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

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

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

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

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

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

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

8. Sequence variants affecting the genome-wide rate of germline microsatellite mutations

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

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

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

12. Genetic architecture of band neutrophil fraction in Iceland

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

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

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

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

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

18. Differences between germline genomes of monozygotic twins

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

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

21. The nature of nurture : Effects of parental genotypes

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

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

24. Multiple transmissions of de novo mutations in families

25. Meta-analysis of Icelandic and UK data sets identifies missense variants in SMO, IL11, COL11A1 and 13 more new loci associated with osteoarthritis

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

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

28. Selection against variants in the genome associated with educational attainment

29. Clonal hematopoiesis, with and without candidate driver mutations, is common in the elderly

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

32. Publisher Correction: GWAS of bone size yields twelve loci that also affect height, BMD, osteoarthritis or fractures

33. GWAS of bone size yields twelve loci that also affect height, BMD, osteoarthritis or fractures

34. A PRPH splice-donor variant associates with reduced sural nerve amplitude and risk of peripheral neuropathy

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

36. A homozygous loss-of-function mutation leading to CYBC1 deficiency causes chronic granulomatous disease

37. Variants associating with uterine leiomyoma highlight genetic background shared by various cancers and hormone-related traits

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

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

40. Sequence variants affect the genome-wide rate of germline microsatellite mutations

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

42. Multiomics analysis of rheumatoid arthritis yields sequence variants that have large effects on risk of the seropositive subset

43. Parental influence on human germline de novo mutations in 1,548 trios from Iceland

44. Symptoms, physical measures and cognitive tests after SARS-CoV-2 infection in a large population-based case-control study

45. Large-scale comparison of immunoassay- and aptamer-based plasma proteomics through genetics and disease

47. Fourteen sequence variants that associate with multiple sclerosis discovered by meta-analysis informed by genetic correlations

48. Sequence Variants in the RNF212 Gene Associate with Genome-Wide Recombination Rate

49. Common Sequence Variants in the LOXL1 Gene Confer Susceptibility to Exfoliation Glaucoma

50. A Common Variant on Chromosome 9p21 Affects the Risk of Myocardial Infarction

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