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

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

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

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

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

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

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

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

10. Biological insights from 108 schizophrenia-associated genetic loci

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

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

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

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

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

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

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

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

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

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

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

25. Copy number variations in DISC1 and DISC1 - interacting partners in major mental illness

26. Free Recall Episodic Memory Performance Predicts Dementia 10 Years Prior to Clinical Diagnosis : Findings from the Betula Longitudinal Study

27. Loss of Nicastrin from Oligodendrocytes Results in Hypomyelination and Schizophrenia with Compulsive Behavior

28. Higher diurnal salivary cortisol levels are related to smaller prefrontal cortex surface area in elderly men and women

29. Serum metabolomic biomarkers of dementia

30. Biological insights from 108 schizophrenia-associated genetic loci

32. Loss of Nicastrin from Oligodendrocytes Results in Hypomyelination and Schizophrenia with Compulsive Behavior

33. Schizophrenia-Associated MIR204 Regulates Noncoding RNAs and Affects Neurotransmitter and Ion Channel Gene Sets

34. Free Recall Episodic Memory Performance Predicts Dementia Ten Years prior to Clinical Diagnosis : Findings from the Betula Longitudinal Study

35. Free Recall Episodic Memory Performance Predicts Dementia Ten Years prior to Clinical Diagnosis:Findings from the Betula Longitudinal Study

37. Policy Reform in Egypt? : A case study

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

39. Modeling Linkage Disequilibrium Increases Accuracy of Polygenic Risk Scores

41. Copy Number Variations in DISC1 and DISC1-Interacting Partners in Major Mental Illness

42. En litteraturstudie om att leva med diabetes typ 2

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

44. Multiplex amplicon quantification screening the ABCA13 gene for copy number variation in schizophrenia and bipolar disorder

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

46. Rare copy number variants in neuropsychiatric disorders: Specific phenotype or not?

47. Sequencing of DISC1 pathway genes reveals increased burden of rare missense variants in schizophrenia patients from a northern Swedish population.

49. Multiplex amplicon quantification screening the ABCA13 gene for copy number variation in schizophrenia and bipolar disorder

50. Sequencing of DISC1 Pathway Genes Reveals Increased Burden of Rare Missense Variants in Schizophrenia Patients from a Northern Swedish Population

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