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

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

3. Investigating rare pathogenic/likely pathogenic exonic variation in bipolar disorder.

4. Author Correction: Divergent landscapes of A-to-I editing in postmortem and living human brain

5. Divergent landscapes of A-to-I editing in postmortem and living human brain

6. Schizophrenia-associated somatic copy-number variants from 12,834 cases reveal recurrent NRXN1 and ABCB11 disruptions

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

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

9. Analysis of Genetically Regulated Gene Expression Identifies a Prefrontal PTSD Gene, SNRNP35, Specific to Military Cohorts

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

11. Divergent landscapes of A-to-I editing in postmortem and living human brain

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

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

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

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

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

17. Discovery of the first genome-wide significant risk loci for attention deficit/hyperactivity disorder.

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

19. Translating genome-wide association findings into new therapeutics for psychiatry

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

22. Characterization of Single Gene Copy Number Variants in Schizophrenia

23. Analysis of protein-coding genetic variation in 60,706 humans.

24. Nicotine dependence and psychosis in Bipolar disorder and Schizoaffective disorder, Bipolar type.

25. Polygenic overlap between schizophrenia risk and antipsychotic response: a genomic medicine approach

26. Rare loss-of-function variants in SETD1A are associated with schizophrenia and developmental disorders

27. Odorant-Binding Protein

28. The PsychENCODE project

29. Correction: Improved Detection of Common Variants Associated with Schizophrenia and Bipolar Disorder Using Pleiotropy-Informed Conditional False Discovery Rate.

30. Synergistic effects of common schizophrenia risk variants

32. Conserved Higher-Order Chromatin Regulates NMDA Receptor Gene Expression and Cognition

33. Polygenic dissection of diagnosis and clinical dimensions of bipolar disorder and schizophrenia.

34. Schizophrenia-associated somatic copy-number variants from 12,834 cases reveal recurrent NRXN1 and ABCB11 disruptions

35. Improved detection of common variants associated with schizophrenia and bipolar disorder using pleiotropy-informed conditional false discovery rate.

37. Correction: Investigating rare pathogenic/likely pathogenic exonic variation in bipolar disorder

38. Evidence for Genetic Association of RORB with Bipolar Disorder

39. A study of gene expression in the living human brain

40. Practical Guidelines for High-Resolution Epigenomic Profiling of Nucleosomal Histones in Postmortem Human Brain Tissue

42. Cell-specific histone modification maps in the human frontal lobe link schizophrenia risk to the neuronal epigenome

48. A polygenic resilience score moderates the genetic risk for schizophrenia

50. Mutation intolerant genes and targets of FMRP are enriched for nonsynonymous alleles in schizophrenia

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