Ragnhild W. Jansson

Bergen, Norway

Last Updated: 09/26/2026

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Found 12 publications

Loss of ATRAID in Late-Onset, Non-Syndromic Retinitis Pigmentosa.

Loss of ATRAID in Late-Onset, Non-Syndromic Retinitis Pigmentosa.

Journal: Investigative ophthalmology & visual science

Published: July 08, 2026

Biallelic loss-of-function variants in DSCAM cause a neurodevelopmental syndrome with nystagmus and retinal dysfunction.

Biallelic loss-of-function variants in DSCAM cause a neurodevelopmental syndrome with nystagmus and retinal dysfunction.

Journal: HGG advances

Published: January 17, 2026

Adalimumab in the management of refractory idiopathic retinal vasculitis, aneurysms, and neuroretinitis (IRVAN) syndrome: a case report and literature review.

Adalimumab in the management of refractory idiopathic retinal vasculitis, aneurysms, and neuroretinitis (IRVAN) syndrome: a case report and literature review.

Journal: BMC ophthalmology

Published: November 15, 2025

Fundus hypopigmentation and choroidal thinning associated with tebentafusp therapy: report of a case and literature review.

Fundus hypopigmentation and choroidal thinning associated with tebentafusp therapy: report of a case and literature review.

Journal: BMC ophthalmology

Published: April 21, 2025

Functional Characterization of ABCA4 Missense Variants Aids Variant Interpretation and Phenotype Prediction in Patients With ABCA4-Retinal Dystrophies.

Functional Characterization of ABCA4 Missense Variants Aids Variant Interpretation and Phenotype Prediction in Patients With ABCA4-Retinal Dystrophies.

Journal: Investigative ophthalmology & visual science

Published: August 01, 2024

Gain-of-function mutations in ALPK1 cause an NF-κB-mediated autoinflammatory disease: functional assessment, clinical phenotyping and disease course of patients with ROSAH syndrome.

Gain-of-function mutations in ALPK1 cause an NF-κB-mediated autoinflammatory disease: functional assessment, clinical phenotyping and disease course of patients with ROSAH syndrome.

Journal: Annals of the rheumatic diseases

Published: April 08, 2022

Clinical features and molecular genetics of patients with ABCA4-retinal dystrophies.

Clinical features and molecular genetics of patients with ABCA4-retinal dystrophies.

Journal: Acta ophthalmologica

Published: June 09, 2020

Diabetic retinopathy in type 1 diabetes patients in Western Norway.

Diabetic retinopathy in type 1 diabetes patients in Western Norway.

Journal: Acta ophthalmologica

Published: June 26, 2017

The intronic ABCA4 c.5461-10T>C variant, frequently seen in patients with Stargardt disease, causes splice defects and reduced ABCA4 protein level.

The intronic ABCA4 c.5461-10T>C variant, frequently seen in patients with Stargardt disease, causes splice defects and reduced ABCA4 protein level.

Journal: Acta ophthalmologica

Published: July 08, 2016

Photopic full-field electroretinography and optical coherence tomography in type 1 diabetic retinopathy.

Photopic full-field electroretinography and optical coherence tomography in type 1 diabetic retinopathy.

Journal: Graefe's archive for clinical and experimental ophthalmology = Albrecht von Graefes Archiv fur klinische und experimentelle Ophthalmologie

Published: November 20, 2014

Topographical distribution of retinal and optic disc neovascularization in early stages of proliferative diabetic retinopathy.

Topographical distribution of retinal and optic disc neovascularization in early stages of proliferative diabetic retinopathy.

Journal: Investigative ophthalmology & visual science

Published: November 22, 2012

Early panretinal photocoagulation for ERG-verified ischaemic central retinal vein occlusion.

Early panretinal photocoagulation for ERG-verified ischaemic central retinal vein occlusion.

Journal: Acta ophthalmologica

Published: December 20, 2011

Showing 1-12 of 12

Last Updated: 09/26/2026