Personal profile
Expertises
Inborn metabolic diseases; biochemical genetics
Main research areas
Inborn metabolic diseases; diagnostic methods in biochemical genetics
Current research
Mitochondrial and lysosomal diseases; diagnostic methods in biochemical genetics
Potential conflicts of interest
None
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Dive into the research topics where Flemming Wibrand is active. These topic labels come from the works of this person. Together they form a unique fingerprint.
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Collaborations and top research areas from the last five years
Recent external collaboration on country/territory level. Dive into details by clicking on the dots or
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A diagnostic algorithm for inherited metabolic disorders using untargeted metabolomics
Gao, Q., Khan, A., Christensen, M., Zhou, X., Lund, A., Grønborg, S. W., Wibrand, F., Østergaard, E. & Moritz, T., 27 Jul 2025, In: Metabolomics : Official journal of the Metabolomic Society. 21, 4, p. 101 101.Research output: Contribution to journal › Journal article › Research › peer-review
2 Citations (Scopus) -
Human D-Lactate Dehydrogenase Deficiency: A Case Report in a Young Boy
Sloth, T. B., Ørngreen, M. C., Ek, J., Bache, I., Wibrand, F. & Lund, A. M., Jul 2025, In: JIMD Reports. 66, 4, p. e70039 e70039.Research output: Contribution to journal › Journal article › Research › peer-review
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Correction: Systematic cascade screening in the Danish Fabry Disease Centre: 20 years of a national single-centre experience
Effraimidis, G., Rasmussen, Å. K., Dunoe, M., Hasholt, L. F., Wibrand, F., Sorensen, S. S., Lund, A. M., Kober, L., Bundgaard, H., Yazdanfard, P. D. W., Oturai, P., Larsen, V. A., de Abreu, V. H. F., Enevoldsen, L. H., Kristensen, T., Svenstrup, K., Bille, M. B., Arif, F., Mogensen, M. & Klokker, M. & 3 others, , 2023Research output: Other contribution › Research
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Multi-omics identifies large mitoribosomal subunit instability caused by pathogenic MRPL39 variants as a cause of pediatric onset mitochondrial disease
Amarasekera, S. S. C., Hock, D. H., Lake, N. J., Calvo, S. E., Grønborg, S. W., Krzesinski, E. I., Amor, D. J., Fahey, M. C., Simons, C., Wibrand, F., Mootha, V. K., Lek, M., Lunke, S., Stark, Z., Østergaard, E., Christodoulou, J., Thorburn, D. R., Stroud, D. A. & Compton, A. G., 20 Jul 2023, In: Human Molecular Genetics. 32, 15, p. 2441-2454 14 p.Research output: Contribution to journal › Journal article › Research › peer-review
19 Citations (Scopus) -
Elucidating the molecular mechanisms associated with TARS2-related mitochondrial disease
Zheng, W.-Q., Pedersen, S. V., Thompson, K., Bellacchio, E., French, C. E., Munro, B., Pearson, T. S., Vogt, J., Diodato, D., Diemer, T., Ernst, A., Horvath, R., Chitre, M., Ek, J., Wibrand, F., Grange, D. K., Raymond, L., Zhou, X.-L., Taylor, R. W. & Ostergaard, E., 21 Feb 2022, In: Human Molecular Genetics. 31, 4, p. 523-534 12 p.Research output: Contribution to journal › Journal article › Research › peer-review
17 Citations (Scopus)