Julie De Zaeytijd

7PUBLICATIONS
189CO-AUTHORS
Gene expression (incl. microarray and other genome-wide approaches)Neurology and neuromuscular diseasesAtmospheric aerosolsOphthalmology and optometry not elsewhere classifiedLinguistic structures (incl. phonology, morphology and syntax)
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Publications (7)

|May 19, 2025
RPE65 variant p.(E519K) causes a novel dominant adult-onset maculopathy in 83 affected individuals.

Eline Van Vooren, Filip Van den Broeck, Quinten Mahieu

|Jan 20, 2025
De novo and inherited dominant variants in U4 and U6 snRNAs cause retinitis pigmentosa.

Mathieu Quinodoz, Kim Rodenburg, Zuzana Cvackova

|Apr 05, 2022
Intravitreal antisense oligonucleotide sepofarsen in Leber congenital amaurosis type 10: a phase 1b/2 trial.

Stephen R Russell, Arlene V Drack, Artur V Cideciyan

|May 05, 2021
Longitudinal phenotypic study of late-onset retinal degeneration due to a founder variant c.562C>A p.(Pro188Thr) in the C1QTNF5 gene.

Julie De Zaeytijd, Frauke Coppieters, Marieke De Bruyne

|Apr 16, 2021
Mild Leber hereditary optic neuropathy (LHON) in a Western European family due to the rare Asian m.14502T>C variant in the MT-ND6 gene.

Justine Vandeputte, Mattias Van Heetvelde, Caroline Van Cauwenbergh

|Jan 23, 2019
The N-terminal p.(Ser38Cys) TIMP3 mutation underlying Sorsby fundus dystrophy is a founder mutation disrupting an intramolecular disulfide bond.

Sarah Naessens, Julie De Zaeytijd, Delfien Syx

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Frequent Collaborators

6 joint publications

Bart P Leroy

4 joint publications

Elfride De Baere

3 joint publications

Caroline Van Cauwenbergh

2 joint publications

Artur V Cideciyan