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

2. 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.

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

19. Multiomics study of nonalcoholic fatty liver disease

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

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

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

23. Genome-wide association meta-analyses and fine-mapping elucidate pathways influencing albuminuria.

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

25. Genetic architecture of band neutrophil fraction in Iceland

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

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

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

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

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

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

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

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

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

35. PR interval genome-wide association meta-analysis identifies 50 loci associated with atrial and atrioventricular electrical activity

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

37. Obesity variants in the GIPR gene do not associate with risk of fracture or bone mineral density

38. Polygenic risk scores associate with blood pressure traits across the lifespan

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

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

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

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

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

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

46. Predicting the probability of death using proteomics

47. Combining Polygenic and Proteomic Risk Scores With Clinical Risk Factors to Improve Performance for Diagnosing Absence of Coronary Artery Disease in Patients With De Novo Chest Pain

48. Evaluation of Large-Scale Proteomics for Prediction of Cardiovascular Events

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

50. Variants at the Interleukin 1 Gene Locus and Pericarditis

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