Publications
Identification of genetic risk loci associated with aquaporin 4-positive neuromyelitis optica spectrum disorder: a genome-wide association study
Journal article
Attfield KE. et al, (2026), The Lancet Neurology, 25, 482 - 491
A Network Approach to Developmental Differences and Disorders.
Journal article
Deniz E. et al, (2026), Dev Sci, 29
'Everyday genetics' in the Mass Observation Project: insights on genetics from people writing for an archive of everyday life in Britain.
Journal article
Horton R. et al, (2026), Eur J Hum Genet
Targeted removal of soluble Fms-like tyrosine kinase 1 in very preterm preeclampsia: a pilot trial.
Journal article
Thadhani R. et al, (2026), Nat Med
News
Dr Alexander Mentzer Named NIHR Oxford Senior Research Fellow
22 January 2026
Seminars
Role of Dysregulated Angiotensin II Signaling in Maternal Microvascular Dysfunction After Preeclampsia
Monday, 11 May 2026, 2pm to 3.30pm
The Biobank Rare Variant consortium powers the discovery of rare genetic associations through global collaboration
Tuesday, 26 May 2026, 9.30am to 10.30am
