Publications by authors named "C Condroyer"

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EGFLAM Pathogenic Variants and Congenital Stationary Night Blindness.
Sanja Boranijasevic, Vasily Smirnov, Julien Navarro, Martha Tjon-Fo-Sang, Christel Condroyer

JAMA Ophthalmol· December 2025

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Autosomal Recessive Bestrophinopathy - Phenotypic variability, Natural History, and Genotype-phenotype correlations.
Lorenzo Bianco, Alessio Antropoli, Elise Boulanger-Scemama, Marco Nassisi, Amine Benadji, Christel Condroyer

Am J Ophthalmol· December 2025

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Variants in the ciliopathy gene SCLT1 are associated with non-syndromic retinal degeneration.
Riccardo Sangermano, Kaoru Fujinami, Suk Ho Byeon, Emily M Place, Julien Navarro, Christel Condroyer

Res Sq· May 2025

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Phenotypic and Genotypic Characterization of RP1L1-Associated Retinopathy.
Alessio Antropoli, Lorenzo Bianco, Xavier Zanlonghi, Amine Benadji, Christel Condroyer

Invest Ophthalmol Vis Sci· April 2025

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PCARE-Associated Retinopathy - Genetics, Clinical Characteristics, and Natural History.
Lorenzo Bianco, Alessio Antropoli, Amine Benadji, Raphaël Atia, Oana Palacci, Christel Condroyer

Invest Ophthalmol Vis Sci· April 2025

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