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1. X-chromosome and kidney function: evidence from a multi-trait genetic analysis of 908,697 individuals reveals sex-specific and sex-differential findings in genes regulated by androgen response elements.

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

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

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

5. A partial loss-of-function variant in STAT6 protects against type 2 asthma

6. Physical and cognitive impact following SARS-CoV-2 infection in a large population-based case-control study

7. Genome-wide meta-analysis identifies 93 risk loci and enables risk prediction equivalent to monogenic forms of venous thromboembolism

8. Complex effects of sequence variants on lipid levels and coronary artery disease

9. Multiomics study of nonalcoholic fatty liver disease

10. The sequences of 150,119 genomes in the UK Biobank

11. Genetic loci and prioritization of genes for kidney function decline derived from a meta-analysis of 62 longitudinal genome-wide association studies

12. Monoclonal gammopathy of undetermined significance with multiple paraproteins: A population‐based screening study.

13. Genetic architecture of band neutrophil fraction in Iceland

14. HLA alleles, disease severity, and age associate with T-cell responses following infection with SARS-CoV-2

15. Differential and shared genetic effects on kidney function between diabetic and non-diabetic individuals

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

17. Genetic propensities for verbal and spatial ability have opposite effects on body mass index and risk of schizophrenia

18. Defining new reference intervals for serum free light chains in individuals with chronic kidney disease: Results of the iStopMM study

19. Variants at the Interleukin 1 Gene Locus and Pericarditis

20. Long-read sequencing of 3,622 Icelanders provides insight into the role of structural variants in human diseases and other traits

21. Monoclonal gammopathy of undetermined significance and COVID-19: a population-based cohort study

22. Genetic variants associated with platelet count are predictive of human disease and physiological markers

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

24. Association Between Autoimmune Diseases and Monoclonal Gammopathy of Undetermined Significance: An Analysis From a Population-Based Screening Study.

25. Development of a Multivariable Model to Predict the Need for Bone Marrow Sampling in Persons With Monoclonal Gammopathy of Undetermined Significance: A Cohort Study Nested in a Clinical Trial.

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

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

28. Predicted loss and gain of function mutations in ACO1 are associated with erythropoiesis

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

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

32. The complexity of kidney disease and diagnosing it - Cystatin C, selective glomerular hypofiltration syndromes and proteome regulation.

33. Genome-wide association meta-analyses and fine-mapping elucidate pathways influencing albuminuria

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

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

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

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

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

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

40. Cholesterol not particle concentration mediates the atherogenic risk conferred by apolipoprotein B particles:A Mendelian randomization analysis

41. The complexity of kidney disease and diagnosing it – cystatin C, selective glomerular hypofiltration syndromes and proteome regulation

42. Prevalence of MGUS Is High in the Istopmm Study but the Prevalence of IgA MGUS Does Not Increase with Age in the Way Other Immunoglobulin Subtypes Do

43. Transient M-Proteins: Epidemiology, Causes, and the Impact of Mass Spectrometry: The Istopmm Study

44. Sars-Cov-2 Vaccinations Do Not Lead to Progression of Monoclonal Gammopathy of Undetermined Significance: Results from the Population-Based Istopmm Screening Study

45. Monoclonal Gammopathy of Undetermined Significance (MGUS) with Multiple Paraproteins: Results from the Population-Based Istopmm Screening Study

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

47. A truncating mutation in EPOR leads to hypo-responsiveness to erythropoietin with normal haemoglobin

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

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