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

2. Sequence variants associated with BMI affect disease risk through BMI itself

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

4. Loss-of-function variants in ITSN1 confer high risk of Parkinson’s disease

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. GWAS meta-analysis reveals key risk loci in essential tremor pathogenesis

8. X-chromosome and kidney function: evidence from a multi-trait genetic analysis of 908,697 individuals reveals sex-specific and sex-differential findings in genes regulated by androgen response elements

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

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

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

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

17. Genetic architecture of band neutrophil fraction in Iceland

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

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

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

22. Differential and shared genetic effects on kidney function between diabetic and non-diabetic individuals

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

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

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

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

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

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

30. Predicting the probability of death using proteomics

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

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

33. Multi-ancestry GWAS of the electrocardiographic PR interval identifies 202 loci underlying cardiac conduction

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

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

36. Associations of autozygosity with a broad range of human phenotypes

37. Sequence variants with large effects on cardiac electrophysiology and disease

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

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

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

41. Sequence variation at ANAPC1 accounts for 24% of the variability in corneal endothelial cell density

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

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

44. Coding variants in RPL3L and MYZAP increase risk of atrial fibrillation

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

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

47. A rare missense mutation in CHRNA4 associates with smoking behavior and its consequences

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

49. Nonsense mutation in the LGR4 gene is associated with several human diseases and other traits

50. Rate of de novo mutations and the importance of father’s age to disease risk

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