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
21 - 30 of 65
- De novo intrachromosomal gene conversion from OPN1MW to OPN1LW in the male germline results in Blue Cone Monochromacy(2016)
Authors: Elena Buena-Atienza, Klaus Rüther, Britta Baumann, Richard Bergholz, David Birch, Elfride De Baere, Helene Dollfus, Marie T Greally, Peter Gustavsson, Christian P Hamel, et al.
- Advancing Therapeutic Strategies for Inherited Retinal Degeneration: Recommendations From the Monaciano Symposium(2015)
Authors: Debra A Thompson, Robin R Ali, Eyal Banin, Kari E Branham, John G Flannery, David M Gamm, William W Hauswirth, John R Heckenlively, Alessandro Iannaccone, K Thiran Jayasundera, et al.
Pages: 918 - 931 - SF3B2, a novel candidate gene for autosomal dominant retinitis pigmentosa, encodes a component of the U2 small nuclear ribonucleoprotein(2015)Volume: 56
Authors: Caroline Van Cauwenbergh, Kris Vleminckx, Frauke Coppieters, Marcus Karlstetter, Thomas Langmann, Gael Manes, Christian P Hamel, Bart Leroy, Elfride De Baere
Number of pages: 1 - Refsum disease(2015)
Authors: Ronald JA Wanders, Hans R Waterham, Bart Leroy, RA Pagon, TC Bird, CR Dolan, K Stephens
Number of pages: 1 - SF3B2, a novel candidate gene for autosomal dominant retinitis pigmentosa, encodes a component of the U2 small nuclear ribonucleoprotein(2015)Volume: 23
Authors: Caroline Van Cauwenbergh, Marcus Karlstetter, Kris Vleminckx, Gael Manes, Thomas Langmann, Christian Hamel, Bart Leroy, Frauke Coppieters, Elfride De Baere
Pages: 73 - 73 - Mutations in IFT172 cause isolated retinal degeneration and Bardet-Biedl syndrome(2015)
Authors: Kinga M Bujakowska, Qi Zhang, Anna M Siemiatkowska, Qin Liu, Emily Place, Marni J Falk, Mark Consugar, Marie-Elise Lancelot, Aline Antonio, Christine Lonjou, et al.
Pages: 230 - 242 - Retinal development in infants and young children with achromatopsia(2015)
Authors: Helena Lee, Ravi Purohit, Viral Sheth, Rebecca J McLean, Susanne Kohl, Bart Leroy, Venki Sundaram, Michel Michaelides, Frank A Proudlock, Irene Gottlob
Pages: 2145 - 2147 - SLC24A5 Mutations are associated with non-syndromic oculocutaneous albinism(2014)
Authors: Fanny Morice-Picard, Eulalie Lasseaux, Stéphane François, Delphine Simon, Caroline Rooryck, Eric Bieth, Estelle Colin, Dominique Bonneau, Hubert Journel, SOPHIE WALRAEDT, et al.
Pages: 568 - 571 - Abnormal retinal development associated with FRMD7 mutations(2014)
Authors: Mervyn G Thomas, Moira Crosier, Susan Lindsay, Anil Kumar, Masasuke Araki, Bart Leroy, Rebecca J McLean, Viral Sheth, Gail Maconachie, Shery Thomas, et al.
Pages: 4086 - 4089 - Spectrum of Cav1.4 dysfunction in congenital stationary night blindness type 2(2014)
Authors: Verena Burtscher, Klaus W Schicker, Elena Novikova, Birgit Pöhn, Thomas Stockner, Christof Kugler, Anamika Singh, Christina Zeitz, Marie-Elise Lancelot, Isabelle Audo, et al.
Pages: 2053 - 2065