Researcher
Bart Leroy
- Disciplines:Optometry, Ophthalmology, Optical technology, Epigenetics, Molecular medicine, Ophthalmology and optometry not elsewhere classified, Clinical genetics and molecular diagnostics, Immunogenetics, Genetics
Affiliations
- Department of Head and Skin (Department)
Member
From1 Oct 2018 → Today - Department of Ophthalmology (Department)
Responsible
From1 Oct 2014 → 30 Sep 2018 - Department of Ophthalmology (Department)
Member
From1 Oct 2014 → 30 Sep 2018 - Department of Ophthalmology (Department)
Member
From1 Oct 1998 → 30 Sep 2018
Projects
1 - 4 of 4
- An integrated CRISPR/iPSC-based approach to elucidate uncertain variation in RPE65, a target for gene therapyFrom1 Nov 2022 → TodayFunding: FWO Strategic Basic Research Grant
- Holistic mixed approaches to capture the real life of children with Rare Eye Diseases (SeeMyLife).From1 Nov 2022 → TodayFunding: FWO research project (including WEAVE projects)
- Precision medicine in inherited blindness using integrated omics in human and animal modelsFrom1 Jan 2020 → TodayFunding: BOF - projects
- Cis-regulatorische mapping van de RPE-geexpresseerde transcriptie factor OTX2From1 Nov 2012 → 31 Oct 2016Funding: Marie Curie - People
Publications
11 - 20 of 66
- 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 - The phenotypic spectrum of patients with PHARC syndrome due to variants in ABHD12 : an ophthalmic perspective(2021)
Authors: Xuan-Thanh-An Nguyen, Hind Almushattat, Ine Strubbe, Michalis Georgiou, Catherina H. Z. Li, Mary J. van Schooneveld, Inge Joniau, Elfride De Baere, Ralph J. Florijn, Arthur A. Bergen, et al.
- Vitreous hemorrhage as presenting sign of retinal arteriovenous malformation(2020)
Authors: Geraldine Accou, Fanny Nerinckx, Bart Leroy, Julie De Zaeytijd
- Long-term follow-up of retinal degenerations associated with LRAT mutations and their comparability to phenotypes associated with RPE65 mutations(2019)
Authors: Mays Talib, Mary J. van Schooneveld, Roos J. G. van Duuren, Caroline Van Cauwenbergh, Jacoline B. ten Brink, Elfride De Baere, Ralph J. Florijn, Nicoline E. Schalij-Delfos, Bart Leroy, Arthur A. Bergen, et al.
- Abetalipoproteinemia from previously unreported gene mutations(2019)
Authors: Xavier-Philippe Aers, Bart Leroy, Joep C Defesche, Samiah Shadid
Pages: 211 - 213 - Biallelic loss-of-function variants in RAX2, encoding a homeobox-containing Rax transcription factor, cause autosomal recessive inherited retinal disease(2018)
Authors: Stijn Van de Sompele, Claire Smith, Marianthi Karali, Marta Corton, Kristof Van Schil, Frank Peelman, Timothy Cherry, Toon Rosseel, Hannah Verdin, Julien Derolez, et al.
Number of pages: 1 - Homozygosity mapping-guided exome sequencing in LCA patients of consanguineous origin reveals mutations in known genes and a novel candidate gene(2017)Volume: 58
Authors: Basamat Almoallem Mohammed H, Kristof Van Schil, Laila Jeddawi, Bart Leroy, Frauke Coppieters, Elfride De Baere
Pages: 1242 - 1242 - Who stole my cholesterol? : a case report of night blindness and virtually absent serum betalipoproteins(2017)Volume: 72
Authors: Xavier-Philippe Aers, Bart Leroy, Samiah Shadid
Pages: 2 - 2 - Biallelic mutations in GNB3 cause a unique form of autosomal-recessive congenital stationary night blindness(2016)
Authors: Ajoy Vincent, Isabelle Audo, Erika Tavares, Jason T Maynes, Anupreet Tumber, Thomas Wright, Shuning Li, Christelle Michiels, Christel Condroyer, Heather MacDonald, et al.
Pages: 1011 - 1019 - Mutations in CTNNA1 cause butterfly-shaped pigment dystrophy and perturbed retinal pigment epithelium integrity(2016)
Authors: Nicole TM Saksens, Mark P Krebs, Frederieke E Schoenmaker-Koller, Wanda Hicks, Minzhong Yu, Lanying Shi, Lucy Rowe, Gayle B Collin, Jeremy R Charette, Stef J Letteboer, et al.
Pages: 144 - 151