Search

Your search keyword '"Eyjolfsson, Gi"' showing total 44 results

Search Constraints

Start Over You searched for: Author "Eyjolfsson, Gi" Remove constraint Author: "Eyjolfsson, Gi"
44 results on '"Eyjolfsson, Gi"'

Search Results

1. Genome-wide association study identifies loci influencing concentrations of liver enzymes in plasma

2. New genetic loci link adipose and insulin biology to body fat distribution.

3. New genetic loci link adipose and insulin biology to body fat distribution

4. Nonsense mutation in the LGR4 gene is associated with several human diseases and other traits

5. Genome-wide association study identifies loci influencing concentrations of liver enzymes in plasma

6. Genetic studies of body mass index yield new insights for obesity biology

7. New genetic loci link adipose and insulin biology to body fat distribution

8. Seventy-five genetic loci influencing the human red blood cell

9. Sequence variants influencing the regulation of serum IgG subclass levels.

10. Lifelong Reduction in LDL (Low-Density Lipoprotein) Cholesterol due to a Gain-of-Function Mutation in LDLR .

11. Eighty-eight variants highlight the role of T cell regulation and airway remodeling in asthma pathogenesis.

12. Common and Rare Sequence Variants Influencing Tumor Biomarkers in Blood.

13. Lipoprotein(a) Concentration and Risks of Cardiovascular Disease and Diabetes.

14. Sequence variants associating with urinary biomarkers.

15. A loss-of-function variant in ALOX15 protects against nasal polyps and chronic rhinosinusitis.

16. Genome-wide association meta-analysis yields 20 loci associated with gallstone disease.

17. Genome-wide associations for benign prostatic hyperplasia reveal a genetic correlation with serum levels of PSA.

18. Insights into imprinting from parent-of-origin phased methylomes and transcriptomes.

19. Rare SCARB1 mutations associate with high-density lipoprotein cholesterol but not with coronary artery disease.

20. A rare missense variant in NR1H4 associates with lower cholesterol levels.

21. Identification of sequence variants influencing immunoglobulin levels.

22. A rare splice donor mutation in the haptoglobin gene associates with blood lipid levels and coronary artery disease.

23. A rare IL33 loss-of-function mutation reduces blood eosinophil counts and protects from asthma.

24. A genome-wide association study yields five novel thyroid cancer risk loci.

25. Variant ASGR1 Associated with a Reduced Risk of Coronary Artery Disease.

26. Variants with large effects on blood lipids and the role of cholesterol and triglycerides in coronary disease.

27. Identification of Common Genetic Variants Influencing Spontaneous Dizygotic Twinning and Female Fertility.

28. Common and rare variants associating with serum levels of creatine kinase and lactate dehydrogenase.

29. Common and rare variants associated with kidney stones and biochemical traits.

30. Large-scale whole-genome sequencing of the Icelandic population.

31. Rare mutations associating with serum creatinine and chronic kidney disease.

32. The germline sequence variant rs2736100_C in TERT associates with myeloproliferative neoplasms.

33. Common variants associated with plasma triglycerides and risk for coronary artery disease.

34. Genetic architecture of vitamin B12 and folate levels uncovered applying deeply sequenced large datasets.

35. Nonsense mutation in the LGR4 gene is associated with several human diseases and other traits.

36. Seventy-five genetic loci influencing the human red blood cell.

37. Discovery of common variants associated with low TSH levels and thyroid cancer risk.

38. Identification of low-frequency variants associated with gout and serum uric acid levels.

39. Genetic correction of PSA values using sequence variants associated with PSA levels.

40. Association of variants at UMOD with chronic kidney disease and kidney stones-role of age and comorbid diseases.

41. Genome-wide meta-analysis for serum calcium identifies significantly associated SNPs near the calcium-sensing receptor (CASR) gene.

42. Common variants on 9q22.33 and 14q13.3 predispose to thyroid cancer in European populations.

43. Sequence variants affecting eosinophil numbers associate with asthma and myocardial infarction.

44. Epidemiology of hairy cell leukemia in Iceland.

Catalog

Books, media, physical & digital resources