Interpreting the impact of noncoding structural variation in neurodevelopmental disorders

por D’haene, Eva, Vergult, Sarah
Publicado 2020

Identification of long non-coding RNAs involved in neuronal development and intellectual disability

por D’haene, Eva, Jacobs, Eva Z., Volders, Pieter-Jan, De Meyer, Tim, Menten, Björn, Vergult, Sarah
Publicado 2016

CRISPR/Cas9-mediated genome editing in naïve human embryonic stem cells

por Jacobs, Eva Z., Warrier, Sharat, Volders, Pieter-Jan, D’haene, Eva, Van Lombergen, Eva, Vantomme, Lies, Van der Jeught, Margot, Heindryckx, Björn, Menten, Björn, Vergult, Sarah
Publicado 2017

A neuronal enhancer network upstream of MEF2C is compromised in patients with Rett-like characteristics

por D’haene, Eva, Bar-Yaacov, Reut, Bariah, Inbar, Vantomme, Lies, Van Loo, Sien, Cobos, Francisco Avila, Verboom, Karen, Eshel, Reut, Alatawna, Rawan, Menten, Björn, Birnbaum, Ramon Y, Vergult, Sarah
Publicado 2019

HDAC9 structural variants disrupting TWIST1 transcriptional regulation lead to craniofacial and limb malformations

por Hirsch, Naama, Dahan, Idit, D'haene, Eva, Avni, Matan, Vergult, Sarah, Vidal-García, Marta, Magini, Pamela, Graziano, Claudio, Severi, Giulia, Bonora, Elena, Nardone, Anna Maria, Brancati, Francesco, Fernández-Jaén, Alberto, Rory, Olson J., Hallgrímsson, Benedikt, Birnbaum, Ramon Y.
Publicado 2022

SOX11 regulates SWI/SNF complex components as member of the adrenergic neuroblastoma core regulatory circuitry

por Decaesteker, Bieke, Louwagie, Amber, Loontiens, Siebe, De Vloed, Fanny, Bekaert, Sarah-Lee, Roels, Juliette, Vanhauwaert, Suzanne, De Brouwer, Sara, Sanders, Ellen, Berezovskaya, Alla, Denecker, Geertrui, D’haene, Eva, Van Haver, Stéphane, Van Loocke, Wouter, Van Dorpe, Jo, Creytens, David, Van Roy, Nadine, Pieters, Tim, Van Neste, Christophe, Fischer, Matthias, Van Vlierberghe, Pieter, Roberts, Stephen S., Schulte, Johannes, Ek, Sara, Versteeg, Rogier, Koster, Jan, van Nes, Johan, Zimmerman, Mark, De Preter, Katleen, Speleman, Frank
Publicado 2023

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

por Van de Sompele, Stijn, Small, Kent W., Cicekdal, Munevver Burcu, Soriano, Víctor López, D’haene, Eva, Shaya, Fadi S., Agemy, Steven, Van der Snickt, Thijs, Rey, Alfredo Dueñas, Rosseel, Toon, Van Heetvelde, Mattias, Vergult, Sarah, Balikova, Irina, Bergen, Arthur A., Boon, Camiel J.F., De Zaeytijd, Julie, Inglehearn, Chris F., Kousal, Bohdan, Leroy, Bart P., Rivolta, Carlo, Vaclavik, Veronika, van den Ende, Jenneke, van Schooneveld, Mary J., Gómez-Skarmeta, José Luis, Tena, Juan J., Martinez-Morales, Juan R., Liskova, Petra, Vleminckx, Kris, De Baere, Elfride
Publicado 2022