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Author Details
Full Name
Claire Lentaigne
Affiliation
ORCID
Career Start Year
2010
Papers
11
H Index
9
Expertise
CM4AI Collaborator
PMID
Paper Title
Journal Title
Published Year
34500500
Clinical outcomes and the impact of prior oral anticoagulant use in patients with coronavirus disease 2019 admitted to hospitals in the UKâ¿¿-â¿¿a multicentre observational study.
British Journal of Haematology
2022
31217188
Germline mutations in the transcription factor IKZF5 cause thrombocytopenia.
Blood
2019
30573501
Inherited missense variants that affect GFI1B function do not necessarily cause bleeding diatheses.
Haematologica
2019
28064200
Rare variants in GP1BB are responsible for autosomal dominant macrothrombocytopenia.
Blood
2017
26936507
A dominant gain-of-function mutation in universal tyrosine kinase SRC causes thrombocytopenia, myelofibrosis, bleeding, and bone pathologies.
Sci Transl Med
2016
27095789
Inherited platelet disorders: toward DNA-based diagnosis.
Blood
2016
26912466
A gain-of-function variant in DIAPH1 causes dominant macrothrombocytopenia and hearing loss.
Blood
2016
27084890
A high-throughput sequencing test for diagnosing inherited bleeding, thrombotic, and platelet disorders.
Blood
2016
25949529
Human phenotype ontology annotation and cluster analysis to unravel genetic defects in 707 cases with unexplained bleeding and platelet disorders.
Genome Med
2015
25258084
Transcriptional diversity during lineage commitment of human blood progenitors.
Science
2014
20038268
Chronic lymphocytic leukemia can cause acute renal failure even in early stage patients.
Leukemia and Lymphoma
2010
1 - 11 of 11
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