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ARVO Annual Meeting Abstract June 2020

Single-nuclei RNA-seq provides comprehensive transcriptomic classification of human retinal cell types.

Xuesen Cheng; Qingnan Liang; Leah A. Owen; Akbar Shakoor; Albert T Vitale; Ivana K Kim; Denise J. Morgan; Yumei Li; Margaret M DeAngelis; Rui Chen

Invest. Ophthalmol. Vis. Sci.. 2020; 61(7):1956. doi:

ARVO Annual Meeting Abstract June 2020

Retinal and systemic disease of Native Americans in the Intermountain West

Patrice M Hicks; Benjamin Haaland; Michael Feehan; Alan S Crandall; Jeff H Pettey; Albert T Vitale; M Elizabeth Hartnett; Paul S Bernstein; Akbar Shakoor; Sandra F Sieminski; Julia P Shulman; Ivana K Kim; Leah A. Owen; Maureen Murtaugh; Albert Noyes; Margaret M DeAngelis

Invest. Ophthalmol. Vis. Sci.. 2020; 61(7):3340. doi:

ARVO Annual Meeting Abstract June 2020

A multi-generational family affected by cavitary optic disc anomaly

Bradley Jacobsen; Moussa A. Zouache; Margaret M DeAngelis; Paul S Bernstein

Invest. Ophthalmol. Vis. Sci.. 2020; 61(7):2696. doi:

ARVO Annual Meeting Abstract July 2019

HTRA1 gene interaction network informs Age-Related Macular Degeneration (AMD) risk

Leah Owen; Patrice Marie Hicks; Denise J Morgan; Jeeyun Ahn; Giuliana Silvestri; Joan W Miller; Kyu Hyung Park; maria G Kotoula; Ivana K Kim; Lindsay A Farrer; Neena B Haider; Margaret M DeAngelis

Invest. Ophthalmol. Vis. Sci.. 2019; 60(9):4895. doi:

ARVO Annual Meeting Abstract July 2019

Genetic Epidemiologic Analysis of Hypertensive Retinopathy (HTR) Reveals Unique Risk in a Native American Population

Patrice Marie Hicks; Samuel Collazo-Melendez; Albert T Vitale; William Self; M Elizabeth Hartnett; Paul S Bernstein; Denise J Morgan; Michael Feehan; Akbar Shakoor; Ivana K Kim; Leah A. Owen; Margaret M. DeAngelis

Invest. Ophthalmol. Vis. Sci.. 2019; 60(9):5225. doi:

Retina March 2019

The Utah Protocol for Postmortem Eye Phenotyping and Molecular Biochemical Analysis

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Leah A. Owen; Akbar Shakoor; Denise J. Morgan; Andre A. Hejazi; M. Wade McEntire; Jared J. Brown; Lindsay A. Farrer; Ivana Kim; Albert Vitale; Margaret M. DeAngelis
TAGS: autopsy, body tissue, donors, eye, phenotype determination, phenotype
Invest. Ophthalmol. Vis. Sci.. 2019; 60(4):1204-1212. doi: https://doi.org/10.1167/iovs.18-24254

Includes: Supplemental Content

ARVO Annual Meeting Abstract July 2018

Long-range polymerase chain reaction validates copy number variation in autosomal dominant optic pit

Eileen Hwang; Denise Morgan; Leah Owen; John H Fingert; Paul S Bernstein; Margaret M DeAngelis

Invest. Ophthalmol. Vis. Sci.. 2018; 59(9):5402. doi:

ARVO Annual Meeting Abstract July 2018

An integrative approach to identify transcript isoforms essential for retina function

Jun Wang; Rachayata Dharmat; Yumei Li; Leah Owen; Margaret M DeAngelis; Rui Chen

Invest. Ophthalmol. Vis. Sci.. 2018; 59(9):2350. doi:

Retina March 2018

Genetic Risk Factors for Radiation Vasculopathy

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Thanos D. Papakostas; Margaux A. Morrison; Anne Marie Lane; Caroline Awh; Margaret M. DeAngelis; Evangelos S. Gragoudas; Ivana K. Kim
TAGS: genetic risk, radiation, single nucleotide polymorphism, vascular diseases, visual impairment, visual acuity
Invest. Ophthalmol. Vis. Sci.. 2018; 59(3):1547-1553. doi: https://doi.org/10.1167/iovs.17-22791

ARVO Annual Meeting Abstract June 2017

An Alu-mediated copy number variation mediates progressive optic nerve cupping in autosomal dominant optic pit

Eileen Hwang; Denise Morgan; James L Zimmerman; Claude F Burgoyne; Paul S Bernstein; Margaret M DeAngelis

Invest. Ophthalmol. Vis. Sci.. 2017; 58(8):576. doi:

ARVO Annual Meeting Abstract June 2017

Master Modifier Nr2e3 Rescues Disease and Promotes Retina Homeostasis in Multiple Models of RP

Neena B Haider; Ana Maria Olivares; Kyle Flattery; Yinan Han; Jessica Capri; Margaret M DeAngelis

Invest. Ophthalmol. Vis. Sci.. 2017; 58(8):1575. doi:

ARVO Annual Meeting Abstract September 2016

Genetic Risk Factors for Radiation Vasculopathy

Thanos D Papakostas; Anne Marie Lane; Caroline Awh; Margaux Morrison; Margaret M DeAngelis; Evangelos S Gragoudas; Ivana K Kim

Invest. Ophthalmol. Vis. Sci.. 2016; 57(12):4096. doi:

ARVO Annual Meeting Abstract September 2016

CRISPR/dCas9 to treat neovascular age-related macular degeneration

Katie L Pennington; Sandeep Kumar; Alex Jones; Margaret M DeAngelis; Yingbin Fu

Invest. Ophthalmol. Vis. Sci.. 2016; 57(12):4436. doi:

ARVO Annual Meeting Abstract September 2016

A Predictive Model of Retinopathy of Prematurity Risk and Severity

Leah Owen; Margaux Morrisson; Bradley Yoder; Margaret M DeAngelis

Invest. Ophthalmol. Vis. Sci.. 2016; 57(12) doi:

ARVO Annual Meeting Abstract September 2016

Identifying Signature Profiles of Transcription Factors in Human and Mouse Models of Retinal Disease

Ana Maria Olivares; Juliana Veira; Kyle Flattery; Margaux Morrisson; Margaret M DeAngelis; Neena B Haider

Invest. Ophthalmol. Vis. Sci.. 2016; 57(12) doi:

ARVO Annual Meeting Abstract June 2015

The nuclear hormone receptor gene Nr2c1 ( Tr2 ) is a Critical Regulator of Cone Photoreceptor Cell Patterning

Ana Maria Olivares; Yinan Han; David Soto; Kyle Flattery; Joe Marini; Pascal Escher; Margaret M DeAngelis; Neena B Haider

Invest. Ophthalmol. Vis. Sci.. 2015; 56(7 ):4639. doi:

Clinical and Epidemiologic Research October 2014

Genetic Variants Associated With Severe Retinopathy of Prematurity in Extremely Low Birth Weight Infants

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M. Elizabeth Hartnett; Margaux A. Morrison; Silvia Smith; Tammy L. Yanovitch; Terri L. Young; Tarah Colaizy; Allison Momany; John Dagle; Waldemar A. Carlo; Erin A. S. Clark; Grier Page; Jeff Murray; Margaret M. DeAngelis; C. Michael Cotten
TAGS: brain-derived neurotrophic factor, cohort studies, extremely low birth weight infant, genes, genetics, infant, retinopathy of prematurity, universities, meta-analysis, single nucleotide polymorphism
Invest. Ophthalmol. Vis. Sci.. 2014; 55(10):6194-6203. doi: https://doi.org/10.1167/iovs.14-14841

Genetics June 2014

FLT1 Genetic Variation Predisposes to Neovascular AMD in Ethnically Diverse Populations and Alters Systemic FLT1 Expression

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Leah A. Owen; Margaux A. Morrison; Jeeyun Ahn; Se Joon Woo; Hajime Sato; Rosann Robinson; Denise J. Morgan; Fani Zacharaki; Marina Simeonova; Hironori Uehara; Usha Chakravarthy; Ruth E. Hogg; Balamurali K. Ambati; Maria Kotoula; Wolfgang Baehr; Neena B. Haider; Giuliana Silvestri; Joan W. Miller; Evangelia E. Tsironi; Lindsay A. Farrer; Ivana K. Kim; Kyu Hyung Park; Margaret M. DeAngelis
TAGS: cohort studies, exudative age-related macular degeneration, genetics, single nucleotide polymorphism, vascular endothelial growth factor a
Invest. Ophthalmol. Vis. Sci.. 2014; 55(6):3543-3554. doi: https://doi.org/10.1167/iovs.14-14047

Includes: Supplemental Content

ARVO Annual Meeting Abstract April 2014

Clinical characteristics of uveal melanoma in patients with germline BAP1 mutations

Mrinali Patel; Margaret M DeAngelis; Anne Marie Lane; Katie Mayne; Evangelos S Gragoudas; Ivana K Kim

Invest. Ophthalmol. Vis. Sci.. 2014; 55(13):6443. doi:

ARVO Annual Meeting Abstract April 2014

Nuclear Hormone Receptors are Potent Genetic Modifiers that Rescue Multiple Models of Retinal Degeneration

Neena B Haider; Ana B Olivares; Nelly M Cruz; Pascal Escher; Margaret M DeAngelis

Invest. Ophthalmol. Vis. Sci.. 2014; 55(13):2182. doi:

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Single-nuclei RNA-seq provides comprehensive transcriptomic classification of human retinal cell types.

Retinal and systemic disease of Native Americans in the Intermountain West

A multi-generational family affected by cavitary optic disc anomaly

HTRA1 gene interaction network informs Age-Related Macular Degeneration (AMD) risk

Genetic Epidemiologic Analysis of Hypertensive Retinopathy (HTR) Reveals Unique Risk in a Native American Population

The Utah Protocol for Postmortem Eye Phenotyping and Molecular Biochemical Analysis

Long-range polymerase chain reaction validates copy number variation in autosomal dominant optic pit

An integrative approach to identify transcript isoforms essential for retina function

Genetic Risk Factors for Radiation Vasculopathy

An Alu-mediated copy number variation mediates progressive optic nerve cupping in autosomal dominant optic pit

Master Modifier Nr2e3 Rescues Disease and Promotes Retina Homeostasis in Multiple Models of RP

Genetic Risk Factors for Radiation Vasculopathy

CRISPR/dCas9 to treat neovascular age-related macular degeneration

A Predictive Model of Retinopathy of Prematurity Risk and Severity

Identifying Signature Profiles of Transcription Factors in Human and Mouse Models of Retinal Disease

The nuclear hormone receptor gene Nr2c1 ( Tr2 ) is a Critical Regulator of Cone Photoreceptor Cell Patterning

Genetic Variants Associated With Severe Retinopathy of Prematurity in Extremely Low Birth Weight Infants

FLT1 Genetic Variation Predisposes to Neovascular AMD in Ethnically Diverse Populations and Alters Systemic FLT1 Expression

Clinical characteristics of uveal melanoma in patients with germline BAP1 mutations

Nuclear Hormone Receptors are Potent Genetic Modifiers that Rescue Multiple Models of Retinal Degeneration

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