Claire E. Lentaigne

Plymouth, ENG, United Kingdom

Last Updated: 09/26/2026

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Found 13 publications

Prevalence and outcomes of antiphospholipid syndrome after unprovoked venous thromboembolism: a multicenter real-world data analysis.

Prevalence and outcomes of antiphospholipid syndrome after unprovoked venous thromboembolism: a multicenter real-world data analysis.

Journal: Journal of thrombosis and haemostasis : JTH

Published: December 22, 2025

Current gynaecological management of women and girls with bleeding disorders in the United Kingdom: A UKHCDO haemophilia treatment centre survey and evaluation of real-world clinical practice for the British Journal of Haematology.

Current gynaecological management of women and girls with bleeding disorders in the United Kingdom: A UKHCDO haemophilia treatment centre survey and evaluation of real-world clinical practice for the British Journal of Haematology.

Journal: British journal of haematology

Published: October 30, 2025

Clinical outcomes and the impact of prior oral anticoagulant use in patients with coronavirus disease 2019 admitted to hospitals in the UK - a multicentre observational study.

Clinical outcomes and the impact of prior oral anticoagulant use in patients with coronavirus disease 2019 admitted to hospitals in the UK - a multicentre observational study.

Journal: British journal of haematology

Published: July 10, 2021

Identification of a homozygous recessive variant in PTGS1 resulting in a congenital aspirin-like defect in platelet function.

Identification of a homozygous recessive variant in PTGS1 resulting in a congenital aspirin-like defect in platelet function.

Journal: Haematologica

Published: September 18, 2019

Germline mutations in the transcription factor IKZF5 cause thrombocytopenia.

Germline mutations in the transcription factor IKZF5 cause thrombocytopenia.

Journal: Blood

Published: March 26, 2019

Inherited missense variants that affect GFI1B function do not necessarily cause bleeding diatheses.

Inherited missense variants that affect GFI1B function do not necessarily cause bleeding diatheses.

Journal: Haematologica

Published: December 22, 2018

Rare variants in GP1BB are responsible for autosomal dominant macrothrombocytopenia.

Rare variants in GP1BB are responsible for autosomal dominant macrothrombocytopenia.

Journal: Blood

Published: August 10, 2016

Inherited platelet disorders: toward DNA-based diagnosis.

Inherited platelet disorders: toward DNA-based diagnosis.

Journal: Blood

Published: March 29, 2016

A high-throughput sequencing test for diagnosing inherited bleeding, thrombotic, and platelet disorders.

A high-throughput sequencing test for diagnosing inherited bleeding, thrombotic, and platelet disorders.

Journal: Blood

Published: December 24, 2015

A dominant gain-of-function mutation in universal tyrosine kinase SRC causes thrombocytopenia, myelofibrosis, bleeding, and bone pathologies.

A dominant gain-of-function mutation in universal tyrosine kinase SRC causes thrombocytopenia, myelofibrosis, bleeding, and bone pathologies.

Journal: Science translational medicine

Published: October 28, 2015

A gain-of-function variant in DIAPH1 causes dominant macrothrombocytopenia and hearing loss.

A gain-of-function variant in DIAPH1 causes dominant macrothrombocytopenia and hearing loss.

Journal: Blood

Published: October 14, 2015

Human phenotype ontology annotation and cluster analysis to unravel genetic defects in 707 cases with unexplained bleeding and platelet disorders.

Human phenotype ontology annotation and cluster analysis to unravel genetic defects in 707 cases with unexplained bleeding and platelet disorders.

Journal: Genome medicine

Published: November 24, 2014

Showing 1-12 of 13

Last Updated: 09/26/2026