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133 results on '"Mühleisen, TW"'

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1. Large-scale gene-centric analysis identifies novel variants for coronary artery disease

2. Genome-wide association identifies nine common variants associated with fasting proinsulin levels and provides new insights into the pathophysiology of type 2 diabetes

3. Large recurrent microdeletions associated with schizophrenia

4. Genome-wide analysis implicates microRNAs and their target genes in the development of bipolar disorder

5. A reappraisal of the association between Dysbindin (DTNBP1) and schizophrenia in a large combined case-control and family-based sample of German ancestry.

6. Psychiatric genome-wide association study analyses implicate neuronal, immune and histone pathways

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

8. Genome-wide meta-analysis identifies 11 new loci for anthropometric traits and provides insights into genetic architecture

9. Genomic analysis of intracranial and subcortical brain volumes yields polygenic scores accounting for variation across ancestries.

10. Associations between antagonistic SNPs for neuropsychiatric disorders and human brain structure.

12. Genetic variants for head size share genes and pathways with cancer.

13. Beyond the Global Brain Differences: Intraindividual Variability Differences in 1q21.1 Distal and 15q11.2 BP1-BP2 Deletion Carriers.

14. Relationships between neurotransmitter receptor densities and expression levels of their corresponding genes in the human hippocampus.

15. Associations of common genetic risk variants of the muscarinic acetylcholine receptor M2 with cardiac autonomic dysfunction in patients with schizophrenia.

16. Analysis of CACNA1C and KCNH2 Risk Variants on Cardiac Autonomic Function in Patients with Schizophrenia.

17. Genetic variants associated with longitudinal changes in brain structure across the lifespan.

18. Effects of copy number variations on brain structure and risk for psychiatric illness: Large-scale studies from the ENIGMA working groups on CNVs.

19. A GWAS top hit for circulating leptin is associated with weight gain but not with leptin protein levels in lithium-augmented patients with major depression.

20. Identification of Phonology-Related Genes and Functional Characterization of Broca's and Wernicke's Regions in Language and Learning Disorders.

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

22. Genetic factors influencing a neurobiological substrate for psychiatric disorders.

23. 1q21.1 distal copy number variants are associated with cerebral and cognitive alterations in humans.

24. A common variation in HCN1 is associated with heart rate variability in schizophrenia.

25. Association of Copy Number Variation of the 15q11.2 BP1-BP2 Region With Cortical and Subcortical Morphology and Cognition.

26. Pathway-Specific Genetic Risk for Alzheimer's Disease Differentiates Regional Patterns of Cortical Atrophy in Older Adults.

27. The genetic architecture of the human cerebral cortex.

28. Dose response of the 16p11.2 distal copy number variant on intracranial volume and basal ganglia.

29. Correction: Dose response of the 16p11.2 distal copy number variant on intracranial volume and basal ganglia.

30. Leptin gene polymorphisms are associated with weight gain during lithium augmentation in patients with major depression.

31. Genetic architecture of subcortical brain structures in 38,851 individuals.

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

33. Combining lifestyle risks to disentangle brain structure and functional connectivity differences in older adults.

34. Effects of BDNF Val 66 Met genotype and schizophrenia familial risk on a neural functional network for cognitive control in humans.

35. Efficient region-based test strategy uncovers genetic risk factors for functional outcome in bipolar disorder.

36. Detecting significant genotype-phenotype association rules in bipolar disorder: market research meets complex genetics.

37. Using coordinate-based meta-analyses to explore structural imaging genetics.

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

39. Integration of transcriptomic and cytoarchitectonic data implicates a role for MAOA and TAC1 in the limbic-cortical network.

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

41. An Expanded Genome-Wide Association Study of Type 2 Diabetes in Europeans.

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

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

44. Novel genetic loci associated with hippocampal volume.

45. Functional neuroimaging effects of recently discovered genetic risk loci for schizophrenia and polygenic risk profile in five RDoC subdomains.

46. Novel genetic loci underlying human intracranial volume identified through genome-wide association.

47. Genome-wide association study of 40,000 individuals identifies two novel loci associated with bipolar disorder.

48. Altered Functional Subnetwork During Emotional Face Processing: A Potential Intermediate Phenotype for Schizophrenia.

49. Impact of a cis-associated gene expression SNP on chromosome 20q11.22 on bipolar disorder susceptibility, hippocampal structure and cognitive performance.

50. A common risk variant in CACNA1C supports a sex-dependent effect on longitudinal functioning and functional recovery from episodes of schizophrenia-spectrum but not bipolar disorder.

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