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
11 - 20 of 63
- Vitreous hemorrhage as presenting sign of retinal arteriovenous malformation(2020)
Authors: Geraldine Accou, Fanny Nerinckx, Bart Leroy, Julie De Zaeytijd
- Unraveling complex structural variants of CEP78 leading to cone-rod dystrophy and hearing loss using long-read sequencing(2020)
Authors: Giulia Ascari, Nanna D. Rendtorff, Julie Jacob, Julie De Zaeytijd, Valerie Baumont, Marieke De Bruyne, Toon Rosseel, Mattias Van Heetvelde, Tim De Pooter, Wouter De Coster, et al.
Number of pages: 1 - VEGFA variants as prognostic markers for the retinopathy in pseudoxanthoma elasticum(2020)
Authors: Eva De Vilder, Mohammad Jakir Hosen, Ludovic Martin, Julie De Zaeytijd, Jean-Marc Ebran, Olivier Vanakker
Pages: 74 - 79 - Whole genome sequencing and 4C techniques provide novel insights into the genetic architecture and mechanisms underlying North Carolina macular dystrophy, a cis-regulatory disease(2020)
Authors: Stijn Van de Sompele, Thijs Van der Snickt, Eva D'haene, Sarah Vergult, Petra Liskova, Carlo Rivolta, Jenneke van den Ende, Arthur Bergen, Irina Balikova, Julie De Zaeytijd, et al.
Number of pages: 1 - The majority of autosomal recessive nanophthalmos and posterior microphthalmia can be attributed to biallelic sequence and structural variants in MFRP and PRSS56(2020)
Authors: Basamat Almoallem Mohammed H, Gavin Arno, Julie De Zaeytijd, Hannah Verdin, Irina Balikova, Ingele Casteels, Thomy de Ravel, Sarah Hull, Martina Suzani, Anne Destrée, et al.
- Worsening of cluster headache with intravenous dihydroergotamine? Think out of the box!(2019)Volume: 39
Authors: Julie De Zaeytijd, Dimitri Roels
Pages: 316 - 316 - ABCA4-associated disease as a model for missing heritability in autosomal recessive disorders : novel noncoding splice, cis-regulatory, structural, and recurrent hypomorphic variants(2019)
Authors: Miriam Bauwens, Alejandro Garanto, Riccardo Sangermano, Sarah Naessens, Nicole Weisschuh, Julie De Zaeytijd, Mubeen Khan, Françoise Sadler, Irina Balikova, Toon Rosseel, et al.
Pages: 1761 - 1771 - Coding and non-coding structural variants of ABCA4 contribute to the missing heritability in Stargardt disease, a prevalent inherited retinal disease(2019)Volume: 27
Authors: Miriam Bauwens, Sarah Naessens, Sarah De Jaegere, Irina Balikova, Yves Sznajer, Julie De Zaeytijd
Pages: 42 - 43 - The N‐terminal p.(Ser38Cys) TIMP3 mutation underlying Sorsby fundus dystrophy is a founder mutation disrupting an intramolecular disulfide bond(2019)
Authors: Sarah Naessens, Julie De Zaeytijd, Frédéric Smeets
Pages: 539 - 551 - Biallelic sequence and structural variants in RAX2 are a novel cause for autosomal recessive inherited retinal disease(2019)
Authors: Stijn Van de Sompele, Claire Smith, Marianthi Karali, Marta Corton, Kristof Van Schil, Timothy Cherry, Toon Rosseel, Hannah Verdin, Julien Derolez, Kamron N. Khan, et al.
Pages: 1319 - 1329