Andrew R. Wood

Genetic susceptibility to earlier ovarian ageing increases de novo mutation rate in offspring

M. Hurles, M. Weedon, K. Ong, 2022, medRxiv.

Insights into the genetics of menopausal vasomotor symptoms: genome-wide analyses of routinely-collected primary care health records

T. Frayling, M. Weedon, K. Ruth, 2023, BMC Medical Genomics.

Whole genome sequencing analysis identifies rare, large-effect non-coding variants and regions associated with circulating protein levels

T. Frayling, M. Weedon, R. Beaumont, 2023, bioRxiv.

Whole genome association testing in 333,100 individuals across three biobanks identifies rare non-coding single variant and genomic aggregate associations with height

Nicholette D. Palmer, J. Murabito, S. Redline, 2023, bioRxiv.

Genome-wide association study identifies genetic loci for self-reported habitual sleep duration supported by accelerometer-derived estimates

Max A. Little, J. Lane, S. Anderson, 2019, Nature Communications.