Daniel F Schorderet (Daniel Schorderet)

ORCID

Publication Activity (10 Years)

Years Active: 2018-2022
Publications (10 Years): 9

Top Venues

Human mutation

Genes

Journal of ophthalmology

Scientific reports

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

Publications

Denisa Džulová, Dylan Lawless, Gaëtan G Pinton, Nicole A Renner, Daniel F Schorderet
Incomplete Recovery of Zebrafish Retina Following Cryoinjury. Cells 11 (8) (2022)
Anaïs F Poncet, Olivier Grunewald, Veronika Vaclavik, Isabelle Meunier, Isabelle Drumare, Valérie Pelletier, Béatrice Bocquet, Margarita G Todorova, Anne-Gaëlle Le Moing, Aurore Devos, Daniel F Schorderet, Florence Jobic, Sabine Defoort-Dhellemmes, Hélène Dollfus, Vasily M Smirnov, Claire-Marie Dhaenens
Contribution of Whole-Genome Sequencing and Transcript Analysis to Decipher Retinal Diseases Associated with MFSD8 Variants. International journal of molecular sciences 23 (8) (2022)
Khaled El Matri, Yousra Falfoul, Imen Habibi, Ahmed Chebil, Daniel F Schorderet, Leila El Matri
Macular Dystrophy with Bilateral Macular Telangiectasia Related to the CYP2U1 Pathogenic Variant Assessed with Multimodal Imaging Including OCT-Angiography. Genes 12 (11) (2021)
Imen Habibi, Yousra Falfoul, Margarita G Todorova, Stefan Wyrsch, Veronika Vaclavik, Maria Helfenstein, Ahmed Turki, Khaled El Matri, Leila El Matri, Daniel F Schorderet
Correction: Habibi I. et al. "Clinical and Genetic Findings of Autosomal Recessive Bestrophinopathy (ARB)" Genes, 2019, 10, 953. Genes 11 (5) (2020)
Imen Habibi, Yosra Falfoul, Ahmed Turki, Asma Hassairi, Khaled El Matri, Ahmed Chebil, Daniel F Schorderet, Leila El Matri
Genetic spectrum of retinal dystrophies in Tunisia. Scientific reports 10 (1) (2020)
Christina Zeitz, Christelle Michiels, Marion Neuillé, Christoph Friedburg, Christel Condroyer, Fiona Boyard, Aline Antonio, Nassima Bouzidi, Diana Milicevic, Robin Veaux, Aurore Tourville, Axelle Zoumba, Imene Seneina, Marine Foussard, Camille Andrieu, Markus N Preising, Steven Blanchard, Jean-Paul Saraiva, Lilia Mesrob, Edith Le Floch, Claire Jubin, Vincent Meyer, Hélène Blanché, Anne Boland, Jean-François Deleuze, Dror Sharon, Isabelle Drumare, Sabine Defoort-Dhellemmes, Elfride De Baere, Bart P Leroy, Xavier Zanlonghi, Ingele Casteels, Thomy J de Ravel, Irina Balikova, Rob K Koenekoop, Fanny Laffargue, Rebecca McLean, Irene Gottlob, Dominique Bonneau, Daniel F Schorderet, Francis L Munier, Martin McKibbin, Katrina Prescott, Valerie Pelletier, Hélène Dollfus, Yaumara Perdomo-Trujillo, Céline Faure, Charlotte Reiff, Bernd Wissinger, Isabelle Meunier, Susanne Kohl, Eyal Banin, Eberhart Zrenner, Bernhard Jurklies, Birgit Lorenz, José Alain Sahel, Isabelle Audo
Where are the missing gene defects in inherited retinal disorders? Intronic and synonymous variants contribute at least to 4% of CACNA1F-mediated inherited retinal disorders. Human mutation 40 (6) (2019)
Valeria Kheir, Vianney Cortés-González, Juan Carlos Zenteno Ruiz, Daniel F Schorderet
Mutation update: TGFBI pathogenic and likely pathogenic variants in corneal dystrophies. Human mutation 40 (6) (2019)
Rossiana I Bojinova, Daniel F Schorderet, Christophe Valmaggia, Cengiz Türksever, Andreas Schoetzau, Margarita G Todorova
Higher retinal vessel oxygen saturation: investigating its relationship with macular oedema in retinitis pigmentosa patients. Eye (London, England) 32 (7) (2018)
Yousra Falfoul, Imen Habibi, Ahmed Turki, Ahmed Chebil, Asma Hassairi, Daniel F Schorderet, Leila El Matri
Phenotypic Progression of Stargardt Disease in a Large Consanguineous Tunisian Family Harboring New ABCA4 Mutations. Journal of ophthalmology 2018 (2018)

Daniel F Schorderet.css-eqlu8i{font-size:small;padding-left:4px;} (Daniel Schorderet)

Publication Activity (10 Years)

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Daniel F Schorderet (Daniel Schorderet)