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1. High incidence and geographic distribution of cleft palate in Finland are associated with the IRF6 gene.

2. Genetic contribution to disease-course severity and progression in the SUPER-Finland study, a cohort of 10,403 individuals with psychotic disorders

3. Proteomic aging clock predicts mortality and risk of common age-related diseases in diverse populations

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

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

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

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

8. Genome-wide meta-analysis of myasthenia gravis uncovers new loci and provides insights into polygenic prediction

9. High incidence and geographic distribution of cleft palate in Finland are associated with the IRF6 gene

10. Genome-wide meta-analysis of myasthenia gravis uncovers new loci and provides insights into polygenic prediction

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

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

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

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

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

19. Genome-wide association study indicates novel associations of annexin A13 to secretory and GAS2L2 with mucous otitis media

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

21. Polygenic risk scores as a marker for epilepsy risk across lifetime and after unspecified seizure events

22. Whole-genome sequencing identifies variants in ANK1, LRRN1, HAS1, and other genes and regulatory regions for stroke in type 1 diabetes

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

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

25. Taurine deficiency as a driver of aging.

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

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

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

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

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

31. Genome-wide association studies highlight novel risk loci for septal defects and left-sided congenital heart defects

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

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

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

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

37. 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

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

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

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

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

44. Genetic causal relationship between immune diseases and migraine: a Mendelian randomization study

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

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

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

48. Use of electronic health record data mining for heart failure subtyping

50. Antipsychotic medications and sleep problems in patients with schizophrenia

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