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72 results on '"Holm, Hilma"'

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

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

3. 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

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

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

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

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

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

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

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

11. Genetic architecture of band neutrophil fraction in Iceland

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

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

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

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

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

17. Predicting the probability of death using proteomics

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

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

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

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

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

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

24. Genome-wide association study identifies six new loci influencing pulse pressure and mean arterial pressure

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

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

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

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

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

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

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

32. Genome-wide associations for benign prostatic hyperplasia reveal a genetic correlation with serum levels of PSA

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

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

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

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

37. Exome-chip meta-analysis identifies novel loci associated with cardiac conduction, including ADAMTS6

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

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

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

41. Genome-wide analysis yields new loci associating with aortic valve stenosis

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

43. Effect of sequence variants on variance in glucose levels predicts type 2 diabetes risk and accounts for heritability

44. Identification of sequence variants influencing immunoglobulin levels

45. Sequence variant at 4q25 near PITX2 associates with appendicitis

46. Diversity in non-repetitive human sequences not found in the reference genome

47. Epigenetic and genetic components of height regulation

48. Variants with large effects on blood lipids and the role of cholesterol and triglycerides in coronary disease

49. Common and rare variants associating with serum levels of creatine kinase and lactate dehydrogenase

50. Genome-wide association study identifies six new loci influencing pulse pressure and mean arterial pressure

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