Search

Your search keyword '"Pato, CN"' showing total 138 results

Search Constraints

Start Over You searched for: Author "Pato, CN" Remove constraint Author: "Pato, CN"
138 results on '"Pato, CN"'

Search Results

1. Evidence for genetic heterogeneity between clinical subtypes of bipolar disorder.

2. GWAS meta-analysis of over 29,000 people with epilepsy identifies 26 risk loci and subtype-specific genetic architecture

3. Interaction Testing and Polygenic Risk Scoring to Estimate the Association of Common Genetic Variants With Treatment Resistance in Schizophrenia

4. GWA study data mining and independent replication identify cardiomyopathy-associated 5 (CMYA5) as a risk gene for schizophrenia

5. Genome-wide association study reveals greater polygenic loading for schizophrenia in cases with a family history of illness

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

7. Partitioning heritability of regulatory and cell-type-specific variants across 11 common diseases

8. Variability in Working Memory Performance Explained by Epistasis vs Polygenic Scores in the ZNF804A Pathway

9. Age at first birth in women is genetically associated with increased risk of schizophrenia

10. Genetic schizophrenia risk variants jointly modulate total brain and white matter volume

11. Biological insights from 108 schizophrenia-associated genetic loci

12. Partitioning the Heritability of Tourette Syndrome and Obsessive Compulsive Disorder Reveals Differences in Genetic Architecture

13. Support for involvement of neuregulin 1 in schizophrenia pathophysiology.

14. Editors' Introduction

15. Psychiatric genome-wide association study analyses implicate neuronal, immune and histone pathways

16. Copy number variation in obsessive-compulsive disorder and tourette syndrome: a cross-disorder study

17. Genetic relationship between five psychiatric disorders estimated from genome-wide SNPs

18. Partitioning the heritability of Tourette syndrome and obsessive compulsive disorder reveals differences in genetic architecture

19. Genomics yields biological and phenotypic insights into bipolar disorder.

20. Identifying genetic differences between bipolar disorder and major depression through multiple genome-wide association analyses.

21. Whole genome sequence-based association analysis of African American individuals with bipolar disorder and schizophrenia.

22. Scaled and efficient derivation of loss-of-function alleles in risk genes for neurodevelopmental and psychiatric disorders in human iPSCs.

23. Phenotype harmonization and analysis for The Populations Underrepresented in Mental illness Association Studies (the PUMAS Project).

24. A blended genome and exome sequencing method captures genetic variation in an unbiased, high-quality, and cost-effective manner.

25. Biological Insights from Schizophrenia-associated Loci in Ancestral Populations.

26. Identifying genetic differences between bipolar disorder and major depression through multiple GWAS.

27. BCFtools/liftover: an accurate and comprehensive tool to convert genetic variants across genome assemblies.

28. Cultured Mesenchymal Cells from Nasal Turbinate as a Cellular Model of the Neurodevelopmental Component of Schizophrenia Etiology.

29. Traumatic events in childhood and adulthood in a diverse-ancestry sample and their role in bipolar disorder.

30. Investigation of convergent and divergent genetic influences underlying schizophrenia and alcohol use disorder.

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

32. Systematic Review and Meta-Analysis on MS-Based Proteomics Applied to Human Peripheral Fluids to Assess Potential Biomarkers of Bipolar Disorder.

33. Systematic Review and Meta-Analysis of Mass Spectrometry Proteomics Applied to Human Peripheral Fluids to Assess Potential Biomarkers of Schizophrenia.

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

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

36. Interaction Testing and Polygenic Risk Scoring to Estimate the Association of Common Genetic Variants With Treatment Resistance in Schizophrenia.

37. What Have We Learned About the Genetics of Obsessive-Compulsive and Related Disorders in Recent Years?

38. Prognostic value of polygenic risk scores for adults with psychosis.

39. The epidemiology of psychiatric disorders in Africa: a scoping review.

40. Genome-Wide Association Studies of Schizophrenia and Bipolar Disorder in a Diverse Cohort of US Veterans.

41. Extensions of Multiple-Group Item Response Theory Alignment: Application to Psychiatric Phenotypes in an International Genomics Consortium.

42. Contributions of common genetic variants to risk of schizophrenia among individuals of African and Latino ancestry.

43. Gene Expression in Patient-Derived Neural Progenitors Implicates WNT5A Signaling in the Etiology of Schizophrenia.

44. Complement genes contribute sex-biased vulnerability in diverse disorders.

45. Ancestry-agnostic estimation of DNA sample contamination from sequence reads.

46. Contribution of Rare Copy Number Variants to Bipolar Disorder Risk Is Limited to Schizoaffective Cases.

47. Interrogating the Genetic Determinants of Tourette's Syndrome and Other Tic Disorders Through Genome-Wide Association Studies.

48. Publisher Correction: Whole genome sequencing in psychiatric disorders: the WGSPD consortium.

49. Genetic validation of bipolar disorder identified by automated phenotyping using electronic health records.

50. Genetic correlation between smoking behaviors and schizophrenia.

Catalog

Books, media, physical & digital resources