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  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 journal › Article › Academic › peer-review

  3. The Ambiguous Role of NKX2-5 Mutations in Thyroid Dysgenesis

    van Engelen, K., Mommersteeg, M. T. M., Baars, M. J. H., Lam, J., Ilgun, A., van Trotsenburg, A. S. P., Smets, A. M. J. B., Christoffels, V. M., Mulder, B. J. M. & Postma, A. V., 2012, In: PLoS ONE. 7, 12, p. e52685

    Research output: Contribution to journal › Article › Academic › peer-review

  4. 2011

  5. 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 journal › Article › Academic › peer-review

  6. A novel autosomal dominant condition consisting of congenital heart defects and low atrial rhythm maps to chromosome 9q

    van de Meerakker, J. B. A., van Engelen, K., Mathijssen, I. B., Lekanne dit Deprez, R. H., Lam, J., Wilde, A. A. M., Baars, M. J. H., Mannens, M. M. A. M., Mulder, B. J. M., Moorman, A. F. M. & Postma, A. V., 2011, In: European journal of human genetics. 19, 7, p. 820-826

    Research output: Contribution to journal › Article › Academic › peer-review

  7. 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 journal › Review article › Academic › peer-review

  8. 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 journal › Comment/Letter to the editor › Academic

  9. 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 journal › Article › Academic › peer-review

  10. 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 journal › Comment/Letter to the editor › Academic

  11. 2010

  12. 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 journal › Article › Academic › peer-review

  13. 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 journal › Article › Academic › peer-review

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