Koenraad Devriendt

Deletion of thyroid transcription factor-1 gene in an infant with neonatal thyroid dysfunction and respiratory failure.

K. Devriendt, F. de Zegher, G. Matthijs, 1998, The New England journal of medicine.

The neurobeachin gene is disrupted by a translocation in a patient with idiopathic autism

K. Devriendt, J. Steyaert, W. V. D. Van de Ven, 2003, Journal of medical genetics.

Mutations in ISPD cause Walker-Warburg syndrome and defective glycosylation of α-dystroglycan

Christian Gilissen, Han G. Brunner, Michael F. Buckley, 2012, Nature Genetics.

Evaluating offspring Genomic and Epigenomic alterations after prenatal exposure to Cancer treatment In Pregnancy (GE-CIP): a multicentric observational study

B. Thienpont, R. van Boxtel, K. Van Calsteren, 2024, BMJ open.

Investigating the etiology of multiple tooth agenesis in three sisters with severe oligodontia.

K. Devriendt, C. Carels, I. Bailleul-Forestier, 2008, Orthodontics & craniofacial research.