Boon CJF - Search Results

1

Prevalence of Myopic Macular Features in Dutch Individuals of European Ancestry With High Myopia.

Haarman AEG, Tedja MS, Brussee C, Enthoven CA, van Rijn GA, Vingerling JR, Keunen JEE, Boon CJF, Geerards AJM, Luyten GPM, Verhoeven VJM, Klaver CCW. Haarman AEG, et al. Among authors: boon cjf. JAMA Ophthalmol. 2022 Feb 1;140(2):115-123. doi: 10.1001/jamaophthalmol.2021.5346. JAMA Ophthalmol. 2022. PMID: 34913968 Free PMC article.

2

Fundus autofluorescence imaging of retinal dystrophies.

Boon CJ, Jeroen Klevering B, Keunen JE, Hoyng CB, Theelen T. Boon CJ, et al. Vision Res. 2008 Nov;48(26):2569-77. doi: 10.1016/j.visres.2008.01.010. Epub 2008 Mar 4. Vision Res. 2008. PMID: 18289629 Free article.

3

The spectrum of retinal dystrophies caused by mutations in the peripherin/RDS gene.

Boon CJ, den Hollander AI, Hoyng CB, Cremers FP, Klevering BJ, Keunen JE. Boon CJ, et al. Prog Retin Eye Res. 2008 Mar;27(2):213-35. doi: 10.1016/j.preteyeres.2008.01.002. Epub 2008 Jan 26. Prog Retin Eye Res. 2008. PMID: 18328765 Review.

4

The spectrum of phenotypes caused by variants in the CFH gene.

Boon CJ, van de Kar NC, Klevering BJ, Keunen JE, Cremers FP, Klaver CC, Hoyng CB, Daha MR, den Hollander AI. Boon CJ, et al. Mol Immunol. 2009 May;46(8-9):1573-94. doi: 10.1016/j.molimm.2009.02.013. Epub 2009 Mar 17. Mol Immunol. 2009. PMID: 19297022 Review.

5

Clinical and molecular genetic analysis of best vitelliform macular dystrophy.

Boon CJ, Theelen T, Hoefsloot EH, van Schooneveld MJ, Keunen JE, Cremers FP, Klevering BJ, Hoyng CB. Boon CJ, et al. Retina. 2009 Jun;29(6):835-47. doi: 10.1097/IAE.0b013e31819d4fda. Retina. 2009. PMID: 19357557

6

The spectrum of ocular phenotypes caused by mutations in the BEST1 gene.

Boon CJ, Klevering BJ, Leroy BP, Hoyng CB, Keunen JE, den Hollander AI. Boon CJ, et al. Prog Retin Eye Res. 2009 May;28(3):187-205. doi: 10.1016/j.preteyeres.2009.04.002. Epub 2009 Apr 16. Prog Retin Eye Res. 2009. PMID: 19375515 Review.

7

Course of visual decline in relation to the Best1 genotype in vitelliform macular dystrophy.

Booij JC, Boon CJ, van Schooneveld MJ, ten Brink JB, Bakker A, de Jong PT, Hoyng CB, Bergen AA, Klaver CC. Booij JC, et al. Ophthalmology. 2010 Jul;117(7):1415-22. doi: 10.1016/j.ophtha.2009.11.044. Epub 2010 Apr 9. Ophthalmology. 2010. PMID: 20381869

8

Risk alleles in CFH and ARMS2 are independently associated with systemic complement activation in age-related macular degeneration.

Smailhodzic D, Klaver CC, Klevering BJ, Boon CJ, Groenewoud JM, Kirchhof B, Daha MR, den Hollander AI, Hoyng CB. Smailhodzic D, et al. Ophthalmology. 2012 Feb;119(2):339-46. doi: 10.1016/j.ophtha.2011.07.056. Epub 2011 Nov 30. Ophthalmology. 2012. PMID: 22133792

9

Clinical course, genetic etiology, and visual outcome in cone and cone-rod dystrophy.

Thiadens AA, Phan TM, Zekveld-Vroon RC, Leroy BP, van den Born LI, Hoyng CB, Klaver CC; Writing Committee for the Cone Disorders Study Group Consortium; Roosing S, Pott JW, van Schooneveld MJ, van Moll-Ramirez N, van Genderen MM, Boon CJ, den Hollander AI, Bergen AA, De Baere E, Cremers FP, Lotery AJ. Thiadens AA, et al. Ophthalmology. 2012 Apr;119(4):819-26. doi: 10.1016/j.ophtha.2011.10.011. Epub 2012 Jan 20. Ophthalmology. 2012. PMID: 22264887

10

Clinical and genetic characteristics of late-onset Stargardt's disease.

Westeneng-van Haaften SC, Boon CJ, Cremers FP, Hoefsloot LH, den Hollander AI, Hoyng CB. Westeneng-van Haaften SC, et al. Ophthalmology. 2012 Jun;119(6):1199-210. doi: 10.1016/j.ophtha.2012.01.005. Epub 2012 Mar 24. Ophthalmology. 2012. PMID: 22449572

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