Birgitte Rode Diness

Birgitte Rode Diness

Clinical Associate Professor

Member of:

  • Clinical Genetics


  1. 2024
  2. Published

    Aortic dissection in a young male with persistent ductus arteriosus and a novel variant in MYLK

    Boelman, M. B., Hansen, Thomas van Overeem, Smith, M. N., Hammer-Hansen, S., Christensen, Alex Hørby & Diness, Birgitte Rode, 2024, In: American Journal of Medical Genetics, Part A. 194, 3, 6 p., e63458.

    Research output: Contribution to journalJournal articleResearchpeer-review

  3. 2023
  4. Published

    National clinical Genetic Networks - GENets - Establishment of expert collaborations in Denmark

    Lildballe, D. L., Frederiksen, A. L., Schönewolf-Greulich, B., Brasch-Andersen, C., Lautrup, C. K., Karstensen, H. G., Pedersen, I. S., Sunde, Lone, Risom, L., Rasmussen, M., Bertelsen, M., Andersen, M. K., Rendtorff, N. D., Gregersen, P. A., Tørring, P. M., Hammer-Hansen, S., Boonen, S. E., Lindquist, Suzanne Granhøj, Hammer, T. B. & Diness, Birgitte Rode, 2023, In: European Journal of Medical Genetics. 66, 12, 5 p., 104872.

    Research output: Contribution to journalJournal articleResearchpeer-review

  5. 2022
  6. Published

    Carriers of COL3A1 pathogenic variants in Denmark: Interfamilial variability in severity and outcome of elective surgical procedures

    Sølyst, S., Oksjoki, R., Farholt, S., Nielsen, D. G., Christensen, Alex Hørby, Fagerberg, C. R., Risom, L., Gregersen, P. A., Christensen, M. B., Rasmussen, T. B. & Diness, Birgitte Rode, 2022, In: Clinical Genetics. 102, 3, p. 191-200

    Research output: Contribution to journalJournal articleResearchpeer-review

  7. Published

    Early diagnosis enabling precision medicine treatment in a young boy with PIK3R1-related overgrowth

    Schönewolf-Greulich, B., Karstensen, H. G., Hjortshøj, T. D., Jørgensen, Finn Stener, Harder, K. M., Frevert, S., Hove, H. & Diness, Birgitte Rode, 2022, In: European Journal of Medical Genetics. 65, 10, 104590.

    Research output: Contribution to journalJournal articleResearchpeer-review

  8. Published

    Hjertesygdomme

    Frederiksen, A. L. & Diness, Birgitte Rode, 2022, Medicinsk genetik. FADL's Forlag, p. 262-274

    Research output: Chapter in Book/Report/Conference proceedingBook chapterEducation

  9. 2021
  10. Published

    Direct to consumer genetic testing in Denmark—public knowledge, use, and attitudes

    Gerdes, Anne-Marie Axø, Nicolaisen, L., Husum, E., Andersen, J. B., Gantzhorn, M. D., Roos, L. & Diness, Birgitte Rode, May 2021, In: European Journal of Human Genetics. 29, 5, p. 851-860 10 p.

    Research output: Contribution to journalJournal articleResearchpeer-review

  11. Published

    Genetisk screening af adopterede raske individer

    Wriedt, T. R., Gerdes, Anne-Marie Axø, Roos, L. K., Hammer-Hansen, S., Christensen, M. B. & Diness, Birgitte Rode, 29 Mar 2021, In: Ugeskrift for Laeger. 183, 13, 7 p., V11200810.

    Research output: Contribution to journalJournal articleResearchpeer-review

  12. Published

    Genetisk screening af kommende forældre

    Smed, V. M., Petersen, Olav Bennike Bjørn, Gerdes, Anne-Marie Axø, Diness, Birgitte Rode & Roos, L. S., 29 Mar 2021, In: Ugeskrift for Laeger. 183, 13, 9 p., V12200933.

    Research output: Contribution to journalJournal articleResearchpeer-review

  13. Published

    Det danske screeningsprogram for hæmoglobinopatier

    Glenthøj, Andreas Birkedal, Samson, M., Toft, N., Diness, Birgitte Rode, Askj R, N., Vojdeman, F. J., Birgens, H., Sørensen, M. B. & Petersen, J., 18 Jan 2021, In: Ugeskrift for Laeger. 183, 3, 8 p., V07200536.

    Research output: Contribution to journalJournal articleResearchpeer-review

  14. Published

    Novel lox variants in five families with aortic/arterial aneurysm and dissection with variable connective tissue findings

    Van Gucht, I., Krebsova, A., Diness, Birgitte Rode, Laga, S., Adlam, D., Kempers, M., Samani, N. J., Webb, T. R., Baranowska, A. A., Van Den Heuvel, L., Perik, M., Luyckx, I., Peeters, N., Votypka, P., Macek, M., Meester, J., Van Laer, L., Verstraeten, A. & Loeys, B. L., 2021, In: International Journal of Molecular Sciences. 22, 13, 7111.

    Research output: Contribution to journalJournal articleResearchpeer-review

  15. Published

    Severe congenital cutis laxa: Identification of novel homozygous LOX gene variants in two families

    McKenzie, F., Mina, K., Callewaert, B., Beyens, A., Dickinson, J. E., Jevon, G., Papadimitriou, J., Diness, Birgitte Rode, Steensberg, J. N., Ek, J. & Baynam, G., 2021, In: Clinical Genetics. 100, 2, p. 168-175

    Research output: Contribution to journalJournal articleResearchpeer-review

  16. 2020
  17. Published

    Phenotypic presentations of Hajdu-Cheney syndrome according to age - 5 distinct clinical presentations

    Graversen, L., Handrup, M. M., Irving, M., Hove, H., Diness, Birgitte Rode, Risom, L., Svaneby, D., Aagaard, M. M., Vogel, I., Gjørup, H., Davidsen, M., Hellfritzsch, M. B., Lauridsen, E. & Gregersen, P. A., Feb 2020, In: European Journal of Medical Genetics. 63, 2, 8 p., 103650.

    Research output: Contribution to journalJournal articleResearchpeer-review

  18. Published

    Expanding the cerebrovascular phenotype of the p.R258H variant in ACTA2 related hereditary thoracic aortic disease (HTAD)

    Diness, Birgitte Rode, Palmquist, R. N., Norling, R., Hove, H., Bundgård, Henning, Hertz, J. M., Kondziella, Daniel, Krieger, D., Dunø, M. & Grønborg, S., 2020, In: Journal of the Neurological Sciences. 415, 116897.

    Research output: Contribution to journalJournal articleResearchpeer-review

  19. 2019
  20. Published

    Aortic aneurysm: An underestimated serious finding in the EP300 mutation phenotypical spectrum

    Luyckx, I., Bolar, N., Diness, Birgitte Rode, Hove, H. B., Verstraeten, A. & Loeys, B. L., Feb 2019, In: European Journal of Medical Genetics. 62, 2, p. 96 1 p.

    Research output: Contribution to journalComment/debateResearchpeer-review

  21. 2018
  22. Published

    A complex phenotype in a family with a pathogenic SOX3 missense variant

    Jelsig, A. M., Diness, Birgitte Rode, Kreiborg, Sven, Main, Katharina Maria, Larsen, V. A. & Hove, H., Mar 2018, In: European Journal of Medical Genetics. 61, 3, p. 168-172

    Research output: Contribution to journalJournal articleResearchpeer-review

  23. Published

    A mutation update on the LDS-associated genes TGFB2/3 and SMAD2/3

    Schepers, D., Tortora, G., Morisaki, H., MacCarrick, G., Lindsay, M., Liang, D., Mehta, S. G., Hague, J., Verhagen, J., van de Laar, I., Wessels, M., Detisch, Y., van Haelst, M., Baas, A., Lichtenbelt, K., Braun, K., van der Linde, D., Roos-Hesselink, J., McGillivray, G., Meester, J. & 22 others, Maystadt, I., Coucke, P., El-Khoury, E., Parkash, S., Diness, Birgitte Rode, Risom, L., Scurr, I., Hilhorst-Hofstee, Y., Morisaki, T., Richer, J., Désir, J., Kempers, M., Rideout, A. L., Horne, G., Bennett, C., Rahikkala, E., Vandeweyer, G., Alaerts, M., Verstraeten, A., Dietz, H., Van Laer, L. & Loeys, B., 2018, In: Human Mutation. 39, 5, p. 621-634 14 p.

    Research output: Contribution to journalJournal articleResearchpeer-review

  24. Published

    First reported adult patient with TARP syndrome: A case report

    Højland, A. T., Lolas, I., Okkels, H., Lautrup, C. K., Diness, Birgitte Rode, Petersen, M. B. & Nielsen, I. K., 2018, In: American Journal of Medical Genetics. Part A. 176, 12, p. 2915-2918 4 p.

    Research output: Contribution to journalJournal articleResearchpeer-review

  25. Published

    Putative new childhood leukemia cancer predisposition syndrome caused by germline bi-allelic missense mutations in DDX41

    Diness, Birgitte Rode, Risom, L., Frandsen, T. L., Hansen, B., Andersen, M. K., Schmiegelow, Kjeld & Wadt, Karin Anna Wallentin, 2018, In: Genes Chromosomes and Cancer. 57, 12, p. 670-674 5 p.

    Research output: Contribution to journalJournal articleResearchpeer-review

  26. 2017
  27. Published

    Translation and Adaptation of the Genetic Counselling Outcome Scale (GCOS-24) for Use in Denmark

    Diness, Birgitte Rode, Overbeck, Gritt, Hjortshøj, T. D., Hammer, T. B., Timshel, S., Sørensen, E. & McAllister, M., Oct 2017, In: Journal of Genetic Counseling. 26, 5, p. 1080–1089 10 p.

    Research output: Contribution to journalJournal articleResearchpeer-review

  28. Published

    Prenatal genetic testing by late amniocentesis to guide delivery management in haemophilia carriers

    Ingerslev, M. D., Langhoff-Roos, J., Soegaard, K., Funding, Eva & Diness, Birgitte Rode, 2017, In: Haemophilia. 23, 5, p. e466-e468

    Research output: Contribution to journalLetterResearchpeer-review

  29. 2014
  30. Published

    Grundig familieanamnese og et multidisciplinært samarbejde er vigtigt ved udredning af årsager til pludselig hjertedød

    Sørensen, C., Diness, Birgitte Rode, Hansen, Steen Holger, Bundgård, Henning & Steensberg, J., 10 Feb 2014, In: Ugeskrift for Laeger. 176, 7, p. V08130505

    Research output: Contribution to journalJournal articleResearchpeer-review

  31. Published

    Genomet i kardiologien

    Bundgård, Henning, Diness, Birgitte Rode, Tfelt-Hansen, Jacob, Henriksen, F. L., Eschen, O., Skovby, F., Havndrup, O., Jensen, H. K. & Tybjærg-Hansen, Anne, 2014, In: Ugeskrift for Laeger. 176, 46, 5 p., V06140376.

    Research output: Contribution to journalJournal articleResearchpeer-review

  32. 2009
  33. Published

    Pre-pregnancy transabdominal cerclage

    Thuesen, Lea Langhoff, Diness, Birgitte Rode & Langhoff-Roos, J., 2009, In: Acta Obstetricia et Gynecologica Scandinavica. 88, 4, p. 483-6 3 p.

    Research output: Contribution to journalJournal articleResearchpeer-review

  34. 2006
  35. Published

    Højdosis vitamin-A-tilskud sænker børnedødeligheden i lavindkomstlande - kan det blive bedre?

    Benn, C. S., Diness, Birgitte Rode, Fisker, A. B., Christoffersen, D. & Friis, Henrik, 2006, In: Ugeskrift for læger. 168 (25), p. 2442-5

    Research output: Contribution to journalJournal articleResearchpeer-review

ID: 156582356