Ulrich Kellner

Publication Activity (10 Years)

Years Active: 2019-2022
Publications (10 Years): 14

Top Topics

Diabetic Retinopathy

Top Venues

International journal of molecular sciences

Proceedings of the National Academy of Sciences of the United States of America

Der Ophthalmologe : Zeitschrift der Deutschen Ophthalmologischen Gesellschaft

This page only lists publications with an associated author ORCID identifier.

Publications

Julia Gersch, Katerina Hufendiek, Julien Delarocque, Carsten Framme, Christina Jacobsen, Heidi Stöhr, Ulrich Kellner, Karsten Hufendiek
Investigation of Structural Alterations in Inherited Retinal Diseases: A Quantitative SD-OCT-Analysis of Retinal Layer Thicknesses in Light of Underlying Genetic Mutations. International journal of molecular sciences 23 (24) (2022)
Julia Gersch, Katerina Hufendiek, Julien Delarocque, Carsten Framme, Christina Jacobsen, Heidi Stöhr, Ulrich Kellner, Karsten Hufendiek
Investigation of Structural Alterations in Inherited Retinal Diseases: A Quantitative SD-OCT-Analysis of Retinal Layer Thicknesses in Light of Underlying Genetic Mutations. International journal of molecular sciences 23 (24) (2022)
Maria Solaki, Britta Baumann, Peggy Reuter, Sten Andreasson, Isabelle Audo, Carmen Ayuso, Ghassan Balousha, Francesco Benedicenti, David Geoffrey Birch, Pierre Bitoun, Delphine Blain, Beatrice Bocquet, Kari Branham, Jaume Catala, Elfride De Baere, Helene Dollfus, Mohammed Falana, Roberto Giorda, Irina Golovleva, Irene Gottlob, John R Heckenlively, Samuel G Jacobson, Kaylie D Jones, Herbert Jägle, Andreas R Janecke, Ulrich Kellner, Petra Liskova, Birgit Lorenz, Loreto Martorell, André M Vieira Messias, Isabelle Meunier, Fernanda Belga Ottoni Porto, Eleni Papageorgiou, Astrid S Plomp, Thomy J L de Ravel, Charlotte M Reiff, Agnes B Renner, Thomas Rosenberg, Günther Rudolph, Roberto Salati, E Cumhur Sener, Paul A Sieving, Franco Stanzial, Elias I Traboulsi, Stephen H Tsang, Balázs Varsanyi, Richard G Weleber, Ditta Zobor, Katarina Stingl, Bernd Wissinger, Susanne Kohl
Comprehensive variant spectrum of the CNGA3 gene in patients affected by achromatopsia. Human mutation 43 (7) (2022)
Julia Gersch, Katerina Hufendiek, Julien Delarocque, Carsten Framme, Christina Jacobsen, Heidi Stöhr, Ulrich Kellner, Karsten Hufendiek
Investigation of Structural Alterations in Inherited Retinal Diseases: A Quantitative SD-OCT-Analysis of Retinal Layer Thicknesses in Light of Underlying Genetic Mutations. International journal of molecular sciences 23 (24) (2022)
Julia Gersch, Katerina Hufendiek, Julien Delarocque, Carsten Framme, Christina Jacobsen, Heidi Stöhr, Ulrich Kellner, Karsten Hufendiek
Investigation of Structural Alterations in Inherited Retinal Diseases: A Quantitative SD-OCT-Analysis of Retinal Layer Thicknesses in Light of Underlying Genetic Mutations. International journal of molecular sciences 23 (24) (2022)
Julia Gersch, Katerina Hufendiek, Julien Delarocque, Carsten Framme, Christina Jacobsen, Heidi Stöhr, Ulrich Kellner, Karsten Hufendiek
Investigation of Structural Alterations in Inherited Retinal Diseases: A Quantitative SD-OCT-Analysis of Retinal Layer Thicknesses in Light of Underlying Genetic Mutations. International journal of molecular sciences 23 (24) (2022)
Julia Gersch, Katerina Hufendiek, Julien Delarocque, Carsten Framme, Christina Jacobsen, Heidi Stöhr, Ulrich Kellner, Karsten Hufendiek
Investigation of Structural Alterations in Inherited Retinal Diseases: A Quantitative SD-OCT-Analysis of Retinal Layer Thicknesses in Light of Underlying Genetic Mutations. International journal of molecular sciences 23 (24) (2022)
Bernd Wissinger, Britta Baumann, Elena Buena-Atienza, Zeinab Ravesh, Artur V Cideciyan, Katarina Stingl, Isabelle Audo, Isabelle Meunier, Béatrice Bocquet, Elias I Traboulsi, Alison J Hardcastle, Jessica C Gardner, Michel Michaelides, Kari E Branham, Thomas Rosenberg, Sten Andreasson, Hélène Dollfus, David Birch, Andrea L Vincent, Loreto Martorell, Jaume Catala, Ulrich Kellner, Klaus Rüther, Birgit Lorenz, Markus N Preising, Emanuela Manfredini, Yuri A Zarate, Raymon Vijzelaar, Eberhart Zrenner, Samuel G Jacobson, Susanne Kohl
The landscape of submicroscopic structural variants at the OPN1LW/OPN1MW gene cluster on Xq28 underlying blue cone monochromacy. Proceedings of the National Academy of Sciences of the United States of America 119 (27) (2022)
Mohammad Seleman Bedar, Ulrich Kellner
Digital 3D "Heads-up" Cataract Surgery: Safety Profile and Comparison with the Conventional Microscope System. Klinische Monatsblatter fur Augenheilkunde 239 (8) (2022)
Ulrich Kellner, Nicole Weisschuh, Silke Weinitz, Ghazaleh Farmand, Sebastian Deutsch, Friederike Kortüm, Pascale Mazzola, Karin Schäferhoff, Valerio Marino, Daniele Dell'Orco
Autosomal Dominant Gyrate Atrophy-Like Choroidal Dystrophy Revisited: 45 Years Follow-Up and Association with a Novel C1QTNF5 Missense Variant. International journal of molecular sciences 22 (4) (2021)
Majida Charif, Naïg Gueguen, Marc Ferré, Zouhair Elkarhat, Salim Khiati, Morgane LeMao, Arnaud Chevrollier, Valerie Desquiret-Dumas, David Goudenège, Céline Bris, Selma Kane, Jennifer Alban, Stéphanie Chupin, Céline Wetterwald, Leonardo Caporali, Francesca Tagliavini, Chiara LaMorgia, Michele Carbonelli, Neringa Jurkute, Abdelhamid Barakat, Philippe Gohier, Christophe Verny, Magalie Barth, Vincent Procaccio, Dominique Bonneau, Xavier Zanlonghi, Isabelle Meunier, Nicole Weisschuh, Simone Schimpf-Linzenbold, Felix Tonagel, Ulrich Kellner, Patrick Yu-Wai-Man, Valerio Carelli, Bernd Wissinger, Patrizia Amati-Bonneau, Pascal Reynier, null null, Guy Lenaers
Dominant ACO2 mutations are a frequent cause of isolated optic atrophy. Brain communications 3 (2) (2021)
Karsten Hufendiek, Katerina Hufendiek, Herbert Jägle, Heidi Stöhr, Marius Book, Georg Spital, Günay Rustambayova, Carsten Framme, Bernhard Heinrich Friedrich Weber, Agnes B Renner, Ulrich Kellner
Clinical Heterogeneity in Autosomal Recessive Bestrophinopathy with Biallelic Mutations in the BEST1 Gene. International journal of molecular sciences 21 (24) (2020)
Ulrich Kellner, Simone Kellner, Silke Weinitz, Ghazaleh Farmand
[Toxic retinopathies]. Der Ophthalmologe : Zeitschrift der Deutschen Ophthalmologischen Gesellschaft 117 (12) (2020)
Julia Felden, Britta Baumann, Manir Ali, Isabelle Audo, Carmen Ayuso, Beatrice Bocquet, Ingele Casteels, Blanca Garcia-Sandoval, Samuel G Jacobson, Bernhard Jurklies, Ulrich Kellner, Line Kessel, Birgit Lorenz, Martin McKibbin, Isabelle Meunier, Thomy de Ravel, Thomas Rosenberg, Klaus Rüther, Maria Vadala, Bernd Wissinger, Katarina Stingl, Susanne Kohl
Mutation spectrum and clinical investigation of achromatopsia patients with mutations in the GNAT2 gene. Human mutation 40 (8) (2019)