1. 2020
  2. Variable phenotypes in hereditary cardiomyopathies

    Jansweijer, J. A., 2020, 162 p.

    Research output: ThesisPhd-Thesis - Research and graduation internal

  3. 2019
  4. Heritability in genetic heart disease: The role of genetic background

    Jansweijer, J. A., van Spaendonck-Zwarts, K. Y., Tanck, M. W. T., Peter van Tintelen, J., Christiaans, I., van der Smagt, J., Vermeer, A., Bos, J. M., Moss, A. J., Swan, H., Priori, S., Rydberg, A., Tfelt-Hansen, J., Ackerman, M., Olivotto, I., Charron, P., Gimeno, J. R., van den Berg, M., Wilde, A. & Pinto, Y. M., 2019, In: Open heart. 6, 1, e000929.

    Research output: Contribution to journalArticleAcademicpeer-review

  5. 2018
  6. 2017
  7. A Comparison of Heritability Estimates by Classical Twin Modeling and Based on Genome-Wide Genetic Relatedness for Cardiac Conduction Traits

    Nolte, I. M., Jansweijer, J. A., Riese, H., Asselbergs, F. W., van der Harst, P., Spector, T. D., Pinto, Y. M., Snieder, H. & Jamshidi, Y., 2017, In: Twin research and human genetics. 20, 6, p. 489-498

    Research output: Contribution to journalArticleAcademicpeer-review

  8. Lamin A/C-Related Cardiac Disease: Late Onset With a Variable and Mild Phenotype in a Large Cohort of Patients With the Lamin A/C p.(Arg331Gln) Founder Mutation

    Hoorntje, E. T., Bollen, I. A., Barge-Schaapveld, D. Q., van Tienen, F. H., te Meerman, G. J., Jansweijer, J. A., van Essen, A. J., Volders, P. G., Constantinescu, A. A., van den Akker, P. C., van Spaendonck-Zwarts, K. Y., Oldenburg, R. A., Marcelis, C. L., van der Smagt, J. J., Hennekam, E. A., Vink, A., Bootsma, M., Aten, E., Wilde, A. A., van den Wijngaard, A. & 5 others, Broers, J. L., Jongbloed, J. D., van der Velden, J., van den Berg, M. P. & van Tintelen, J. P., 2017, In: Circulation. Cardiovascular genetics. 10, 4, e001631.

    Research output: Contribution to journalArticleAcademicpeer-review

  9. Truncating titin mutations are associated with a mild and treatable form of dilated cardiomyopathy

    Jansweijer, J. A., Nieuwhof, K., Russo, F., Hoorntje, E. T., Jongbloed, J. D. H., Lekanne Deprez, R. H., Postma, A. V., Bronk, M., van Rijsingen, I. A. W., de Haij, S., Biagini, E., van Haelst, P. L., van Wijngaarden, J., van den Berg, M. P., Wilde, A. A. M., Mannens, M. M. A. M., de Boer, R. A., van Spaendonck-Zwarts, K. Y., van Tintelen, J. P. & Pinto, Y. M., 2017, In: European journal of heart failure. 19, 4, p. 512-521

    Research output: Contribution to journalArticleAcademicpeer-review

  10. 2016
  11. European cardiomyopathy pilot registry: EURObservational research programme of the European society of cardiology

    on behalf of the EORP Cardiomyopathy Registry Pilot Investigators, 2016, In: European heart journal. 37, 2, p. 164-173 10 p.

    Research output: Contribution to journalArticleAcademicpeer-review

  12. 2015
  13. Tricky ticks: the importance of Lyme carditis recognition

    Jansweijer, J. A. & van Oort, R. J., 2015, In: Netherlands heart journal. 23, 11, p. 531-532

    Research output: Contribution to journalEditorialAcademicpeer-review

  14. 2014
  15. Loss of nuclear TDP-43 in amyotrophic lateral sclerosis (ALS) causes altered expression of splicing machinery and widespread dysregulation of RNA splicing in motor neurones

    Highley, J. R., Kirby, J., Jansweijer, J. A., Webb, P. S., Hewamadduma, C. A., Heath, P. R., Higginbottom, A., Raman, R., Ferraiuolo, L., Cooper-Knock, J., McDermott, C. J., Wharton, S. B., Shaw, P. J. & Ince, P. G., 2014, In: Neuropathology and applied neurobiology. 40, 6, p. 670-685

    Research output: Contribution to journalArticleAcademicpeer-review

ID: 63280