Retrieved from Lund University's publications database
- Age-dependent variation of genotypes in MHC II transactivator gene (CIITA) in controls and association to type 1 diabetes
- Large-scale association analysis provides insights into the genetic architecture and pathophysiology of type 2 diabetes
- Worse glycaemic control in LADA patients than in those with type 2 diabetes, despite a longer time on insulin therapy.
- Common variants in CNDP1 and CNDP2, and risk of nephropathy in type 2 diabetes.
- Minor amputation in patients with diabetes mellitus and severe foot ulcers achieves good outcomes.
- Power in the Phenotypic Extremes: A Simulation Study of Power in Discovery and Replication of Rare Variants
- Uromodulin gene variant is associated with type 2 diabetic nephropathy.
- Association between LTA, TNF and AGER polymorphisms and late diabetic complications.
- Common Missense Variant in the Glucokinase Regulatory Protein Gene Is Associated With Increased Plasma Triglyceride and C-Reactive Protein but Lower Fasting Glucose Concentrations
- Common variants in or around the JAZF1, CDKN2A/2B, CDKAL1 and WFS1 genes discriminate between autoimmune and non-autoimmune diabetes
- Common variants in the TCF7L2 gene help to differentiate autoimmune from non-autoimmune diabetes in young (15-34 years) but not in middle-aged (40-59 years) diabetic patients.
- Genetic similarities between latent autoimmune diabetes in adults, type 1 diabetes, and type 2 diabetes
- Immigrants from the Middle-East have a different form of Type 2 diabetes compared with Swedish patients.
- Polymorphism in the MHC2TA gene is associated with features of the metabolic syndrome and cardiovascular mortality.
- The -374 T/A polymorphism in the gene encoding RAGE is associated with diabetic nephropathy and retinopathy in type 1 diabetic patients.
- Type 2 diabetes and risk for periodontal disease: a role for dental health awareness