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143 results on '"Sparsø, T."'

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1. Whole-Exome Sequencing of 2,000 Danish Individuals and the Role of Rare Coding Variants in Type 2 Diabetes

2. Exome sequencing-driven discovery of coding polymorphisms associated with common metabolic phenotypes

7. dsSwissKnife: An R package for federated data analysis

13. Differential DNA methylation at birth associated with mental disorder in individuals with 22q11.2 deletion syndrome

14. CNV-association meta-analysis in 191,161 European adults reveals new loci associated with anthropometric traits

15. Differential DNA methylation at birth associated with mental disorder in individuals with 22q11.2 deletion syndrome

16. The Lin28/let-7 axis regulates glucose metabolism

17. A principal component meta-analysis on multiple anthropometric traits identifies novel loci for body shape

18. Bayesian inference analyses of the polygenic architecture of rheumatoid arthritis

19. Genome-wide association identifies nine common variants associated with fasting proinsulin levels and provides new insights into the pathophysiology of type 2 diabetes

20. The Influence of Age and Sex on Genetic Associations with Adult Body Size and Shape: A Large-Scale Genome-Wide Interaction Study

21. Trans-ancestry genome-wide association study identifies 12 genetic loci influencing blood pressure and implicates a role for DNA methylation

22. Genetic fine mapping and genomic annotation defines causal mechanisms at type 2 diabetes susceptibility loci

23. Erratum: New genetic loci implicated in fasting glucose homeostasis and their impact on type 2 diabetes risk (Nature Genetics (2010) 42 (105-116))

24. Whole-Exome Sequencing of 2,000 Danish Individuals and the Role of Rare Coding Variants in Type 2 Diabetes

25. A genome-wide approach accounting for body mass index identifies genetic variants influencing fasting glycemic traits and insulin resistance.

26. Novel loci for adiponectin levels and their influence on type 2 diabetes and metabolic traits: a multi-ethnic meta-analysis of 45,891 individuals.

27. Genome-wide association for abdominal subcutaneous and visceral adipose reveals a novel locus for visceral fat in women.

28. The diabetogenic VPS13C/C2CD4A/C2CD4B rs7172432 variant impairs glucose-stimulated insulin response in 5,722 non-diabetic Danish individuals

29. Type 2 diabetes risk allele near CENTD2 is associated with decreased glucose-stimulated insulin release

30. New genetic loci implicated in fasting glucose homeostasis and their impact on type 2 diabetes risk

31. Twelve type 2 diabetes susceptibility loci identified through large-scale association analysis

32. Combined analysis of 19 common validated type 2 diabetes susceptibility gene variants shows moderate discriminative value and no evidence of gene-gene interaction

33. Impact of polymorphisms in WFS1 on prediabetic phenotypes in a population-based sample of middle-aged people with normal and abnormal glucose regulation

34. Genetic analysis of the estrogen-related receptor alpha and studies of association with obesity and type 2 diabetes

35. The GCKR rs780094 polymorphism is associated with elevated fasting serum triacylglycerol, reduced fasting and OGTT-related insulinaemia, and reduced risk of type 2 diabetes

36. Large-scale study of the -232C> G polymorphism of PCK1 in Type 2 diabetes

38. Erratum: Corrigendum: Twelve type 2 diabetes susceptibility loci identified through large-scale association analysis

39. Impact of polymorphisms in WFS1 on prediabetic phenotypes in a population-based sample of middle-aged people with normal and abnormal glucose regulation

40. The GCKR rs780094 polymorphism is associated with elevated fasting serum triacylglycerol, reduced fasting and OGTT-related insulinaemia, and reduced risk of type 2 diabetes

41. Genetic analysis of the estrogen-related receptor α and studies of association with obesity and type 2 diabetes

42. The diabetogenic VPS13C/ C2CD4A/ C2CD4B rs7172432 variant impairs glucose-stimulated insulin response in 5,722 non-diabetic Danish individuals.

43. Physiologic characterization of type 2 diabetes-related loci.

44. G-allele of intronic rs10830963 in MTNR1B confers increased risk of impaired fasting glycemia and type 2 diabetes through an impaired glucose-stimulated insulin release: studies involving 19,605 Europeans.

45. AHSG tag single nucleotide polymorphisms associate with type 2 diabetes and dyslipidemia: studies of metabolic traits in 7,683 white Danish subjects.

49. Genetic evidence that raised sex hormone binding globulin (SHBG) levels reduce the risk of type 2 diabetes

50. A genome-wide approach accounting for body mass index identifies genetic variants influencing fasting glycemic traits and insulin resistance

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