Fadi Nasser

10PUBLICATIONS
11CO-AUTHORS
Gene expression (incl. microarray and other genome-wide approaches)Vision sciencePhotography, video and lens-based practiceGene mappingOptical technology
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Publications (10)

|Jul 30, 2021
Disease expression caused by different variants in the BEST1 gene: genotype and phenotype findings in bestrophinopathies.

Katarzyna Nowomiejska, Fadi Nasser, Katarina Stingl

|Mar 06, 2021
Clinical Phenotype of PDE6B-Associated Retinitis Pigmentosa.

Laura Kuehlewein, Ditta Zobor, Katarina Stingl

|Jan 21, 2021
Spatial and temporal resolution of the photoreceptors rescue dynamics after treatment with voretigene neparvovec.

Krunoslav Stingl, Melanie Kempf, Karl U Bartz-Schmidt

|Oct 04, 2019
Ophthalmic features of retinitis pigmentosa in Cohen syndrome caused by pathogenic variants in the VPS13B gene.

Fadi Nasser, Anne Kurtenbach, Saskia Biskup

|Apr 22, 2019
A case of X-linked retinoschisis with atypical fundus appearance.

F Nasser, S Kohl, L Kuehlewein

|Apr 05, 2019
Retinal dystrophies with bull's-eye maculopathy along with negative ERGs.

F Nasser, A Kurtenbach, S Kohl

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Frequent Collaborators

3 joint publications

Katarina Stingl

2 joint publications

Eberhart Zrenner

2 joint publications

Friederike Charlotte Kortüm

1 joint publications

Torsten Strasser