Denise J. Morgan

Department of Ophthalmology and Visual Sciences, University of Utah

Affiliated withUniversity of Utah

Research Area

Biography

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JoVE Journal Publications

ArticleTotal : 1	Year
Publication title	2025

Other Publications

Article	Year
Influence of ROBO1 and RORA on risk of age-related macular degeneration reveals genetically distinct phenotypes in disease pathophysiology. PloS one\| PubMed ID: 21998696	2011
Identification of a rare coding variant in complement 3 associated with age-related macular degeneration. Nature genetics\| PubMed ID: 24036949	2013
FLT1 genetic variation predisposes to neovascular AMD in ethnically diverse populations and alters systemic FLT1 expression. Investigative ophthalmology & visual science\| PubMed ID: 24812550	2014
Rare and common variants in extracellular matrix gene Fibrillin 2 (FBN2) are associated with macular degeneration. Human molecular genetics\| PubMed ID: 24899048	2014
Differential Gene Expression in Age-Related Macular Degeneration. Cold Spring Harbor perspectives in medicine\| PubMed ID: 25342062	2014
Ancestry of the Timorese: age-related macular degeneration associated genotype and allele sharing among human populations from throughout the world. Frontiers in genetics\| PubMed ID: 26217379	2015
A large genome-wide association study of age-related macular degeneration highlights contributions of rare and common variants. Nature genetics\| PubMed ID: 26691988	2016
Genetics of age-related macular degeneration (AMD). Human molecular genetics\| PubMed ID: 28854576	2017
Genetics of age-related macular degeneration (AMD). Human molecular genetics\| PubMed ID: 28977452	2017
The Utah Protocol for Postmortem Eye Phenotyping and Molecular Biochemical Analysis. Investigative ophthalmology & visual science\| PubMed ID: 30924847	2019
ALPK1 missense pathogenic variant in five families leads to ROSAH syndrome, an ocular multisystem autosomal dominant disorder. Genetics in medicine : official journal of the American College of Medical Genetics\| PubMed ID: 30967659	2019
Progressive optic nerve changes in cavitary optic disc anomaly: integration of copy number alteration and cis-expression quantitative trait loci to assess disease etiology. BMC medical genetics\| PubMed ID: 31029096	2019
Generation, transcriptome profiling, and functional validation of cone-rich human retinal organoids. Proceedings of the National Academy of Sciences of the United States of America\| PubMed ID: 31072937	2019
Genetic Epidemiologic Analysis of Hypertensive Retinopathy in an Underrepresented and Rare Federally Recognized Native American Population of the Intermountain West. Journal of community medicine & public health\| PubMed ID: 31475247	2019
Structure and mechanics of the vitreoretinal interface. Journal of the mechanical behavior of biomedical materials\| PubMed ID: 35963021	2022
Confocal reflectance microscopy for mapping collagen fiber organization in the vitreous gel of the eye. Biomedical optics express\| PubMed ID: 36874496	2023