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1. Genetic regulation of cell type–specific chromatin accessibility shapes brain disease etiology

2. Transcriptomic sex differences in postmortem brain samples from patients with psychiatric disorders

3. Alzheimer's disease transcriptional landscape in ex-vivo human microglia

5. List of contributors

6. Transcriptomic profiling of prefrontal cortex reveals shared mechanisms underlying Alzheimer’s and Parkinson’s Diseases

7. Unraveling the transcriptomic landscape of healthy aging

8. Plasticity of Human Microglia and Brain Perivascular Macrophages in Aging and Alzheimer’s Disease

9. A public resource of single cell transcriptomes and multiscale networks from persons with and without Alzheimer’s disease

10. Multi-omic profiling of the developing human cerebral cortex at the single-cell level

11. Lineage specific 3D genome structure in the adult human brain and neurodevelopmental changes in the chromatin interactome

12. The neuronal chromatin landscape in adult schizophrenia brains is linked to early fetal development

13. The neuronal chromatin landscape in adult schizophrenia brains is linked to early fetal development

14. FUNCTIONAL CHARACTERIZATION OF GENETIC LIABILITY FOR AUTISM SPECTRUM DISORDER

15. Multi-omic atlas of the parahippocampal gyrus in Alzheimer’s disease

16. Genome-wide analysis of a model-derived binge eating disorder phenotype identifies risk loci and implicates iron metabolism

17. The stability of the myelinating oligodendrocyte transcriptome is regulated by the nuclear lamina

18. Depression pathophysiology, risk prediction of recurrence and comorbid psychiatric disorders using genome-wide analyses

19. ZBTB7A regulates MDD-specific chromatin signatures and astrocyte-mediated stress vulnerability in orbitofrontal cortex

20. Efficient differential expression analysis of large-scale single cell transcriptomics data using dreamlet

21. Extending Human Genome-Wide “Omics” Data With Mechanistic Studies in Rodent Models Identifies an Astrocyte-specific Mechanism of Orbitofrontal Cortex Dysfunction in Major Depressive Disorder

22. A study of gene expression in the living human brain

23. Efficient differential expression analysis of large-scale single cell transcriptomics data using dreamlet

24. Genetic regulation of cell-type specific chromatin accessibility shapes the etiology of brain diseases

25. Genome‐wide methylomic regulation of multiscale gene networks in Alzheimer's disease

26. Automatic Detection of Complex Structural Genome Variation Across Human Populations and in Brains of Individuals with Psychiatric Disorders

27. Rescue of deficits by Brwd1 copy number restoration in the Ts65Dn mouse model of Down syndrome

28. Multi-omic profiling of the developing human cerebral cortex at the single cell level

29. The three-dimensional landscape of cortical chromatin accessibility in Alzheimer’s disease

30. Identification of shared and differentiating genetic architecture for autism spectrum disorder, attention-deficit hyperactivity disorder and case subgroups

31. Transcriptome and chromatin accessibility landscapes across 25 distinct human brain regions expand the susceptibility gene set for neuropsychiatric disorders

32. DeepGAMI: Deep biologically guided auxiliary learning for multimodal integration and imputation to improve phenotype prediction

33. Genetics of the human microglia regulome refines Alzheimer’s disease risk loci

34. Impact of schizophrenia GWAS loci converge onto distinct pathways in cortical interneurons vs glutamatergic neurons during development

35. Genome-wide analysis of binge-eating disorder identifies the first three risk loci and implicates iron metabolism

36. Common variants contribute to intrinsic human brain functional networks

38. Sex Differences in the Human Brain Transcriptome of Cases With Schizophrenia

39. From compartments to gene loops: Functions of the 3D genome in the human brain

40. Genetics of the human microglia regulome refines Alzheimer’s disease risk loci

41. From compartments to gene loops: Functions of the 3D genome in the human brain

42. Unbiased identification of novel transcription factors in striatal compartmentation and striosome maturation

45. Author response: Unbiased identification of novel transcription factors in striatal compartmentation and striosome maturation

46. Common genetic variation influencing human white matter microstructure

47. Identification of shared and differentiating genetic risk for autism spectrum disorder, attention deficit hyperactivity disorder and case subgroups

48. Integration of Alzheimer’s disease genetics and myeloid genomics identifies disease risk regulatory elements and genes

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