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1. Characterization of genetic variants of GIPR reveals a contribution of β-arrestin to metabolic phenotypes

4. Multi-trait analysis characterizes the genetics of thyroid function and identifies causal associations with clinical implications

5. Genetic drivers of heterogeneity in type 2 diabetes pathophysiology

6. The interplay between birth weight and obesity in determining childhood and adolescent cardiometabolic risk

8. Evidence of a causal and modifiable relationship between kidney function and circulating trimethylamine N-oxide

9. Genetic analysis of blood molecular phenotypes reveals common properties in the regulatory networks affecting complex traits

10. The gut microbiota in multiple sclerosis varies with disease activity

11. The gut microbiota contributes to the pathogenesis of anorexia nervosa in humans and mice

13. FGL1 as a modulator of plasma D‐dimer levels: Exome‐wide marker analysis of plasma tPA, PAI‐1, and D‐dimer

14. Discovery of drug–omics associations in type 2 diabetes with generative deep-learning models

15. Determinants of penetrance and variable expressivity in monogenic metabolic conditions across 77,184 exomes.

16. Large-scale association analyses identify host factors influencing human gut microbiome composition

17. Microbially Produced Imidazole Propionate Is Associated With Heart Failure and Mortality

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

19. Alteration of Gut Microbiome in Patients With Schizophrenia Indicates Links Between Bacterial Tyrosine Biosynthesis and Cognitive Dysfunction

20. Trans-ethnic and Ancestry-Specific Blood-Cell Genetics in 746,667 Individuals from 5 Global Populations

21. Genome-wide meta-analysis of macronutrient intake of 91,114 European ancestry participants from the cohorts for heart and aging research in genomic epidemiology consortium

22. Genome-wide association analyses of physical activity and sedentary behavior provide insights into underlying mechanisms and roles in disease prevention

24. Author Correction: Discovery of drug–omics associations in type 2 diabetes with generative deep-learning models

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

26. 14-fold increased prevalence of rare glucokinase gene variant carriers in unselected Danish patients with newly diagnosed type 2 diabetes

27. Exome-chip meta-analysis identifies novel loci associated with cardiac conduction, including ADAMTS6

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

29. Microbiome and metabolome features of the cardiometabolic disease spectrum

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

33. Four groups of type 2 diabetes contribute to the etiological and clinical heterogeneity in newly diagnosed individuals: An IMI DIRECT study

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

35. Combinatorial, additive and dose-dependent drug–microbiome associations

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

37. Genome‐Wide Interactions with Dairy Intake for Body Mass Index in Adults of European Descent

38. ExomeChip-Wide Analysis of 95 626 Individuals Identifies 10 Novel Loci Associated With QT and JT Intervals

39. Dairy Consumption and Body Mass Index Among Adults: Mendelian Randomization Analysis of 184802 Individuals from 25 Studies

43. Large-scale GWAS identifies multiple loci for hand grip strength providing biological insights into muscular fitness.

44. Selection in Europeans on Fatty Acid Desaturases Associated with Dietary Changes

45. The Association of Cardiometabolic, Diet and Lifestyle Parameters With Plasma Glucagon-like Peptide-1: An IMI DIRECT Study

46. Genome-Wide Association Study of the Modified Stumvoll Insulin Sensitivity Index Identifies BCL2 and FAM19A2 as Novel Insulin Sensitivity Loci

48. Obesity treatment effect in Danish children and adolescents carrying Melanocortin-4 Receptor mutations

49. Altered Glucagon and GLP-1 Responses to Oral Glucose in Children and Adolescents With Obesity and Insulin Resistance.

50. Meta-analysis of rare and common exome chip variants identifies S1PR4 and other loci influencing blood cell traits

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