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Ulrich Kellner

Free University of Berlin
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386

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9564

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Dominant ACO2 mutations are a frequent cause of isolated optic atrophy

2021
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Autosomal dominant gyrate atrophy-like choroidal dystrophy revisited: 45 years follow-up and association with a novel missense variant

2021 Investigative Ophthalmology & Visual Science
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Treatment contentment and preference of patients undergoing intravitreal anti-VEGF therapy.

2021 Graefes Archive for Clinical and Experimental Ophthalmology
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Autosomal Dominant Gyrate Atrophy-Like Choroidal Dystrophy Revisited: 45 Years Follow-Up and Association with a Novel C1QTNF5 Missense Variant.

2021 International Journal of Molecular Sciences
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Screening auf Frühgeborenenretinopathie – die wichtigsten Änderungen in der neuen deutschen Leitlinie 2020

2021 Ophthalmologe
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[Guidelines for ophthalmological screening of premature infants in Germany (S2k level, AWMF guidelines register no. 024/010, March 2020) : Joint recommendation of the German Ophthalmological Society (DOG), Retinological Society (RG), Professional Association of Ophthalmologists in Germany e. V. (BVA), German Society of Paediatrics and Adolescent Medicine (DGKJ), Professional Association of Pediatricians (BVKJ), Federal Association "The Premature Child" , Society for Neonatology and Paediatric Intensive Care Medicine (GNPI)].

2021 Ophthalmologe
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Wide-field optical coherence tomography in ABCA4 -associated inherited retinal dystrophies

2021
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Augenärztliche Screening-Untersuchung bei Frühgeborenen (S2k-Level, AWMF-Leitlinien-Register-Nr. 024/010, März 2020): Gemeinsame Empfehlung von Deutsche Ophthalmologische Gesellschaft (DOG), Retinologische Gesellschaft (RG), Berufsverband der Augenärzte Deutschlands (BVA), Deutsche Gesellschaft für Kinder- und Jugendmedizin (DGKJ), Berufsverband der Kinder- und Jugendärzte e.V. (BVKJ), Bundesverband „Das frühgeborene Kind“ e.V., Gesellschaft für Neonatologie und Pädiatrische Intensivmedizin (GNPI)

2021 Zeitschrift Fur Geburtshilfe Und Neonatologie
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Mutation spectrum of the OPA1 gene in a large cohort of patients with suspected dominant optic atrophy: Identification and classification of 48 novel variants.

2021 PLOS ONE
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Resolving the dark matter of ABCA4 for 1054 Stargardt disease probands through integrated genomics and transcriptomics.

2020 Genetics in Medicine
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Citations (39)