| A randomized, double‐blind, phase 2 study of erythropoietin in optic neuritis KW Sühs, K Hein, MB Sättler, A Görlitz, C Ciupka, K Scholz, ... Annals of neurology 72 (2), 199-210, 2012 | 171 | 2012 |
| Mutations in the MATP gene in five German patients affected by oculocutaneous albinism type 4 U Rundshagen, C Zühlke, S Opitz, E Schwinger, B Käsmann‐Kellner Human Mutation 23 (2), 106-110, 2004 | 115 | 2004 |
| Configuration of the optic chiasm in humans with albinism as revealed by magnetic resonance imaging B Schmitz, T Schaefer, CM Krick, W Reith, M Backens, ... Investigative ophthalmology & visual science 44 (1), 16-21, 2003 | 96 | 2003 |
| Novel and recurrent mutations in the tyrosinase gene and the P gene in the German albino population L Passmore, B Kaesmann-Kellner, B Weber Human genetics 105, 200-210, 1999 | 93 | 1999 |
| Biomechanical profile of the cornea in primary congenital glaucoma Z Gatzioufas, G Labiris, O Stachs, M Hovakimyan, A Schnaidt, A Viestenz, ... Acta ophthalmologica 91 (1), e29-e34, 2013 | 73 | 2013 |
| Ocular changes in mucopolysaccharidosis IV A (Morquio A syndrome) and long-term results of perforating keratoplasty B Käsmann-Kellner, J Weindler, B Pfau, KW Ruprecht Ophthalmologica 213 (3), 200-205, 1999 | 73 | 1999 |
| Eye movement in amyotrophic lateral sclerosis: a longitudinal study. A Palmowski, WH Jost, J Prudlo, J Osterhage, B Käsmann, K Schimrigk, ... German journal of ophthalmology 4 (6), 355-362, 1995 | 61 | 1995 |
| Screening-Untersuchung auf Amblyopie, Strabismus und Refraktionsanomalie bei 1030 Kindergartenkindern B Käsmann-Kellner, M Heine, B Pfau, A Singer, KW Ruprecht Klinische Monatsblätter für Augenheilkunde 213 (09), 166-173, 1998 | 60 | 1998 |
| Ocular manifestations in a father and son with EEC syndrome B Käsmann, KW Ruprecht Graefe's archive for clinical and experimental ophthalmology 235 (8), 512-516, 1997 | 60 | 1997 |
| Monocular visual activation patterns in albinism as revealed by functional magnetic resonance imaging B Schmitz, B Käsmann‐Kellner, T Schäfer, CM Krick, G Grön, M Backens, ... Human brain mapping 23 (1), 40-52, 2004 | 57 | 2004 |
| Molecular analysis of patients with aniridia in Russian Federation broadens the spectrum of PAX6 mutations TA Vasilyeva, AA Voskresenskaya, B Käsmann‐Kellner, OV Khlebnikova, ... Clinical genetics 92 (6), 639-644, 2017 | 50 | 2017 |
| PAX6 mutational status determines aniridia-associated keratopathy phenotype N Lagali, B Wowra, FN Fries, L Latta, K Moslemani, TP Utheim, ... Ophthalmology 127 (2), 273-275, 2020 | 45 | 2020 |
| Detection of 53 novel DNA variations within the tyrosinase gene and accumulation of mutations in 17 patients with albinism S Opitz, B Käsmann‐Kellner, M Kaufmann, E Schwinger, C Zühlke Human mutation 23 (6), 630-631, 2004 | 44 | 2004 |
| Can retinoscopy keep up in keratoconus diagnosis? S Goebels, B Käsmann-Kellner, T Eppig, B Seitz, A Langenbucher Contact Lens and Anterior Eye 38 (4), 234-239, 2015 | 42 | 2015 |
| Aniridia syndrome: clinical findings, problematic courses and suggestions for optimization of care (“aniridia guide”) B Käsmann-Kellner, B Seitz Der Ophthalmologe 111, 1145-1156, 2014 | 42* | 2014 |
| Early phenotypic features of aniridia-associated keratopathy and association with PAX6 coding mutations N Lagali, B Wowra, FN Fries, L Latta, K Moslemani, TP Utheim, ... The ocular surface 18 (1), 130-140, 2020 | 38 | 2020 |
| Vision screening survey of all children starting primary school in 1998 in the Federal State of Saarland, Germany B Käsmann-Kellner, KW Ruprecht Strabismus 8 (3), 201-207, 2000 | 35 | 2000 |
| Human aniridia limbal epithelial cells lack expression of keratins K3 and K12 L Latta, A Viestenz, T Stachon, S Colanesi, N Szentmáry, B Seitz, ... Experimental Eye Research 167, 100-109, 2018 | 33 | 2018 |
| Abnormal neovascular and proliferative conjunctival phenotype in limbal stem cell deficiency is associated with altered microRNA and gene expression modulated by PAX6 … L Latta, N Ludwig, L Krammes, T Stachon, FN Fries, A Mukwaya, ... The Ocular Surface 19, 115-127, 2021 | 32 | 2021 |
| Case Reports-Incontinentia pigmenti (Bloch-Sulzberger-Syndrome): Case Report and Differential Diagnosis to Related Dermato-Ocular Syndromes B Kasmann-Kellner, B Jurin-Bunte, KW Ruprecht Ophthalmologica 213 (1), 63-69, 1999 | 31* | 1999 |
Fabian N. FriesKlinik für Augenheilkunde, Universitätsklinikum des Saarlandes, Universität des SaarlandesVerified email at uks.eu
