Birgitte Rode Diness
Clinical Associate Professor
- 2024
- 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 journal › Journal article › Research › peer-review
- 2023
- 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 journal › Journal article › Research › peer-review
- 2022
- 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. 191-200Research output: Contribution to journal › Journal article › Research › peer-review
- 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 journal › Journal article › Research › peer-review
- Published
Hjertesygdomme
Frederiksen, A. L. & Diness, Birgitte Rode, 2022, Medicinsk genetik. FADL's Forlag, p. 262-274Research output: Chapter in Book/Report/Conference proceeding › Book chapter › Education
- 2021
- 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 journal › Journal article › Research › peer-review
- 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 journal › Journal article › Research › peer-review
- 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 journal › Journal article › Research › peer-review
- 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 journal › Journal article › Research › peer-review
- 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 journal › Journal article › Research › peer-review
- 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. 168-175Research output: Contribution to journal › Journal article › Research › peer-review
- 2020
- 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 journal › Journal article › Research › peer-review
- 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 journal › Journal article › Research › peer-review
- 2019
- 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 journal › Comment/debate › Research › peer-review
- 2018
- 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. 168-172Research output: Contribution to journal › Journal article › Research › peer-review
- 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, , 2018, In: Human Mutation. 39, 5, p. 621-634 14 p.Research output: Contribution to journal › Journal article › Research › peer-review
- 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 journal › Journal article › Research › peer-review
- 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 journal › Journal article › Research › peer-review
- 2017
- 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 journal › Journal article › Research › peer-review
- 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-e468Research output: Contribution to journal › Letter › Research › peer-review
- 2014
- 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. V08130505Research output: Contribution to journal › Journal article › Research › peer-review
- 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 journal › Journal article › Research › peer-review
- 2009
- 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 journal › Journal article › Research › peer-review
- 2006
- 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. 2442-5Research output: Contribution to journal › Journal article › Research › peer-review
ID: 156582356
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First reported adult patient with TARP syndrome: A case report
Research output: Contribution to journal › Journal article › Research › peer-review
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63
downloads
A mutation update on the LDS-associated genes TGFB2/3 and SMAD2/3
Research output: Contribution to journal › Journal article › Research › peer-review
Published -
11
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Early diagnosis enabling precision medicine treatment in a young boy with PIK3R1-related overgrowth
Research output: Contribution to journal › Journal article › Research › peer-review
Published