Andrew Mumford
14PUBLICATIONS
107CO-AUTHORS
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Publications (14)
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|Sep 05, 2025
Biallelic variants in RNU2-2 cause the most prevalent known recessive neurodevelopmental disorder.Daniel Greene, Rodrigo Mendez, Jon Lees
|Sep 16, 2024
Mutations in the U2 snRNA gene RNU2-2P cause a severe neurodevelopmental disorder with prominent epilepsy.Daniel Greene, Koenraad De Wispelaere, Jon Lees
|Sep 13, 2024
Clinical and cost-effectiveness of clopidogrel resistance genotype testing after ischaemic stroke or transient ischaemic attack: a systematic review and economic model.Joe Carroll, Catalina Lopez Manzano, Eve Tomlinson
|Jan 29, 2024
Congenital fibrinogen disorders: a retrospective clinical and genetic analysis of the Prospective Rare Bleeding Disorders Database.Samin Mohsenian, Roberta Palla, Marzia Menegatti
|Aug 30, 2023
A signature of platelet reactivity in CBC scattergrams reveals genetic predictors of thrombotic disease risk.Hippolyte Verdier, Patrick Thomas, Joana Batista
|Aug 30, 2023
The effects of pathogenic and likely pathogenic variants for inherited hemostasis disorders in 140 214 UK Biobank participants.Luca Stefanucci, Janine Collins, Matthew C Sims
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Frequent Collaborators
3 joint publications
Ernest Turro
2 joint publications
Janine Collins
2 joint publications
William J Astle
2 joint publications
Laura J Corbin
2 joint publications
Nick Gleadall
2 joint publications
Willem H Ouwehand
1 joint publications
Penny Whiting
1 joint publications
Kurt Taylor
1 joint publications
Marion T van den Bosch
1 joint publications
Josine L Min
