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1. Genetic drivers of heterogeneity in type 2 diabetes pathophysiology.

4. Multi-ancestry genetic study of type 2 diabetes highlights the power of diverse populations for discovery and translation

7. A saturated map of common genetic variants associated with human height

9. 14-fold increased prevalence of rare glucokinase gene variant carriers in unselected Danish patients with newly diagnosed type 2 diabetes

12. Implicating genes, pleiotropy, and sexual dimorphism at blood lipid loci through multi-ancestry meta-analysis

13. Protein-coding variants implicate novel genes related to lipid homeostasis contributing to body-fat distribution

14. A multi-layer functional genomic analysis to understand noncoding genetic variation in lipids

15. The power of genetic diversity in genome-wide association studies of lipids

16. A Genome-Wide Association Study of Diabetic Kidney Disease in Subjects With Type 2 Diabetes

17. Publisher Correction: Protein-altering variants associated with body mass index implicate pathways that control energy intake and expenditure in obesity.

18. Refining the accuracy of validated target identification through coding variant fine-mapping in type 2 diabetes.

19. Protein-altering variants associated with body mass index implicate pathways that control energy intake and expenditure in obesity

22. A Low-Frequency Inactivating Akt2 Variant Enriched in the Finnish Population is Associated With Fasting Insulin Levels and Type 2 Diabetes Risk.

23. Rare and low-frequency coding variants alter human adult height

24. Proteomic analysis of diabetic retinopathy identifies potential plasma-protein biomarkers for diagnosis and prognosis.

29. Identification and functional characterization of G6PC2 coding variants influencing glycemic traits define an effector transcript at the G6PC2-ABCB11 locus.

30. Blood-Biomarkers for Glucose Metabolism in Preterm Infants

31. Cardiolipin Synthesis in Brown and Beige Fat Mitochondria Is Essential for Systemic Energy Homeostasis

33. A novel rare CUBN variant and three additional genes identified in Europeans with and without diabetes: results from an exome-wide association study of albuminuria

34. Fine-mapping type 2 diabetes loci to single-variant resolution using high-density imputation and islet-specific epigenome maps

38. C-reactive Protein, C-peptide, and Risk of First-time Cardiovascular Events and Mortality in Early Type 2 Diabetes: A Danish Cohort Study

39. CRP, C-Peptide, and Risk of First-Time Cardiovascular Events and Mortality in Early Type 2 Diabetes: A Danish Cohort Study

42. Multi-ancestry genome-wide study in >2.5 million individuals reveals heterogeneity in mechanistic pathways of type 2 diabetes and complications

43. A Review of Major Danish Biobanks: Advantages and Possibilities of Health Research in Denmark

45. Additional file 26 of Implicating genes, pleiotropy, and sexual dimorphism at blood lipid loci through multi-ancestry meta-analysis

46. Additional file 34 of Implicating genes, pleiotropy, and sexual dimorphism at blood lipid loci through multi-ancestry meta-analysis

47. Additional file 16 of Implicating genes, pleiotropy, and sexual dimorphism at blood lipid loci through multi-ancestry meta-analysis

48. Author Correction : The power of genetic diversity in genome-wide association studies of lipids

49. Additional file 6 of Implicating genes, pleiotropy, and sexual dimorphism at blood lipid loci through multi-ancestry meta-analysis

50. Additional file 9 of Implicating genes, pleiotropy, and sexual dimorphism at blood lipid loci through multi-ancestry meta-analysis

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