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Eva D'haene
Eva D'haene
Postdoctoral researcher | De Baere lab | Ghent University
Verified email at ugent.be
Title
Cited by
Cited by
Year
Identification of long non-coding RNAs involved in neuronal development and intellectual disability
E D’haene, EZ Jacobs, PJ Volders, T De Meyer, B Menten, S Vergult
Scientific Reports 6 (1), 28396, 2016
562016
Interpreting the impact of noncoding structural variation in neurodevelopmental disorders
E D’haene, S Vergult
Genetics in Medicine 23 (1), 34-46, 2021
352021
A neuronal enhancer network upstream of MEF2C is compromised in patients with Rett-like characteristics
E D’haene, R Bar-Yaacov, I Bariah, L Vantomme, S Van Loo, FA Cobos, ...
Human molecular genetics 28 (5), 818-827, 2019
192019
CRISPR/Cas9-mediated genome editing in naïve human embryonic stem cells
EZ Jacobs, S Warrier, PJ Volders, E D’haene, E Van Lombergen, ...
Scientific Reports 7 (1), 16650, 2017
122017
Transcriptional and functional consequences of alterations to MEF2C and its topological organization in neuronal models
K Mohajeri, R Yadav, E D'haene, PM Boone, S Erdin, D Gao, ...
The American Journal of Human Genetics 109 (11), 2049-2067, 2022
112022
Multi-omics approach dissects cis-regulatory mechanisms underlying North Carolina macular dystrophy, a retinal enhanceropathy
S Van de Sompele, KW Small, MB Cicekdal, VL Soriano, E D’haene, ...
The American Journal of Human Genetics 109 (11), 2029-2048, 2022
102022
SOX11 regulates SWI/SNF complex components as member of the adrenergic neuroblastoma core regulatory circuitry
B Decaesteker, A Louwagie, S Loontiens, F De Vloed, SL Bekaert, ...
Nature communications 14 (1), 1267, 2023
92023
A distant global control region is essential for normal expression of anterior HOXA genes during mouse and human craniofacial development
A Wilderman, E D’haene, M Baetens, TN Yankee, EW Winchester, ...
Nature Communications 15 (1), 136, 2024
82024
HDAC9 structural variants disrupting TWIST1 transcriptional regulation lead to craniofacial and limb malformations
N Hirsch, I Dahan, E D'haene, M Avni, S Vergult, M Vidal-García, P Magini, ...
Genome Research 32 (7), 1242-1253, 2022
72022
SOX11 is a lineage-dependency factor and master epigenetic regulator in neuroblastoma
B Decaesteker, A Louwagie, S Loontiens, F De Vloed, J Roels, ...
bioRxiv, 2020.08. 21.261131, 2020
72020
Multi-omics profiling, in vitro and in vivo enhancer assays dissect the cis-regulatory mechanisms underlying North Carolina macular dystrophy, a retinal …
S Van de Sompele, KW Small, MB Cicekdal, VL Soriano, E D’haene, ...
bioRxiv, 2022.03. 08.481329, 2022
22022
Regulation of non-canonical expression of ABCA4 by an RPE-specific enhancer with implications in ABCA4-associated disease
VL Soriano, AD Rey, G Ascari, M Cicekdal, E D'haene, Q Mahieu, ...
EUROPEAN JOURNAL OF HUMAN GENETICS 32, 39-40, 2024
2024
Differential 3D genome topology shapes the regulatory landscapes of IRD genes in human neural retina and retinal pigment epithelium
E D'haene, PM Martínez-García, V López-Soriano, M Bauwens, ...
Investigative Ophthalmology & Visual Science 64 (8), 2849-2849, 2023
2023
Comparative 3D genome analysis between neural retina and RPE reveals differential cis-regulatory interactions at retinal disease loci
E D'haene, VL Soriano, PM Martínez-García, S Kalayanamontri, AD Rey, ...
bioRxiv, 2023.06. 20.543842, 2023
2023
Identification and characterization of a novel retina-specific lncRNA upstream ABCA4 with a potential role in ABCA4-associated inherited retinal disease
AD Rey, V López-Soriano, Z Corradi, CM Dhaenens, M Bouckaert, ...
Investigative Ophthalmology & Visual Science 63 (7), 2628-2628, 2022
2022
An optimized workflow for CRISPR/Cas9-mediated generation of indels and large deletions in induced pluripotent stem cells and neural stem cells.
L Hamerlinck, MR Pérez Baca, E D'haene, L Vantomme, S Vergult
RARE-MED symposium, 2022
2022
Mapping the 3D genome of the human retina and its role in retinal disease
E D'haene, V Lopez Soriano, L Vantomme, B Wissinger, S Kohl, S Vergult, ...
Joint BeSHG/NVHG meeting 2022, 2022
2022
The adrenergic-specific long non-coding RNA NESPR controls survival of neuroblastoma cells
L Delhaye, E de Bony de Lavergne, D Rombaut, L Fang Qi, ...
OncoPoint Symposium 2022, 2022
2022
Whole genome sequencing and UMI-4C provide novel insights into the genetic architecture and mechanisms underlying North Carolina macular dystrophy, a cis-regulatory disease
S Van de Sompele, E D'haene, T Van der Snickt, S Vergult, P Liskova, ...
Investigative Ophthalmology & Visual Science 62 (8), 3-3, 2021
2021
Mapping the cis-regulatory landscape of ABCA4 in adult human retina
V López-Soriano, S Van de Sompele, E D'haene, JJ Tena-Aguilar, ...
Investigative Ophthalmology & Visual Science 62 (8), 2611-2611, 2021
2021
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