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

2. Genetic links between ovarian ageing, cancer risk and de novo mutation rates

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

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

9. Histopathology and levels of proteins in plasma associate with survival after colorectal cancer diagnosis

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

11. Cross-ancestry genome-wide meta-analysis of 61,047 cases and 947,237 controls identifies new susceptibility loci contributing to lung cancer.

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

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. Genome-wide Association Study of Bladder Cancer Reveals New Biological and Translational Insights

17. Multiomics study of nonalcoholic fatty liver disease

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

19. Genetic architecture of band neutrophil fraction in Iceland

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

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

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

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

24. Identification of a novel susceptibility locus at 13q34 and refinement of the 20p12.2 region as a multi-signal locus associated with bladder cancer risk in individuals of European ancestry

25. Common variants at 19p13 are associated with susceptibility to ovarian cancer (vol 42, pg 880, 2010)

26. Corrigendum: Common variants at 19p13 are associated with susceptibility to ovarian cancer.

27. Estimating robustness of the tileShuffle method with repeated probes

28. Identification of 22 susceptibility loci associated with testicular germ cell tumors

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

30. Predicting the probability of death using proteomics

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

32. Author Correction: Germline variants at SOHLH2 influence multiple myeloma risk

33. A Missense Variant in PTPN22 is a Risk Factor for Drug-induced Liver Injury

34. Germline variants at SOHLH2 influence multiple myeloma risk

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

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

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

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

39. Common variants at 19p13 are associated with susceptibility to ovarian cancer.

40. Evaluation of association of HNF1B variants with diverse cancers: collaborative analysis of data from 19 genome-wide association studies.

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

42. Author Correction: Identification of multiple risk loci and regulatory mechanisms influencing susceptibility to multiple myeloma

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

44. Supplementary Table 1 from Cross-Cancer Genome-Wide Analysis of Lung, Ovary, Breast, Prostate, and Colorectal Cancer Reveals Novel Pleiotropic Associations

45. Data from Cross-Cancer Genome-Wide Analysis of Lung, Ovary, Breast, Prostate, and Colorectal Cancer Reveals Novel Pleiotropic Associations

46. Supplementary Table 1 from Association of Folate-Pathway Gene Polymorphisms with the Risk of Prostate Cancer: a Population-Based Nested Case-Control Study, Systematic Review, and Meta-analysis

47. Supplementary Table 2 and Supplemental Figures from Cross-Cancer Genome-Wide Analysis of Lung, Ovary, Breast, Prostate, and Colorectal Cancer Reveals Novel Pleiotropic Associations

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

49. Data from Association of Folate-Pathway Gene Polymorphisms with the Risk of Prostate Cancer: a Population-Based Nested Case-Control Study, Systematic Review, and Meta-analysis

50. Supplementary Table 2 from Association of Folate-Pathway Gene Polymorphisms with the Risk of Prostate Cancer: a Population-Based Nested Case-Control Study, Systematic Review, and Meta-analysis

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