Ulrich Kellner

OPA1, encoding a dynamin-related GTPase, is mutated in autosomal dominant optic atrophy linked to chromosome 3q28

Christiane Alexander, Marcela Votruba, Ulrike E. A. Pesch et al. · Nature Genetics · 2000 · 1.3K citations

Mendelian Disorder, Dynamin-related Gtpase, Genetic Disorder +6

Recommendations on Screening for Chloroquine and Hydroxychloroquine Retinopathy (2016 Revision)

Michael F. Marmor, Ulrich Kellner, Timothy Y. Y. Lai et al. · Ophthalmology · 2016 · 1.1K citations · Full text

Ocular Disease, Ophthalmology, Ocular Pathology +3

Revised Recommendations on Screening for Chloroquine and Hydroxychloroquine Retinopathy

Michael F. Marmor, Ulrich Kellner, Timothy Y. Y. Lai et al. · Ophthalmology · 2011 · 683 citations

Ocular Disease, Ophthalmology, Laboratory Medicine +3

Mutations in a human homologue of Drosophila crumbs cause retinitis pigmentosa (RP12)

Anneke I. den Hollander, Jacoline B. ten Brink, Yvette J.M. de Kok et al. · Nature Genetics · 1999 · 470 citations

Biology, Developmental Biology, Genetics +6

Safety and Efficacy of a Flexible Dosing Regimen of Ranibizumab in Neovascular Age-Related Macular Degeneration: The SUSTAIN Study

Frank G. Holz, Winfried M. K. Amoaku, Robyn H. Guymer et al. · Ophthalmology · 2011 · 410 citations

Ocular Disease, Ophthalmology, Medicine +5