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Genome Medicine|April 26, 2024
Clustering of predicted loss-of-function variants in genes linked with monogenic disease can explain incomplete penetranceRobin N Beaumont, Gareth Hawkes, Adam C Gunning, et al.
Diabetologia|July 13, 2023
Utility of genetic risk scores in type 1 diabetesAmber M Luckett, Michael N Weedon, Gareth Hawkes, et al.
Neuroendocrinology|March 13, 2025
Clinical and Genetic Factors Associated with Neuroendocrine Neoplasms: A UK Biobank StudyHarry David Green, Marie Line El-Asmar, Brian Rous, et al.
European Journal of Epidemiology|March 19, 2025
Effects of childhood and adult height on later life cardiovascular disease risk estimated through Mendelian randomizationTom G Richardson, Helena Urquijo, Laurence J Howe, et al.
Journal of Neuroendocrinology|June 16, 2026
Sex-differential associations of MC3R p.F45S with human metabolic profileTanya C Kaur, Andrew R Wood, Gareth Hawkes, et al.
Plos Genetics|September 21, 2023
Identification and analysis of individuals who deviate from their genetically-predicted phenotypeGareth Hawkes, Loic Yengo, Sailaja Vedantam, et al.
Biorxiv : the Preprint Server for Biology|February 17, 2023
Identification and analysis of individuals who deviate from their genetically-predicted phenotypeGareth Hawkes, Loic Yengo, Sailaja Vedantam, et al.
Human Molecular Genetics|June 9, 2026
Limited penetrance of dominantly inherited AIRE variants in a population-based cohortSuraj N Ramchand, Jacques Murray Leech, Luke N Sharp, et al.
JHEP Reports : Innovation in Hepatology|April 8, 2026
Genetic and lifestyle modifiers of haemochromatosis-related clinical outcomes in HFE C282Y homozygotesMitchell R Lucas, João Delgado, Robin N Beaumont, et al.
Diabetes|November 12, 2024
Type 1 Diabetes Genetic Risk Contributes to Phenotypic Presentation in Monogenic Autoimmune DiabetesAmber M Luckett, Gareth Hawkes, Harry D Green, et al.
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