Onderzoeker
Lies Vantomme
- Disciplines:Palliatieve zorg en zorg rond het levenseinde, Laboratoriumgeneeskunde, Andere translationele wetenschappen, Regeneratieve geneeskunde, Verpleegkunde, Andere klinische wetenschappen, Andere basiswetenschappen, Andere paramedische wetenschappen, Andere gezondheidswetenschappen, Andere medische en gezondheidswetenschappen
Affiliaties
- Vakgroep Biomoleculaire Geneeskunde (Departement)
Lid
Vanaf1 okt 2018 → Heden - Vakgroep Pediatrie en genetica (Departement)
Lid
Vanaf1 okt 2006 → 30 sep 2018
Publicaties
1 - 9 van 9
- Structural variants disrupt a critical regulatory region downstream of FOXG1(2023)Volume: 31
Auteurs: Eva D'haene, Lies Vantomme, Björn Menten, Bert Callewaert, Elfride De Baere, Sarah Vergult
Pagina's: 28 - 28 - Comparative 3D genome analysis between neural retina and RPE reveals differential cis-regulatory interactions at retinal disease loci(2023)
Auteurs: 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.
Aantal pagina's: 1 - Differential 3D genome topology shapes the regulatory landscapes of IRD genes in human neural retina and retinal pigment epithelium(2023)Volume: 64
Auteurs: Eva D'haene, Pedro Martinez-Garcia, Victor Lopez Soriano, Miriam Bauwens, Lies Vantomme, Sarah Vergult, Juan Martinez-Morales, Juan Tena, Elfride De Baere
Aantal pagina's: 1 - Mapping the 3D genome of the human retina and its role in retinal disease(2023)Volume: 31
Auteurs: Eva D'haene, Victor Lopez Soriano, Lies Vantomme, Bernd Wissinger, Susanne Kohl, Sarah Vergult, Elfride De Baere
Pagina's: 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)
Auteurs: Lisa Hamerlinck, Maria del Rocio Pérez Baca, Lies Vantomme, Eva D'haene, Sarah Vergult
Pagina's: 38 - 38 - Mapping the 3D genome of the human retina and its role in retinal disease(2022)
Auteurs: Eva D'haene, Victor Lopez Soriano, Lies Vantomme, Bernd Wissinger, Susanne Kohl, Sarah Vergult, Elfride De Baere
Aantal pagina's: 1 - A novel neurodevelopmental syndrome caused by loss-of-function of the Zinc Finger Homeobox 3 (ZFHX3) gene(2022)
Auteurs: Maria del Rocio Pérez Baca, Eva Jacobs, Lies Vantomme, Pontus LeBlanc, Elke Bogaert, Annelies Dheedene, Laurenz De Cock, Bart Dermaut, Aidin Foroutan, Jennifer Kerkhof, et al.
Aantal pagina's: 1 - Benchmarking of long-read structural variant callers on a recently released truth set using Oxford Nanopore data(2021)
Auteurs: Griet De Clercq, Bram Van Gaever, Lies Vantomme, Annelies Dheedene, Björn Menten
Aantal pagina's: 1 - A neuronal enhancer network upstream of MEF2C is compromised in patients with Rett-like characteristics(2018)
Auteurs: 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.
Aantal pagina's: 1