dr. Caroline Van Cauwenbergh

CRB1-associated retinal dystrophies in a Belgian cohort : genetic characteristics and long-term clinical follow-up

Mays Talib, Caroline Van Cauwenbergh (UGent) , Julie De Zaeytijd (UGent) , David Van Wynsberghe, Elfride De Baere (UGent) , Camiel J F Boon and Bart Leroy (UGent)

(2021) BRITISH JOURNAL OF OPHTHALMOLOGY. 106(5). p.696-704

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A qualitative study among patients with an inherited retinal disease on the meaning of genomic unsolicited findings

Marlies Saelaert (UGent) , Heidi Mertes (UGent) , Tania Moerenhout, Caroline Van Cauwenbergh (UGent) , Bart Leroy (UGent) , Ignaas Devisch (UGent) and Elfride De Baere (UGent)

(2021) SCIENTIFIC REPORTS. 11(1).

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The need for widely available genomic testing in rare eye diseases : an ERN-EYE position statement

Graeme C. Black, [missing] ERN-EYE study group, Panagiotis Sergouniotis, Andrea Sodi, Bart Leroy (UGent) , Caroline Van Cauwenbergh (UGent) , Petra Liskova, Karen Grønskov, Artur Klett, Susanne Kohl, et al.

(2021) ORPHANET JOURNAL OF RARE DISEASES. 16(1).

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Isolated maculopathy and moderate rod-cone dystrophy represent the milder end of the RDH12-related retinal dystrophy spectrum

Julie De Zaeytijd (UGent) , Caroline Van Cauwenbergh (UGent) , Marieke De Bruyne (UGent) , Mattias Van Heetvelde (UGent) , Elfride De Baere (UGent) , Frauke Coppieters (UGent) and Bart Leroy (UGent)

(2021) RETINA-THE JOURNAL OF RETINAL AND VITREOUS DISEASES. 41(6). p.1346-1355

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Phenocopy of a heterozygous carrier of X-linked retinitis pigmentosa due to mosaicism for a RHO variant

Ine Strubbe (UGent) , Caroline Van Cauwenbergh (UGent) , Julie De Zaeytijd (UGent) , Sarah De Jaegere (UGent) , Marieke De Bruyne (UGent) , Toon Rosseel (UGent) , Stijn Van de Sompele (UGent) , Elfride De Baere (UGent) and Bart Leroy (UGent)

(2021) SCIENTIFIC REPORTS. 11.

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Clinical characteristics and natural history of rho-associated retinitis pigmentosa : a long-term follow-up study

Xuan-Thanh-An Nguyen, Mays Talib, Caroline Van Cauwenbergh (UGent) , Mary J. van Schooneveld, Marta Fiocco, Jan Wijnholds, Jacoline B. ten Brink, Ralph J. Florijn, Nicoline E. Schalij-Delfos, Gislin Dagnelie, et al.

(2021) RETINA -THE JOURNAL OF RETINAL AND VITREOUS DISEASES. 41(1). p.213-223

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Charting extracellular transcriptomes in the human biofluid RNA atlas

Eva Hulstaert, Annelien Morlion (UGent) , Francisco Avila Cobos (UGent) , Kimberly Verniers (UGent) , Justine Nuytens (UGent) , Eveline Vanden Eynde (UGent) , Nurten Yigit (UGent) , Jasper Anckaert (UGent) , Anja Geerts (UGent) , Pieter Hindryckx (UGent) , et al.

(2020) CELL REPORTS. 33(13).

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Expanded phenotypic spectrum of retinopathies associated with autosomal recessive and dominant mutations in PROM1

Marta Del Pozo-Valero, Inmaculada Martin-Merida, Belen Jimenez-Rolando, Ana Arteche, Almudena Avila-Fernandez, Fiona Blanco-Kelly, Rosa Riveiro-Alvarez, Caroline Van Cauwenbergh (UGent) , Elfride De Baere (UGent) , Carlo Rivolta, et al.

(2019) AMERICAN JOURNAL OF OPHTHALMOLOGY. 207. p.204-214

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Effect of an intravitreal antisense oligonucleotide on vision in Leber congenital amaurosis due to a photoreceptor cilium defect

Artur V. Cideciyan, Samuel G. Jacobson, Arlene V. Drack, Allen C. Ho, Jason Charng, Alexandra V. Garafalo, Alejandro J. Roman, Alexander Sumaroka, Ian C. Han, Maria D. Hochstedler, et al.

(2019) NATURE MEDICINE. 25(2). p.225-228

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Long-term follow-up of retinal degenerations associated with LRAT mutations and their comparability to phenotypes associated with RPE65 mutations

Mays Talib, Mary J. van Schooneveld, Roos J. G. van Duuren, Caroline Van Cauwenbergh (UGent) , Jacoline B. ten Brink, Elfride De Baere (UGent) , Ralph J. Florijn, Nicoline E. Schalij-Delfos, Bart Leroy (UGent) , Arthur A. Bergen, et al.

(2019) TRANSLATIONAL VISION SCIENCE & TECHNOLOGY. 8(4).

Academic Bibliography

dr. Caroline Van Cauwenbergh

CRB1-associated retinal dystrophies in a Belgian cohort : genetic characteristics and long-term clinical follow-up

A qualitative study among patients with an inherited retinal disease on the meaning of genomic unsolicited findings

The need for widely available genomic testing in rare eye diseases : an ERN-EYE position statement

Isolated maculopathy and moderate rod-cone dystrophy represent the milder end of the RDH12-related retinal dystrophy spectrum

Phenocopy of a heterozygous carrier of X-linked retinitis pigmentosa due to mosaicism for a RHO variant

Clinical characteristics and natural history of rho-associated retinitis pigmentosa : a long-term follow-up study

Charting extracellular transcriptomes in the human biofluid RNA atlas

Expanded phenotypic spectrum of retinopathies associated with autosomal recessive and dominant mutations in PROM1

Effect of an intravitreal antisense oligonucleotide on vision in Leber congenital amaurosis due to a photoreceptor cilium defect

Long-term follow-up of retinal degenerations associated with LRAT mutations and their comparability to phenotypes associated with RPE65 mutations

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