Exome-wide analysis of rare coding variation identifies novel associations with COPD and airflow limitation in MOCS3, IFIT3 and SERPINA12
Genetic variants associated with subjective well-being, depressive symptoms, and neuroticism identified through genome-wide analyses
Recurrent short sleep, chronic insomnia symptoms and salivary cortisol: a 10-year follow-up in the Whitehall II study
Proinflammatory genotype is associated with the frailty phenotype in the English Longitudinal Study of Ageing
Never too early, never too late: social and biological influences on health and disease over the lifecourse
The genetics of blood pressure regulation and its target organs from association studies in 342,415 individuals
Circulating apolipoprotein E concentration and cardiovascular disease risk: meta-analysis of results from three studies
Equity of utilisation of cardiovascular care and mental health services in England: a cohort-based cross-sectional study using small-area estimation