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Association of a polymorphism in the BIRC6 gene with pseudoexfoliative glaucoma.
PLoS One. 2014 Aug 13;9(8):e105023. doi: 10.1371/journal.pone.0105023. eCollection 2014.
PLoS One. 2014.
PMID: 25118708
Free PMC article.
Association of known common genetic variants with primary open angle, primary angle closure, and pseudoexfoliation glaucoma in Pakistani cohorts.
Micheal S, Ayub H, Khan MI, Bakker B, Schoenmaker-Koller FE, Ali M, Akhtar F, Khan WA, Qamar R, den Hollander AI.
Micheal S, et al. Among authors: schoenmaker koller fe.
Mol Vis. 2014 Nov 4;20:1471-9. eCollection 2014.
Mol Vis. 2014.
PMID: 25489222
Free PMC article.
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Analyses of Sequence Variants in the MYOC Gene and of Single Nucleotide Polymorphisms in the NR3C1 and FKBP5 Genes in Corticosteroid-Induced Ocular Hypertension.
Hogewind BF, Micheal S, Schoenmaker-Koller FE, Hoyng CB, den Hollander AI.
Hogewind BF, et al. Among authors: schoenmaker koller fe.
Ophthalmic Genet. 2015;36(4):299-302. doi: 10.3109/13816810.2013.879598. Epub 2015 Aug 28.
Ophthalmic Genet. 2015.
PMID: 24417561
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Analysis of rare variants in the C3 gene in patients with age-related macular degeneration.
Duvvari MR, Paun CC, Buitendijk GH, Saksens NT, Volokhina EB, Ristau T, Schoenmaker-Koller FE, van de Ven JP, Groenewoud JM, van den Heuvel LP, Hofman A, Fauser S, Uitterlinden AG, Klaver CC, Hoyng CB, de Jong EK, den Hollander AI.
Duvvari MR, et al. Among authors: schoenmaker koller fe.
PLoS One. 2014 Apr 15;9(4):e94165. doi: 10.1371/journal.pone.0094165. eCollection 2014.
PLoS One. 2014.
PMID: 24736606
Free PMC article.
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A functional variant in the CFI gene confers a high risk of age-related macular degeneration.
van de Ven JP, Nilsson SC, Tan PL, Buitendijk GH, Ristau T, Mohlin FC, Nabuurs SB, Schoenmaker-Koller FE, Smailhodzic D, Campochiaro PA, Zack DJ, Duvvari MR, Bakker B, Paun CC, Boon CJ, Uitterlinden AG, Liakopoulos S, Klevering BJ, Fauser S, Daha MR, Katsanis N, Klaver CC, Blom AM, Hoyng CB, den Hollander AI.
van de Ven JP, et al. Among authors: schoenmaker koller fe.
Nat Genet. 2013 Jul;45(7):813-7. doi: 10.1038/ng.2640. Epub 2013 May 19.
Nat Genet. 2013.
PMID: 23685748
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Mutations in CTNNA1 cause butterfly-shaped pigment dystrophy and perturbed retinal pigment epithelium integrity.
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.
Saksens NT, et al. Among authors: schoenmaker koller fe.
Nat Genet. 2016 Feb;48(2):144-51. doi: 10.1038/ng.3474. Epub 2015 Dec 21.
Nat Genet. 2016.
PMID: 26691986
Free PMC article.
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A rare nonsynonymous sequence variant in C3 is associated with high risk of age-related macular degeneration.
Helgason H, Sulem P, Duvvari MR, Luo H, Thorleifsson G, Stefansson H, Jonsdottir I, Masson G, Gudbjartsson DF, Walters GB, Magnusson OT, Kong A, Rafnar T, Kiemeney LA, Schoenmaker-Koller FE, Zhao L, Boon CJ, Song Y, Fauser S, Pei M, Ristau T, Patel S, Liakopoulos S, van de Ven JP, Hoyng CB, Ferreyra H, Duan Y, Bernstein PS, Geirsdottir A, Helgadottir G, Stefansson E, den Hollander AI, Zhang K, Jonasson F, Sigurdsson H, Thorsteinsdottir U, Stefansson K.
Helgason H, et al. Among authors: schoenmaker koller fe.
Nat Genet. 2013 Nov;45(11):1371-4. doi: 10.1038/ng.2740. Epub 2013 Sep 15.
Nat Genet. 2013.
PMID: 24036950
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Clinical evaluation of 3 families with basal laminar drusen caused by novel mutations in the complement factor H gene.
van de Ven JP, Boon CJ, Fauser S, Hoefsloot LH, Smailhodzic D, Schoenmaker-Koller F, Klevering J, Klaver CC, den Hollander AI, Hoyng CB.
van de Ven JP, et al.
Arch Ophthalmol. 2012 Aug;130(8):1038-47. doi: 10.1001/archophthalmol.2012.265.
Arch Ophthalmol. 2012.
PMID: 22491393
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