James R Staley

PhenoScanner V2: an expanded tool for searching human genotype–phenotype associations

Stephen Burgess, Mihir A Kamat, James A Blackshaw, 2019, Bioinform..

MendelianRandomization v0.5.0: updates to an R package for performing Mendelian randomization analyses using summarized data

Stephen Burgess, Andrew J. Grant, James R Staley, 2020, Wellcome open research.

Longitudinal analysis strategies for modelling epigenetic trajectories

Tom R. Gaunt, Tom R Gaunt, Kate Tilling, 2018, International journal of epidemiology.

Phenome-wide Mendelian randomization mapping the influence of the plasma proteome on complex diseases

Valeriia Haberland, Stephen Burgess, Jie Zheng, 2020, Nature genetics.

A comparison of Cox and logistic regression for use in genome-wide association studies of cohort and case-cohort design

Edmund Jones, Stephen Kaptoge, Angela M Wood, 2017, European Journal of Human Genetics.

Trans-ancestry meta-analyses identify rare and common variants associated with blood pressure and hypertension

He Zhang, Andres Metspalu, Fotios Drenos, 2016, Nature Genetics.

A fast and efficient colocalization algorithm for identifying shared genetic risk factors across multiple traits

Stephen Burgess, Paul D W Kirk, James R Staley, 2019, Nature Communications.

A robust and efficient method for Mendelian randomization with hundreds of genetic variants: unravelling mechanisms linking HDL-cholesterol and coronary heart disease

Stephen Burgess, James R Staley, Elias Allara, 2019, bioRxiv.