Andrew D. Mumford

Bristol, ENG, United Kingdom

Last Updated: 09/26/2026

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Found 121 publications

Purified zymogens reveal mechanisms of snake venom metalloproteinase auto-activation.

Purified zymogens reveal mechanisms of snake venom metalloproteinase auto-activation.

Journal: eLife

Published: June 10, 2026

Publisher Correction: Biallelic variants in RNU2-2 cause the most prevalent known recessive neurodevelopmental disorder.

Publisher Correction: Biallelic variants in RNU2-2 cause the most prevalent known recessive neurodevelopmental disorder.

Journal: Nature genetics

Published: April 23, 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

Biallelic variants in RNU2-2 cause the most prevalent known recessive neurodevelopmental disorder.

Biallelic variants in RNU2-2 cause the most prevalent known recessive neurodevelopmental disorder.

Journal: medRxiv : the preprint server for health sciences

Published: September 05, 2025

Biallelic variants in RNU2-2 cause the most prevalent known recessive neurodevelopmental disorder.

Biallelic variants in RNU2-2 cause the most prevalent known recessive neurodevelopmental disorder.

Journal: Nature genetics

Published: August 21, 2025

Predictive accuracy of diagnostic tests for excessive bleeding in cardiac surgery: The COPTIC-C study.

Predictive accuracy of diagnostic tests for excessive bleeding in cardiac surgery: The COPTIC-C study.

Journal: Transfusion

Published: May 19, 2025

A comprehensive phenome wide analysis of the role of neutrophils in health and disease.

A comprehensive phenome wide analysis of the role of neutrophils in health and disease.

Journal: Journal of leukocyte biology

Published: February 07, 2025

Leber hereditary optic neuropathy: utilities and carer burden from British and Irish participants.

Leber hereditary optic neuropathy: utilities and carer burden from British and Irish participants.

Journal: Orphanet journal of rare diseases

Published: January 22, 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

Mutations in the U2 snRNA gene RNU2-2P cause a severe neurodevelopmental disorder with prominent epilepsy.

Mutations in the U2 snRNA gene RNU2-2P cause a severe neurodevelopmental disorder with prominent epilepsy.

Journal: medRxiv : the preprint server for health sciences

Published: September 16, 2024

Clinical and cost-effectiveness of clopidogrel resistance genotype testing after ischaemic stroke or transient ischaemic attack: a systematic review and economic model.

Clinical and cost-effectiveness of clopidogrel resistance genotype testing after ischaemic stroke or transient ischaemic attack: a systematic review and economic model.

Journal: Health technology assessment (Winchester, England)

Published: September 13, 2024

Mutations in the small nuclear RNA gene RNU2-2 cause a severe neurodevelopmental disorder with prominent epilepsy.

Mutations in the small nuclear RNA gene RNU2-2 cause a severe neurodevelopmental disorder with prominent epilepsy.

Journal: Nature genetics

Published: September 13, 2024

Showing 1-12 of 121

Last Updated: 09/26/2026