Camille Andrieu

Paris, France

Last Updated: 09/26/2026

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Found 22 publications

Identification and functional validation of a novel disease-causing variant in the noncoding region of NYX.

Identification and functional validation of a novel disease-causing variant in the noncoding region of NYX.

Journal: Acta ophthalmologica

Published: October 17, 2025

Autosomal Recessive Bestrophinopathy-Phenotypic Variability, Natural History, and Genotype-Phenotype Correlations.

Autosomal Recessive Bestrophinopathy-Phenotypic Variability, Natural History, and Genotype-Phenotype Correlations.

Journal: American journal of ophthalmology

Published: October 08, 2025

Identification of IDH3G, encoding the gamma subunit of mitochondrial isocitrate dehydrogenase, as a novel candidate gene for X-linked retinitis pigmentosa.

Identification of IDH3G, encoding the gamma subunit of mitochondrial isocitrate dehydrogenase, as a novel candidate gene for X-linked retinitis pigmentosa.

Journal: Genetics in medicine : official journal of the American College of Medical Genetics

Published: December 12, 2024

Expanding the genetic landscape of Usher syndrome type IV caused by pathogenic ARSG variants.

Expanding the genetic landscape of Usher syndrome type IV caused by pathogenic ARSG variants.

Journal: Clinical genetics

Published: May 13, 2024

Voretigene neparvovec in RPE65-related inherited retinal dystrophy: the 1-year real-world study LIGHT.

Voretigene neparvovec in RPE65-related inherited retinal dystrophy: the 1-year real-world study LIGHT.

Journal: Eye (London, England)

Published: February 19, 2024

Variants in UBAP1L lead to autosomal recessive rod-cone and cone-rod dystrophy.

Variants in UBAP1L lead to autosomal recessive rod-cone and cone-rod dystrophy.

Journal: Genetics in medicine : official journal of the American College of Medical Genetics

Published: July 17, 2023

Salmonella Typhimurium uses the Cpx stress response to detect N-chlorotaurine and promote the repair of oxidized proteins.

Salmonella Typhimurium uses the Cpx stress response to detect N-chlorotaurine and promote the repair of oxidized proteins.

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

Published: March 28, 2023

Large Benefit from Simple Things: High-Dose Vitamin A Improves RBP4-Related Retinal Dystrophy.

Large Benefit from Simple Things: High-Dose Vitamin A Improves RBP4-Related Retinal Dystrophy.

Journal: International journal of molecular sciences

Published: April 22, 2022

HprSR Is a Reactive Chlorine Species-Sensing, Two-Component System in Escherichia coli.

HprSR Is a Reactive Chlorine Species-Sensing, Two-Component System in Escherichia coli.

Journal: Journal of bacteriology

Published: December 13, 2021

Novel TTLL5 Variants Associated with Cone-Rod Dystrophy and Early-Onset Severe Retinal Dystrophy.

Novel TTLL5 Variants Associated with Cone-Rod Dystrophy and Early-Onset Severe Retinal Dystrophy.

Journal: International journal of molecular sciences

Published: May 19, 2021

Mutated CCDC51 Coding for a Mitochondrial Protein, MITOK Is a Candidate Gene Defect for Autosomal Recessive Rod-Cone Dystrophy.

Mutated CCDC51 Coding for a Mitochondrial Protein, MITOK Is a Candidate Gene Defect for Autosomal Recessive Rod-Cone Dystrophy.

Journal: International journal of molecular sciences

Published: April 26, 2021

Retinal Phenotype of Patients With Isolated Retinal Degeneration Due to CLN3 Pathogenic Variants in a French Retinitis Pigmentosa Cohort.

Retinal Phenotype of Patients With Isolated Retinal Degeneration Due to CLN3 Pathogenic Variants in a French Retinitis Pigmentosa Cohort.

Journal: JAMA ophthalmology

Published: January 28, 2021

Showing 1-12 of 22

Last Updated: 09/26/2026