Translational Metabolic Genomics in the Grarup Group
The goal of the Grarup Group is to define the genetic determinants of diabetes-related phenotypes and to perform detailed physiological characterization of these variants in humans. The ambition is to translate this knowledge into clinically relevant interventions.
The overarching goal of the Grarup Group is to gain a deeper understanding of the genetic architecture of type 2 diabetes, to expand our insights into diabetes pathogenesis and pathophysiology and thereby derive novel drug targets for diabetes and advances in clinical diabetes management and prevention.
One major focus area is to define the genetic determinants of diabetes-related phenotypes. Other focus areas include the application of recall-by-genotype principles to investigate the physiological impact on genetic variation related to metabolism and to determine the genetic determinants of food preferences and taste perception.
“FGF21 Is a Sugar-Induced Hormone Associated with Sweet Intake and Preference in Humans”
Published in Cell Metabolism in 2017 this study identifies variation near FGF21 (the hepatokine fibroblast growth factor) in relation to food intake, especially sugar-containing items in Danish individuals. The findings suggest that the liver may secrete hormones that influence eating behavior
“Loss-of-function variants in ADCY3 increase risk of obesity and type 2 diabetes”
Published in Nature Genetics in 2018 this study identified a loss-of-function variant in ADCY3 (encoding adenylate cyclase 3) in Greenlanders, which had a high impact on obesity and type 2 diabetes. The findings provide new information on disease etiology relevant for future treatment strategies.
“Increasing insulin resistance accentuates the effect of triglyceride-associated loci on serum triglycerides during 5 years”
Published in the Journal of Lipid Research in 2016 this study investigates the association between a serum triglyceride weighted genetic risk score and changes in fasting serum triglyceride level over 5 years. The findings suggest that increased genetic risk load is associated with a larger increase in fasting serum triglyceride levels in nondiabetic individuals.
|Grarup, Niels||Associate professor||Platform Coordinator, Phenomics; Group Leader, Grarup Group, Translational Metabolic Genomics||+45 353-37126|
|Haydar, Sara||Postdoc||Grarup Group, Translational Metabolic Genomics||+45 353-25072|
|Justesen, Johanne Marie||International Researcher||Grarup Group, Translational Metabolic Genomics|
|Suleman, Sufyan||Research assistant||Grarup Group, Translational Metabolic Genomics||+45 29 42 05 55|
|Sørensen, Kimmie Vestergaard||PhD student||Grarup Group, Translational Metabolic Genomics||+45 353-30742|
|Torresano Lominchar, Jesus Vicente||Research assistant||Grarup Group, Translational Metabolic Genomics||+45 353-34601|
|Zilhao Nogueira, Nuno Rodrigues||Postdoc||Grarup Group, Translational Metabolic Genomics||+45 353-35456|