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Optical Coherence Tomography–Defined Changes Preceding the Development of Drusen-Associated Atrophy in Age-Related Macular Degeneration

Ophthalmology (Rochester, Minn.), 2014-12, Vol.121 (12), p.2415-2422

2014

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Associations of human retinal very long-chain polyunsaturated fatty acids with dietary lipid biomarkers

Journal of lipid research, 2016-03, Vol.57 (3), p.499-508

2016

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Macular retinal thickness differs markedly in age-related macular degeneration driven by risk polymorphisms on chromosomes 1 and 10

Scientific reports, 2020-12, Vol.10 (1), p.21093-21093, Article 21093

2020

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Perifoveal Müller Cell Depletion in a Case of Macular Telangiectasia Type 2

Ophthalmology (Rochester, Minn.), 2010-12, Vol.117 (12), p.2407-2416

2010

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n‐3 PUFA Supplementation Alters Retinal Very‐Long‐Chain‐PUFA Levels and Ratios in Diabetic Animal Models

Molecular nutrition & food research, 2019-08, Vol.63 (15), p.e1801058-n/a

2019

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Protective chromosome 1q32 haplotypes mitigate risk for age-related macular degeneration associated with the CFH-CFHR5 and ARMS2/HTRA1 loci

Human genomics, 2021-09, Vol.15 (1), p.60-60, Article 60

2021

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A role for local inflammation in the formation of drusen in the aging eye

American journal of ophthalmology, 2002-09, Vol.134 (3), p.411-431

2002

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Author Correction: Macular retinal thickness differs markedly in age-related macular degeneration driven by risk polymorphisms on chromosomes 1 and 10

Scientific reports, 2021-05, Vol.11 (1), p.11164-11164, Article 11164

2021

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Mapping the Complement Factor H-Related Protein 1 (CFHR1):C3b/C3d Interactions

PloS one, 2016-11, Vol.11 (11), p.e0166200

2016

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Y402H Polymorphism of Complement Factor H Affects Binding Affinity to C-Reactive Protein

Journal of Immunology, 2007-03, Vol.178 (6), p.3831-3836

2007

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Clinical, histological and genetic findings in a donor with a clinical history of type 1 Autoimmune Polyendocrinopathy Syndrome

American journal of ophthalmology case reports, 2022-03, Vol.25, p.101266, Article 101266

2022

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Inclusion of Genotype with Fundus Phenotype Improves Accuracy of Predicting Choroidal Neovascularization and Geographic Atrophy

Ophthalmology (Rochester, Minn.), 2013-09, Vol.120 (9), p.1880-1892

2013

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From Genes, Proteins, and Clinical Manifestation: Why Do We Need to Better Understand Age-Related Macular Degeneration?

Ophthalmology science (Online), 2022-06, Vol.2 (2), p.100174-100174, Article 100174

2022

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Cell atlas of the human ocular anterior segment: Tissue-specific and shared cell types

Proceedings of the National Academy of Sciences - PNAS, 2022-07, Vol.119 (29), p.e2200914119-e2200914119

2022

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Hypertensive disorders of pregnancy increase the risk of developing neovascular age-related macular degeneration in later life

Hypertension in pregnancy, 2019-07, Vol.38 (3), p.141-148

2019

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Extended haplotypes in the complement factor H (CFH) and CFH-related (CFHR) family of genes protect against age-related macular degeneration: Characterization, ethnic distribution and evolutionary implications

Annals of medicine (Helsinki), 2006, Vol.38 (8), p.592-604

2006

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Local cellular sources of apolipoprotein E in the human retina and retinal pigmented epithelium: implications for the process of drusen formation

American journal of ophthalmology, 2001-06, Vol.131 (6), p.767-781

2001

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Influence of ROBO1 and RORA on risk of age-related macular degeneration reveals genetically distinct phenotypes in disease pathophysiology

PloS one, 2011-10, Vol.6 (10), p.e25775-e25775

2011

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Reticular pseudodrusen: a risk factor for geographic atrophy in fellow eyes of individuals with unilateral choroidal neovascularization

Ophthalmology (Rochester, Minn.), 2014-06, Vol.121 (6), p.1252-1256

2014

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Patterns of Fundus Autofluorescence Lifetimes In Eyes of Individuals With Nonexudative Age-Related Macular Degeneration

Investigative ophthalmology & visual science, 2018-03, Vol.59 (4), p.AMD65-AMD77

2018

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Ultrastructural analysis of submacular choriocapillaris and its transport systems in AMD and aged control eyes

Experimental eye research, 2019-04, Vol.181, p.252-262

2019

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Clinical validation of a genetic model to estimate the risk of developing choroidal neovascular age-related macular degeneration

Human genomics, 2011-07, Vol.5 (5), p.420-440

2011

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Progression of Age-Related Macular Degeneration Among Individuals Homozygous for Risk Alleles on Chromosome 1 (CFH-CFHR5) or Chromosome 10 (ARMS2/HTRA1) or Both

JAMA ophthalmology, 2022-03, Vol.140 (3), p.252

2022

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The vascular geometry of the choriocapillaris is associated with spatially heterogeneous molecular exchange with the outer retina

The Journal of physiology, 2024-04, Vol.602 (7), p.1273-1295

2024

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Levels of the HtrA1 Protein in Serum and Vitreous Humor Are Independent of Genetic Risk for Age-Related Macular Degeneration at the 10q26 Locus

Investigative ophthalmology & visual science, 2024-04, Vol.65 (4), p.34-34

2024

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Optical Coherence Tomography–Defined Changes Preceding the Development of Drusen-Associated Atrophy in Age-Related Macular Degeneration

Associations of human retinal very long-chain polyunsaturated fatty acids with dietary lipid biomarkers

Macular retinal thickness differs markedly in age-related macular degeneration driven by risk polymorphisms on chromosomes 1 and 10

Perifoveal Müller Cell Depletion in a Case of Macular Telangiectasia Type 2

n‐3 PUFA Supplementation Alters Retinal Very‐Long‐Chain‐PUFA Levels and Ratios in Diabetic Animal Models

Protective chromosome 1q32 haplotypes mitigate risk for age-related macular degeneration associated with the CFH-CFHR5 and ARMS2/HTRA1 loci

A role for local inflammation in the formation of drusen in the aging eye

Author Correction: Macular retinal thickness differs markedly in age-related macular degeneration driven by risk polymorphisms on chromosomes 1 and 10

Mapping the Complement Factor H-Related Protein 1 (CFHR1):C3b/C3d Interactions

Y402H Polymorphism of Complement Factor H Affects Binding Affinity to C-Reactive Protein

Clinical, histological and genetic findings in a donor with a clinical history of type 1 Autoimmune Polyendocrinopathy Syndrome

Inclusion of Genotype with Fundus Phenotype Improves Accuracy of Predicting Choroidal Neovascularization and Geographic Atrophy

From Genes, Proteins, and Clinical Manifestation: Why Do We Need to Better Understand Age-Related Macular Degeneration?

Cell atlas of the human ocular anterior segment: Tissue-specific and shared cell types

Hypertensive disorders of pregnancy increase the risk of developing neovascular age-related macular degeneration in later life

Extended haplotypes in the complement factor H (CFH) and CFH-related (CFHR) family of genes protect against age-related macular degeneration: Characterization, ethnic distribution and evolutionary implications

Local cellular sources of apolipoprotein E in the human retina and retinal pigmented epithelium: implications for the process of drusen formation

Influence of ROBO1 and RORA on risk of age-related macular degeneration reveals genetically distinct phenotypes in disease pathophysiology

Reticular pseudodrusen: a risk factor for geographic atrophy in fellow eyes of individuals with unilateral choroidal neovascularization

Patterns of Fundus Autofluorescence Lifetimes In Eyes of Individuals With Nonexudative Age-Related Macular Degeneration

Ultrastructural analysis of submacular choriocapillaris and its transport systems in AMD and aged control eyes

Clinical validation of a genetic model to estimate the risk of developing choroidal neovascular age-related macular degeneration

Progression of Age-Related Macular Degeneration Among Individuals Homozygous for Risk Alleles on Chromosome 1 (CFH-CFHR5) or Chromosome 10 (ARMS2/HTRA1) or Both

The vascular geometry of the choriocapillaris is associated with spatially heterogeneous molecular exchange with the outer retina

Levels of the HtrA1 Protein in Serum and Vitreous Humor Are Independent of Genetic Risk for Age-Related Macular Degeneration at the 10q26 Locus

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