متابعة
Arthur Bergen
Arthur Bergen
Hoogleraar complexe Ophthalmogenetica
بريد إلكتروني تم التحقق منه على amc.uva.nl
عنوان
عدد مرات الاقتباسات
عدد مرات الاقتباسات
السنة
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
8301998
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
7272010
Mutations in ABCC6 cause pseudoxanthoma elasticum
AAB Bergen, AS Plomp, EJ Schuurman, S Terry, M Breuning, ...
Nature genetics 25 (2), 228-231, 2000
7182000
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
6571998
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
6122017
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
5691999
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
5522013
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
4501998
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
4452006
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
4272000
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
3701999
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
3452018
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
3171999
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
3051992
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
3022014
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
2852010
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
2662013
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
2652009
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
2502010
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
2461995
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مقالات 1–20