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

5. How Real-World Data Can Facilitate the Development of Precision Medicine Treatment in Psychiatry

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

12. Schizophrenia risk conferred by rare protein-truncating variants is conserved across diverse human populations

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

15. Genome-wide analyses of smoking behaviors in schizophrenia: Findings from the Psychiatric Genomics Consortium

17. Pathogenic Mis-splicing of CPEB4 in Schizophrenia

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

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

22. Comparative genetic architectures of schizophrenia in East Asian and European populations

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

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

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

27. Rare coding variants in ten genes confer substantial risk for schizophrenia

28. GWAS of Suicide Attempt in Psychiatric Disorders and Association With Major Depression Polygenic Risk Scores

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

30. Publisher Correction: Gene expression imputation across multiple brain regions provides insights into schizophrenia risk

31. Population‐based identity‐by‐descent mapping combined with exome sequencing to detect rare risk variants for schizophrenia

32. Gene expression imputation across multiple brain regions provides insights into schizophrenia risk

33. Integrative functional genomic analysis of human brain development and neuropsychiatric risks

35. Identifying the Common Genetic Basis of Antidepressant Response

36. Transcriptome-wide association study of schizophrenia and chromatin activity yields mechanistic disease insights.

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

38. Psychiatric Genomics: An Update and an Agenda

40. Gene prioritization in GWAS loci using multimodal evidence

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

44. Genome-wide association study of more than 40,000 bipolar disorder cases provides new insights into the underlying biology

47. Genome-wide analyses of smoking behaviors in schizophrenia: Findings from the Psychiatric Genomics Consortium

48. Genetic Implication of Prenatal GABAergic and Cholinergic Neuron Development in Susceptibility to Schizophrenia.

49. The Genetics of the Mood Disorder Spectrum: Genome-wide Association Analyses of More Than 185,000 Cases and 439,000 Controls

50. Classical Human Leukocyte Antigen Alleles and C4 Haplotypes Are Not Significantly Associated With Depression

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