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Dive into the research topics where Andreas Ørslev Rasmussen 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
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Case Series: Clinical Significance of Heterozygous Pathogenic RTEL1 Variants Identified via Routine Clinical Genetic Diagnostics
Wedge, E., Rasmussen, A. Ø., Borgwardt, L., Cowland, J. B., Grønbæk, K., Issa, I. I., Friis, L. S., Andersen, M. K., Hvidbjerg, M. S. & Jelsig, A. M., Apr 2026, In: American Journal of Medical Genetics, Part A. 200, 4, p. 959-965 7 p.Research output: Contribution to journal › Journal article › Research › peer-review
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A Novel Case of Biallelic MLH3 Variants in a Patient With Rectal Cancer and Polyps
Johannesen, K. M., Karstensen, J. G., Rasmussen, A. Ø., Scott, E. A. H., Birkedal, U., Hansen, T. V. O., Steenholdt, C. & Jelsig, A. M., Apr 2025, In: Clinical Genetics. 107, 4, p. 480-482 3 p.Research output: Contribution to journal › Journal article › Research › peer-review
3 Citations (Scopus) -
Hereditary stomatocytosis in the general population: A genetically based prevalence estimate from a 109 039 individual Danish cohort
Mottelson, M., Helby, J., Petersen, J., Nordestgaard, B. G., Bojesen, S. E., Bendtsen, S. K., Rossing, M., Rasmussen, A. Ø. & Glenthøj, A., Jan 2025, In: American Journal of Hematology. 100, 1, p. 152-157 6 p.Research output: Contribution to journal › Comment/debate › Research › peer-review
1 Citation (Scopus) -
A Rare Case of De Novo Beta-Thalassemia Diagnosed by Whole-Genome Sequencing in an Ethnically Danish Newborn
Ravichandran, S., Hoffmann, M., Petersen, J., Sjø, L., Rasmussen, A. Ø., Eidesgaard, A. & Glenthøj, A., 2024, In: Hemoglobin. 48, 3, p. 196-199 4 p.Research output: Contribution to journal › Journal article › Research › peer-review
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Dahean: A Danish nationwide study ensuring quality assurance through real-world data for suspected hereditary anemia patients
Glenthøj, A., Rasmussen, A. Ø., Bendtsen, S. K., Hasle, H., Hoffmann, M., Rieneck, K., Dziegiel, M. H., Sjö, L. D., Frederiksen, H., Hansen, D. L., Fassi, D. E., Rathe, M., Jensen, P.-D. M., Winther-Larsen, A., Nielsen, C., Olsen, M., Toft, N., Lorenzen, M. O. B., Jensen, L. H. & Gudbrandsdottir, S. & 4 others, , 31 Jul 2024, In: Orphanet Journal of Rare Diseases. 19, 1, p. 284 284.Research output: Contribution to journal › Journal article › Research › peer-review