Researcher
Julie De Zaeytijd
- Disciplines:Ophthalmology and optometry, Palliative care and end-of-life care, Laboratory medicine, Other translational sciences, Regenerative medicine, Nursing, Other clinical sciences, Other basic sciences, Other paramedical sciences, Other health sciences, Other medical and health sciences
Affiliations
- Department of Head and Skin (Department)
Member
From1 Oct 2018 → 25 Sep 2022 - Department of Ophthalmology (Department)
Member
From18 Feb 2016 → 30 Sep 2018
Publications
1 - 10 of 63
- Long-read sequencing to unravel complex structural variants of CEP78 leading to cone-rod dystrophyand hearing loss(2022)Volume: 30
Authors: Giulia Ascari, Nanna D. Rendtorff, Marieke De Bruyne, Julie De Zaeytijd, Michel Van Lint, Gavin Arno, Julie Jacob, Toon Rosseel, Tim De Pooter, Peter De Rijk, et al.
Pages: 45 - 45 - Serum calcification propensity T50 associates with disease severity in patients with pseudoxanthoma elasticum(2022)
Authors: Lukas Nollet, Matthias Van Gils, Suzanne Fischer, Swapna Karthik, Andreas Pasch, Julie De Zaeytijd, Daniel Devos, Olivier Vanakker
- Clinical and subclinical findings in heterozygous ABCC6 carriers : results from a Belgian cohort and clinical practice guidelines(2022)
Authors: Lukas Nollet, Laurence Campens, Julie De Zaeytijd, Dimitri Hemelsoet, Olivier Vanakker
Pages: 496 - 504 - Long-term deep phenotyping in inherited ocular disease novel genotype-phenotype correlations(2022)
Authors: Julie De Zaeytijd
- Phenocopy of a heterozygous carrier of X-linked retinitis pigmentosa due to mosaicism for a RHO variant(2021)
Authors: Ine Strubbe, Julie De Zaeytijd, Sarah De Jaegere, Marieke De Bruyne, Toon Rosseel, Stijn Van de Sompele
- 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(2021)
Authors: Justine Vandeputte, Sara Seneca, Julie De Zaeytijd
Pages: 440 - 445 - Isolated maculopathy and moderate rod-cone dystrophy represent the milder end of the RDH12-related retinal dystrophy spectrum(2021)
Authors: Julie De Zaeytijd, Marieke De Bruyne
Pages: 1346 - 1355 - Longitudinal phenotypic study of late-onset retinal degeneration due to a founder variant c.562C > A p.(Pro188Thr) in the C1QTNF5 gene(2021)
Authors: Julie De Zaeytijd, Frauke Coppieters, Marieke De Bruyne, Jasper Van Royen, Dimitri Roels, Rani Six, Caroline Van Cauwenbergh, Elfride De Baere, Bart Leroy
Pages: 521 - 532 - Long-read sequencing to unravel complex structural variants of CEP78 leading to cone-rod dystrophy and hearing loss(2021)
Authors: Giulia Ascari, Nanna D. Rendtorff, Marieke De Bruyne, Julie De Zaeytijd, Michel Van Lint, Miriam Bauwens, Gavin Arno, Julie Jacob, Toon Rosseel, Tim De Pooter, et al.
- Scheimpflug-based analysis of the reflectivity of the cornea in Marfan syndrome(2021)
Authors: Michèle Tack, Elke O. Kreps, Julie De Zaeytijd, Alejandra Consejo