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Your search keyword '"Michael, J Owen"' showing total 324 results

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324 results on '"Michael, J Owen"'

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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. Severe psychiatric disorders are associated with increased risk of dementia

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

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

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

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

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

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

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

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

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

17. Identifying the Common Genetic Basis of Antidepressant Response

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

19. Genomic insights into schizophrenia

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

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

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

23. Sleep EEG in young people with 22q11.2 deletion syndrome: A cross-sectional study of slow-waves, spindles and correlations with memory and neurodevelopmental symptoms

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

25. 1q21.1 distal copy number variants are associated with cerebral and cognitive alterations in humans

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

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

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

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

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

31. Psychopathology in adults with copy number variants

32. Brain functional connectivity mirrors genetic pleiotropy in psychiatric conditions

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

35. Association of genetic liability for psychiatric disorders with accelerometer-assessed physical activity in the UK Biobank.

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

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

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

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

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

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

42. Area Deprivation, Urbanicity and Severe Mental Illness – A Population-Based Linkage Study Using Routinely Collected Primary and Secondary Care Data

43. Genetic Overlap Between Alzheimer’s Disease and Bipolar Disorder Implicates the MARK2 and VAC14 Genes

44. Using rare genetic mutations to revisit structural brain asymmetry

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

47. Pathogenic Mis-splicing of CPEB4 in Schizophrenia

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

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

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

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