Anzahl der Einträge: 14.
Artikel
Fritsche, L. G. ,
Igl, Wilmar,
Bailey, J. N.,
Grassmann, Felix ,
Sengupta, Sebanti,
Bragg-Gresham, Jennifer L.,
Burdon, Kathryn P.,
Hebbring, Scott J.,
Weber, Bernhard H. F. und
Heid, Iris M.
(2016)
A large genome-wide association study of age-related macular degeneration highlights contributions of rare and common variants.
Nature Genetics 48, S. 134-143.
Volltext nicht vorhanden.
Baas, D. C.,
Ho, L.,
Tanck, M. W.,
Fritsche, L. G.,
Merriam, J. E.,
van het Slot, R.,
Koeleman, B. P.,
Gorgels, T. G.,
van Duijn, C. M.,
Uitterlinden, A. G.,
de Jong, P. T.,
Hofman, A.,
ten Brink, J. B.,
Vingerling, J. R.,
Klaver, C. C.,
Dean, M.,
Weber, Bernhard H. F. und
et al, .
(2012)
Multicenter cohort association study of SLC2A1 single nucleotide polymorphisms and age-related macular degeneration.
Molecular vision 18, S. 657-674.
Friedrich, U.,
Myers, C. A.,
Fritsche, L. G.,
Milenkovic, Andrea,
Wolf, A.,
Corbo, J. C. und
Weber, Bernhard H. F.
(2011)
Risk- and non-risk-associated variants at the 10q26 AMD locus influence ARMS2 mRNA expression but exclude pathogenic effects due to protein deficiency.
Human Molecular Genetics 20, S. 1387-1399.
Volltext nicht vorhanden.
McKay, G. J.,
Silvestri, G.,
Chakravarthy, U.,
Dasari, S.,
Fritsche, L. G.,
Weber, Bernhard H. F. und
et al, .
(2011)
Variations in apolipoprotein E frequency with age in a pooled analysis of a large group of older people.
American Journal of Epidemiology 173 (12), S. 1357-1364.
Volltext nicht vorhanden.
Fritsche, L. G.,
Freitag-Wolf, S.,
Bettecken, T.,
Meitinger, T.,
Keilhauer, C. N.,
Krawczak, Michael und
Weber, Bernhard H. F.
(2009)
Age-related macular degeneration and functional promoter and coding variants of the apolipoprotein E gene.
Human Mutation 30, S. 1048-1053.
Volltext nicht vorhanden.
Scholl, H. P.,
Fleckenstein, M.,
Fritsche, L. G.,
Schmitz-Valckenberg, S.,
Göbel, A.,
Adrion, C.,
Herold, C.,
Keilhauer, C. N.,
Mackensen, F.,
Mössner, A.,
Pauleikhoff, D.,
Weinberger, A. W.,
Mansmann, U.,
Holz, F. G.,
Becker, T. und
Weber, Bernhard H. F.
(2009)
CFH, C3 and ARMS2 are significant risk loci for susceptibility but not for disease progression of geographic atrophy due to AMD.
PLoS one 4 (10), e7418.
Fritsche, L. G.,
Loenhardt, T.,
Janssen, A.,
Fisher, S. A.,
Rivera, A.,
Keilhauer, C. N. und
Weber, Bernhard H. F.
(2008)
Age-related macular degeneration is associated with an unstable ARMS2 (LOC387715) mRNA.
Nature Genetics 40, S. 892-896.
Volltext nicht vorhanden.
Scholl, H. P.,
Charbel Issa, P.,
Walier, M.,
Janzer, S.,
Pollok-Kopp, B.,
Börncke, F.,
Fritsche, L. G.,
Chong, N. V.,
Fimmers, R.,
Wienker, T.,
Holz, F. G.,
Weber, Bernhard H. F. und
Oppermann, M.
(2008)
Systemic complement activation in age-related macular degeneration.
PLoS one 3 (7), e2593.
Fisher, S. A.,
Rivera, A.,
Fritsche, L. G.,
Babadjanova, G.,
Petrov, S. und
Weber, Bernhard H. F.
(2007)
Assessment of the contribution of CFH and chromosome 10q26 AMD susceptibility loci in a Russian population isolate.
British Journal of Ophthalmology 91 (5), S. 576-578.
Volltext nicht vorhanden.
Fisher, S. A.,
Rivera, A.,
Fritsche, L. G.,
Keilhauer, C. N.,
Lichtner, P.,
Meitinger, T.,
Rudolph, G. und
Weber, Bernhard H. F.
(2007)
Case–control genetic association study of fibulin-6 (FBLN6 or HMCN1) variants in age-related macular degeneration (AMD).
Human Mutation 28 (4), S. 406-413.
Volltext nicht vorhanden.
Rivera, A.,
Fisher, Sheila A.,
Fritsche, L. G.,
Keilhauer, Claudia N.,
Lichtner, Peter,
Meitinger, Thomas und
Weber, Bernhard H. F.
(2005)
Hypothetical LOC387715 is a second major susceptibility gene for age-related macular degeneration, contributing independently of complement factor H to disease risk.
Human Molecular Genetics 14, S. 3227-3236.
Volltext nicht vorhanden.
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