Papers authored by Keilhauer CN

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Age-related macular degeneration and functional promoter and coding variants of the apolipoprotein E gene.
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Fritsche LG, Freitag-Wolf S, Bettecken T, Meitinger T, Keilhauer CN, Krawczak M, and Weber BH
Human mutation 30(7):1048-53, 2009 Jul - Who cited this? | PubMed ID: 19384966 | Fulltext
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CFH, C3 and ARMS2 are significant risk loci for susceptibility but not for disease progression of geographic atrophy due to AMD.
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Scholl HP, Fleckenstein M, Fritsche LG, Schmitz-Valckenberg S, Göbel A, Adrion C, Herold C, Keilhauer CN, Mackensen F, Mössner A, Pauleikhoff D, Weinberger AW, Mansmann U, Holz FG, Becker T, and Weber BH
PLoS ONE 4(10):e7418, 2009 - Who cited this? | PubMed ID: 19823576 | Fulltext
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Age-related macular degeneration is associated with an unstable ARMS2 (LOC387715) mRNA.
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Fritsche LG, Loenhardt T, Janssen A, Fisher SA, Rivera A, Keilhauer CN, and Weber BH
Nature genetics 40(7):892, 2008 Jul - Who cited this? | PubMed ID: 18511946 | Fulltext
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Defective complement control of factor H (Y402H) and FHL-1 in age-related macular degeneration.
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Skerka C, Lauer N, Weinberger AA, Keilhauer CN, Sühnel J, Smith R, Schlötzer-Schrehardt U, Fritsche L, Heinen S, Hartmann A, Weber BH, and Zipfel PF
Molecular immunology 44(13):3398-406, 2007 Jul - Who cited this? | PubMed ID: 17399790 | Fulltext
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Case-control genetic association study of fibulin-6 (FBLN6 or HMCN1) variants in age-related macular degeneration (AMD).
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Fisher SA, Rivera A, Fritsche LG, Keilhauer CN, Lichtner P, Meitinger T, Rudolph G, and Weber BH
Human mutation 28(4):406-13, 2007 Apr - Who cited this? | PubMed ID: 17216616 | Fulltext
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[Clinical findings in a patient with Lowe syndrome and a splice site mutation in the OCRL1 gene].
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Keilhauer CN, Gal A, Sold JE, Zimmermann J, Netzer KO, and Schramm L
Klinische Monatsblatter fur Augenheilkunde 224(3):207-9, 2007 Mar - Who cited this? | PubMed ID: 17385124 | Fulltext
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Late-onset central areolar choroidal dystrophy caused by a heterozygous frame-shift mutation affecting codon 307 of the peripherin/RDS gene.
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Keilhauer CN, Meigen T, Stöhr H, and Weber BH
Ophthalmic genetics 27(4):139-44, 2006 Dec - Who cited this? | PubMed ID: 17148040 | Fulltext
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Near-infrared autofluorescence imaging of the fundus: visualization of ocular melanin.
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Keilhauer CN and Delori FC
Investigative ophthalmology & visual science 47(8):3556, 2006 Aug - Who cited this? | PubMed ID: 16877429 | Fulltext
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Clinical findings in a multigeneration family with autosomal dominant central areolar choroidal dystrophy associated with an Arg195Leu mutation in the peripherin/RDS gene.
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Keilhauer CN, Meigen T, and Weber BH
Archives of ophthalmology 124(7):1020, 2006 Jul - Who cited this? | PubMed ID: 16832026 | Fulltext
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Hypothetical LOC387715 is a second major susceptibility gene for age-related macular degeneration, contributing independently of complement factor H to disease risk.
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Rivera A, Fisher SA, Fritsche LG, Keilhauer CN, Lichtner P, Meitinger T, and Weber BH
Human molecular genetics 14(21):3227-36, 2005 Nov 1 - Who cited this? | PubMed ID: 16174643 | Fulltext
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