1. 2012
  2. Identifying the Evolutionary Building Blocks of the Cardiac Conduction System

    Jensen, B., Boukens, B. J. D., Postma, A. V., Gunst, Q. D., van den Hoff, M. J. B., Moorman, A. F. M., Wang, T. & Christoffels, V. M., 2012, In: PLoS ONE. 7, 9, p. e44231

    Research output: Contribution to journalArticleAcademicpeer-review

  3. 2011
  4. A complex double deletion in LMNA underlies progressive cardiac conduction disease, atrial arrhythmias, and sudden death

    Marsman, R. F., Bardai, A., Postma, A. V., Res, J. C. J., Koopmann, T. T., Beekman, L., van der Wal, A. C., Pinto, Y. M., Lekanne Deprez, R. H., Wilde, A. A. M., Jordaens, L. J. & Bezzina, C. R., 2011, In: Circulation. Cardiovascular genetics. 4, 3, p. 280-287

    Research output: Contribution to journalArticleAcademicpeer-review

  5. Developmental aspects of cardiac arrhythmogenesis

    Postma, A. V., Christoffels, V. M. & Bezzina, C. R., 2011, In: Cardiovascular research. 91, 2, p. 243-251

    Research output: Contribution to journalReview articleAcademicpeer-review

  6. Functional analysis of novel TBX5 T-box mutations associated with Holt-Oram syndrome (vol 88, pg 130, 2010)

    Boogerd, C. J. J., Dooijes, D., Ilgun, A., Mathijssen, I. B., Hordijk, R., van de Laar, I. M. B. H., Rump, P., Veenstra-Knol, H. E., Moorman, A. F. M., Barnett, P. & Postma, A. V., 2011, In: Cardiovascular research. 89, 1, p. 253

    Research output: Contribution to journalComment/Letter to the editorAcademic

  7. Mutations in the Sarcomere Gene MYH7 in Ebstein Anomaly

    Postma, A. V., van Engelen, K., van de Meerakker, J., Rahman, T., Probst, S., Baars, M. J. H., Bauer, U., Pickardt, T., Sperling, S. R., Berger, F., Moorman, A. F. M., Mulder, B. J. M., Thierfelder, L., Keavney, B., Goodship, J. & Klaassen, S., 2011, In: Circulation. Cardiovascular genetics. 4, 1, p. 43-50

    Research output: Contribution to journalArticleAcademicpeer-review

  8. Screening for 22q11.2 microdeletion in adults with tetralogy of Fallot Reply

    van Engelen, K., Baars, M. J. H., Postma, A. V. & Mulder, B. J. M., 2011, In: Heart (British Cardiac Society). 97, 10, p. 860

    Research output: Contribution to journalComment/Letter to the editorAcademic

  9. 2010
  10. 22q11.2 Deletion Syndrome is under-recognised in adult patients with tetralogy of Fallot and pulmonary atresia

    van Engelen, K., Topf, A., Keavney, B. D., Goodship, J. A., van der Velde, E. T., Baars, M. J. H., Snijder, S., Moorman, A. F., Postma, A. V. & Mulder, B. J. M., 2010, In: Heart (British Cardiac Society). 96, 8, p. 621-624

    Research output: Contribution to journalArticleAcademicpeer-review

  11. Functional analysis of novel TBX5 T-box mutations associated with Holt-Oram syndrome

    Boogerd, C. J. J., Dooijes, D., Ilgun, A., Hordijk, R., van de Laar, I. M. B. H., Rump, P., Veenstra-Knol, H. E., Moorman, A. F. M., Barnett, P. & Postma, A. V., 2010, In: Cardiovascular research. 88, 1, p. 130-139

    Research output: Contribution to journalArticleAcademicpeer-review

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