| Identification of the gene responsible for Best macular dystrophy K Petrukhin, MJ Koisti, B Bakall, W Li, G Xie, T Marknell, O Sandgren, ... Nature genetics 19 (3), 241-247, 1998 | 814 | 1998 |
| The dynamic nature of Bruch's membrane JC Booij, DC Baas, J Beisekeeva, TGMF Gorgels, AAB Bergen Progress in retinal and eye research 29 (1), 1-18, 2010 | 712 | 2010 |
| Mutations in ABCC6 cause pseudoxanthoma elasticum AAB Bergen, AS Plomp, EJ Schuurman, S Terry, M Breuning, ... Nature genetics 25 (2), 228-231, 2000 | 708 | 2000 |
| Autosomal Recessive Retinitis Pigmentosa and Cone-rod Dystrophy Caused by Splice Site Mutations in the Stargardt's Disease Gene ABCR FPM Cremers, DJR van de Pol, M van Driel, AI den Hollander, ... Human molecular genetics 7 (3), 355-362, 1998 | 650 | 1998 |
| Prevalence of age-related macular degeneration in Europe: the past and the future JM Colijn, GHS Buitendijk, E Prokofyeva, D Alves, ML Cachulo, ... Ophthalmology 124 (12), 1753-1763, 2017 | 586 | 2017 |
| Mutations in a human homologue of Drosophila crumbs cause retinitis pigmentosa (RP12) AI den Hollander, JB ten Brink, YJM de Kok, S van Soest, LI van den Born, ... Nature genetics 23 (2), 217-221, 1999 | 565 | 1999 |
| Genome-wide meta-analyses of multiancestry cohorts identify multiple new susceptibility loci for refractive error and myopia VJM Verhoeven, PG Hysi, R Wojciechowski, Q Fan, JA Guggenheim, ... Nature genetics 45 (3), 314-318, 2013 | 546 | 2013 |
| Complement factor H polymorphism, complement activators, and risk of age-related macular degeneration DDG Despriet, CCW Klaver, JCM Witteman, AAB Bergen, I Kardys, ... Jama 296 (3), 301-309, 2006 | 448 | 2006 |
| Positional cloning of the gene for X-linked retinitis pigmentosa 2 U Schwahn, S Lenzner, J Dong, S Feil, B Hinzmann, G Van Duijnhoven, ... Nature genetics 19 (4), 327-332, 1998 | 446 | 1998 |
| Mutations in NYX, encoding the leucine-rich proteoglycan nyctalopin, cause X-linked complete congenital stationary night blindness NT Bech-Hansen, MJ Naylor, TA Maybaum, RL Sparkes, B Koop, ... Nature genetics 26 (3), 319-323, 2000 | 422 | 2000 |
| Retinitis pigmentosa: defined from a molecular point of view S Van Soest, A Westerveld, PTVM De Jong, EM Bleeker-Wagemakers, ... Survey of ophthalmology 43 (4), 321-334, 1999 | 367 | 1999 |
| Genome-wide association meta-analysis highlights light-induced signaling as a driver for refractive error MS Tedja, R Wojciechowski, PG Hysi, N Eriksson, NA Furlotte, ... Nature genetics 50 (6), 834-848, 2018 | 318 | 2018 |
| The 2588G→ C mutation in the ABCR gene is a mild frequent founder mutation in the Western European population and allows the classification of ABCR mutations in patients with … A Maugeri, MA van Driel, DJR van de Pol, BJ Klevering, FJJ van Haren, ... The American Journal of Human Genetics 64 (4), 1024-1035, 1999 | 316 | 1999 |
| Isolation of a candidate gene for Norrie disease by positional cloning W Berger, A Meindl, TJR Van de Pol, FPM Cremers, HH Ropers, ... Nature genetics 1 (3), 199-203, 1992 | 308 | 1992 |
| ABCC6–mediated ATP secretion by the liver is the main source of the mineralization inhibitor inorganic pyrophosphate in the systemic circulation—brief report RS Jansen, S Duijst, S Mahakena, D Sommer, F Szeri, A Váradi, A Plomp, ... Arteriosclerosis, thrombosis, and vascular biology 34 (9), 1985-1989, 2014 | 298 | 2014 |
| A genome-wide association study identifies a susceptibility locus for refractive errors and myopia at 15q14 AM Solouki, VJM Verhoeven, CM Van Duijn, AJMH Verkerk, MK Ikram, ... Nature genetics 42 (10), 897-901, 2010 | 283 | 2010 |
| Mutations in TRPM1 are a common cause of complete congenital stationary night blindness MM van Genderen, MMC Bijveld, YB Claassen, RJ Florijn, JN Pearring, ... The American Journal of Human Genetics 85 (5), 730-736, 2009 | 265 | 2009 |
| ABCC6 prevents ectopic mineralization seen in pseudoxanthoma elasticum by inducing cellular nucleotide release RS Jansen, A Küçükosmanoğlu, M De Haas, S Sapthu, JA Otero, ... Proceedings of the National Academy of Sciences 110 (50), 20206-20211, 2013 | 258 | 2013 |
| A genome-wide association study of optic disc parameters WD Ramdas, LME van Koolwijk, MK Ikram, NM Jansonius, PTVM de Jong, ... PLoS genetics 6 (6), e1000978, 2010 | 248 | 2010 |
| Cloning of the gene for ocular albinism type 1 from the distal short arm of the X chromosome MT Bassi, MV Schiaffino, A Renieri, FD Nigris, L Galli, M Bruttini, ... Nature genetics 10 (1), 13-19, 1995 | 247 | 1995 |
