81 results on '"O'Donovan, Michael"'
Search Results
2. Mediation and longitudinal analysis to interpret the association between clozapine pharmacokinetics, pharmacogenomics, and absolute neutrophil count
3. Genomic findings in schizophrenia and their implications
4. Schizophrenia risk conferred by rare protein-truncating variants is conserved across diverse human populations
5. Family-based analysis of the contribution of rare and common genetic variants to school performance in schizophrenia
6. Golgi apparatus, endoplasmic reticulum and mitochondrial function implicated in Alzheimer’s disease through polygenic risk and RNA sequencing
7. Age- and sex-specific associations between risk scores for schizophrenia and self-reported health in the general population
8. Multiscale simulations of uni-polar hole transport in (In,Ga)N quantum well systems
9. Exome sequencing in bipolar disorder identifies AKAP11 as a risk gene shared with schizophrenia
10. Rare coding variants in ten genes confer substantial risk for schizophrenia
11. Transcriptional programs regulating neuronal differentiation are disrupted in DLG2 knockout human embryonic stem cells and enriched for schizophrenia and related disorders risk variants
12. Schizophrenia, autism spectrum disorders and developmental disorders share specific disruptive coding mutations
13. HLA-DQB1 6672G>C (rs113332494) is associated with clozapine-induced neutropenia and agranulocytosis in individuals of European ancestry
14. Correction: Investigating rare pathogenic/likely pathogenic exonic variation in bipolar disorder
15. Neurotrophin receptor activation rescues cognitive and synaptic abnormalities caused by hemizygosity of the psychiatric risk gene Cacna1c
16. Investigating rare pathogenic/likely pathogenic exonic variation in bipolar disorder
17. Genetic association of FMRP targets with psychiatric disorders
18. A brief report: de novo copy number variants in children with attention deficit hyperactivity disorder
19. Cis-effects on gene expression in the human prenatal brain associated with genetic risk for neuropsychiatric disorders
20. Using Genetics to Examine a General Liability to Childhood Psychopathology
21. Rare loss-of-function variants in SETD1A are associated with schizophrenia and developmental disorders
22. Correction: The genomic basis of mood instability: identification of 46 loci in 363,705 UK Biobank participants, genetic correlation with psychiatric disorders, and association with gene expression and function
23. The genomic basis of mood instability: identification of 46 loci in 363,705 UK Biobank participants, genetic correlation with psychiatric disorders, and association with gene expression and function
24. Dye-coupling between neonatal spinal motoneurons and interneurons revealed by prolonged back-filling of a ventral root with a low molecular weight tracer in the mouse
25. Dynamic expression of genes associated with schizophrenia and bipolar disorder across development
26. A genome-wide association study in individuals of African ancestry reveals the importance of the Duffy-null genotype in the assessment of clozapine-related neutropenia
27. Genetic liability to schizophrenia is negatively associated with educational attainment in UK Biobank
28. Effects of pathogenic CNVs on physical traits in participants of the UK Biobank
29. Expression quantitative trait loci in the developing human brain and their enrichment in neuropsychiatric disorders
30. Genetics of self-reported risk-taking behaviour, trans-ethnic consistency and relevance to brain gene expression
31. Publisher Correction: Common schizophrenia alleles are enriched in mutation-intolerant genes and in regions under strong background selection
32. Genome-wide analysis of self-reported risk-taking behaviour and cross-disorder genetic correlations in the UK Biobank cohort
33. Pamela Sklar 1959–2017
34. Genome-wide analysis in UK Biobank identifies four loci associated with mood instability and genetic correlation with major depressive disorder, anxiety disorder and schizophrenia
35. Genome-wide association analysis identifies 30 new susceptibility loci for schizophrenia
36. Genetic influences on schizophrenia and subcortical brain volumes: large-scale proof of concept
37. Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls
38. Genome-wide analyses for personality traits identify six genomic loci and show correlations with psychiatric disorders
39. The implications of the shared genetics of psychiatric disorders
40. Gender differences in CNV burden do not confound schizophrenia CNV associations
41. Methylation QTLs in the developing brain and their enrichment in schizophrenia risk loci
42. Schizophrenia
43. Novel genetic advances in schizophrenia: an interview with Michael O’Donovan
44. Adverse effects from antidepressant treatment: randomised controlled trial of 601 depressed individuals
45. De novo mutations in schizophrenia implicate synaptic networks
46. Factor Structure of Autistic Traits in Children with ADHD
47. Erratum: Genome-wide association study identifies variants at CLU and PICALM associated with Alzheimer's disease
48. Mosaic copy number variation in schizophrenia
49. Genetic architectures of psychiatric disorders: the emerging picture and its implications
50. Permutation-based approaches do not adequately allow for linkage disequilibrium in gene-wide multi-locus association analysis
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