S. K. Verbakel

Pathogenic variants in IMPG1 cause autosomal dominant and autosomal recessive retinitis pigmentosa

Jeroen B. Klevering, C. Hoyng, P. Sergouniotis, 2020, Journal of Medical Genetics.

Macular Dystrophy and Cone-Rod Dystrophy Caused by Mutations in the RP1 Gene: Extending the RP1 Disease Spectrum.

B. J. Klevering, C. Klaver, A. D. den Hollander, 2019, Investigative ophthalmology & visual science.

Non-syndromic retinitis pigmentosa

B. J. Klevering, Jeroen B. Klevering, C. Klaver, 2018, Progress in Retinal and Eye Research.

The identification of a RNA splice variant in TULP1 in two siblings with early‐onset photoreceptor dystrophy

B. J. Klevering, F. Cremers, C. Hoyng, 2019, Molecular genetics & genomic medicine.

Allogeneic and autologous serum eye drops: a pilot double‐blind randomized crossover trial

R. Thurlings, S. K. Verbakel, J. Jacobs, 2021, Acta ophthalmologica.

Homozygous variants in KIAA1549, encoding a ciliary protein, are associated with autosomal recessive retinitis pigmentosa

H. Kremer, F. Cremers, C. Hoyng, 2018, Journal of Medical Genetics.

Carbonic Anhydrase Inhibitors for the Treatment of Cystic Macular Lesions in Children With X-Linked Juvenile Retinoschisis.

B. J. Klevering, C. Hoyng, E. D. de Jong, 2016, Investigative ophthalmology & visual science.

Analysis of Risk Alleles and Complement Activation Levels in Familial and Non-Familial Age-Related Macular Degeneration

A. D. den Hollander, C. Hoyng, M. Daha, 2016, PloS one.