Anneke den Hollander - Selected Publications#

Number of publications: 198
H-index: 43
Number of citations: 5783
ResearcherID: N‐4911‐2014

1. den Hollander AI. (2016) Omics in Ophthalmology: Advances in genomics and precision medicine for Leber congenital amaurosis and age-related macular degeneration. Invest Ophthalmol Vis Sci, 57:1378-87 (IF 3.4, ranking 7/57 in ophthalmology, printed version of Cogan Award lecture)

2. Saksens NT, Krebs MP, Schoenmaker-Koller FE, Hicks W, Yu M, Shi L, Rowe L, Collin GB, Charette JR, Letteboer SJ, Neveling K, van Moorsel TW, Abu-Ltaif S, De Baere E, Walraedt S, Banfi S, Simonelli F, Cremers FP, Boon CJ, Roepman R, Leroy BP, Peachey NS, Hoyng CB, Nishina PM, den Hollander AI. (2016) Mutations in CTNNA1 cause butterfly-shaped pigment dystrophy and perturbed retinal pigment epithelium integrity. Nature Genet 48:144-151 (IF 29.3, ranking 2/167 in genetics)

3. den Hollander AI, de Jong EK. (2014) Highly penetrant alleles in age-related macular degeneration. Cold Spring Harb Perspect Med 5:a017202. (IF 9.4, 7/123 in medicine)

4. Roosing S, Lamers IJ, de Vrieze E, van den Born LI, Lambertus S, Arts HH; POC1B Study Group., Peters TA, Hoyng CB, Kremer H, Hetterschijt L, Letteboer SJ, van Wijk E, Roepman R, den Hollander AI, Cremers FP. (2014) Disruption of the basal body protein POC1B results in autosomal-recessive cone-rod dystrophy. Am J Hum Genet 95:131-42. (impact factor 10.9, 6/167 in genetics)

5. Siemiatkowska AM, Collin RW, den Hollander AI, Cremers FP. (2014) Genomic approaches for the discovery of genes mutated in inherited retinal degeneration. Cold Spring Harb Perspect Med 4:a017137. (IF 9.4, 7/123 in medicine)

6. Boon CFJ, van de Ven JPH, Hoyng CB, den Hollander AI, Klevering BJ. (2013) Cuticular drusen: Stars in the sky. Prog Retin Eye Res 37:90-113 (impact factor 8.7, 1st in ophthalmology)

7. Roosing S, Rohrschneider K, Beryozkin A, Sharon D, Weisshuh N, Staller J, Kohl S, Zelinger L, Neveling K, Strom TM, European Retinal Disease Consortium, Hoyng CB, Klaver CCW, Wissinger B, Banin E, Cremers FPM, den Hollander AI. (2013) The farnesylated small GTPase RAB28 is mutated in autosomal recessive cone-rod dystrophy. Am J Hum Genet 93:110-117 (IF 10.9, ranking 6/167 in genetics)

8. van de Ven JPH, Nilsson SC, Tan PL, Buitendijk GHS, Ristau T, Mohlin FC, Nabuurs SB, Schoenmaker-Koller FE, Smailhodzic D, Campochiarro PA, Zack DJ, Duvvari MR, Bakker B, Paun CC, Boon CJF, Uitterlinden AG, Liakopoulos S, Klevering BJ, Fauser S, Daha MR, Katsanis N, Klaver CCW, Blom AM, Hoyng CB, den Hollander AI. (2013) A functional variant in the CFI gene confers a high risk of age-related macular degeneration. Nature Genet 45:813-817 (IF 29.3, ranking 2/167 in genetics)

9. den Hollander AI, Koenekoop RK, Mohamed MD, Arts HH, Boldt K, Towns KV, Sedmak T, Beer M, Nagel-Wolfrum K, McKibbin M, Dharmaraj S, Lopez I, Ivings L, Williams GA, Springell K, Woods CG, Jafri H, Rashid Y, Strom TM, van der Zwaag B, Gosens I, Kersten FFJ, van Wijk E, Veltman JA, Zonneveld MN, van Beersum SEC, Maumenee IH, Wolfrum U, Cheetham ME, Ueffing M, Cremers FPM, Inglehearn CF, Roepman R. (2007) Mutations in LCA5, encoding the ciliary protein lebercilin, cause Leber congenital amaurosis. Nature Genet 39:889-895 (IF 29.3, ranking 2/167 in genetics)

10. den Hollander AI, ten Brink JB, de Kok YJM, van Soest S, van den Born LI, van Driel MA, van de Pol DJR, Payne AM, Bhattacharya SS, Kellner U, Hoyng CB, Westerveld A, Brunner HG, Bleeker-Wagemakers EM, Deutman AF, Heckenlively JR, Cremers FPM, Bergen AAB. (1999) Mutations in a human homologue of Drosophila crumbs cause retinitis pigmentosa (RP12). Nature Genet 23:217-221 (IF 29.3, ranking 2/167 in genetics)