Zeitz Christina

31PUBLICATIONS
75CO-AUTHORS
Neurology and neuromuscular diseasesOptical technologyCellular nervous systemNeurogeneticsVision science
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Publications (31)

|Feb 23, 2026
Identification and functional validation of a novel disease-causing variant in the noncoding region of NYX.

Filip Spanic, Christelle Michiels, Julien Navarro

|Nov 19, 2025
Increased sensitivity to myopia and altered retinal ON/OFF balance in a mouse model lacking <i>Dusp4</i>.

Baptiste Wilmet, Christelle Michiels, Jingyi Zhang

|Mar 15, 2025
Voretigene neparvovec in RPE65-related inherited retinal dystrophy: the 1-year real-world study LIGHT.

Isabelle Audo, Pierre-Olivier Barale, Céline Devisme

|Nov 08, 2024
Coding and non-coding variants in the ciliopathy gene CFAP410 cause early-onset non-syndromic retinal degeneration.

Riccardo Sangermano, Priya Gupta, Cherrell Price

|Jul 30, 2024
Characterising the refractive error in paediatric patients with congenital stationary night blindness: a multicentre study.

Austin D Igelman, Elizabeth White, Alaa Tayyib

|Jan 08, 2023
Mice Lacking <i>Gpr179</i> with Complete Congenital Stationary Night Blindness Are a Good Model for Myopia.

Baptiste Wilmet, Jacques Callebert, Robert Duvoisin

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Frequent Collaborators

25 joint publications

Isabelle Audo

8 joint publications

Said El-Shamieh

7 joint publications

José-Alain Sahel

6 joint publications

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