Works by Rasmussen, Andreas Ørslev

Results: 8

DAHEAN: A Danish nationwide study ensuring quality assurance through real-world data for suspected hereditary anemia patients.

Published in:

Orphanet Journal of Rare Diseases, 2024, v. 19, n. 1, p. 1, doi. 10.1186/s13023-024-03298-4

By:

Glenthøj, Andreas;
Rasmussen, Andreas Ørslev;
Bendtsen, Selma Kofoed;
Hasle, Henrik;
Hoffmann, Marianne;
Rieneck, Klaus;
Dziegiel, Morten Hanefeld;
Sjö, Lene Dissing;
Frederiksen, Henrik;
Hansen, Dennis Lund;
Fassi, Daniel El;
Rathe, Mathias;
Jensen, Peter-Diedrich Matthias;
Winther-Larsen, Anne;
Nielsen, Christian;
Olsen, Marianne;
Toft, Nina;
Lorenzen, Mads Okkels Birk;
Jensen, Lise Heilmann;
Gudbrandsdottir, Sif

Publication type:

Article

Hereditary stomatocytosis in the general population: A genetically based prevalence estimate from a 109 039 individual Danish cohort.

Published in:

American Journal of Hematology, 2025, v. 100, n. 1, p. 152, doi. 10.1002/ajh.27508

By:

Mottelson, Mathis;
Helby, Jens;
Petersen, Jesper;
Nordestgaard, Børge Grønne;
Bojesen, Stig Egil;
Bendtsen, Selma Kofoed;
Rossing, Maria;
Rasmussen, Andreas Ørslev;
Glenthøj, Andreas

Publication type:

Article

Platelet expression of the transcription factor ETV6 associates with ETV6‐related thrombocytopenia and can be detected by immunofluorescence on the blood film.

Published in:

British Journal of Haematology, 2024, v. 204, n. 2, p. 710, doi. 10.1111/bjh.19211

By:

Zaninetti, Carlo;
Baschin, Marcel;
Vater, Leonard;
Karastaneva, Anna;
Holzhauer, Susanne;
Leinøe, Eva;
Ørslev Rasmussen, Andreas;
Wesche, Jan;
Freyer, Carmen;
Seidel, Markus G.;
Greinacher, Andreas

Publication type:

Article

Germline pathogenic variants in RNF43 in patients with and without serrated polyposis syndrome.

Published in:

Familial Cancer, 2025, v. 24, n. 1, p. 1, doi. 10.1007/s10689-024-00428-6

By:

Brinch, Heidi Hesselø;
Byrjalsen, Anna;
Lohse, Zuzana;
Rasmussen, Andreas Ørslev;
Karstensen, John Gásdal;
Kristiansen, Britta Schlott;
Jelsig, Anne Marie

Publication type:

Article

A Rare Case of De Novo Beta-Thalassemia Diagnosed by Whole-Genome Sequencing in an Ethnically Danish Newborn.

Published in:

Hemoglobin, 2024, v. 48, n. 3, p. 196, doi. 10.1080/03630269.2024.2335919

By:

Ravichandran, Stefni;
Hoffmann, Marianne;
Petersen, Jesper;
Sjø, Lene;
Rasmussen, Andreas Ørslev;
Eidesgaard, Annetta;
Glenthøj, Andreas

Publication type:

Article

Glucose phosphate isomerase deficiency demasked by whole-genome sequencing: a case report.

Published in:

Journal of Medical Case Reports, 2024, v. 18, n. 1, p. 1, doi. 10.1186/s13256-024-04466-7

By:

Holme, Sissel;
van Wijk, Richard;
Rasmussen, Andreas Ørslev;
Petersen, Jesper;
Glenthøj, Andreas

Publication type:

Article

A Novel Case of Biallelic MLH3 Variants in a Patient With Rectal Cancer and Polyps.

Published in:

Clinical Genetics, 2025, v. 107, n. 4, p. 480, doi. 10.1111/cge.14689

By:

Johannesen, Katrine M.;
Karstensen, John Gásdal;
Rasmussen, Andreas Ørslev;
Scott, Emma Adine Hoxer;
Birkedal, Ulf;
Hansen, Thomas v. O.;
Steenholdt, Casper;
Jelsig, Anne Marie

Publication type:

Article

Low vitamin C status and hypermobility‐related disorders in patients with bleeding disorder of unknown cause.

Published in:

Haemophilia, 2024, v. 30, n. 6, p. 1366, doi. 10.1111/hae.15099

By:

Leinøe, Eva;
Fridriksdottir, Halla;
Rasmussen, Andreas Ørslev;
Funding, Eva;
Sørensen, Anne Louise Tølbøll;
Kampmann, Peter;
Lykkesfeldt, Jens;
Rossing, Maria

Publication type:

Article