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Researcher
Bart Leroy
Profile
Projects
Publications
Activities
Awards & Distinctions
Results
:
ALL
(
15
)
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Title (a-z)
Title (a-z)
Chronological by starting year (new to old)
As
Promotor-spokesperson
01 November 2022 → 31 December 2025
Holistic mixed approaches to capture the real life of children with Rare Eye Diseases (SeeMyLife).
Funding: Research Foundation - Flanders (FWO)
As
Administrative supervisor
18 September 2020 → 25 September 2022
Doctoral project Ine Strubbe
Doctoral researcher: Ine Strubbe
15 March 2023 → 21 September 2025
Early diagnosis and treatment of immune-mediated ocular surface disease.
Doctoral researcher: Dimitri Roels
23 April 2021 → 21 September 2025
Precision medicine in inherited blindness using integrated omics in humans
Doctoral researcher: Filip Van den Broeck
As
PhD Supervisor
16 December 2022 → 21 September 2025
An integrated CRISPR/iPSC-based approach to elucidate uncertain variation in RPE65, a target for gene therapy
Doctoral researcher: Eline Van Vooren
14 September 2022 → 21 September 2025
Development of a non-invasive prognostic test for Graves' orbitopathy
Doctoral researcher: Virginie Ninclaus
13 January 2025 → 21 September 2025
Development of a novel mutation-agnostic therapy for PRPH2-associated inherited retinal diseases.
Doctoral researcher: Alvaro Gonzalez Cid
12 September 2012 → 19 September 2018
Doctoral project Miriam Bauwens
Doctoral researcher: Miriam Bauwens
14 December 2023 → 21 September 2025
The quest for a generic therapy for inherited blindness: NRF2 upstream open reading frames as a novel therapeutic target
Doctoral researcher: Kyana Van Acker
As
Promotor
01 January 2024 → 31 December 2024
Genotypes, Phenotypes & Treatment in Ophthalmic Genetics
Funding: Regional and community funding: Special Research Fund
01 January 2020 → 31 October 2026
Precision medicine in inherited blindness using integrated omics in human and animal models
Funding: Regional and community funding: Special Research Fund
As
Copromotor
01 November 2022 → 31 October 2026
An integrated CRISPR/iPSC-based approach to elucidate uncertain variation in RPE65, a target for gene therapy
Fellow: Eline Van Vooren
Funding: Research Foundation - Flanders (FWO)
01 November 2012 → 31 October 2016
Cis-regulatorische mapping van de RPE-geexpresseerde transcriptie factor OTX2
Funding: European funding: framework programme
01 November 2023 → 31 October 2025
The quest for a generic therapy for inherited blindness: NRF2 upstream open reading frames as a novel therapeutic target
Fellow: Kyana Van Acker
Funding: Research Foundation - Flanders (FWO)
As
Fellow
16 May 2010 → 30 September 2022
Genotype-phenotype studies and gene therapy for inherited blindness
Fellows: Bart Leroy
Funding: Research Foundation - Flanders (FWO)