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The Capital Region of Denmark - a part of Copenhagen University Hospital
  1. 2018
  2. Published

    Exome data clouds the pathogenicity of genetic variants in Pulmonary Arterial Hypertension

    Abbasi, Y., Jabbari, J., Jabbari, R., Glinge, C., Izadyar, S. B., Spiekerkoetter, E., Zamanian, R. T., Carlsen, J. & Tfelt-Hansen, J., Sep 2018, In: Molecular Genetics & Genomic Medicine. 6, 5, p. 835-844 10 p.

    Research output: Contribution to journalReviewpeer-review

  3. 2017
  4. Published
  5. Published

    A Common Variant in SCN5A and the Risk of Ventricular Fibrillation Caused by First ST-Segment Elevation Myocardial Infarction

    Jabbari, R., Glinge, C., Jabbari, J., Risgaard, B., Winkel, B. G., Terkelsen, C. J., Tilsted, H-H., Jensen, L. O., Hougaard, M., Haunsø, S., Engstrøm, T., Albert, C. M. & Tfelt-Hansen, J., 2017, In: P L o S One. 12, 1, p. e0170193

    Research output: Contribution to journalJournal articleResearchpeer-review

  6. Published
  7. Published

    Stability of Circulating Blood-Based MicroRNAs - Pre-Analytic Methodological Considerations

    Glinge, C., Clauss, S., Boddum, K., Jabbari, R., Jabbari, J., Risgaard, B., Tomsits, P., Hildebrand, B., Kääb, S., Wakili, R., Jespersen, T. & Tfelt-Hansen, J., 2017, In: P L o S One. 12, 2, p. e0167969

    Research output: Contribution to journalJournal articleResearchpeer-review

  8. 2015
  9. Published

    Role of common and rare variants in SCN10A: results from the Brugada syndrome QRS locus gene discovery collaborative study

    Behr, E. R., Savio-Galimberti, E., Barc, J., Holst, A. G., Petropoulou, E., Prins, B. P., Jabbari, J., Torchio, M., Berthet, M., Mizusawa, Y., Yang, T., Nannenberg, E. A., Dagradi, F., Weeke, P., Bastiaenan, R., Ackerman, M. J., Haunso, S., Leenhardt, A., Kääb, S., Probst, V., Redon, R., Sharma, S., Wilde, A., Tfelt-Hansen, J., Schwartz, P., Roden, D. M., Bezzina, C., Olesen, M., Darbar, D., Guicheney, P., Crotti, L., Jamshidi, Y. & UK10K Consortium, 1 Jun 2015, In: Cardiovascular Research. 106, 3, p. 520-9 10 p.

    Research output: Contribution to journalJournal articleResearchpeer-review

  10. Published

    The pathogenicity of genetic variants previously associated with left ventricular non-compaction

    Abbasi, Y., Jabbari, J., Jabbari, R., Yang, R-Q., Risgaard, B., Køber, L., Haunsø, S. & Tfelt-Hansen, J., Mar 2015, In: Molecular Genetics & Genomic Medicine. 4, 2, p. 135-42 8 p.

    Research output: Contribution to journalJournal articleResearchpeer-review

  11. Published

    Common and rare variants in SCN10A modulate the risk of atrial fibrillation

    Jabbari, J., Olesen, M. S., Yuan, L., Nielsen, J. B., Liang, B., Macri, V., Christophersen, I. E., Nielsen, N., Sajadieh, A., Ellinor, P. T., Grunnet, M., Haunsø, S., Holst, A. G., Svendsen, J. H. & Jespersen, T., Feb 2015, In: Circulation. Cardiovascular genetics. 8, 1, p. 64-73 10 p.

    Research output: Contribution to journalJournal articleResearchpeer-review

  12. Published
  13. 2014
  14. Published

    Brugada syndrome risk loci seem protective against atrial fibrillation

    Andreasen, L., Nielsen, J. B., Darkner, S., Christophersen, I. E., Jabbari, J., Refsgaard, L., Thiis, J. J., Sajadieh, A., Tveit, A., Haunsø, S., Svendsen, J. H., Schmitt, N. & Olesen, M. S., Dec 2014, In: European journal of human genetics : EJHG. 22, 12, p. 1357-61 5 p.

    Research output: Contribution to journalJournal articleResearchpeer-review

  15. Published

    Genetics of cardiac arrhythmias (Ph.d.-afhandling)

    Jabbari, J., 18 Jul 2014, 1 ed. København: Eget forlag Københavns University. 138 p.

    Research output: Book/ReportPh.D. thesis

  16. Published
  17. Published
  18. 2013
  19. Published
  20. Published

    Rare variants in GJA5 are associated with early-onset lone atrial fibrillation

    Christophersen, I. E., Holmegard, H. N., Jabbari, J., Sajadieh, A., Haunsø, S., Tveit, A., Svendsen, J. H. & Olesen, M. S., Jan 2013, In: The Canadian journal of cardiology. 29, 1, p. 111-6 6 p.

    Research output: Contribution to journalJournal articleResearchpeer-review

  21. 2012
  22. Published
  23. Published

    Mutations in the potassium channel subunit KCNE1 are associated with early-onset familial atrial fibrillation

    Olesen, M. S., Bentzen, B. H., Nielsen, J. B., Steffensen, A. B., David, J-P., Jabbari, J., Jensen, P. H., Haunsø, S., Svendsen, J. H. & Schmitt, N., 2012, In: B M C Medical Genetics. 13, p. 24

    Research output: Contribution to journalJournal articleResearchpeer-review

  24. 2011
  25. Published

    Common polymorphisms in KCNJ5 [corrected] are associated with early-onset lone atrial fibrillation in Caucasians

    Jabbari, J., Olesen, M. S., Holst, A. G., Nielsen, J. B., Haunso, S. & Svendsen, J. H., 2011, In: Cardiology. 118, 2, p. 116-20 5 p.

    Research output: Contribution to journalJournal articleResearchpeer-review

  26. Published

    Screening of KCNN3 in patients with early-onset lone atrial fibrillation

    Olesen, M. S., Jabbari, J., Holst, A. G., Nielsen, J. B., Steinbrüchel, D. A., Jespersen, T., Haunsø, S. & Svendsen, J. H., 2011, In: Europace. 13, 7, p. 963-7 5 p.

    Research output: Contribution to journalJournal articleResearchpeer-review

ID: 16254