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Scholar Results 1 - 10 of about 16 citing Fisher: Assessment of the contribution of CFH and chromosome 10q26 AMD susceptibility loci.... (0.09 sec) 

Genetic susceptibility to age-related macular degeneration: a paradigm for dissecting …

- oxfordjournals.org
A Swaroop, KEH Branham, W Chen, G … - Human molecular genetics, 2007 - Oxford Univ Press
Age-related macular degeneration (AMD) is a progressive neurodegenerative
disease, which affects quality of life for millions of elderly individuals
worldwide. AMD is associated with a diverse spectrum of clinical ...
Cited by 46 - Related articles - BL Direct - All 6 versions

Association of complement factor H and LOC387715 genotypes with response of exudative …


MA Brantley, AM Fang, JM King, A Tewari, SM … - Ophthalmology, 2007 - Elsevier
Cited by 20 - Related articles - All 5 versions

Genetic markers and biomarkers for age-related macular degeneration


RJ Ross, V Verma, KI Rosenberg, CC Chan, J … - Expert review of ophthalmology, 2007 - pubmedcentral.nih.gov
Age-related macular degeneration (AMD) is the leading cause of visual impairment
and blindness in the USA. Although the treatment of AMD has evolved to include
laser photocoagulation, photodynamic therapy, surgical macular ...
Cited by 15 - Related articles - BL Direct - All 4 versions

C2 and CFB genes in age-related maculopathy and joint action with CFH and LOC387715 …


J Jakobsdottir, YP Conley, DE Weeks, RE … - PloS one, 2008 - pubmedcentral.nih.gov
Age-related maculopathy (ARM) is a common cause of visual impairment in the
elderly populations of industrialized countries and significantly affects the
quality of life of those suffering from the disease. Variants within two ...
Cited by 11 - Related articles - All 7 versions

Variants in the 10q26 gene cluster (LOC387715 and HTRA1) exhibit enhanced risk of age- …

- iovs.org
I Kaur, S Katta, A Hussain, N Hussain, A … - Investigative Ophthalmology & Visual Science, 2008 - ARVO
RESULTS. Resequencing revealed seven different SNPs in these genes, of which
significant associations were noted with the risk alleles of rs10490924 (T
allele; P = 5.34 x 10 –12 ) in LOC387715, and rs11200638 (A allele; P = ...
Cited by 7 - Related articles - BL Direct - All 2 versions

Complement factor H polymorphisms, renal phenotypes and age-related macular …


C Xing, TA Sivakumaran, JJ Wang, E … - Genes and Immunity, 2008 - nature.com
Complement factor H (CFH) is a key regulator of the alternative pathway of
complement and its mutations have been associated with membranoproliferative
glomerulonephritis type II, atypical hemolytic uremic syndrome and ...
Cited by 6 - Related articles - BL Direct - All 3 versions

Phenotype analysis of patients with the risk variant LOC387715 (A69S) in age-related …


RK Shuler, S Schmidt, P Gallins, MA Hauser, … - American Journal of Ophthalmology, 2007 - Elsevier
The number of AMD cases in each group was 164 cases (two risk alleles), 330
cases (one risk allele), and 281 cases (zero risk allele). The mean age at
examination for homozygous carriers of the LOC387715 risk allele was ...
Cited by 5 - Related articles - All 22 versions

Genotype–phenotype correlation of age-related macular degeneration: influence of …


I Droz, I Mantel, A Ambresin, M Faouzi, DF … - British Journal of Ophthalmology, 2008 - bjo.bmj.com
Results: In this Swiss population, an OR of 2.95 was confirmed for AMD in the
presence of at least one risk C allele and OR of 9.05 for the CC homozygotes,
corrected for age and sex. No difference was found between the AMD stages. ...
Cited by 4 - Related articles - BL Direct - All 4 versions

Association of complement factor H Y402H polymorphism with phenotype of neovascular age …


I Chowers, Y Cohen, N Goldenberg-Cohen, J … - Molecular Vision, 2008 - pubmedcentral.nih.gov
The Tyr402His variant of complement factor H (CFH) is associated with
age-related macular degeneration (AMD) in several populations. Our aim was to
evaluate if this single nucleotide polymorphism (SNP) is associated with ...
Cited by 3 - Related articles - All 6 versions

ARMS2/HTRA1 and CFH polymorphisms are not associated with choroidal neovascularization …


H Nakanishi, N Gotoh, R Yamada, K Yamashiro, … - Eye, 2009 - nature.com
Highly myopic elderly Japanese patients with and without CNV were genotyped for
three AMD-associated single nucleotide polymorphisms (SNPs), namely rs10490924
(A69S) of ARMS2, rs11200638 of HTRA1, and rs1061170 (Y402H) of complement ...
Related articles - All 3 versions


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