Koenraad Devriendt

25PUBLICATIONS
222CO-AUTHORS
Psychosocial aspects of childbirth and perinatal mental healthGene expression (incl. microarray and other genome-wide approaches)NeurogeneticsDevelopmental genetics (incl. sex determination)Cardiology (incl. cardiovascular diseases)
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Publications (25)

|Aug 19, 2026
Cell-free DNA fragmentome analysis informs pregnancy outcome in patients with immune-mediated disease.

|Aug 10, 2026
An episignature informed systematic analysis to ascertain the clinical significance and consequences of CHD8 missense variants.

|Jul 09, 2026
Copy number variant analysis by exome sequencing is an effective approach to optimize diagnostic yield for developmental disorders-the DDD-Africa study.

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

|Mar 27, 2026
Deletion size and background genetic variation shape congenital heart disease phenotypes in 3,016 individuals with 22q11.2 deletion syndrome.

Jhih-Rong Lin, Daniella Miller, Dana Luong

|Aug 12, 2025
Non-isolated tetralogy of fallot (TOF+): exome sequencing efficacy and phenotypic expansions.

Julia Volpi, Xiaonan Zhao, Nichole Owen

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Frequent Collaborators

4 joint publications

Jeroen Breckpot

4 joint publications

Joris Robert Vermeesch

3 joint publications

Bernard Thienpont

3 joint publications

Lore Lannoo