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1. Deep learning of left atrial structure and function provides link to atrial fibrillation risk.

2. Genetic drivers and cellular selection of female mosaic X chromosome loss

3. Understanding the genetic complexity of puberty timing across the allele frequency spectrum

4. Polygenic liability for antipsychotic dosage and polypharmacy - a real-world registry and biobank study

5. Evidence for the additivity of rare and common variant burden throughout the spectrum of intellectual disability

6. Publisher Correction: Understanding the genetic complexity of puberty timing across the allele frequency spectrum

9. Complex trait susceptibilities and population diversity in a sample of 4,145 Russians

10. A unified framework for estimating country-specific cumulative incidence for 18 diseases stratified by polygenic risk

12. Multi-omics and pathway analyses of genome-wide associations implicate regulation and immunity in verbal declarative memory performance

13. Distinct and shared genetic architectures of gestational diabetes mellitus and type 2 diabetes

14. Taurine deficiency as a driver of aging.

15. Genome-wide meta-analyses reveal novel loci for verbal short-term memory and learning

16. Integrating transcriptomics, metabolomics, and GWAS helps reveal molecular mechanisms for metabolite levels and disease risk

17. Genetic and functional analysis of Raynaud’s syndrome implicates loci in vasculature and immunity

18. Association of early blood-based biomarkers and six-month functional outcomes in conventional severity categories of traumatic brain injury: capturing the continuous spectrum of injury

19. Depression pathophysiology, risk prediction of recurrence and comorbid psychiatric disorders using genome-wide analyses

20. Rare coding variants in ten genes confer substantial risk for schizophrenia.

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

22. Prioritization of Kidney Cell Types Highlights Myofibroblast Cells in Regulating Human Blood Pressure

23. Antipsychotic medications and sleep problems in patients with schizophrenia

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

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

28. Genome-wide screen of otosclerosis in population biobanks: 27 loci and shared associations with skeletal structure

30. A genome-wide association study of outcome from traumatic brain injury

31. Sex-Dependent Shared and Nonshared Genetic Architecture Across Mood and Psychotic Disorders.

32. Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci

34. Clinical descriptors of disease trajectories in patients with traumatic brain injury in the intensive care unit (CENTER-TBI): a multicentre observational cohort study

35. Mitochondrial genome copy number measured by DNA sequencing in human blood is strongly associated with metabolic traits via cell-type composition differences

36. Identifying nootropic drug targets via large-scale cognitive GWAS and transcriptomics.

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

39. Genetic predictors of lifelong medication-use patterns in cardiometabolic diseases

40. Chromosome Xq23 is associated with lower atherogenic lipid concentrations and favorable cardiometabolic indices.

41. Association of structural variation with cardiometabolic traits in Finns

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

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

44. Genome-wide meta-analysis identifies 127 open-angle glaucoma loci with consistent effect across ancestries.

45. Combined effects of genotype and childhood adversity shape variability of DNA methylation across age.

46. Genome-wide association study identifies 48 common genetic variants associated with handedness

47. Comparative effectiveness of decompressive craniectomy versus craniotomy for traumatic acute subdural hematoma (CENTER-TBI): an observational cohort study

48. Schizophrenia-associated somatic copy-number variants from 12,834 cases reveal recurrent NRXN1 and ABCB11 disruptions

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