alexander Goloborodko, Sanne Broekman, et al.
International Journal of Molecular Sciences|September 10, 2021
Efficient Generation of Knock-In Zebrafish Models for Inherited Disorders Using CRISPR-Cas9 Ribonucleoprotein ComplexesErik de Vrieze, Suzanne E de Bruijn, Janine Reurink, et al.
Molecular Therapy. Nucleic Acids|June 14, 2023
A protein domain-oriented approach to expand the opportunities of therapeutic exon skipping for USH2A-associated retinitis pigmentosaRenske T W Schellens, Sanne Broekman, Theo Peters, et al.
International Journal of Molecular Sciences|September 10, 2021
Zebrafish as a Model to Evaluate a CRISPR/Cas9-Based Exon Excision Approach as a Future Treatment Option for EYS-Associated Retinitis PigmentosaRenske Schellens, Erik de Vrieze, Pam Graave, et al.
Molecular Therapy. Nucleic Acids|October 2, 2025
Exploring exon excision as a therapeutic intervention strategy for the future treatment of ADGRV1-associated retinitis pigmentosaMerel Stemerdink, Lucija Malinar, Sanne Broekman, et al.
Plos One|July 28, 2018
Eyes shut homolog is important for the maintenance of photoreceptor morphology and visual function in zebrafishMuriël Messchaert, Margo Dona, Sanne Broekman, et al.
American Journal of Physiology. Heart and Circulatory Physiology|September 27, 2024
RRAGD variants cause cardiac dysfunction in a zebrafish modelAnastasia Adella, Faris Tengku, Francisco J Arjona, et al.
Hearing Research|January 13, 2024
Rational design of a genomically humanized mouse model for dominantly inherited hearing loss, DFNA9Dorien Verdoodt, Erwin van Wijk, Sanne Broekman, et al.
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