Stijn Van de Sompele

6PUBLICATIONS
59CO-AUTHORS
Genetic immunologyMedical biotechnology not elsewhere classifiedGene expression (incl. microarray and other genome-wide approaches)Developmental genetics (incl. sex determination)Epigenetics (incl. genome methylation and epigenomics)
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Publications (6)

|May 08, 2026
Variant Curation of the Largest Compendium of FOXL2 Coding and Noncoding Sequence and Structural Variants in BPES.

|Oct 23, 2025
Late diagnosis of Heimler syndrome and review of the genetic and phenotypic spectrum.

Miel Theunis, Stijn Van De Sompele, Julie Jacob

|May 19, 2025
RPE65 variant p.(E519K) causes a novel dominant adult-onset maculopathy in 83 affected individuals.

Eline Van Vooren, Filip Van den Broeck, Quinten Mahieu

|Feb 27, 2025
Autistic behavior is a common outcome of biallelic disruption of PDZD8 in humans and mice.

Andreea D Pantiru, Stijn Van de Sompele, Clemence Ligneul

|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

|Dec 23, 2017
Functional characterization of a novel non-coding mutation "Ghent +49A > G" in the iron-responsive element of L-ferritin causing hereditary hyperferritinaemia-cataract syndrome.

Stijn Van de Sompele, Lucie Pécheux, Jorge Couso

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Frequent Collaborators

5 joint publications

Elfride De Baere

3 joint publications

Sascha Vermeer

3 joint publications

Miriam Bauwens

2 joint publications

Eva D'haene