B. F. Hogewind

Analyses of Sequence Variants in the MYOC Gene and of Single Nucleotide Polymorphisms in the NR3C1 and FKBP5 Genes in Corticosteroid-Induced Ocular Hypertension

A. D. den Hollander, C. Hoyng, S. Micheal, 2015, Ophthalmic genetics.

Autosomal dominant optic neuropathy and sensorineual hearing loss associated with a novel mutation of WFS1

C. Cremers, J. Cruysberg, R. Pennings, 2010, Molecular vision.

Variants in the PRPF8 Gene are Associated with Glaucoma

A. D. den Hollander, C. Hoyng, R. Qamar, 2017, Molecular Neurobiology.

Identification of TP53BP2 as a Novel Candidate Gene for Primary Open Angle Glaucoma by Whole Exome Sequencing in a Large Multiplex Family

A. D. den Hollander, C. Hoyng, Nicole T. M. Saksens, 2017, Molecular Neurobiology.

Intravitreal Triamcinolone for the Treatment of Refractory Macular Edema in Idiopathic Intermediate or Posterior Uveitis

B. J. Klevering, C. Hoyng, C. Zijlstra, 2008, European journal of ophthalmology.