- ORCID iD
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0000-0002-1835-2405
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Evaluation of a novel antisense oligonucleotide therapy targeting a 5’UTR variant in the RDH12 gene
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Design and evaluation of universal control antisense oligonucleotides across cellular models
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BioID reveals that NR2E3 mediates transcriptional repression through the AP-1 complex
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- Journal Article
- A1
- open access
RetiGene, a comprehensive gene atlas for inherited retinal diseases (IRDs)
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- Journal Article
- A1
- open access
Generation of two iPSC lines (UGENTi003 and UGENTi004) from patients with intermediate rod-cone dystrophy carrying the c.[-123C>T;701G>A]; [806_810del] variants in the RDH12 gene
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- Journal Article
- A1
- open access
Non-coding single-nucleotide and structural variants affecting the EYS putative promoter cause autosomal recessive retinitis pigmentosa
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Unravelling the proxisome of photoreceptor-specific nuclear receptor NR2E3 reveals a potential molecular link between transcriptional regulation and splicing in human retina
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Evaluation of a novel antisense oligonucleotide therapy targeting a 5’UTR mutation in the RDH12 gene
-
Evaluation of a novel antisense oligonucleotide therapy targeting a 5’UTR mutation in the RDH12 gene
-
Evaluation of a novel antisense oligonucleotide therapy targeting a 5’UTR mutation in the RDH12 gene