Katarina Stingl

30PUBLICATIONS
217CO-AUTHORS
Neurology and neuromuscular diseasesEndocrinologyVision scienceInfant and child healthGene expression (incl. microarray and other genome-wide approaches)
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Publications (30)

|Jul 17, 2026
Missense variants in KATNA1 alter microtubule dynamics and underlie dominant macular dystrophy.

|May 20, 2026
Clinical endpoints special session, ISCEV 2025, Utrecht.

|Sep 16, 2025
OCT Biomarkers in a Cohort of Patients With PRPF31-Associated Retinitis Pigmentosa.

Jan-Philipp Bodenbender, Katarina Stingl, Susanne Kohl

|Aug 18, 2025
Safety and vision outcomes of subretinal gene supplementation therapy in PDE6A-associated retinitis pigmentosa: a non-randomised controlled trial.

Felix F Reichel, M Dominik Fischer, Katarina Stingl

|Jul 11, 2025
ABCA4-associated disease in childhood and adolescence- a phenotype study.

Jan-Philipp Bodenbender, Annekatrin Rickmann, Katarina Stingl

|Apr 24, 2025
Clinical manifestations of dual-gene variants involving ABCA4 in retinal dystrophies.

Lasse Wolfram, David A Merle, Laura Kühlewein

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Frequent Collaborators

15 joint publications

Susanne Kohl

8 joint publications

Laura Kühlewein

7 joint publications

Tobias Haack

6 joint publications

Nicole Weisschuh