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

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

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

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

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

6. Predicting the presence of coronary plaques featuring high-risk characteristics using polygenic risk scores and targeted proteomics in patients with suspected coronary artery disease

7. 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

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

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

10. Genome-wide association meta-analysis identifies risk loci for abdominal aortic aneurysm and highlights PCSK9 as a therapeutic target

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

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

13. Genetic insights into resting heart rate and its role in cardiovascular disease

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

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

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

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

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

19. Abstract 18244: A Multi-Ancestry GWAS of Calcific Aortic Stenosis Among 2.7 Million Individuals

20. Abstract 16950: The Genetic Basis of Atrial Fibrillation in a Large-Scale Multi-Ancestry Sample

21. Discovery and systematic characterization of risk variants and genes for coronary artery disease in over a million participants

22. Multiomics study of nonalcoholic fatty liver disease

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

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

25. A multi-layer functional genomic analysis to understand noncoding genetic variation in lipids

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

27. Genetic architecture of band neutrophil fraction in Iceland

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

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

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

31. Implicating genes, pleiotropy, and sexual dimorphism at blood lipid loci through multi-ancestry meta-analysis

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

33. The power of genetic diversity in genome-wide association studies of lipids

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

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

36. Distinction between the effects of parental and fetal genomes on fetal growth

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

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

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

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

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

43. Predicting the probability of death using proteomics

44. Lipoprotein(a) Concentration and Risks of Cardiovascular Disease and Diabetes

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

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

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

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

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

50. Biobank-driven genomic discovery yields new insight into atrial fibrillation biology

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