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49 results on '"Wolen, Aaron R"'

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1. A genome sequencing system for universal newborn screening, diagnosis, and precision medicine for severe genetic diseases

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

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

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

6. Response to Grosse et al.

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

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

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

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

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

17. Replicated umbilical cord blood DNA methylation loci associated with gestational age at birth

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

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

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

21. Genetic influences on schizophrenia and subcortical brain volumes: large-scale proof of concept

22. Replicated Umbilical Cord Blood DNA Methylation Loci Associated with Gestational Age at Birth

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

27. Incorporating Functional Genomic Information to Enhance Polygenic Signal and Identify Variants Involved in Gene-by-Environment Interaction for Young Adult Alcohol Problems

28. Contribution of copy number variants to schizophrenia from a genome-wide study of 41,321 subjects

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

32. Estimation of Genetic Correlation via Linkage Disequilibrium Score Regression and Genomic Restricted Maximum Likelihood

33. Incorporating Functional Genomic Information to Enhance Polygenic Signal and Identify Variants Involved in Gene-by-Environment Interaction for Young Adult Alcohol Problems

34. Contribution of copy number variants to schizophrenia from a genome-wide study of 41,321 subjects

35. No Reliable Association between Runs of Homozygosity and Schizophrenia in a Well-Powered Replication Study

36. Identification of Quantitative Trait Loci and Candidate Genes for an Anxiolytic-like Response to Ethanol in BXD Recombinant Inbred Strains

37. Molecular Genetic Influences on Normative and Problematic Alcohol Use in a Population-Based Sample of College Students

39. Sphingosine‐1‐phosphate phosphatase 2 promotes disruption of mucosal integrity, and contributes to ulcerative colitis in mice and humans

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

43. Modeling Linkage Disequilibrium Increases Accuracy of Polygenic Risk Scores

45. Molecular Genetic Influences on Normative and Problematic Alcohol Use in a Population-Based Sample of College Students.

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

47. Genetic correlation between amyotrophic lateral sclerosis and schizophrenia

48. The allostatic impact of chronic ethanol on gene expression: A genetic analysis of chronic intermittent ethanol treatment in the BXD cohort.

49. Contribution of copy number variants to schizophrenia from a genome-wide study of 41,321 subjects.

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