502 results on '"Masson, Gisli"'
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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
31. Relatedness disequilibrium regression estimates heritability without environmental bias
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
46. Author Correction: The rate of meiotic gene conversion varies by sex and age
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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