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1. Gene-based burden tests of rare germline variants identify six cancer susceptibility genes

2. Homozygosity for a stop-gain variant in CCDC201 causes primary ovarian insufficiency

3. The correlation between CpG methylation and gene expression is driven by sequence variants

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

5. Deciphering the genetics and mechanisms of predisposition to multiple myeloma

6. Start codon variant in LAG3 is associated with decreased LAG-3 expression and increased risk of autoimmune thyroid disease

7. Variant in the synaptonemal complex protein SYCE2 associates with pregnancy loss through effect on recombination

8. Genetics and epidemiology of mutational barcode-defined clonal hematopoiesis

9. Author Correction: Large-scale plasma proteomics comparisons through genetics and disease associations

10. Rare variants with large effects provide functional insights into the pathology of migraine subtypes, with and without aura

11. Large-scale plasma proteomics comparisons through genetics and disease associations

12. Sequence variant affects GCSAML splicing, mast cell specific proteins, and risk of urticaria

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

14. Publisher Correction: Deficit of homozygosity among 1.52 million individuals and genetic causes of recessive lethality

15. Deficit of homozygosity among 1.52 million individuals and genetic causes of recessive lethality

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

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

18. Multiomics study of nonalcoholic fatty liver disease

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

20. Reconstruction of a large-scale outbreak of SARS-CoV-2 infection in Iceland informs vaccination strategies

21. Genetic architecture of band neutrophil fraction in Iceland

22. A genome-wide meta-analysis identifies 50 genetic loci associated with carpal tunnel syndrome

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

25. Population-level deficit of homozygosity unveils CPSF3 as an intellectual disability syndrome gene

26. Author Correction: Rare SLC13A1 variants associate with intervertebral disc disorder highlighting role of sulfate in disc pathology

27. Rare SLC13A1 variants associate with intervertebral disc disorder highlighting role of sulfate in disc pathology

28. Author Correction: Functional dissection of inherited non-coding variation influencing multiple myeloma risk

29. Functional dissection of inherited non-coding variation influencing multiple myeloma risk

30. Genetic Associations and Architecture of Asthma-COPD Overlap

31. Large-scale integration of the plasma proteome with genetics and disease

32. Short Vi-polysaccharide abrogates T-independent immune response and hyporesponsiveness elicited by long Vi-CRM 197 conjugate vaccine

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

34. Genome-Wide Association Study of Accessory Atrioventricular Pathways

35. Homozygosity for a stop-gain variant in CCDC201causes primary ovarian insufficiency

36. Distinction between the effects of parental and fetal genomes on fetal growth

37. Genome-wide investigation of persistence with methotrexate treatment in early rheumatoid arthritis

38. Variants at the Interleukin 1 Gene Locus and Pericarditis

39. Differences between germline genomes of monozygotic twins

40. A protein-truncating R179X variant in RNF186 confers protection against ulcerative colitis.

41. Molecular benchmarks of a SARS-CoV-2 epidemic

42. A meta-analysis uncovers the first sequence variant conferring risk of Bell’s palsy

43. The genetic architecture of age-related hearing impairment revealed by genome-wide association analysis

44. A genome-wide meta-analysis uncovers six sequence variants conferring risk of vertigo

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

46. Predicting the probability of death using proteomics

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

48. FLT3 stop mutation increases FLT3 ligand level and risk of autoimmune thyroid disease

49. A meta-analysis of genome-wide association studies identifies novel variants associated with osteoarthritis of the hip

50. Genome-wide investigation of persistence with methotrexate treatment in early rheumatoid arthritis.

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