Search

Your search keyword '"Pietiläinen, Olli"' showing total 568 results

Search Constraints

Start Over You searched for: Author "Pietiläinen, Olli" Remove constraint Author: "Pietiläinen, Olli"
568 results on '"Pietiläinen, Olli"'

Search Results

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

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

7. A novel variant in SMG9 causes intellectual disability, confirming a role for nonsense-mediated decay components in neurocognitive development

8. Mapping genomic loci implicates genes and synaptic biology in schizophrenia

9. The 22q11.2 region regulates presynaptic gene-products linked to schizophrenia

10. Astrocytes regulate neuronal network burst frequency through NMDA receptors in species and donor-specific manner

12. Polygenic burden has broader impact on health, cognition, and socioeconomic outcomes than most rare and high-risk copy number variants

14. Antipsychotic medications and sleep problems in patients with schizophrenia

15. Genomic, molecular, and cellular divergence of the human brain.

16. Rare loss-of-function variants in SETD1A are associated with schizophrenia and developmental disorders

18. Long working hours and change in body weight: analysis of individual-participant data from 19 cohort studies

20. W88. PHENOTYPIC AND GENETIC CHARACTERIZATION OF INDIVIDUALS WITH SCHIZOPHRENIA AND HIGH PSYCHIATRIC HOSPITALIZATION BURDEN

21. Deletion of TOP3β, a component of FMRP-containing mRNPs, contributes to neurodevelopmental disorders

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

24. Robust induction of functional astrocytes using NGN2 expression in human pluripotent stem cells

26. Contribution of rare and common variants to intellectual disability in a sub-isolate of Northern Finland

27. SARS-CoV-2 Infection of Human Neurons Is TMPRSS2 Independent, Requires Endosomal Cell Entry, and Can Be Blocked by Inhibitors of Host Phosphoinositol-5 Kinase

31. Impact of constitutional TET2 haploinsufficiency on molecular and clinical phenotype in humans

32. Astrocytic cell adhesion genes linked to schizophrenia correlate with synaptic programs in neurons

33. Efficient generation of lower induced motor neurons by coupling Ngn2 expression with developmental cues

34. Kartasta tuli uutinen: liikkuvien karttojen nousu datajournalismissa ja verkon uudet karttatoteutukset

37. SARS-CoV-2 infection of human neurons requires endosomal cell entry and can be blocked by inhibitors of host phosphoinositol-5 kinase

38. Robust induction of functional astrocytes using NGN2 expression in human pluripotent stem cells

42. Associations between low parental education, childhood adversities and sickness absence in midlife public sector employees.

43. A polygenic resilience score moderates the genetic risk for schizophrenia

44. Association of alcohol use with years lived without major chronic diseases: A multicohort study from the IPD-Work consortium and UK Biobank

46. Association of alcohol use with years lived without major chronic diseases : A multicohort study from the IPD-Work consortium and UK Biobank

47. Mapping genomic loci implicates genes and synaptic biology in schizophrenia

48. Changes in occupational class differences in leisure‐time physical activity and the contribution of retirement.

49. Life-course socioeconomic circumstances in acute, chronic and disabling pain among young employees: a double suffering.

Catalog

Books, media, physical & digital resources