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

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

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

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

9. Bipolar multiplex families have an increased burden of common risk variants for psychiatric disorders

10. Bipolar multiplex families have an increased burden of common risk variants for psychiatric disorders

11. Rare copy number variants: a point of rarity in genetic risk for bipolar diosrder and schizophrenia

12. Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls

13. Variation at the DAOA/G30 locus influences susceptibility to major mood episodes but not psychosis in schizophrenia and bipolar disorder

14. Operation of the schizophrenia susceptibility gene, Neuregulin 1, across traditional diagnostic boundaries to increase risk for Bipolar Disorder

16. Identification of a CACNA2D4 deletion in late onset bipolar disorder patients and implications for the involvement of voltage-dependent calcium channels in psychiatric disorders

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

18. Association of Polygenic Liabilities for Major Depression, Bipolar Disorder, and Schizophrenia With Risk for Depression in the Danish Population

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

22. Applying polygenic risk scoring for psychiatric disorders to a large family with bipolar disorder and major depressive disorder

23. Improving genetic prediction by leveraging genetic correlations among human diseases and traits

24. Improving genetic prediction by leveraging genetic correlations among human diseases and traits

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

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

27. Localization of type 1 diabetes susceptibility to the MHC class I genes HLA-B and HLA-A

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

29. Replication of bipolar disorder susceptibility alleles and identification of 2 novel genome-wide significant associations in a new bipolar disorder case-control sample

30. Joint Analysis of Psychiatric Disorders Increases Accuracy of Risk Prediction for Schizophrenia, Bipolar Disorder, and Major Depressive Disorder

34. Variation at the GABAA receptor gene, Rho 1 (GABRR1) associated with susceptibility to bipolar schizoaffective disorder

35. P2RX7: A bipolar and unipolar disorder candidate susceptibility gene?

37. Bipolar disorder and polymorphisms in the dysbindin gene (DTNBP1)

39. Allele-Specific Oligonucleotide PCR.

40. Fluorescent In Situ Hybridization.

41. Genomic organization and chromosomal localization of the humanCUL2 gene and the role of von Hippel-Lindau tumor suppressor-binding protein (CUL2 and VBP1) mutation and loss in renal-cell carcinoma development

42. Genomic organization and chromosomal localization of the human CUL2 gene and the role of von Hippel‐Lindau tumor suppressor‐binding protein (CUL2 and VBP1) mutation and loss in renal‐cell carcinoma development

43. Restriction Fragment-Length Polymorphisms.

44. Identification of a CACNA2D4deletion in late onset bipolar disorder patients and implications for the involvement of voltage‐dependent calcium channels in psychiatric disorders

45. Localization of type 1 diabetes susceptibility to the MHC class I genes HLA-B and HLA-A

46. Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls

47. Association scan of 14,500 nonsynonymous SNPs in four diseases identifies autoimmunity variants

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

49. Collaborative genome-wide association analysis supports a role for ANK3 and CACNA1C in bipolar disorder.

50. Association scan of 14,500 nonsynonymous SNPs in four diseases identifies autoimmunity variants.

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