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Your search keyword '"Strohmaier J"' showing total 286 results

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286 results on '"Strohmaier J"'

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1. Genome-wide association study of borderline personality disorder reveals genetic overlap with bipolar disorder, major depression and schizophrenia.

4. Response to the letter by Esteves et al.

5. Assessment of Bidirectional Relationships Between Physical Activity and Depression Among Adults A 2-Sample Mendelian Randomization Study

8. Shared genetic risk between eating disorder- and substance-use-related phenotypes: Evidence from genome-wide association studies

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

10. Shared genetic risk between eating disorder- and substance-use-related phenotypes: Evidence from genome-wide association studies

11. Association between genetic variation in a region on chromosome 11 and schizophrenia in large samples from Europe

12. TMEM132D, a new candidate for anxiety phenotypes: evidence from human and mouse studies

13. Polymorphisms in SREBF1 and SREBF2, two antipsychotic-activated transcription factors controlling cellular lipogenesis, are associated with schizophrenia in German and Scandinavian samples

15. Classical Human Leukocyte Antigen Alleles and C4 Haplotypes Are Not Significantly Associated With Depression

16. Genome-wide gene-environment analyses of major depressive disorder and reported lifetime traumatic experiences in UK Biobank

18. Identification of common genetic risk variants for autism spectrum disorder

19. Genome-wide by environment interaction studies of depressive symptoms and psychosocial stress in UK Biobank and Generation Scotland

20. Evidence for increased genetic risk load for major depression in patients assigned to electroconvulsive therapy

21. [Erratum to:] Does Childhood Trauma Moderate Polygenic Risk for Depression? A Meta-analysis of 5765 Subjects From the Psychiatric Genomics Consortium (vol 84, pg 138, 2018)

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

23. Classical Human Leukocyte Antigen Alleles and C4 Haplotypes Are Not Significantly Associated With Depression

24. Investigating polygenic burden in age at disease onset in bipolar disorder: Findings from an international multicentric study

25. Integrated analysis of environmental and genetic influences on cord blood DNA methylation in new-borns

26. Evidence for increased genetic risk load for major depression in patients assigned to electroconvulsive therapy

27. Genome-wide by environment interaction studies of depressive symptoms and psychosocial stress in UK Biobank and Generation Scotland

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

29. Integrated analysis of environmental and genetic influences on cord blood DNA methylation in new-borns

30. Genome-wide association study reveals greater polygenic loading for schizophrenia in cases with a family history of illness

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

33. Analysis of shared heritability in common disorders of the brain

34. The protocadherin 17 gene affects cognition, personality, amygdala structure and function, synapse development and risk of major mood disorders

35. Genome-wide interaction study of a proxy for stress-sensitivity and its prediction of major depressive disorder

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

37. The protocadherin 17 gene affects cognition, personality, amygdala structure and function, synapse development and risk of major mood disorders

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

39. Gene set enrichment analysis and expression pattern exploration implicate an involvement of neurodevelopmental processes in bipolar disorder

40. Exome sequencing of multiply affected bipolar disorder families and follow-up resequencing implicate rare variants in neuronal genes contributing to disease etiology

41. Large family-based exome sequencing study provides new insight into schizophrenia

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

43. Analysis of shared heritability in common disorders of the brain

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

45. Genetic Effects Influencing Risk For Major Depressive Disorder In China And Europe

46. Partitioning heritability of regulatory and cell-type-specific variants across 11 common diseases

47. Genome-wide association study of borderline personality disorder reveals genetic overlap with bipolar disorder, major depression and schizophrenia

48. Identification of shared risk loci and pathways for bipolar disorder and schizophrenia

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

50. Common variants at 2q11.2, 8q21.3, and 11q13.2 are associated with major mood disorders

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