Researcher
Eva D'haene
- Disciplines:Analysis of next-generation sequence data, Epigenetics, Laboratory medicine, Other basic sciences, Genetics, Computational transcriptomics and epigenomics
Affiliations
- Department of Biomolecular Medicine (Department)
Member
From1 Oct 2018 → Today - Department of Pediatrics and medical genetics (Department)
Member
From17 Aug 2015 → 30 Sep 2018
Projects
1 - 4 of 4
- 3D genome topology and multi-omics in granulosa cells to decipher the regulation of FOXL2, a key factor in ovarian development and maintenanceFrom1 Nov 2023 → TodayFunding: FWO fellowships
- Role of the ultraconserved IRXA cluster in North Carolina Macular Dystrophy, a retinal enhanceropathyFrom1 Nov 2023 → TodayFunding: FWO fellowships
- 3D-RET: unlocking 3D genome architecture in human retina using C-technologiesFrom1 Oct 2022 → TodayFunding: FWO junior postdoctoral fellowship
- Elucidating the dark matter of the genome in central nervous system disorders.From1 Jan 2016 → 31 Dec 2017Funding: Foundations, funds and other with scientific goal
Publications
1 - 10 of 11
- Structural variants disrupt a critical regulatory region downstream of FOXG1(2023)Volume: 31
Authors: Eva D'haene, Lies Vantomme, Björn Menten, Bert Callewaert, Elfride De Baere, Sarah Vergult
Pages: 28 - 28 - Comparative 3D genome analysis between neural retina and RPE reveals differential cis-regulatory interactions at retinal disease loci(2023)
Authors: Eva D'haene, Pedro Manuel Martinez-Garcia, Victor Lopez Soriano, Soraya Kalayanamontri, Alfredo Dueñas Rey, Lies Vantomme, Sarah Vergult, Ana Bastos Neto, José Luis Gomez-Skarmeta, Juan Ramon Martinez-Morales, et al.
Number of pages: 1 - Differential 3D genome topology shapes the regulatory landscapes of IRD genes in human neural retina and retinal pigment epithelium(2023)Volume: 64
Authors: Eva D'haene, Pedro Martinez-Garcia, Victor Lopez Soriano, Miriam Bauwens, Lies Vantomme, Sarah Vergult, Juan Martinez-Morales, Juan Tena, Elfride De Baere
Number of pages: 1 - Mapping the 3D genome of the human retina and its role in retinal disease(2023)Volume: 31
Authors: Eva D'haene, Victor Lopez Soriano, Lies Vantomme, Bernd Wissinger, Susanne Kohl, Sarah Vergult, Elfride De Baere
Pages: 57 - 57 - An optimized workflow for CRISPR/Cas9-mediated generation of indels and large deletions in induced pluripotent stem cells and neural stem cells(2022)
Authors: Lisa Hamerlinck, Maria del Rocio Pérez Baca, Lies Vantomme, Eva D'haene, Sarah Vergult
Pages: 38 - 38 - Mapping the 3D genome of the human retina and its role in retinal disease(2022)
Authors: Eva D'haene, Victor Lopez Soriano, Lies Vantomme, Bernd Wissinger, Susanne Kohl, Sarah Vergult, Elfride De Baere
Number of pages: 1 - Transcriptional and functional consequences of alterations to MEF2C and its topological organization in neuronal models(2022)
Authors: Kiana Mohajeri, Rachita Yadav, Eva D'haene, Philip M. Boone, Serkan Erdin, Dadi Gao, Mariana Moyses-Oliveira, Riya Bhavsar, Benjamin B. Currall, Kathryn O'Keefe, et al.
Pages: 2049 - 2067 - Neurodevelopmental disorders in 3D : interpreting the impact of non-coding structural variation on gene regulation and 3D chromatin structure(2021)
Authors: Eva D'haene
- Whole genome sequencing and 4C techniques provide novel insights into the genetic architecture and mechanisms underlying North Carolina macular dystrophy, a cis-regulatory disease(2020)
Authors: Stijn Van de Sompele, Thijs Van der Snickt, Eva D'haene, Sarah Vergult, Petra Liskova, Carlo Rivolta, Jenneke van den Ende, Arthur Bergen, Irina Balikova, Julie De Zaeytijd, et al.
Number of pages: 1 - A neuronal enhancer network upstream of MEF2C is compromised in patients with Rett-like characteristics(2018)
Authors: Eva D'haene, Reut Bar-Yaacov, Inbar Bariah, Lies Vantomme, Sien Van Loo, Francisco Avila Cobos, Karen Verboom, Reut Eshel, Rawan Alatawna, Björn Menten, et al.
Number of pages: 1