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121 results on '"Palotie, Aarno"'

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

2. Global Biobank Meta-analysis Initiative: Powering genetic discovery across human disease

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

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

5. Health care utilization and outcomes in older adults after Traumatic Brain Injury: A CENTER-TBI study

6. Measurement invariance of six language versions of the post-traumatic stress disorder checklist for DSM-5 in civilians after traumatic brain injury

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

8. Genome-wide association study of varicose veins identifies a protective missense variant in GJD3 enriched in the Finnish population

9. Supplementary figures for 'Depression pathophysiology, risk prediction of recurrence and comorbid psychiatric disorders using genome-wide analyses'

10. Supplementary figures for 'Pathophysiologic inferences from 243 genetic loci for depression and risk prediction of recurrence and comorbid psychiatric disorders'

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

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

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

14. Reaction Time and Visual Memory in Connection to Hazardous Drinking Polygenic Scores in Schizophrenia, Schizoaffective Disorder and Bipolar Disorder

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

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

17. sj-pdf-7-cep-10.1177_03331024211068065 - Supplemental material for NCOR2 is a novel candidate gene for migraine-epilepsy phenotype

18. sj-pdf-2-cep-10.1177_03331024211068065 - Supplemental material for NCOR2 is a novel candidate gene for migraine-epilepsy phenotype

19. sj-pdf-1-cep-10.1177_03331024211068065 - Supplemental material for NCOR2 is a novel candidate gene for migraine-epilepsy phenotype

20. sj-pdf-3-cep-10.1177_03331024211068065 - Supplemental material for NCOR2 is a novel candidate gene for migraine-epilepsy phenotype

21. sj-pdf-7-cep-10.1177_03331024211068065 - Supplemental material for NCOR2 is a novel candidate gene for migraine-epilepsy phenotype

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

23. Additional file 1 of Whole-exome sequencing identifies novel protein-altering variants associated with serum apolipoprotein and lipid concentrations

24. sj-pdf-5-cep-10.1177_03331024211068065 - Supplemental material for NCOR2 is a novel candidate gene for migraine-epilepsy phenotype

25. sj-pdf-6-cep-10.1177_03331024211068065 - Supplemental material for NCOR2 is a novel candidate gene for migraine-epilepsy phenotype

26. sj-pdf-6-cep-10.1177_03331024211068065 - Supplemental material for NCOR2 is a novel candidate gene for migraine-epilepsy phenotype

27. sj-pdf-3-cep-10.1177_03331024211068065 - Supplemental material for NCOR2 is a novel candidate gene for migraine-epilepsy phenotype

28. sj-pdf-2-cep-10.1177_03331024211068065 - Supplemental material for NCOR2 is a novel candidate gene for migraine-epilepsy phenotype

29. Inframe insertion and splice site variants in MFGE8 associate with protection against coronary atherosclerosis

30. Comprehensive genome-wide association study of different forms of hernia identifies more than 80 associated loci

31. sj-pdf-1-cep-10.1177_03331024211045651 - Supplemental material for Polygenic risk provides biological validity for the ICHD-3 criteria among Finnish migraine families

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

33. Additional file 3 of Mitochondrial genome copy number measured by DNA sequencing in human blood is strongly associated with metabolic traits via cell-type composition differences

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

35. Additional file 1 of Mitochondrial genome copy number measured by DNA sequencing in human blood is strongly associated with metabolic traits via cell-type composition differences

36. Extensions of Multiple-Group Item Response Theory Alignment: Application to Psychiatric Phenotypes in an International Genomics Consortium

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

38. How do 66 European institutional review boards approve one protocol for an international prospective observational study on traumatic brain injury? Experiences from the CENTER-TBI study

39. Supplemental_Material_B_-_Putative_Harmonized_Items_and_Parameters – Supplemental material for Extensions of Multiple-Group Item Response Theory Alignment: Application to Psychiatric Phenotypes in an International Genomics Consortium

40. Supplemental_Material_A_-_WGSPD_Inclusion-Exclusion_Criteria – Supplemental material for Extensions of Multiple-Group Item Response Theory Alignment: Application to Psychiatric Phenotypes in an International Genomics Consortium

41. Additional file 1 of Gene family information facilitates variant interpretation and identification of disease-associated genes in neurodevelopmental disorders

42. Narrow-sense heritability estimation of complex traits using identity-by-descent information

43. Gene discovery and polygenic prediction from a genome-wide association study of educational attainment in 1.1 million individuals

44. Polygenic burden in focal and generalized epilepsies

45. CCR5-del32 is not deleterious in the homozygous state in humans

46. Exome sequencing of Finnish isolates enhances rare-variant association power

47. Identification of common genetic risk variants for autism spectrum disorder

48. Disentangling the genetics of lean mass

49. Hundreds of genes could lie behind a single disease

50. Transancestral GWAS of alcohol dependence reveals common genetic underpinnings with psychiatric disorders

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