Key publications
All Publications
- Ellesøe Sabrina G., Workman Christopher T., Bouvagnet Patrice, Loffredo Christopher A., McBride Kim L., Hinton Robert B., van Engelen Klaartje, Gertsen Emma C., Mulder Barbara J. M., Postma Alex V., Anderson Robert H., Hjortdal Vibeke E., Brunak Søren, Larsen Lars A. Familial co-occurrence of congenital heart defects follows distinct patterns European heart journal 2018;39 (12):1015-1022 [PubMed]
- Postma A. V., Alders M., Sylva M., Bilardo C. M., Pajkrt E., van Rijn R. R., Schulte-Merker S., Bulk S., Stefanovic S., Ilgun A., Barnett P., Mannens M. M. A. M., Moorman A. F. M., Oostra R. J., van Maarle M. C. Mutations in the T (brachyury) gene cause a novel syndrome consisting of sacral agenesis, abnormal ossification of the vertebral bodies and a persistent notochordal canal Journal of medical genetics 2014;51 (2):90-97 [PubMed]
- Postma Alex V., van Engelen Klaartje, van de Meerakker Judith, Rahman Thahira, Probst Susanne, Baars Marieke J. H., Bauer Ulrike, Pickardt Thomas, Sperling Silke R., Berger Felix, Moorman Antoon F. M., Mulder Barbara J. M., Thierfelder Ludwig, Keavney Bernard, Goodship Judith, Klaassen Sabine Mutations in the Sarcomere Gene MYH7 in Ebstein Anomaly Circulation. Cardiovascular genetics 2011;4 (1):43-50 [PubMed]
- Postma Alex V., van de Meerakker Judith B. A., Mathijssen Inge B., Barnett Phil, Christoffels Vincent M., Ilgun Aho, Lam Jan, Wilde Arthur A. M., Lekanne Deprez Ronald H., Moorman Antoon F. M. A gain-of-function TBX5 mutation is associated with atypical Holt-Oram syndrome and paroxysmal atrial fibrillation Circulation research 2008;102 (11):1433-1442 [PubMed]
Research programmes
Prof. PhD M.M.A.M. Mannens (Genome diagnostics i.p. epigenetics of disease)
Prof. PhD V.M. Christoffels (Transcriptional mechanism controlling heart development, regeneration and rhythm)
PhD A.V. Postma (Promoties)