Daniel F. Schorderet

Institut de Recherche en Opthalmologie — Switzerland

Biochemistry, Genetics and Molecular Biology · Life Sciences

61h-index23.4kcitations410works0.02yr avg
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Research Topics

Retinal Development and Disorders(144), Retinal Diseases and Treatments(80), Connexins and lens biology(48), Corneal Surgery and Treatments(38), Glaucoma and retinal disorders(33)

Publications406 total

Characterization of the Retinal Phenotype Using Multimodal Imaging in Novel Compound Heterozygote Variants of CYP2U1
Ophthalmology Science·2024Open Access
Genetics of retinitis pigmentosa and other hereditary retinal disorders in Western Switzerland
Ophthalmic Research·2023· 8 citedOpen Access
Analysis of Suspected Achromatopsia by Multimodal Diagnostic Testing
Klinische Monatsblätter für Augenheilkunde·2023· 2 citedOpen Access
Characterisation of the retinal phenotype using multimodal imaging in novel compound heterozygote variants of <i>CYP2U1</i>
2023· 1 citedOpen Access
Incomplete Recovery of Zebrafish Retina Following Cryoinjury
Cells·2022· 2 citedOpen Access
Contribution of Whole-Genome Sequencing and Transcript Analysis to Decipher Retinal Diseases Associated with MFSD8 Variants
International Journal of Molecular Sciences·2022· 14 citedOpen Access
New<i>COL6A6</i>Variant Causes Autosomal Dominant Retinitis Pigmentosa in a Four-Generation Family
Investigative Ophthalmology & Visual Science·2022· 4 citedOpen Access
Premature Vertebral Mineralization in hmx1-Mutant Zebrafish
Cells·2022· 7 citedOpen Access
Macular Dystrophy with Bilateral Macular Telangiectasia Related to the CYP2U1 Pathogenic Variant Assessed with Multimodal Imaging Including OCT-Angiography
Genes·2021· 5 citedOpen Access
Crystals deposits in the anterior and posterior lens cortex in Bietti corneo-retinal dystrophy
Ophthalmic Genetics·2021· 1 cited
Piperlongumine promotes death of retinoblastoma cancer cells
Oncotarget·2021· 8 citedOpen Access
OCT-angiography assessing quiescent and active choroidal neovascularization in retinitis pigmentosa associated with <i>PRPH2</i> pathogenic variant
European Journal of Ophthalmology·2021· 10 citedOpen Access
Different Phenotypes in Pseudodominant Inherited Retinal Dystrophies
Frontiers in Cell and Developmental Biology·2021· 6 citedOpen Access
Homozygous mutation in ABCA4 associated with cone rod dystrophy in a patient with Turner syndrome.
PubMed·2021Open Access
Hmx1 regulates urfh1 expression in the craniofacial region in zebrafish
PLoS ONE·2021· 6 citedOpen Access
Malattia Leventinese: EFEMP1 R345W Variant Is a Hot Spot Mutation, Not a Founder Mutation
Ophthalmology Retina·2020· 4 citedOpen Access
Genetic spectrum of retinal dystrophies in Tunisia
Scientific Reports·2020· 14 citedOpen Access
Report of a Tunisian family with phenotypic variability linked to BEST 1mutation
2020
Whole exome sequencing identified novel homozygous ALMS1 mutations in a Tunisian family with Alström syndrome
Investigative Ophthalmology & Visual Science·2020Open Access
Correction: Habibi I. et al. “Clinical and Genetic Findings of Autosomal Recessive Bestrophinopathy (ARB)” Genes, 2019, 10, 953
Genes·2020· 2 citedOpen Access
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Frequent Co-authors

Francis L. Munier(24), Pascal Escher(6), Christophe Bonny(5), Léonidas Zografos(5), Elena Korvatska(4), Anne Oberson(4), Graeme C. Black(4), Yvan Arsenijévic(4), Leila Tiab(4), Hana Abouzeid(4), Elise Héon(3), Pascal Cousin(3), Xiaodong Jiao(3), Fumino Iwata(3), J. Fielding Hejtmancik(3), Michel Michaelides(3), Béatrice E. Frueh(3), S. Uffer(3), Birgit Lorenz(3), Susanne Kohl(3)