Suzanne E de Bruijn

9PUBLICATIONS
179CO-AUTHORS
Sensory systemsGene expression (incl. microarray and other genome-wide approaches)Neurology and neuromuscular diseasesGene mappingWastewater treatment processes
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Publications (9)

|Jan 09, 2026
De novo and inherited dominant variants in U4 and U6 snRNA genes cause retinitis pigmentosa.

Mathieu Quinodoz, Kim Rodenburg, Zuzana Cvackova

|Mar 04, 2025
Deciphering the largest disease-associated transcript isoforms in the human neural retina with advanced long-read sequencing approaches.

Merel Stemerdink, Tabea Riepe, Nick Zomer

|Jan 20, 2025
De novo and inherited dominant variants in U4 and U6 snRNAs cause retinitis pigmentosa.

Mathieu Quinodoz, Kim Rodenburg, Zuzana Cvackova

|Aug 26, 2023
Combined Single Gene Testing and Genome Sequencing as an Effective Diagnostic Approach for Anophthalmia and Microphthalmia Patients.

Rabia Basharat, Kim Rodenburg, María Rodríguez-Hidalgo

|Oct 05, 2021
Correction to: Exploring the missing heritability in subjects with hearing loss, enlarged vestibular aqueducts, and a single or no pathogenic SLC26A4 variant.

Jeroen J Smits, Suzanne E de Bruijn, Cornelis P Lanting

|Sep 10, 2021
Efficient Generation of Knock-In Zebrafish Models for Inherited Disorders Using CRISPR-Cas9 Ribonucleoprotein Complexes.

Erik de Vrieze, Suzanne E de Bruijn, Janine Reurink

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Frequent Collaborators

5 joint publications

Frans P M Cremers

5 joint publications

Hannie Kremer

4 joint publications

Susanne Roosing

3 joint publications

Jeroen J Smits