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Author Details
Full Name
Andrea J Richardson
Affiliation
Royal Victorian Eye and Ear Hospital
ORCID
Career Start Year
2003
Papers
50
H Index
28
Expertise
CM4AI Collaborator
PMID
Paper Title
Journal Title
Published Year
33649486
A multi-ethnic genome-wide association study implicates collagen matrix integrity and cell differentiation pathways in keratoconus.
Commun Biol
2021
31855235
Association of Genetic Variation With Keratoconus.
JAMA Ophthalmol
2020
31819893
Do age-related macular degeneration genes show association with keratoconus?
Eye Vis (Lond)
2019
29625465
Gene Expression and Pathways Underlying Form Deprivation Myopia in the Guinea Pig Sclera.
Invest Ophthalmol Vis Sci
2018
29852030
Association of Genetic Variants With Response to Anti-Vascular Endothelial Growth Factor Therapy in Age-Related Macular Degeneration.
JAMA Ophthalmol
2018
29686068
Recurrent structural variation, clustered sites of selection, and disease risk for the complement factor H (<i>CFH</i>) gene family.
Proc Natl Acad Sci U S A
2018
26691988
A large genome-wide association study of age-related macular degeneration highlights contributions of rare and common variants.
Nat Genet
2016
27892514
GWAS study using DNA pooling strategy identifies association of variant rs4910623 in OR52B4 gene with anti-VEGF treatment response in age-related macular degeneration.
Sci Rep
2016
27090374
Multiallelic copy number variation in the complement component 4A (C4A) gene is associated with late-stage age-related macular degeneration (AMD).
J Neuroinflammation
2016
25823570
Identification of myopia-associated WNT7B polymorphisms provides insights into the mechanism underlying the development of myopia.
Nat Commun
2015
26207622
Association Study of Mannose-Binding Lectin Levels and Genetic Variants in Lectin Pathway Proteins with Susceptibility to Age-Related Macular Degeneration: A Case-Control Study.
PLoS One
2015
25627090
Age-related macular degeneration phenotypes associated with mutually exclusive homozygous risk variants in CFH and HTRA1 genes.
Retina
2015
24416191
Association of the hepatocyte growth factor gene with keratoconus in an Australian population.
PLoS One
2014
25077528
Polymorphisms in the APOE gene and the location of retinal fluid in eyes with neovascular age-related macular degeneration.
Retina
2014
23131718
Genetic association of refractive error and axial length with 15q14 but not 15q25 in the Blue Mountains Eye Study cohort.
Ophthalmology
2013
24391822
Proof of concept, randomized, placebo-controlled study of the effect of simvastatin on the course of age-related macular degeneration.
PLoS One
2013
24036949
Identification of a rare coding variant in complement 3 associated with age-related macular degeneration.
Nat Genet
2013
24265017
Evaluating the association between keratoconus and the corneal thickness genes in an independent Australian population.
Invest Ophthalmol Vis Sci
2013
23592919
Association of the del443ins54 at the ARMS2 locus in Indian and Australian cohorts with age-related macular degeneration.
Mol Vis
2013
23474815
Meta-analysis of genome-wide association studies in five cohorts reveals common variants in RBFOX1, a regulator of tissue-specific splicing, associated with refractive error.
Hum Mol Genet
2013
23455636
Seven new loci associated with age-related macular degeneration.
Nat Genet
2013
23582991
Genetic influences on the outcome of anti-vascular endothelial growth factor treatment in neovascular age-related macular degeneration.
Ophthalmology
2013
23303206
A rare functional haplotype of the P2RX4 and P2RX7 genes leads to loss of innate phagocytosis and confers increased risk of age-related macular degeneration.
FASEB J
2013
23149126
Variants in the VEGFA gene and treatment outcome after anti-VEGF treatment for neovascular age-related macular degeneration.
Ophthalmology
2013
22328704
Apolipoprotein E gene associations in age-related macular degeneration: the Melbourne Collaborative Cohort Study.
Am J Epidemiol
2012
22936692
Can genetic associations change with age? CFH and age-related macular degeneration.
Hum Mol Genet
2012
22705344
Heritability and genome-wide association study to assess genetic differences between advanced age-related macular degeneration subtypes.
Ophthalmology
2012
22558131
Comprehensive analysis of Copy Number Variation of genes at chromosome 1 and 10 loci associated with late age related macular degeneration.
PLoS One
2012
21245410
Variants in the APOE gene are associated with improved outcome after anti-VEGF treatment for neovascular AMD.
Invest Ophthalmol Vis Sci
2011
21665990
Common variants near FRK/COL10A1 and VEGFA are associated with advanced age-related macular degeneration.
Hum Mol Genet
2011
21498607
Identification of urinary biomarkers for age-related macular degeneration.
Invest Ophthalmol Vis Sci
2011
20605213
C-reactive protein levels and complement factor H polymorphism interaction in age-related macular degeneration and its progression.
Ophthalmology
2010
20445115
An intergenic region between the tagSNP rs3793917 and rs11200638 in the HTRA1 gene indicates association with age-related macular degeneration.
Invest Ophthalmol Vis Sci
2010
20499266
Analysis of glutathione S-transferase Pi isoform (GSTP1) single-nucleotide polymorphisms and macular telangiectasia type 2.
Int Ophthalmol
2010
18806293
Analysis of rare variants in the complement component 2 (C2) and factor B (BF) genes refine association for age-related macular degeneration (AMD).
Invest Ophthalmol Vis Sci
2009
19365569
Fine mapping linkage analysis identifies a novel susceptibility locus for myopia on chromosome 2q37 adjacent to but not overlapping MYP12.
Mol Vis
2009
18203751
Gene-environment interaction in progression of AMD: the CFH gene, smoking and exposure to chronic infection.
Hum Mol Genet
2008
17205325
Heritability and shared environment estimates for myopia and associated ocular biometric traits: the Genes in Myopia (GEM) family study.
Hum Genet
2007
17962440
Genetic mapping of myopia susceptibility loci.
Invest Ophthalmol Vis Sci
2007
17898262
Linkage replication of the MYP12 locus in common myopia.
Invest Ophthalmol Vis Sci
2007
18079689
A tag-single nucleotide polymorphisms approach to the vascular endothelial growth factor-A gene in age-related macular degeneration.
Mol Vis
2007
17568317
Evaluation of accuracy in proband-reported family history and its determinants: the Genes in Myopia family study.
Optom Vis Sci
2007
17362467
Analysis of the RDS/peripherin gene in age-related macular degeneration.
Clin Exp Ophthalmol
2007
16453339
Apolipoprotein (APOE) gene is associated with progression of age-related macular degeneration (AMD).
Hum Mutat
2006
17003406
Analysis of the Y402H variant of the complement factor H gene in age-related macular degeneration.
Invest Ophthalmol Vis Sci
2006
16750666
Blood storage at 4 degrees C-factors involved in DNA yield and quality.
J Lab Clin Med
2006
15953455
The Q368STOP myocilin mutation in a population-based cohort: the Blue Mountains Eye Study.
Am J Ophthalmol
2005
16226543
A common disease haplotype for the Q368STOP mutation of the myocilin gene in Australian and Canadian glaucoma families.
Am J Ophthalmol
2005
15498064
Analysis of optineurin (OPTN) gene mutations in subjects with and without glaucoma: the Blue Mountains Eye Study.
Clin Exp Ophthalmol
2004
12522550
Analysis of 15 primary open-angle glaucoma families from Australia identifies a founder effect for the Q368STOP mutation of myocilin.
Hum Genet
2003
1 - 50 of 50
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Columbia University Medical Center
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