Sarah Vergult

14PUBLICATIONS
68CO-AUTHORS
NeurogeneticsDevelopmental genetics (incl. sex determination)Epigenetics (incl. genome methylation and epigenomics)Genome structure and regulationGene and molecular therapy
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Publications (14)

|Jun 03, 2026
Non-coding structural variants disrupt FOXG1 transcriptional regulation in early neurodevelopment.

|Jan 27, 2025
RNA-sequencing unveils FLT4 splice site variants in variable congenital heart disease.

Maxim Verlee, Erika D'haenens, Laurenz De Cock

|Aug 16, 2024
Loss-of-function of the Zinc Finger Homeobox 4 (ZFHX4) gene underlies a neurodevelopmental disorder.

Pérez Baca María Del Rocío, María Palomares Bralo, Michiel Vanhooydonck

|May 17, 2024
Comparative 3D genome analysis between neural retina and retinal pigment epithelium reveals differential cis-regulatory interactions at retinal disease loci.

Eva D'haene, Víctor López-Soriano, Pedro Manuel Martínez-García

|Jan 03, 2024
A distant global control region is essential for normal expression of anterior HOXA genes during mouse and human craniofacial development.

Andrea Wilderman, Eva D'haene, Machteld Baetens

|Jun 09, 2023
A novel neurodevelopmental syndrome caused by loss-of-function of the Zinc Finger Homeobox 3 (ZFHX3) gene.

María Del Rocío Pérez Baca, Eva Z Jacobs, Lies Vantomme

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Frequent Collaborators

7 joint publications

Bert Callewaert

4 joint publications

Eva D'haene

3 joint publications

Pérez Baca María Del Rocío

3 joint publications

Laura Muiño Mosquera