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

9. The Relationship Between Polygenic Risk Scores and Cognition in Schizophrenia

10. Using brain cell-type-specific protein interactomes to interpret neurodevelopmental genetic signals in schizophrenia

11. Publisher Correction: Common schizophrenia alleles are enriched in mutation-intolerant genes and in regions under strong background selection

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

13. Transcriptional programs regulating neuronal differentiation are disrupted in DLG2 knockout human embryonic stem cells and enriched for schizophrenia and related disorders risk variants

15. Common schizophrenia alleles are enriched in mutation-intolerant genes and in regions under strong background selection

16. Genetic and Phenotypic Features of Schizophrenia in the UK Biobank

18. Assessing the validity of a self-reported clinical diagnosis of schizophrenia

19. Examining treatment response and adverse effects of clozapine

20. HLA-DQB1 6672G>C (rs113332494) is associated with clozapine-induced neutropenia and agranulocytosis in individuals of European ancestry

23. Mediation and Longitudinal Analysis to interpret the association between clozapine pharmacokinetics, pharmacogenomics, and absolute neutrophil count

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

26. Contributors

27. Examining cognition across the bipolar/schizophrenia diagnostic spectrum

29. Genomic Stratification of Clozapine Prescription Patterns Using Schizophrenia Polygenic Scores

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

34. Mapping genomic loci prioritises genes and implicates synaptic biology in schizophrenia

35. Interaction Testing and Polygenic Risk Scoring to Estimate the Association of Common Genetic Variants With Treatment Resistance in Schizophrenia

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

37. Interaction Testing and Polygenic Risk Scoring to Estimate the Association of Common Genetic Variants With Treatment Resistance in Schizophrenia

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

39. De novo mutations identified by exome sequencing implicate rare missense variants in SLC6A1 in schizophrenia

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

42. A Comparison of Ten Polygenic Score Methods for Psychiatric Disorders Applied Across Multiple Cohorts

44. Associations Between Schizophrenia Polygenic Liability, Symptom Dimensions, and Cognitive Ability in Schizophrenia

46. Rare Copy Number Variants Are Associated With Poorer Cognition in Schizophrenia

47. Biological insights from 108 schizophrenia-associated genetic loci

48. CNV analysis in a large schizophrenia sample implicates deletions at 16p12.1 and SLC1A1 and duplications at 1p36.33 and CGNL1

49. Analysis of copy number variations at 15 schizophrenia-associated loci

50. Lack of Support for the Genes by Early Environment Interaction Hypothesis in the Pathogenesis of Schizophrenia

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