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

2. Irritability in young people with copy number variants associated with neurodevelopmental disorders (ND-CNVs)

3. Linking haploinsufficiency of the autism- and schizophrenia-associated gene Cyfip1 with striatal-limbic-cortical network dysfunction and cognitive inflexibility

4. Using rare genetic mutations to revisit structural brain asymmetry

5. Rare X-linked variants carry predominantly male risk in autism, Tourette syndrome, and ADHD

6. Mediation and longitudinal analysis to interpret the association between clozapine pharmacokinetics, pharmacogenomics, and absolute neutrophil count

7. Chromatin regulators in the TBX1 network confer risk for conotruncal heart defects in 22q11.2DS

8. Author Correction: Using rare genetic mutations to revisit structural brain asymmetry

9. Sleep disturbance as a transdiagnostic marker of psychiatric risk in children with neurodevelopmental risk genetic conditions

10. Neurodevelopmental dimensional assessment of young children at high genomic risk of neuropsychiatric conditions

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

12. The contribution of Neanderthal introgression and natural selection to neurodegenerative diseases

13. Mental health impact of autism on families of children with intellectual and developmental disabilities of genetic origin

14. DRAGON-Data: a platform and protocol for integrating genomic and phenotypic data across large psychiatric cohorts

15. Identifying the Common Genetic Basis of Antidepressant Response

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

17. Genomic insights into schizophrenia

18. Schizophrenia, autism spectrum disorders and developmental disorders share specific disruptive coding mutations

19. Autism: A model of neurodevelopmental diversity informed by genomics

20. Effects of eight neuropsychiatric copy number variants on human brain structure

21. Haploinsufficiency of the schizophrenia and autism risk gene Cyfip1 causes abnormal postnatal hippocampal neurogenesis through microglial and Arp2/3 mediated actin dependent mechanisms

22. 1q21.1 distal copy number variants are associated with cerebral and cognitive alterations in humans

23. The psychiatric phenotypes of 1q21 distal deletion and duplication

24. Translating insights from neuropsychiatric genetics and genomics for precision psychiatry

25. Cyfip1 haploinsufficient rats show white matter changes, myelin thinning, abnormal oligodendrocytes and behavioural inflexibility

26. Using kinematic analyses to explore sensorimotor control impairments in children with 22q11.2 deletion syndrome

27. Effects of pathogenic CNVs on physical traits in participants of the UK Biobank

28. Clozapine Metabolism is Associated With Absolute Neutrophil Count in Individuals With Treatment-Resistant Schizophrenia

29. Impact of schizophrenia genetic liability on the association between schizophrenia and physical illness: data-linkage study

30. Expression quantitative trait loci in the developing human brain and their enrichment in neuropsychiatric disorders

31. Formalising recall by genotype as an efficient approach to detailed phenotyping and causal inference

32. Correction: The psychiatric phenotypes of 1q21 distal deletion and duplication

33. Schizophrenia risk variants modulate white matter volume across the psychosis spectrum: Evidence from two independent cohorts

34. Molecular investigation of TBP allele length

35. Correction: Genetic Evidence Implicates the Immune System and Cholesterol Metabolism in the Aetiology of Alzheimer's Disease.

37. Psychopathology in adults with copy number variants

38. Brain functional connectivity mirrors genetic pleiotropy in psychiatric conditions

41. Neuropsychiatric risk in children with intellectual disability of genetic origin: IMAGINE, a UK national cohort study

42. Schizophrenia Polygenic Risk and Experiences of Childhood Adversity: A Systematic Review and Meta-analysis

43. Using rare genetic mutations to revisit structural brain asymmetry

45. Rare CNVs and phenome-wide profiling highlight brain structural divergence and phenotypical convergence

46. Pathogenic Mis-splicing of CPEB4 in Schizophrenia

47. Exome sequencing in bipolar disorder identifies AKAP11 as a risk gene shared with schizophrenia

48. New insights into the genetic etiology of Alzheimer's disease and related dementias

49. Using induced pluripotent stem cells to investigate human neuronal phenotypes in 1q21.1 deletion and duplication syndrome

50. Genetic Heterogeneity Shapes Brain Connectivity in Psychiatry

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