Devriendt, Koenraad

The annual incidence of DiGeorge/velocardiofacial syndrome

Devriendt, K., Fryns, J. P., Mortier, G., van Thienen, M. N., & Keymolen, K. (1998) · Journal of Medical Genetics

Intracranial Aneurysms: Treatment and ComplicationsImmunodeficiency and Autoimmune Disorders

Cited by 330

Contribution of Global Rare Copy-Number Variants to the Risk of Sporadic Congenital Heart Disease

Soemedi, R., Wilson, I. J., Bentham, J., Darlay, R., Töpf, A., Zelenika, D., Cosgrove, C., Setchfield, K., Thornborough, C., Granados-Riveron, J., et al. (2012) · The American Journal of Human Genetics

Genomic variations and chromosomal abnormalitiesCongenital heart defects research

Cited by 315

Deletion of Thyroid Transcription Factor-1 Gene in an Infant with Neonatal Thyroid Dysfunction and Respiratory Failure

Devriendt, K., Vanhole, C., Matthijs, G., & de Zegher, F. (1998) · New England Journal of Medicine

Thyroid Disorders and TreatmentsHead and Neck Anomalies

Cited by 263

Whole exome sequencing reveals the major genetic contributors to nonsyndromic tetralogy of Fallot

Page, D. J., Miossec, M. J., Williams, S. G., Monaghan, R. M., Fotiou, E., Cordell, H. J., Sutcliffe, L., Topf, A., Bourgey, M., Bourque, G., et al. (2019) · Circulation Research

Congenital heart defects researchCongenital Heart Disease Studies

Cited by 189

Neuropsychopathology in 7 patients with the 22q13 deletion syndrome: Presence of bipolar disorder and progressive loss of skills

Denayer, A., Van Esch, H., de Ravel, T., Frijns, J.-P., Van Buggenhout, G., Vogels, A., Devriendt, K., Geutjens, J., Thiry, P., & Swillen, A. (2012) · Molecular Syndromology

Genetics and Neurodevelopmental DisordersGenomic variations and chromosomal abnormalities

Cited by 99

A nationwide prospective randomized trial for diagnosing developmental disorders demonstrates genome sequencing outperforms standard of care

Geysens, M., Souche, E., Baroni, M. C., Benoit, V., Beyltjens, T., Bossuyt, W., Bours, V., Crabbé, M., Croes, D., De Smet, M., et al. (2026) · Genome Medicine

Genomics and Rare DiseasesGenetics and Neurodevelopmental Disorders

Cited by 0