Elsebet Østergaard
Clinical Associate Professor
- 2023
- Published
The postgraduate medical educational climate assessed by the Danish Residency Educational Climate Test (DK-RECT): a validation and cross-sectional observational study
Jacobsen, Rikke Vita Borre, Boor, K., Christensen, Karl Bang, Ung, V. H., Carlsen, Jørn, Kirk, Ole, Dziegiel, Morten Hanefeld, Østergaard, Elsebet, Rochat, Per Bjørnstad, Albrecht-Beste, Elisabeth, Droogh, M., Lapperre, T. S., Scheele, F. & Sorensen, Jette Led , 2023, In: BMC Medical Education. 23, 1, 13 p., 943.Research output: Contribution to journal › Journal article › Research › peer-review
- 2022
- Published
Mitokondriesygdomme
Duno, M. & Østergaard, Elsebet, 2022, Medicinsk genetik. FADL's Forlag, p. 385-392Research output: Chapter in Book/Report/Conference proceeding › Book chapter › Education
- Published
Bi-allelic LETM1 variants perturb mitochondrial ion homeostasis leading to a clinical spectrum with predominant nervous system involvement
Kaiyrzhanov, R., Mohammed, S. E. M., Maroofian, R., Husain, R. A., Catania, A., Torraco, A., Alahmad, A., Dutra-Clarke, M., Grønborg, S., Sudarsanam, A., Vogt, J., Arrigoni, F., Baptista, J., Haider, S., Feichtinger, R. G., Bernardi, P., Zulian, A., Gusic, M., Efthymiou, S., Bai, R. & 34 others, , 2022, In: American Journal of Human Genetics. 109, 9, p. 1692-1712 21 p.Research output: Contribution to journal › Journal article › Research › peer-review
- Published
The clinical and molecular spectrum of QRICH1 associated neurodevelopmental disorder
Kumble, S. & Undiagnosed Diseases Network, U. D. N., 2022, In: Human Mutation. 43, 2, p. 266-282Research output: Contribution to journal › Journal article › Research › peer-review
- Published
Functional correlation of genome-wide DNA methylation profiles in genetic neurodevelopmental disorders
Levy, M. A., Relator, R., McConkey, H., Pranckeviciene, E., Kerkhof, J., Barat-Houari, M., Bargiacchi, S., Biamino, E., Palomares Bralo, M., Cappuccio, G., Ciolfi, A., Clarke, A., DuPont, B. R., Elting, M. W., Faivre, L., Fee, T., Ferilli, M., Fletcher, R. S., Cherick, F., Foroutan, A. & 72 others, , 2022, In: Human Mutation. 43, 11, p. 1609-1628Research output: Contribution to journal › Journal article › Research › peer-review
- Published
Novel diagnostic DNA methylation episignatures expand and refine the epigenetic landscapes of Mendelian disorders
Levy, M. A., McConkey, H., Kerkhof, J., Barat-Houari, M., Bargiacchi, S., Biamino, E., Cappuccio, G., Ciolfi, A., Clarke, A., DuPont, B. R., Elting, M. W., Faivre, L., Fee, T., Fletcher, R. S., Cherik, F., Foroutan, A., Friez, M. J., Gervasini, C., Haghshenas, S., Hilton, B. A. & 66 others, , 13 Jan 2022, In: Human Genetics and Genomics Advances. 3, 1, 18 p., 100075.Research output: Contribution to journal › Journal article › Research › peer-review
- Published
Biallelic Loss-of-Function NDUFA12 Variants Cause a Wide Phenotypic Spectrum from Leigh/Leigh-Like Syndrome to Isolated Optic Atrophy
Magrinelli, F., Cali, E., Braga, V. L., Yis, U., Tomoum, H., Shamseldin, H., Raiman, J., Kernstock, C., Rezende Filho, F. M., Povoas Barsottini, O. G., Taylor, R. W., Ostergaard, E., Tamim, A., Schaeferhoff, K., Ferraz Sallum, J. M., Zaki, M. S., Kok, F., Bhatia, K. P., Wissinger, B., Sergeant, K. & 7 others, , 2022, In: Movement Disorders Clinical Practice. 9, 2, p. 218-228Research output: Contribution to journal › Journal article › Research › peer-review
- Published
Renal Phenotype in Mitochondrial Diseases: A Multicenter Study
Parasyri, M., Brandstroem, P., Uusimaa, J., Østergaard, Elsebet, Hikmat, O., Isohanni, P., Naess, K., de Coo, I. F. M., Nascimento Osorio, A., Nuutinen, M., Lindberg, C., Bindoff, L. A., Tulinius, M., Darin, N. & Sofou, K., 2022, In: Kidney diseases. 8, 2, 12 p.Research output: Contribution to journal › Journal article › Research › peer-review
- Published
Genetisk variation
Pedersen, Inge Søkilde & Østergaard, Elsebet, 2022, Medicinsk genetik. 3 ed. FADL's Forlag, p. 67-97Research output: Chapter in Book/Report/Conference proceeding › Book chapter › Education
- Published
Medicinsk genetik
Sunde, Lone (ed.) & Østergaard, Elsebet (ed.), 2022, 3 ed. FADL's Forlag.Research output: Book/Report › Anthology › Communication
ID: 33970574
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203
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Two transgenic mouse models for β-subunit components of succinate-CoA ligase yielding pleiotropic metabolic alterations
Research output: Contribution to journal › Journal article › Research › peer-review
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133
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A scoring system predicting the clinical course of CLPB defect based on the foetal and neonatal presentation of 31 patients
Research output: Contribution to journal › Journal article › Research › peer-review
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70
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Clinical, biochemical and genetic spectrum of 70 patients with ACAD9 deficiency: is riboflavin supplementation effective?
Research output: Contribution to journal › Journal article › Research › peer-review
Published