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

4. Genetic drivers of heterogeneity in type 2 diabetes pathophysiology

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

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

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

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

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

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

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

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

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

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

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

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

18. 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

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

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

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

22. Microbiome and metabolome features of the cardiometabolic disease spectrum

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

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

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

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

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

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

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

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

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

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

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

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

38. Exome Genotyping Identifies Pleiotropic Variants Associated with Red Blood Cell Traits

41. Trans-ethnic gut microbial signatures of prediabetic subjects from India and Denmark

42. Trans-ethnic gut microbiota signatures of type 2 diabetes in Denmark and India

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

47. Uncovering the Genetic History of the Present-Day Greenlandic Population

48. Habitual sleep duration is associated with BMI and macronutrient intake and may be modified by CLOCK genetic variants 2–4

49. Pleiotropic genes for metabolic syndrome and inflammation

50. Variation and association to diabetes in 2000 full mtDNA sequences mined from an exome study in a Danish population

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