Birgitte Rode Diness

Birgitte Rode Diness

Clinical Associate Professor

Member of:

  • Clinical Genetics


  1. 2021
  2. 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

  3. 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

  4. 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

  5. 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

  6. 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

  7. 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

ID: 156582356