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Journal Articles (5)
Meeting Abstract (2)

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Investigative Ophthalmology & Visual Science (5)
Journal of Vision (1)
Translational Vision Science & Technology (1)

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ARVO Annual Meeting Abstract (2)
Article (1)
Articles (1)
Biochemistry and Molecular Biology (1)
Retina (1)
Visual Psychophysics and Physiological Optics (1)

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Genetics (4)
Eye Anatomy and Disorders (3)
Retina (3)
Biochemistry and Molecular Biology (1)
Low Vision (1)
Nanotechnology and Regenerative Medicine (1)
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Visual Psychophysics and Physiological Optics (1)

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mutation (3)
eye (2)
leber's amaurosis (2)
photopsia (2)
retinal cone (2)
anesthetics (1)
bleach (1)
blindness (1)
calibration (1)
congenital abnormality (1)

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ARVO Annual Meeting Abstract June 2022

High myopia and vitreal veils in a patient with Poretti-Boltshauser syndrome due to a novel homozygous LAMA1 mutation

Irina Balikova; Nawid Faizi; Paul Coucke; Marieke De Bruyne; Elfride De Baere; Ingele Casteels

Invest. Ophthalmol. Vis. Sci.. 2022; 63(7):493 – A0070. doi:

Articles March 2022

The Effect of Topical Anesthetics on 16S Ribosomal Ribonucleic Acid Amplicon Sequencing Results in Ocular Surface Microbiome Research

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Heleen Delbeke; Ingele Casteels; Marie Joossens
TAGS: anesthetics, microbiome, ocular surfaces, ribosomal rna, topical anesthetics
Trans. Vis. Sci. Tech.. 2022; 11(3):2. doi: https://doi.org/10.1167/tvst.11.3.2

Article November 2015

Spectral sensitivity measurements reveal partial success in restoring missing rod function with gene therapy

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Caterina Ripamonti; G. Bruce Henning; Scott J. Robbie; Venki Sundaram; L. Ingeborgh van den Born; Ingele Casteels; Thomy J. L. de Ravel; Anthony T. Moore; Alexander J. Smith; James W. Bainbridge; Robin R. Ali; Andrew Stockman
TAGS: gene therapy, retinal cone, rod photoreceptors, bleach, photopsia
Journal of Vision. 2015; 15(15):20. doi: https://doi.org/10.1167/15.15.20

Visual Psychophysics and Physiological Optics October 2014

Nature of the Visual Loss in Observers With Leber's Congenital Amaurosis Caused by Specific Mutations in RPE65

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Caterina Ripamonti; G. Bruce Henning; Robin R. Ali; James W. Bainbridge; Scott J. Robbie; Venki Sundaram; Vy A. Luong; L. Ingeborgh van den Born; Ingele Casteels; Thomy J. L. de Ravel; Anthony T. Moore; Andrew Stockman
TAGS: blindness, contrast sensitivity, eye, flicker fusion, leber's amaurosis, mutation, retinal cone, visual impairment, filters, luminance
Invest. Ophthalmol. Vis. Sci.. 2014; 55(10):6817-6828. doi: https://doi.org/10.1167/iovs.14-14923

ARVO Annual Meeting Abstract March 2012

Combined Identity-by-descent Mapping And Exome Sequencing Identifies A Novel MERTK Mutation In Autosomal Recessive Retinitis Pigmentosa

Frauke Coppieters; Kristof Van Schil; Steve Lefever; Julie De Zaeytijd; Bart P. Leroy; Ingele Casteels; Thomy de Ravel; Elfride De Baere

Invest. Ophthalmol. Vis. Sci.. 2012; 53(14):4521. doi:

Biochemistry and Molecular Biology January 2011

Expanding the Spectrum of FOXC1 and PITX2 Mutations and Copy Number Changes in Patients with Anterior Segment Malformations

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Barbara D'haene; Françoise Meire; Ilse Claerhout; Hester Y. Kroes; Astrid Plomp; Yvonne H. Arens; Thomy de Ravel; Ingele Casteels; Sarah De Jaegere; Sally Hooghe; Wim Wuyts; Jenneke van den Ende; Françoise Roulez; Hermine E. Veenstra-Knol; Rogier A. Oldenburg; Jacques Giltay; Johanna B. G. M. Verheij; Jan-Tjeerd de Faber; Björn Menten; Anne De Paepe; Philippe Kestelyn; Bart P. Leroy; Elfride De Baere
TAGS: congenital abnormality, mutation, screening
Invest. Ophthalmol. Vis. Sci.. 2011; 52(1):324-333. doi: https://doi.org/10.1167/iovs.10-5309

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Retina March 2006

Microarray-Based Mutation Detection and Phenotypic Characterization of Patients with Leber Congenital Amaurosis

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Suzanne Yzer; Bart P. Leroy; Elfride De Baere; Thomy J. de Ravel; Marijke N. Zonneveld; Krysta Voesenek; Ulrich Kellner; Jose P. Martinez Ciriano; Jan-Tjeerd H. N. de Faber; Klaus Rohrschneider; Ronald Roepman; Anneke I. den Hollander; Johannes R. Cruysberg; Françoise Meire; Ingele Casteels; Norka G. van Moll-Ramirez; Rando Allikmets; L. Ingeborgh van den Born; Frans P. M. Cremers
TAGS: genotype, leber's amaurosis, mutation, phenotype, genes, ophthalmoscopy, eye
Invest. Ophthalmol. Vis. Sci.. 2006; 47(3):1167-1176. doi: https://doi.org/10.1167/iovs.05-0848

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