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  1. 2010

  2. Haploinsufficiency of TAB2 causes congenital heart defects in humans

    Thienpont, B., Zhang, L., Postma, A. V., Breckpot, J., Tranchevent, L-C., van Loo, P., Møllgård, K., Tommerup, N., Bache, I., Tümer, Z., van Engelen, K., Menten, B., Mortier, G., Waggoner, D., Gewillig, M., Moreau, Y., Devriendt, K. & Larsen, L. A., 2010, In: American journal of human genetics. 86, 6, p. 839-849

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

  3. The human CASQ2 mutation K206N is associated with hyperglycosylation and altered cellular calcium handling

    Kirchhefer, U., Wehrmeister, D., Postma, A. V., Pohlentz, G., Mormann, M., Kucerova, D., Müller, F. U., Schmitz, W., Schulze-Bahr, E., Wilde, A. A. & Neumann, J., 2010, In: Journal of molecular and cellular cardiology. 49, 1, p. 95-105

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

  4. 2009

  5. Developmental and genetic aspects of atrial fibrillation

    Postma, A. V., Dekker, L. R. C., Soufan, A. T. & Moorman, A. F. M., 2009, In: Trends in cardiovascular medicine. 19, 4, p. 123-130

    Research output: Contribution to journal › Review article › Academic › peer-review

  6. Prevalence of congenital heart defects in neuroblastoma patients: a cohort study and systematic review of literature

    van Engelen, K., Merks, J. H. M., Lam, J., Kremer, L. C. M., Backes, M., Baars, M. J. H., van der Pal, H. J. H., Postma, A. V., Versteeg, R., Caron, H. N. & Mulder, B. J. M., 2009, In: European journal of pediatrics. 168, 9, p. 1081-1090

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

  7. 2008

  8. A case of catecholaminergic polymorphic ventricular tachycardia caused by two calsequestrin 2 mutations

    de la Fuente, S., van Langen, I. M., Postma, A. V., Bikker, H. & Meijer, A., 2008, In: Pacing and clinical electrophysiology. 31, 7, p. 916-919

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

  9. A gain-of-function TBX5 mutation is associated with atypical Holt-Oram syndrome and paroxysmal atrial fibrillation

    Postma, A. V., van de Meerakker, J. B. A., Mathijssen, I. B., Barnett, P., Christoffels, V. M., Ilgun, A., Lam, J., Wilde, A. A. M., Lekanne Deprez, R. H. & Moorman, A. F. M., 2008, In: Circulation research. 102, 11, p. 1433-1442

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

  10. Developmental aspects of the electrophysiology of the heart: function follows form

    Postma, A. V., Christoffels, V. M. & Moorman, A. F. M., 2008, Electrical diseases of the heart. Genetics, mechanisms, treatment, prevention.. Gussak, I., Antzelevitch, C., Wilde, A. A. M., Friedman, P. A., Ackerman, M. J. & Shen, W-K. (eds.). London: Springer, p. 24-36

    Research output: Chapter in Book/Report/Conference proceeding › Chapter › Academic › peer-review

  11. 2007

  12. A novel early onset lethal form of catecholaminergic polymorphic ventricular tachycardia maps to chromosome 7p14-p22

    Bhuiyan, Z. A., Hamdan, M. A., Shamsi, E. T. A., Postma, A. V., Mannens, M. M. A. M., Wilde, A. A. M. & Al-Gazali, L., 2007, In: Journal of cardiovascular electrophysiology. 18, 10, p. 1060-1066

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

  13. Expanding spectrum of human RYR2-related disease: new electrocardiographic, structural, and genetic features

    Bhuiyan, Z. A., van den Berg, M. P., van Tintelen, J. P., Bink-Boelkens, M. T. E., Wiesfeld, A. C. P., Alders, M., Postma, A. V., van Langen, I., Mannens, M. M. A. M. & Wilde, A. A. M., 2007, In: Circulation. 116, 14, p. 1569-1576

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

  14. 2006

  15. Candidate genes for the hereditary component of cardiac hypertrophy

    van den Hoff, M. J. B., Postma, A. V. & Michel, M. C., 2006, In: Journal of hypertension. 24, 2, p. 273-277

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

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