Ghent University Academic Bibliography

Your filters: cql: jcr.category exact "OPHTHALMOLOGY"

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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

V Carelli, NJ Newman, P Yu-Wai-Man, V Biousse, ML Moster, PS Subramanian, C Vignal-Clermont, AG Wang, SP Donahue, Bart Leroy (UGent) , et al.

(2023) OPHTHALMOLOGY AND THERAPY. 12. p.401-429
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Resolution of outer retinal abnormalities in eyes with vitreomacular traction without macular hole in the OASIS trial

Akshay S Thomas, Luc Duchateau (UGent) , Petra Kozma-Wiebe and Glenn Jaffe

(2023) BRITISH JOURNAL OF OPHTHALMOLOGY. 107(7). p.1012-1017
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Ligneous conjunctivitis mimicking preseptal cellulitis in a 3-month-old infant

Valentien Merlevede, Virginie Ninclaus (UGent) , Dimitri Roels (UGent) , Liesbeth Huys (UGent) , Bert Callewaert (UGent) and Elke O. Kreps (UGent)

(2023) OPHTHALMIC GENETICS. 44(1). p.103-106
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- Conference Paper
- C3
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Results of Belgian patients with RPE65-related inherited retinal dystrophy 6 months after treatment with voretigene neparvovec

Leen Hertens (UGent) , Caroline Van Cauwenbergh (UGent) , Filip Van Den Broeck (UGent) , Julie Sambaer (UGent) , Manon Van Haute (UGent) , Pieter Hertens (UGent) , Elfride De Baere (UGent) , Geraldine Accou (UGent) , Fanny Nerinckx (UGent) and Bart Leroy (UGent)

(2023) INVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCE. In Investigative Ophthalmology & Visual Science 64(8).
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- Conference Paper
- C3
Differential 3D genome topology shapes the regulatory landscapes of IRD genes in human neural retina and retinal pigment epithelium

Eva D'haene (UGent) , Pedro Martinez-Garcia, Victor Lopez Soriano (UGent) , Miriam Bauwens (UGent) , Lies Vantomme (UGent) , Sarah Vergult (UGent) , Juan Martinez-Morales, Juan Tena and Elfride De Baere (UGent)

(2023) INVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCE. In Investigative Ophthalmology & Visual Science 64(8).
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- Conference Paper
- C3
A systematic approach to characterize the contribution of 5'UTR variation to inherited retinal disease

Alfredo Dueñas Rey (UGent) , Manon Bouckaert (UGent) , Marta del Pozo Valero (UGent) , Marieke De Bruyne (UGent) , Mattias Van Heetvelde (UGent) , Jamie Ellingford, Gavin Arno, Andrew Webster, Carmen Ayuso, Carlo Rivolta, et al.

(2023) INVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCE. In Investigative Ophthalmology & Visual Science 64(8).
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- Conference Paper
- C3
- open access
Targeted sequencing using single-molecule Molecular Inversion Probes reveals severe bi-allelic ABCA4 alleles in probands diagnosed with Leber congenital amaurosis

Daan Panneman, Susanne Roosing, Erica Boonen, Chris Inglehearn, Martin McKibbin, Elfride De Baere (UGent) , Thomy de Ravel, Sascha Vermeer, Andrea Vincent, Robert Koenekoop, et al.

(2023) INVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCE. In Investigative Ophthalmology & Visual Science 64(8).
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- Conference Paper
- C3
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Multi-omics profiling, in vitro and in vivo approaches to interpret non-coding variation in inherited retinal diseases

Elfride De Baere (UGent)

(2023) INVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCE. In Investigative Ophthalmology & Visual Science 64(8).
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An application of causal inference in vitreomacular traction : how does the effect of ocriplasmin on functional and patient-reported outcomes occur

Benedicte Lescrauwaet, Luc Duchateau, Stijn Vansteelandt (UGent) , SriniVas Sadda and Timothy Jackson

(2023) INVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCE. 64(8).
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Whole genome sequencing delineates novel non-coding variants and candidate genes in inherited retinal diseases

Marta del Pozo Valero (UGent) , Miriam Bauwens (UGent) , Marieke De Bruyne (UGent) , Filip Van Den Broeck (UGent) , Stephanie Dulst, Quinten Quinten, Audrey Meunier, Thomy de Ravel, Joke Ruys, Mattias Van Heetvelde (UGent) , et al.

(2023) INVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCE. In Investigative Ophthalmology & Visual Science 64(8).

Academic Bibliography

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

Resolution of outer retinal abnormalities in eyes with vitreomacular traction without macular hole in the OASIS trial

Ligneous conjunctivitis mimicking preseptal cellulitis in a 3-month-old infant

Results of Belgian patients with RPE65-related inherited retinal dystrophy 6 months after treatment with voretigene neparvovec

Differential 3D genome topology shapes the regulatory landscapes of IRD genes in human neural retina and retinal pigment epithelium

A systematic approach to characterize the contribution of 5'UTR variation to inherited retinal disease

Targeted sequencing using single-molecule Molecular Inversion Probes reveals severe bi-allelic ABCA4 alleles in probands diagnosed with Leber congenital amaurosis

Multi-omics profiling, in vitro and in vivo approaches to interpret non-coding variation in inherited retinal diseases

An application of causal inference in vitreomacular traction : how does the effect of ocriplasmin on functional and patient-reported outcomes occur

Whole genome sequencing delineates novel non-coding variants and candidate genes in inherited retinal diseases

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