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185 related items for PubMed ID: 34508573

  • 1. Systemic complement levels in patients with age-related macular degeneration carrying rare or low-frequency variants in the CFH gene.
    de Jong S, de Breuk A, Volokhina EB, Bakker B, Garanto A, Fauser S, Katti S, Hoyng CB, Lechanteur YTE, van den Heuvel LP, den Hollander AI.
    Hum Mol Genet; 2022 Feb 03; 31(3):455-470. PubMed ID: 34508573
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  • 2. The Functional Effect of Rare Variants in Complement Genes on C3b Degradation in Patients With Age-Related Macular Degeneration.
    Geerlings MJ, Kremlitzka M, Bakker B, Nilsson SC, Saksens NT, Lechanteur YT, Pauper M, Corominas J, Fauser S, Hoyng CB, Blom AM, de Jong EK, den Hollander AI.
    JAMA Ophthalmol; 2017 Jan 01; 135(1):39-46. PubMed ID: 27918759
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  • 3. Common haplotypes at the CFH locus and low-frequency variants in CFHR2 and CFHR5 associate with systemic FHR concentrations and age-related macular degeneration.
    Lorés-Motta L, van Beek AE, Willems E, Zandstra J, van Mierlo G, Einhaus A, Mary JL, Stucki C, Bakker B, Hoyng CB, Fauser S, Clark SJ, de Jonge MI, Nogoceke E, Koertvely E, Jongerius I, Kuijpers TW, den Hollander AI.
    Am J Hum Genet; 2021 Aug 05; 108(8):1367-1384. PubMed ID: 34260947
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  • 6. Consequences of a Rare Complement Factor H Variant for Age-Related Macular Degeneration in the Amish.
    Waksmunski AR, Miskimen K, Song YE, Grunin M, Laux R, Fuzzell D, Fuzzell S, Adams LD, Caywood L, Prough M, Stambolian D, Scott WK, Pericak-Vance MA, Haines JL.
    Invest Ophthalmol Vis Sci; 2022 Aug 02; 63(9):8. PubMed ID: 35930268
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  • 7. 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.
    Ophthalmology; 2012 Feb 02; 119(2):339-46. PubMed ID: 22133792
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  • 8. Phenotype Characteristics of Patients With Age-Related Macular Degeneration Carrying a Rare Variant in the Complement Factor H Gene.
    Kersten E, Geerlings MJ, den Hollander AI, de Jong EK, Fauser S, Peto T, Hoyng CB.
    JAMA Ophthalmol; 2017 Oct 01; 135(10):1037-1044. PubMed ID: 28859202
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  • 10. Evaluating the Occurrence of Rare Variants in the Complement Factor H Gene in Patients With Early-Onset Drusen Maculopathy.
    de Breuk A, Heesterbeek TJ, Bakker B, Verzijden T, Lechanteur YTE, Klaver CCW, den Hollander AI, Hoyng CB.
    JAMA Ophthalmol; 2021 Nov 01; 139(11):1218-1226. PubMed ID: 34647987
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  • 11. Genetic Risk in Families with Age-Related Macular Degeneration.
    de Breuk A, Lechanteur YTE, Heesterbeek TJ, Fauser S, Klaver CCW, Hoyng CB, den Hollander AI.
    Ophthalmol Sci; 2021 Dec 01; 1(4):100087. PubMed ID: 36246952
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  • 12. Plasma complement components and activation fragments: associations with age-related macular degeneration genotypes and phenotypes.
    Reynolds R, Hartnett ME, Atkinson JP, Giclas PC, Rosner B, Seddon JM.
    Invest Ophthalmol Vis Sci; 2009 Dec 01; 50(12):5818-27. PubMed ID: 19661236
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  • 20. Genetic influences on plasma CFH and CFHR1 concentrations and their role in susceptibility to age-related macular degeneration.
    Ansari M, McKeigue PM, Skerka C, Hayward C, Rudan I, Vitart V, Polasek O, Armbrecht AM, Yates JR, Vatavuk Z, Bencic G, Kolcic I, Oostra BA, Van Duijn CM, Campbell S, Stanton CM, Huffman J, Shu X, Khan JC, Shahid H, Harding SP, Bishop PN, Deary IJ, Moore AT, Dhillon B, Rudan P, Zipfel PF, Sim RB, Hastie ND, Campbell H, Wright AF.
    Hum Mol Genet; 2013 Dec 01; 22(23):4857-69. PubMed ID: 23873044
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