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ARVO Annual Meeting Abstract June 2024

Choroidal Imaging Biomarkers as Predictors of Conversion to Neovascular Age-related Macular Degeneration

Arman Zarnegar; Stavan V Shah; Nicola Valsecchi; Shiva Deena Yagobian; Anthony Tang; Danilo Iannetta; Jay Chhablani

Invest. Ophthalmol. Vis. Sci.. 2024; 65(7):2272.

ARVO Annual Meeting Abstract June 2024

Analysis of Biomarkers Predictive of Neovascular Age-Related Macular Degeneration

Stavan V Shah; Nicola Valsecchi; Arman Zarnegar; Shiva Deena Yagobian; Anthony Tang; Amrish Selvam; Nikita Kedia; Danilo Iannetta; Jay Chhablani

Invest. Ophthalmol. Vis. Sci.. 2024; 65(7):4364.

ARVO Annual Meeting Abstract June 2024

Assessment of clinical and Optical Coherence Tomography findings in patients with dry Age-related Macular Degeneration (AMD) converting to wet AMD according to the condition of the fellow eye

Nicola Valsecchi; Arman Zarnegar; Stavan V Shah; Anthony Tang; Shiva Deena Yagobian; Luigi Fontana; Danilo Iannetta; Jay Chhablani

Invest. Ophthalmol. Vis. Sci.. 2024; 65(7):5704.

ARVO Annual Meeting Abstract June 2023

Optical coherence tomography analysis of patients with newly neovascular age-related macular degeneration in one eye and dry age-related macular degeneration in the fellow eye.

Sonny Caplash; Doowon Huh; Stavan V Shah; Shiva Yagobian; Anthony Tang; Jay Chhablani

Invest. Ophthalmol. Vis. Sci.. 2023; 64(8):2192.

Special Issue May 2023

IMI—Management and Investigation of High Myopia in Infants and Young Children

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Ian Flitcroft; John Ainsworth; Audrey Chia; Susan Cotter; Elise Harb; Zi-Bing Jin; Caroline C. W. Klaver; Anthony T. Moore; Ken K. Nischal; Kyoko Ohno-Matsui; Evelyn A. Paysse; Michael X. Repka; Irina Y. Smirnova; Martin Snead; Virginie J. M. Verhoeven; Pavan K. Verkicharla
TAGS: child, myopia
Invest. Ophthalmol. Vis. Sci.. 2023; 64(6):3. https://doi.org/10.1167/iovs.64.6.3

Genetics August 2022

Dominant Cone Rod Dystrophy, Previously Assigned to a Missense Variant in RIMS1 , Is Fully Explained by Co-Inheritance of a Dominant Allele of PROM1

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Maria Pilar Martin-Gutierrez; Elena R. Schiff; Genevieve Wright; Naushin Waseem; Omar A. Mahroo; Michel Michaelides; Anthony T. Moore; Andrew R. Webster; Gavin Arno; for the Genomics England Research Consortium
TAGS: alleles, genetic inheritance, progressive cone-rod dystrophy, retinitis pigmentosa, family, macular dystrophy, datasets
Invest. Ophthalmol. Vis. Sci.. 2022; 63(9):14. https://doi.org/10.1167/iovs.63.9.14

ARVO Annual Meeting Abstract June 2022

The Summation of Diverse Synaptic and Intrinsic Drives across M1 Ganglion Cell Photoreceptors

Elliott Milner; Hannah Blume; Michael Charles Brown; Todd Anthony; Michael Tri Hoang Do

Invest. Ophthalmol. Vis. Sci.. 2022; 63(7):4578 – F0440.

ARVO Annual Meeting Abstract June 2022

Using human LCA7 retinal organoids to establish allele-specific editing as a therapy

Kathleen R Chirco; Shereen Chew; Anthony T Moore; Jacque L Duncan; Renee Christine Ryals; Martha Neuringer; Deepak A Lamba

Invest. Ophthalmol. Vis. Sci.. 2022; 63(7):81 – A0054.

ARVO Annual Meeting Abstract June 2022

Long-term efficacy and safety of satralizumab in adults with AQP4-IgG-seropositive neuromyelitis optica spectrum disorder (NMOSD): results from the Phase 3 SAkura studies

Shervin Gholizadeh Moghaddam; Jeffrey L Bennett; Edward Fox; Benjamin Greenberg; Brian G Weinshenker; Anthony Traboulsee; Michael R Yeaman; Kathleen Blondeau; Kristina Weber; Ivana Vodopivec; Michael Levy

Invest. Ophthalmol. Vis. Sci.. 2022; 63(7):1585 – A0374.

Genetics December 2021

SSBP1 -Disease Update: Expanding the Genetic and Clinical Spectrum, Reporting Variable Penetrance and Confirming Recessive Inheritance

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Neringa Jurkute; Fabiana D'Esposito; Anthony G. Robson; Robert D. S. Pitceathly; Francesca Cordeiro; F. Lucy Raymond; Anthony T. Moore; Michel Michaelides; Patrick Yu-Wai-Man; Andrew R. Webster; Gavin Arno; for the Genomics England Research Consortium
TAGS: family, genetics, optic atrophy, penetrance, genetic, phenotype, proteins, recessive inheritance, retinal dystrophies, dna, mitochondrial, phenotype determination
Invest. Ophthalmol. Vis. Sci.. 2021; 62(15):12. https://doi.org/10.1167/iovs.62.15.12

ARVO Annual Meeting Abstract June 2021

Establishing an in vitro human Leber congenital amaurosis model system

Kathleen R Chirco; Shereen Chew; Jacque L Duncan; Anthony T Moore; Deepak A Lamba

Invest. Ophthalmol. Vis. Sci.. 2021; 62(8):1693.

ARVO Annual Meeting Abstract June 2021

Investigating the genotype-phenotype relationships of patient specific PNPLA6 mutations

James Liu; Cara Lwin; Yi He; Gavin Arno; Anthony T Moore; Andrew Webster; Laryssa A Huryn; Bin Guan; Robert B Hufnagel

Invest. Ophthalmol. Vis. Sci.. 2021; 62(8):1519.

ARVO Annual Meeting Abstract June 2021

Efficacy and safety of satralizumab in neuromyelitis optica spectrum disorder (NMOSD): Results from open-label extension periods of SAkuraSky and SAkuraStar

Zdenka Haskova; Benjamin Greenberg; Jeffrey Bennett; Brian G. Weinshenker; Anthony Traboulsee; Michael R. Yeaman; Kristina Weber; Kathleen Blondeau; H-Christian von Büdingen; Daniela Stokmaier; Gaëlle Klingelschmitt

Invest. Ophthalmol. Vis. Sci.. 2021; 62(8):3475.

ARVO Annual Meeting Abstract June 2021

Preoperative Imaging and Surgical Outcomes After Epiretinal Membrane Peeling in Pediatric Combined Hamartoma of the Retina and Retinal Pigment Epithelium

Anthony Therattil; Sophie Cai; Arathi Ponugoti; Cynthia A Toth; Lejla Vajzovic

Invest. Ophthalmol. Vis. Sci.. 2021; 62(8):3678.

Genetics May 2021

Expanding the FDXR -Associated Disease Phenotype: Retinal Dystrophy Is a Recurrent Ocular Feature

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Neringa Jurkute; Priya D. Shanmugarajah; Marios Hadjivassiliou; Jenny Higgs; Miodrag Vojcic; Iain Horrocks; Yann Nadjar; Valerie Touitou; Guy Lenaers; Roy Poh; James Acheson; Anthony G. Robson; F. Lucy Raymond; Mary M. Reilly; Patrick Yu-Wai-Man; Anthony T. Moore; Andrew R. Webster; Gavin Arno; for the Genomics England Research Consortium
TAGS: family, optic atrophy, phenotype, recurrence, retinal dystrophies
Invest. Ophthalmol. Vis. Sci.. 2021; 62(6):2. https://doi.org/10.1167/iovs.62.6.2

Includes: Supplemental Content

ARVO Annual Meeting Abstract June 2020

Efficacy and safety of satralizumab from two phase 3 trials in neuromyelitis optica spectrum disorder

Zdenka Haskova; Benjamin Frishberg; Jerome de Seze; Brian Weinshenker; Yusuke Terada; Yuichi Kawata; Athos Gianella-Borradori; Christian von Büdingen; Gaelle Klingelschmitt; Anthony Traboulsee; Takashi Yamamura

Invest. Ophthalmol. Vis. Sci.. 2020; 61(7):3173.

ARVO Annual Meeting Abstract June 2020

Measuring Volume of Subretinal Injections with Commercial Intraoperative OCT

Anthony Therattil; William Raynor; Jianwei David Li; Christian Viehland; Joseph A Izatt; Cynthia Toth; Lejla Vajzovic

Invest. Ophthalmol. Vis. Sci.. 2020; 61(7):791.

Articles May 2020

Quantifying the Separation Between the Retinal Pigment Epithelium and Bruch's Membrane using Optical Coherence Tomography in Patients with Inherited Macular Degeneration

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Kamron N. Khan; Shyamanga Borooah; Leonardo Lando; Kunny Dans; Omar A. Mahroo; Amit Meshi; Angelos Kalitzeos; Georgios Agorogiannis; Sasan Moghimi; William R. Freeman; Andrew R. Webster; Anthony T. Moore; Martin McKibbin; Michel Michaelides
TAGS: bruch's basal membrane, macular degeneration, optical coherence tomography, retinal pigment epithelium, spectral domain-optical coherence tomography, eye, drusen
Trans. Vis. Sci. Tech.. 2020; 9(6):26. https://doi.org/10.1167/tvst.9.6.26

Includes: Supplemental Content

ARVO Annual Meeting Abstract July 2019

Progression to blindness in 20 years among patients with glaucomatous visual fields in a tertiary hospital in the Philippines

Cathleen Camille Narciso Cabrera; Joseph Anthony Tumbocon; John Mark de Leon

Invest. Ophthalmol. Vis. Sci.. 2019; 60(9):2474.

ARVO Annual Meeting Abstract July 2019

Portable VEP Diagnostics for NeuroVisual Disorders

Srinivas Sridhar; Craig Versek; Ali Banijamali; Anthony Tran; Armando Cardozo; Kameran Lashkari; Peter Bex

Invest. Ophthalmol. Vis. Sci.. 2019; 60(9):3591.

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Choroidal Imaging Biomarkers as Predictors of Conversion to Neovascular Age-related Macular Degeneration

Analysis of Biomarkers Predictive of Neovascular Age-Related Macular Degeneration

Assessment of clinical and Optical Coherence Tomography findings in patients with dry Age-related Macular Degeneration (AMD) converting to wet AMD according to the condition of the fellow eye

Optical coherence tomography analysis of patients with newly neovascular age-related macular degeneration in one eye and dry age-related macular degeneration in the fellow eye.

IMI—Management and Investigation of High Myopia in Infants and Young Children

Dominant Cone Rod Dystrophy, Previously Assigned to a Missense Variant in RIMS1 , Is Fully Explained by Co-Inheritance of a Dominant Allele of PROM1

The Summation of Diverse Synaptic and Intrinsic Drives across M1 Ganglion Cell Photoreceptors

Using human LCA7 retinal organoids to establish allele-specific editing as a therapy

Long-term efficacy and safety of satralizumab in adults with AQP4-IgG-seropositive neuromyelitis optica spectrum disorder (NMOSD): results from the Phase 3 SAkura studies

SSBP1 -Disease Update: Expanding the Genetic and Clinical Spectrum, Reporting Variable Penetrance and Confirming Recessive Inheritance

Establishing an in vitro human Leber congenital amaurosis model system

Investigating the genotype-phenotype relationships of patient specific PNPLA6 mutations

Efficacy and safety of satralizumab in neuromyelitis optica spectrum disorder (NMOSD): Results from open-label extension periods of SAkuraSky and SAkuraStar

Preoperative Imaging and Surgical Outcomes After Epiretinal Membrane Peeling in Pediatric Combined Hamartoma of the Retina and Retinal Pigment Epithelium

Expanding the FDXR -Associated Disease Phenotype: Retinal Dystrophy Is a Recurrent Ocular Feature

Efficacy and safety of satralizumab from two phase 3 trials in neuromyelitis optica spectrum disorder

Measuring Volume of Subretinal Injections with Commercial Intraoperative OCT

Quantifying the Separation Between the Retinal Pigment Epithelium and Bruch's Membrane using Optical Coherence Tomography in Patients with Inherited Macular Degeneration

Progression to blindness in 20 years among patients with glaucomatous visual fields in a tertiary hospital in the Philippines

Portable VEP Diagnostics for NeuroVisual Disorders

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