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1. A multi-ancestry genetic study of pain intensity in 598,339 veterans

2. A large meta-analysis identifies genes associated with anterior uveitis

3. Rare coding variants in CHRNB2 reduce the likelihood of smoking

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

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

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

7. Characterisation of age and polarity at onset in bipolar disorder.

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

9. Identifying nootropic drug targets via large-scale cognitive GWAS and transcriptomics.

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

11. “PMS2CL interference leading to erroneous identification of a pathogenic PMS2 variant in Black Patients”

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

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

14. Impact of schizophrenia GWAS loci converge onto distinct pathways in cortical interneurons vs glutamatergic neurons during development

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

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

17. Genomic Relationships, Novel Loci, and Pleiotropic Mechanisms across Eight Psychiatric Disorders

18. ANGPTL7, a therapeutic target for increased intraocular pressure and glaucoma

19. Population-scale analysis of common and rare genetic variation associated with hearing loss in adults

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

21. Genome-wide analysis provides genetic evidence that ACE2 influences COVID-19 risk and yields risk scores associated with severe disease

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

23. Pleiotropic Meta-Analysis of Cognition, Education, and Schizophrenia Differentiates Roles of Early Neurodevelopmental and Adult Synaptic Pathways.

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

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

26. Genetic analyses of diverse populations improves discovery for complex traits.

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

28. Genome-wide association study identifies 30 loci associated with bipolar disorder

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

30. Distinct genetic liability profiles define clinically relevant patient strata across common diseases.

31. Exome sequencing and analysis of 454,787 UK Biobank participants

32. Genomic Dissection of Bipolar Disorder and Schizophrenia, Including 28 Subphenotypes

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

34. Shared activity patterns arising at genetic susceptibility loci reveal underlying genomic and cellular architecture of human disease.

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

36. Fine-mapping of lipid regions in global populations discovers ethnic-specific signals and refines previously identified lipid loci

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

39. Characterization of Single Gene Copy Number Variants in Schizophrenia

42. New data and an old puzzle: the negative association between schizophrenia and rheumatoid arthritis

43. Synergistic effects of common schizophrenia risk variants

45. Genomic architecture of pharmacological efficacy and adverse events

46. Partitioning Heritability of Regulatory and Cell-Type-Specific Variants across 11 Common Diseases

48. Genetics of rheumatoid arthritis contributes to biology and drug discovery.

49. Whole-Exome Sequencing Identifies Rare and Low-Frequency Coding Variants Associated with LDL Cholesterol

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

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