Project
Genotype-phenotype studies and gene therapy for inherited blindness
Genotype-phenotype studies and gene therapy for inherited blindness
Researchers
- Alain Van Hiel (Promoter)
Department of Developmental, Personality and Social Psychology
Duration: 1 Oct 2013 → 30 Sep 2022 - Philippe Kestelyn (Promoter)Duration: 16 May 2010 → 30 Sep 2013
- Alain Van Hiel (Co-promoter)
Department of Developmental, Personality and Social Psychology
Duration: 16 May 2010 → 30 Sep 2013 - Bart Leroy (Fellow)Duration: 1 Oct 2018 → 30 Sep 2022
Project partners
- Department of Developmental, Personality and Social Psychology (Department)From16 May 2010 → 30 Sep 2013
- Department of Ophthalmology (Department)From16 May 2010 → 30 Sep 2013
Funding
1 - 1 of 1 results
- Funding: FWO fellowships(Principal funding)
Funding party: Research Foundation Flanders
Policy level funding: Flemish
Publications
1 - 7 of 7
- Multi-omics approach dissects cis-regulatory mechanisms underlying North Carolina macular dystrophy, a retinal enhanceropathy
Authors: Stijn Van de Sompele, Kent W. Small, Münevver Burcu Cicekdal, Victor Lopez Soriano, Fadi S. Shaya, Steven Agemy, Thijs Van der Snickt, Alfredo Dueñas Rey, Toon Rosseel, Sarah Vergult, et al.
Pages: 2029 - 2048 - Intravitreal antisense oligonucleotide sepofarsen in Leber congenital amaurosis type 10 : a phase 1b/2 trial
Authors: Stephen R. Russell, Arlene V. Drack, Artur V. Cideciyan, Samuel G. Jacobson, Allen C. Ho, Alina V. Dumitrescu, Ian C. Han, Mitchell Martin, Wanda L. Pfeifer, Elliott H. Sohn, et al.
Pages: 1014 - 1021 - 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
- 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 - Cost-effective sequence analysis of 113 genes in 1,192 probands with retinitis pigmentosa and Leber congenital amaurosis(2023)
Authors: Daan M. Panneman, Rebekkah J. Hitti-Malin, Lara K. Holtes, Suzanne E. de Bruijn, Janine Reurink, Erica G. M. Boonen, Muhammad Imran Khan, Manir Ali, Sten Andréasson, Sandro Banfi, et al.
- Randomized trial of bilateral gene therapy injection for m.11778G>A MT-ND4 Leber optic neuropathy
Authors: Nancy J. Newman, Patrick Yu-Wai-Man, Prem S. Subramanian, Mark L. Moster, An-Guor Wang, Sean P. Donahue, Bart Leroy, Valerio Carelli, Valerie Biousse, Catherine Vignal-Clermont, et al.
Pages: 1328 - 1341 - The natural history of leber congenital amaurosis and cone–rod dystrophy associated with variants in the GUCY2D gene
Authors: Leo C. Hahn, Michalis Georgiou, Hind Almushattat, Mary J. van Schooneveld, Emanuel R. de Carvalho, Nieneke L. Wesseling, Jacoline B. ten Brink, Ralph J. Florijn, Birgit I. Lissenberg-Witte, Ine Strubbe, et al.
Pages: 711 - 722