Association Between X-Linked Mixed Deafness and Mutations in the POU Domain Gene <i>POU3F4</i>Yvette J.M. de Kok, Frans P.M. Cremers, Silvère M. van der Maarel et al.|Science|1995Cited by 449
Cloning of a gene that is rearranged in patients with choroideraemiaFrans P.M. Cremers, Hans‐Hilger Ropers, Dorien J.R. van de Pol et al.|Nature|1990Cited by 334
Clinical spectrum, genetic complexity and therapeutic approaches for retinal disease caused by ABCA4 mutationsFrans P.M. Cremers, Rando Allikmets, Winston Lee et al.|Progress in Retinal and Eye Research|2020Cited by 311
AHI1 is required for photoreceptor outer segment development and is a modifier for retinal degeneration in nephronophthisisCarrie M Louie, Joseph G. Gleeson, Madeline A. Lancaster et al.|Nature Genetics|2010Cited by 189
Long-read technologies identify a hidden inverted duplication in a family with choroideremiaZeinab Fadaie, Susanne Roosing, Kornelia Neveling et al.|Human Genetics and Genomics Advances|2021Cited by 24