Anna L Gloyn, DPhil

Professor, Department of Pediatrics and Department of Genetics, Stanford University

Dr Anna Gloyn joined the faculty at Stanford University in February 2020 as Professor of Pediatrics & Genetics.   She completed her DPhil at the University of Oxford under the supervision of the late Professor Robert C. Turner, followed by post-doctoral training with Professors Andrew Hattersley & Sian Ellard (University of Exeter, UK) and Professor Franz Matschinsky (University of Pennsylvania, USA). Her DPhil and post-doctoral research were both focused on the role of genetic variation in the genes encoding the KATP channel initially in type 2 diabetes and subsequently in neonatal diabetes. 

 In 2004 she returned to Oxford where she established an independent research group focused on understanding beta-cell function through the functional characterization of genetic variants causally implicated in monogenic diabetes.  For the past 10 years a major focus of her work has been on translating discoveries from genome-wide association studies into biological and clinical insights.  Her research combines genetic discovery and functional genomics with clinical phenotyping and disease modelling in human cell models to elucidate how changes in DNA sequence alter diabetes risk. 

 Her work is highly collaborative, she plays roles in multiple international consortia including the Accelerated Medicines Partnership for Common Metabolic Disease (AMP-CMD) and the Human Islet Research Network (HIRN). 

 Dr Gloyn is the recipient of multiple national and international awards for her research including the European Association for the Study of Diabetes (EASD) Rising Star (2005) and Minkowski (2014) awards and the American Diabetes Association Outstanding Scientific Achievement Award (2022).