Irina Balikova

Miscellaneous

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. 64(8).

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Conference Paper

Whole genome sequencing sheds light on the dark matter of the genome in patients with inherited retinal diseases

Miriam Bauwens (UGent) , Marta del Pozo Valero (UGent) , Marieke De Bruyne (UGent) , Filip Van Den Broeck (UGent) , Quinten Mahieu (UGent) , Mattias Van Heetvelde (UGent) , Irina Balikova (UGent) , Sascha Vermeer, Julie De Zaeytijd (UGent) , Bart Leroy (UGent) , et al.

(2023)

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Journal Article
A1
open access

Paediatric cataract surgery with 27G vitrectomy instrumentation : the Ghent University Hospital experience

Hwei Wuen Chan, Filip Van Den Broeck (UGent) , Axelle Cools (UGent) , SOPHIE WALRAEDT (UGent) , Inge Joniau (UGent) , Hannah Verdin (UGent) , Irina Balikova (UGent) , Stefaan Van Nuffel, Patricia Delbeke, Elfride De Baere (UGent) , et al.

(2023) FRONTIERS IN MEDICINE. 10.

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Journal Article
A1
open access

Multi-omics approach dissects cis-regulatory mechanisms underlying North Carolina macular dystrophy, a retinal enhanceropathy

Stijn Van de Sompele (UGent) , Kent W. Small, Münevver Burcu Cicekdal (UGent) , Victor Lopez Soriano (UGent) , Eva D'haene (UGent) , Fadi S. Shaya, Steven Agemy, Thijs Van der Snickt (UGent) , Alfredo Dueñas Rey (UGent) , Toon Rosseel (UGent) , et al.

(2022) AMERICAN JOURNAL OF HUMAN GENETICS. 109(11). p.2029-2048

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Expanding the clinical spectrum and management of traboulsi syndrome : report on two siblings homozygous for a novel pathogenic variant in ASPH

Tom Van Hoorde (UGent) , Fanny Nerinckx (UGent) , Elke O. Kreps (UGent) , Dimitri Roels (UGent) , Philippe Huyghe, Mattias Van Heetvelde (UGent) , Hannah Verdin (UGent) , Elfride De Baere (UGent) , Irina Balikova (UGent) and Bart Leroy (UGent)

(2021) OPHTHALMIC GENETICS. 42(4). p.493-499

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Journal Article
A1
open access

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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Whole genome sequencing and 4C techniques provide novel insights into the genetic architecture and mechanisms underlying North Carolina macular dystrophy, a cis-regulatory disease

Stijn Van de Sompele (UGent) , Thijs Van der Snickt (UGent) , Eva D'haene (UGent) , Sarah Vergult (UGent) , Petra Liskova, Carlo Rivolta, Jenneke van den Ende, Arthur A. Bergen, Irina Balikova (UGent) , Julie De Zaeytijd (UGent) , et al.

(2020) Retina Meeting, Abstracts.

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Whole genome sequencing and 4C techniques provide novel insights into the genetic architecture and mechanisms underlying North Carolina macular dystrophy, a cis-regulatory disease

Stijn Van de Sompele (UGent) , Thijs Van der Snickt (UGent) , Eva D'haene (UGent) , Sarah Vergult (UGent) , Petra Liskova, Carlo Rivolta, Jenneke Van den Ende, Arthur A. Bergen, Irina Balikova (UGent) , Julie De Zaeytijd (UGent) , et al.

(2020) European Human Genetics Virtual Conference ESHG 2020.2, Abstracts.

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Whole genome sequencing and 4C techniques provide novel insights into the genetic architecture and mechanisms underlying North Carolina macular dystrophy, a cis-regulatory disease

Stijn Van de Sompele (UGent) , Thijs Van der Snickt (UGent) , Eva D'haene (UGent) , Sarah Vergult (UGent) , Petra Liskova, Carlo Rivolta, Jenneke van den Ende, Arthur Bergen, Irina Balikova (UGent) , Julie De Zaeytijd (UGent) , et al.

(2020) Belgian Society for Human Genetics, 20th Annual meeting, Abstracts.

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Exome-based panel testing as an efficient method to diagnose the highly heterogeneous ocular disorder spectrum Microphthalmia, Anophthalmia, Coloboma and Anterior Segment Dysgenesis (MAC-ASD)

Hannah Verdin (UGent) , Toon Rosseel (UGent) , Sascha Vermeer, Irina Balikova (UGent) , Philippe Kestelyn (UGent) , Colombine Meunier, Françoise Meire (UGent) , Julie Van De Velde (UGent) , Olivier Vanakker (UGent) , Jenneke Van Den Ende, et al.

(2020) Belgian Society for Human Genetics, 20th Annual meeting, Abstracts.

Academic Bibliography

Irina Balikova

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

Whole genome sequencing sheds light on the dark matter of the genome in patients with inherited retinal diseases

Paediatric cataract surgery with 27G vitrectomy instrumentation : the Ghent University Hospital experience

Multi-omics approach dissects cis-regulatory mechanisms underlying North Carolina macular dystrophy, a retinal enhanceropathy

Expanding the clinical spectrum and management of traboulsi syndrome : report on two siblings homozygous for a novel pathogenic variant in ASPH

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

Whole genome sequencing and 4C techniques provide novel insights into the genetic architecture and mechanisms underlying North Carolina macular dystrophy, a cis-regulatory disease

Whole genome sequencing and 4C techniques provide novel insights into the genetic architecture and mechanisms underlying North Carolina macular dystrophy, a cis-regulatory disease

Whole genome sequencing and 4C techniques provide novel insights into the genetic architecture and mechanisms underlying North Carolina macular dystrophy, a cis-regulatory disease

Exome-based panel testing as an efficient method to diagnose the highly heterogeneous ocular disorder spectrum Microphthalmia, Anophthalmia, Coloboma and Anterior Segment Dysgenesis (MAC-ASD)

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