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
1 - 10 of 65
- An in vitro enzymatic assay to elucidate the VUS problem in RPE65, a target for retinal gene therapy(2023)
Authors: Eline Van Vooren, Suzanne Kohl, Carlo Rivolta, Bart Leroy, Miriam Bauwens, Elfride De Baere
Number of pages: 1 - Outcome of cataract surgery in patients with retinitis pigmentosa(2023)
Authors: Xuan-Thanh-An Nguyen, Alberta A.H.J. Thiadens, Marta Fiocco, Weijen Tan, Martin McKibbin, Caroline C.W. Klaver, Magda A. Meester-Smoor, Caroline Van Cauwenbergh, Ine Strubbe, Andrea Vergaro, et al.
Pages: 1 - 9 - Indirect comparison of lenadogene nolparvovec gene therapy versus natural history in patients with Leber hereditary optic neuropathy carrying the m.11778G>A MT-ND4 mutation(2023)
Authors: V Carelli, NJ Newman, P Yu-Wai-Man, V Biousse, ML Moster, PS Subramanian, C Vignal-Clermont, AG Wang, SP Donahue, Bart Leroy, et al.
Pages: 401 - 429 - Restoration of cone sensitivity to individuals with congenital photoreceptor blindness within the phase 1/2 sepofarsen trial(2022)
Authors: Artur V. Cideciyan, Samuel G. Jacobson, Allen C. Ho, Arun K. Krishnan, Alejandro J. Roman, Alexandra V. Garafalo, Vivian Wu, Malgorzata Swider, Alexander Sumaroka, Caroline Van Cauwenbergh, et al.
- Evaluation of visual outcome following cataract surgery in patients with retinitis pigmentosa(2022)Volume: 100
Authors: Xuan-Thanh-An Nguyen, Alberta A. H. J Thiadens, Marta Fiocco, Weijen Tan, Martin McKibbin, Caroline C. W Klaver, Magda A Meester-Smoor, Caroline Van Cauwenbergh, Ine Strubbe, Andrea Vergaro, et al.
Pages: 21 - 21 - An in vitro enzymatic assay to elucidate the VUS problem in RPE65, a target for retinal gene therapy(2022)
Authors: Eline Van Vooren, Suzanne Kohl, Bart Leroy, Miriam Bauwens, Elfride De Baere
Pages: 27 - 27 - A virtual reality orientation and mobility test for inherited retinal degenerations : testing a proof-of-concept after gene therapy(2021)
Authors: Tomas S. Aleman, Alexander J. Miller, Katherine H. Maguire, Elena M. Aleman, Leona W. Serrano, Keli B. O'Connor, Emma C. Bedoukian, Bart Leroy, Albert M. Maguire, Jean Bennett
Pages: 939 - 952 - Comparative natural history of visual function from patients with biallelic variants in BBS1 and BBS10(2021)
Authors: Monika K. Grudzinska Pechhacker, Samuel G. Jacobson, V Drack, Arlene, Matteo Di Scipio, Ine Strubbe, Wanda Pfeifer, Jacque L. Duncan, Helene Dollfus, Nathalie Goetz, Jean Muller, et al.
- The need for widely available genomic testing in rare eye diseases : an ERN-EYE position statement(2021)
Authors: Graeme C. Black, [missing] ERN-EYE study group, Panagiotis Sergouniotis, Andrea Sodi, Bart Leroy, Caroline Van Cauwenbergh, Petra Liskova, Karen Grønskov, Artur Klett, Susanne Kohl, et al.
- 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