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1. Complete human recombination maps

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

20. Max Point-Tolerance Graphs

21. PopIns: population-scale detection of novel sequence insertions

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

23. Sequence Variants in TAAR5 and Other Loci Affect Human Odor Perception and Naming

25. Differences between germline genomes of monozygotic twins

26. Variants at the Interleukin 1 Gene Locus and Pericarditis

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

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

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

31. Characterizing mutagenic effects of recombination through a sequence-level genetic map

32. Crucial words for abelian powers

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

34. The nature of nurture : Effects of parental genotypes

36. Whole-Genome Shotgun Assembly and Comparison of Human Genome Assemblies

38. Genome-wide association identifies seven loci for pelvic organ prolapse in Iceland and the UK Biobank

39. Multiple transmissions of de novo mutations in families

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

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

44. Data from Loss-of-Function Variants in the Tumor-Suppressor Gene PTPN14 Confer Increased Cancer Risk

45. The Minimum Vulnerability Problem on Graphs

46. Estimating Population Size via Line Graph Reconstruction

47. A Mixed Integer Programming Model for the Parsimonious Loss of Heterozygosity Problem

48. Streaming Algorithms for Independent Sets

49. The Clark Phase-able Sample Size Problem: Long-Range Phasing and Loss of Heterozygosity in GWAS

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

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