Search | IOVS | ARVO Journals

Showing 1 – 20 of 35

SORT: Best Match Most Recent Oldest

VIEW: Basic | Expanded

ARVO Annual Meeting Abstract June 2024

The role of somatic chromosomal abundance in risk and prognosis of age-related macular degeneration

Anastasios Papadam; Bernhard Hf Weber; Emily Y Chew; Claudia Strachwitz; Felix Grassmann

Invest. Ophthalmol. Vis. Sci.. 2024; 65(7):1353.

ARVO Annual Meeting Abstract June 2024

AI-based identification of photoreceptor degeneration and retinal pigment epithelial atrophy in inherited macular dystrophies

Ulrich Kellner; Simone Kellner; Heidi Stöhrq; Christina Kiel; Silke Weinitz; Ghazaleh Farmand; Bernhard Hf Weber

Invest. Ophthalmol. Vis. Sci.. 2024; 65(7):3099.

ARVO Annual Meeting Abstract June 2024

Exploring the Genetic Landscape of Geographic Atrophy Progression: A GWAS in 2,472 Individuals with AMD

Amy Stockwell; Anastasios Papadam; Tiarnan D L Keenan; Catherine Cukras; Elvira Agron; Emily Y Chew; Bernhard Hf Weber; Brian Yaspan; Felix Grassmann

Invest. Ophthalmol. Vis. Sci.. 2024; 65(7):4237.

ARVO Annual Meeting Abstract June 2023

Near-infrared autofluorescence in inherited retinal dystrophies

Simone Kellner; Heidi Stoehr; Christina Kiel; Silke Weinitz; Ghazaleh Farmand; Bernhard HF Weber; Ulrich Kellner

Invest. Ophthalmol. Vis. Sci.. 2023; 64(8):4656.

ARVO Annual Meeting Abstract June 2023

Wide-field optical coherence tomography in retinitis pigmentosa

Ulrich Kellner; Heidi Stoehr; Christina Kiel; Simone Kellner; Silke Weinitz; Ghazaleh Farmand; Bernhard HF Weber

Invest. Ophthalmol. Vis. Sci.. 2023; 64(8):4655.

ARVO Annual Meeting Abstract June 2022

Nicotinamide and its role in reducing complement activation and oxidative stress in age-related macular degeneration

Karolina Ploessl; Anna Eifler; Ardita Ramadani; Florian Schaetzler; Bernhard HF Weber

Invest. Ophthalmol. Vis. Sci.. 2022; 63(7):469 – A0006.

ARVO Annual Meeting Abstract June 2022

Vitronectin and its interaction with plasminogen activator inhibitor 1 - a possible link to vascular changes in AMD pathology

Fabiola Biasella; Christina Kiel; Tobias Strunz; Ulrike Friedrich; Bernhard HF Weber

Invest. Ophthalmol. Vis. Sci.. 2022; 63(7):468 – A0005.

ARVO Annual Meeting Abstract June 2022

Global methylation status of induced pluripotent stem cells, their origins and final differentiations

Christina Kiel; Patricia Berber; Karolina Plössl; Armin Wolf; Thomas Langmann; Bernhard HF Weber

Invest. Ophthalmol. Vis. Sci.. 2022; 63(7):3734 – F0340.

ARVO Annual Meeting Abstract June 2021

Effect of retinoschisin on compartmentalization on novel interaction partners of the retinal Na/K-ATPase-retinoschisin complex

Verena Schmid; Astrid Bruckmann; Bernhard HF Weber; Ulrike Friedrich

Invest. Ophthalmol. Vis. Sci.. 2021; 62(8):3053.

ARVO Annual Meeting Abstract June 2021

Gene expression in liver is influenced by coordinated activities at genetic loci associated with age-related macular degeneration

Tobias Strunz; Christina Kiel; Christoph A Nebauer; Simon Stelzl; Bernhard HF Weber

Invest. Ophthalmol. Vis. Sci.. 2021; 62(8):1449.

ARVO Annual Meeting Abstract June 2021

Allele-specific influence of seed polymorphism rs2168518 in hsa-miR-4513 on expression of neovascularization-associated genes

Christina Kiel; Tobias Strunz; Daniele Hasler; Gunter Meister; Felix Grassmann; Bernhard HF Weber

Invest. Ophthalmol. Vis. Sci.. 2021; 62(8):531.

ARVO Annual Meeting Abstract June 2020

Variation of Clinical Findings in Choroideremia Carriers - From normal to severe

Ulrich Kellner; Heidi Stoehr; Simone Kellner; Silke Weinitz; Ghazaleh Farmand; Bernhard HF Weber

Invest. Ophthalmol. Vis. Sci.. 2020; 61(7):3039.

ARVO Annual Meeting Abstract June 2020

Long-term follow-up and variable progression of ocular signs in two sisters with AHI1-gene associated Joubert syndrome

Simone Kellner; Heidi Stoehr; Silke Weinitz; Ghazaleh Farmand; Bernhard HF Weber; Ulrich Kellner

Invest. Ophthalmol. Vis. Sci.. 2020; 61(7):3041.

ARVO Annual Meeting Abstract July 2019

Towards comprehensive identification and functional characterization of deep-intronic ABCA4 variants in 1000 Stargardt disease cases

Mubeen Khan; Stephanie Cornelis; Marta del Pozo Valero; Muhammad Imran Khan; Heidi Stohr; Felix Grassmann; Marloes Steehouwer; Alexander Hoischen; Carmen Ayuso; Raj Ramesar; Isabelle Anne Meunier; Sabine defoort; Bernhard HF Weber; Claire-Marie Dhaenens; Frans P Cremers

Invest. Ophthalmol. Vis. Sci.. 2019; 60(9):2813.

ARVO Annual Meeting Abstract July 2019

North-Carolina Macular dystrophy like phenotype in a three generation pedigree wit autosomal dominant inheritance and exclusion of MCRD1

Ulrich Kellner; Heidi Stohr; Birgit Budde; Simone Kellner; Silke Weinitz; Ghazaleh Farmand; Birgit Lindau; Bernhard HF Weber

Invest. Ophthalmol. Vis. Sci.. 2019; 60(9):4482.

ARVO Annual Meeting Abstract July 2019

An iPSC-derived RPE cell repository with high and low genetic AMD risk as model systems to study AMD pathology in vitro

Karolina Ploessl; Annie Lauer; Christina Kiel; Caroline Brandl; Felix Grassmann; Bernhard HF Weber

Invest. Ophthalmol. Vis. Sci.. 2019; 60(9):4916.

ARVO Annual Meeting Abstract July 2019

CRISPR/Cas9-Mediated Genome Editing to Treat Best Vitelliforme Macular Dystrophy

Andrea Milenkovic; Bernhard HF Weber

Invest. Ophthalmol. Vis. Sci.. 2019; 60(9):4922.

ARVO Annual Meeting Abstract July 2019

Vitreo-retinal interface abnormalities in an older European population: results from the AugUR study

Caroline Brandl; Felicitas Borgmann; Martina E Zimmermann; Horst Helbig; Bernhard HF Weber; Iris M Heid; Klaus J Stark

Invest. Ophthalmol. Vis. Sci.. 2019; 60(9):2007.

ARVO Annual Meeting Abstract July 2018

Molecular Genetic Screening In A Series Of 852 Patients With Inherited Retinal Dystrophies From One German Reference Center

Ulrich Kellner; Heidi Stoehr; Simone Kellner; Silke Weinitz; Ghazaleh Farmand; Birgit Lindau; Bernhard HF Weber

Invest. Ophthalmol. Vis. Sci.. 2018; 59(9):18.

ARVO Annual Meeting Abstract July 2018

Retinal layer thicknesses in early age-related macular degeneration: results from the German AugUR-study

Caroline Brandl; Christiane Brücklmayer; Martina E Zimmermann; Felix Günther; Helmut Küchenhoff; Horst Helbig; Bernhard HF Weber; Iris M Heid; Klaus J Stark

Invest. Ophthalmol. Vis. Sci.. 2018; 59(9):2407.

1 2

Next 20 Results »

NARROW

Content Type

Journal

Article Type

Specify Date Range

The role of somatic chromosomal abundance in risk and prognosis of age-related macular degeneration

AI-based identification of photoreceptor degeneration and retinal pigment epithelial atrophy in inherited macular dystrophies

Exploring the Genetic Landscape of Geographic Atrophy Progression: A GWAS in 2,472 Individuals with AMD

Near-infrared autofluorescence in inherited retinal dystrophies

Wide-field optical coherence tomography in retinitis pigmentosa

Nicotinamide and its role in reducing complement activation and oxidative stress in age-related macular degeneration

Vitronectin and its interaction with plasminogen activator inhibitor 1 - a possible link to vascular changes in AMD pathology

Global methylation status of induced pluripotent stem cells, their origins and final differentiations

Effect of retinoschisin on compartmentalization on novel interaction partners of the retinal Na/K-ATPase-retinoschisin complex

Gene expression in liver is influenced by coordinated activities at genetic loci associated with age-related macular degeneration

Allele-specific influence of seed polymorphism rs2168518 in hsa-miR-4513 on expression of neovascularization-associated genes

Variation of Clinical Findings in Choroideremia Carriers - From normal to severe

Long-term follow-up and variable progression of ocular signs in two sisters with AHI1-gene associated Joubert syndrome

Towards comprehensive identification and functional characterization of deep-intronic ABCA4 variants in 1000 Stargardt disease cases

North-Carolina Macular dystrophy like phenotype in a three generation pedigree wit autosomal dominant inheritance and exclusion of MCRD1

An iPSC-derived RPE cell repository with high and low genetic AMD risk as model systems to study AMD pathology in vitro

CRISPR/Cas9-Mediated Genome Editing to Treat Best Vitelliforme Macular Dystrophy

Vitreo-retinal interface abnormalities in an older European population: results from the AugUR study

Molecular Genetic Screening In A Series Of 852 Patients With Inherited Retinal Dystrophies From One German Reference Center

Retinal layer thicknesses in early age-related macular degeneration: results from the German AugUR-study

To View More...

You must be signed into an individual account to use this feature.