Christina Zeitz

Paris, France

Last Updated: 09/26/2026

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Found 137 publications

Combined Expression of hRdCVF and hRdCVFL Through AAV-Mediated Delivery for the Treatment of Retinitis Pigmentosa.

Combined Expression of hRdCVF and hRdCVFL Through AAV-Mediated Delivery for the Treatment of Retinitis Pigmentosa.

Journal: Investigative ophthalmology & visual science

Published: March 02, 2026

Biallelic germline variants in the hematologic malignancy predisposition gene DDX41 cause retinal dystrophy through dysregulation of retinal homeostasis.

Biallelic germline variants in the hematologic malignancy predisposition gene DDX41 cause retinal dystrophy through dysregulation of retinal homeostasis.

Journal: medRxiv : the preprint server for health sciences

Published: February 06, 2026

Retinal Impairments in Mice Lacking Both Nxnl1 and Nxnl2 Genes.

Retinal Impairments in Mice Lacking Both Nxnl1 and Nxnl2 Genes.

Journal: Investigative ophthalmology & visual science

Published: December 12, 2025

EGFLAM Pathogenic Variants and Congenital Stationary Night Blindness.

EGFLAM Pathogenic Variants and Congenital Stationary Night Blindness.

Journal: JAMA ophthalmology

Published: December 04, 2025

Increased sensitivity to myopia and altered retinal ON/OFF balance in a mouse model lacking Dusp4.

Increased sensitivity to myopia and altered retinal ON/OFF balance in a mouse model lacking Dusp4.

Journal: bioRxiv : the preprint server for biology

Published: November 19, 2025

Identification of a novel CABP4 frameshift variant and a secondary USH2A missense variant in congenital cone-rod synaptic disorder.

Identification of a novel CABP4 frameshift variant and a secondary USH2A missense variant in congenital cone-rod synaptic disorder.

Journal: Ophthalmic genetics

Published: October 23, 2025

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

Eyes shut homolog (EYS): Connecting molecule to disease.

Eyes shut homolog (EYS): Connecting molecule to disease.

Journal: Progress in retinal and eye research

Published: June 23, 2025

Development of RS1-specific ACMG/AMP variant classification criteria with pilot variant curation.

Development of RS1-specific ACMG/AMP variant classification criteria with pilot variant curation.

Journal: Human genetics

Published: June 20, 2025

Variants in the ciliopathy gene SCLT1 are associated with non-syndromic retinal degeneration.

Variants in the ciliopathy gene SCLT1 are associated with non-syndromic retinal degeneration.

Journal: Research square

Published: June 05, 2025

Variants in the ciliopathy gene SCLT1 are associated with non-syndromic and syndromic retinal degeneration of variable severity.

Variants in the ciliopathy gene SCLT1 are associated with non-syndromic and syndromic retinal degeneration of variable severity.

Journal: NPJ genomic medicine

Published: April 22, 2025

Showing 1-12 of 137

Last Updated: 09/26/2026