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

3. Genomics yields biological and phenotypic insights into bipolar disorder

4. Fine-mapping across diverse ancestries drives the discovery of putative causal variants underlying human complex traits and diseases

7. Trans-ancestry genome-wide study of depression identifies 697 associations implicating cell types and pharmacotherapies

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

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

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

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

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

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

23. Pathogenic Mis-splicing of CPEB4 in Schizophrenia

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

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

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

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

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

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

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

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

38. Identifying the Common Genetic Basis of Antidepressant Response

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

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

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

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

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

44. Dissecting the Shared Genetic Architecture of Suicide Attempt, Psychiatric Disorders, and Known Risk Factors

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

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

49. Psychiatric Genomics: An Update and an Agenda

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