Search

Your search keyword '"Holm, Hilma"' showing total 521 results

Search Constraints

Start Over You searched for: Author "Holm, Hilma" Remove constraint Author: "Holm, Hilma" Publication Year Range Last 10 years Remove constraint Publication Year Range: Last 10 years
521 results on '"Holm, Hilma"'

Search Results

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

2. Homozygosity for a stop-gain variant in CCDC201 causes primary ovarian insufficiency

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

4. 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.

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

33. Loss-of-function variants in ITSN1 confer high risk of Parkinson's disease.

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

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

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

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

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

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

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

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

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

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

44. Variants at the Interleukin 1 Gene Locus and Pericarditis

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

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

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

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

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

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

Catalog

Books, media, physical & digital resources