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1. Genetic Overlap Between Alzheimer’s Disease and Bipolar Disorder Implicates the MARK2 and VAC14 Genes

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

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

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

5. Genome-wide association study identifies new locus associated with OCD

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

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

8. Characterization of Age and Polarity at Onset in Bipolar Disorder

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

10. Distinct gene-set burden patterns underlie common generalized and focal epilepsies

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

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

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

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

15. Genome-wide Burden of Rare Short Deletions is Enriched in Major Depressive Disorder in Four Cohorts

16. Ultra-Rare Genetic Variation in the Epilepsies: A Whole-Exome Sequencing Study of 17,606 Individuals

17. LINE1 insertions as a genomic risk factor for schizophrenia: Preliminary evidence from an affected family

18. Contribution of rare copy number variants to bipolar disorder risk is limited to schizoaffective cases

19. Substance use associated with short sleep duration in patients with schizophrenia or schizoaffective disorder

20. Paternal age effect: Replication in schizophrenia with intriguing dissociation between bipolar with and without psychosis

21. Obsessive-Compulsive Disorder Genetics: Current and Future Directions

22. Transcriptomic Imputation of Bipolar Disorder and Bipolar subtypes reveals 29 novel associated genes

23. Gene expression in patient-derived neural progenitors implicates WNT5A signaling in the etiology of schizophrenia

24. Genome-wide association study identifies 30 Loci Associated with Bipolar Disorder

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

26. 48 GENE EXPRESSION OF PATIENT-DERIVED NEURAL PROGENITOR CELL LINES DEVELOPED FROM OLFACTORY NEUROEPITHELIUM IMPLICATES WNT SIGNALING IN THE ETIOLOGY OF SCHIZOPHRENIA

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

28. F118CONTRIBUTIONS OF COMMON GENETIC VARIANTS TO SCHIZOPHRENIA RISK IN INDIVIDUALS WITH AFRICAN AND LATINO ANCESTRY

29. Association of DNA Methylation Differences With Schizophrenia in an Epigenome-Wide Association Study

30. Epigenetic Alterations in Schizophrenia

31. Genetic Strategies in Psychiatric Disorders

33. Failure to confirm association between RGS4 haplotypes and schizophrenia in Caucasians

34. Alteration of branch site consensus sequence and enhanced pre-mRNA splicing of an NMDAR1 intron not associated with schizophrenia

35. Identification of single nucleotide polymorphisms (SNPs) and other sequence changes and estimation of nucleotide diversity in coding and flanking regions of the NMDAR1 receptor gene in schizophrenic patients

36. Variants in the ?2A AR adrenergic receptor gene in psychiatric patients

37. Scanning of the dopamine D1 and D5 receptor genes by REF in neuropsychiatric patients reveals a novel missense change at a highly conserved amino acid

38. Screening the monoamine oxidase B gene in 100 male patients with schizophrenia: A cluster of polymorphisms in African-Americans but lack of functionally significant sequence changes

39. Transposable elements and psychiatric disorders

40. The genomic psychiatry cohort: Partners in discovery

41. Identification of a missense mutation and several polymorphisms in the proenkephalin A gene of schizophrenic patients

42. Genotype-to-phenotype analysis: Search for clinical characteristics of a missense change in the GABAA-β1 receptor gene

43. Screening the dopamine D1 receptor gene in 131 schizophrenics and eight alcoholics: Identification of polymorphisms but lack of functionally significant sequence changes

44. The D5 dopamine receptor gene in schizophrenia: identification of a nonsense change and multiple missense changes but lack of association with disease

45. Infrastructure for sharing standardized clinical brain scans across hospitals

46. Dopamine D4 receptor variants in unrelated schizophrenic cases and controls

47. Novel association approach for determining the genetic predisposition to schizophrenia: Case-control resource and testing of a candidate gene

50. Histamine N-methyltransferase functional polymorphism: Lack of association with schizophrenia

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