Sarah Finer
London, ENG, United Kingdom
Last Updated: 09/26/2026
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Found 81 publications
Selection-guided discovery in South Asians implicates the MAPT locus in insulin resistance.
Journal: medRxiv : the preprint server for health sciences
Published: July 03, 2026
An ancestry-enriched HNF4A variant and GP2 reveal distinct mechanisms of type 2 diabetes in exome-wide study of 13,674 cases and 41,024 controls.
Journal: medRxiv : the preprint server for health sciences
Published: June 04, 2026
The Biobank Rare Variant consortium powers the discovery of rare genetic associations through global collaboration.
Journal: medRxiv : the preprint server for health sciences
Published: June 04, 2026
Multi-ancestry, trans-generational GWAS meta-analysis of gestational diabetes and glycaemic traits during pregnancy reveals limited evidence of pregnancy-specific genetic effects.
Journal: Nature communications
Published: December 14, 2025
Improving type 2 diabetes polygenic risk scores by incorporating rare, low-frequency, and population-specific variants.
Journal: medRxiv : the preprint server for health sciences
Published: December 08, 2025
Equity and impact of social prescribing in type 2 diabetes prevention: cross-sectional and cohort study using national primary care data.
Journal: The British journal of general practice : the journal of the Royal College of General Practitioners
Published: November 19, 2025
Genetic and sociodemographic factors associated with trajectories of physical and mental health multimorbidity in a South Asian cohort in the UK: A multistate modelling analysis.
Journal: PLoS medicine
Published: November 11, 2025
Genetics of Cholesterol and Coronary Disease Risk across Six Global Ancestries.
Journal: NEJM evidence
Published: October 28, 2025
Combining polygenic risk scores to understand genetic liability to physical-mental health multimorbidity in UK Biobank.
Journal: Human molecular genetics
Published: October 09, 2025
The genetic architecture of fibromyalgia across 2.5 million individuals.
Journal: Nature medicine
Published: September 18, 2025
Meta-analysis across six global biobanks identifies recessive coding associations with complex traits and diseases.
Journal: American journal of human genetics
Published: September 15, 2025
The contribution of apolipoprotein E genetic variation to dementia risk in British South Asians.
Journal: Brain communications
Published: September 08, 2025
Last Updated: 09/26/2026