Robert K Koenekoop

Oral 9-cis retinoid for childhood blindness due to Leber congenital amaurosis caused by RPE65 or LRAT mutations: an open-label phase 1b trial

Gislin Dagnelie, Ava K. Bittner, Ronald A Schuchard, 2014, The Lancet.

Leveraging splice‐affecting variant predictors and a minigene validation system to identify Mendelian disease‐causing variants among exon‐captured variants of uncertain significance

Hui Li, Rui Chen, Yumei Li, 2017, Human mutation.

Mutations in IMPG1 cause vitelliform macular dystrophies.

Xavier Zanlonghi, Joe G Hollyfield, Gilles Labesse, 2013, American journal of human genetics.

Next-generation sequencing-based molecular diagnosis of a Chinese patient cohort with autosomal recessive retinitis pigmentosa.

Fei Xu, Yumei Li, Feng Wang, 2013, Investigative ophthalmology & visual science.

PDZD7 is a modifier of retinal disease and a contributor to digenic Usher syndrome.

Monte Westerfield, Peter Nürnberg, Bernhard Schermer, 2010, The Journal of clinical investigation.

Optimal compliance for amblyopia therapy: occlusion with a translucent tape on the lens.

Robert K Koenekoop, Raquel G Beneish, Robert C Polomeno, 2009, Canadian journal of ophthalmology. Journal canadien d'ophtalmologie.