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1. Integrative common and rare variant analyses provide insights into the genetic architecture of liver cirrhosis.

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

3. Understanding the genetic complexity of puberty timing across the allele frequency spectrum

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

5. Publisher Correction: Understanding the genetic complexity of puberty timing across the allele frequency spectrum

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

7. Deciphering the genetics and mechanisms of predisposition to multiple myeloma

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

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

10. 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

11. A population-based survey of FBN1 variants in Iceland reveals underdiagnosis of Marfan syndrome

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

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

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

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

16. PSMD11 loss-of-function variants correlate with a neurobehavioral phenotype, obesity, and increased interferon response

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

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

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

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

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

22. Genome-wide meta-analysis identifies 93 risk loci and enables risk prediction equivalent to monogenic forms of venous thromboembolism

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

24. Multiomics study of nonalcoholic fatty liver disease

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

26. Genetic loci and prioritization of genes for kidney function decline derived from a meta-analysis of 62 longitudinal genome-wide association studies

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

28. Genetic architecture of band neutrophil fraction in Iceland

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

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

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

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

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

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

36. Obesity Variants in the GIPR Gene Are not Associated With Risk of Fracture or Bone Mineral Density.

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

38. Sequence variants in malignant hyperthermia genes in Iceland: classification and actionable findings in a population database

39. Genetic inactivation of ANGPTL4 improves glucose homeostasis and is associated with reduced risk of diabetes

40. Genetic insights into biological mechanisms governing human ovarian ageing

41. Genetic propensities for verbal and spatial ability have opposite effects on body mass index and risk of schizophrenia

43. Genomic analyses identify hundreds of variants associated with age at menarche and support a role for puberty timing in cancer risk.

44. Obesity Variants in the GIPRGene Are not Associated With Risk of Fracture or Bone Mineral Density

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

46. Differences between germline genomes of monozygotic twins

47. A protein-truncating R179X variant in RNF186 confers protection against ulcerative colitis.

48. 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

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

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

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