Eva B. Leinoe

Copenhagen, Denmark

Last Updated: 09/26/2026

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Found 33 publications

Genetic screening alters diagnosis and management in patients with immune thrombocytopenia.

Genetic screening alters diagnosis and management in patients with immune thrombocytopenia.

Journal: Haematologica

Published: March 03, 2026

Recurrent Venous Thrombosis in a Hypofibrinogenemic Patient Despite a Heterozygous Deletion of the Fibrinogen Gene Cluster and Hemizygous FGB p.Pro265Leu Variant Mimicking a Homozygous Genotype.

Recurrent Venous Thrombosis in a Hypofibrinogenemic Patient Despite a Heterozygous Deletion of the Fibrinogen Gene Cluster and Hemizygous FGB p.Pro265Leu Variant Mimicking a Homozygous Genotype.

Journal: Hamostaseologie

Published: August 07, 2025

Title Not Found

Title Not Found

Journal: Ugeskrift for laeger

Published: November 12, 2024

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

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

Journal: Haemophilia : the official journal of the World Federation of Hemophilia

Published: July 15, 2024

Aggregates of nonmuscular myosin IIA in erythrocytes associate with GATA1- and GFI1B-related thrombocytopenia.

Aggregates of nonmuscular myosin IIA in erythrocytes associate with GATA1- and GFI1B-related thrombocytopenia.

Journal: Journal of thrombosis and haemostasis : JTH

Published: September 11, 2023

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

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

Journal: British journal of haematology

Published: August 24, 2023

Corrigendum to GoldVariants, a resource for sharing rare genetic variants detected in bleeding, thrombotic, and platelet disorders: Communication from the ISTH SSC Subcommittee on Genomics in Thrombosis and Hemostasis [J Thromb Haemost. 2021 Oct;19(10):2612-2617].

Corrigendum to GoldVariants, a resource for sharing rare genetic variants detected in bleeding, thrombotic, and platelet disorders: Communication from the ISTH SSC Subcommittee on Genomics in Thrombosis and Hemostasis [J Thromb Haemost. 2021 Oct;19(10):2612-2617].

Journal: Journal of thrombosis and haemostasis : JTH

Published: February 03, 2023

Validation of immunofluorescence analysis of blood smears in patients with inherited platelet disorders.

Validation of immunofluorescence analysis of blood smears in patients with inherited platelet disorders.

Journal: Journal of thrombosis and haemostasis : JTH

Published: October 08, 2022

Genome-wide meta-analysis identifies 93 risk loci and enables risk prediction equivalent to monogenic forms of venous thromboembolism.

Genome-wide meta-analysis identifies 93 risk loci and enables risk prediction equivalent to monogenic forms of venous thromboembolism.

Journal: Nature genetics

Published: August 09, 2022

Platelet function testing: Current practice among clinical centres in Northern Europe.

Platelet function testing: Current practice among clinical centres in Northern Europe.

Journal: Haemophilia : the official journal of the World Federation of Hemophilia

Published: February 06, 2022

Inherited platelet disorders

Inherited platelet disorders

Journal: Ugeskrift for laeger

Published: October 28, 2021

Severe Congenital Thrombocytopenia Characterized by Decreased Platelet Sialylation and Moderate Complement Activation Caused by Novel Compound Heterozygous Variants in GNE.

Severe Congenital Thrombocytopenia Characterized by Decreased Platelet Sialylation and Moderate Complement Activation Caused by Novel Compound Heterozygous Variants in GNE.

Journal: Frontiers in immunology

Published: September 15, 2021

Showing 1-12 of 33

Last Updated: 09/26/2026