Sarah K. Westbury

Bristol, ENG, United Kingdom

Last Updated: 09/26/2026

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Found 34 publications

Testing for Non-Severe Heritable Platelet Function Disorders.

Testing for Non-Severe Heritable Platelet Function Disorders.

Journal: International journal of laboratory hematology

Published: January 09, 2026

Associations of tumor somatic mutations with cancer-associated venous thromboembolism.

Associations of tumor somatic mutations with cancer-associated venous thromboembolism.

Journal: Journal of thrombosis and haemostasis : JTH

Published: September 18, 2025

Germline genomic testing to assess the suitability of stem cell donors in the treatment of haematological malignancy: clinical ethics commentary.

Germline genomic testing to assess the suitability of stem cell donors in the treatment of haematological malignancy: clinical ethics commentary.

Journal: Journal of medical ethics

Published: June 12, 2025

Association between tumour somatic mutations and venous thromboembolism in the 100,000 Genomes Project cancer cohort: a study protocol.

Association between tumour somatic mutations and venous thromboembolism in the 100,000 Genomes Project cancer cohort: a study protocol.

Journal: Wellcome open research

Published: December 20, 2024

Human and mouse platelet transcriptomes and proteomes for phenotyping 3474 genes with hemostatic and platelet traits.

Human and mouse platelet transcriptomes and proteomes for phenotyping 3474 genes with hemostatic and platelet traits.

Journal: Blood vessels, thrombosis & hemostasis

Published: September 03, 2024

Rare disease gene association discovery in the 100,000 Genomes Project.

Rare disease gene association discovery in the 100,000 Genomes Project.

Journal: Nature

Published: December 19, 2023

Functional filter for whole-genome sequencing data identifies HHT and stress-associated non-coding SMAD4 polyadenylation site variants >5 kb from coding DNA.

Functional filter for whole-genome sequencing data identifies HHT and stress-associated non-coding SMAD4 polyadenylation site variants >5 kb from coding DNA.

Journal: American journal of human genetics

Published: May 28, 2023

Platelet VPS16B is dependent on VPS33B expression, as determined in two siblings with arthrogryposis, renal dysfunction, and cholestasis syndrome.

Platelet VPS16B is dependent on VPS33B expression, as determined in two siblings with arthrogryposis, renal dysfunction, and cholestasis syndrome.

Journal: Journal of thrombosis and haemostasis : JTH

Published: February 04, 2022

Inherited platelet disorders: From new variants to new knowledge.

Inherited platelet disorders: From new variants to new knowledge.

Journal: British journal of haematology

Published: January 21, 2022

Haematology morphology teaching during the COVID-19 pandemic: a UK teaching hospital experience.

Haematology morphology teaching during the COVID-19 pandemic: a UK teaching hospital experience.

Journal: Future healthcare journal

Published: April 01, 2021

Specifications of the variant curation guidelines for ITGA2B/ITGB3: ClinGen Platelet Disorder Variant Curation Panel.

Specifications of the variant curation guidelines for ITGA2B/ITGB3: ClinGen Platelet Disorder Variant Curation Panel.

Journal: Blood advances

Published: October 29, 2020

FLNA variants associated with disorders of platelet number or function.

FLNA variants associated with disorders of platelet number or function.

Journal: Platelets

Published: April 18, 2020

Showing 1-12 of 34

Last Updated: 09/26/2026