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1. Whole-exome sequencing in UK Biobank reveals rare genetic architecture for depression.

4. Genome-wide association analyses identify 95 risk loci and provide insights into the neurobiology of post-traumatic stress disorder

5. Collective genomic segments with differential pleiotropic patterns between cognitive dimensions and psychopathology.

6. Rare variant associations with plasma protein levels in the UK Biobank

7. Author Correction: New genetic signals for lung function highlight pathways and chronic obstructive pulmonary disease associations across multiple ancestries

8. Thrombosis risk in single- and double-heterozygous carriers of factor V Leiden and prothrombin G20210A in FinnGen and the UK Biobank

10. A FinnGen pilot clinical recall study for Alzheimer’s disease

13. High-Resolution Genotyping of Formalin-Fixed Tissue Accurately Estimates Polygenic Risk Scores in Human Diseases

14. Brain expression quantitative trait locus and network analyses reveal downstream effects and putative drivers for brain-related diseases

15. Genome-Wide Association Study Identifies 4 Novel Risk Loci for Small Intestinal Neuroendocrine Tumors Including a Missense Mutation in LGR5

16. FinnGen provides genetic insights from a well-phenotyped isolated population

17. Risk of Midlife Stroke After Adverse Pregnancy Outcomes: The FinnGen Study

18. The public health impact of poor sleep on severe COVID-19, influenza and upper respiratory infections

20. TWINGEN: protocol for an observational clinical biobank recall and biomarker cohort study to identify Finnish individuals with high risk of Alzheimer’s disease

21. Adaptive and Innate Immunity Are Key Drivers of Age at Onset of Multiple Sclerosis

22. Systematic single-variant and gene-based association testing of thousands of phenotypes in 394,841 UK Biobank exomes

26. Genome-wide meta-analysis conducted in three large biobanks expands the genetic landscape of lumbar disc herniations.

27. The Parkinson’s disease-associated gene ITPKB protects against α-synuclein aggregation by regulating ER-to-mitochondria calcium release

28. Common and rare variant association analyses in amyotrophic lateral sclerosis identify 15 risk loci with distinct genetic architectures and neuron-specific biology

29. Comprehensive Inherited Risk Estimation for Risk-Based Breast Cancer Screening in Women

30. Identification of plasma proteomic markers underlying polygenic risk of type 2 diabetes and related comorbidities

31. Thrombosis risk in single- and double-heterozygous carriers of factor V Leiden and prothrombin G20210A in FinnGen and the UK Biobank

32. Author Correction: FinnGen provides genetic insights from a well-phenotyped isolated population

33. Plasma proteomic evidence for increased Alzheimer’s disease-related brain pathology after SARS-CoV-2 infection

35. Phenome-wide Mendelian randomization mapping the influence of the plasma proteome on complex diseases

36. Transmembrane Protein 55B Is a Novel Regulator of Cellular Cholesterol Metabolism

37. Genetic determinants of blood gene expression and splicing and their contribution to molecular phenotypes and health outcomes

38. Author Correction: Common and rare variant association analyses in amyotrophic lateral sclerosis identify 15 risk loci with distinct genetic architectures and neuron-specific biology

39. New genetic signals for lung function highlight pathways and chronic obstructive pulmonary disease associations across multiple ancestries

41. The public health impact of poor sleep on severe COVID-19, influenza and upper respiratory infections

42. Genomic atlas of the human plasma proteome

43. Genetic map of regional sulcal morphology in the human brain from UK biobank data

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

45. NTHL1 is a recessive cancer susceptibility gene.

46. A FinnGen pilot clinical recall study for Alzheimer’s disease

47. Genetic associations of protein-coding variants in human disease

48. FinnGen provides genetic insights from a well-phenotyped isolated population

49. Genetic associations of protein-coding variants in human disease

50. Recontacting biobank participants to collect lifestyle, behavioural and cognitive information via online questionnaires: lessons from a pilot study within FinnGen

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