41 - 50 out of 81Page size: 10
  1. 2013

  2. Developmental aspects of the electrophysiology of the heart: Function follows form

    Postma, A. V., Christoffels, V. M. & Moorman, A. F. M., 1 Jan 2013, Electrical Diseases of the Heart: Volume 1: Basic Foundations and Primary Electrical Diseases. Springer-Verlag London Ltd, Vol. 1. p. 25-45 21 p.

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

  3. A novel alpha-tropomyosin mutation associates with dilated and non-compaction cardiomyopathy and diminishes actin binding

    van de Meerakker, J. B. A., Christiaans, I., Barnett, P., Lekanne Deprez, R. H., Ilgun, A., Mook, O. R. F., Mannens, M. M. A. M., Lam, J., Wilde, A. A. M., Moorman, A. F. M. & Postma, A. V., 2013, In: BIOCHIMICA ET BIOPHYSICA ACTA-MOLECULAR CELL RESEARCH. 1833, 4, p. 833-839

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

  4. Association between C677T polymorphism of methylene tetrahydrofolate reductase and congenital heart disease: meta-analysis of 7697 cases and 13,125 controls

    Mamasoula, C., Prentice, R. R., Pierscionek, T., Pangilinan, F., Mills, J. L., Druschel, C., Pass, K., Russell, M. W., Hall, D., Töpf, A., Brown, D. L., Zelenika, D., Bentham, J., Cosgrove, C., Bhattacharya, S., Riveron, J. G., Setchfield, K., Brook, J. D., Bu'lock, F. A., Thornborough, C., & 22 othersRahman, T. J., Doza, J. P., Tan, H. L., O'Sullivan, J., Stuart, A. G., Blue, G., Winlaw, D., Postma, A. V., Mulder, B. J. M., Zwinderman, A. H., van Engelen, K., Moorman, A. F. M., Rauch, A., Gewillig, M., Breckpot, J., Devriendt, K., Lathrop, G. M., Farrall, M., Goodship, J. A., Cordell, H. J., Brody, L. C. & Keavney, B. D., 2013, In: Circulation. Cardiovascular genetics. 6, 4, p. 347-353

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

  5. Ebstein anomaly associated with left ventricular noncompaction: an autosomal dominant condition that can be caused by mutations in MYH7

    Vermeer, A. M. C., van Engelen, K., Postma, A. V., Baars, M. J. H., Christiaans, I., de Haij, S., Klaassen, S., Mulder, B. J. M. & Keavney, B., 2013, In: American journal of medical genetics. Part C, Seminars in medical genetics. 163, 3, p. 178-184

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

  6. Ebstein's anomaly may be caused by mutations in the sarcomere protein gene MYH7

    van Engelen, K., Postma, A. V., van de Meerakker, J. B. A., Roos-Hesselink, J. W., Helderman-van den Enden, A. T. J. M., Vliegen, H. W., Rahman, T., Baars, M. J. H., Sels, J-W., Bauer, U., Pickardt, T., Sperling, S. R., Moorman, A. F. M., Keavney, B., Goodship, J., Klaassen, S. & Mulder, B. J. M., 2013, In: Netherlands heart journal. 21, 3, p. 113-117

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

  7. Genome-wide association study identifies loci on 12q24 and 13q32 associated with tetralogy of Fallot

    Cordell, H. J., Töpf, A., Mamasoula, C., Postma, A. V., Bentham, J., Zelenika, D., Heath, S., Blue, G., Cosgrove, C., Granados Riveron, J., Darlay, R., Soemedi, R., Wilson, I. J., Ayers, K. L., Rahman, T. J., Hall, D., Mulder, B. J. M., Zwinderman, A. H., van Engelen, K., Brook, J. D., & 17 othersSetchfield, K., Bu'lock, F. A., Thornborough, C., O'Sullivan, J., Stuart, A. G., Parsons, J., Bhattacharya, S., Winlaw, D., Mital, S., Gewillig, M., Breckpot, J., Devriendt, K., Moorman, A. F. M., Rauch, A., Lathrop, G. M., Keavney, B. D. & Goodship, J. A., 2013, In: Human molecular genetics. 22, 7, p. 1473-1481

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

  8. Genome-wide association study of multiple congenital heart disease phenotypes identifies a susceptibility locus for atrial septal defect at chromosome 4p16

    Cordell, H. J., Bentham, J., Topf, A., Zelenika, D., Heath, S., Mamasoula, C., Cosgrove, C., Blue, G., Granados-Riveron, J., Setchfield, K., Thornborough, C., Breckpot, J., Soemedi, R., Martin, R., Rahman, T. J., Hall, D., van Engelen, K., Moorman, A. F. M., Zwinderman, A. H., Barnett, P., & 21 othersKoopmann, T. T., Adriaens, M. E., Varro, A., George, A. L., Dos Remedios, C., Bishopric, N. H., Bezzina, C. R., O'Sullivan, J., Gewillig, M., Bu'lock, F. A., Winlaw, D., Bhattacharya, S., Devriendt, K., Brook, J. D., Mulder, B. J. M., Mital, S., Postma, A. V., Lathrop, G. M., Farrall, M., Goodship, J. A. & Keavney, B. D., 2013, In: Nature genetics. 45, 7, p. 822-824

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

  9. The clinical and molecular relations between idiopathic preterm labor and maternal congenital heart defects

    de Laat, M. W. M., Pieper, P. G., Oudijk, M. A., Mulder, B. J. M., Christoffels, V. M., Afink, G. B., Postma, A. V. & Ris-Stalpers, C., 2013, In: Reproductive sciences (Thousand Oaks, Calif.). 20, 2, p. 190-201

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

  10. The value of the clinical geneticist caring for adults with congenital heart disease: diagnostic yield and patients' perspective

    van Engelen, K., Baars, M. J. H., Felix, J. P., Postma, A. V., Mulder, B. J. M. & Smets, E. M. A., 2013, In: American journal of medical genetics. Part A. 161AA, 7, p. 1628-1637

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

  11. 2012

  12. Decreased inward rectification of Kir2.1 channels is a novel mechanism underlying the short QT syndrome

    Casini, S. & Postma, A. V., 2012, In: Cardiovascular research. 93, 4, p. 535-536

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

Previous 1 2 3 4 5 6 7 8 9 Next

ID: 79221