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ARVO Annual Meeting Abstract June 2025

A comparison of the effect of endotamponade devices on macular thickness in eyes with macula-on rhegmatogenous retinal detachment treated with pars plana vitrectomy.

Kwame A Baffour-Awuah; Amandeep Josan; Robert E MacLaren; Imran H Yusuf

Invest. Ophthalmol. Vis. Sci.. 2025; 66(8):222.

ARVO Annual Meeting Abstract June 2025

DEFINING A NOVEL RPGR PHENOTYPE OF SECTOR RETINITIS PIGMENTOSA WITH CONE DYSTROPHY.

Olha Chorna; Maram E A Abdalla Elsayed; Robert E MacLaren

Invest. Ophthalmol. Vis. Sci.. 2025; 66(8):4352.

ARVO Annual Meeting Abstract June 2025

Analysis of candidate genes rescuable by CRISPR activation in monogenic cases of inherited retinal degenerations and optic neuropathies

Benjamin Wei Jie Ng; Robert E MacLaren; Stephan Sanders; Jasmina Cehajic Kapetanovic

Invest. Ophthalmol. Vis. Sci.. 2025; 66(8):5961.

ARVO Annual Meeting Abstract June 2025

Determining optimal timepoint and dosing strategy for transduction of an AAV5 viral vector in wild-type retinal organoids

Sylvia Franklin; Qingyun Zheng; Valeria Chichagova; Michelle McClements; Robert E MacLaren

Invest. Ophthalmol. Vis. Sci.. 2025; 66(8):5940.

ARVO Annual Meeting Abstract June 2025

Novel ETNK1 and NR2E3 variants associated with inherited retinal dystrophy in dogs and humans

Sara Mikkonen; Inka-Tuulevi Vähämäki; Jonas Donner; Susan Pearce-Kelling; Sruthi Hundi; Claire M. Wade; Kaisa Wickström; Sanna Elfving; Päivi Vanhapelto; Imran H Yusuf; Jasmina Cehajic Kapetanovic; Robert E MacLaren; Eeva-Marja Sankila; Joni Turunen; Maria Kaukonen; Hannes Lohi

Invest. Ophthalmol. Vis. Sci.. 2025; 66(8):5132.

ARVO Annual Meeting Abstract June 2025

Comparison of near-infrared reflectance and blue autofluorescence imaging for diagnosis and monitoring of geographic atrophy

Grace A Borchert; Kanmin Xue; Jasmina Cehajic Kapetanovic; Robert E MacLaren; Susan M Downes; Samantha R De Silva

Invest. Ophthalmol. Vis. Sci.. 2025; 66(8):705.

ARVO Annual Meeting Abstract June 2025

Global inequity in retinal gene therapy development for recessive inherited retinal degenerations

Imran H Yusuf; Robert E MacLaren

Invest. Ophthalmol. Vis. Sci.. 2025; 66(8):6065.

ARVO Annual Meeting Abstract June 2025

Natural History of Central Retinal Sensitivity Decline in RPGR related Retinitis Pigmentosa: A Comprehensive Analysis

Amandeep Josan; laura taylor; Shabnam Raji; Jasmina Cehajic Kapetanovic; Robert E MacLaren

Invest. Ophthalmol. Vis. Sci.. 2025; 66(8):6049.

ARVO Annual Meeting Abstract June 2025

Female carriers of RPGR ORF1 5 variants causing X-linked cone dystrophy have a distinct phenotype

Shabnam Raji; Robert E MacLaren; Peter Charbel Issa; Jasmina Cehajic-Kapetanovic

Invest. Ophthalmol. Vis. Sci.. 2025; 66(8):3148.

ARVO Annual Meeting Abstract June 2025

To report a novel OCT clinical sign in choroideremia patients associated with a focal outer foveal defect

Maram E A Abdalla Elsayed; Robert E MacLaren

Invest. Ophthalmol. Vis. Sci.. 2025; 66(8):4350.

ARVO Annual Meeting Abstract June 2025

RPGR-associated advanced retinitis pigmentosa with unusually preserved cone function

Cristina Martinez-Fernandez dela Camara; Benjamin WJ NG; Robert E MacLaren; Jasmina Cehajic Kapetanovic

Invest. Ophthalmol. Vis. Sci.. 2025; 66(8):1449.

ARVO Annual Meeting Abstract June 2025

Ocular phenotype of a European cohort of patients with Usher syndrome type 1B associated with pathogenic variants in MYO7A

Vasil Kostin; Amandeep S. Josan; Shabnam Raji; Telma Machado; Ana Luísa Carvalho; João Pedro Marques; Susan M Downes; Robert E MacLaren; Kanmin Xue

Invest. Ophthalmol. Vis. Sci.. 2025; 66(8):1441.

ARVO Annual Meeting Abstract June 2025

Genetic Characterization of Inherited Retinal Diseases in a Finnish Cohort of 497 Patients

Joni Turunen; Julia Krootila; Maria Kaukonen; Eeva-Marja Sankila; Maarjaliis Paavo; Sanna Seitsonen; Pauliina Repo; Michael Backlund; Anna Majander; Päivi Lindhal; Kristiina Vasara; Robert E MacLaren; Tero T Kivelä

Invest. Ophthalmol. Vis. Sci.. 2025; 66(8):1436.

ARVO Annual Meeting Abstract June 2025

Background blood-retinal barrier breakdown in rapid inherited retinal degeneration could exacerbate gene therapy-associated uveitis (GTAU)

Molly John; Cristina Martinez-Fernandez Dela Camara; Hoda Shamsnajafabadi; Jasmina Cehajic Kapetanovic; Alissa Bray; Andrew D Dick; M Dominik Fischer; Robert E MacLaren; Kanmin Xue

Invest. Ophthalmol. Vis. Sci.. 2025; 66(8):3048.

Retina June 2025

An Analysis of Scotopic Microperimetry in Healthy Adults

PDF

Daniel A. O. Adeyoju; Amandeep S. Josan; Laura J. Taylor; Robert E. MacLaren
TAGS: adult, eye, reliability, rod photoreceptors, eye diseases, vision, perimetry, age-related macular degeneration, retinal diseases
Trans. Vis. Sci. Tech.. 2025; 14(6):18. https://doi.org/10.1167/tvst.14.6.18

Retina June 2025

Characterizing Inner Retinal Changes in End-Stage Inherited Retinal Diseases That Might be Suitable for Optogenetic Therapies

PDF

Benjamin W. J. Ng; Tien-En Tan; Vasil Kostin; Robert E. MacLaren; Jasmina Cehajic-Kapetanovic
TAGS: optogenetics, retinal diseases, spectral domain-optical coherence tomography, macular dystrophy, retina, retinitis pigmentosa
Trans. Vis. Sci. Tech.. 2025; 14(6):2. https://doi.org/10.1167/tvst.14.6.2

Includes: Supplemental Content

Clinical and Epidemiologic Research November 2024

Ranked Importance of Visual Function Outcome Measures in Choroideremia Clinical Trials

PDF

Amandeep Singh Josan; Laura Jayne Taylor; Kanmin Xue; Jasmina Cehajic-Kapetanovic; Robert Edward MacLaren
TAGS: choroideremia, functional measures, outcome measures, vision
Invest. Ophthalmol. Vis. Sci.. 2024; 65(13):58. https://doi.org/10.1167/iovs.65.13.58

Includes: Supplemental Content

Retina September 2024

Exploring Scotopic Microperimetry as an Outcome Measure in Choroideremia

PDF

Laura J. Taylor; Amandeep S. Josan; Daniel Adeyoju; Jasleen K. Jolly; Robert E. MacLaren
TAGS: choroideremia, outcome measures, rod photoreceptors, volume
Trans. Vis. Sci. Tech.. 2024; 13(9):29. https://doi.org/10.1167/tvst.13.9.29

Includes: Supplemental Content

Retina September 2024

Establishing Clinical Trial Endpoints in Selecting Patients for RPGR Retinal Gene Therapy

PDF

Evita Evangelia Christou; Amandeep S. Josan; Jasmina Cehajic-Kapetanovic; Robert E. MacLaren
TAGS: gene therapy, retinitis pigmentosa, surrogate endpoints
Trans. Vis. Sci. Tech.. 2024; 13(9):18. https://doi.org/10.1167/tvst.13.9.18

Review June 2024

Robot-Assisted Eye Surgery: A Systematic Review of Effectiveness, Safety, and Practicality in Clinical Settings

PDF

Arun J. Thirunavukarasu; Monica L. Hu; William P. Foster; Kanmin Xue; Jasmina Cehajic-Kapetanovic; Robert E. MacLaren
TAGS: ophthalmologic surgical procedures, safety, surgical procedures, operative, systematic reviews, surgeons, robotic surgery, screening, healthcare quality assessment, laparotomy
Trans. Vis. Sci. Tech.. 2024; 13(6):20. https://doi.org/10.1167/tvst.13.6.20

Includes: Supplemental Content

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A comparison of the effect of endotamponade devices on macular thickness in eyes with macula-on rhegmatogenous retinal detachment treated with pars plana vitrectomy.

DEFINING A NOVEL RPGR PHENOTYPE OF SECTOR RETINITIS PIGMENTOSA WITH CONE DYSTROPHY.

Analysis of candidate genes rescuable by CRISPR activation in monogenic cases of inherited retinal degenerations and optic neuropathies

Determining optimal timepoint and dosing strategy for transduction of an AAV5 viral vector in wild-type retinal organoids

Novel ETNK1 and NR2E3 variants associated with inherited retinal dystrophy in dogs and humans

Comparison of near-infrared reflectance and blue autofluorescence imaging for diagnosis and monitoring of geographic atrophy

Global inequity in retinal gene therapy development for recessive inherited retinal degenerations

Natural History of Central Retinal Sensitivity Decline in RPGR related Retinitis Pigmentosa: A Comprehensive Analysis

Female carriers of RPGR ORF1 5 variants causing X-linked cone dystrophy have a distinct phenotype

To report a novel OCT clinical sign in choroideremia patients associated with a focal outer foveal defect

RPGR-associated advanced retinitis pigmentosa with unusually preserved cone function

Ocular phenotype of a European cohort of patients with Usher syndrome type 1B associated with pathogenic variants in MYO7A

Genetic Characterization of Inherited Retinal Diseases in a Finnish Cohort of 497 Patients

Background blood-retinal barrier breakdown in rapid inherited retinal degeneration could exacerbate gene therapy-associated uveitis (GTAU)

An Analysis of Scotopic Microperimetry in Healthy Adults

Characterizing Inner Retinal Changes in End-Stage Inherited Retinal Diseases That Might be Suitable for Optogenetic Therapies

Ranked Importance of Visual Function Outcome Measures in Choroideremia Clinical Trials

Exploring Scotopic Microperimetry as an Outcome Measure in Choroideremia

Establishing Clinical Trial Endpoints in Selecting Patients for RPGR Retinal Gene Therapy

Robot-Assisted Eye Surgery: A Systematic Review of Effectiveness, Safety, and Practicality in Clinical Settings

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